Publications by authors named "Helen Hanson"

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Quantifying evidence for phenotypic specificity (PP4) for syndromic phenotypes: Large-scale integration of rare germline FH variants from diagnostic laboratory testing for HLRCC and renal cancer.
Sophie Allen, Charlie F Rowlands, Samantha Butler, Miranda Durkie, Carrie Horton, Helen Hanson

Genet Med· November 2025

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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).
Joanne Ngeow, Jianbang Chiang, Esteban Astiazaran-Symonds, Judith Balmaña, Ilana Cass, Helen Hanson

Genet Med· November 2025

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Germline genomic testing to assess the suitability of stem cell donors in the treatment of haematological malignancy: clinical ethics commentary.
Helena Carley, Kate Sahan, Helen Hanson, Katie Snape, Sarah Westbury

J Med Ethics· November 2025

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Proposed framework for triage of putative germline variants detected via tumour genomic testing in UK oncology practice.
Terri Patricia McVeigh, Helen Hanson, George J Burghel, Clare Turnbull, Katie Snape

J Med Genet· October 2025

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Availability of benign missense variant "truthsets" for validation of functional assays: Current status and a systematic approach.
Charlie F Rowlands, Sophie Allen, Alice Garrett, Miranda Durkie, George J Burghel, Helen Hanson

Am J Hum Genet· October 2025

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Recontact and follow-up for individuals with germline pathogenic variants in hereditary breast and ovarian cancer susceptibility genes: a UK Cancer Genetics Group consensus meeting.
Joseph Christopher, Katharine Edgerley, Beth McIldowie, Rosalyn Jewell, Zoe Kemp, Helen Hanson

J Med Genet· October 2025

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Estimands for Clinical Effectiveness of Risk-Reducing Early Salpingectomy in Women With High Risk of Ovarian Cancer.
Jacqueline Sia, Emily F Lane, Caitlin T Fierheller, Samuel Oxley, Ashwin Kalra, Helen Hanson

JAMA Netw Open· September 2025

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UK clinical practice guidelines for the management of patients with constitutional pathogenic variants.
Olga Tsoulaki, D Gareth Evans, Khushboo Sinha, Neil Rajan, Farah Bakr, Helen Hanson

J Med Genet· August 2025

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Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study.
Kelly Kohut, Kate Morton, Lesley Turner, Rebecca Foster, Elizabeth K Bancroft, Helen Hanson

J Genet Couns· August 2025

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Surveillance for individuals with a strong family history of kidney cancer but no identified heritable disease: a UK consensus.
James Whitworth, Helen Hanson, Alice Youngs, Terri McVeigh,

BJU Int· June 2025

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Validating data from multiplex assays of variant effect: A CanVIG-UK national survey of NHS clinical scientists.
Sophie Allen, Alice Garrett, Charlie F Rowlands, Miranda Durkie, George J Burghel, Helen Hanson

Am J Hum Genet· June 2025

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Impact of NICE Guideline NG241 'Ovarian Cancer: identifying and managing familial and genetic risk' on a regional NHS family history and clinical genetics service.
Alexander Roe, Andrea Forman, Fiona Lalloo, Terri P McVeigh, Helen Hanson

J Med Genet· April 2025

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Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK).
Alice Garrett, Sophie Allen, Miranda Durkie, George J Burghel, Rachel Robinson, Helen Hanson

Genet Med· February 2025

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Management of individuals with heterozygous germline pathogenic variants in ATM: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Tuya Pal, Katherine R Schon, Esteban Astiazaran-Symonds, Judith Balmaña, William D Foulkes, Helen Hanson

Genet Med· January 2025

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Digital innovation for cancer risk assessment allows large-scale service redevelopment of regional cancer genetics service delivery.
Alice Youngs, Andrea Forman, Marisa Elms, Kelly Kohut, Min Theik Hlaing, Helen Hanson

Fam Cancer· November 2024

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Corrigendum to "Development of an international glossary for clinical guidelines collaboration" "[Journal of Clinical Epidemiology 158 (2023) 84-91]".
Rachel E Christensen, Michael D Yi, Bianca Y Kang, Sarah A Ibrahim, Noor Anvery, Helen Hanson

J Clin Epidemiol· November 2024

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The PS4-likelihood ratio calculator: flexible allocation of evidence weighting for case-control data in variant classification.
Charlie F Rowlands, Alice Garrett, Sophie Allen, Miranda Durkie, George J Burghel, Helen Hanson

J Med Genet· September 2024

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'I Live With Lynch. Cancer Worry Ebbs Into the Background, Then Something Brings It to the Fore.' A Qualitative Interview Study Exploring How Lynch Syndrome Carriers Make Sense of Their Cancer Risks and Implications to Support Decision Making.
Kelly Kohut, Kate Morton, Lesley Turner, Rebecca Foster, Elizabeth K Bancroft, Helen Hanson

Psychooncology· September 2024

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Correction: EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer.
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George J Burghel, Samantha Butler, Helen Hanson

Eur J Hum Genet· August 2024

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Carrier testing for partners of variant carriers: UK Cancer Genetics Group recommendations.
Terri Patricia McVeigh, Fiona Lalloo, Kevin J Monahan, Andrew Latchford, Miranda Durkie, Helen Hanson

J Med Genet· July 2024

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Validation of the BOADICEA model in a prospective cohort of pathogenic variant carriers.
Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Helen Hanson

J Med Genet· July 2024

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Saturation genome editing of BAP1 functionally classifies somatic and germline variants.
Andrew J Waters, Timothy Brendler-Spaeth, Danielle Smith, Victoria Offord, Hong Kee Tan, Helen Hanson

Nat Genet· July 2024

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Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice.
Olga Tsoulaki, Marc Tischkowitz, Antonis C Antoniou, Hannah Musgrave, Gillian Rea, Helen Hanson

Br J Cancer· June 2024

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