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Author Details
Full Name
Erika Kleiderman
Affiliation
Universite de Montreal.
ORCID
Career Start Year
2012
Papers
36
H Index
11
Expertise
CM4AI Collaborator
Vardit Ravitsky (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36919551
Going Back to Basics: What is the Target of Prenatal Screening?
Am J Bioeth
2023
37192471
Developing Policy for the Healthy Life Trajectories Initiative: Going from National to International.
Biopreserv Biobank
2023
35089840
The Serious Factor in Expanded Prenatal Genetic Testing.
Am J Bioeth
2022
35125311
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries.
Genet Med
2022
34034801
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries.
Genome Med
2021
34711210
The impact of reporting magnetic resonance imaging incidental findings in the Canadian alliance for healthy hearts and minds cohort.
BMC Med Ethics
2021
31420817
Human germline genome editing is illegal in Canada, but could it be desirable for some members of the rare disease community?
J Community Genet
2020
31784701
Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data.
Eur J Hum Genet
2020
31694871
'Serious' factor-a relevant starting point for further debate: a response.
J Med Ethics
2020
32946764
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
Am J Hum Genet
2020
32804063
Of the Rights and Best Interests of Future Generations.
Am J Bioeth
2020
30361155
Pre-implantation Genetic Diagnosis: The Road Forward in Canada.
J Obstet Gynaecol Can
2019
31531740
Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia.
Hum Genet
2019
31326898
The 'serious' factor in germline modification.
J Med Ethics
2019
31355201
Canada's <i>Assisted Human Reproduction Act:</i> Pragmatic Reforms in Support of Research.
Front Med (Lausanne)
2019
31599679
Heritable Genome Editing: Who Speaks for "Future" Children?
CRISPR J
2019
31068009
Realigning gene editing with clinical research ethics: What the "CRISPR Twins" debacle means for Chinese and international research ethics governance.
Account Res
2019
30692104
"CRISPR babies": What does this mean for science and Canada?
CMAJ
2019
30476628
Attitudes of publics who are unwilling to donate DNA data for research.
Eur J Med Genet
2019
29454384
APPLaUD: access for patients and participants to individual level uninterpreted genomic data.
Hum Genomics
2018
29856292
'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods.
Per Med
2018
30043682
Bridging stem cell research and medicine: a learning health system.
Regen Med
2018
29852118
Genetically Enhanced Minors: Whose Responsibility?
Am J Bioeth
2018
30409192
Overcoming barriers to facilitate the regulation of multi-centre regenerative medicine clinical trials.
Stem Cell Res Ther
2018
29570738
The author who wasn't there? Fairness and attribution in publications following access to population biobanks.
PLoS One
2018
29595433
Research on Human Embryos and Reproductive Materials: Revisiting Canadian Law and Policy.
Healthc Policy
2018
28733061
Mitochondrial Replacement Therapy: The Road to the Clinic in Canada.
J Obstet Gynaecol Can
2017
28443132
Disease Resistance and the Definition of Genetic Enhancement.
Front Genet
2017
29302357
A blueprint for the next generation of ELSI research, training, and outreach in regenerative medicine.
NPJ Regen Med
2017
29302340
Human gene editing: revisiting Canadian policy.
NPJ Regen Med
2017
28946923
Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic.
Genome Med
2017
26797999
GENETIC TECHNOLOGY REGULATION. Editing policy to fit the genome?
Science
2016
25492269
Disclosure of incidental findings in cancer genomic research: investigators' perceptions on obligations and barriers.
Clin Genet
2015
24356209
Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases.
J Med Ethics
2014
23340514
Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk.
Eur J Hum Genet
2013
23216847
Recruiting terminally ill patients into non-therapeutic oncology studies: views of health professionals.
BMC Med Ethics
2012
1 - 36 of 36
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Anne-Marie Laberge
UNIVERSITY OF MONTREAL
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Erick R Scott
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Minh Thu Nguyen
Institute of Medical Microbiology, University Hospital of Munster
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Christine Patch
Queen Mary University of London, United Kingdom Society and Ethics Research
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Jason Bobe
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