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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

European journal of human genetics : EJHG, 2023-12, Vol.31 (12), p.1348-1349

Clarke, Angus J

2023

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Rett syndrome: Revised diagnostic criteria and nomenclature

Annals of neurology, 2010-12, Vol.68 (6), p.944-950

2010

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Managing the ethical challenges of next-generation sequencing in genomic medicine

British medical bulletin, 2014-09, Vol.111 (1), p.17-30

Clarke, Angus J

2014

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Ethics in genetic counselling

Journal of community genetics, 2019-01, Vol.10 (1), p.3-33

2019

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Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis

BMJ open, 2016-01, Vol.6 (1), p.e010002-e010002

2016

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Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK)

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1049-1053

2013

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Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway

American journal of medical genetics. Part A, 2019-03, Vol.179 (3), p.442-447

2019

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Ethics experts and fetal patients: a proposal for modesty

BMC medical ethics, 2021-12, Vol.22 (1), p.161-161, Article 161

2021

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Peter S. Harper: obituary

Human genetics, 2021-07, Vol.140 (7), p.981-983

2021

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Communication of Information about Genetic Risks: Putting Families at the Center

Family process, 2018-09, Vol.57 (3), p.836-846

2018

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Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

European journal of human genetics : EJHG, 2021-03, Vol.29 (3), p.365-377

2021

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The evolving role of medical geneticists in the era of gene therapy: An urgency to prepare

Genetics in medicine, 2023-04, Vol.25 (4), p.100022-100022, Article 100022

2023

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Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases

Journal of genetic counseling, 2021-10, Vol.30 (5), p.1480-1490

2021

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For Your Interest? The Ethical Acceptability of Using Non-Invasive Prenatal Testing to Test 'Purely for Information'

Bioethics, 2015-01, Vol.29 (1), p.19-25

2015

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Harper's Practical Genetic Counselling, Eighth Edition

Clarke, Angus

8th edition., 2019

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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.169-182

2019

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Response to Beretich and Beretich

Genetics in medicine, 2023-10, Vol.25 (10), p.100903-100903, Article 100903

2023

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International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency Disorder

Frontiers in neurology, 2022-06, Vol.13, p.874695

2022

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Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom

European journal of human genetics : EJHG, 2017-02, Vol.25 (3), p.275-279

2017

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The Fetus as a Patient: A Contested Concept and its Normative Implications

1, 2018

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A Historical and Current Review of Newborn Screening for Neuromuscular Disorders From Around the World: Lessons for the United States

Pediatric neurology, 2017-12, Vol.77, p.12-22

2017

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GWAS: heritability missing in action?

European journal of human genetics : EJHG, 2010-08, Vol.18 (8), p.859-861

2010

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Process and outcome in communication of genetic information within families: a systematic review

European journal of human genetics : EJHG, 2007-10, Vol.15 (10), p.999-1011

2007

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Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom

Genetics in medicine, 2016-09, Vol.18 (9), p.876-881

2016

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"A very big challenge": a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England

Frontiers in genetics, 2024-01, Vol.14, p.1282034-1282034

2024

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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

Rett syndrome: Revised diagnostic criteria and nomenclature

Managing the ethical challenges of next-generation sequencing in genomic medicine

Ethics in genetic counselling

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis

Newborn bloodspot screening for Duchenne muscular dystrophy: 21 years experience in Wales (UK)

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway

Ethics experts and fetal patients: a proposal for modesty

Peter S. Harper: obituary

Communication of Information about Genetic Risks: Putting Families at the Center

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

The evolving role of medical geneticists in the era of gene therapy: An urgency to prepare

Between responsibility and desire: Accounts of reproductive decisions from those at risk for or affected by late‐onset neurological diseases

For Your Interest? The Ethical Acceptability of Using Non-Invasive Prenatal Testing to Test 'Purely for Information'

Harper's Practical Genetic Counselling, Eighth Edition

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

Response to Beretich and Beretich

International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency Disorder

Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom

The Fetus as a Patient: A Contested Concept and its Normative Implications

A Historical and Current Review of Newborn Screening for Neuromuscular Disorders From Around the World: Lessons for the United States

GWAS: heritability missing in action?

Process and outcome in communication of genetic information within families: a systematic review

Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom

"A very big challenge": a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England

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