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Sociology of Health & Illness|January 29, 2026
Non-Directiveness and Authenticity in the Predictive Genetic ClinicShane Doheny, Rebecca Dimond, Lisa Ballard, et al.Social Science & Medicine (1982)|April 7, 2009
Distinguishing research from clinical care in cancer genetics: theoretical justifications and practical strategiesNina Hallowell, Sarah Cooke, Gill Crawford, et al.European Journal of Human Genetics : EJHG|May 23, 2025
Determining a role for Patient and Public Involvement and Engagement (PPIE) in genomic data governance for cancer careKatherine Sahan, Lesley Turner, Nina Hallowell, et al.Advances in Health Sciences Education : Theory and Practice|April 27, 2023
Using collaborative autoethnography to explore the teaching of qualitative research methods in medicineKinda Ibrahim, Susie Weller, Elissa Elvidge, et al.Quality & Quantity|April 2, 2019
Big data, qualitative style: a breadth-and-depth method for working with large amounts of secondary qualitative dataEmma Davidson, Rosalind Edwards, Lynn Jamieson, et al.BMC Medical Ethics|August 10, 2017
Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approachGabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, et al.Journal of Medical Genetics|September 18, 2014
Defining and managing incidental findings in genetic and genomic practiceShiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2015
Health-care professionals' responsibility to patients' relatives in genetic medicine: a systematic review and synthesis of empirical researchSandi Dheensa, Angela Fenwick, Shiri Shkedi-Rafid, et al.Familial Cancer|April 14, 2017
How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods studySandi Dheensa, Gillian Crawford, Claire Salter, et al.Journal of Genetic Counseling|June 4, 2026
Counseling patients in the predictive genetics clinic for Huntington's disease: A qualitative analysis of ethnographic observationsShane Doheny, Rebecca Dimond, Lisa Ballard, et al.Pageof 11