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|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
2009-01-16 | 19,010,793 | Baranzini SE | 2008-11-14 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/19010793 | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. | Brain lesion load | 791 European ancestry cases, 883 European ancestry controls | NA | Illumina [551642] | 4 | multiple sclerosis | http://purl.obolibrary.org/obo/MONDO_0005301 | GCST000265 | Genome-wide genotyping array | null | false | NA | false |
2009-01-16 | 19,010,793 | Baranzini SE | 2008-11-14 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/19010793 | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. | Multiple sclerosis (severity) | 794 European ancestry cases, 883 European ancestry controls | NA | Illumina [551642] | 11 | multiple sclerosis | http://purl.obolibrary.org/obo/MONDO_0005301 | GCST000266 | Genome-wide genotyping array | null | false | NA | false |
2009-01-12 | 19,079,261 | Willer CJ | 2008-12-14 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/19079261 | Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. | Body mass index | 32,387 European ancestry individuals | 59,082 European ancestry individuals | Affymetrix, Illumina [2399588] (imputed) | 11 | body mass index | http://www.ebi.ac.uk/efo/EFO_0004340 | GCST000298 | Genome-wide genotyping array | null | false | NA | false |
2011-01-16 | 21,177,295 | Panoutsopoulou K | 2010-12-21 | Ann Rheum Dis | www.ncbi.nlm.nih.gov/pubmed/21177295 | Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study. | Osteoarthritis | 3,177 European ancestry cases, 4,894 European ancestry controls | 10,312 European ancestry cases, 45,861 European ancestry controls, 213 cases, 2,531 controls | Illumina [514898] | 0 | osteoarthritis | http://purl.obolibrary.org/obo/MONDO_0005178 | GCST000923 | Genome-wide genotyping array | null | false | NA | false |
2008-12-09 | 18,985,386 | Pankratz N | 2008-11-06 | Hum Genet | www.ncbi.nlm.nih.gov/pubmed/18985386 | Genomewide association study for susceptibility genes contributing to familial Parkinson disease. | Parkinson's disease (familial) | 1,119 European ancestry cases, 1,127 European ancestry controls | NA | Illumina [328189] | 1 | Parkinson disease | http://purl.obolibrary.org/obo/MONDO_0005180 | GCST000261 | Genome-wide genotyping array | null | false | NA | false |
2009-01-15 | 19,079,260 | Thorleifsson G | 2008-12-14 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/19079260 | Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. | Weight | 72,598 European ancestry individuals, 1,160 African American individuals | Up to 11,036 European ancestry individuals, 32,615 individuals | Illumina [305846] | 17 | body weight | http://www.ebi.ac.uk/efo/EFO_0004338 | GCST000299 | Genome-wide genotyping array | null | false | NA | false |
2009-01-15 | 19,079,260 | Thorleifsson G | 2008-12-14 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/19079260 | Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. | Body mass index | 72,598 European ancestry individuals, 1,160 African American individuals | Up to 11,036 European ancestry individuals, 32,615 individuals | Illumina [305846] | 14 | body mass index | http://www.ebi.ac.uk/efo/EFO_0004340 | GCST000296 | Genome-wide genotyping array | null | false | NA | false |
2015-05-23 | 21,208,937 | Pichler I | 2011-01-04 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/21208937 | Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. | Iron status biomarkers | Up to 5,633 European ancestry individuals | Up to 3,457 European ancestry individuals | Affymetrix, Illumina [~ 2500000] (imputed) | 5 | iron biomarker measurement | http://www.ebi.ac.uk/efo/EFO_0004461 | GCST000935 | Genome-wide genotyping array | null | false | NA | false |
2009-09-28 | 18,403,759 | Ober C | 2008-04-09 | N Engl J Med | www.ncbi.nlm.nih.gov/pubmed/18403759 | Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. | YKL-40 levels | 632 Hutterite individuals | 443 European ancestry cases, 491 European ancestry controls, 206 European ancestry individuals | Affymetrix [290325] | 1 | YKL40 measurement | http://www.ebi.ac.uk/efo/EFO_0004869 | GCST000177 | Genome-wide genotyping array | null | false | NA | false |
2008-07-22 | 18,332,876 | Kirov G | 2008-03-11 | Mol Psychiatry | www.ncbi.nlm.nih.gov/pubmed/18332876 | A genome-wide association study in 574 schizophrenia trios using DNA pooling. | Schizophrenia | 574 European ancestry trios, 605 European ancestry controls | NA | Illumina [~ 550000] | 1 | schizophrenia | http://purl.obolibrary.org/obo/MONDO_0005090 | GCST000163 | Genome-wide genotyping array | null | false | NA | false |
2008-09-15 | 17,903,295 | Lunetta KL | 2007-09-19 | BMC Med Genet | www.ncbi.nlm.nih.gov/pubmed/17903295 | Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. | Aging traits | 1,345 individuals from 330 families | NA | Affymetrix [70897] | 10 | aging, age at menopause, exercise test, age at death | http://www.ebi.ac.uk/efo/EFO_0022597, http://www.ebi.ac.uk/efo/EFO_0004704, http://www.ebi.ac.uk/efo/EFO_0004328, http://www.ebi.ac.uk/efo/EFO_0005056 | GCST000096 | Genome-wide genotyping array | null | false | NA | false |
2008-09-10 | 17,903,295 | Lunetta KL | 2007-09-19 | BMC Med Genet | www.ncbi.nlm.nih.gov/pubmed/17903295 | Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. | Morbidity-free survival | 558 individuals | NA | Affymetrix [70897] | 5 | disease free survival | http://www.ebi.ac.uk/efo/EFO_0000409 | GCST000103 | Genome-wide genotyping array | null | false | NA | false |
2008-06-16 | 17,603,485 | Gudmundsson J | 2007-07-01 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/17603485 | Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. | Prostate cancer | 1,501 European ancestry cases, 11,290 European ancestry controls | 1,992 European ancestry cases, 3,058 European ancestry controls | Illumina [310520] | 2 | prostate carcinoma | http://www.ebi.ac.uk/efo/EFO_0001663 | GCST000050 | Genome-wide genotyping array | null | false | NA | false |
