Helen Hanson

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 55

Top Venues

Journal of medical genetics

European journal of human genetics : EJHG

British journal of cancer

The British journal of general practice : the journal of the Royal College of General Practitioners

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

Publications

Catherine Huntley, Bethany Torr, Grace L Kavanaugh, Angela George, Helen Hanson, Katie M Snape, John Broggio, Louise Glasgow, Marc Tischkowitz, Dafydd Gareth Evans, Antonis C Antoniou, Clare Turnbull
Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study. The British journal of general practice : the journal of the Royal College of General Practitioners 74 (746) (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)
Catherine Huntley, Bethany Torr, Grace L Kavanaugh, Angela George, Helen Hanson, Katie M Snape, John Broggio, Louise Glasgow, Marc Tischkowitz, Dafydd Gareth Evans, Antonis C Antoniou, Clare Turnbull
Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study. The British journal of general practice : the journal of the Royal College of General Practitioners 74 (746) (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)
Sophie Allen, Lucy Loong, Alice Garrett, Bethany Torr, Miranda Durkie, James Drummond, Alison Callaway, Rachel Robinson, George Joseph Burghel, Helen Hanson, Joanne Field, Trudi McDevitt, Terri P McVeigh, Tina Bedenham, Christopher Bowles, Kirsty Bradshaw, Claire Brooks, Samantha Butler, Juan Carlos Del Rey Jimenez, Lorraine Hawkes, Victoria Stinton, Suzanne MacMahon, Martina Owens, Sheila Palmer-Smith, Kenneth Smith, James Tellez, Mikel Valganon-Petrizan, Erik Waskiewicz, Michael Yau, Diana M Eccles, Marc Tischkowitz, Shilpi Goel, Fiona McRonald, Antonis C Antoniou, Eva Morris, Steven Hardy, Catherine Huntley
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of medical genetics 61 (4) (2024)
Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Karin Kast, Christian F Singer, Anna Jakubowska, Carla H van Gils, Yen Y Tan, Christoph Engel, Muriel A Adank, Christi J van Asperen, Margreet G E M Ausems, Pascaline Berthet, null null, Margriet J Collee, Jackie A Cook, Jacqueline Eason, Karin Y van Spaendonck-Zwarts, D Gareth Evans, Encarna B Gómez García, Helen Hanson, Louise Izatt, Zoe Kemp, Fiona Lalloo, Christine Lasset, Fabienne Lesueur, Hannah Musgrave, Sophie Nambot, Catherine Noguès, Jan C Oosterwijk, Dominique Stoppa-Lyonnet, Marc Tischkowitz, Vishakha Tripathi, Marijke R Wevers, Emily Zhao, Flora E van Leeuwen, Marjanka K Schmidt, Douglas F Easton, Matti A Rookus, Antonis C Antoniou
Validation of the BOADICEA model in a prospective cohort of BRCA1/2 pathogenic variant carriers. 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)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (2024)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (2024)
Catherine Huntley, Bethany Torr, Grace L Kavanaugh, Angela George, Helen Hanson, Katie M Snape, John Broggio, Louise Glasgow, Marc Tischkowitz, Dafydd Gareth Evans, Antonis C Antoniou, Clare Turnbull
Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study. The British journal of general practice : the journal of the Royal College of General Practitioners (2024)
Catherine Huntley, Bethany Torr, Grace L Kavanaugh, Angela George, Helen Hanson, Katie M Snape, John Broggio, Louise Glasgow, Marc Tischkowitz, Dafydd Gareth Evans, Antonis C Antoniou, Clare Turnbull
Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study. The British journal of general practice : the journal of the Royal College of General Practitioners (2024)
