Author details

Full Name

Karine SÃ©nÃ©cal

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33868358	Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.	Front Genet	2021
34276804	Corrigendum: Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.	Front Genet	2021
31472303	Exploration of genetic health professional - laboratory specialist interactions in diagnostic genomic sequencing.	Eur J Med Genet	2020
31856387	Genetic health professionals' experiences returning results from diagnostic genomic sequencing to patients.	J Genet Couns	2020
32200539	Genetic health professionals' experiences with initiating reanalysis of genomic sequence data.	Fam Cancer	2020
29554172	Key Implications of Data Sharing in Pediatric Genomics.	JAMA Pediatr	2018
29184171	Points to consider for laboratories reporting results from diagnostic genomic sequencing.	Eur J Hum Genet	2018
28132577	Unsolved challenges in pediatric whole-exome sequencing: A literature analysis.	Crit Rev Clin Lab Sci	2017
28774848	Reporting practices for variants of uncertain significance from next generation sequencing technologies.	Eur J Med Genet	2017
28406189	Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing.	Eur J Hum Genet	2017
28561019	Reply to C Harling.	Eur J Hum Genet	2017
28512758	Reporting practices for unsolicited and secondary findings from next-generation sequencing technologies: Perspectives of laboratory personnel.	Hum Mutat	2017
28222731	Genomic newborn screening: public health policy considerations and recommendations.	BMC Med Genomics	2017
27876816	Reply to Kranendonk et al.	Eur J Hum Genet	2017
27599532	Next-Generation Sequencing and the Return of Results.	Cold Spring Harb Perspect Med	2016
30088377	Recontacting Pediatric Research Participants for Consent When They Reach the Age of Majority.	IRB	2016
27302841	Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencing.	Eur J Hum Genet	2016
27111240	Do It Yourself Newborn Screening.	JAMA Pediatr	2016
27654498	Participation of Children in Medical Decision-Making: Challenges and Potential Solutions.	J Bioeth Inq	2016
24916647	To disclose, or not to disclose? Context matters.	Eur J Hum Genet	2015
29749887	Genome-based newborn screening: a conceptual analysis of the best interests of the child standard.	Per Med	2015
25626707	Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.	Eur J Hum Genet	2015
25533753	Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities.	Journal of Community Genetics	2015
26613133	Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process.	Genome	2015
26239711	Return of genetic testing results in the era of whole-genome sequencing.	Nat Rev Genet	2015
26061751	Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.	N Engl J Med	2015
24670681	Whole-genome sequencing in newborn screening programs.	Sci Transl Med	2014
26767472	Defining the Scope of Public Engagement: Examining the "Right Not to Know" in Public Health Genomics.	Journal of Law, Medicine and Ethics	2014
23921532	Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform.	Eur J Hum Genet	2014
24558742	[Promoting public involvement to increase the legitimacy in health policy decisions].		2013
22084845	Pediatric research and the return of individual research results.	J Law Med Ethics	2011
19488835	Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minors.	Fam Cancer	2010
19030022	Direct-to-consumer genome scanning services. Also for children?	Nat Rev Genet	2009