Detalhe da pesquisa
1.
Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates.
Genet Med
; 24(2): 454-462, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906510
2.
Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test.
Genet Med
; 23(9): 1689-1696, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33976420
3.
VisCap: inference and visualization of germ-line copy-number variants from targeted clinical sequencing data.
Genet Med
; 18(7): 712-9, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26681316
4.
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
Genet Med
; 16(8): 601-8, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24503780
5.
The Evolution of a Large Biobank at Mass General Brigham.
J Pers Med
; 12(8)2022 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36013271
6.
Remote Fingerstick Blood Collection for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Antibody Testing.
Arch Pathol Lab Med
; 145(4): 415-418, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33264390
7.
Next generation sequencing-based copy number analysis reveals low prevalence of deletions and duplications in 46 genes associated with genetic cardiomyopathies.
Mol Genet Genomic Med
; 4(2): 143-51, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27066507