2008-06-16 | 17,603,472 | Gudbjartsson DF | 2007-07-01 | Nature | www.ncbi.nlm.nih.gov/pubmed/17603472 | Variants conferring risk of atrial fibrillation on chromosome 4q25. | Atrial fibrillation/atrial flutter | 550 European ancestry cases, 4,476 European ancestry controls | 3,030 European ancestry cases, 14,780 European ancestry controls, 333 Han Chinese ancestry cases, 2,836 Han Chinese ancestry controls | Illumina [316515] | 2 | atrial fibrillation | http://www.ebi.ac.uk/efo/EFO_0000275 | GCST000051 | Genome-wide genotyping array | null | false | NA | false |
2011-03-02 | 21,273,288 | Del Greco M F | 2011-01-27 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/21273288 | Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. | Natriuretic peptide levels | 1,325 European ancestry individuals | 1,746 European ancestry individuals | Illumina [~ 2500000] (imputed) | 3 | NT-proBNP measurement | http://www.ebi.ac.uk/efo/EFO_0004745 | GCST000957 | Genome-wide genotyping array | null | false | NA | false |
2011-03-28 | 21,270,382 | Baik I | 2011-01-26 | Am J Clin Nutr | www.ncbi.nlm.nih.gov/pubmed/21270382 | Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. | Alcohol consumption | 1,721 Korean ancestry male individuals | 1,113 Korean ancestry male individuals | Affymetrix [315914] | 4 | alcohol drinking | http://www.ebi.ac.uk/efo/EFO_0004329 | GCST000954 | Genome-wide genotyping array | null | false | NA | false |
2011-05-02 | 21,460,840 | Hollingworth P | 2011-04-03 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/21460840 | Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. | Alzheimer's disease | 6,688 European ancestry cases, 13,685 European ancestry controls | 13,182 European ancestry cases, 26,161 European ancestry controls | Affymetrix, Illumina [496763] | 4 | Alzheimer disease | http://purl.obolibrary.org/obo/MONDO_0004975 | GCST001025 | Genome-wide genotyping array | null | false | NA | false |
2015-04-22 | 21,305,692 | Belmonte Mahon P | 2011-02-08 | Am J Med Genet B Neuropsychiatr Genet | www.ncbi.nlm.nih.gov/pubmed/21305692 | Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. | Bipolar disorder (age of onset and psychotic symptoms) | 2,836 European ancestry cases, 2,744 European ancestry controls | 3,916 European cases, 5,112 controls | Affymetrix, Illumina [2373895] (imputed) | 2 | psychotic symptoms, age of onset of bipolar disorder | http://www.ebi.ac.uk/efo/EFO_0005940, http://purl.obolibrary.org/obo/OBA_2001019 | GCST000969 | Genome-wide genotyping array | null | false | NA | false |
2010-02-05 | 20,070,850 | Edwards TL | 2010-01-13 | Ann Hum Genet | www.ncbi.nlm.nih.gov/pubmed/20070850 | Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. | Parkinson's disease | 1,752 European ancestry cases, 1,745 European ancestry controls | NA | Illumina [495715] (imputed) | 6 | Parkinson disease | http://purl.obolibrary.org/obo/MONDO_0005180 | GCST000567 | Genome-wide genotyping array | null | false | NA | false |
2010-02-04 | 20,068,591 | Van Laer L | 2010-01-13 | Eur J Hum Genet | www.ncbi.nlm.nih.gov/pubmed/20068591 | A genome-wide association study for age-related hearing impairment in the Saami. | Hearing impairment | 347 Finnish Saami individuals | NA | Affymetrix [83381] | 2 | hearing loss | http://www.ebi.ac.uk/efo/EFO_0004238 | GCST000566 | Genome-wide genotyping array | null | false | NA | false |
2010-06-18 | 20,520,587 | Nielsen DA | 2010-06-01 | Psychiatr Genet | www.ncbi.nlm.nih.gov/pubmed/20520587 | Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. | Heroin addiction | 200 European ancestry cases, 150 European ancestry controls, 125 African American cases, 100 African American controls | NA | Affymetrix [up to 113174] | 0 | heroin dependence | http://www.ebi.ac.uk/efo/EFO_0004240 | GCST000690 | Genome-wide genotyping array | null | false | NA | false |
2011-04-06 | 21,383,967 | Zhernakova A | 2011-02-24 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/21383967 | Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. | Celiac disease or Rheumatoid arthritis | 4,533 European ancestry celiac disease cases, 5,539 European ancestry rheumatoid arthritis cases, 27,981 European ancestry controls | 2,169 European ancestry celiac disease cases, 2,845 European ancestry rheumatoid arthritis cases, 7,199 European ancestry controls | Illumina [472854] | 15 | immune system disease | http://www.ebi.ac.uk/efo/EFO_0000540 | GCST000987 | Genome-wide genotyping array | null | false | NA | false |
2010-01-19 | 20,009,918 | Shrestha S | 2010-01-01 | AIDS | www.ncbi.nlm.nih.gov/pubmed/20009918 | A genome-wide association study of carotid atherosclerosis in HIV-infected men. | Carotid atherosclerosis in HIV infection | 177 European ancestry individuals | NA | Illumina [311194] | 7 | internal carotid artery thickness, carotid artery disease, carotid artery thickness | http://purl.obolibrary.org/obo/OBA_2050107, http://www.ebi.ac.uk/efo/EFO_0003781, http://purl.obolibrary.org/obo/OBA_2050108 | GCST000555 | Genome-wide genotyping array | null | false | NA | false |
2010-03-17 | 20,174,558 | Tsai FJ | 2010-02-19 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/20174558 | A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. | Type 2 diabetes | 995 Han Chinese ancestry cases, 894 Han Chinese ancestry controls | 1,803 Han Chinese ancestry cases, 1,473 Han Chinese ancestry controls | Illumina [516737] | 3 | type 2 diabetes mellitus | http://purl.obolibrary.org/obo/MONDO_0005148 | GCST000601 | Genome-wide genotyping array | null | false | NA | false |
2010-01-28 | 20,072,603 | Guo Y | 2010-01-08 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/20072603 | Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. | Osteoporosis | 350 Han Chinese ancestry cases, 350 Han Chinese ancestry controls | 390 Han Chinese ancestry cases, 516 Han Chinese ancestry controls | Affymetrix [281533] | 1 | osteoporosis | http://www.ebi.ac.uk/efo/EFO_0003882 | GCST000560 | Genome-wide genotyping array | null | false | NA | false |
