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Public Health Genomics
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October 24, 2024
"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes
Ridhi Gopalakrishnan, Jordan Sam, Carly Butkowsky, et al.
European Journal of Human Genetics : EJHG
|
October 11, 2023
"I just wanted more": Hereditary cancer syndromes patients' perspectives on the utility of circulating tumour DNA testing for cancer screening
Ella Adi-Wauran, Marc Clausen, Salma Shickh, et al.
BMJ Open
|
April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial
Salma Shickh, Marc Clausen, Chloe Mighton, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2026
"Where do I go from here?" Navigating a lifelong road without a map: the care experiences of hereditary cancer patients
Carly Butkowsky, June C Carroll, Melyssa Aronson, et al.
European Journal of Human Genetics : EJHG
|
March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing results
Chloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
Human Genetics
|
June 23, 2022
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings
Jordan Sam, Emma Reble, Rita Kodida, et al.
Clinical Biochemistry
|
July 5, 2023
Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey
Gregory Morgan, Laurent Briollais, Marc Clausen, et al.
BMJ Open
|
October 1, 2021
Implementation of serological and molecular tools to inform COVID-19 patient management: protocol for the GENCOV prospective cohort study
Jennifer Taher, Chloe Mighton, Sunakshi Chowdhary, et al.
Journal of Medical Genetics
|
May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencing
Rita Kodida, Emma Reble, Marc Clausen, et al.
BMJ Open
|
April 3, 2024
Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol
Sebastian Lunke, Sophie E Bouffler, Lilian Downie, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 52) with videos related to
Sort By:
Page
of 6
Public Health Genomics
|
October 24, 2024
"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes
Ridhi Gopalakrishnan, Jordan Sam, Carly Butkowsky, et al.
European Journal of Human Genetics : EJHG
|
October 11, 2023
"I just wanted more": Hereditary cancer syndromes patients' perspectives on the utility of circulating tumour DNA testing for cancer screening
Ella Adi-Wauran, Marc Clausen, Salma Shickh, et al.
BMJ Open
|
April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial
Salma Shickh, Marc Clausen, Chloe Mighton, et al.
European Journal of Human Genetics : EJHG
|
March 3, 2026
"Where do I go from here?" Navigating a lifelong road without a map: the care experiences of hereditary cancer patients
Carly Butkowsky, June C Carroll, Melyssa Aronson, et al.
European Journal of Human Genetics : EJHG
|
March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing results
Chloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
Human Genetics
|
June 23, 2022
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings
Jordan Sam, Emma Reble, Rita Kodida, et al.
Clinical Biochemistry
|
July 5, 2023
Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey
Gregory Morgan, Laurent Briollais, Marc Clausen, et al.
BMJ Open
|
October 1, 2021
Implementation of serological and molecular tools to inform COVID-19 patient management: protocol for the GENCOV prospective cohort study
Jennifer Taher, Chloe Mighton, Sunakshi Chowdhary, et al.
Journal of Medical Genetics
|
May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencing
Rita Kodida, Emma Reble, Marc Clausen, et al.
BMJ Open
|
April 3, 2024
Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol
Sebastian Lunke, Sophie E Bouffler, Lilian Downie, et al.
Page
of 6