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“Ethical responsibility very often gets drowned out”: A qualitative interview study of genome scientists’ and ELSI scholars’ perspectives on the role and relevance of ELSI expertise

AJOB Empirical Bioethics

Daphne O. Martschenko, Anna Granucci, Mildred K. Cho

2024

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Study of the impact of ClinGen Revisions on ACMG/AMP variant semi-automatic classification for rare diseases diagnosis

Clin Chim Acta

Ana Rius, Nicolas Aguirre, Lorenzo Erra, Franco Gino Brunello, German Biagioli, Jonathan Zaiat, Marcelo A. Marti

2024

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Population-based genetic carrier screening. A consensus statement from the Spanish societies: AEGH, AEDP, ASEBIR, SEAGEN, SEF and SEGCD

European Journal of Human Genetics

Xavier Vendrell, Anna Abulí, Clara Serra, Juan José Guillén, Joaquín Rueda, Javier García-Planells, Fernando Santos-Simarro, Ramiro Quiroga, Fernando Abellán, Raluca Oancea-Ionescu, Encarna Guillén-Navarro

2024

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Profiling public perception of emerging technologies: Gene editing, brain chips and exoskeletons. A data-analytics framework

Heliyon

Simona-Vasilica Oprea, Adela Bâra

2024

Publication

The European Health Data Space as a case study

Ethics & Human Research

Edward S. Dove

2024

Publication

The ethics of synthetic DNA

J Med Ethics

Adrian Villalba, Anna Smajdor, Iain Brassington, Daniela Cutas

2024

Publication

Who has the responsibility to inform relatives at risk of hereditary cancer? A population-based survey in Sweden

BMJ Open

Kalle Grill, Amicia Phillips, Barbro Numan Hellquist, Anna Rosén

2024

Publication

A qualitative study of the experiences of patients with prostate cancer when receiving negative genetic results: "I still don't have a grasp of what it all means"

Journal of Genetic Counseling

Kimberly Zayhowski, Catharine Wang, Mary Nahorniak, Stephanie Loo, Gretchen Gignac, Christine Gunn

2024

Publication

The health information management professionals' role in supporting individuals considering genetic testing: An exploratory study

Health Information Management Journal

Christina Turrietta, Barbara Hewitt, Jackie Moczygemba, Alexander McLeod

2024

Publication

Culturally responsive strategies and practical considerations for live tissue studies in Māori participant cohorts

Front Res Metr Anal

Helena Abolins-Thompson, Kimiora L. Henare, Bridget Simonson, Mark Chaffin, Patrick T. Ellinor, Claire Henry, Mairarangi Haimona, Jake Aitken, Taku Parai, Bianca Elkington, Michael Rongo, Kirsty M. Danielson, Megan P. Leask

2024

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“Ethical responsibility very often gets drowned out”: A qualitative interview study of genome scientists’ and ELSI scholars’ perspectives on the role and relevance of ELSI expertise

Study of the impact of ClinGen Revisions on ACMG/AMP variant semi-automatic classification for rare diseases diagnosis

Population-based genetic carrier screening. A consensus statement from the Spanish societies: AEGH, AEDP, ASEBIR, SEAGEN, SEF and SEGCD

Profiling public perception of emerging technologies: Gene editing, brain chips and exoskeletons. A data-analytics framework

The European Health Data Space as a case study

The ethics of synthetic DNA

Who has the responsibility to inform relatives at risk of hereditary cancer? A population-based survey in Sweden

A qualitative study of the experiences of patients with prostate cancer when receiving negative genetic results: "I still don't have a grasp of what it all means"

The health information management professionals' role in supporting individuals considering genetic testing: An exploratory study

Culturally responsive strategies and practical considerations for live tissue studies in Māori participant cohorts

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731 - 740 of 31758 Topics

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