2010-06-23 | 20,528,957 | Oedegaard KJ | 2010-06-07 | Genes Brain Behav | www.ncbi.nlm.nih.gov/pubmed/20528957 | A genome-wide association study of bipolar disorder and comorbid migraine. | Migraine in psychiatric disorder | 56 European ancestry bipolar disorder cases, 699 European ancestry bipolar disorder controls | 131 European ancestry attention deficit hyperactivity disorder cases, 324 European ancestry attention deficit hyperactivity disorder controls | Affymetrix [724067] | 0 | migraine disorder | http://purl.obolibrary.org/obo/MONDO_0005277 | GCST000695 | Genome-wide genotyping array | null | false | NA | false |
2015-05-13 | 21,347,282 | Lettre G | 2011-02-10 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/21347282 | Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. | Coronary heart disease | 260 African American cases, 5,053 African American controls | 621 African American cases, 1,629 African American controls | Affymetrix [~ 2740000] (imputed) | 3 | coronary artery disease | http://www.ebi.ac.uk/efo/EFO_0001645 | GCST000972 | Genome-wide genotyping array | null | false | NA | false |
2015-05-13 | 21,347,282 | Lettre G | 2011-02-10 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/21347282 | Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. | Type 2 diabetes | 1,264 African American cases, 5,678 African American controls | 503 African American cases, 1,656 African American controls | Affymetrix [~ 2740000] (imputed) | 2 | type 2 diabetes mellitus | http://purl.obolibrary.org/obo/MONDO_0005148 | GCST000976 | Genome-wide genotyping array | null | false | NA | false |
2015-05-13 | 21,347,282 | Lettre G | 2011-02-10 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/21347282 | Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. | LDL cholesterol | 7,565 African American individuals | 3,789 African American and Afro-Caribbean individuals | Affymetrix [~ 2740000] (imputed) | 17 | low density lipoprotein cholesterol measurement | http://www.ebi.ac.uk/efo/EFO_0004611 | GCST000975 | Genome-wide genotyping array | null | false | NA | false |
2015-05-13 | 21,347,282 | Lettre G | 2011-02-10 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/21347282 | Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. | HDL cholesterol | 7,813 African American individuals | 4,323 African American and Afro-Caribbean individuals | Affymetrix [~ 2740000] (imputed) | 18 | high density lipoprotein cholesterol measurement | http://www.ebi.ac.uk/efo/EFO_0004612 | GCST000974 | Genome-wide genotyping array | null | false | NA | false |
2015-05-13 | 21,347,282 | Lettre G | 2011-02-10 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/21347282 | Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. | Hypertension | 4,069 African American cases, 3,848 African American controls | 1,372 African American cases, 1,482 African American controls | Affymetrix [~ 2740000] (imputed) | 8 | hypertension | http://www.ebi.ac.uk/efo/EFO_0000537 | GCST000973 | Genome-wide genotyping array | null | false | NA | false |
2010-09-07 | 20,639,881 | Conde L | 2010-07-18 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20639881 | Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. | Follicular lymphoma | 681 European ancestry cases, 750 European ancestry controls | up to 3,164 European ancestry cases, 6,208 European ancestry controls | Illumina [312768] | 3 | neoplasm of mature B-cells | http://www.ebi.ac.uk/efo/EFO_0000096 | GCST000734 | Genome-wide genotyping array | null | false | NA | false |
2013-04-24 | 23,354,978 | Rinella ES | 2013-01-25 | Hum Genet | www.ncbi.nlm.nih.gov/pubmed/23354978 | Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation. | Breast cancer | 477 Ashkenazi Jewish cases, 524 Ashkenazi Jewish controls | 203 Ashkenazi Jewish cases, 263 Ashkenazi Jewish contols | Affymetrix [435632] | 3 | breast carcinoma | http://www.ebi.ac.uk/efo/EFO_0000305 | GCST001831 | Genome-wide genotyping array | null | false | NA | false |
2010-07-04 | 20,487,506 | Joubert BR | 2010-03-01 | Genome Med | www.ncbi.nlm.nih.gov/pubmed/20487506 | A whole genome association study of mother-to-child transmission of HIV in Malawi. | HIV (mother-to-child transmission) | 100 Malawian ancestry infant cases, 126 Malawian ancestry infant controls | NA | Illumina [586681] | 0 | HIV mother to child transmission | http://www.ebi.ac.uk/efo/EFO_0004595 | GCST000613 | Genome-wide genotyping array | null | false | NA | false |
2012-01-07 | 22,137,330 | Sanchez-Juan P | 2011-11-30 | Neurobiol Aging | www.ncbi.nlm.nih.gov/pubmed/22137330 | Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. | Creutzfeldt-Jakob disease (variant) | 93 European ancestry cases, 1,504 European ancestry controls | 42 European ancestry cases | Affymetrix [287554] | 6 | Creutzfeldt Jacob Disease | http://www.ebi.ac.uk/efo/EFO_0004226 | GCST001334 | Genome-wide genotyping array | null | false | NA | false |
2010-09-02 | 20,639,880 | Liu X | 2010-07-18 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20639880 | Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. | Primary biliary cholangitis | 453 European ancestry cases, 945 European ancestry controls, | 481 European ancestry cases, 3,706 European ancestry controls | Illumina [276459] | 6 | biliary liver cirrhosis | http://www.ebi.ac.uk/efo/EFO_0004267 | GCST000733 | Genome-wide genotyping array | null | false | NA | false |
2010-01-29 | 20,062,061 | Chambers JC | 2010-01-10 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20062061 | Genetic variation in SCN10A influences cardiac conduction. | Electrocardiographic traits | 6,543 Indian Asian ancestry individuals | 6,243 Indian Asian ancestry individuals, 5,370 European ancestry individuals | Illumina [303309] | 3 | electrocardiography | http://www.ebi.ac.uk/efo/EFO_0004327 | GCST000564 | Genome-wide genotyping array | null | false | NA | false |
2013-04-04 | 23,328,707 | Tin A | 2013-01-16 | Nephrol Dial Transplant | www.ncbi.nlm.nih.gov/pubmed/23328707 | Genome-wide significant locus of beta-trace protein, a novel kidney function biomarker, identified in European and African Americans. | Beta-trace protein levels | 6,720 European ancestry individuals | 1,734 African American individuals | Affymetrix [~ 2500000] (imputed) | 1 | urinary system trait | http://purl.obolibrary.org/obo/OBA_VT1000777 | GCST001825 | Genome-wide genotyping array | null | false | NA | false |
