"Genome-wide era" association studies

A listing of studies identified as genetic association studies with robust p-values since 2007.

Publication Title SNPs
Nat Genet. 2010 Sep 26. [Epub ahead of print] Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. rs2736100 rs10937405 rs4488809
Genes Immun. 2010 Sep 23. [Epub ahead of print] Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. rs429608 rs429608 rs2679798
Nat Genet. 2010 Sep 19. [Epub ahead of print] A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. rs8170 rs2363956 rs2363956 rs2363956
Cytometry B Clin Cytom. 2010;78 Suppl 1:S24-34. Non-CLL-like monoclonal B-cell lymphocytosis in the general population: prevalence and phenotypic/genetic characteristics.
Inflamm Bowel Dis. 2010 May 18. [Epub ahead of print] Genetic predictors of medically refractory ulcerative colitis. rs17207986 rs11554257
Hum Genet. 2010 Sep 14. [Epub ahead of print] Association of common DNA sequence variants at 33 genetic loci with blood lipids in individuals of African ancestry from Jamaica.
Hum Genet. 2010 Sep 14. [Epub ahead of print] The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes.
PLoS Genet. 2010 Sep 9;6(9). pii: e1001094. Longitudinal genome-wide association of cardiovascular disease risk factors in the bogalusa heart study. rs247616 rs445925
roc Natl Acad Sci U S A. 2010 Sep 13. [Epub ahead of print] Shared molecular amino acid signature in the HLA-DR peptide binding pocket predisposes to both autoimmune diabetes and thyroiditis.
Nat Genet. 2010 Sep 12. [Epub ahead of print] A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. rs8027411
Am J Hum Genet. 2010 Sep 10;87(3):430-5. A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study. rs10917469 rs10917469
PLoS Med. 2010 Aug 31;7(8). pii: e1000332. Physical activity attenuates the genetic predisposition to obesity in 20,000 men and women from EPIC-Norfolk prospective population study.
Nat Genet. 2010 Aug 29. [Epub ahead of print] Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. rs1835740 rs1835740 rs1835740 rs1835740
Diabetes. 2010 Aug 26. [Epub ahead of print] HLA Class I and Genetic Susceptibility to Type 1 Diabetes: Results from the Type 1 Diabetes Genetics Consortium.
Rev Esp Cardiol. 2010 Aug;63(8):925-33. Additive effect of multiple genetic variants on the risk of coronary artery disease.
Circulation. 2010 Sep 7;122(10):976-84. Epub 2010 Aug 23. Independent susceptibility markers for atrial fibrillation on chromosome 4q25. rs2200733 rs2200733 rs17570669 rs3853445
Nat Genet. 2010 Sep;42(9):759-63. Epub 2010 Aug 22. Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54.
Nat Genet. 2010 Sep;42(9):764-7. Epub 2010 Aug 22. A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. rs2274223
Genet Test Mol Biomarkers. 2010 Aug;14(4):577-84. Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients.
Am J Nephrol. 2010;32(3):279-86. Epub 2010 Aug 13. Association of four genetic loci with uric acid levels and reduced renal function: the J-SHIPP Suita study. rs11231825 rs1014290 rs2231142
Nat Genet. 2010 Sep;42(9):781-5. Epub 2010 Aug 15. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. rs3129882 rs3129882
Nat Genet. 2010 Sep;42(9):768-71. Epub 2010 Aug 15. A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. rs873549 rs1511412 rs940187 rs8032158
Nat Genet. 2010 Sep;42(9):786-9. Epub 2010 Aug 15. Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy. rs2858884 rs2858884
Gastroenterology. 2010 Aug 11. [Epub ahead of print] Genome-Wide Association Study Identifies Variants Associated With Histologic Features of Nonalcoholic Fatty Liver Disease. rs2645424 rs343062 rs1227756 rs6591182 rs887304 rs2499604 rs6487679 rs1421201 rs2710833
J Infect Dis. 2010 Sep 15;202(6):908-15. Multiple-cohort genetic association study reveals CXCR6 as a new chemokine receptor involved in long-term nonprogression to AIDS. rs2234358
PLoS Genet. 2010 Aug 5;6(8). pii: e1001045. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
PLoS Genet. 2010 Aug 5;6(8). pii: e1001051. The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. rs2736100 rs2736100
Nat Genet. 2010 Sep;42(9):739-41. Epub 2010 Aug 8. Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. rs4331426
Nat Genet. 2010 Sep;42(9):772-6. Epub 2010 Aug 8. Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. rs1065489 rs426736
Nat Genet. 2010 Sep;42(9):777-80. Epub 2010 Aug 8. Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. rs1990760 rs6498142
Nature. 2010 Aug 5;466(7307):707-13. Biological, clinical and population relevance of 95 loci for blood lipids.
Nat Genet. 2010 Sep;42(9):751-4. Epub 2010 Aug 1. Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.
Nat Genet. 2010 Sep;42(9):755-8. Epub 2010 Aug 1. Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers. rs17401966 rs17401966
Hum Mol Genet. 2010 Aug 24. [Epub ahead of print] The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. rs713598 rs10772420
J Invest Dermatol. 2010 Jul 29. [Epub ahead of print] Carriers of Rare Missense Variants in IFIH1 Are Protected from Psoriasis. rs35667974 rs10930046
J Hum Genet. 2010 Jul 22. [Epub ahead of print] Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population: a case-control study.
Hum Mol Genet. 2010 Aug 16. [Epub ahead of print] A genome-wide scan for common alleles affecting risk for autism. rs4141463 rs4141463
Arthritis Rheum. 2010 Jul 26. [Epub ahead of print] Genome-wide association study of cardiac manifestations of neonatal lupus identifies candidate loci at 6p21 and 21q22. rs3099844 rs7775397 rs2857595 rs2230365 rs3128982 rs743446
Int J Colorectal Dis. 2010 Jul 27. [Epub ahead of print] Correlating of GSTM1, GSTT1, and GSTP1 genetic polymorphisms with the risk and expressions in children with isolated Hirschsprung disease.
Nat Genet. 2010 Aug;42(8):684-7. Epub 2010 Jul 25. Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Hepatology. 2010 Sep;52(3):904-12. PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease. rs738409 rs738409
Diabetologia. 2010 Jul 17. [Epub ahead of print] Disease-associated loci are significantly over-represented among genes bound by transcription factor 7-like 2 (TCF7L2) in vivo.
Nat Genet. 2010 Aug;42(8):661-4. Epub 2010 Jul 18. Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. rs10484561 rs7755224 rs735665
Nat Genet. 2010 Aug;42(8):655-7. Epub 2010 Jul 18. Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis.
Hum Mol Genet. 2010 Sep 15;19(18):3672-8. Epub 2010 Jul 16. Genome-wide association of serum bilirubin levels in Korean population. rs11891311 rs2417940 rs11891311 rs2417940 rs11891311 rs4148323 rs4148323 rs2417940 rs2417940 rs17680137 rs2117032
Hum Mol Genet. 2010 Oct 1;19(19):3885-94. Epub 2010 Jul 16. Genome-wide association analysis identifies multiple loci related to resting heart rate.
PLoS Pathog. 2010 Jul 1;6:e1000979. Leprosy and the adaptation of human toll-like receptor 1. rs1071630
Carcinogenesis. 2010 Sep;31(9):1612-9. Epub 2010 Jul 7. Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. rs12701937 rs6038071 rs11014993
Am J Hum Genet. 2010 Jul 9;87(1):6-16. Epub 2010 Jun 17. IRF4 variants have age-specific effects on nevus count and predispose to melanoma. rs12203592 rs12203592 rs12203592 rs872071 rs872071 rs12203592
Nat Genet. 2010 Aug;42(8):707-10. Epub 2010 Jul 4. A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. rs10965235 rs16826658
Am J Hum Genet. 2010 Jul 9;87(1):60-74. Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability. rs2435357
J Am Soc Nephrol. 2010 Jul 29. [Epub ahead of print] HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis.
PLoS One. 2010 Jun 25;5(6):e11296. A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01. rs3135391 rs4959039
PLoS Genet. 2010 Jun 24;6(6):e1001002. Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium. rs4784227 rs4784227 rs4784227
Mol Psychiatry. 2010 Jun 29. [Epub ahead of print] Genome-wide association study of conduct disorder symptomatology.
BMC Cancer. 2010 Jun 18;10:303. Mutations in TGFbeta-RII and BAX mediate tumor progression in the later stages of colorectal cancer with microsatellite instability.
J Bone Miner Res. 2010 Jun 18. [Epub ahead of print] Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone. rs35211496 rs1805034 rs35211496 rs1805034
J Lipid Res. 2010 Sep;51(9):2766-74. Epub 2010 Jun 19. FADS genetic variants and omega-6 polyunsaturated fatty acid metabolism in a homogeneous island population. rs174537 rs174545 rs174546 rs174553 rs174556 rs174561 rs174568 rs99780
J Am Soc Nephrol. 2010 Jul;21(7):1223-32. Epub 2010 Jun 17. Common genetic variants associate with serum phosphorus concentration.
Diabetologia. 2010 Oct;53(10):2163-6. Epub 2010 Jun 17. Combined effects of 17 common genetic variants on type 2 diabetes risk in a Han Chinese population.
Br J Haematol. 2010 Aug;150(4):473-9. Epub 2010 Jun 10. Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk. rs17483466 rs13397985 rs872071 rs735665 rs7176508 rs11083846 rs13397985 rs872071 rs735665 rs7176508 rs11083846
J Natl Cancer Inst. 2010 Jul 7;102(13):959-71. Epub 2010 Jun 14. Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium. rs16969968 rs8034191 rs2736100 rs402710 rs2256543 rs4324798 rs16969968 rs2736100 rs402710 rs2736100 rs402710 rs2736100 rs402710
Gastroenterology. 2010 Jun 12. [Epub ahead of print] Variants in the ITPA Gene Protect Against Ribavirin-Induced Hemolytic Anemia and Decrease the Need for Ribavirin Dose Reduction. rs1127354 rs7270101 rs1127354 rs7270101
Cancer Epidemiol Biomarkers Prev. 2010 Jul;19(7):1855-61. Epub 2010 Jun 8. Risk of genome-wide association study-identified genetic variants for colorectal cancer in a Chinese population. rs6983267 rs4939827 rs10795668 rs3802842 rs961253 rs10795668 rs3802842 rs6983267 rs4939827 rs10795668 rs3802842 rs961253
Circ Cardiovasc Genet. 2010 Aug;3(4):331-9. Epub 2010 Jun 7. Genetic regulation of serum phytosterol levels and risk of coronary artery disease. rs4245791 rs41360247 rs4245791 rs657152 rs4245791 rs657152 rs41360247
Genes Brain Behav. 2010 Jun 7. [Epub ahead of print] A genome-wide association study of bipolar disorder and comorbid migraine. rs9566845 rs9566867 rs9566845 rs9566867 rs9566845
Cold Spring Harb Protoc. 2010 Jun;2010(6):pdb.top81. Meta-analysis of genome-wide association studies.
Breast Cancer Res Treat. 2010 May 28. [Epub ahead of print] Centrosome-related genes, genetic variation, and risk of breast cancer. rs10145182 rs2134808
Int J Cancer. 2010 May 25. [Epub ahead of print] Allergy and glioma risk: Test of association by genotype. rs7216389
Tissue Antigens. 2010 Sep;76(3):208-15. An influence of HLA-A, B, DR, DQ, and MICA on the occurrence of Celiac disease in patients with type 1 diabetes.
Hum Mol Genet. 2010 Aug 1;19(15):3089-101. Epub 2010 May 19. A comprehensive analysis of common IGF1, IGFBP1 and IGFBP3 genetic variation with prospective IGF-I and IGFBP-3 blood levels and prostate cancer risk among Caucasians. rs2854746 rs2854744 rs4764695
J Natl Cancer Inst. 2010 Jul 7;102(13):972-81. Epub 2010 May 18. Genetic and clinical predictors for breast cancer risk assessment and stratification among Chinese women. rs2046210 rs1219648 rs3817198 rs8051542 rs3803662 rs889312 rs10941679 rs13281615
Hum Mol Genet. 2010 Jul 15;19(14):2917-25. Epub 2010 May 11. Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. rs17095355
Nat Genet. 2010 Jun;42(6):508-14. Epub 2010 May 9. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.
Nat Genet. 2010 Jun;42(6):515-9. Epub 2010 May 9. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. rs3093024 rs3093024
Nat Genet. 2010 Jun;42(6):495-7. Epub 2010 May 9. Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. rs9657904
Nat Genet. 2010 Jun;42(6):492-4. Epub 2010 May 9. Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk. rs3731217
Nat Genet. 2010 Jun;42(6):504-7. Epub 2010 May 9. Genome-wide association study identifies five new breast cancer susceptibility loci. rs3757318 rs1562430 rs909116
PLoS Genet. 2010 Apr 29;6(4):e1000928. Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.
Nat Genet. 2010 Jun;42(6):520-4. Epub 2010 May 2. Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. rs484959 rs1561570 rs3018362
Nat Genet. 2010 Jun;42(6):525-9. Epub 2010 May 2. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. rs13041247 rs560426
Mol Vis. 2010 Apr 21;16:705-12. Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. rs1048661 rs3825942 rs41435250 rs13329473 rs3825942 rs1048661 rs1048661 rs3825942 rs3825942
Seizure. 2010 Jun;19(5):303-5. Epub 2010 Apr 28. A patient with DiGeorge syndrome with spina bifida and sacral myelomeningocele, who developed both hypocalcemia-induced seizure and epilepsy.
