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European Journal of Human Genetics : EJHG
|
January 5, 2017
Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, et al.
BMC Women'S Health
|
December 17, 2017
Health care professionals' attitudes towards population-based genetic testing and risk-stratification for ovarian cancer: a cross-sectional survey
Katie E J Hann, Lindsay Fraser, Lucy Side, et al.
European Journal of Human Genetics : EJHG
|
March 10, 2022
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
Michelle Peter, Jennifer Hammond, Saskia C Sanderson, et al.
Journal of Genetic Counseling
|
February 23, 2016
Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project
Sabrina A Suckiel, Michael D Linderman, Saskia C Sanderson, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2023
Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project
Michelle Peter, Jennifer Hammond, Saskia C Sanderson, et al.
Atherosclerosis
|
November 21, 2008
Association between IL6 gene variants -174G>C and -572G>C and serum IL-6 levels: interactions with social position in the Whitehall II cohort
Saskia C Sanderson, Meena Kumari, Eric J Brunner, et al.
Journal of Community Genetics
|
November 24, 2011
Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study
Samantha A Streicher, Saskia C Sanderson, Ethylin Wang Jabs, et al.
Journal of Community Genetics
|
June 25, 2013
Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study
Saskia C Sanderson, Michael A Diefenbach, Randi Zinberg, et al.
Public Health Genomics
|
January 31, 2015
Factors affecting recall of different types of personal genetic information about Alzheimer's disease risk: the REVEAL study
Andria G Besser, Saskia C Sanderson, J Scott Roberts, et al.
Pharmacogenomics
|
December 6, 2023
Pharmacogenomic knowledge and awareness among diverse patients treated with angiotensin converting enzyme inhibitors
Hetanshi Naik, Michelle Y O'Connor, Saskia C Sanderson, et al.
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Search research articles
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Showing results (41-50 of 71) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
January 5, 2017
Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, et al.
BMC Women'S Health
|
December 17, 2017
Health care professionals' attitudes towards population-based genetic testing and risk-stratification for ovarian cancer: a cross-sectional survey
Katie E J Hann, Lindsay Fraser, Lucy Side, et al.
European Journal of Human Genetics : EJHG
|
March 10, 2022
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
Michelle Peter, Jennifer Hammond, Saskia C Sanderson, et al.
Journal of Genetic Counseling
|
February 23, 2016
Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project
Sabrina A Suckiel, Michael D Linderman, Saskia C Sanderson, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2023
Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project
Michelle Peter, Jennifer Hammond, Saskia C Sanderson, et al.
Atherosclerosis
|
November 21, 2008
Association between IL6 gene variants -174G>C and -572G>C and serum IL-6 levels: interactions with social position in the Whitehall II cohort
Saskia C Sanderson, Meena Kumari, Eric J Brunner, et al.
Journal of Community Genetics
|
November 24, 2011
Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study
Samantha A Streicher, Saskia C Sanderson, Ethylin Wang Jabs, et al.
Journal of Community Genetics
|
June 25, 2013
Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study
Saskia C Sanderson, Michael A Diefenbach, Randi Zinberg, et al.
Public Health Genomics
|
January 31, 2015
Factors affecting recall of different types of personal genetic information about Alzheimer's disease risk: the REVEAL study
Andria G Besser, Saskia C Sanderson, J Scott Roberts, et al.
Pharmacogenomics
|
December 6, 2023
Pharmacogenomic knowledge and awareness among diverse patients treated with angiotensin converting enzyme inhibitors
Hetanshi Naik, Michelle Y O'Connor, Saskia C Sanderson, et al.
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of 8