2010-09-27 | 20,802,204 | Baranzini SE | 2010-09-01 | Brain | www.ncbi.nlm.nih.gov/pubmed/20802204 | Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. | Multiple sclerosis--Brain Glutamate Levels | 382 cases | NA | Illumina [~ 500000] | 5 | multiple sclerosis | http://purl.obolibrary.org/obo/MONDO_0005301 | GCST000783 | Genome-wide genotyping array | null | false | NA | false |
2010-06-14 | 20,512,145 | Bei JX | 2010-05-30 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20512145 | A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. | Nasopharyngeal carcinoma | 1,583 Chinese ancestry cases, 1,894 Chinese ancestry controls | 3,507 Chinese ancestry cases, 3,063 Chinese ancestry controls, 284 Chinese ancestry trios | Illumina [464328] | 7 | nasopharyngeal neoplasm | http://www.ebi.ac.uk/efo/EFO_0004252 | GCST000687 | Genome-wide genotyping array | null | false | NA | false |
2010-09-23 | 20,801,718 | Laaksovirta H | 2010-08-27 | Lancet Neurol | www.ncbi.nlm.nih.gov/pubmed/20801718 | Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. | Amyotrophic lateral sclerosis | 405 European ancestry cases, 497 European ancestry controls | NA | Illumina [318167] | 2 | amyotrophic lateral sclerosis | http://purl.obolibrary.org/obo/MONDO_0004976 | GCST000781 | Genome-wide genotyping array | null | false | NA | false |
2009-05-07 | 19,389,651 | Smith JG | 2009-02-15 | Heart Rhythm | www.ncbi.nlm.nih.gov/pubmed/19389651 | Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. | Electrocardiographic conduction measures | 1,262 Kosraen individuals | NA | Affymetrix [338049] | 7 | electrocardiography | http://www.ebi.ac.uk/efo/EFO_0004327 | GCST000344 | Genome-wide genotyping array | null | false | NA | false |
2009-09-09 | 19,714,205 | Hancock DB | 2009-08-28 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/19714205 | Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. | Asthma (childhood onset) | 492 Mexican ancestry trios | 177 Mexican ancestry trios | Illumina [520767] | 1 | childhood onset asthma | http://purl.obolibrary.org/obo/MONDO_0005405 | GCST000468 | Genome-wide genotyping array | null | false | NA | false |
2009-05-07 | 18,839,057 | Lesch KP | 2008-10-07 | J Neural Transm (Vienna) | www.ncbi.nlm.nih.gov/pubmed/18839057 | Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. | Attention deficit hyperactivity disorder | 343 European ancestry cases, 250 European ancestry controls, 54 controls | NA | Affymetrix [504219] | 26 | attention deficit hyperactivity disorder | http://www.ebi.ac.uk/efo/EFO_0003888 | GCST000246 | Genome-wide genotyping array | null | false | NA | false |
2009-11-18 | 19,851,299 | Johansson A | 2009-10-22 | Obesity (Silver Spring) | www.ncbi.nlm.nih.gov/pubmed/19851299 | Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. | Weight | Up to 3,925 European individuals | NA | Illumina [318237] | 9 | body weight | http://www.ebi.ac.uk/efo/EFO_0004338 | GCST000511 | Genome-wide genotyping array | null | false | NA | false |
2009-11-18 | 19,851,299 | Johansson A | 2009-10-22 | Obesity (Silver Spring) | www.ncbi.nlm.nih.gov/pubmed/19851299 | Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. | Body mass index | 1,079 South Tyrolean individuals, 790 Dutch founder individuals, 2,060 European ancestry individuals | NA | Illumina [318237] | 10 | body mass index | http://www.ebi.ac.uk/efo/EFO_0004340 | GCST000512 | Genome-wide genotyping array | null | false | NA | false |
2009-12-04 | 19,897,590 | Schaefer AS | 2009-11-06 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/19897590 | A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis. | Periodontitis | 283 European ancestry cases, 972 European ancestry controls | 155 European ancestry cases, 341 European ancestry controls | Affymetrix [345646] | 1 | periodontitis | http://www.ebi.ac.uk/efo/EFO_0000649 | GCST000521 | Genome-wide genotyping array | null | false | NA | false |
2009-08-21 | 19,620,980 | Skibola CF | 2009-07-20 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/19620980 | Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. | Follicular lymphoma | 189 European ancestry cases, 592 European controls | 456 European ancestry cases, 2,785 European ancestry controls | Illumina [~ 500000] | 1 | neoplasm of mature B-cells | http://www.ebi.ac.uk/efo/EFO_0000096 | GCST000448 | Genome-wide genotyping array | null | false | NA | false |
2010-09-28 | 20,838,585 | Smith EN | 2010-09-09 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/20838585 | Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. | Cardiovascular risk factors (age interaction) | 525 European ancestry individuals | 2,442 Finnish ancestry individuals | Illumina [2173391] (imputed) | 4 | triglyceride measurement, low density lipoprotein cholesterol measurement, waist circumference, cardiovascular disease, high density lipoprotein cholesterol measurement, age at assessment | http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://purl.obolibrary.org/obo/OBA_1001085, http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0008007 | GCST000789 | Genome-wide genotyping array | null | false | NA | true |
2017-09-12 | 20,838,585 | Smith EN | 2010-09-09 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/20838585 | Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. | Cardiovascular risk factors | 525 European ancestry individuals | 2,442 Finnish ancestry individuals | Illumina [2173391] (imputed) | 2 | triglyceride measurement, low density lipoprotein cholesterol measurement, waist circumference, cardiovascular disease, high density lipoprotein cholesterol measurement | http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://purl.obolibrary.org/obo/OBA_1001085, http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0004612 | GCST004704 | Genome-wide genotyping array | null | false | NA | false |
