Detalhe da pesquisa
1.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
Cell
; 167(5): 1415-1429.e19, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27863252
2.
The impact of fatty acids biosynthesis on the risk of cardiovascular diseases in Europeans and East Asians: a Mendelian randomization study.
Hum Mol Genet
; 31(23): 4034-4054, 2022 11 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35796550
3.
Genomic atlas of the human plasma proteome.
Nature
; 558(7708): 73-79, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875488
4.
Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses.
Circulation
; 146(20): 1507-1517, 2022 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36314129
5.
A robust mean and variance test with application to high-dimensional phenotypes.
Eur J Epidemiol
; 37(4): 377-387, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34651232
6.
The Effect of Attention Deficit/Hyperactivity Disorder on Physical Health Outcomes: A 2-Sample Mendelian Randomization Study.
Am J Epidemiol
; 190(6): 1047-1055, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33324987
7.
PhenoScanner V2: an expanded tool for searching human genotype-phenotype associations.
Bioinformatics
; 35(22): 4851-4853, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31233103
8.
Semiparametric methods for estimation of a nonlinear exposure-outcome relationship using instrumental variables with application to Mendelian randomization.
Genet Epidemiol
; 41(4): 341-352, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28317167
9.
PhenoScanner: a database of human genotype-phenotype associations.
Bioinformatics
; 32(20): 3207-3209, 2016 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27318201
10.
Coding and regulatory variants are associated with serum protein levels and disease.
Nat Commun
; 13(1): 481, 2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079000
11.
The EWAS Catalog: a database of epigenome-wide association studies.
Wellcome Open Res
; 7: 41, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35592546
12.
A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits.
Nat Commun
; 12(1): 764, 2021 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33536417
13.
Sclerostin Downregulation Globally by Naturally Occurring Genetic Variants, or Locally in Atherosclerotic Plaques, Does Not Associate With Cardiovascular Events in Humans.
J Bone Miner Res
; 36(7): 1326-1339, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33784435
14.
DNA methylation signatures of adolescent victimization: analysis of a longitudinal monozygotic twin sample.
Epigenetics
; 16(11): 1169-1186, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33371772
15.
A robust and efficient method for Mendelian randomization with hundreds of genetic variants.
Nat Commun
; 11(1): 376, 2020 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31953392
16.
MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data.
Wellcome Open Res
; 5: 252, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33381656
17.
Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases.
Nat Genet
; 52(10): 1122-1131, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32895551
18.
Body mass index and all cause mortality in HUNT and UK Biobank studies: linear and non-linear mendelian randomisation analyses.
BMJ
; 364: l1042, 2019 03 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30957776
19.
Genetic data do not provide evidence that lower sclerostin is associated with increased risk of atherosclerosis: comment on the article by Zheng et al.
Arthritis Rheumatol
; 2023 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37942677
20.
Longitudinal analysis strategies for modelling epigenetic trajectories.
Int J Epidemiol
; 47(2): 516-525, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29462323