Diabetes. 2010 Aug;59(8):2068-74. Epub 2010 Apr 27. Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians. rs1801282 rs5219 rs7903146 rs13266634 rs1111875 rs10811661 rs4402960 rs10946398
Proc Natl Acad Sci U S A. 2010 May 18;107(20):9293-8. Epub 2010 Apr 26. Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. rs4387287 rs4452212
Nat Genet. 2010 May;42(5):441-7. Epub 2010 Apr 25. Genome-wide meta-analyses identify multiple loci associated with smoking behavior. rs1051730 rs1329650 rs1028936 rs3733829 rs6265 rs3025343
Nat Genet. 2010 May;42(5):436-40. Epub 2010 Apr 25. Meta-analysis and imputation refines the association of 15q25 with smoking quantity. rs55853698 rs6495308
Nat Genet. 2010 May;42(5):448-53. Epub 2010 Apr 25. Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. rs1051730 rs4105144 rs6474412 rs6474412 rs4105144
Bone. 2010 Jul;47(1):156-63. Epub 2010 Apr 18. Chronic kidney disease bone and mineral disorder (CKD-MBD) in apolipoprotein E-deficient mice with chronic renal failure.
J Biol Chem. 2010 Jun 11;285(24):18496-504. Epub 2010 Apr 16. DNA binding by the ETS protein TEL (ETV6) is regulated by autoinhibition and self-association.
Am J Hum Genet. 2010 May 14;86(5):773-82. Epub 2010 Apr 15. Distinct variants at LIN28B influence growth in height from birth to adulthood. rs7759938 rs314277 rs7759938 rs314277 rs7759938 rs314277 rs7759938
Cancer Res. 2010 Apr 15;70(8):3170-6. Telomere length in prospective and retrospective cancer case-control studies.
Cancer Res. 2010 Apr 15;70(8):3128-35. A second genetic variant on chromosome 15q24-25.1 associates with lung cancer. rs1051730 rs1051730 rs481134 rs1051730 rs481134 rs1051730 rs481134 rs481134
Proc Biol Sci. 2010 Aug 22;277(1693):2531-40. Epub 2010 Apr 14. Inferred relatedness and heritability in malaria parasites.
Int J Obes (Lond). 2010 Apr 13. [Epub ahead of print] Genes and lifestyle factors in obesity: results from 12 462 subjects from MONICA/KORA. rs6548238 rs9935401 rs7498665
Proc Natl Acad Sci U S A. 2010 Apr 20;107(16):7401-6. Epub 2010 Apr 12. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.
Nat Genet. 2010 May;42(5):426-9. Epub 2010 Apr 11. Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. rs2056626
Nat Genet. 2010 May;42(5):376-84. Epub 2010 Apr 11. New loci associated with kidney function and chronic kidney disease.
at Genet. 2010 May;42(5):373-5. Epub 2010 Apr 11. Genetic loci influencing kidney function and chronic kidney disease. rs10206899 rs4805834
Nat Genet. 2010 May;42(5):430-5. Epub 2010 Apr 6. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. rs900400 rs9883204
BMC Med Genet. 2010 Apr 6;11:55. Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data. rs599839 rs4970834 rs4245791
Mol Psychiatry. 2010 Apr 6. [Epub ahead of print] Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. rs1344706 rs1344706 rs1344706
Nat Genet. 2010 May;42(5):420-5. Epub 2010 Apr 4. Genome-wide association study of intracranial aneurysm identifies three new risk loci.
Ophthalmology. 2010 Jul;117(7):1331-8.e5. Epub 2010 Apr 3. Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. rs3213787 rs735860
Hum Hered. 2010;69(4):268-84. Epub 2010 Mar 31. Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.
Med Oncol. 2010 Mar 31. [Epub ahead of print] Mutation of FLT3 gene in acute myeloid leukemia with normal cytogenetics and its association with clinical and immunophenotypic features.
BMC Med Genet. 2010 Mar 30;11:51. Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study. rs3886223
Hum Mol Genet. 2010 Jun 15;19(12):2516-23. Epub 2010 Mar 29. The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. rs965513 rs944289
Nat Genet. 2010 May;42(5):415-9. Epub 2010 Mar 28. A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. rs798766 rs798766 rs798766 rs798766
Epilepsia. 2010 May;51(5):926-30. Epub 2010 Mar 19. Association between HLA-B*1502 and carbamazepine-induced severe cutaneous adverse drug reactions in a Thai population.
Rheumatology (Oxford). 2010 Jul;49(7):1239-44. Epub 2010 Mar 24. Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases. rs763361 rs763361 rs763361 rs763361 rs763361 rs763361
Cancer Epidemiol Biomarkers Prev. 2010 Apr;19(4):1140-3. Epub 2010 Mar 23. A genome-wide association study of prognosis in breast cancer.
Blood. 2010 Jun 3;115(22):4517-23. Epub 2010 Mar 19. The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms.
Am J Hum Genet. 2010 Apr 9;86(4):519-25. Epub 2010 Mar 18. A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. rs314277 rs314277
Genes Immun. 2010 Apr;11(3):232-8. Epub 2010 Mar 18. New genetic associations detected in a host response study to hepatitis B vaccine. rs5000563
Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3509-14. Epub 2010 Mar 17. The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness.
J Clin Endocrinol Metab. 2010 May;95(5):2476-85. Epub 2010 Mar 17. Chemerin, a novel adipokine in the regulation of angiogenesis. rs347344
Hepatology. 2010 Jun;51(6):1904-11. Interferon-lambda genotype and low serum low-density lipoprotein cholesterol levels in patients with chronic hepatitis C infection. rs12979860 rs12979860 rs12979860 rs12979860 rs12979860
Nat Genet. 2010 Apr;42(4):332-7. Epub 2010 Mar 14. Genome-wide association identifies multiple ulcerative colitis susceptibility loci.
Nat Genet. 2010 Apr;42(4):292-4. Epub 2010 Mar 14. Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). rs7809799 rs5771069 rs7809799 rs5771069
Am J Hum Genet. 2010 Apr 9;86(4):592-5. Epub 2010 Mar 11. A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. rs169713
J Bone Miner Res. 2010 Sep;25(9):1980-7. The T-13910C polymorphism in the lactase phlorizin hydrolase gene is associated with differences in serum calcium levels and calcium intake. rs4988235 rs4988235
Science. 2010 Apr 30;328(5978):636-9. Epub 2010 Mar 10. Analysis of genetic inheritance in a family quartet by whole-genome sequencing.
J Clin Endocrinol Metab. 2010 May;95(5):2418-25. Epub 2010 Mar 9. Implication of genetic variants near NEGR1, SEC16B, TMEM18, ETV5/DGKG, GNPDA2, LIN7C/BDNF, MTCH2, BCDIN3D/FAIM2, SH2B1, FTO, MC4R, and KCTD15 with obesity and type 2 diabetes in 7705 Chinese.
BMC Infect Dis. 2010 Mar 7;10:52. Latent tuberculosis among pregnant mothers in a resource poor setting in Northern Tanzania: a cross-sectional study.
J Bone Miner Res. 2010 Aug;25(8):1830-8. Genetic variation in the RANKL/RANK/OPG signaling pathway is associated with bone turnover and bone mineral density in men. rs2073618 rs9594759 rs2073618 rs9594759
Br J Dermatol. 2010 May;162(5):1038-43. Epub 2010 Mar 1. Polymorphisms in human histamine receptor H4 gene are associated with atopic dermatitis.
Hum Mol Genet. 2010 Jun 1;19(11):2303-12. Epub 2010 Feb 26. A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. rs12338076 rs17032362 rs17032362 rs1457595 rs17032362 rs1457595
Respir Res. 2010 Feb 26;11:25. Different HLA-DRB1 allele distributions in distinct clinical subgroups of sarcoidosis patients.
J Interferon Cytokine Res. 2010 May;30(5):291-8. Interleukin 7 receptor alpha chain haplotypes vary in their influence on multiple sclerosis susceptibility and response to interferon Beta.
Diabetes. 2010 May;59(5):1266-75. Epub 2010 Feb 25. Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans.
J Psychiatr Res. 2010 Sep;44(12):748-53. Epub 2010 Feb 24. Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. rs7045881 rs433598 rs10761482
Metabolism. 2010 Oct;59(10):1520-7. Epub 2010 Feb 23. Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypes. rs3213448 rs315952 rs315949 rs1143642
Nat Genet. 2010 Mar;42(3):200-2. Epub 2010 Feb 21. Variants in FAM13A are associated with chronic obstructive pulmonary disease. rs7671167
Nat Genet. 2010 Mar;42(3):240-4. Epub 2010 Feb 21. Common variants in KCNN3 are associated with lone atrial fibrillation. rs13376333 rs13376333
Hum Mol Genet. 2010 May 15;19(10):2079-85. Epub 2010 Feb 18. Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. rs4794822 rs2072910 rs4794822 rs2072910 rs4794822 rs2072910
PLoS Genet. 2010 Feb 12;6(2):e1000842. A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes. rs2268388 rs2268388 rs2268388 rs2268388
Hum Mol Genet. 2010 May 15;19(10):2068-78. Epub 2010 Feb 18. Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk. rs429358 rs2230805 rs3183702 rs3183702
Circ Cardiovasc Genet. 2010 Feb 1;3(1):31-8. Epub 2009 Dec 11. Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples. rs964184 rs964184
Hum Mol Genet. 2010 May 15;19(10):1921-9. Epub 2010 Feb 16. Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK. rs7298565 rs11067231 rs7298565
Am J Hum Genet. 2010 Feb 12;86(2):285-91. Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. rs744166
Twin Res Hum Genet. 2010 Feb;13(1):10-29. A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. rs964170 rs7530302 rs1784300 rs12882384
J Ocul Biol Dis Infor. 2009 Dec 22;2(4):164-175. Genetic analysis of typical wet-type age-related macular degeneration and polypoidal choroidal vasculopathy in Japanese population. rs10490924 rs10490924 rs800292 rs2241394
Nat Genet. 2010 Mar;42(3):234-9. Epub 2010 Feb 14. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. rs1990622 rs1990622
Hum Mol Genet. 2010 May 15;19(10):2050-8. Epub 2010 Feb 13. Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. rs7422339 rs1801133
Arterioscler Thromb Vasc Biol. 2010 Apr;30(4):885-90. Epub 2010 Feb 11. Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. rs2115763 rs2115763 rs1834481 rs7106524 rs2115763 rs1834481
Hum Mol Genet. 2010 May 1;19(9):1856-62. Epub 2010 Feb 10. Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes. rs651007 rs651007
Neurology. 2010 Feb 9;74(6):480-6. Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease. rs7910977 rs7910977
Mol Genet Metab. 2010 May;100(1):77-82. Epub 2010 Jan 15. Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets. rs13266634 rs13266634 rs13266634 rs13266634 rs13266634
Arch Dermatol Res. 2010 Oct;302(8):619-24. Epub 2010 Feb 4. The association of the BLK gene with SLE was replicated in Chinese Han. rs2248932 rs2248932 rs2248932
Nature. 2010 Feb 4;463(7281):671-5. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
Hum Mol Genet. 2010 May 1;19(9):1805-15. Epub 2010 Feb 2. Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15. rs5750250 rs2413396 rs5750248 rs11912763 rs4821480 rs11912763
Arthritis Rheum. 2010 Feb;62(2):323-9. Confirmation of an association between rs6822844 at the Il2-Il21 region and multiple autoimmune diseases: evidence of a general susceptibility locus. rs6822844 rs6822844 rs6822844 rs6822844 rs6822844 rs6822844 rs6822844
Arthritis Rheum. 2010 Feb;62(2):574-9. The association of a nonsynonymous single-nucleotide polymorphism in TNFAIP3 with systemic lupus erythematosus and rheumatoid arthritis in the Japanese population. rs10499194 rs2230926 rs10499194
Arthritis Rheum. 2010 Feb;62(2):499-510. A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22. rs3815148 rs3757713
J Allergy Clin Immunol. 2010 Jan;125(1):170-4.e1-2. Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutations. rs7927894 rs877776 rs7927894 rs877776 rs7927894 rs7927894 rs877776 rs7927894
Am J Clin Nutr. 2010 Mar;91(3):662-71. Epub 2010 Jan 27. Adiposity is inversely related to insulin sensitivity in relatively lean Chinese adolescents: a population-based twin study.
Invest Ophthalmol Vis Sci. 2010 Jun;51(6):3055-60. Epub 2010 Jan 27. Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population.
Hum Mol Genet. 2010 May 1;19(9):1828-39. Epub 2010 Jan 27. Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
Nat Genet. 2010 Mar;42(3):224-8. Epub 2010 Jan 24. A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. rs9543325 rs9564966 rs3790844 rs401681
J Immunol. 2010 Mar 1;184(5):2512-7. Epub 2010 Jan 22. Functionally significant differences in expression of disease-associated IL-7 receptor alpha haplotypes in CD4 T cells and dendritic cells.
