Author

Ruth Armstrong

Observed name: RUTH ARMSTRONG

Institution: Cambridge University Hospitals NHS Foundation Trust

Observed institutions: Royal Free London NHS Foundation Trust, University of Cambridge, Great Ormond Street Hospital, Great Ormond Street Hospital for Children NHS Foundation Trust, East London NHS Foundation Trust, Southmead Hospital, Cancer Research UK, Cambridge University Hospitals NHS Foundation Trust, University of Manchester, National Institute for Health and Care Research, Cancer Research UK Cambridge Center, Papworth Hospital NHS Foundation Trust, Addenbrooke's Hospital, Liverpool Womens NHS Foundation Trust, Alder Hey Children's Hospital, NIHR BioResource, NIHR Cambridge Biomedical Research Centre, University College London

ORCID: 0000-0002-7958-2829

Observed ORCID: 0000-0002-7958-2829

OpenAlex ID: A5118941433

Whole-genome sequencing of patients with rare diseases in a national health system

2020 · Ernest Turro, William J. Astle, et al. · Nature · 564

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort

2020 · James E. D. Thaventhiran, Hana Lango Allen, et al. · Nature · 242

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Germline selection shapes human mitochondrial DNA diversity

2019 · Wei Wei, Salih Tuna, et al. · Science · 239

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KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants

2018 · Joanna Kennedy, David Goudie, et al. · Genetics in Medicine · 106

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‘F*ck It!’: Matza and the Mood of Fatalism in the Desistance Process

2016 · Mark Halsey, Ruth Armstrong, et al. · The British Journal of Criminology · 82

Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

2018 · James Whitworth, Philip S. Smith, et al. · The American Journal of Human Genetics · 68

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Trusting the Untrustworthy: The Theology, Practice and Implications of Faith-Based Volunteers’ Work with Ex-Prisoners

2014 · Ruth Armstrong · Studies in Christian Ethics · 48

Benefits for children with suspected cancer from routine whole-genome sequencing

2024 · Angus Hodder, Sarah M. Leiter, et al. · Nature Medicine · 46

Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

2017 · Gavin Arno, Keren J. Carss, et al. · The American Journal of Human Genetics · 33

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What’s so good about participation? Politics, ethics and love in Learning Together

2020 · Ruth Armstrong, Amy Ludlow · Methodological Innovations · 16

From Paper Ethics to Real-World Research: Supervising Ethical Reflexivity When Taking Risks in Research with ‘the Risky’

2014 · Ruth Armstrong, Loraine Gelsthorpe, et al. · Palgrave Macmillan UK eBooks · 16

Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

2023 · Lauren Jeffries, Emily K. Mis, et al. · Genetics in Medicine · 14

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Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child

2017 · Katherine Schon, Olivera Spasic-Boskovic, et al. · Neurogenetics · 9

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Parole and Beyond: International Experiences of Life After Prison

2016 · Ruth Armstrong, Ioan Durnescu · Palgrave Macmillan UK eBooks · 8

Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort

2020 · James E. D. Thaventhiran, Hana Lango Allen, et al. · Nature · 7

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Examining Imprisonment Through a Social Justice Lens

2016 · Ruth Armstrong, Shadd Maruna · Routledge eBooks · 7

Validation of a new scale Evaluating the Personal, Interpersonal and Contextual dimensions of growth through learning – the EPIC scale

2022 · Ingrid Obsuth, Ruth Harriet Brown, et al. · Studies In Educational Evaluation · 6

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Outcomes from the English National Lynch Syndrome transformation project

2026 · Kevin J. Monahan, Paul Fleming, et al. · International Journal of Cancer · 5

Outlining a model of social journalism for health

2017 · Melissa Sweet, Lynore Geia, et al. · UWA Profiles and Research Repository (UWA) · 5

Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trial

2026 · John Burn, Gillian M Borthwick, et al. · The Lancet. Gastroenterology & hepatology · 4

Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practice

2024 · Michelle Bishop, Aditi Vedi, et al. · BMC Medical Education · 3

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Interstitial deletion of the short arm of chromosome 2 in a mother and child, with facial dysmorphism and mild learning difficulties

2006 · Ruth Armstrong, Ian Ellis, et al. · Clinical Dysmorphology · 3

Approach to the Paediatric Patient With Suspected Pheochromocytoma or Paraganglioma Versus Neuroblastoma

2024 · A Emile J Hendriks, Charlotte Burns, et al. · The Journal of Clinical Endocrinology & Metabolism · 2

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Living in Faith on Parole in Bible Belt USA

2016 · Ruth Armstrong · Palgrave Macmillan UK eBooks · 1

Self‐determination: more than politics

2012 · Ruth Armstrong, Noel E Hayman · The Medical Journal of Australia · 1

Works count: 71

Citation count: 1,604

H-index: 13

I10-index: 13