Detalhe da pesquisa
1.
Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study.
J Med Genet
; 58(4): 275-283, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32581083
2.
Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings.
Hum Genet
; 140(3): 493-504, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32892247
3.
Variant classification changes over time in BRCA1 and BRCA2.
Genet Med
; 21(10): 2248-2254, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30971832
4.
Correction: Variant classification changes over time in BRCA1 and BRCA2.
Genet Med
; 21(10): 2406-2407, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31043710
5.
Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).
Genet Med
; 20(3): 294-302, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28726806
6.
Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
BMJ Open
; 9(10): e031092, 2019 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31594892