Am J Hum Genet. 2010 Feb 12;86(2):229-39. Epub 2010 Jan 21. Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. rs2273061 rs2273061 rs2273061 rs2273061
World J Gastroenterol. 2010 Jan 21;16(3):359-64. NOD2, IL23R and ATG16L1 polymorphisms in Lithuanian patients with inflammatory bowel disease. rs2066844 rs2066845 rs2066847 rs11209026 rs2241880
Nat Genet. 2010 Feb;42(2):142-8. Epub 2010 Jan 17. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. rs10423928 rs2877716 rs17271305 rs1260326 rs7903146
Nat Genet. 2010 Feb;42(2):128-31. Epub 2010 Jan 17. Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. rs2251219
Ann Hum Genet. 2010 Mar;74(2):97-109. Epub 2010 Jan 8. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. rs2736990 rs11012
Nat Genet. 2010 Feb;42(2):132-6. Epub 2010 Jan 10. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk. rs757978 rs2456449 rs7169431 rs305061 rs783540 rs1036935
Nat Genet. 2010 Feb;42(2):123-7. Epub 2010 Jan 10. Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. rs10865331 rs2242944 rs4333130 rs2310173 rs11209026 rs27434
Nat Genet. 2010 Feb;42(2):149-52. Epub 2010 Jan 10. Genetic variation in SCN10A influences cardiac conduction. rs6795970 rs6795970 rs6795970
Nat Genet. 2010 Feb;42(2):153-9. Epub 2010 Jan 10. Genome-wide association study of PR interval.
Carcinogenesis. 2010 May;31(5):834-41. Epub 2010 Jan 8. Individuals susceptible to lung adenocarcinoma defined by combined HLA-DQA1 and TERT genotypes. rs2736100
Gastroenterology. 2010 Apr;138(4):1338-45, 1345.e1-7. Epub 2010 Jan 11. Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. rs8099917 rs8099917
Genes Immun. 2010 Apr;11(3):209-18. Epub 2010 Jan 7. Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes. rs4151659 rs7762619 rs4151659
Am J Hum Genet. 2010 Jan;86(1):88-92. Epub 2009 Dec 31. Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. rs2524054 rs1838149
Blood. 2010 Mar 4;115(9):1765-7. Epub 2009 Dec 30. Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood.
Nat Genet. 2010 Feb;42(2):137-41. Epub 2009 Dec 27. A genome-wide perspective of genetic variation in human metabolism.
Immunogenetics. 2010 Feb;62(2):101-7. Epub 2009 Dec 23. Single-nucleotide polymorphisms in the IL2RA gene are associated with age at diagnosis in late-onset Finnish type 1 diabetes subjects. rs11594656 rs41295061
Circ Cardiovasc Genet. 2009 Dec;2(6):607-13. Epub 2009 Sep 5. Association of AHSG gene polymorphisms with fetuin-A plasma levels and cardiovascular diseases in the EPIC-Potsdam study. rs2248690 rs2070633 rs2070635 rs4917 rs6787344 rs6787344 rs4917 rs4917
Circ Cardiovasc Genet. 2009 Aug;2(4):338-46. Epub 2009 May 28. 9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population. rs2383206 rs1004638 rs10757278
Circ Cardiovasc Genet. 2009 Aug;2(4):329-37. Epub 2009 May 14. Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. rs495366 rs12289128 rs11226373 rs495366
Circ Cardiovasc Genet. 2009 Aug;2(4):322-8. Epub 2009 May 15. A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. rs885389 rs2880058 rs2478333
Circ Cardiovasc Genet. 2009 Apr;2(2):151-8. Epub 2009 Feb 18. COL4A1 is associated with arterial stiffness by genome-wide association scan. rs3742207 rs1495448 rs3742207
Circ Cardiovasc Genet. 2009 Apr;2(2):142-50. Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study. rs1801133 rs6586282 rs7422339 rs4267943 rs11018628 rs1126464
Circ Cardiovasc Genet. 2009 Apr;2(2):134-41. Epub 2009 Feb 12. Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.
Circ Cardiovasc Genet. 2009 Apr;2(2):125-33. Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. rs1800789 rs2522056 rs511154 rs1539019
J Med Virol. 2010 Feb;82(2):282-8. Human bocavirus infection in young children with acute respiratory tract infection in Lanzhou, China.
Nat Genet. 2010 Jan;42(1):24-6. Epub 2009 Dec 20. Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. rs227731 rs7078160
Atherosclerosis. 2010 Feb;208(2):412-20. Epub 2009 Dec 2. Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals.
BMC Proc. 2009 Dec 15;3 Suppl 7:S84. Effects of covariates and interactions on a genome-wide association analysis of rheumatoid arthritis.
BMC Proc. 2009 Dec 15;3 Suppl 7:S51. Transmission-ratio distortion in the Framingham Heart Study. rs1000548
BMC Proc. 2009 Dec 15;3 Suppl 7:S46. Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study.
BMC Proc. 2009 Dec 15;3 Suppl 7:S42. Multivariate association analysis of the components of metabolic syndrome from the Framingham Heart Study.
BMC Proc. 2009 Dec 15;3 Suppl 7:S37. Armitage's trend test for genome-wide association analysis: one-sided or two-sided? rs12380341 rs872863 rs1953126 rs10985073 rs881375 rs3761847 rs10760130 rs2900180
BMC Proc. 2009 Dec 15;3 Suppl 7:S115. A multilevel linear mixed model of the association between candidate genes and weight and body mass index using the Framingham longitudinal family data. rs1121980 rs9939609 rs17782313 rs17700633 rs9939609
BMC Proc. 2009 Dec 15;3 Suppl 7:S114. Growth mixture modelling in families of the Framingham Heart Study. rs1445404
Rheumatol Int. 2009 Dec 13. [Epub ahead of print] A single-nucleotide polymorphism of the TNFSF4 gene is associated with systemic lupus erythematosus in Chinese Han population. rs1234315 rs1234315
Nat Genet. 2010 Jan;42(1):45-52. Epub 2009 Dec 13. Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
Hum Mol Genet. 2010 Mar 1;19(5):953-62. Epub 2009 Dec 9. Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. rs12122721 rs1132200
Eur Respir J. 2010 Jul;36(1):89-95. Epub 2009 Dec 8. Hedgehog-interacting protein is a COPD susceptibility gene: the Rotterdam Study. rs1828591 rs13118928
Hum Mol Genet. 2010 Mar 1;19(5):953-62. Epub 2009 Dec 9. Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. rs12122721 rs1132200
Eur Respir J. 2010 Jul;36(1):89-95. Epub 2009 Dec 8. Hedgehog-interacting protein is a COPD susceptibility gene: the Rotterdam Study. rs1828591 rs13118928
Blood. 2010 Jan 28;115(4):778-82. Epub 2009 Nov 20. Thrombosis in primary myelofibrosis: incidence and risk factors.
J Hum Hypertens. 2010 Jun;24(6):367-72. Epub 2009 Nov 19. Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts. rs17249754 rs1378942 rs12945290 rs17249754 rs995322
Genes Immun. 2009 Dec;10 Suppl 1:S74-84. Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families. rs689 rs689 rs2476601 rs1990760 rs1427676
Eur J Clin Nutr. 2010 Mar;64(3):253-8. Epub 2009 Dec 2. Dairy intake associates with the IGF rs680 polymorphism to height variation in periadolescent children. rs680 rs680 rs680 rs680 rs680 rs680 rs680
Eur Child Adolesc Psychiatry. 2010 Jul;19(7):549-57. Epub 2009 Nov 28. COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10-14.
Nat Genet. 2010 Jan;42(1):21-3. Epub 2009 Nov 29. Variant in PNPLA3 is associated with alcoholic liver disease. rs738409
Gastroenterology. 2010 Mar;138(3):1102-11. Epub 2009 Nov 26. Genome-wide association analysis in primary sclerosing cholangitis. rs3099844 rs2844559 rs9524260 rs12612347 rs3197999
Diabetologia. 2010 Feb;53(2):299-308. Epub 2009 Nov 25. Common variants at the GCK, GCKR, G6PC2-ABCB11 and MTNR1B loci are associated with fasting glucose in two Asian populations. rs1799884 rs780094 rs560887 rs1387153 rs10830963 rs3755157 rs3755157 rs560887
J Mol Evol. 2009 Dec;69(6):579-88. Epub 2009 Nov 24. Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group.
Mol Vis. 2009 Nov 14;15:2349-57. Evaluation of LOXL1 polymorphisms in exfoliation syndrome in a Chinese population. rs1048661 rs3825942 rs2165241 rs3825942 rs2165241 rs1048661 rs1048661 rs2165241 rs1048661 rs3825942 rs1048661 rs2165241 rs1048661 rs1048661 rs2165241
Ann Hum Genet. 2010 Jan;74(1):11-6. Epub 2009 Nov 20. HMGA2 is confirmed to be associated with human adult height. rs1042725 rs1042725 rs7968902 rs7968682 rs1042725 rs1042725
Congenit Heart Dis. 2009 Nov;4(6):459-63. Population-based assessment of familial inheritance and neurologic comorbidities among patients with an isolated atrial septal defect.
Hum Genet. 2009 Nov 19. [Epub ahead of print] A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E. rs2071348 rs9376092 rs766432
Oncogene. 2010 Feb 18;29(7):1041-9. Epub 2009 Nov 16. Genetic variants cis-regulating Xrn2 expression contribute to the risk of spontaneous lung tumor. rs27328255 rs27328255 rs2025811
Nat Genet. 2009 Dec;41(12):1303-7. Epub 2009 Nov 15. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.
Nat Genet. 2009 Dec;41(12):1308-12. Epub 2009 Nov 15. Genome-wide association study reveals genetic risk underlying Parkinson's disease. rs2736990 rs393152 rs823128 rs1491923
Nat Genet. 2009 Dec;41(12):1335-40. Epub 2009 Nov 15. Common variants at five new loci associated with early-onset inflammatory bowel disease. rs8049439 rs2412973 rs1250550 rs4676410 rs10500264
Nat Genet. 2009 Dec;41(12):1325-9. Epub 2009 Nov 15. A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. rs1801274 rs17085007 rs2108225 rs1801274
Nat Genet. 2009 Dec;41(12):1330-4. Epub 2009 Nov 15. Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
Arthritis Res Ther. 2009;11(6):R171. Epub 2009 Nov 13. HLA-E gene polymorphism associates with ankylosing spondylitis in Sardinia. rs1264457 rs1264457
Genes Immun. 2010 Mar;11(2):173-80. Epub 2009 Nov 12. HLA-class I markers and multiple sclerosis susceptibility in the Italian population.
Prostate. 2010 Feb 15;70(3):270-5. Replication of prostate cancer risk loci on 8q24, 11q13, 17q12, 19q33, and Xp11 in African Americans. rs10896449 rs2735839 rs443076 rs5945572
J Clin Oncol. 2009 Dec 10;27(35):5972-8. Epub 2009 Nov 9. Germline genetic variation in an organic anion transporter polypeptide associated with methotrexate pharmacokinetics and clinical effects. rs11045879 rs4149081 rs4149056 rs11045879 rs4149081
Nat Genet. 2009 Dec;41(12):1313-8. Epub 2009 Nov 8. Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. rs11586238 rs1980422 rs548234 rs394581 rs10919563 rs540386 rs12746613
J Clin Endocrinol Metab. 2010 Jan;95(1):100-8. Epub 2009 Nov 6. Increased Prevalance of the -211 T allele of follicle stimulating hormone (FSH) beta subunit promoter polymorphism and lower serum FSH in infertile men. rs10835638 rs10835638 rs10835638 rs10835638
Hum Mol Genet. 2010 Feb 1;19(3):553-62. Epub 2009 Nov 6. A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis. rs1537415 rs1537415 rs1537415 rs1537415
Eur J Hum Genet. 2010 Apr;18(4):502-4. Epub 2009 Nov 4. A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. rs34536443
Blood. 2010 Jan 7;115(1):94-6. Epub 2009 Oct 30. A genome-wide association analysis of serum iron concentrations. rs4820268
Diabetes. 2010 Feb;59(2):539-49. Epub 2009 Oct 29. A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose.
Biol Psychiatry. 2010 Feb 1;67(3):279-82. Epub 2009 Oct 28. Genomewide association study of movement-related adverse antipsychotic effects. rs17022444 rs2126709 rs7669317 rs17022444 rs7669317 rs2126709
Hum Mol Genet. 2010 Jan 15;19(2):387-95. Epub 2009 Oct 27. Replication of the five novel loci for uric acid concentrations and potential mediating mechanisms. rs12129861 rs780094 rs742132 rs17300741 rs742132
Nat Genet. 2009 Nov;41(11):1223-7. Epub 2009 Oct 25. Microduplications of 16p11.2 are associated with schizophrenia.
PLoS Genet. 2009 Oct;5(10):e1000696. Epub 2009 Oct 23. High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. rs3117103 rs362521 rs8283 rs7769979 rs10947345 rs3828903
Obesity (Silver Spring). 2010 Apr;18(4):803-8. Epub 2009 Oct 22. Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. rs12517906
Nat Genet. 2009 Nov;41(11):1228-33. Epub 2009 Oct 18. A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.
Nat Genet. 2009 Nov;41(11):1234-7. Epub 2009 Oct 18. Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus.
J Hum Genet. 2009 Dec;54(12):749-52. Epub 2009 Oct 16. Evaluation of genetic loci influencing adult height in the Japanese population.
Arch Ophthalmol. 2009 Oct;127(10):1368-72. Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population.
Am J Clin Nutr. 2010 Jan;91(1):184-90. Epub 2009 Oct 7. Cumulative effects and predictive value of common obesity-susceptibility variants identified by genome-wide association studies. rs1121980 rs7132908 rs17782313
Acta Neurol Scand. 2010 Feb;121(2):114-9. Epub 2009 Oct 5. Endothelial nitric oxide synthase Glu298Asp, 4b/a, and -786T>C gene polymorphisms and the risk of ischemic stroke.
