Angus Clarke

Cardiff University

United Kingdom

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Articles (15)

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2025

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2025

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2025

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2023

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2023

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2023

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2023

Collaborators (8)

Anneke Lucassen

University of Oxford

UNITED KINGDOM

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Jorge Sequeiros

PORTUGAL

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Liliana Sousa

Associate Professor

Universidade de Aveiro

PORTUGAL

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Fiona Ulph

UNITED KINGDOM

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Yalda Jamshidi

Reader in Genomic Medicine

St George’s, University of London

UNITED KINGDOM

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Lisa Ballard

University of Southampton

UNITED KINGDOM

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Encarna Guillén-Navarro

Profesora titular vinculada

Universidad de Murcia

SPAIN

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Celine Lewis

UNITED KINGDOM

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Angus Clarke

Research Interests

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Articles (15)

Addressing family communication in genetic counseling: A scoping review of process studies

Genetic tests as prophecy: understanding self-defeating and self-fulfilling mechanisms in (predictive) genetic testing

The value of large-scale programmes in human genomics

Communicating Genetic Information in Families with Inherited Late-Onset Neurodegenerative Diseases: A Scoping Review

Ethical and social implications of public–private partnerships in the context of genomic/big health data collection

Written communication of whole genome sequencing results in the NHS Genomic Medicine Service: a multi-centre service evaluation

Predictive genetic testing for Huntington's disease: Exploring participant experiences of uncertainty and ambivalence between clinic appointments

Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions

Review of a specialist Rett syndrome clinic from 2003 to the COVID pandemic: clinic experience and carer perspectives

Protocol for the Phase 2 EDELIFE Trial Investigating the Efficacy and Safety of Intra-Amniotic ER004 Administration to Male Subjects with X-Linked Hypohidrotic Ectodermal Dysplasia.

Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’

Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’

Börjeson–Forssman–Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families

Commentary on Eichinger J, Zimmermann B, Elger B, McLennan S, Filges I, Koné I. 2023. ‘It’s a nightmare’: informed consent in paediatric genome-wide sequencing. A qualitative expert interview study from Germany and Switzerland

Terminology and Consistency

Collaborators (8)

Anneke Lucassen

Jorge Sequeiros

Liliana Sousa

Fiona Ulph

Yalda Jamshidi

Lisa Ballard

Encarna Guillén-Navarro

Celine Lewis

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