2012-01-27 | 22,199,011 | Murabito JM | 2011-12-23 | Circ Cardiovasc Genet | www.ncbi.nlm.nih.gov/pubmed/22199011 | Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. | Ankle-brachial index | 38,376 European ancestry individuals, 2,133 Erasmus Rucphen individuals, 1,183 Old Order Amish individuals | 16,717 European ancestry individuals | Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) | 2 | ankle brachial index | http://www.ebi.ac.uk/efo/EFO_0003912 | GCST001361 | Genome-wide genotyping array | null | false | NA | false |
2009-08-07 | 19,584,346 | Vasan RS | 2009-07-08 | JAMA | www.ncbi.nlm.nih.gov/pubmed/19584346 | Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. | Aortic root size | 12,612 European ancestry individuals | 4,094 European ancestry individuals | Affymetrix, Illumina [~ 2500000] (imputed) | 6 | bulb of aorta size | http://purl.obolibrary.org/obo/OBA_0005483 | GCST000442 | Genome-wide genotyping array | null | false | NA | false |
2009-08-07 | 19,584,346 | Vasan RS | 2009-07-08 | JAMA | www.ncbi.nlm.nih.gov/pubmed/19584346 | Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. | Cardiac structure and function | 12,612 European ancestry individuals | 4,094 European ancestry individuals | Affymetrix, Illumina [~ 2500000] (imputed) | 4 | cardiovascular measurement | http://www.ebi.ac.uk/efo/EFO_0004298 | GCST000441 | Genome-wide genotyping array | null | false | NA | false |
2010-09-23 | 20,729,853 | Wang LD | 2010-08-22 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20729853 | Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54. | Esophageal cancer | 1,077 Han Chinese ancestry cases, 1,733 Han Chinese ancestry controls | 7,673 Han Chinese ancestry cases, 11,013 Han Chinese ancestry controls, 303 Uygur-Kazakh Chinese ancestry cases, 537 Uygur-Kazakh Chinese ancestry controls | Illumina [506666] | 0 | esophageal carcinoma | http://www.ebi.ac.uk/efo/EFO_0002916 | GCST000776 | Genome-wide genotyping array | null | false | NA | false |
2009-12-01 | 19,874,204 | Guo Y | 2009-10-29 | J Bone Miner Res | www.ncbi.nlm.nih.gov/pubmed/19874204 | IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. | Bone mineral density | 983 European ancestry individuals | 2,557 European ancestry individuals from 750 families | Affymetrix [342854] | 2 | bone tissue density | http://purl.obolibrary.org/obo/OBA_1000110 | GCST000515 | Genome-wide genotyping array | null | false | NA | false |
2009-11-12 | 19,850,125 | Kim HJ | 2009-10-19 | Neurobiol Dis | www.ncbi.nlm.nih.gov/pubmed/19850125 | Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica. | Neuromyelitis optica | 53 Korean ancestry cases, 240 Korean ancestry controls | 37 Korean ancestry cases | Illumina [288025] | 0 | neuromyelitis optica | http://www.ebi.ac.uk/efo/EFO_0004256 | GCST000508 | Genome-wide genotyping array | null | false | NA | false |
2008-06-16 | 18,311,140 | Hunt KA | 2008-03-02 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/18311140 | Newly identified genetic risk variants for celiac disease related to the immune response. | Celiac disease | 767 European ancestry cases, 1,422 European ancestry controls | 1,643 European ancestry cases, 3,406 European ancestry controls | Illumina [310605] | 8 | celiac disease | http://www.ebi.ac.uk/efo/EFO_0001060 | GCST000157 | Genome-wide genotyping array | null | false | NA | false |
2008-06-16 | 18,264,096 | Thomas G | 2008-02-10 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/18264096 | Multiple loci identified in a genome-wide association study of prostate cancer. | Prostate cancer | 1,172 European ancestry cases, 1,157 European ancestry controls | 3,941 European ancestry cases, 3,964 European ancestry controls | Illumina [527869] | 7 | prostate carcinoma | http://www.ebi.ac.uk/efo/EFO_0001663 | GCST000154 | Genome-wide genotyping array | null | false | NA | false |
2009-12-18 | 19,944,697 | Karlsen TH | 2009-11-25 | Gastroenterology | www.ncbi.nlm.nih.gov/pubmed/19944697 | Genome-wide association analysis in primary sclerosing cholangitis. | Primary sclerosing cholangitis | 285 European ancestry cases, 298 European ancestry controls | 766 European ancestry cases, 2,935 European ancestry controls | Affymetrix [375487] | 0 | sclerosing cholangitis | http://www.ebi.ac.uk/efo/EFO_0004268 | GCST000534 | Genome-wide genotyping array | null | false | NA | false |
2015-04-23 | 19,875,614 | Paterson AD | 2009-10-29 | Diabetes | www.ncbi.nlm.nih.gov/pubmed/19875614 | A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. | Glycemic control in type 1 diabetes (HbA1c) | 667 European ancestry conventional treatment cases, 637 European ancestry intensive treatment cases | 1,382 European ancestry cases | Affymetrix, Illumina [2518578] (imputed) | 0 | HbA1c measurement | http://www.ebi.ac.uk/efo/EFO_0004541 | GCST000516 | Genome-wide genotyping array | null | false | NA | false |
2008-09-17 | 18,325,910 | Liu YJ | 2008-03-05 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/18325910 | Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. | Obesity | 1,000 European ancestry individuals | 896 European ancestry cases, 2,916 European ancestry controls | Affymetrix [379319] | 0 | obesity | http://www.ebi.ac.uk/efo/EFO_0001073 | GCST000159 | Genome-wide genotyping array | null | false | NA | false |
2008-09-17 | 18,327,256 | Doring A | 2008-03-09 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/18327256 | SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. | Urate levels | 1,644 European ancestry individuals | 9,947 European ancestry individuals | Affymetrix [335152] | 1 | urate measurement | http://www.ebi.ac.uk/efo/EFO_0004531 | GCST000161 | Genome-wide genotyping array | null | false | NA | false |
2009-09-04 | 19,648,919 | Song H | 2009-08-02 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/19648919 | A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. | Ovarian cancer | 1,817 European ancestry cases, 2,353 European ancestry controls | 6,944 European ancestry cases, 9,477 European ancestry controls | Illumina [up to 2000000] (imputed) | 1 | ovarian carcinoma | http://www.ebi.ac.uk/efo/EFO_0001075 | GCST000455 | Genome-wide genotyping array | null | false | NA | false |
