Melissa Martyn

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

Top Topics

Cross Sectional

Palliative Care

Top Venues

European journal of human genetics : EJHG

JCO precision oncology

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Melissa Martyn, Ling Lee, Alli Jan, Elly Lynch, Rona Weerasuriya, Anaita Kanga-Parabia, Clara L Gaff
Evaluation of a two-step model of opportunistic genomic screening. European journal of human genetics : EJHG 32 (6) (2024)
Melissa Martyn, Emily Forbes, Ling Lee, Anaita Kanga-Parabia, Rona Weerasuriya, Elly Lynch, Penny Gleeson, Clara L Gaff
Secondary use of genomic data: patients' decisions at point of testing and perspectives to inform international data sharing. European journal of human genetics : EJHG (2024)
Kortnye Smith, Sophie O'Haire, Benjamin Markman, Hui Kong Gan, Kenneth J O'Byrne, Michael Millward, Ben Tran, Benjamin J Solomon, Clare L Scott, Damien Kee, Grant A McArthur, Andrew P Fellowes, Dong Anh K Khoung-Quang, Paul G Ekert, Paul A James, Huiling Xu, Melissa Martyn, Elly Lynch, Rona Weerasuriya, Clara L Gaff, Stephen B Fox, Jayesh Desai
Patient Experience of Complex Genomic Sequencing Exploring Patient Preference, Barriers, and Enablers for Delivery. JCO precision oncology 8 (2024)
Melissa Martyn, Emily Forbes, Ling Lee, Anaita Kanga-Parabia, Rona Weerasuriya, Elly Lynch, Penny Gleeson, Clara L Gaff
Secondary use of genomic data: patients' decisions at point of testing and perspectives to inform international data sharing. European journal of human genetics : EJHG 32 (6) (2024)
Melissa Martyn, Emily Forbes, Ling Lee, Anaita Kanga-Parabia, Rona Weerasuriya, Elly Lynch, Penny Gleeson, Clara L Gaff
Secondary use of genomic data: patients' decisions at point of testing and perspectives to inform international data sharing. European journal of human genetics : EJHG 32 (6) (2024)
Melissa Martyn, Ling Lee, Alli Jan, Elly Lynch, Rona Weerasuriya, Anaita Kanga-Parabia, Clara L Gaff
Evaluation of a two-step model of opportunistic genomic screening. European journal of human genetics : EJHG (2024)
Melissa Martyn, Ling Lee, Alli Jan, Elly Lynch, Rona Weerasuriya, Anaita Kanga-Parabia, Clara L Gaff
Evaluation of a two-step model of opportunistic genomic screening. European journal of human genetics : EJHG 32 (6) (2024)
Thu Trang Do, Melissa Martyn, Belinda J McClaren, Alison McEwen, Clara L Gaff
Becoming agents for genomic change: genetic counsellors' views of patient care and implementation influences when genomics is mainstreamed. European journal of human genetics : EJHG (2024)
Melissa Martyn, Ling Lee, Alli Jan, Elly Lynch, Rona Weerasuriya, Anaita Kanga-Parabia, Clara L Gaff
Evaluation of a two-step model of opportunistic genomic screening. European journal of human genetics : EJHG 32 (6) (2024)
Melissa Martyn, Emily Forbes, Ling Lee, Anaita Kanga-Parabia, Rona Weerasuriya, Elly Lynch, Penny Gleeson, Clara L Gaff
Secondary use of genomic data: patients' decisions at point of testing and perspectives to inform international data sharing. European journal of human genetics : EJHG 32 (6) (2024)
Erin Crellin, Melissa Martyn, Belinda McClaren, Clara L Gaff
What matters to parents? A scoping review of parents' service experiences and needs regarding genetic testing for rare diseases. European journal of human genetics : EJHG (2023)
Hilary Bowman-Smart, Danya F Vears, Gemma R Brett, Melissa Martyn, Zornitza Stark, Christopher Gyngell
'Diagnostic shock': the impact of results from ultrarapid genomic sequencing of critically unwell children on aspects of family functioning. European journal of human genetics : EJHG 30 (9) (2022)
Max Catchpool, Jay Ramchand, Melissa Martyn, David L Hare, Paul A James, Alison H Trainer, Josh Knight, Ilias Goranitis
A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)