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Laura A Zahavich
Observed names:
L Zahavich,
L. Zahavich,
Laura Zahavich,
Zahavich, Laura,
Zahavich, Laura A
Institutions:
University of Toronto,
Great Ormond Street Hospital,
Hospital for Sick Children
Observed institutions:
University of Toronto,
Great Ormond Street Hospital,
Hospital for Sick Children,
Princess Margaret Cancer Centre,
Princess Margaret Hospital
ORCID:
0000-0002-5337-6349
Observed ORCID:
0000-0002-5337-6349
OpenAlex ID:
A5043040146
Family screening for hypertrophic cardiomyopathy: Is it time to change practice guidelines?
2019
·
Myriam Lafreniere-Roula
, Yoav Bolkier
, et al.
·
European Heart Journal
·
100
PDF
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
2018
·
Carol-Anne Martin
, Kata Sarlós
, et al.
·
The American Journal of Human Genetics
·
98
PDF
Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy
2017
·
J. Mathew
, L. Zahavich
, et al.
·
Clinical Genetics
·
84
PDF
SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups
2018
·
Alban-Elouen Baruteau
, Florence Kyndt
, et al.
·
European Heart Journal
·
49
PDF
Clinical genetic testing in pediatric cardiomyopathy: Is bigger better?
2017
·
A.C. Ouellette
, J. Mathew
, et al.
·
Clinical Genetics
·
49
PDF
Return of genetic and genomic research findings: experience of a pediatric biorepository
2019
·
Tanya Papaz
, Eriskay Liston
, et al.
·
BMC Medical Genomics
·
33
PDF
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease
2024
·
Kaitlin J. Stanley
, Kelsey J. Kalbfleisch
, et al.
·
European Journal of Human Genetics
·
25
Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy
2018
·
Laura Zahavich
, Mark Tarnopolsky
, et al.
·
Circulation Genomic and Precision Medicine
·
17
Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease
2017
·
Laura Zahavich
, Sarah Bowdin
, et al.
·
Circulation Cardiovascular Genetics
·
14
PDF
Exploring Barriers and Facilitators to Indirect Cascade Screening for Familial Hypercholesteraemia in a Paediatric/Parent Population
2023
·
Megan A. Dickson
, Laura Zahavich
, et al.
·
CJC Pediatric and Congenital Heart Disease
·
11
PDF
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
2018
·
Carol-Anne Martin
, Kata Sarlós
, et al.
·
The American Journal of Human Genetics
·
11
PDF
Development and Evaluation of Decision Aids to Guide Families’ Predictive Testing Choices for Children at Risk for Arrhythmia or Cardiomyopathy
2021
·
Susan Christian
, Alicia Welsh
, et al.
·
Canadian Journal of Cardiology
·
9
The Use of Family History Questionnaires: An Examination of Genetic Risk Estimates and Genetic Testing Eligibility in the Non‐responder Population
2011
·
Susan Randall Armel
, Kara Hitchman
, et al.
·
Journal of Genetic Counseling
·
9
Barriers in applying to genetic counseling Master's degree programs: Perceptions of prospective applicants when compared with Canadian admissions committee members
2023
·
Laura Zahavich
, Riyana Babul‐Hirji
·
Journal of Genetic Counseling
·
6
PDF
Heart Failure with Recovered Ejection Fraction in Patients with Vinculin Loss-of-function Variants
2023
·
Laura Zahavich
, Rajadurai Akilen
, et al.
·
Journal of Cardiovascular Translational Research
·
5
PDF
Return of Results Policies for Genomic Research: Current Practices and the Hearts in Rhythm Organization (HiRO) Approach
2021
·
Drake A. Comber
, Brianna Davies
, et al.
·
Canadian Journal of Cardiology
·
5
Yield on Reinterpretation of Genetic Variants in Pediatric Cardiomyopathy
2025
·
Takanori Suzuki
, Robert Lesurf
, et al.
·
Journal of the American Heart Association
·
2
PDF
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
2024
·
Carol-Anne Martin
, Kata Sarlós
, et al.
·
The American Journal of Human Genetics
·
2
An Inherited Arrhythmia Syndrome with Long QT, Sudden Death and Depolarization Disorder Due to an In-Frame Deletion in Exon 16 of the CACNA1C Gene
2017
·
Muhammad Arshad Rafiq
, Tamara T Koopmann
, et al.
·
Journal of Next Generation Sequencing & Applications
·
2
PDF
Canadian Cardiovascular Society Clinical Practice Update on Cardiogenetic Testing
2025
·
Melanie Care
, Laura Arbour
, et al.
·
Canadian Journal of Cardiology
·
1
P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing
2024
·
Katharine Fooks
, Lydia Vermeer
, et al.
·
Genetics in Medicine Open
·
1
PDF
ALU transposition induces familial hypertrophic cardiomyopathy
2019
·
Landry Nfonsam
, Lijia Huang
, et al.
·
Molecular Genetics & Genomic Medicine
·
1
PDF
SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups
2019
·
Alban-Elouen Baruteau
, Florence Kyndt
, et al.
·
Archives of Cardiovascular Diseases Supplements
·
1
PDF
A Generalizable, Governance-Embedded Pathway for Assessing Patient-Level Opportunities for Genetic Medicines
2026
·
David Cheerie
, Amy Y. Pan
, et al.
·
medRxiv
The Patient-reported Genetic testing Utility InDEx (P-GUIDE): A novel measure of personal utility
2026
·
Elise Poole
, Bowen Xiao
, et al.
·
Genetics in Medicine
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Works count:
49
Citation count:
534
H-index:
11
I10-index:
11
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