2009-09-28 | 19,729,612 | Paterson AD | 2009-09-03 | Arterioscler Thromb Vasc Biol | www.ncbi.nlm.nih.gov/pubmed/19729612 | Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. | Soluble E-selectin levels | 685 European ancestry individuals with type 1 diabetes | 477 European ancestry individuals | Illumina [~ 841000] | 1 | E-selectin amount | http://purl.obolibrary.org/obo/OBA_2050324 | GCST000476 | Genome-wide genotyping array | null | false | NA | false |
2008-09-17 | 18,327,257 | Vitart V | 2008-03-09 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/18327257 | SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout. | Urate levels | 794 European ancestry individuals | 706 European ancestry individuals | Illumina [308140] | 1 | urate measurement | http://www.ebi.ac.uk/efo/EFO_0004531 | GCST000160 | Genome-wide genotyping array | null | false | NA | false |
2009-07-24 | 19,587,794 | Nolte IM | 2009-07-09 | PLoS One | www.ncbi.nlm.nih.gov/pubmed/19587794 | Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. | QT interval | 3,558 European ancestry individuals | 29,527 European ancestry individuals | Affymetrix, Illumina [~ 2399142] (imputed) | 2 | QT interval | http://www.ebi.ac.uk/efo/EFO_0004682 | GCST000444 | Genome-wide genotyping array | null | false | NA | false |
2013-11-29 | 23,727,862 | Savage SA | 2013-06-02 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/23727862 | Genome-wide association study identifies two susceptibility loci for osteosarcoma. | Osteosarcoma | 694 European ancestry cases, 2,703 European ancestry controls | 247 European ancestry cases, 550 European ancestry controls | Illumina [698968] | 6 | osteosarcoma | http://www.ebi.ac.uk/efo/EFO_0000637 | GCST002056 | Genome-wide genotyping array | null | false | NA | false |
2010-03-29 | 20,304,703 | Li Y | 2010-03-19 | Lancet Oncol | www.ncbi.nlm.nih.gov/pubmed/20304703 | Genetic variants and risk of lung cancer in never smokers: a genome-wide association study. | Lung cancer | 364 European ancestry cases, 364 European ancestry controls, 13 cases, 13 controls | 446 European ancestry cases, 853 European ancestry controls, 65 cases, 154 controls | Illumina [331918] | 1 | lung carcinoma | http://www.ebi.ac.uk/efo/EFO_0001071 | GCST000633 | Genome-wide genotyping array | null | false | NA | false |
2013-11-15 | 23,698,163 | Gong J | 2013-05-21 | Nutrients | www.ncbi.nlm.nih.gov/pubmed/23698163 | Genome-wide association study of serum selenium concentrations. | Serum selenium levels | 582 European ancestry individuals | 621 European ancestry individuals | Illumina [2474333] | 4 | serum selenium amount | http://purl.obolibrary.org/obo/OBA_2050059 | GCST002028 | Genome-wide genotyping array | null | false | NA | false |
2013-02-27 | 23,284,291 | Hancock DB | 2012-12-20 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/23284291 | Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. | Pulmonary function (smoking interaction) | 50,047 European ancestry individuals | NA | NR [~ 2500000] (imputed) | 53 | pulmonary function measurement, smoking behavior trait | http://www.ebi.ac.uk/efo/EFO_0003892, http://purl.obolibrary.org/obo/OBA_2050116 | GCST001784 | Genome-wide genotyping array | null | false | NA | true |
2008-09-25 | 18,794,855 | Kiemeney LA | 2008-09-14 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/18794855 | Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. | Urinary bladder cancer | 1,803 European ancestry cases, 34,336 European ancestry controls | 2,165 European ancestry cases, 3,800 European ancestry controls | Illumina [302140] | 2 | urinary bladder carcinoma | http://purl.obolibrary.org/obo/MONDO_0004986 | GCST000231 | Genome-wide genotyping array | null | false | NA | false |
2010-05-24 | 20,418,889 | Liu JZ | 2010-04-25 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20418889 | Meta-analysis and imputation refines the association of 15q25 with smoking quantity. | Smoking behavior | 41,150 European ancestry individuals | 120,516 European ancestry individuals | Affymetrix, Illumina [NR] (imputed) | 1 | smoking behavior | http://www.ebi.ac.uk/efo/EFO_0004318 | GCST000668 | Genome-wide genotyping array | null | false | NA | false |
2009-10-06 | 19,779,542 | Nakanishi H | 2009-09-25 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/19779542 | A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1. | Myopia (pathological) | 297 Japanese ancestry cases, 934 Japanese ancestry controls | 533 Japanese ancestry cases, 977 Japanese ancestry controls | Illumina [411777] | 1 | pathological myopia | http://www.ebi.ac.uk/efo/EFO_0004207 | GCST000491 | Genome-wide genotyping array | null | false | NA | false |
2009-12-03 | 19,902,172 | Palmer ND | 2009-11-10 | Diabetologia | www.ncbi.nlm.nih.gov/pubmed/19902172 | Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study. | Insulin-related traits | 229 Hispanic individuals from 34 families | 814 Hispanic family members | Illumina [309200] | 0 | insulin measurement | http://www.ebi.ac.uk/efo/EFO_0004467 | GCST000526 | Genome-wide genotyping array | null | false | NA | false |
2010-03-22 | 20,175,129 | Zhao LJ | 2009-12-11 | J Bone Miner Res | www.ncbi.nlm.nih.gov/pubmed/20175129 | Genome-wide association study for femoral neck bone geometry. | Femoral neck bone geometry | 987 European ancestry individuals | 1,488 European ancestry individuals, 2,118 Chinese ancestry individuals | Affymetrix [379319] | 0 | femoral neck bone geometry | http://www.ebi.ac.uk/efo/EFO_0004511 | GCST000541 | Genome-wide genotyping array | null | false | NA | false |
2011-04-11 | 21,378,988 | Coronary Artery Disease (C4D) Genetics Consortium | 2011-03-06 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/21378988 | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. | Coronary heart disease | 8,424 European ancestry cases, 7,268 European ancestry controls, 6,996 South Asian ancestry cases, 7,794 South Asian ancestry controls | 18,049 European ancestry cases, 16,357 European ancestry controls, 3,359 South Asian ancestry cases, 2,828 South Asian ancestry controls | Illumina [574919] | 19 | coronary artery disease | http://www.ebi.ac.uk/efo/EFO_0001645 | GCST000999 | Genome-wide genotyping array | null | false | NA | false |
