Detalhe da pesquisa
1.
A deep catalogue of protein-coding variation in 983,578 individuals.
Nature
; 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38768635
2.
POLG2 disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity.
Hum Mol Genet
; 24(18): 5184-97, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26123486
3.
The Ethical, Legal, and Social Implications Program of the National Human Genome Research Institute: reflections on an ongoing experiment.
Annu Rev Genomics Hum Genet
; 15: 481-505, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24773317
4.
Evolving approaches to the ethical management of genomic data.
Trends Genet
; 29(6): 375-82, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23453621
5.
A deep catalog of protein-coding variation in 985,830 individuals.
bioRxiv
; 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37214792
6.
Bayesian modeling of skewed X inactivation in genetically diverse mice identifies a novel Xce allele associated with copy number changes.
Genetics
; 218(1)2021 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33693696
7.
Lung cancer mutation profile of EGFR, ALK, and KRAS: Meta-analysis and comparison of never and ever smokers.
Lung Cancer
; 102: 122-134, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27987580