Detalhe da pesquisa
1.
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
Brain
; 140(11): 2860-2878, 2017 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29053796
2.
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
Nat Commun
; 14(1): 3453, 2023 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37301908
3.
Improving the diagnostic yield of exome- sequencing by predicting gene-phenotype associations using large-scale gene expression analysis.
Nat Commun
; 10(1): 2837, 2019 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31253775
4.
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
Nat Commun
; 14(1): 3923, 2023 Jul 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37400429
5.
Biological interpretation of genome-wide association studies using predicted gene functions.
Nat Commun
; 6: 5890, 2015 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25597830
6.
Gene expression analysis identifies global gene dosage sensitivity in cancer.
Nat Genet
; 47(2): 115-25, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25581432
7.
Genome-wide association analyses identify variants in developmental genes associated with hypospadias.
Nat Genet
; 46(9): 957-63, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25108383