Helen M. Hanson

Heavitree Road
Exeter, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 89 publications

'Truthsets' for clinical validation of large-scale functional assays: Practice recommendations from Cancer Variant Interpretation Group UK (CanVIG-UK).

'Truthsets' for clinical validation of large-scale functional assays: Practice recommendations from Cancer Variant Interpretation Group UK (CanVIG-UK).

Journal: medRxiv : the preprint server for health sciences

Published: July 30, 2026

Integrating enriched case data from national laboratory testing with population-based case-control analyses: a novel statistical likelihood-ratio methodology for PS4 applied to 325,345 breast cancer cases and 671,006 controls.

Integrating enriched case data from national laboratory testing with population-based case-control analyses: a novel statistical likelihood-ratio methodology for PS4 applied to 325,345 breast cancer cases and 671,006 controls.

Journal: medRxiv : the preprint server for health sciences

Published: May 25, 2026

A national survey of UK Family History services.

A national survey of UK Family History services.

Journal: British journal of cancer

Published: April 15, 2026

Guidance on the reporting and clinical follow up of individuals with incidentally discovered germline RET variants in the UK.

Guidance on the reporting and clinical follow up of individuals with incidentally discovered germline RET variants in the UK.

Journal: Endocrine-related cancer

Published: April 10, 2026

Cancer Variant Interpretation Group UK (CanVIG-UK): updates on an exemplar national subspecialty multidisciplinary network.

Cancer Variant Interpretation Group UK (CanVIG-UK): updates on an exemplar national subspecialty multidisciplinary network.

Journal: Journal of medical genetics

Published: March 22, 2026

Health-related quality of life after risk-reducing hysterectomy (PRESCORES): a cross-sectional study.

Health-related quality of life after risk-reducing hysterectomy (PRESCORES): a cross-sectional study.

Journal: EClinicalMedicine

Published: February 15, 2026

The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.

The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.

Journal: Journal of medical genetics

Published: January 22, 2026

Consideration of inherited cancer risk on a continuum: An international and multidisciplinary perspective: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).

Consideration of inherited cancer risk on a continuum: An international and multidisciplinary perspective: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 21, 2025

The SINEs were there: identification of a pathogenic Alu insertion in a patient with DICER1-related tumour predisposition.

The SINEs were there: identification of a pathogenic Alu insertion in a patient with DICER1-related tumour predisposition.

Journal: Journal of medical genetics

Published: November 13, 2025

Estimands for Clinical Effectiveness of Risk-Reducing Early Salpingectomy in Women With High Risk of Ovarian Cancer.

Estimands for Clinical Effectiveness of Risk-Reducing Early Salpingectomy in Women With High Risk of Ovarian Cancer.

Journal: JAMA network open

Published: September 16, 2025

Management of individuals with heterozygous germline pathogenic variants in RAD51C, RAD51D, and BRIP1: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).

Management of individuals with heterozygous germline pathogenic variants in RAD51C, RAD51D, and BRIP1: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 08, 2025

Germline genomic testing to assess the suitability of stem cell donors in the treatment of haematological malignancy: clinical ethics commentary.

Germline genomic testing to assess the suitability of stem cell donors in the treatment of haematological malignancy: clinical ethics commentary.

Journal: Journal of medical ethics

Published: June 12, 2025

Showing 1-12 of 89

Last Updated: 09/26/2026