2010-05-06 | 20,385,826 | Neale BM | 2010-04-12 | Proc Natl Acad Sci U S A | www.ncbi.nlm.nih.gov/pubmed/20385826 | Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). | Age-related macular degeneration | 979 cases, 1,709 controls | 868 European ancestry cases, 410 European ancestry controls, 4,921 cases, 3,824 controls | Affymetrix [632932] | 11 | age-related macular degeneration | http://www.ebi.ac.uk/efo/EFO_0001365 | GCST000653 | Genome-wide genotyping array | null | false | NA | false |
2010-07-04 | 20,548,944 | Hsu YH | 2010-06-10 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/20548944 | An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. | Osteoporosis-related phenotypes | 2,038 European ancestry female individuals, 1,531 European ancestry male individuals | 5,595 European ancestry female individuals, 2,126 European ancestry male individuals | Affymetrix [433510] | 7 | osteoporosis | http://www.ebi.ac.uk/efo/EFO_0003882 | GCST000698 | Genome-wide genotyping array | null | false | NA | false |
2010-04-12 | 20,304,771 | Newman AB | 2010-03-18 | J Gerontol A Biol Sci Med Sci | www.ncbi.nlm.nih.gov/pubmed/20304771 | A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. | Longevity | 1,836 European ancestry long-lived individuals, 1,955 European ancestry controls | 2,594 European ancestry long-lived individuals, 3,431 European ancestry controls | Affymetrix, Illumina [2287520] (imputed) | 1 | life span determination trait | http://purl.obolibrary.org/obo/OBA_VT0005372 | GCST000632 | Genome-wide genotyping array | null | false | NA | false |
2009-11-04 | 19,798,445 | Hicks AA | 2009-10-02 | PLoS Genet | www.ncbi.nlm.nih.gov/pubmed/19798445 | Genetic determinants of circulating sphingolipid concentrations in European populations. | Sphingolipid levels | 4,110 European ancestry individuals | NA | Illumina [318237] | 5 | sphingolipid level | http://purl.obolibrary.org/obo/OBA_1000965 | GCST000493 | Genome-wide genotyping array | null | false | NA | false |
2010-06-22 | 20,526,339 | Quan C | 2010-06-06 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/20526339 | Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. | Vitiligo | 1,117 Han Chinese ancestry cases, 1,429 Han Chinese ancestry controls | 6,623 East Asian ancestry cases, 10,740 East Asian ancestry controls | Illumina [493909] | 4 | Vitiligo | http://www.ebi.ac.uk/efo/EFO_0004208 | GCST000692 | Genome-wide genotyping array | null | false | NA | false |
2011-05-11 | 21,483,023 | Wu X | 2011-04-11 | J Natl Cancer Inst | www.ncbi.nlm.nih.gov/pubmed/21483023 | Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. | Response to platinum-based chemotherapy in non-small-cell lung cancer | 327 European ancestry individuals | 735 European ancestry individuals | Illumina [307260] | 1 | trait in response to platinum | http://purl.obolibrary.org/obo/OBA_2040037 | GCST001035 | Genome-wide genotyping array | null | false | NA | false |
2011-01-11 | 21,150,878 | Ferreira MA | 2010-12-08 | Eur J Hum Genet | www.ncbi.nlm.nih.gov/pubmed/21150878 | Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. | Asthma | 986 European ancestry cases, 1,846 European ancestry controls | 391 European ancestry cases, 213 European ancestry controls | Illumina [~ 2380000] (imputed) | 1 | asthma | http://purl.obolibrary.org/obo/MONDO_0004979 | GCST000910 | Genome-wide genotyping array | null | false | NA | false |
2013-05-02 | 18,514,160 | Arnaud-Lopez L | 2008-06-01 | Am J Hum Genet | www.ncbi.nlm.nih.gov/pubmed/18514160 | Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function. | Thyroid stimulating hormone levels | 4,300 Sardinian indivduals | 1,164 European ancestry individuals, 1,136 Old Order Amish individuals, 1,858 Sardinian individuals | Affymetrix [362129] | 1 | thyroid function | http://www.ebi.ac.uk/efo/EFO_0004296 | GCST000199 | Genome-wide genotyping array | null | false | NA | false |
2011-04-11 | 21,378,990 | Schunkert H | 2011-03-06 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/21378990 | Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. | Coronary heart disease | 22,233 European ancestry cases, 64,762 European ancestry controls | 56,682 European ancestry cases and controls | Affymetrix, Illumina [~ 2300000] (imputed) | 30 | coronary artery disease | http://www.ebi.ac.uk/efo/EFO_0001645 | GCST000998 | Genome-wide genotyping array | null | true | http://ftp.ebi.ac.uk/pub/databases/gwas/summary_statistics/GCST000001-GCST001000/GCST000998 | false |
2009-03-31 | 19,260,141 | Zemunik T | 2009-02-01 | Croat Med J | www.ncbi.nlm.nih.gov/pubmed/19260141 | Genome-wide association study of biochemical traits in Korcula Island, Croatia. | Biochemical measures | 898 Korculan (founder/genetic isolate) individuals | NA | Illumina [316730] | 17 | total cholesterol measurement, serum albumin amount, triglyceride measurement, low density lipoprotein cholesterol measurement, circulating fibrinogen levels, uric acid measurement, high density lipoprotein cholesterol measurement | http://www.ebi.ac.uk/efo/EFO_0004574, http://purl.obolibrary.org/obo/OBA_2050068, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://purl.obolibrary.org/obo/OBA_0000061, http://www.ebi.ac.uk/efo/EFO_0004761, http://www.ebi.ac.uk/efo/EFO_0004612 | GCST000328 | Genome-wide genotyping array | null | false | NA | false |
2010-11-15 | 20,932,654 | Kerns SL | 2010-10-05 | Int J Radiat Oncol Biol Phys | www.ncbi.nlm.nih.gov/pubmed/20932654 | Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. | Erectile dysfunction and prostate cancer treatment | 27 African American cases, 52 African American controls | NA | Affymetrix [512497] | 23 | response to radiation, prostate carcinoma, erectile dysfunction | http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_0004234 | GCST000824 | Genome-wide genotyping array | null | false | NA | false |
2010-06-21 | 20,516,156 | Lewis CM | 2010-06-01 | Am J Psychiatry | www.ncbi.nlm.nih.gov/pubmed/20516156 | Genome-wide association study of major recurrent depression in the U.K. population. | Major depressive disorder | 1,636 European ancestry cases, 1,594 European ancestry controls | 1,418 European ancestry cases, 1,918 European ancestry controls | Illumina [471747] | 4 | major depressive disorder | http://purl.obolibrary.org/obo/MONDO_0002009 | GCST000689 | Genome-wide genotyping array | null | false | NA | false |
