Detalhe da pesquisa
1.
A deep catalogue of protein-coding variation in 983,578 individuals.
Nature
; 2024 May 20.
Artigo
Inglês
| MEDLINE | ID: mdl-38768635
2.
Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 622(7984): 784-793, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37821707
3.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34662886
4.
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Nature
; 586(7831): 749-756, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-33087929
5.
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 626(8001): E18, 2024 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-38332034
6.
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.
Am J Hum Genet
; 108(7): 1350-1355, 2021 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34115965
7.
Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals.
Genet Epidemiol
; 45(6): 664-681, 2021 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34184762
8.
Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation.
Platelets
; 30(2): 164-173, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-29185836
9.
Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response.
Pharmacogenet Genomics
; 27(4): 159-163, 2017 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28207573
10.
Familial aggregation of tobacco use behaviors among Amish men.
Nicotine Tob Res
; 16(7): 923-30, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24583363
11.
A deep catalog of protein-coding variation in 985,830 individuals.
bioRxiv
; 2023 Nov 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37214792
12.
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.
Nat Commun
; 13(1): 6914, 2022 11 14.
Artigo
Inglês
| MEDLINE | ID: mdl-36376295
13.
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease.
Nat Genet
; 54(4): 382-392, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35241825
14.
Computationally efficient whole-genome regression for quantitative and binary traits.
Nat Genet
; 53(7): 1097-1103, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34017140
15.
The genomics of heart failure: design and rationale of the HERMES consortium.
ESC Heart Fail
; 8(6): 5531-5541, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34480422
16.
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk.
Nat Commun
; 11(1): 4093, 2020 10 23.
Artigo
Inglês
| MEDLINE | ID: mdl-33097703
17.
Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium.
Clin Pharmacol Ther
; 108(5): 1067-1077, 2020 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32472697
18.
Pharmacogenomic polygenic response score predicts ischaemic events and cardiovascular mortality in clopidogrel-treated patients.
Eur Heart J Cardiovasc Pharmacother
; 6(4): 203-210, 2020 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31504375
19.
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nat Commun
; 11(1): 163, 2020 01 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31919418
20.
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nat Genet
; 50(9): 1234-1239, 2018 09.
Artigo
Inglês
| MEDLINE | ID: mdl-30061737