Danya F Vears (D F Vears, Danya Vears)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 45

Top Topics

High Throughput Sequencing

Muscular Dystrophy

Top Venues

European journal of human genetics : EJHG

Familial cancer

International journal of neonatal screening

Twin research and human genetics : the official journal of the International Society for Twin Studies

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

Publications

Danya F Vears, Alison McLean, Chloe La Spina, Aideen M McInerney-Leo, null null
Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children. Twin research and human genetics : the official journal of the International Society for Twin Studies (2024)
Danya F Vears, Alison McLean, Chloe La Spina, Aideen M McInerney-Leo, null null
Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children. Twin research and human genetics : the official journal of the International Society for Twin Studies 27 (2) (2024)
Amicia Phillips, Danya F Vears, Nozomi Mizushima, Pascal Borry
Clinician perspectives on policy approaches to genetic risk disclosure in families. Familial cancer 23 (2) (2024)
Amicia Phillips, Danya F Vears, Nozomi Mizushima, Pascal Borry
Clinician perspectives on policy approaches to genetic risk disclosure in families. Familial cancer (2024)
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison Dalton Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F Vears
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International journal of neonatal screening 10 (1) (2024)
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison Dalton Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F Vears
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International journal of neonatal screening 10 (1) (2024)
Amicia Phillips, Danya F Vears, Nozomi Mizushima, Pascal Borry
Clinician perspectives on policy approaches to genetic risk disclosure in families. Familial cancer 23 (2) (2024)
Amicia Phillips, Danya F Vears, Nozomi Mizushima, Pascal Borry
Clinician perspectives on policy approaches to genetic risk disclosure in families. Familial cancer 23 (2) (2024)
Stephanie Best, Zoe Fehlberg, Christopher Richards, Michael C J Quinn, Sebastian Lunke, Amanda B Spurdle, Karin S Kassahn, Chirag Patel, Danya F Vears, Ilias Goranitis, Fiona Lynch, Alan Robertson, Emma Tudini, John Chrisodoulou, Hamish S Scott, Julie McGaughran, Zornitza Stark
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services. European journal of human genetics : EJHG (2024)
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison Dalton Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F Vears
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International journal of neonatal screening 10 (1) (2024)
Amicia Phillips, Danya F Vears, Nozomi Mizushima, Pascal Borry
Clinician perspectives on policy approaches to genetic risk disclosure in families. Familial cancer 23 (2) (2024)
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison Dalton Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F Vears
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International journal of neonatal screening 10 (1) (2024)
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison Dalton Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F Vears
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International journal of neonatal screening 10 (1) (2024)
Erin Tutty, Alison D Archibald, Lilian Downie, Clara L Gaff, Sebastian Lunke, Danya F Vears, Zornitza Stark, Stephanie Best
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework. European journal of human genetics : EJHG (2024)
Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison Dalton Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F Vears
Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International journal of neonatal screening 10 (1) (2024)
Simon Coghlan, Christopher Gyngell, Danya F Vears
Ethics of artificial intelligence in prenatal and pediatric genomic medicine. Journal of community genetics (2023)
Danya F Vears, Julian Savulescu, John Chrisodoulou, Meaghan Wall, Ainsley Janelle Newson
Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns? Pharmacogenomics and personalized medicine 16 (2023)
Sachini Poogoda, Fiona Lynch, Zornitza Stark, Dominic Wilkinson, Julian Savulescu, Danya F Vears, Christopher Gyngell
Intensive Care Clinicians' Perspectives on Ethical Challenges Raised by Rapid Genomic Testing in Critically Ill Infants. Children (Basel, Switzerland) 10 (6) (2023)
Danya F Vears, Jackie Boyle, Chris Jacobs, Aideen M McInerney-Leo, Ainsley Janelle Newson, null null
Human Genetics Society of Australasia Position Statement: Genetic Carrier Testing for Recessive Conditions. Twin research and human genetics : the official journal of the International Society for Twin Studies (2023)
Sachini Poogoda, Fiona Lynch, Zornitza Stark, Dominic Wilkinson, Julian Savulescu, Danya F Vears, Christopher Gyngell
Intensive Care Clinicians' Perspectives on Ethical Challenges Raised by Rapid Genomic Testing in Critically Ill Infants. Children (Basel, Switzerland) 10 (6) (2023)
Fiona Lynch, Yan Meng, Stephanie Best, Ilias Goranitis, Julian Savulescu, Christopher Gyngell, Danya F Vears
Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations. European journal of human genetics : EJHG (2023)
Danya F Vears, Fiona Lynch, Amy Nisselle, Samantha Ayres, Zornitza Stark
Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia. European journal of human genetics : EJHG (2023)
Fiona Lynch, Lynn Gillam, Danya F Vears
Alleviating the confusion around content analysis: A comment in response to Wainstein, Elliott & Austin 2023. Journal of genetic counseling (2023)
