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.
Genomic atlas of the human plasma proteome.
Nature
; 558(7708): 73-79, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29875488
3.
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
4.
PhenoScanner: a database of human genotype-phenotype associations.
Bioinformatics
; 32(20): 3207-3209, 2016 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27318201
5.
A Role for Non-B DNA Forming Sequences in Mediating Microlesions Causing Human Inherited Disease.
Hum Mutat
; 37(1): 65-73, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26466920
6.
Remotely acting SMCHD1 gene regulatory elements: in silico prediction and identification of potential regulatory variants in patients with FSHD.
Hum Genomics
; 9: 25, 2015 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26446085