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

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

2022

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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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Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update

Genes, 2022-12, Vol.13 (12), p.2327

2022

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Somatic mutations in salivary duct carcinoma and potential therapeutic targets

Oncotarget, 2017-09, Vol.8 (44), p.75893-75903

2017

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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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A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti

PloS one, 2013-12, Vol.8 (12), p.e81625-e81625

2013

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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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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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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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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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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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Response to Beretich and Beretich

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

2023

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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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GWAS: heritability missing in action?

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

2010

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

European journal of human genetics : EJHG, 2023-12, Vol.31 (12), p.1421-1429

2023

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Recontacting in clinical practice: the views and expectations of patients in the United Kingdom

European journal of human genetics : EJHG, 2017-10, Vol.25 (10), p.1106-1112

2017

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Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe

European journal of human genetics : EJHG, 2018-07, Vol.26 (7), p.946-954

2018

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A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice

European journal of human genetics : EJHG, 2019-08, Vol.27 (8), p.1215-1224

2019

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Recontacting in clinical genetics and genomic medicine? We need to talk about it

European journal of human genetics : EJHG, 2017-05, Vol.25 (5), p.520-521

2017

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Commentary on predictive genetic testing of minors: by Mand et al

Journal of medical ethics, 2012-09, Vol.38 (9), p.527-528

Clarke, Angus J

2012

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Rett syndrome: Revised diagnostic criteria and nomenclature

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

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

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

Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update

Somatic mutations in salivary duct carcinoma and potential therapeutic targets

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

A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti

Ethics in genetic counselling

Peter S. Harper: obituary

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

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

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

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

Response to Beretich and Beretich

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

GWAS: heritability missing in action?

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

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

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

Recontacting in clinical practice: the views and expectations of patients in the United Kingdom

Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe

A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice

Recontacting in clinical genetics and genomic medicine? We need to talk about it

Commentary on predictive genetic testing of minors: by Mand et al

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