Detalhe da pesquisa
1.
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Am J Hum Genet
; 109(5): 857-870, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35385699
2.
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.
Am J Med Genet A
; 161A(7): 1523-30, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23704059
3.
Multiset correlation and factor analysis enables exploration of multi-omics data.
Cell Genom
; 3(8): 100359, 2023 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37601969
4.
Quality control and quality assurance in genotypic data for genome-wide association studies.
Genet Epidemiol
; 34(6): 591-602, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20718045
5.
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene.
PLoS One
; 9(2): e87645, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24520335
6.
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Science
; 343(6170): 506-511, 2014 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-24482476