Detalhe da pesquisa
1.
The human genetic epidemiology of COVID-19.
Nat Rev Genet
; 23(9): 533-546, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35501396
2.
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature
; 604(7906): 509-516, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396579
3.
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets.
Nature
; 595(7865): 107-113, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33915569
4.
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
5.
Fast estimation of genetic correlation for biobank-scale data.
Am J Hum Genet
; 109(1): 24-32, 2022 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34861179
6.
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
PLoS Genet
; 18(11): e1010367, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36327219
7.
Detailed stratified GWAS analysis for severe COVID-19 in four European populations.
Hum Mol Genet
; 31(23): 3945-3966, 2022 11 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35848942
8.
HAPNEST: efficient, large-scale generation and evaluation of synthetic datasets for genotypes and phenotypes.
Bioinformatics
; 39(9)2023 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37647640
9.
Patterns of reproductive health in inflammatory rheumatic diseases and other immune-mediated diseases: a nationwide registry study.
Rheumatology (Oxford)
; 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38503536
10.
The impact of rare variation on gene expression across tissues.
Nature
; 550(7675): 239-243, 2017 10 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29022581
11.
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
12.
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
13.
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 15(5): e1008190, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31145742
14.
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Am J Hum Genet
; 102(6): 1204-1211, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29861106
15.
Discriminating bipolar depression from major depressive disorder with polygenic risk scores.
Psychol Med
; 51(9): 1451-1458, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32063240
16.
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 14(5): e1007329, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29795570
17.
Variant Score Ranker-a web application for intuitive missense variant prioritization.
Bioinformatics
; 35(21): 4478-4479, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31086968
18.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
Nature
; 514(7520): 92-97, 2014 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25231870
19.
Correction: Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study.
PLoS Genet
; 13(9): e1007002, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28910285
20.
A Multi-Cohort Metabolomics Analysis Discloses Sphingomyelin (32:1) Levels to be Inversely Related to Incident Ischemic Stroke.
J Stroke Cerebrovasc Dis
; 29(2): 104476, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31806450