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Cancer
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June 11, 2005
Screening and preventive behaviors one year after predictive genetic testing for hereditary nonpolyposis colorectal carcinoma
Veronica Collins, Bettina Meiser, Clara Gaff, et al.
Journal of Behavioral Medicine
|
February 16, 2017
Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining
Louise A Keogh, Heather Niven, Alison Rutstein, et al.
European Journal of Human Genetics : EJHG
|
January 3, 2025
Non-geneticist champions are essential to the mainstreaming of genomic medicine
Michael P Mackley, Emma Weisz, Robin Z Hayeems, et al.
BMJ Open
|
July 10, 2021
Measuring physician practice, preparedness and preferences for genomic medicine: a national survey
Amy Nisselle, Emily A King, Belinda McClaren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 12, 2009
A comparison of male attendees and nonattendees at a familial cancer clinic
Elizabeth A Lobb, Clara Gaff, Bettina Meiser, et al.
European Journal of Human Genetics : EJHG
|
February 5, 2025
Utilisation of subsidised genetic and genomic testing in a publicly funded healthcare system 2014-2023
Chris Schilling, Florencia Sjaaf, Ilias Goranitis, et al.
Patient Education and Counseling
|
November 25, 2020
Introducing Edna: A trainee chatbot designed to support communication about additional (secondary) genomic findings
David Ireland, DanaKai Bradford, Emma Szepe, et al.
Midwifery
|
October 1, 2019
Lessons learnt from implementing change in newborn bloodspot screening processes over more than a decade: Midwives, genetics and education
Amy Nisselle, Michelle Bishop, Taryn Charles, et al.
AJOB Empirical Bioethics
|
December 31, 2019
From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
Jacqueline Savard, Chriselle Hickerton, Sylvia A Metcalfe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 20, 2020
Evaluating the resource implications of different service delivery models for offering additional genomic findings
Martin Vu, Koen Degeling, Melissa Martyn, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 109) with videos related to
Sort By:
Page
of 11
Cancer
|
June 11, 2005
Screening and preventive behaviors one year after predictive genetic testing for hereditary nonpolyposis colorectal carcinoma
Veronica Collins, Bettina Meiser, Clara Gaff, et al.
Journal of Behavioral Medicine
|
February 16, 2017
Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining
Louise A Keogh, Heather Niven, Alison Rutstein, et al.
European Journal of Human Genetics : EJHG
|
January 3, 2025
Non-geneticist champions are essential to the mainstreaming of genomic medicine
Michael P Mackley, Emma Weisz, Robin Z Hayeems, et al.
BMJ Open
|
July 10, 2021
Measuring physician practice, preparedness and preferences for genomic medicine: a national survey
Amy Nisselle, Emily A King, Belinda McClaren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 12, 2009
A comparison of male attendees and nonattendees at a familial cancer clinic
Elizabeth A Lobb, Clara Gaff, Bettina Meiser, et al.
European Journal of Human Genetics : EJHG
|
February 5, 2025
Utilisation of subsidised genetic and genomic testing in a publicly funded healthcare system 2014-2023
Chris Schilling, Florencia Sjaaf, Ilias Goranitis, et al.
Patient Education and Counseling
|
November 25, 2020
Introducing Edna: A trainee chatbot designed to support communication about additional (secondary) genomic findings
David Ireland, DanaKai Bradford, Emma Szepe, et al.
Midwifery
|
October 1, 2019
Lessons learnt from implementing change in newborn bloodspot screening processes over more than a decade: Midwives, genetics and education
Amy Nisselle, Michelle Bishop, Taryn Charles, et al.
AJOB Empirical Bioethics
|
December 31, 2019
From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
Jacqueline Savard, Chriselle Hickerton, Sylvia A Metcalfe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 20, 2020
Evaluating the resource implications of different service delivery models for offering additional genomic findings
Martin Vu, Koen Degeling, Melissa Martyn, et al.
Page
of 11