Detalhe da pesquisa
1.
Significance tests for R2 of out-of-sample prediction using polygenic scores.
Am J Hum Genet
; 110(2): 349-358, 2023 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36702127
2.
Mitigating type 1 error inflation and power loss in GxE PRS: Genotype-environment interaction in polygenic risk score models.
Genet Epidemiol
; 48(2): 85-100, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38303123
3.
Genetic correlations of polygenic disease traits: from theory to practice.
Nat Rev Genet
; 20(10): 567-581, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31171865
4.
Phenotypic variance partitioning by transcriptomic gene expression levels and environmental variables for anthropometric traits using GTEx data.
Genet Epidemiol
; 47(7): 465-474, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37318147
5.
Unraveling phenotypic variance in metabolic syndrome through multi-omics.
Hum Genet
; 143(1): 35-47, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38095720
6.
Cross-ancestry genetic architecture and prediction for cholesterol traits.
Hum Genet
; 143(5): 635-648, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38536467
7.
Host genetic determinants of COVID-19 susceptibility and severity: A systematic review and meta-analysis.
Rev Med Virol
; 33(5): e2466, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37303119
8.
Integrative analysis of genomic and exposomic influences on youth mental health.
J Child Psychol Psychiatry
; 63(10): 1196-1205, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35946823
9.
Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.
Am J Hum Genet
; 102(6): 1185-1194, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754766
10.
Adiposity and cancer: a Mendelian randomization analysis in the UK biobank.
Int J Obes (Lond)
; 45(12): 2657-2665, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34453097
11.
RICOPILI: Rapid Imputation for COnsortias PIpeLIne.
Bioinformatics
; 36(3): 930-933, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31393554
12.
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.
Am J Hum Genet
; 96(2): 283-94, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25640677
13.
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
Am J Hum Genet
; 95(5): 535-52, 2014 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-25439723
14.
Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.
Am J Hum Genet
; 93(3): 463-70, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23954163
15.
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
PLoS Genet
; 9(10): e1003864, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24204291
16.
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.
Hum Mol Genet
; 22(4): 832-41, 2013 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23193196
17.
Heterogeneity of genetic architecture of body size traits in a free-living population.
Mol Ecol
; 24(8): 1810-30, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25753777
18.
GCTA: a tool for genome-wide complex trait analysis.
Am J Hum Genet
; 88(1): 76-82, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21167468
19.
GCTA-GREML accounts for linkage disequilibrium when estimating genetic variance from genome-wide SNPs.
Proc Natl Acad Sci U S A
; 113(32): E4579-80, 2016 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27457963
20.
A Metabolome-Wide Mendelian Randomization Study Identifies Dysregulated Arachidonic Acid Synthesis as a Potential Causal Risk Factor for Bipolar Disorder.
Biol Psychiatry
; 2024 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38401803