Summary statistics are available for download from the GWAS Catalog.
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.
Levin MG, et al.
Nat Commun. 2022 Nov 14;13(1):6914. doi: 10.1038/s41467-022-34216-6.
PMID: 36376295
Summary statistics are available for download from the GWAS Catalog.
Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
Hübel C, et al.
Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):428-438. doi: 10.1002/ajmg.b.32709.
PMID: 30593698
Summary statistics are available for download from the GWAS Catalog.
Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
Hübel C, et al.
Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):428-438. doi: 10.1002/ajmg.b.32709.
PMID: 30593698
Summary statistics are available for download from the GWAS Catalog.
Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
Hübel C, et al.
Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):428-438. doi: 10.1002/ajmg.b.32709.
PMID: 30593698
Summary statistics are available for download from the GWAS Catalog.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Helgeland Ø, et al.
Nat Commun. 2019 Oct 1;10(1):4448. doi: 10.1038/s41467-019-12308-0.
PMID: 31575865
Summary statistics are available for download from the GWAS Catalog.
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes.
Forgetta V, et al.
Diabetes. 2020 Apr;69(4):784-795. doi: 10.2337/db19-0831.
PMID: 32005708
Summary statistics are available for download from the GWAS Catalog.
Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits.
Choudhury A, Brandenburg J-T, et al.
Nat Commun. 2022 May 11;13(1):2578. doi: 10.1038/s41467-022-30098-w.
PMID: 35546142
Summary statistics are available for download from the GWAS Catalog.
Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study.
Cai L, et al.
Sci Data. 2020 Nov 13;7(1):393. doi: 10.1038/s41597-020-00716-7.
PMID: 33188205
Summary statistics are available for download from the GWAS Catalog.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Barton AR, et al.
Nat Genet. 2021 Aug;53(8):1260-1269. doi: 10.1038/s41588-021-00892-1.
PMID: 34226706
This dataset was generated by members of the Global Parkinson's Genetics Program (GP2). Find more information at the GP2 website. If you wish to publish analyses using these results, please see the GP2 publication policy.