Terri Patricia McVeigh (Terri P McVeigh, Terri P McVeigh, Terri McVeigh, T P McVeigh)

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 32

Top Venues

Journal of medical genetics

Familial cancer

JMIR biomedical engineering

American journal of medical genetics. Part A

Royal Marsden Hospital

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Royal Marsden Hospital Jul 11 2018

United Kingdom

Consultant Clinical Geneticist :: Cancer Genetics

Institute of Cancer Research Mar 01 2017

United Kingdom

Tutor, Masters in Genomics (Cancer) :: Cancer Genetics

National University of Ireland - Galway Mar 01 2015

Ireland

Tutor, Masters of Health Sciences :: Clinical Education

Our Lady's Children's Hospital Jan 10 2015 - Jul 10 2018

Ireland

Specialist Registrar :: Clinical Genetics

Mater Misericordiae University Hospital Jul 11 2014 - Jan 10 2015

Ireland

Specialist Registrar :: Metabolic Medicine

Publications

Terri Patricia McVeigh, Fiona Lalloo, Ian M Frayling, Andrew Latchford, Katie Snape, Miranda Durkie, Kevin J Monahan, Helen Hanson
Challenges in developing and implementing international best practice guidance for intermediate-risk variants in cancer susceptibility genes: APC c.3920T>A p.(Ile1307Lys) as an exemplar. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Ian M Frayling, Andrew Latchford, Katie Snape, Miranda Durkie, Kevin J Monahan, Helen Hanson
Challenges in developing and implementing international best practice guidance for intermediate-risk variants in cancer susceptibility genes: APC c.3920T>A p.(Ile1307Lys) as an exemplar. Journal of medical genetics (2024)
Terri Patricia McVeigh, Kevin J Monahan, Joseph Christopher, Nick West, Malcolm Scott, Jennie Murray, Helen Hanson, null null
Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of medical genetics 61 (7) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Kevin J Monahan, Andrew Latchford, Miranda Durkie, Rachael Mein, Andrew H Crosby, Helen Hanson
Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Kevin J Monahan, Andrew Latchford, Miranda Durkie, Rachael Mein, Andrew H Crosby, Helen Hanson
Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Kevin J Monahan, Andrew Latchford, Miranda Durkie, Rachael Mein, Andrew H Crosby, Helen Hanson
Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Kevin J Monahan, Andrew Latchford, Miranda Durkie, Rachael Mein, Andrew H Crosby, Helen Hanson
Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Kevin J Monahan, Joseph Christopher, Nick West, Malcolm Scott, Jennie Murray, Helen Hanson, null null
Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of medical genetics 61 (7) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Ian M Frayling, Andrew Latchford, Katie Snape, Miranda Durkie, Kevin J Monahan, Helen Hanson
Challenges in developing and implementing international best practice guidance for intermediate-risk variants in cancer susceptibility genes: APC c.3920T>A p.(Ile1307Lys) as an exemplar. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Kevin J Monahan, Joseph Christopher, Nick West, Malcolm Scott, Jennie Murray, Helen Hanson, null null
Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of medical genetics (2024)
Terri Patricia McVeigh, Kevin J Monahan, Joseph Christopher, Nick West, Malcolm Scott, Jennie Murray, Helen Hanson, null null
Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of medical genetics (2024)
Terri Patricia McVeigh, Fiona Lalloo, Ian M Frayling, Andrew Latchford, Katie Snape, Miranda Durkie, Kevin J Monahan, Helen Hanson
Challenges in developing and implementing international best practice guidance for intermediate-risk variants in cancer susceptibility genes: APC c.3920T>A p.(Ile1307Lys) as an exemplar. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Ian M Frayling, Andrew Latchford, Katie Snape, Miranda Durkie, Kevin J Monahan, Helen Hanson
Challenges in developing and implementing international best practice guidance for intermediate-risk variants in cancer susceptibility genes: APC c.3920T>A p.(Ile1307Lys) as an exemplar. Journal of medical genetics 61 (8) (2024)
Terri Patricia McVeigh, Fiona Lalloo, Kevin J Monahan, Andrew Latchford, Miranda Durkie, Rachael Mein, Andrew H Crosby, Helen Hanson
Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations. Journal of medical genetics (2024)
Terri Patricia McVeigh, Kevin J Monahan, Joseph Christopher, Nick West, Malcolm Scott, Jennie Murray, Helen Hanson, null null
Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of medical genetics 61 (7) (2024)
Hemendra Worlikar, Sean Coleman, Jack Kelly, Sadhbh O'Connor, Aoife Murray, Terri Patricia McVeigh, Jennifer Doran, Ian McCabe, Derek T O'Keeffe
