Detalhe da pesquisa
1.
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.
Nucleic Acids Res
; 49(D1): D1311-D1320, 2021 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33045747
2.
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.
PLoS Genet
; 16(11): e1009077, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33175840
3.
Genes for Good: Engaging the Public in Genetics Research via Social Media.
Am J Hum Genet
; 105(1): 65-77, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204010
4.
Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative.
Am J Hum Genet
; 102(6): 1048-1061, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29779563
5.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
; 102(1): 103-115, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29290336
6.
New genetic loci link adipose and insulin biology to body fat distribution.
Nature
; 518(7538): 187-196, 2015 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25673412
7.
Genetic studies of body mass index yield new insights for obesity biology.
Nature
; 518(7538): 197-206, 2015 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25673413
8.
A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWAS.
Am J Hum Genet
; 101(1): 37-49, 2017 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28602423
9.
Genes for Good: Engaging the Public in Genetics Research via Social Media.
Am J Hum Genet
; 105(2): 441-442, 2019 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31374205
10.
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Am J Hum Genet
; 94(2): 233-45, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24507775
11.
GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach.
Bioinformatics
; 31(16): 2601-6, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25886982
12.
The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients.
Cell Genom
; 3(2): 100257, 2023 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36819667
13.
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
; 54(5): 560-572, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35551307
14.
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.
Nat Genet
; 53(11): 1527-1533, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34711957
15.
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.
Nat Commun
; 11(1): 4432, 2020 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32887874
16.
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry.
Nat Neurosci
; 22(3): 503, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30622366
17.
Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection.
Circ Genom Precis Med
; 12(6): e002476, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31211624
18.
Genetic variants and acute kidney injury: A review of the literature.
J Crit Care
; 44: 203-211, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29161666
19.
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry.
Nat Neurosci
; 21(1): 16-18, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29230059
20.
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry.
Nat Neurosci
; 21(7): 1018, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29752479