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Genome Medicine|June 23, 2012
Integrating stakeholder perspectives into the translation of cell-free fetal DNA testing for aneuploidyLauren C Sayres, Megan Allyse, Mildred K Cho
Clinical Trials (London, England)|September 15, 2016
A randomized study of multimedia informational aids for research on medical practices: Implications for informed consentStephanie A Kraft, Melissa Constantine, David Magnus, et al.
Pharmacogenomics|February 28, 2003
Privacy issues in personalized medicineLaszlo T Vaszar, Mildred K Cho, Thomas A Raffin
JMIR Mhealth and Uhealth|July 28, 2021
Ethical Development of Digital Phenotyping Tools for Mental Health Applications: Delphi StudyNicole Martinez-Martin, Henry T Greely, Mildred K Cho
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 2, 2021
Taking an antiracist posture in scientific publications in human genetics and genomicsKyle B Brothers, Robin L Bennett, Mildred K Cho
Science and Engineering Ethics|November 20, 2014
Reporting Race and Ethnicity in Genetics Research: Do Journal Recommendations or Resources Matter?Pamela Sankar, Mildred K Cho, Keri Monahan, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|August 14, 2003
Financial conflict-of-interest policies in clinical research: issues for clinical investigatorsElizabeth A Boyd, Mildred K Cho, Lisa A Bero
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2006
What is in a cause? Exploring the relationship between genetic cause and felt stigmaPamela Sankar, Mildred K Cho, Paul Root Wolpe, et al.
Cell Genomics|August 8, 2022
Three decades of ethical, legal, and social implications research: Looking back to chart a path forwardDeanne Dunbar Dolan, Sandra Soo-Jin Lee, Mildred K Cho
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