Detalhe da pesquisa
1.
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.
Cell
; 179(3): 589-603, 2019 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31607513
2.
The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature
; 581(7809): 434-443, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32461654
3.
Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder.
Psychol Med
; 53(4): 1196-1204, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34231451
4.
Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature
; 597(7874): E3-E4, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34373650
5.
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature
; 590(7846): E53, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33536625
6.
RICOPILI: Rapid Imputation for COnsortias PIpeLIne.
Bioinformatics
; 36(3): 930-933, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31393554
7.
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.
Mol Psychiatry
; 25(8): 1673-1687, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32099098
8.
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Addict Biol
; 26(1): e12880, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32064741
9.
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Am J Hum Genet
; 100(4): 635-649, 2017 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28366442
10.
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Am J Hum Genet
; 107(4): 788-789, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33007199
11.
Epi2Loc: an R package to investigate two-locus epistatic models.
Twin Res Hum Genet
; 17(4): 272-8, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24983251
12.
Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes.
Nat Genet
; 56(3): 377-382, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38182742
13.
An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data.
Bioinformatics
; 28(20): 2615-23, 2012 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22847933
14.
Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci.
Nat Hum Behav
; 7(8): 1371-1387, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37386106
15.
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
Nat Genet
; 55(2): 198-208, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36702997
16.
The addiction risk factor: A unitary genetic vulnerability characterizes substance use disorders and their associations with common correlates.
Neuropsychopharmacology
; 47(10): 1739-1745, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34750568
17.
The female protective effect against autism spectrum disorder.
Cell Genom
; 2(6): 100134, 2022 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36778135
18.
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups.
Nat Genet
; 54(10): 1470-1478, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36163277
19.
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.
Nat Commun
; 12(1): 576, 2021 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33495439
20.
Genetic analyses identify widespread sex-differential participation bias.
Nat Genet
; 53(5): 663-671, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888908