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Plos One
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July 1, 2025
Vulnerability in research ethics: A systematic review of policy guidelines and documents
Asia Grigis, Giorgia Beretta, Pascal Borry, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
January 18, 2008
Attitudes regarding predictive genetic testing in minors: a survey of European clinical geneticists
Pascal Borry, Tom Goffin, Herman Nys, et al.
Heliyon
|
May 9, 2024
Opt-in or out? Public perspectives on forensic DNA kinship investigations within the Dutch-speaking community
Sofie Claerhout, Hanna Noppe, Betty Cohn, et al.
Personalized Medicine
|
May 15, 2018
Designing expanded carrier screening panels: results of a qualitative study with European geneticists
Davit Chokoshvili, Sandra Janssens, Danya Vears, et al.
Xenotransplantation
|
December 1, 2021
Should you need an organ… Flemish secondary school students' attitudes toward xenotransplantation and transgenetic organ donation
Maryn Reyneke, Nel Kerckhof, Rachna Dherwani, et al.
The Mount Sinai Journal of Medicine, New York
|
August 16, 2008
Predictive genetic testing in minors for adult-onset genetic diseases
Pascal Borry, Tom Goffin, Herman Nys, et al.
Critical Reviews in Clinical Laboratory Sciences
|
January 31, 2017
Unsolved challenges in pediatric whole-exome sequencing: A literature analysis
Gabrielle Bertier, Karine Sénécal, Pascal Borry, et al.
Journal of Community Genetics
|
October 12, 2012
The challenge of implementing genetic tests with clinical utility while avoiding unsound applications
Martina C Cornel, Carla G van El, Pascal Borry
Nature Reviews. Genetics
|
November 26, 2008
Direct-to-consumer genome scanning services. Also for children?
Pascal Borry, Heidi C Howard, Karine Sénécal, et al.
Human Mutation
|
September 21, 2016
Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies
Emilia Niemiec, Pascal Borry, Wim Pinxten, et al.
Page
of 24
Search research articles
Search
Showing results (91-100 of 236) with videos related to
Sort By:
Page
of 24
Plos One
|
July 1, 2025
Vulnerability in research ethics: A systematic review of policy guidelines and documents
Asia Grigis, Giorgia Beretta, Pascal Borry, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
January 18, 2008
Attitudes regarding predictive genetic testing in minors: a survey of European clinical geneticists
Pascal Borry, Tom Goffin, Herman Nys, et al.
Heliyon
|
May 9, 2024
Opt-in or out? Public perspectives on forensic DNA kinship investigations within the Dutch-speaking community
Sofie Claerhout, Hanna Noppe, Betty Cohn, et al.
Personalized Medicine
|
May 15, 2018
Designing expanded carrier screening panels: results of a qualitative study with European geneticists
Davit Chokoshvili, Sandra Janssens, Danya Vears, et al.
Xenotransplantation
|
December 1, 2021
Should you need an organ… Flemish secondary school students' attitudes toward xenotransplantation and transgenetic organ donation
Maryn Reyneke, Nel Kerckhof, Rachna Dherwani, et al.
The Mount Sinai Journal of Medicine, New York
|
August 16, 2008
Predictive genetic testing in minors for adult-onset genetic diseases
Pascal Borry, Tom Goffin, Herman Nys, et al.
Critical Reviews in Clinical Laboratory Sciences
|
January 31, 2017
Unsolved challenges in pediatric whole-exome sequencing: A literature analysis
Gabrielle Bertier, Karine Sénécal, Pascal Borry, et al.
Journal of Community Genetics
|
October 12, 2012
The challenge of implementing genetic tests with clinical utility while avoiding unsound applications
Martina C Cornel, Carla G van El, Pascal Borry
Nature Reviews. Genetics
|
November 26, 2008
Direct-to-consumer genome scanning services. Also for children?
Pascal Borry, Heidi C Howard, Karine Sénécal, et al.
Human Mutation
|
September 21, 2016
Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies
Emilia Niemiec, Pascal Borry, Wim Pinxten, et al.
Page
of 24