Detalhe da pesquisa
1.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450978
2.
Divergent role of Mitochondrial Amidoxime Reducing Component 1 (MARC1) in human and mouse.
PLoS Genet
; 20(3): e1011179, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38437227
3.
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies.
Am J Hum Genet
; 109(9): 1638-1652, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055212
4.
Germline Mutations in CIDEB and Protection against Liver Disease.
N Engl J Med
; 387(4): 332-344, 2022 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939579
5.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
6.
Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals.
Arterioscler Thromb Vasc Biol
; 42(4): 484-501, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34852643
7.
Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration-Brief Report.
Arterioscler Thromb Vasc Biol
; 41(5): 1792-1800, 2021 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33730874
8.
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
Am J Hum Genet
; 103(5): 691-706, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30388399
9.
Directional dominance on stature and cognition in diverse human populations.
Nature
; 523(7561): 459-462, 2015 Jul 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26131930
10.
A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans.
Nutr J
; 20(1): 71, 2021 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34315477
11.
Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples.
J Nutr
; 150(10): 2635-2645, 2020 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32840624
12.
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
Circ Res
; 122(3): 433-443, 2018 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29212778
13.
Circulating total bilirubin and risk of non-alcoholic fatty liver disease in the PREVEND study: observational findings and a Mendelian randomization study.
Eur J Epidemiol
; 35(2): 123-137, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31773475
14.
Genetics and the heart rate response to exercise.
Cell Mol Life Sci
; 76(12): 2391-2409, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30919020
15.
Discovery of novel heart rate-associated loci using the Exome Chip.
Hum Mol Genet
; 26(12): 2346-2363, 2017 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28379579
16.
Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci.
Am J Nephrol
; 49(3): 193-202, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30808845
17.
Genetic Obesity and the Risk of Atrial Fibrillation: Causal Estimates from Mendelian Randomization.
Circulation
; 135(8): 741-754, 2017 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-27974350
18.
Genetic Risk Prediction of Atrial Fibrillation.
Circulation
; 135(14): 1311-1320, 2017 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27793994
19.
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.
Hum Mol Genet
; 25(10): 2093-2103, 2016 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26962151
20.
FTO genotype is associated with phenotypic variability of body mass index.
Nature
; 490(7419): 267-72, 2012 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-22982992