Detalhe da pesquisa
1.
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.
Nature
; 559(7714): 350-355, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29995854
2.
Annotations capturing cell type-specific TF binding explain a large fraction of disease heritability.
Hum Mol Genet
; 29(7): 1057-1067, 2020 05 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31595288
3.
Motif-Raptor: a cell type-specific and transcription factor centric approach for post-GWAS prioritization of causal regulators.
Bioinformatics
; 37(15): 2103-2111, 2021 Aug 09.
Artigo
Inglês
| MEDLINE | ID: mdl-33532840
4.
Sequential regulatory activity prediction across chromosomes with convolutional neural networks.
Genome Res
; 28(5): 739-750, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29588361
5.
Estimating cross-population genetic correlations of causal effect sizes.
Genet Epidemiol
; 43(2): 180-188, 2019 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-30474154
6.
Interaction Patterns of Men Who Have Sex With Men on a Geosocial Networking Mobile App in Seven United States Metropolitan Areas: Observational Study.
J Med Internet Res
; 21(9): e13766, 2019 09 12.
Artigo
Inglês
| MEDLINE | ID: mdl-31516124
7.
Cleaning up the record on the maximal information coefficient and equitability.
Proc Natl Acad Sci U S A
; 111(33): E3362-3, 2014 Aug 19.
Artigo
Inglês
| MEDLINE | ID: mdl-25139972
8.
Co-varying neighborhood analysis identifies cell populations associated with phenotypes of interest from single-cell transcriptomics.
Nat Biotechnol
; 40(3): 355-363, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34675423
9.
Functionally informed fine-mapping and polygenic localization of complex trait heritability.
Nat Genet
; 52(12): 1355-1363, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33199916
10.
Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits.
Nat Genet
; 50(7): 1041-1047, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29942083
11.
Identifying genetic variants that influence the abundance of cell states in single-cell data.
bioRxiv
; 2023 Nov 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38014313
12.
Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk.
Nat Genet
; 50(10): 1483-1493, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30177862
13.
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
Nat Genet
; 50(4): 621-629, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29632380
14.
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Nat Genet
; 50(4): 538-548, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29632383
15.
Reference-based phasing using the Haplotype Reference Consortium panel.
Nat Genet
; 48(11): 1443-1448, 2016 11.
Artigo
Inglês
| MEDLINE | ID: mdl-27694958
16.
Partitioning heritability by functional annotation using genome-wide association summary statistics.
Nat Genet
; 47(11): 1228-35, 2015 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-26414678
17.
Comparing pedigree graphs.
J Comput Biol
; 19(9): 998-1014, 2012 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-22897201
18.
Detecting novel associations in large data sets.
Science
; 334(6062): 1518-24, 2011 Dec 16.
Artigo
Inglês
| MEDLINE | ID: mdl-22174245