Lauren Notini, Clara L Gaff, Julian Savulescu, Danya F Vears
Offering and Returning Secondary Findings in the Context of Exome Sequencing for Hearing Loss: Clinicians' Views and Experiences. AJOB empirical bioethics (2023)
Janneke M L Kuiper, Pascal Borry, Danya F Vears, Hilde Van Esch, Martina Cornelia Cornel, Nozomi Mizushima
Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography. European journal of human genetics : EJHG (2023)
Christopher Gyngell, Fiona Lynch, Danya F Vears, Hilary Bowman-Smart, Julian Savulescu, John Christodoulou
Storing paediatric genomic data for sequential interrogation across the lifespan. Journal of medical ethics (2023)
Danya F Vears, Nina Hallowell, Heidi Beate Bentzen, Bridget Ellul, Therese Haugdahl Nøst, Angeliki Kerasidou, Shona M Kerr, Michaela Th Mayrhofer, Signe Mezinska, Elizabeth Ormondroyd, Berge Solberg, Birgitte Wirum Sand, Isabelle Budin-Ljøsne
A practical checklist for return of results from genomic research in the European context. European journal of human genetics : EJHG (2023)
Katie Arkell, Christopher Gyngell, Zornitza Stark, Danya F Vears
Rapid Genomic Testing in Intensive Care: Health Professionals' Perspectives on Ethical Challenges. Children (Basel, Switzerland) 10 (5) (2023)
Janneke M L Kuiper, Pascal Borry, Danya F Vears, Hilde Van Esch, Nozomi Mizushima
Navigating the uncertainties of next-generation sequencing in the genetics clinic. Sociology of health & illness (2022)
Kayla Elliott, Danya F Vears, Valerie Sung, Zeffie Poulakis, Jane Sheehan
Exploring Parent Support Needs during the Newborn Hearing Diagnosis Pathway. Journal of clinical medicine 11 (5) (2022)
Amicia Phillips, Thomas Bronselaer, Pascal Borry, Nozomi Mizushima, Danya F Vears, Laurent Pasquier, Stefaan Callens
Informing relatives of their genetic risk: an examination of the Belgian legal context. European journal of human genetics : EJHG 30 (7) (2022)
Michelle Cao, Lauren Notini, Samantha Ayres, Danya F Vears
Australian healthcare professionals' perspectives on the ethical and practical issues associated with genomic newborn screening. Journal of genetic counseling (2022)
Danya F Vears, Joel T Minion, Stephanie J Roberts, James Cummings, Mavis Machirori, Madeleine J Murtagh
Views on genomic research result delivery methods and informed consent: a review. Personalized medicine 18 (3) (2021)
Danya F Vears
Should we respect parents' views about which results to return from genomic sequencing? Human genetics (2021)
Danya F Vears, Joel T Minion, Stephanie J Roberts, James Cummings, Mavis Machirori, Mwenza Blell, Isabelle Budin-Ljøsne, Lorraine Cowley, Stephanie O M Dyke, Clara Gaff, Robert Green, Alison Hall, Amber L Johns, Bartha M Knoppers, Stephanie Mulrine, Christine Patch, Eva Winkler, Madeleine J Murtagh
Return of individual research results from genomic research: A systematic review of stakeholder perspectives. PloS one 16 (11) (2021)
Lauren Notini, Clara L Gaff, Julian Savulescu, Danya F Vears
Clinicians' Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss. Journal of clinical medicine 11 (1) (2021)
Danya F Vears, Karine Sénécal, Pascal Borry
Genetic health professionals' experiences with initiating reanalysis of genomic sequence data. Familial cancer 19 (3) (2021)
Amicia Phillips, Emilia Niemiec, Heidi Carmen Howard, Kalliopi Kagkelari, Pascal Borry, Danya F Vears
Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing. European journal of human genetics : EJHG 28 (9) (2020)
Danya F Vears, Martin Elferink, Marjolein Kriek, Pascal Borry, Koen L van Gassen
Analysis of laboratory reporting practices using a quality assessment of a virtual patient. Genetics in medicine : official journal of the American College of Medical Genetics 23 (3) (2020)
Middleton Anna, Richard Milne, Heidi Howard, Emilia Niemiec, Lauren Robarts, Christine Critchley, Dianne Nicol, Barbara Prainsack, Jerome Atutornu, Danya F Vears, James Smith, Claire Steed, Paul Bevan, Erick R Scott, Jason Bobe, Peter Goodhand, Erika Kleiderman, Adrian Thorogood, Katherine I Morley, null null
Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data. European journal of human genetics : EJHG 28 (4) (2019)
Bertrand Isidor, Sophie Julia, Pascale Saugier-Veber, Paul-Loup Weil-Dubuc, Stephane Bezieau, Eric Bieth, Jean-Paul Bonnefont, Arnold Munnich, Franck Bourdeaut, Catherine Bourgain, Nicolas Chassaing, Nadège Corradini, Damien Haye, Julie Plaisancie, Delphine Dupin-Deguine, Patrick Calvas, Cyril Mignot, Benjamin Cogné, Sylvie Manouvrier, Laurent Pasquier, Delphine Héron, Kym M Boycott, Mauro Turrini, Danya F Vears, Mathilde Nizon, Marie Vincent
Searching for secondary findings: considering actionability and preserving the right not to know. European journal of human genetics : EJHG 27 (10) (2019)
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry
Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms. European journal of human genetics : EJHG 26 (12) (2018)
Danya F Vears, E Niemiec, H C Howard, P Borry
How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis. Clinical genetics 94 (3-4) (2018)
Danya F Vears, Karine Sénécal, Pascal Borry
Reporting practices for unsolicited and secondary findings from next-generation sequencing technologies: Perspectives of laboratory personnel. Human mutation 38 (8) (2017)
Danya F Vears, K Sénécal, Angus John Clarke, L Jackson, A M Laberge, L Lovrecic, Amelie Piton, K L I Van Gassen, H G Yntema, B M Knoppers, P Borry
Points to consider for laboratories reporting results from diagnostic genomic sequencing. European journal of human genetics : EJHG 26 (1) (2017)