Circ Cardiovasc Genet. 2008 Oct;1(1):21-30. Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication.
Nat Genet. 2009 Nov;41(11):1199-206. Epub 2009 Oct 4. Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
Int J Epidemiol. 2010 Apr;39(2):563-77. Epub 2009 Sep 23. Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals. rs16969968
Mol Biol Rep. 2010 Jan;37(1):389-94. A single-nucleotide polymorphism of the TNFAIP3 gene is associated with systemic lupus erythematosus in Chinese Han population. rs2230926 rs2230926 rs2230926 rs2230926
Nat Genet. 2009 Oct;41(10):1055-7. Epub 2009 Sep 20. Identification of a new prostate cancer susceptibility locus on chromosome 8q24. rs620861
Nat Genet. 2009 Oct;41(10):1116-21. Epub 2009 Sep 20. Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.
Nat Genet. 2009 Oct;41(10):1058-60. Epub 2009 Sep 20. Multiple loci on 8q24 associated with prostate cancer susceptibility. rs1006908 rs620861
J Intern Med. 2010 Mar;267(3):287-94. Epub 2009 Jun 11. Circulating high molecular weight adiponectin isoform is heritable and shares a common genetic background with insulin resistance in nondiabetic White Caucasians from Italy: evidence from a family-based study. rs17300539 rs1501299 rs677395 rs17300539 rs1501299 rs6773957 rs17300539 rs1501299 rs1501299
Mol Vis. 2009 Sep 4;15:1774-80. Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia. rs11823728 rs544978 rs2186410 rs542269
Nat Genet. 2009 Oct;41(10):1100-4. Epub 2009 Sep 13. IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. rs8099917
Hum Mol Genet. 2009 Dec 1;18(23):4677-87. Epub 2009 Sep 10. Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway. rs602662 rs492602 rs601338 rs1801133
Diabetes. 2009 Dec;58(12):2946-53. Epub 2009 Sep 9. Additive effects of genetic variation in GCK and G6PC2 on insulin secretion and fasting glucose. rs1799884 rs560887 rs1799884 rs560887 rs1799884 rs560887
Nat Genet. 2009 Oct;41(10):1094-9. Epub 2009 Sep 6. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. rs11136000 rs6656401
Nat Genet. 2009 Oct;41(10):1088-93. Epub 2009 Sep 6. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. rs2075650 rs11136000 rs3851179 rs11136000 rs3851179
Nat Genet. 2009 Oct;41(10):1110-5. Epub 2009 Sep 6. Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. rs2943641 rs2943641
Am J Hum Genet. 2009 Sep;85(3):377-93. Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. rs12936231
Hum Mol Genet. 2009 Dec 1;18(23):4662-8. Epub 2009 Sep 3. Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs. rs1569019 rs1976930 rs1569019
J Natl Cancer Inst. 2009 Oct 7;101(19):1330-6. Epub 2009 Sep 2. Replication of prostate cancer risk loci in a Japanese case-control association study. rs6983561 rs4430796
Arthritis Rheum. 2009 Sep;60(9):2577-84. TRAF1 polymorphisms associated with rheumatoid arthritis susceptibility in Asians and in Caucasians. rs7021206 rs6457617 rs7021206 rs3761847 rs3761847 rs7021206 rs3761847 rs7021206 rs3761847 rs7021206 rs1953126 rs2900180 rs7021206 rs3761847
J Hum Genet. 2009 Nov;54(11):642-6. Epub 2009 Aug 28. Validation of eight genetic risk factors in East Asian populations replicated the association of BRAP with coronary artery disease. rs11066001
Hum Genet. 2009 Aug 26. [Epub ahead of print] Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population. rs2200733 rs2200733 rs2200733 rs2200733 rs2200733 rs2200733 rs2200733
Cancer Res. 2009 Sep 1;69(17):6848-56. Epub 2009 Aug 25. The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. rs16969968 rs578776 rs16969968 rs16969968
Gastroenterology. 2009 Nov;137(5):1768-75. Epub 2009 Aug 19. Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. rs1229984 rs671 rs671 rs1229984
Hum Mol Genet. 2009 Nov 1;18(21):4204-12. Epub 2009 Aug 18. Investigating the genetic association between ERAP1 and ankylosing spondylitis. rs30187 rs27044 rs27434
Nat Genet. 2009 Sep;41(9):1006-10. Epub 2009 Aug 16. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. rs4132601 rs7089424 rs2239633
Nat Genet. 2009 Sep;41(9):1001-5. Epub 2009 Aug 16. Germline genomic variants associated with childhood acute lymphoblastic leukemia. rs10821936 rs10994982 rs10821936 rs10994982
Nature. 2009 Sep 17;461(7262):399-401. Epub 2009 Aug 16. Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.
J Cancer Res Clin Oncol. 2010 Feb;136(2):249-59. Epub 2009 Aug 12. Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers.
Am J Hum Genet. 2009 Aug;85(2):194-203. Epub 2009 Aug 6. Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. rs2517713 rs2975042 rs29232 rs3129055 rs9258122 rs29232
Br J Dermatol. 2009 Dec;161(6):1387-90. Epub 2009 Aug 7. FLG mutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema.
Atherosclerosis. 2010 Jan;208(1):183-9. Epub 2009 Jul 8. Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. rs599839 rs599839 rs599839 rs599839 rs599839
J Pediatr. 2009 Dec;155(6):909-13. Epub 2009 Aug 4. A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24. rs987525
Genome Res. 2009 Nov;19(11):1942-52. Epub 2009 Aug 4. Population genomics in a disease targeted primary cell model. rs3744270
Cancer Res. 2009 Aug 15;69(16):6633-41. Epub 2009 Aug 4. Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. rs12914385 rs4975616 rs3117582 rs8034191 rs4975616 rs3117582 rs748404 rs1926203
Diabetes. 2009 Nov;58(11):2703-8. Epub 2009 Aug 3. Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians. rs2166706 rs1387153 rs10830963 rs2166706 rs2166706 rs1260326 rs560887
Nat Genet. 2009 Sep;41(9):991-5. Epub 2009 Aug 2. Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. rs2294008 rs2294008 rs2294008 rs2294008
Nat Genet. 2009 Sep;41(9):996-1000. Epub 2009 Aug 2. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. rs3814113
Nat Genet. 2009 Sep;41(9):986-90. Epub 2009 Aug 2. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. rs505922
J Anim Sci. 2009 Nov;87(11):3470-6. Epub 2009 Jul 31. The effects of single and epistatic quantitative trait loci for fatty acid composition in a Meishan x Duroc crossbred population.
Hum Mol Genet. 2009 Nov 1;18(21):4219-25. Epub 2009 Jul 31. Replication of celiac disease UK genome-wide association study results in a US population.
Hum Mol Genet. 2009 Nov 1;18(21):4195-203. Epub 2009 Jul 31. Common and different genetic background for rheumatoid arthritis and coeliac disease.
Forensic Sci Int Genet. 2009 Sep;3(4):e127-8. Epub 2008 Dec 19. The Karimojong from Uganda: genetic characterization using an X-STR decaplex system.
Cancer Res. 2009 Aug 1;69(15):6290-8. Epub 2009 Jul 21. Identification of Las2, a major modifier gene affecting the Pas1 mouse lung tumor susceptibility locus. rs30245983 rs13459098
Nat Genet. 2009 Aug;41(8):873-5. Epub 2009 Jul 20. Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. rs6457327
Clin Rheumatol. 2009 Oct;28(10):1187-91. Epub 2009 Jul 17. Evidence of association of vitamin D receptor Apa I gene polymorphism with bone mineral density in postmenopausal women with osteoporosis.
JAMA. 2009 Jul 15;302(3):276-89. Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas.
Nat Genet. 2009 Aug;41(8):879-81. Epub 2009 Jul 13. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. rs2106261
Nat Genet. 2009 Aug;41(8):876-8. Epub 2009 Jul 13. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. rs7193343
Cancer Prev Res (Phila). 2009 Jul;2(7):617-24. Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants.
Arch Gen Psychiatry. 2009 Jul;66(7):773-84. Genome-wide association study of alcohol dependence. rs7590720 rs1344694
Nat Genet. 2009 Aug;41(8):899-904. Epub 2009 Jul 5. Genome-wide association study identifies five susceptibility loci for glioma. rs2736100 rs4295627 rs4977756 rs6010620 rs498872
Nat Genet. 2009 Aug;41(8):905-8. Epub 2009 Jul 5. Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. rs1412829 rs6010620
Nat Genet. 2009 Aug;41(8):915-9. Epub 2009 Jul 5. Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. rs4636294 rs2284063 rs10757257 rs132985
Nat Genet. 2009 Aug;41(8):920-5. Epub 2009 Jul 5. Genome-wide association study identifies three loci associated with melanoma risk. rs258322 rs1393350 rs7023329
Nat Genet. 2009 Aug;41(8):909-14. Epub 2009 Jul 5. New common variants affecting susceptibility to basal cell carcinoma. rs11170164 rs2151280 rs157935 rs157935 rs401681
Hum Mol Genet. 2009 Oct 1;18(19):3758-68. Epub 2009 Jul 4. A genome-wide association study of acenocoumarol maintenance dosage. rs10871454 rs4086116 rs2108622
Brain. 2009 Aug;132(Pt 8):2005-25. Epub 2009 Jul 3. The monogenic primary dystonias.
Nature. 2009 Aug 6;460(7256):753-7. Epub 2009 Jul 1. Common variants on chromosome 6p22.1 are associated with schizophrenia.
Hum Mol Genet. 2009 Sep 15;18(18):3516-24. Epub 2009 Jul 1. A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. rs6717918 rs6718438 rs6717918 rs10472828
Int J Cancer. 2009 Oct 1;125(7):1622-5. The CDH1-160C>A polymorphism is a risk factor for colorectal cancer. rs16260 rs16260
JAMA. 2009 Jul 1;302(1):37-48. Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. rs6700896 rs4537545 rs7553007 rs1183910 rs4420638 rs7553007 rs6700896 rs4537545 rs4420638
J Natl Cancer Inst. 2009 Jul 15;101(14):1012-8. Epub 2009 Jun 30. Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. rs13387042 rs13387042 rs13387042 rs13387042 rs13387042
Nat Genet. 2009 Aug;41(8):926-30. Epub 2009 Jun 28. Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. rs219780 rs219780
J Med Genet. 2010 Feb;47(2):116-9. Epub 2009 Jun 18. A common variant in the adiponutrin gene influences liver enzyme values. rs738409
Genes Immun. 2009 Sep;10(6):559-65. Epub 2009 Jun 18. Sex-specific effect of IL9 polymorphisms on lung function and polysensitization. rs2069885 rs2069882
Diabetologia. 2009 Sep;52(9):1866-70. Epub 2009 Jun 17. Combined effects of single-nucleotide polymorphisms in GCK, GCKR, G6PC2 and MTNR1B on fasting plasma glucose and type 2 diabetes risk.
Nat Genet. 2009 Jul;41(7):824-8. Epub 2009 Jun 14. Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. rs703842 rs10876994 rs12368653 rs6074022 rs1569723
Nat Genet. 2009 Jul;41(7):776-82. Epub 2009 Jun 14. Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. rs1800693 rs4149584
Neurology. 2009 Jun 9;72(23):1984-8. Risk alleles for multiple sclerosis in multiplex families.
Cancer Epidemiol Biomarkers Prev. 2009 Jun;18(6):1815-20. Two independent prostate cancer risk-associated Loci at 11q13. rs10896449 rs12418451 rs10896449 rs12418451
J Hum Genet. 2009 Jul;54(7):433-5. Epub 2009 Jun 5. The E23K variation in the KCNJ11 gene is associated with type 2 diabetes in Chinese and East Asian population. rs1799854
Tissue Antigens. 2009 Jun;73(6):569-74. HLA-B is the best candidate of susceptibility genes in HLA for Japanese ulcerative colitis.
Genes Immun. 2009 Jun;10(4):356-64. Association of ATG16L1 and IRGM genes polymorphisms with inflammatory bowel disease: a meta-analysis approach. rs2241880 rs13361189 rs4958847 rs2241880 rs13361189 rs4958847 rs13361189 rs4958847 rs13361189 rs4958847 rs2241880 rs13361189 rs4958847
Cancer Res. 2009 Jun 15;69(12):5065-72. Epub 2009 Jun 2. Genetic variants on chromosome 15q25 associated with lung cancer risk in Chinese populations. rs2036534 rs667282 rs12910984 rs6495309 rs6495309
Nat Genet. 2009 Jul;41(7):816-9. Epub 2009 May 31. HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. rs2395029 rs10937275
Nat Genet. 2009 Jul;41(7):811-5. Epub 2009 May 31. Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. rs3782179 rs4474514 rs4324715 rs6897876
J Hum Genet. 2009 Jul;54(7):392-7. Epub 2009 May 29. A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. rs2212020 rs189897
Ann Neurol. 2009 May;65(5):610-4. SNCA variants are associated with increased risk for multiple system atrophy.
Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9362-7. Epub 2009 May 27. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
Ann Hum Genet. 2009 May;73(Pt 3):379-81. CALHM1 polymorphism is not associated with late-onset Alzheimer disease. rs2986017
J Med Genet. 2009 Aug;46(8):553-4. Epub 2009 May 21. Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies. rs17574546 rs7171171
Prostate. 2009 Sep 1;69(12):1281-91. Genetic and plasma variation of insulin-like growth factor binding proteins in relation to prostate cancer incidence and survival. rs2854744
Proc Natl Acad Sci U S A. 2009 Jun 2;106(22):9004-9. Epub 2009 May 18. Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. rs1541160 rs1541160 rs522444 rs1541160 rs522444
Nat Genet. 2009 Jun;41(6):729-33. Epub 2009 May 17. Genetic variation in LIN28B is associated with the timing of puberty. rs314276
Nat Genet. 2009 Jun;41(6):724-8. Epub 2009 May 17. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.
Nat Genet. 2009 Jun;41(6):648-50. Epub 2009 May 17. Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. rs7759938
Nat Genet. 2009 Jun;41(6):645-7. Epub 2009 May 17. Loci at chromosomes 13, 19 and 20 influence age at natural menopause. rs1172822 rs236114 rs7333181
Ann Rheum Dis. 2010 May;69(5):813-6. Epub 2009 May 11. Association of CD40 with rheumatoid arthritis confirmed in a large UK case-control study. rs4810485 rs2812378 rs42041 rs6682654 rs42041 rs6682654
Nat Genet. 2009 Jun;41(6):666-76. Epub 2009 May 10. Genome-wide association study identifies eight loci associated with blood pressure.
Nat Genet. 2009 Jun;41(6):712-7. Epub 2009 May 10. Multiple loci associated with indices of renal function and chronic kidney disease.
Nat Genet. 2009 Jun;41(6):703-7. Epub 2009 May 10. Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.
PLoS Genet. 2009 May;5(5):e1000472. Epub 2009 May 8. Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genes.
Clin Appl Thromb Hemost. 2010 Apr;16(2):184-8. Epub 2009 May 5. Plasminogen activator inhibitor-1 (PAI-1) gene 4G/5G promoter polymorphism is seen in higher frequency in the Indian patients with deep vein thrombosis.
Hum Mol Genet. 2009 Jul 15;18(14):2711-8. Epub 2009 May 6. Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
J Clin Oncol. 2009 Jun 1;27(16):2660-7. Epub 2009 May 4. Genome-wide analysis of survival in early-stage non-small-cell lung cancer.
Hum Mol Genet. 2009 Jul 15;18(14):2700-10. Epub 2009 May 4. Genome-wide association meta-analysis for total serum bilirubin levels. rs4149056
J Neurol. 2009 Mar;256(3):483-7. Epub 2009 Mar 24. The leucine rich repeat kinase 2 (LRRK2) G2019S substitution mutation. Association with Parkinson disease, malignant melanoma and prevalence in ethnic groups in Israel.
Nature. 2009 May 28;459(7246):528-33. Epub 2009 Apr 28. Common genetic variants on 5p14.1 associate with autism spectrum disorders. rs4307059
Diabetes. 2009 Jul;58(7):1690-9. Epub 2009 Apr 28. Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.
Ann Rheum Dis. 2010 Mar;69(3):561-6. Epub 2009 Apr 27. Susceptibility variants for rheumatoid arthritis in the TRAF1-C5 and 6q23 loci: a meta-analysis. rs3761847 rs2900180 rs10499194 rs6920220 rs6920220 rs10499194 rs3761847 rs6920220 rs6920220 rs6920220
Neurology. 2009 Apr 28;72(17):1495-503. Neuropathologic intermediate phenotypes enhance association to Alzheimer susceptibility alleles.
Nat Genet. 2009 May;41(5):527-34. Epub 2009 Apr 26. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. rs12731740 rs12110693 rs17249754 rs2074356 rs7776725 rs1721400
Heart Rhythm. 2009 May;6(5):634-41. Epub 2009 Feb 15. Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. rs7638909
Genes Immun. 2009 Jul;10(5):539-45. Epub 2009 Apr 23. Admixture in Hispanic Americans: its impact on ITGAM association and implications for admixture mapping in SLE.
Genes Immun. 2009 Jul;10(5):470-7. Epub 2009 Apr 23. Meta-analysis and imputation identifies a 109 kb risk haplotype spanning TNFAIP3 associated with lupus nephritis and hematologic manifestations. rs5029939 rs5029939 rs5029939
Proc Natl Acad Sci U S A. 2009 May 12;106(19):7933-8. Epub 2009 Apr 21. Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility. rs10993994 rs10993994 rs10993994 rs10993994 rs10993994 rs10993994 rs10993994
Pharmacogenomics. 2009 Apr;10(4):549-63. Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.
Diabetes. 2009 Jul;58(7):1710-4. Epub 2009 Apr 14. Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy.
Clin Lung Cancer. 2009 Mar;10(2):118-23. DNA repair gene polymorphisms predict favorable clinical outcome in advanced non-small-cell lung cancer.
Genes Immun. 2009 Jul;10(5):414-20. Epub 2009 Apr 9. Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese. rs3733197 rs17266594 rs844648 rs2205960 rs4522865 rs3733197 rs17266594 rs2205960 rs844648
Nat Genet. 2009 May;41(5):596-601. Epub 2009 Apr 6. A common variant on chromosome 11q13 is associated with atopic dermatitis. rs7927894 rs7927894
Nat Genet. 2009 May;41(5):591-5. Epub 2009 Apr 6. A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.
PLoS One. 2009;4(4):e5003. Epub 2009 Apr 4. Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion. rs765250 rs765250
J Hum Genet. 2009 May;54(5):289-97. Epub 2009 Apr 3. Association of LOXL1 gene with Finnish exfoliation syndrome patients. rs1048661 rs3825942 rs2165241 rs1048661 rs3825942 rs2165241
J Clin Endocrinol Metab. 2009 Jun;94(6):2123-7. Epub 2009 Mar 31. High-sensitivity C-reactive protein levels and type 2 diabetes in urban North Indians.
Hum Mol Genet. 2009 Jun 15;18(12):2305-16. Epub 2009 Mar 31. Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. rs6046
Arthritis Rheum. 2009 Apr;60(4):1085-95. High-density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups.
Arthritis Rheum. 2009 Apr;60(4):1076-84. Variants within MECP2, a key transcription regulator, are associated with increased susceptibility to lupus and differential gene expression in patients with systemic lupus erythematosus.
Nat Genet. 2009 May;41(5):579-84. Epub 2009 Mar 29. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). rs11249433 rs999737
Nat Genet. 2009 May;41(5):585-90. Epub 2009 Mar 29. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. rs4973768 rs6504950
Proc Natl Acad Sci U S A. 2009 Apr 14;106(15):6256-61. Epub 2009 Mar 27. Identification of IRAK1 as a risk gene with critical role in the pathogenesis of systemic lupus erythematosus.
Brain Dev. 2010 Mar;32(3):171-9. Epub 2009 Mar 27. Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.
Diabetes. 2009 Jun;58(6):1450-6. Epub 2009 Mar 26. G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans. rs10830963 rs10830963 rs10830963 rs10830963
Diabetologia. 2009 Jul;52(7):1322-5. Epub 2009 Mar 24. Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population. rs2074196 rs2237892 rs2237895 rs2237897 rs2237892 rs2237897 rs2237895
Carcinogenesis. 2009 Jun;30(6):968-76. Epub 2009 Mar 23. Aromatic DNA adducts and polymorphisms in metabolic genes in healthy adults: findings from the EPIC-Spain cohort.
Nat Genet. 2009 Apr;41(4):407-14. Epub 2009 Mar 22. Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nat Genet. 2009 Apr;41(4):399-406. Epub 2009 Mar 22. Common variants at ten loci influence QT interval duration in the QTGEN Study.
Hum Mol Genet. 2009 Jun 15;18(12):2288-96. Epub 2009 Mar 20. Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. rs11646213 rs11646213
Am J Hum Genet. 2009 Apr;84(4):477-82. Epub 2009 Mar 19. Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. rs4654748 rs602662
PLoS Genet. 2009 Mar;5(3):e1000433. Epub 2009 Mar 20. A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. rs2108622
PLoS Genet. 2009 Mar;5(3):e1000424. Epub 2009 Mar 20. An African ancestry-specific allele of CTLA4 confers protection against rheumatoid arthritis in African Americans. rs231778 rs3087243 rs231775 rs231778
PLoS Genet. 2009 Mar;5(3):e1000421. Epub 2009 Mar 20. A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. rs8034191 rs1051730 rs8034191
Obesity (Silver Spring). 2009 Aug;17(8):1549-53. Epub 2009 Mar 19. A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity. rs10487818 rs10487818
Curr Opin Lipidol. 2009 Apr;20(2):92-7. Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment.
Nat Genet. 2009 Apr;41(4):473-7. Epub 2009 Mar 8. Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. rs987525
Science. 2009 Apr 17;324(5925):387-9. Epub 2009 Mar 5. Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes.
Croat Med J. 2009 Feb;50(1):23-33. Genome-wide association study of biochemical traits in Korcula Island, Croatia. rs4767631 rs10444502 rs10444502 rs2839619
Am J Hum Genet. 2009 Mar;84(3):388-98. Epub 2009 Feb 26. Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups.
J Hum Genet. 2009 Apr;54(4):236-41. Epub 2009 Feb 27. Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association.
Genes Chromosomes Cancer. 2009 Jun;48(6):468-79. Genomic instability in giant cell tumor of bone. A study of 52 cases using DNA ploidy, relocalization FISH, and array-CGH analysis.
Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5264-9. Epub 2009 Feb 23. The role of the CD58 locus in multiple sclerosis. rs2300747 rs2300747
Am J Hum Genet. 2009 Mar;84(3):328-38. Epub 2009 Feb 19. A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
Eur J Clin Pharmacol. 2009 May;65(5):533-40. Epub 2009 Feb 20. TPMT but not ITPA gene polymorphism influences the risk of azathioprine intolerance in renal transplant recipients.
Genes Immun. 2009 Apr;10(3):219-26. Epub 2009 Feb 19. Population differences in SLE susceptibility genes: STAT4 and BLK, but not PXK, are associated with systemic lupus erythematosus in Hong Kong Chinese. rs7574865 rs13277113 rs7574865 rs7601754 rs7574865 rs6445975
Nat Genet. 2009 Mar;41(3):324-8. Epub 2009 Feb 15. Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. rs2046210
Nat Genet. 2009 Mar;41(3):348-53. Epub 2009 Feb 15. Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure. rs5068 rs198358 rs632793 rs5068 rs198358 rs632793 rs5068 rs198358
Pharmacogenomics. 2009 Feb;10(2):171-9. Genome-wide association study of acute post-surgical pain in humans. rs2562456 rs17122021 rs6693882
Gut. 2009 Jun;58(6):799-804. Epub 2009 Feb 6. Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis. rs13151961 rs13119723 rs6840978 rs6822844
Nat Genet. 2009 Apr;41(4):460-4. Epub 2009 Feb 6. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. rs965513 rs944289
Nat Genet. 2009 Mar;41(3):280-2. Epub 2009 Feb 8. New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Nat Genet. 2009 Mar;41(3):342-7. Epub 2009 Feb 8. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. rs1420101 rs12619285 rs4857855 rs4143832 rs3184504
Nat Genet. 2009 Mar;41(3):329-33. Epub 2009 Feb 8. SNPs in BRAP associated with risk of myocardial infarction in Asian populations.
Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2694-9. Epub 2009 Feb 5. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. rs16879552 rs7835688 rs2435357 rs7835688
Rheumatology (Oxford). 2009 Apr;48(4):386-9. Epub 2009 Feb 2. Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case-control study and meta-analysis of published series. rs11209032 rs11209032 rs11209026 rs11209026 rs11465804
Mol Psychiatry. 2009 Jul;14(7):668-80. Epub 2009 Feb 3. Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15. rs4956302 rs17354547 rs1402812 rs4956396 rs17354547 rs17354547 rs1402812 rs4956396 rs17354547
Clin Cancer Res. 2009 Feb 1;15(3):1105-11. Genetic variants and family history predict prostate cancer similar to prostate-specific antigen.
Am J Hum Genet. 2009 Feb;84(2):123-33. Epub 2009 Jan 29. Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study. rs6564851 rs12272004
Nat Genet. 2009 Mar;41(3):277-9. Epub 2009 Feb 1. Variant in the sequence of the LINGO1 gene confers risk of essential tremor.
Hum Mol Genet. 2009 Apr 15;18(8):1510-7. Epub 2009 Jan 30. Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.
PLoS One. 2009;4(1):e4333. Epub 2009 Jan 30. Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population. rs16847548 rs16856785 rs16847548 rs16856785 rs16847548
Nat Genet. 2009 Feb;41(2):205-10. Epub 2009 Jan 25. Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. rs1265181 rs3213094 rs4085613
Nat Genet. 2009 Feb;41(2):199-204. Epub 2009 Jan 25. Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.
Nat Genet. 2008 Sep;40(9):1103-6. Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis. rs2789679 rs7091565 rs1049550 rs1953600 rs2573346 rs2784773 rs1049550
Nat Genet. 2008 Sep;40(9):1059-61. Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. rs5029939
Arterioscler Thromb Vasc Biol. 2009 May;29(5):774-80. Epub 2009 Jan 22. Large scale association analysis of novel genetic loci for coronary artery disease. rs1333049 rs599839 rs3008621 rs501120 rs6922269 rs2943634
Hum Genomics. 2009 Jan;3(2):128-42. Whole-genome approach implicates CD44 in cellular resistance to carboplatin.
