Detalhe da pesquisa
1.
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members.
J Genet Couns
; 32(4): 896-905, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36945104
2.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 111(5): 996, 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38701747
3.
"Acquired" Brugada syndrome in a cardiac allograft.
Pediatr Transplant
; 26(5): e14276, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35340105
4.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 103(2): 221-231, 2018 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30057030
5.
Family screening for hypertrophic cardiomyopathy: Is it time to change practice guidelines?
Eur Heart J
; 40(45): 3672-3681, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31170284
6.
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
Eur Heart J
; 39(31): 2879-2887, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30059973
7.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 103(3): 456, 2018 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30193137
8.
Heart Failure with Recovered Ejection Fraction in Patients with Vinculin Loss-of-function Variants.
J Cardiovasc Transl Res
; 16(6): 1303-1309, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37548861
9.
Exploring Barriers and Facilitators to Indirect Cascade Screening for Familial Hypercholesteraemia in a Paediatric/Parent Population.
CJC Pediatr Congenit Heart Dis
; 2(5): 211-218, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37970213
10.
Return of Results Policies for Genomic Research: Current Practices and the Hearts in Rhythm Organization (HiRO) Approach.
Can J Cardiol
; 38(4): 526-535, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34715283
11.
The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population.
J Genet Couns
; 20(4): 355-64, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21448763
12.
Development and Evaluation of Decision Aids to Guide Families' Predictive Testing Choices for Children at Risk for Arrhythmia or Cardiomyopathy.
Can J Cardiol
; 37(10): 1586-1592, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34147624
13.
ALU transposition induces familial hypertrophic cardiomyopathy.
Mol Genet Genomic Med
; 8(1): e951, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31568709
14.
Return of genetic and genomic research findings: experience of a pediatric biorepository.
BMC Med Genomics
; 12(1): 173, 2019 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31775751
15.
Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy.
Circ Genom Precis Med
; 11(10): e002255, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30354306
16.
Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease.
Circ Cardiovasc Genet
; 10(3)2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28473349