Summary statistics are available for download from the GWAS Catalog.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
Vuckovic D, et al.
Cell. 2020 Sep 3;182(5):1214-1231.e11. doi: 10.1016/j.cell.2020.08.008.
PMID: 32888494
Summary statistics are available for download from the GWAS Catalog.
Genome-wide association study identifies 48 common genetic variants associated with handedness.
Cuellar-Partida G, et al.
Nat Hum Behav. 2021 Jan;5(1):59-70. doi: 10.1038/s41562-020-00956-y. Epub 2020 Sep 28.
PMID: 32989287
Summary statistics are available for download from the authors.
Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Koyama S, et al.
Nat Genet. 2020 Nov;52(11):1169-1177. doi: 10.1038/s41588-020-0705-3. Epub 2020 Oct 5.
PMID: 33020668
Summary statistics are available for download from the GWAS Catalog.
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.
Vogelezang S, et al.
PLoS Genet. 2020 Oct 12;16(10):e1008718. doi: 10.1371/journal.pgen.1008718. eCollection 2020 Oct.
PMID: 33045005
Summary statistics are available for download from the GWAS Catalog.
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.
Tan MMX, et al.
Mov Disord. 2021 Feb;36(2):424-433. doi: 10.1002/mds.28342. Epub 2020 Oct 28.
PMID: 33111402
Summary statistics are available for download from the authors.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Gorski M, et al.
Kidney Int. 2021 Apr;99(4):926-939. doi: 10.1016/j.kint.2020.09.030. Epub 2020 Oct 31.
PMID: 33137338
Summary statistics are available for download from the GWAS Catalog.
The genetic architecture of sporadic and multiple consecutive miscarriage.
Laisk T, et al.
Nat Commun. 2020 Nov 25;11(1):5980. doi: 10.1038/s41467-020-19742-5.
PMID: 33239672
Summary statistics are available for download from the authors.
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
Lin BM, et al.
EBioMedicine. 2021 Jan;63:103157. doi: 10.1016/j.ebiom.2020.103157. Epub 2021 Jan 6.
PMID: 33418499
Summary statistics are available for download from the GWAS Catalog.
GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility.
Eriksson D, et al.
Nat Commun. 2021 Feb 11;12(1):959. doi: 10.1038/s41467-021-21015-8.
PMID: 33574239
Summary statistics are available for download from the GWAS Catalog.
Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes.
Schwartzentruber J, et al.
Nat Genet. 2021 Mar;53(3):392-402. doi: 10.1038/s41588-020-00776-w. Epub 2021 Feb 15.
PMID: 33589840