BMC Med Genet. 2009 Jan 22;10:6. An open access database of genome-wide association results.
Neoplasma. 2009;56(1):48-55. Clonal analysis of gastric carcinoma and precancerous lesions and its relation to Ki-67 protein expression.
Nat Genet. 2009 Feb;41(2):221-7. Epub 2009 Jan 18. Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. rs401681 rs401681 rs401681 rs2736098 rs2736098 rs401681
Nat Genet. 2009 Feb;41(2):157-9. Epub 2009 Jan 18. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.
PLoS Genet. 2009 Jan;5(1):e1000338. Epub 2009 Jan 16. Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study. rs174537 rs174537 rs953413 rs174537
Eur Heart J. 2009 Apr;30(7):813-9. Epub 2009 Jan 13. Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. rs2200733 rs10033464 rs2200733 rs10033464 rs2200733 rs10033464
Nat Genet. 2009 Feb;41(2):192-8. Epub 2009 Jan 11. Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. rs5984894 rs5984894
PLoS Genet. 2009 Jan;5(1):e1000319. Epub 2009 Jan 9. A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. rs17531088 rs7199343
Lung. 2009 Mar-Apr;187(2):110-5. Epub 2009 Jan 7. Association between p53 codon 72 genetic polymorphism and tobacco use and lung cancer risk.
Hum Mol Genet. 2009 Mar 15;18(6):1171-80. Epub 2009 Jan 6. Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE). rs1143679 rs1143679 rs1143679 rs1143679 rs1143679 rs1143679
J Lipid Res. 2009 May;50(5):798-806. Epub 2009 Jan 5. Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.
Nat Genet. 2009 Feb;41(2):216-20. Epub 2009 Jan 4. Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. rs6426833 rs1558744 rs2395185 rs11209026 rs10889677
Prostate. 2009 Mar 1;69(4):419-27. Association of reported prostate cancer risk alleles with PSA levels among men without a diagnosis of prostate cancer.
J Clin Endocrinol Metab. 2009 Mar;94(3):1033-41. Epub 2008 Dec 30. Genetic variations in sex steroid-related genes as predictors of serum estrogen levels in men. rs2470152 rs2470152 rs2470152
Nat Genet. 2009 Jan;41(1):71-6. Epub 2008 Dec 21. Common variants in the NLRP3 region contribute to Crohn's disease susceptibility. rs10733113
PLoS Genet. 2008 Dec;4(12):e1000312. Epub 2008 Dec 19. Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study. rs730497 rs13266634 rs1402837 rs7072268
Genes Immun. 2009 Jan;10(1):68-76. Epub 2008 Dec 18. Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjögren's syndrome. rs10488631 rs7582694
Am J Hum Genet. 2009 Jan;84(1):60-5. Epub 2008 Dec 11. Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. rs1830084 rs3811647 rs1830084 rs1799852 rs2280673 rs3811647 rs1799852 rs2280673
Lancet Neurol. 2009 Jan;8(1):57-66. Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
Nat Genet. 2009 Jan;41(1):25-34. Epub 2008 Dec 14. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
Gastroenterology. 2009 Feb;136(2):523-9.e3. Epub 2008 Oct 25. Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. rs11205387
Mol Psychiatry. 2009 Apr;14(4):359-75. Epub 2008 Dec 9. Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. rs2715148 rs2522833 rs2522833
Mol Psychiatry. 2009 Mar;14(3):252-60. Epub 2008 Dec 9. Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.
Cancer Genet Cytogenet. 2009 Jan 1;188(1):26-31. Association of DNA repair gene XRCC1 and lung cancer susceptibility among nonsmoking Chinese women.
Nat Genet. 2009 Jan;41(1):47-55. Epub 2008 Dec 7. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Nat Genet. 2009 Jan;41(1):89-94. Epub 2008 Dec 7. A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. rs1387153 rs1387153
Nat Genet. 2009 Jan;41(1):77-81. Epub 2008 Dec 7. Variants in MTNR1B influence fasting glucose levels. rs10830963 rs560887 rs4607517
Diabetes. 2009 Feb;58(2):505-10. Epub 2008 Dec 3. Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. rs8050136 rs7901695
Ann Rheum Dis. 2009 Dec;68(12):1916-20. Epub 2008 Dec 3. Association of the DVWA and GDF5 polymorphisms with osteoarthritis in UK populations. rs11718863 rs7639618 rs143383 rs143383 rs7639618
PLoS One. 2008;3(12):e3833. Epub 2008 Dec 2. Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration.
Hum Mutat. 2009 Feb;30(2):E320-9. Genomic deletions of OFD1 account for 23% of oral-facial-digital type 1 syndrome after negative DNA sequencing.
J Intern Med. 2009 Apr;265(4):448-58. Epub 2009 Oct 25. Common candidate gene variants are associated with QT interval duration in the general population. rs3807375 rs2880058
Nat Genet. 2008 Dec;40(12):1426-35. Epub 2008 Nov 16. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. rs4444235 rs9929218 rs10411210 rs961253
Diabetologia. 2009 Feb;52(2):253-61. Epub 2008 Nov 11. Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population. rs7756992 rs7754840 rs564398 rs1333040 rs10757278 rs10811661 rs8050136 rs1111875 rs5015480 rs7923837 rs4402960 rs13266634 rs7903146 rs12255372 rs5215 rs5219 rs3856806 rs1801282 rs7756992 rs7754840 rs10811661 rs1111875 rs5015480 rs7923837 rs4402960 rs13266634 rs7903146 rs7756992 rs7754840 rs10811661 rs1111875 rs5015480 rs7923837
Nat Genet. 2008 Dec;40(12):1402-3. Epub 2008 Nov 9. Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. rs10492972
Hum Mol Genet. 2009 Feb 1;18(3):580-93. Epub 2008 Nov 7. Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. rs1229984 rs1229984 rs1229984 rs1042026 rs1693482 rs1230165 rs3762894
Hum Mol Genet. 2009 Feb 1;18(3):472-81. Epub 2008 Nov 7. Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.
Ann Neurol. 2008 Oct;64(4):402-9. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. rs2200733 rs10033464 rs2200733 rs2200733 rs2200733 rs10033464 rs2200733 rs10033464 rs2200733 rs2200733 rs10033464
J Hum Genet. 2008;53(11-12):991-8. Epub 2008 Nov 11. Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population. rs13266634 rs1111875 rs10811661 rs4402960 rs8050136 rs734312 rs7754840 rs2237892 rs7754840 rs1111875 rs10811661 rs2237892
Genes Immun. 2009 Jan;10(1):11-4. Epub 2008 Nov 6. The expanding genetic overlap between multiple sclerosis and type I diabetes. rs12708716 rs763361
Inflamm Bowel Dis. 2009 Apr;15(4):501-7. Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children. rs2241880 rs10065172 rs2241880 rs2241880 rs10065172
Nat Genet. 2008 Dec;40(12):1399-401. Epub 2008 Nov 2. Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.
Nat Genet. 2008 Dec;40(12):1407-9. Epub 2008 Nov 2. Common 5p15.33 and 6p21.33 variants influence lung cancer risk. rs8042374 rs3117582 rs401681
Am J Hum Genet. 2008 Nov;83(5):623-32. Epub 2008 Oct 30. Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. rs4420638 rs11159647
Genes Immun. 2009 Jan;10(1):5-10. Epub 2008 Oct 30. CD226 Gly307Ser association with multiple autoimmune diseases. rs763361 rs763361
Mol Vis. 2008;14:1898-905. Epub 2008 Oct 27. LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract. rs1048661 rs3825942 rs2165241 rs1048661 rs3825942 rs2165241 rs1048661 rs3825942 rs1048661 rs2165241
Hum Mol Genet. 2009 Jan 15;18(2):358-65. Epub 2008 Oct 16. IFIH1 polymorphisms are significantly associated with type 1 diabetes and IFIH1 gene expression in peripheral blood mononuclear cells. rs2929366 rs9127 rs1445898 rs2302188 rs1990760
Am Heart J. 2008 Oct;156(4):752-8. Epub 2008 Aug 15. Angiotensin-converting enzyme 2 A1075G polymorphism is associated with survival in an acute coronary syndromes cohort.
Nat Genet. 2008 Nov;40(11):1279-81. Epub 2008 Oct 12. Susceptibility variants for male-pattern baldness on chromosome 20p11. rs2180439
Nat Genet. 2008 Nov;40(11):1313-8. Epub 2008 Oct 12. Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. rs7538876 rs801114
Nat Genet. 2008 Nov;40(11):1282-4. Epub 2008 Oct 12. Male-pattern baldness susceptibility locus at 20p11. rs1160312
PLoS Genet. 2008 Aug;4(8):e1000166. Epub 2008 Aug 22. Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. rs2251746 rs2427837
Diabetes. 2009 Jan;58(1):290-5. Epub 2008 Oct 7. Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. rs9976767 rs3757247
Nat Genet. 2008 Nov;40(11):1319-23. Epub 2008 Oct 5. Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility. rs3024505 rs3024505
J Med Genet. 2008 Oct;45(10):654-6. A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. rs2736100
Lancet. 2008 Dec 6;372(9654):1953-61. Epub 2008 Oct 1. Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. rs16890979 rs2231142 rs1165205 rs16890979 rs2231142 rs1165205 rs2231142
Gut. 2009 Mar;58(3):388-95. Epub 2008 Sep 29. Molecular prediction of disease risk and severity in a large Dutch Crohn's disease cohort.
Nat Genet. 2008 Dec;40(12):1461-5. Epub 2008 Sep 25. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. rs738409 rs738409 rs6006460
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Artif Intell Med. 2009 Jun;46(2):131-8. Epub 2008 Sep 19. Association of genetic profiles to Crohn's disease by linear combinations of single nucleotide polymorphisms. rs124869
Eur J Haematol. 2009 Jan;82(1):54-60. Epub 2008 Sep 17. Aberrant increase in the immature platelet fraction in patients with myelodysplastic syndrome: a marker of karyotypic abnormalities associated with poor prognosis.
Nat Genet. 2008 Oct;40(10):1224-9. Epub 2008 Sep 14. Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population. rs3766379 rs6682654 rs3766379 rs6682654
Nat Genet. 2008 Oct;40(10):1175-84. Epub 2008 Sep 14. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
Nat Genet. 2008 Nov;40(11):1307-12. Epub 2008 Sep 14. Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. rs9642880 rs9642880 rs9642880 rs710521
Nat Genet. 2008 Oct;40(10):1216-23. Epub 2008 Sep 14. Common variants at CD40 and other loci confer risk of rheumatoid arthritis. rs4810485 rs2812378 rs3890745 rs42041 rs4750316 rs1678542
Exp Gerontol. 2008 Dec;43(12):1102-7. Epub 2008 Aug 26. Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease.
Nat Genet. 2008 Oct;40(10):1160-2. Epub 2008 Sep 7. Common variants of FUT2 are associated with plasma vitamin B12 levels. rs492602 rs492602
Diabetes. 2008 Dec;57(12):3353-9. Epub 2008 Sep 5. Common variants in the adiponectin gene (ADIPOQ) associated with plasma adiponectin levels, type 2 diabetes, and diabetes-related quantitative traits: the Framingham Offspring Study. rs17300539 rs822387 rs6773957 rs17366743
Prostate. 2008 Dec 1;68(16):1790-7. Association of HPC2/ELAC2 and RNASEL non-synonymous variants with prostate cancer risk in African American familial and sporadic cases.
Arthritis Rheum. 2008 Sep;58(9):2874-81. Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. rs10489070 rs16890979 rs10489070
Nat Genet. 2008 Oct;40(10):1153-5. Epub 2008 Aug 31. Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12. rs4430796 rs11649743
Nat Genet. 2008 Oct;40(10):1204-10. Epub 2008 Aug 31. A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. rs17483466 rs13397985 rs872071 rs735665 rs7176508 rs11083846
Hum Mol Genet. 2008 Dec 1;17(23):3720-7. Epub 2008 Aug 27. Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. rs3802842 rs3802842 rs3802842
Eur J Neurol. 2008 Oct;15(10):1140-2. Epub 2008 Aug 20. Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation.
Nat Genet. 2008 Sep;40(9):1092-7. Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. rs2237892 rs2237892
Nat Genet. 2008 Sep;40(9):1098-102. SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. rs2283228 rs2237895 rs2237897 rs2237895 rs2237897 rs2237895 rs2237897
Nat Genet. 2008 Sep;40(9):1056-8. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. rs10994336 rs1006737
Cancer Epidemiol Biomarkers Prev. 2008 Aug;17(8):2052-61. Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium. rs2660753
Hum Genet. 2008 Sep;124(2):179-85. Epub 2008 Aug 13. A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia.
