Detalhe da pesquisa
1.
Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network.
Am J Hum Genet
; 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38688278
2.
CANOES: detecting rare copy number variants from whole exome sequencing data.
Nucleic Acids Res
; 42(12): e97, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24771342
3.
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics.
medRxiv
; 2023 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37662324
4.
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.
Am J Med Genet A
; 158A(2): 298-308, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22147502
5.
Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.
PLoS One
; 17(5): e0268725, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35594287