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Frontiers in Public Health
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December 22, 2025
AI-driven tools for the prediction of obesity-related vascular diseases: stakeholder perspectives and challenges
Kaatje Goossens, Pascal Borry, Tessa Marie Forehand, et al.
Accountability in Research
|
November 30, 2022
Assessing the acceptability of individual studies that use deception: A systematic review of normative guidance documents
Kamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 8, 2021
Disclosure of genetic information to family members: a systematic review of normative documents
Amicia Phillips, Pascal Borry, Ine Van Hoyweghen, et al.
European Journal of Human Genetics : EJHG
|
March 9, 2017
Paternity testing under the cloak of recreational genetics
Nathalie Moray, Katherina E Pink, Pascal Borry, et al.
Personalized Medicine
|
May 18, 2018
"It's our DNA, we deserve the right to test!" A content analysis of a petition for the right to access direct-to-consumer genetic testing
Yeyang Su, Pascal Borry, Ina C Otte, et al.
Accountability in Research
|
June 3, 2024
Truthfulness as the basis for ethical safeguards in deceptive research: An interview study with researchers
Kamiel Verbeke, Jan Piasecki, Dieter Baeyens, et al.
AJOB Empirical Bioethics
|
October 5, 2020
Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing
Danya F Vears, Pascal Borry, Julian Savulescu, et al.
Familial Cancer
|
July 9, 2024
Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
Amicia Phillips, Danya F Vears, Ine Van Hoyweghen, et al.
Journal of Community Genetics
|
September 1, 2017
Readability of informed consent forms for whole-exome and whole-genome sequencing
Emilia Niemiec, Danya F Vears, Pascal Borry, et al.
Familial Cancer
|
March 29, 2024
Clinician perspectives on policy approaches to genetic risk disclosure in families
Amicia Phillips, Danya F Vears, Ine Van Hoyweghen, et al.
Page
of 24
Search research articles
Search
Showing results (121-130 of 236) with videos related to
Sort By:
Page
of 24
Frontiers in Public Health
|
December 22, 2025
AI-driven tools for the prediction of obesity-related vascular diseases: stakeholder perspectives and challenges
Kaatje Goossens, Pascal Borry, Tessa Marie Forehand, et al.
Accountability in Research
|
November 30, 2022
Assessing the acceptability of individual studies that use deception: A systematic review of normative guidance documents
Kamiel Verbeke, Tomasz Krawczyk, Dieter Baeyens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 8, 2021
Disclosure of genetic information to family members: a systematic review of normative documents
Amicia Phillips, Pascal Borry, Ine Van Hoyweghen, et al.
European Journal of Human Genetics : EJHG
|
March 9, 2017
Paternity testing under the cloak of recreational genetics
Nathalie Moray, Katherina E Pink, Pascal Borry, et al.
Personalized Medicine
|
May 18, 2018
"It's our DNA, we deserve the right to test!" A content analysis of a petition for the right to access direct-to-consumer genetic testing
Yeyang Su, Pascal Borry, Ina C Otte, et al.
Accountability in Research
|
June 3, 2024
Truthfulness as the basis for ethical safeguards in deceptive research: An interview study with researchers
Kamiel Verbeke, Jan Piasecki, Dieter Baeyens, et al.
AJOB Empirical Bioethics
|
October 5, 2020
Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing
Danya F Vears, Pascal Borry, Julian Savulescu, et al.
Familial Cancer
|
July 9, 2024
Correction: Clinician perspectives on policy approaches to genetic risk disclosure in families
Amicia Phillips, Danya F Vears, Ine Van Hoyweghen, et al.
Journal of Community Genetics
|
September 1, 2017
Readability of informed consent forms for whole-exome and whole-genome sequencing
Emilia Niemiec, Danya F Vears, Pascal Borry, et al.
Familial Cancer
|
March 29, 2024
Clinician perspectives on policy approaches to genetic risk disclosure in families
Amicia Phillips, Danya F Vears, Ine Van Hoyweghen, et al.
Page
of 24