Nat Genet. 2008 Aug 10. [Epub ahead of print] Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis. rs2789679 rs7091565 rs1049550 rs1953600 rs2573346 rs2784773 rs1049550
Carcinogenesis. 2008 Oct;29(10):1973-8. Epub 2008 Aug 5. Genetic variants in RUNX3 and risk of bladder cancer: a haplotype-based analysis. rs760805 rs760805 rs760805 rs11249206 rs11249206 rs1395621 rs760805 rs2236852
Diabetes. 2008 Nov;57(11):3112-21. Epub 2008 Aug 4. Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations. rs780094 rs780094 rs1260326 rs780094
Nat Genet. 2008 Sep;40(9):1053-5. Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Nat Genet. 2008 Aug;40(8):946-8. Epub 2008 Jul 27. PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. rs4626664 rs1975197
Genes Immun. 2008 Oct;9(7):624-30. Epub 2008 Jul 24. Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians. rs6498169 rs2104286 rs6604026 rs12044852 rs6897932
Diabetes. 2008 Oct;57(10):2858-61. Epub 2008 Jul 22. A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3. rs876498
Tissue Antigens. 2008 Oct;72(4):401-3. Epub 2008 Jul 17. A Taqman assay for high-throughput genotyping of the multiple sclerosis-associated HLA-DRB1*1501 allele. rs3135388
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Diabetes. 2008 Oct;57(10):2834-42. Epub 2008 Jul 15. Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population. rs9465871 rs10811661 rs4402960 rs13266634
Nat Genet. 2008 Aug;40(8):994-8. Epub 2008 Jul 11. Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis. rs11718863 rs7639618
Mol Immunol. 2008 Aug;45(14):3827-31. Epub 2008 Jul 7. High-producing MBL2 genotypes increase the risk of acute and chronic carditis in patients with history of rheumatic fever.
Ann Rheum Dis. 2008 Nov;67(11):1578-80. Epub 2008 Jul 1. The TRAF1/C5 region is a risk factor for polyarthritis in juvenile idiopathic arthritis. rs10818488
Arthritis Rheum. 2008 Jul;58(7):2183-8. The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis.
Arthritis Rheum. 2008 Jul;58(7):1940-6. Association of STAT4 with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in the Japanese population. rs7574865
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Blood. 2009 Jan 22;113(4):784-92. Epub 2008 Jun 23. The largest prospective warfarin-treated cohort supports genetic forecasting.
Hum Genet. 2008 Aug;124(1):89-94. Epub 2008 Jun 22. Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease. rs1805874
Diabetes. 2008 Aug;57(8):2253-7. Epub 2008 Jun 12. The common P446L polymorphism in GCKR inversely modulates fasting glucose and triglyceride levels and reduces type 2 diabetes risk in the DESIR prospective general French population. rs1260326 rs1260326 rs1260326 rs1260326
Mol Vis. 2008 Jun 5;14:1037-40. LOXL1 genetic polymorphisms are associated with exfoliation glaucoma in the Japanese population. rs1048661 rs3825942 rs1048661
BMC Med Genet. 2008 Jun 9;9:51. The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. rs572515 rs9288410 rs2014307 rs10801575 rs2014307 rs10801575 rs2014307
Blood. 2008 Aug 15;112(4):1022-7. Epub 2008 Jun 5. A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. rs1057910 rs4917639
J Hum Genet. 2008;53(8):718-27. Epub 2008 Jun 4. Adiponectin gene ADIPOQ SNP associations with serum adiponectin in two female populations and effects of SNPs on promoter activity. rs182052 rs16861209 rs1501299 rs1063537 rs17300539 rs266729
J Clin Invest. 2008 Jul;118(7):2620-8. Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. rs563694 rs563694
Am J Hum Genet. 2008 Jun;82(6):1270-80. Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function. rs4704397 rs1505287 rs10512065 rs2252696 rs1976324 rs27178 rs4903957
JAMA. 2008 May 28;299(20):2423-36. Genetic susceptibility to cancer: the role of polymorphisms in candidate genes.
Ann Hum Genet. 2008 Sep;72(Pt 5):654-7. Epub 2008 May 26. Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest). rs10757274 rs2383206 rs2383207 rs10757278
BMC Med Genet. 2008 May 22;9:45. The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies. rs7903146 rs7903146 rs7903146
Nat Genet. 2008 Jun;40(6):730-40. Epub 2008 May 18. Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer. rs2976392 rs2294008 rs2976392
Nat Genet. 2008 Jul;40(7):886-91. Epub 2008 May 18. ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
Nat Genet. 2008 Jul;40(7):838-40. Epub 2008 May 18. Common sequence variants on 20q11.22 confer melanoma susceptibility. rs910873 rs1885120
Diabetes. 2008 Aug;57(8):2226-33. Epub 2008 May 9. Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. rs8050136
J Appl Physiol. 2008 Oct;105(4):1352-8. Epub 2008 May 8. The Gly482Ser genotype at the PPARGC1A gene and elevated blood pressure: a meta-analysis involving 13,949 individuals. rs8192678
Proc Natl Acad Sci U S A. 2008 May 13;105(19):6998-7003. Epub 2008 May 5. Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. rs1617640 rs1617640 rs1617640
Bull Exp Biol Med. 2007 Sep;144(3):304-8. Peripheral blood serum from healthy donors contains antibodies against the fragment of transcribed region of ribosomal repeat.
Nat Genet. 2008 Jun;40(6):768-75. Epub 2008 May 4. Common variants near MC4R are associated with fat mass, weight and risk of obesity. rs17782313
Nat Genet. 2008 Jun;40(6):716-8. Epub 2008 May 4. Common genetic variation near MC4R is associated with waist circumference and insulin resistance. rs12970134 rs12970134
BMC Biol. 2008 May 1;6:18. Flying lemurs--the 'flying tree shrews'? Molecular cytogenetic evidence for a Scandentia-Dermoptera sister clade.
Science. 2008 May 23;320(5879):1085-8. Epub 2008 May 1. A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels. rs560887 rs560887
Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3976-80. Epub 2008 Apr 30. Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese. rs1048661 rs3825942 rs2165241 rs1048661 rs3825942 rs2165241 rs1048661 rs3825942 rs2165241 rs1048661 rs2165241 rs3825942 rs3825942 rs1048661
Am J Hum Genet. 2008 May;82(5):1202-10. Epub 2008 Apr 24. Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two susceptibility loci harboring CARD9 and IL18RAP. rs917997 rs917997 rs10870077
Am J Hum Genet. 2008 May;82(5):1185-92. Epub 2008 Apr 24. Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
Nat Genet. 2008 Jun;40(6):703-6. Epub 2008 Apr 27. Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. rs4415084 rs10941679 rs10941679
Diabetologia. 2008 Jun;51(6):971-7. Epub 2008 Apr 24. Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study). rs10811661 rs9939609 rs13266634 rs4402960 rs1111875 rs7756992
Invest Ophthalmol Vis Sci. 2008 May;49(5):1771-6. Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age-related macular degeneration along with CFH in Indian patients. rs10490924 rs11200638 rs1061170 rs10490924 rs11200638 rs2672598 rs10490924 rs11200638
Eur J Endocrinol. 2008 May;158(5):R1-5. RANTES/CCL5 gene polymorphisms, serum concentrations, and incident type 2 diabetes: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.
Am J Gastroenterol. 2008 Jun;103(6):1437-42. Epub 2008 Apr 16. Association of TNFSF15 with Crohn's disease in Koreans. rs3810936 rs6478108 rs7848647
J Oral Pathol Med. 2008 May;37(5):271-7. Combinational polymorphisms of four DNA repair genes XRCC1, XRCC2, XRCC3, and XRCC4 and their association with oral cancer in Taiwan. rs2040639 rs2040639 rs861539 rs2040639 rs861539 rs2075685 rs2040639 rs861539 rs2075685 rs1799782
N Engl J Med. 2008 Apr 17;358(16):1682-91. Epub 2008 Apr 9. Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function.
J Allergy Clin Immunol. 2008 May;121(5):1203-1209.e1. Epub 2008 Apr 8. Filaggrin mutations, atopic eczema, hay fever, and asthma in children.
J Allergy Clin Immunol. 2008 Apr;121(4):860-3. A polymorphism controlling ORMDL3 expression is associated with asthma that is poorly controlled by current medications. rs7216389 rs4512342 rs10924993
Nat Genet. 2008 May;40(5):575-83. Epub 2008 Apr 6. Genome-wide association analysis identifies 20 loci that influence adult height.
Nat Genet. 2008 May;40(5):584-91. Epub 2008 Apr 6. Identification of ten loci associated with height highlights new biological pathways in human growth.
Am J Hum Genet. 2008 Apr;82(4):849-58. On the replication of genetic associations: timing can be everything!
Nature. 2008 Apr 3;452(7187):633-7. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.
Nat Genet. 2008 May;40(5):616-22. Epub 2008 Apr 2. Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. rs1051730 rs8034191
Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1459-63. Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. rs2165241 rs1048661 rs3825942 rs2165241 rs1048661 rs3825942 rs1048661 rs3825942
Nat Genet. 2008 May;40(5):623-30. Epub 2008 Mar 30. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. rs10795668 rs16892766
Nat Genet. 2008 May;40(5):638-45. Epub 2008 Mar 30. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.
Nat Genet. 2008 May;40(5):631-7. Epub 2008 Mar 30. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. rs3802842 rs7014346 rs4939827 rs3802842 rs4939827
Hum Mol Genet. 2008 Jul 1;17(13):1938-45. Epub 2008 Mar 25. Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. rs495337 rs495337 rs495337
J Clin Endocrinol Metab. 2008 Jun;93(6):2294-9. Epub 2008 Mar 25. The -250G>A promoter variant in hepatic lipase associates with elevated fasting serum high-density lipoprotein cholesterol modulated by interaction with physical activity in a study of 16,156 Danish subjects. rs2070895 rs2070895
Am J Hum Genet. 2008 Apr;82(4):937-48. Epub 2008 Mar 20. Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. rs2981582 rs3803662 rs889312 rs2981582 rs889312 rs3803662
JAMA. 2008 Mar 19;299(11):1291-305. Association of FKBP5 polymorphisms and childhood abuse with risk of posttraumatic stress disorder symptoms in adults. rs9296158 rs3800373 rs1360780 rs9470080
Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4340-5. Epub 2008 Mar 7. Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. rs1078806 rs2180341
Hum Mol Genet. 2008 Jun 15;17(12):1803-13. Epub 2008 Mar 5. Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. rs6013029 rs6013029 rs6013029
PLoS Med. 2008 Mar 4;5(3):e52. Alcohol intake and blood pressure: a systematic review implementing a Mendelian randomization approach.
Mol Psychiatry. 2008 Jun;13(6):558-69. Epub 2008 Mar 4. Whole-genome association study of bipolar disorder.
Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2357-65. Epub 2008 Mar 3. HTRA1 variants in exudative age-related macular degeneration and interactions with smoking and CFH. rs11200638 rs11200638 rs2672598 rs1049331 rs2293870 rs11200638 rs800292 rs11200638 rs800292 rs11200638
Lancet Neurol. 2008 Apr;7(4):319-26. Epub 2008 Mar 3. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.
J Pediatr Adolesc Gynecol. 2008 Feb;21(1):3-8. Non-chromosomal, non-iatrogenic premature ovarian failure in an adolescent population: a case series.
Stroke. 2008 Apr;39(4):1333-5. Epub 2008 Feb 28. The role of aquaporin-4 polymorphisms in the development of brain edema after middle cerebral artery occlusion. rs9951307
Genet Epidemiol. 2008 Apr;32(3):227-34. Estimation of significance thresholds for genomewide association scans.
Cell Cycle. 2008 Feb 15;7(4):521-4. Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort. rs2165241 rs3825942 rs2165241 rs3825942
Nat Genet. 2008 Mar;40(3):281-3. Epub 2008 Feb 10. Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. rs5945572 rs721048
Nat Genet. 2008 Mar;40(3):316-21. Epub 2008 Feb 10. Multiple newly identified loci associated with prostate cancer susceptibility.
Nat Genet. 2008 Mar;40(3):310-5. Epub 2008 Feb 10. Multiple loci identified in a genome-wide association study of prostate cancer.
BMC Med Genet. 2008 Feb 6;9:5. DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity. rs3825942
Transfusion. 2008 May;48(5):917-24. Epub 2008 Feb 1. Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease. rs2814778
Clin Calcium. 2008 Feb;18(2):162-7. [Genomic approaches to bone and joint diseases. Current status of genetic study of osteoarthritis] rs143383
Hum Genet. 2008 Apr;123(3):273-80. Epub 2008 Jan 26. Haplotypic analysis of Wellcome Trust Case Control Consortium data.
J Invest Dermatol. 2008 Jul;128(7):1653-61. Epub 2008 Jan 24. Polymorphisms of the IL12B and IL23R genes are associated with psoriasis. rs3212227 rs6887695 rs7530511 rs11209026 rs3212227 rs6887695 rs3212227 rs6887695 rs7530511 rs11209026
Dis Markers. 2008;24(2):119-26. A common polymorphism G-50T in cytochrome P450 2J2 gene is associated with increased risk of essential hypertension in a Russian population.
BMC Med Genet. 2008 Jan 24;9:4. FTO gene SNPs associated with extreme obesity in cases, controls and extremely discordant sister pairs. rs1421085 rs17817449 rs9939609 rs1421085 rs17817449
Nat Genet. 2008 Feb;40(2):152-4. Epub 2008 Jan 20. A nonsynonymous functional variant in integrin-alpha(M) (encoded by ITGAM) is associated with systemic lupus erythematosus. rs1143679
Nat Genet. 2008 Feb;40(2):211-6. Epub 2008 Jan 20. Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. rs10516487 rs17266594 rs10516487 rs3733197
Nat Genet. 2008 Feb;40(2):204-10. Epub 2008 Jan 20. Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. rs10798269
Diabetes. 2008 Apr;57(4):1143-6. Epub 2008 Jan 15. A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. rs1701704
Tissue Antigens. 2008 Mar;71(3):206-12. Epub 2007 Jan 8. Genetic analysis of autoimmune regulator haplotypes in alopecia areata.
