Andrew Green

Professor of Medical Genetics

Dublin City University

Ireland

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Articles (10)

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

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2022

Year:

2022

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2021

Year:

2021

Year:

2021

Collaborators (14)

Demetra Georgiou

Imperial College London

UNITED KINGDOM

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Robert Cooper

Professor of Cardiology and Sports Medicine

Liverpool John Moores University

UNITED KINGDOM

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Edward Tobias

University of Glasgow

UNITED KINGDOM

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Ignacio Soriano

University of Oxford

UNITED KINGDOM

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John Burn

UNITED KINGDOM

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Andrew Crosby

Professor of Human Genetics

University of Exeter

UNITED KINGDOM

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Ian Majewski

Laboratory Head

Walter and Eliza Hall Institute of Medical Research

AUSTRALIA

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Sally Ann Lynch

IRELAND

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Nadia Akawi

University of Oxford

UNITED KINGDOM

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Ina Knerr

Consultant Metabolic Paediatrician, Clinical Professor

IRELAND

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Louise Gibson

Senior Lecturer

University College Cork

IRELAND

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Jonathan Neil Berg

Academic, Clinical Reader

University of Dundee

UNITED KINGDOM

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William Cross

Lecturer

University of Westminster

UNITED KINGDOM

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Hannah Deborah West

Senior Lecturer

Cardiff University

UNITED KINGDOM

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Andrew Green

Research Interests

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Articles (10)

An approach to recognising and identifying metabolic presentations in the paediatric Irish Traveller population

Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair (Nature Communications, (2023), 14, 1, (3636), 10.1038/s41467-023-39248-0)

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair

The utility of multiple genomic technologies for interpretation of modern next generation sequencing: A novel case of three FANCA gene variants resulting in autosomal recessive Fanconi anaemia

Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UK

Nicolaides-Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion

Germline MBD4 deficiency causes a multi-tumor predisposition syndrome

The contribution of X-linked coding variation to severe developmental disorders.

Multi-Organ Dysfunction in Cerebral Palsy

An unusual case of tetralogy of Fallot with an absent pulmonary valve associated with a retro-aortic innominate vein in a patient with a 16p12.2 microdeletion

Collaborators (14)

Demetra Georgiou

Robert Cooper

Edward Tobias

Ignacio Soriano

John Burn

Andrew Crosby

Ian Majewski

Sally Ann Lynch

Nadia Akawi

Ina Knerr

Louise Gibson

Jonathan Neil Berg

William Cross

Hannah Deborah West

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