Detalhe da pesquisa
1.
A deep catalogue of protein-coding variation in 983,578 individuals.
Nature
; 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38768635
2.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450978
3.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662886
4.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
5.
Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study.
Psychol Med
; 53(1): 217-226, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33949298
6.
Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci.
Mol Psychiatry
; 27(10): 3970-3979, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35879402
7.
Gene-gene interaction between DRD4 and COMT modulates clinical response to clozapine in treatment-resistant schizophrenia.
Pharmacogenet Genomics
; 28(1): 31-35, 2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29087970
8.
Polygenic Risk of Mental Disorders and Subject-Specific School Grades.
Biol Psychiatry
; 2023 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38061465
9.
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity.
Sci Rep
; 13(1): 429, 2023 01 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36624241
10.
A large meta-analysis identifies genes associated with anterior uveitis.
Nat Commun
; 14(1): 7300, 2023 11 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37949852
11.
Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Nat Genet
; 55(7): 1138-1148, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37308787
12.
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications.
Nat Genet
; 55(12): 2094-2103, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37985822
13.
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.
Nat Med
; 29(7): 1832-1844, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37464041
14.
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
15.
A deep catalog of protein-coding variation in 985,830 individuals.
bioRxiv
; 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37214792
16.
Genome-wide by Environment Interaction Study of Stressful Life Events and Hospital-Treated Depression in the iPSYCH2012 Sample.
Biol Psychiatry Glob Open Sci
; 2(4): 400-410, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36324662
17.
Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder.
Nat Genet
; 54(8): 1117-1124, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35927488
18.
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
19.
Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.
Lancet Child Adolesc Health
; 5(3): 201-209, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33453761
20.
Genetic analyses identify widespread sex-differential participation bias.
Nat Genet
; 53(5): 663-671, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888908