Mixed Reality Platforms in Telehealth Delivery: Scoping Review. JMIR biomedical engineering 8 (2023)
Andrew Clark, Sally Thomas, Angela Hamblin, Polly Talley, Austin G Kulasekararaj, Jacob Grinfeld, Beverley Speight, Katie Snape, Terri Patricia McVeigh, John A Snowden
Management of patients with germline predisposition to haematological malignancies considered for allogeneic blood and marrow transplantation: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene-CanVar, NHS England Genomic Laboratory Hub (GLH) Haematological Malignancies Working Group and the British Society of Blood and Marrow Transplantation and cellular therapy (BSBMTCT). British journal of haematology (2023)
Hemendra Worlikar, Sean Coleman, Jack Kelly, Sadhbh O'Connor, Aoife Murray, Terri Patricia McVeigh, Jennifer Doran, Ian McCabe, Derek T O'Keeffe
Mixed Reality Platforms in Telehealth Delivery: Scoping Review. JMIR biomedical engineering 8 (2023)
Hemendra Worlikar, Sean Coleman, Jack Kelly, Sadhbh O'Connor, Aoife Murray, Terri Patricia McVeigh, Jennifer Doran, Ian McCabe, Derek T O'Keeffe
Mixed Reality Platforms in Telehealth Delivery: Scoping Review. JMIR biomedical engineering 8 (2023)
Terri Patricia McVeigh, Karl J Sweeney, Donal J Brennan, Una M McVeigh, Simon Ward, Ann Strydom, Sheila Seal, Katherine Astbury, Paul Donnellan, Joanne Higgins, Maccon Keane, Michael J Kerin, Carmel Malone, Pauline McGough, Ray McLaughlin, Michael O'Leary, Margaret Rushe, Michael Kevin Barry, Geraldine MacGregor, Michael Sugrue, Ala Yousif, Dhafir Al-Azawi, Eileen Berkeley, Terence J Boyle, Elizabeth M Connolly, Carmel Nolan, Elaine Richardson, Claire Giffney, Samantha B Doyle, Sheila Broderick, William Boyd, Ruaidhri McVey, Thomas Walsh, Michael Farrell, David J Gallagher, Nazneen Rahman, Angela J George
A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland. Familial cancer (2022)
Shahram Aziz, Hazel O'Sullivan, Kara Heelan, Afrina Alam, Terri Patricia McVeigh
Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review. Familial cancer (2022)
Una Mary McVeigh, John William Tepper, Terri Patricia McVeigh
A Review of Breast Cancer Risk Factors in Adolescents and Young Adults. Cancers 13 (21) (2021)
Sarah Wedderburn, Terri Patricia McVeigh
Should All Individuals Be Screened for Genetic Predisposition to Cancer? Genetics research 2021 (2021)
E Cojocaru, S Gennatas, K Thway, C Fisher, A Smrke, D Strauss, A Hayes, M Smith, R L Jones, C Benson, Terri Patricia McVeigh
Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK. Familial cancer (2021)
Hannah Dawson, Alannah Smrke, Peter M Ellery, Nafisa Wilkinson, Adam N Rosenthal, Terri Patricia McVeigh
Fibroadenoma in vulval ectopic breast tissue in a patient with PTEN Hamartoma Tumour Syndrome. Familial cancer (2021)
Patrick W Owens, Terri Patricia McVeigh, Nicola Miller, Carole Guerin, Frederic Sebag, Denis Quill, Marcia Bell, Michael J Kerin, Aoife J Lowery
FOXE1 polymorphism rs965513 predisposes to thyroid cancer in a European cohort. Endocrine oncology (Bristol, England) 1 (1) (2021)
Jana McHugh, Gozie Offiah, Sean Daly, Nazmy El Beltagi, Michael Kevin Barry, Seamus O'Reilly, Terri Patricia McVeigh
Postgraduate training in Cancer Genetics-a cross-specialty survey exploring experience of clinicians in Ireland. Irish journal of medical science (2021)
Xavier Bracke, Jonathan Roberts, Terri Patricia McVeigh
A systematic review and meta-analysis of telephone vs in-person genetic counseling in BRCA1/BRCA2 genetic testing. Journal of genetic counseling 30 (2) (2020)
Catherine Diskin, Terri Patricia McVeigh, Des W Cox
Sleep disordered breathing in children with Down syndrome in the Republic of Ireland. American journal of medical genetics. Part A 182 (12) (2020)
Terri Patricia McVeigh, Deirdre Donnelly, Maryam Al Shehhi, Elizabeth A Jones, Alexandra Murray, Sarah Wedderburn, Mary Porteous, Sally Ann Lynch
Towards establishing consistency in triage in a tertiary specialty. European journal of human genetics : EJHG 27 (4) (2019)
Terri Patricia McVeigh, Luke J Kelly, Elizabeth Whitmore, Tara Clark, Brendan Mullaney, David E Barton, Alana Ward, Sally Ann Lynch
Managing uncertainty in inherited cardiac pathologies-an international multidisciplinary survey. European journal of human genetics : EJHG 27 (8) (2019)
Terri Patricia McVeigh, Jonathan A Soye, Emma Gordon, Sally A Lynch
Non-syndromic bilateral ulnar aplasia with humero-radial synostosis and oligo-ectro-dactyly. American journal of medical genetics. Part A 176 (5) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Terri Patricia McVeigh (Terri P McVeigh, Terri P McVeigh, Terri McVeigh, T P McVeigh)