2009-05-11 | 19,403,135 | Yamada Y | 2009-04-05 | Atherosclerosis | www.ncbi.nlm.nih.gov/pubmed/19403135 | Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. | Stroke (ischemic) | 131 Japanese ancestry cases, 135 Japanese ancestry controls | 776 Japanese ancestry cases, 5,205 Japanese ancestry controls | Affymetrix [~ 520000] | 0 | stroke | http://www.ebi.ac.uk/efo/EFO_0000712 | GCST000373 | Genome-wide genotyping array | null | false | NA | false |
2010-03-15 | 20,167,578 | Barbalic M | 2010-02-18 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/20167578 | Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. | Soluble levels of adhesion molecules | Up to 9,813 European ancestry individuals | NA | Affymetrix, Illumina [~ 2500000] (imputed) | 5 | adhesion molecule measurement | http://www.ebi.ac.uk/efo/EFO_0004522 | GCST000599 | Genome-wide genotyping array | null | false | NA | false |
2009-04-01 | 19,303,062 | Tanaka T | 2009-03-18 | Am J Hum Genet | www.ncbi.nlm.nih.gov/pubmed/19303062 | Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. | Folate pathway vitamin levels | 2,934 European ancestry individuals | 686 European ancestry individuals | Affymetrix, Illumina [~ 2500000] (imputed) | 5 | vitamin B measurement, vitamin B12 measurement, vitamin B6 measurement | http://www.ebi.ac.uk/efo/EFO_0004843, http://www.ebi.ac.uk/efo/EFO_0004620, http://www.ebi.ac.uk/efo/EFO_0004621 | GCST000358 | Genome-wide genotyping array | null | false | NA | false |
2011-04-13 | 21,423,239 | Willour VL | 2011-03-25 | Mol Psychiatry | www.ncbi.nlm.nih.gov/pubmed/21423239 | A genome-wide association study of attempted suicide. | Suicide attempts in bipolar disorder | 1,201 European and unknown ancestry attempters, 1,497 European and unknown ancestry non-attempters | 1,295 attempters, 1,822 non-attempters | Affymetrix, Illumina [2408051] (imputed) | 3 | attempted suicide | http://www.ebi.ac.uk/efo/EFO_0004321 | GCST001015 | Genome-wide genotyping array | null | false | NA | false |
2011-01-03 | 21,041,692 | Denny JC | 2010-11-01 | Circulation | www.ncbi.nlm.nih.gov/pubmed/21041692 | Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. | Atrioventricular conduction | 2,334 European ancestry individuals | NA | Illumina [514999] | 5 | heart function attribute | http://purl.obolibrary.org/obo/OBA_2045275 | GCST000852 | Genome-wide genotyping array | null | false | NA | false |
2011-01-14 | 21,130,836 | Luciano M | 2010-12-03 | Biol Psychol | www.ncbi.nlm.nih.gov/pubmed/21130836 | Whole genome association scan for genetic polymorphisms influencing information processing speed. | Information processing speed | Up to 4,039 European ancestry individuals | NA | Illumina [~ 610000] | 25 | information processing speed | http://www.ebi.ac.uk/efo/EFO_0004363 | GCST000905 | Genome-wide genotyping array | null | false | NA | false |
2011-01-11 | 21,057,379 | Curtis D | 2010-11-04 | Psychiatr Genet | www.ncbi.nlm.nih.gov/pubmed/21057379 | Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. | Bipolar disorder and schizophrenia | 506 European ancestry bipolar 1 disorder cases, 523 European ancestry schizophrenia cases, 505 European ancestry controls | NA | Affymetrix [302482] | 6 | mental or behavioural disorder | http://www.ebi.ac.uk/efo/EFO_0000677 | GCST000862 | Genome-wide genotyping array | null | false | NA | false |
2011-04-13 | 21,441,570 | Grassi MA | 2011-03-26 | Hum Mol Genet | www.ncbi.nlm.nih.gov/pubmed/21441570 | Genome-wide meta-analysis for severe diabetic retinopathy. | Diabetic retinopathy | 973 European ancestry cases, 1,856 European ancestry controls | NA | Affymetrix, Illumina [2543887] (imputed) | 19 | diabetic retinopathy | http://www.ebi.ac.uk/efo/EFO_0003770 | GCST001017 | Genome-wide genotyping array | null | false | NA | false |
2011-01-03 | 21,184,583 | Zlojutro M | 2010-11-02 | Am J Med Genet B Neuropsychiatr Genet | www.ncbi.nlm.nih.gov/pubmed/21184583 | Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. | Event-related brain oscillations | 431 European ancestry alcohol dependence cases, 340 European ancestry controls, 209 African American alcohol dependence cases, 84 African American controls | 683 alcohol dependence cases and 412 controls from multiplex families | Illumina [951071] | 3 | event-related brain oscillation | http://www.ebi.ac.uk/efo/EFO_0004358 | GCST000857 | Genome-wide genotyping array | null | false | NA | false |
2012-02-25 | 22,290,723 | Ryu J | 2012-01-30 | Hum Mutat | www.ncbi.nlm.nih.gov/pubmed/22290723 | Association of glycosylated hemoglobin with the gene encoding CDKAL1 in the Korean Association Resource (KARE) study. | Glycated hemoglobin levels | 4,275 Korean ancestry individuals | 3,782 Korean ancestry individuals | Affymetrix [1693116] (imputed) | 1 | HbA1c measurement | http://www.ebi.ac.uk/efo/EFO_0004541 | GCST001393 | Genome-wide genotyping array | null | false | NA | false |
2013-10-24 | 23,563,609 | Wheeler E | 2013-04-07 | Nat Genet | www.ncbi.nlm.nih.gov/pubmed/23563609 | Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. | Obesity (early onset extreme) | 1,509 European ancestry cases, 5,380 European ancestry controls | 971 European ancestry cases, 1,990 European ancestry controls | Affymetrix [~ 2000000] (imputed) | 18 | obesity | http://www.ebi.ac.uk/efo/EFO_0001073 | GCST001957 | Genome-wide genotyping array | null | false | NA | false |
2009-01-21 | 19,118,814 | Beecham GW | 2009-01-03 | Am J Hum Genet | www.ncbi.nlm.nih.gov/pubmed/19118814 | Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. | Alzheimer's disease | 492 European ancestry cases, 496 European ancestry controls | 238 European ancestry cases, 220 European ancestry controls | Illumina [~ 2500000] (imputed) | 3 | Alzheimer disease | http://purl.obolibrary.org/obo/MONDO_0004975 | GCST000310 | Genome-wide genotyping array | null | false | NA | false |
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