Mol Microbiol. 2008 Mar;67(5):984-95. Epub 2008 Jan 8. Double illegitimate recombination events integrate DNA segments through two different mechanisms during natural transformation of Acinetobacter baylyi.
Nat Genet. 2008 Feb;40(2):149-51. Epub 2008 Jan 13. Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. rs3812316
Nat Genet. 2008 Feb;40(2):189-97. Epub 2008 Jan 13. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Am J Hum Genet. 2008 Jan;82(1):139-49. Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
Acta Derm Venereol. 2008;88(1):15-9. Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families.
Nat Genet. 2008 Feb;40(2):217-24. Epub 2008 Jan 6. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. rs10757278 rs10811661 rs10757278 rs10811661 rs10757278
Nat Genet. 2008 Jan;40(1):29-31. Epub 2007 Dec 16. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
Diabetes. 2008 Mar;57(3):770-6. Epub 2007 Dec 7. Analysis of single nucleotide polymorphisms identifies major type 1A diabetes locus telomeric of the major histocompatibility complex. rs1233478 rs1233478
PLoS Med. 2007 Dec;4(12):e335. N348I in the connection domain of HIV-1 reverse transcriptase confers zidovudine and nevirapine resistance.
Diabetologia. 2008 Mar;51(3):458-63. Epub 2007 Nov 27. Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations. rs10010131 rs6446482 rs752854 rs734312 rs752854 rs10010131
Diabetologia. 2008 Jan;51(1):70-5. Epub 2007 Nov 16. The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes. rs780094 rs780094 rs780094 rs780094 rs780094 rs780094
Nature. 2007 Dec 6;450(7171):887-92. Epub 2007 Nov 14. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A.
Diabetes. 2008 Feb;57(2):509-13. Epub 2007 Nov 14. Association of the ATP-binding cassette transporter A1 R230C variant with early-onset type 2 diabetes in a Mexican population.
Am J Hum Genet. 2007 Dec;81(6):1284-8. Epub 2007 Oct 24. Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases. rs6822844 rs6822844
PLoS Genet. 2007 Nov;3(11):e192. Identification of two independent risk factors for lupus within the MHC in United Kingdom families. rs419788 rs419788
Nat Genet. 2007 Dec;39(12):1477-82. Epub 2007 Nov 4. Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. rs10499194 rs10499194 rs6920220
Nat Genet. 2007 Dec;39(12):1431-3. Epub 2007 Nov 4. Rheumatoid arthritis association at 6q23. rs6920220
Diabetes. 2008 Feb;57(2):494-502. Epub 2007 Oct 31. Association analysis indicates that a variant GATA-binding site in the PIK3CB promoter is a Cis-acting expression quantitative trait locus for this gene and attenuates insulin resistance in obese children. rs361072 rs361072 rs361072 rs361072 rs361072 rs361072
Ann Rheum Dis. 2008 Jul;67(7):972-9. Epub 2007 Oct 29. The Wegener's granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping.
J Thromb Haemost. 2008 Jan;6(1):20-31. Epub 2007 Oct 16. Clinical and genetic correlates of soluble P-selectin in the community. rs6136
Diabetes. 2008 Jan;57(1):95-101. Epub 2007 Oct 17. Low physical activity accentuates the effect of the FTO rs9939609 polymorphism on body fat accumulation. rs9939609 rs9939609 rs9939609 rs9939609 rs9939609
Diabetes. 2008 Jan;57(1):209-17. Epub 2007 Oct 16. Genetic variants within the LPIN1 gene, encoding lipin, are influencing phenotypes of the metabolic syndrome in humans.
Nat Genet. 2007 Nov;39(11):1315-7. Epub 2007 Oct 14. A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. rs4939827
BMC Med Genet. 2007 Sep 19;8 Suppl 1:S15. Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. rs1131497 rs1970546
J Natl Cancer Inst. 2007 Oct 17;99(20):1525-33. Epub 2007 Oct 9. Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans. rs1447295 rs6983267 rs1447295 rs6983267
Reprod Biomed Online. 2007 Oct;15(4):463-7. Prevalence of chromosomal aberrations in Mexican women with primary amenorrhoea.
Anim Genet. 2007 Oct;38(5):491-8. Genome-wide association analysis reveals cryptic alleles as an important factor in heterosis for fatness in chicken F2 population.
Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16227-32. Epub 2007 Sep 20. A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration. rs10490924 rs11200638 rs11200638 rs10490924 rs10490924 rs10490924
Hum Mol Genet. 2007 Dec 15;16(24):3008-16. Epub 2007 Sep 19. An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases.
PLoS Med. 2007 Sep;4(9):e278. A candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritis. rs10818488
Inflamm Bowel Dis. 2007 Dec;13(12):1484-7. Role of the PXR gene locus in inflammatory bowel diseases. rs3814055 rs3814055 rs6784598 rs2276707 rs3789243
Nat Genet. 2007 Oct;39(10):1245-50. Epub 2007 Sep 2. A common variant of HMGA2 is associated with adult and childhood height in the general population. rs1042725 rs1042725 rs1042725
J Clin Oncol. 2007 Sep 1;25(25):3837-45. Clinical implications of CYP2D6 genotypes predictive of tamoxifen pharmacokinetics in metastatic breast cancer.
Ann Rheum Dis. 2008 May;67(5):677-82. Epub 2007 Aug 29. Investigating the role of the HLA-Cw*06 and HLA-DRB1 genes in susceptibility to psoriatic arthritis: comparison with psoriasis and undifferentiated inflammatory arthritis.
Stroke. 2007 Oct;38(10):2663-9. Epub 2007 Aug 16. An interactive association of common sequence variants in the neuropeptide Y gene with susceptibility to ischemic stroke.
Nat Genet. 2007 Sep;39(9):1074-82. Epub 2007 Aug 5. Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.
Genes Immun. 2007 Oct;8(7):552-9. Epub 2007 Aug 2. A common variant of the interleukin 6 receptor (IL-6r) gene increases IL-6r and IL-6 levels, without other inflammatory effects. rs4537545 rs8192284 rs4537545 rs4537545 rs4537545
PLoS Genet. 2007 Jul;3(7):e115. Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. rs9930506 rs6602024 rs9930506 rs6602024
Genes Immun. 2007 Sep;8(6):503-12. Epub 2007 Jul 19. IA-2 autoantibodies in incident type I diabetes patients are associated with a polyadenylation signal polymorphism in GIMAP5. rs6598 rs6598
Nat Genet. 2007 Aug;39(8):995-9. Epub 2007 Jul 15. A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. rs11887534
Hepatology. 2007 Sep;46(3):793-801. Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterol.
Nat Genet. 2007 Aug;39(8):984-8. Epub 2007 Jul 8. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. rs6983267 rs6983267
Nat Genet. 2007 Aug;39(8):989-94. Epub 2007 Jul 8. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.
Inflamm Res. 2007 Jun;56(6):240-5. Effect of rectal administration of rebamipide on dextran sulfate sodium-induced colitis: role of hepatocyte growth factor.
J Allergy Clin Immunol. 2007 Sep;120(3):578-85. Epub 2007 Jun 21. Association between Q551R IL4R genetic variants and atopic asthma risk demonstrated by meta-analysis.
PLoS Genet. 2007 Jun;3(6):e98. A genomic pathway approach to a complex disease: axon guidance and Parkinson disease.
Hum Hered. 2007;64(4):214-9. Epub 2007 Jun 12. Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish. rs1415262 rs10494366 rs10494366 rs10494366
Nat Genet. 2007 Jul;39(7):827-9. Epub 2007 Jun 10. A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. rs13119723 rs6822844
Nat Genet. 2007 Jul;39(7):830-2. Epub 2007 Jun 6. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Nat Genet. 2007 Jul;39(7):857-64. Epub 2007 Jun 6. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
Autoimmun Rev. 2007 Jun;6(6):402-8. Epub 2006 Dec 20. Meta-analysis of HLA-DRB1 polymorphism in Latin American patients with rheumatoid arthritis.
Nat Genet. 2007 Jun;39(6):721-3. Epub 2007 May 21. FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.
Nat Genet. 2007 Jul;39(7):870-4. Epub 2007 May 27. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. rs1219648
Nucleic Acids Res. 2007;35(11):3848-58. Epub 2007 May 25. Single-molecule analysis of 1D diffusion and transcription elongation of T7 RNA polymerase along individual stretched DNA molecules.
J Clin Endocrinol Metab. 2007 Aug;92(8):3162-70. Epub 2007 May 15. Cytotoxic T-lymphocyte associated antigen 4 gene polymorphisms and autoimmune thyroid disease: a meta-analysis.
Mol Psychiatry. 2008 Feb;13(2):197-207. Epub 2007 May 8. A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
Gastroenterology. 2007 May;132(5):1657-64. Epub 2007 Feb 24. IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease.
Hum Genet. 2007 Jul;121(6):721-7. Epub 2007 May 3. Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans. rs2070197
J Mol Med. 2007 Jul;85(7):777-82. Epub 2007 May 3. TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis. rs7903146 rs7903146 rs7903146
J Clin Psychiatry. 2007 Apr;68(4):613-8. A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. rs4420638
Inflamm Bowel Dis. 2007 Aug;13(8):941-6. Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene. rs2 rs2 rs2
PLoS Genet. 2007 Apr 20;3(4):e58. Epub 2007 Mar 5. Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
Carcinogenesis. 2007 Aug;28(8):1659-64. Epub 2007 Apr 13. MC1R: three novel variants identified in a malignant melanoma association study in the Spanish population.
Fertil Steril. 2007 Oct;88(4):900-5. Epub 2007 Apr 16. Lack of association between polycystic ovary syndrome and embryonic aneuploidy.
Diabetologia. 2007 Jun;50(6):1186-91. Epub 2007 Apr 11. TCF7L2 in the Go-DARTS study: evidence for a gene dose effect on both diabetes susceptibility and control of glucose levels. rs12255372 rs7903146 rs7903146
Nat Genet. 2007 May;39(5):650-4. Epub 2007 Apr 8. Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
Diabetes. 2007 Jul;56(7):1943-7. Epub 2007 Apr 6. TCF7L2 polymorphisms modulate proinsulin levels and beta-cell function in a British Europid population. rs7903146 rs7903146
Cancer Res. 2007 Apr 1;67(7):2951-6. A common 8q24 variant in prostate and breast cancer from a large nested case-control study. rs1447295 rs1447295 rs1447295
Nat Genet. 2007 May;39(5):638-44. Epub 2007 Apr 1. Multiple regions within 8q24 independently affect risk for prostate cancer.
Nat Genet. 2007 May;39(5):645-9. Epub 2007 Apr 1. Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. rs1447295 rs6983267 rs1447295 rs6983267 rs6983267 rs1447295
Arthritis Res Ther. 2007;9(2):R32. Replication of the genetic effects of IFN regulatory factor 5 (IRF5) on systemic lupus erythematosus in a Korean population. rs2004640 rs2004640 rs2004640 rs2004640 rs2280714
Nat Genet. 2007 Apr;39(4):529-33. Epub 2007 Mar 25. A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis. rs143383
Diabetologia. 2007 Apr;50(4):741-6. Epub 2007 Feb 14. A type 1 diabetes subgroup with a female bias is characterised by failure in tolerance to thyroid peroxidase at an early age and a strong association with the cytotoxic T-lymphocyte-associated antigen-4 gene. rs3087243 rs2476601
Hum Genet. 2007 May;121(3-4):305-17. Epub 2007 Feb 27. Candidate SNPs for a universal individual identification panel.
Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1128-32. The LOC387715 polymorphism and age-related macular degeneration: replication in three case-control samples. rs10490924
Biol Blood Marrow Transplant. 2007 Mar;13(3):307-14. Pharmacokinetic disposition and clinical outcomes in infants and children receiving intravenous busulfan for allogeneic hematopoietic stem cell transplantation.
Hum Mutat. 2007 May;28(5):431-40. Genetic variants in MGMT and risk of lung cancer in Southeastern Chinese: a haplotype-based analysis. rs1625649 rs1625649
Tissue Antigens. 2007 Feb;69(2):161-9. Primary sclerosing cholangitis is associated with extended HLA-DR3 and HLA-DR6 haplotypes.
Mol Cancer Ther. 2007 Jan;6(1):380-9. A phase I trial of hyperthermia-induced interleukin-12 gene therapy in spontaneously arising feline soft tissue sarcomas.
J Pediatr Surg. 2007 Jan;42(1):160-5; discussion 165. Interferon beta-mediated vessel stabilization improves delivery and efficacy of systemically administered topotecan in a murine neuroblastoma model.
Nat Genet. 2007 Feb;39(2):207-11. Epub 2006 Dec 31. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. rs2241880 rs2241880 rs2241880 rs2241880
Hum Mol Genet. 2007 Mar 15;16(6):579-91. Epub 2006 Dec 22. Association of IRF5 in UK SLE families identifies a variant involved in polyadenylation. rs2004640 rs3807306 rs2004640 rs2280714 rs10954213 rs10954213 rs10954213 rs10954213
J Clin Endocrinol Metab. 2007 Feb;92(2):685-90. Epub 2006 Dec 5. Association of PTPN22 haplotypes with Graves' disease. rs2476601 rs2476601 rs2476601
Diabetologia. 2007 Jan;50(1):68-73. Epub 2006 Dec 2. An association analysis of the HLA gene region in latent autoimmune diabetes in adults.