Detalhe da pesquisa
1.
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease.
Cell
; 184(10): 2633-2648.e19, 2021 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33864768
2.
RNA editing underlies genetic risk of common inflammatory diseases.
Nature
; 608(7923): 569-577, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35922514
3.
Integration of rare expression outlier-associated variants improves polygenic risk prediction.
Am J Hum Genet
; 109(6): 1055-1064, 2022 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35588732
4.
An integrated approach to identify environmental modulators of genetic risk factors for complex traits.
Am J Hum Genet
; 108(10): 1866-1879, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34582792
5.
A single-cell CRISPRi platform for characterizing candidate genes relevant to metabolic disorders in human adipocytes.
Am J Physiol Cell Physiol
; 325(3): C648-C660, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37486064
6.
Transcriptomics and chromatin accessibility in multiple African population samples.
bioRxiv
; 2023 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37986808
7.
Multiple causal variants underlie genetic associations in humans.
Science
; 375(6586): 1247-1254, 2022 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35298243
8.
Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genes.
Genome Med
; 14(1): 31, 2022 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35292083
9.
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics.
Nat Genet
; 53(3): 313-321, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33664507
10.
Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases.
Nat Genet
; 52(11): 1158-1168, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33106633
11.
FAM13A affects body fat distribution and adipocyte function.
Nat Commun
; 11(1): 1465, 2020 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32193374
12.
Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms.
Commun Biol
; 2: 186, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31123710
13.
Genetic regulation of gene expression and splicing during a 10-year period of human aging.
Genome Biol
; 20(1): 230, 2019 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31684996
14.
Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure.
Nat Commun
; 10(1): 2760, 2019 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31235787
15.
Population- and individual-specific regulatory variation in Sardinia.
Nat Genet
; 49(5): 700-707, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28394350
16.
Abundant associations with gene expression complicate GWAS follow-up.
Nat Genet
; 51(5): 768-769, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31043754