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.
Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity.
Am J Hum Genet
; 109(2): 223-239, 2022 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35085493
3.
Single-cell sequencing reveals lineage-specific dynamic genetic regulation of gene expression during human cardiomyocyte differentiation.
PLoS Genet
; 18(1): e1009666, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35061661
4.
The impact of rare variation on gene expression across tissues.
Nature
; 550(7675): 239-243, 2017 10 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29022581
5.
SURGE: uncovering context-specific genetic-regulation of gene expression from single-cell RNA sequencing using latent-factor models.
Genome Biol
; 25(1): 28, 2024 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38254214
6.
Fine-mapping causal tissues and genes at disease-associated loci.
medRxiv
; 2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37961337
7.
Single-cell allele-specific expression analysis reveals dynamic and cell-type-specific regulatory effects.
Nat Commun
; 14(1): 6317, 2023 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37813843
8.
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection.
medRxiv
; 2023 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38106023
9.
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection.
Res Sq
; 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38168385
10.
The functional impact of rare variation across the regulatory cascade.
Cell Genom
; 3(10): 100401, 2023 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37868038
11.
Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types.
Elife
; 112022 02 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35142607
12.
Transcriptomic signatures across human tissues identify functional rare genetic variation.
Science
; 369(6509)2020 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32913073
13.
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.
Nat Med
; 25(6): 911-919, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31160820
14.
A method to predict the impact of regulatory variants from DNA sequence.
Nat Genet
; 47(8): 955-61, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26075791