Charlie F Rowlands, Alice Garrett, Sophie Allen, Miranda Durkie, George Joseph Burghel, Rachel Robinson, Alison Callaway, Joanne Field, Bethan Frugtniet, Sheila Palmer-Smith, Jonathan Grant, Judith Pagan, Trudi McDevitt, Terri P McVeigh, Helen Hanson, Nicola Whiffin, Michael Jones, Catherine Huntley, null null
The PS4-likelihood ratio calculator: flexible allocation of evidence weighting for case-control data in variant classification. Journal of medical genetics (2024)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (2024)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (2024)
Sophie Allen, Lucy Loong, Alice Garrett, Bethany Torr, Miranda Durkie, James Drummond, Alison Callaway, Rachel Robinson, George Joseph Burghel, Helen Hanson, Joanne Field, Trudi McDevitt, Terri P McVeigh, Tina Bedenham, Christopher Bowles, Kirsty Bradshaw, Claire Brooks, Samantha Butler, Juan Carlos Del Rey Jimenez, Lorraine Hawkes, Victoria Stinton, Suzanne MacMahon, Martina Owens, Sheila Palmer-Smith, Kenneth Smith, James Tellez, Mikel Valganon-Petrizan, Erik Waskiewicz, Michael Yau, Diana M Eccles, Marc Tischkowitz, Shilpi Goel, Fiona McRonald, Antonis C Antoniou, Eva Morris, Steven Hardy, Catherine Huntley
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of medical genetics 61 (4) (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)
Olga Tsoulaki, Marc Tischkowitz, Antonis C Antoniou, Hannah Musgrave, Gillian Rea, Ashu Gandhi, Karina Cox, Tracey Irvine, Sue Holcombe, Diana Eccles, Clare Turnbull, Ramsey Cutress, null null, Stephanie Archer, Helen Hanson
Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice. British journal of cancer 130 (12) (2024)
Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Karin Kast, Christian F Singer, Anna Jakubowska, Carla H van Gils, Yen Y Tan, Christoph Engel, Muriel A Adank, Christi J van Asperen, Margreet G E M Ausems, Pascaline Berthet, null null, Margriet J Collee, Jackie A Cook, Jacqueline Eason, Karin Y van Spaendonck-Zwarts, D Gareth Evans, Encarna B Gómez García, Helen Hanson, Louise Izatt, Zoe Kemp, Fiona Lalloo, Christine Lasset, Fabienne Lesueur, Hannah Musgrave, Sophie Nambot, Catherine Noguès, Jan C Oosterwijk, Dominique Stoppa-Lyonnet, Marc Tischkowitz, Vishakha Tripathi, Marijke R Wevers, Emily Zhao, Flora E van Leeuwen, Marjanka K Schmidt, Douglas F Easton, Matti A Rookus, Antonis C Antoniou
Validation of the BOADICEA model in a prospective cohort of BRCA1/2 pathogenic variant carriers. Journal of medical genetics (2024)
Olga Tsoulaki, Marc Tischkowitz, Antonis C Antoniou, Hannah Musgrave, Gillian Rea, Ashu Gandhi, Karina Cox, Tracey Irvine, Sue Holcombe, Diana Eccles, Clare Turnbull, Ramsey Cutress, null null, Stephanie Archer, Helen Hanson
Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice. British journal of cancer (2024)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (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)
Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Karin Kast, Christian F Singer, Anna Jakubowska, Carla H van Gils, Yen Y Tan, Christoph Engel, Muriel A Adank, Christi J van Asperen, Margreet G E M Ausems, Pascaline Berthet, null null, Margriet J Collee, Jackie A Cook, Jacqueline Eason, Karin Y van Spaendonck-Zwarts, D Gareth Evans, Encarna B Gómez García, Helen Hanson, Louise Izatt, Zoe Kemp, Fiona Lalloo, Christine Lasset, Fabienne Lesueur, Hannah Musgrave, Sophie Nambot, Catherine Noguès, Jan C Oosterwijk, Dominique Stoppa-Lyonnet, Marc Tischkowitz, Vishakha Tripathi, Marijke R Wevers, Emily Zhao, Flora E van Leeuwen, Marjanka K Schmidt, Douglas F Easton, Matti A Rookus, Antonis C Antoniou
Validation of the BOADICEA model in a prospective cohort of BRCA1/2 pathogenic variant carriers. 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)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (2024)
Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Karin Kast, Christian F Singer, Anna Jakubowska, Carla H van Gils, Yen Y Tan, Christoph Engel, Muriel A Adank, Christi J van Asperen, Margreet G E M Ausems, Pascaline Berthet, null null, Margriet J Collee, Jackie A Cook, Jacqueline Eason, Karin Y van Spaendonck-Zwarts, D Gareth Evans, Encarna B Gómez García, Helen Hanson, Louise Izatt, Zoe Kemp, Fiona Lalloo, Christine Lasset, Fabienne Lesueur, Hannah Musgrave, Sophie Nambot, Catherine Noguès, Jan C Oosterwijk, Dominique Stoppa-Lyonnet, Marc Tischkowitz, Vishakha Tripathi, Marijke R Wevers, Emily Zhao, Flora E van Leeuwen, Marjanka K Schmidt, Douglas F Easton, Matti A Rookus, Antonis C Antoniou
Validation of the BOADICEA model in a prospective cohort of BRCA1/2 pathogenic variant carriers. 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)
Olga Tsoulaki, Marc Tischkowitz, Antonis C Antoniou, Hannah Musgrave, Gillian Rea, Ashu Gandhi, Karina Cox, Tracey Irvine, Sue Holcombe, Diana Eccles, Clare Turnbull, Ramsey Cutress, null null, Stephanie Archer, Helen Hanson
Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice. British journal of cancer 130 (12) (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)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
Correction: EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG (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)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG (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)
Sophie Allen, Lucy Loong, Alice Garrett, Bethany Torr, Miranda Durkie, James Drummond, Alison Callaway, Rachel Robinson, George Joseph Burghel, Helen Hanson, Joanne Field, Trudi McDevitt, Terri P McVeigh, Tina Bedenham, Christopher Bowles, Kirsty Bradshaw, Claire Brooks, Samantha Butler, Juan Carlos Del Rey Jimenez, Lorraine Hawkes, Victoria Stinton, Suzanne MacMahon, Martina Owens, Sheila Palmer-Smith, Kenneth Smith, James Tellez, Mikel Valganon-Petrizan, Erik Waskiewicz, Michael Yau, Diana M Eccles, Marc Tischkowitz, Shilpi Goel, Fiona McRonald, Antonis C Antoniou, Eva Morris, Steven Hardy, Catherine Huntley
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of medical genetics 61 (4) (2024)
Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Karin Kast, Christian F Singer, Anna Jakubowska, Carla H van Gils, Yen Y Tan, Christoph Engel, Muriel A Adank, Christi J van Asperen, Margreet G E M Ausems, Pascaline Berthet, null null, Margriet J Collee, Jackie A Cook, Jacqueline Eason, Karin Y van Spaendonck-Zwarts, D Gareth Evans, Encarna B Gómez García, Helen Hanson, Louise Izatt, Zoe Kemp, Fiona Lalloo, Christine Lasset, Fabienne Lesueur, Hannah Musgrave, Sophie Nambot, Catherine Noguès, Jan C Oosterwijk, Dominique Stoppa-Lyonnet, Marc Tischkowitz, Vishakha Tripathi, Marijke R Wevers, Emily Zhao, Flora E van Leeuwen, Marjanka K Schmidt, Douglas F Easton, Matti A Rookus, Antonis C Antoniou
Validation of the BOADICEA model in a prospective cohort of BRCA1/2 pathogenic variant carriers. 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)
Trudi McDevitt, Miranda Durkie, Norbert Arnold, George Joseph Burghel, Samantha Butler, Kathleen B M Claes, Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, Helen Hanson, Clare Turnbull, Stacey Hume
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European journal of human genetics : EJHG 32 (5) (2024)
Olga Tsoulaki, Marc Tischkowitz, Antonis C Antoniou, Hannah Musgrave, Gillian Rea, Ashu Gandhi, Karina Cox, Tracey Irvine, Sue Holcombe, Diana Eccles, Clare Turnbull, Ramsey Cutress, null null, Stephanie Archer, Helen Hanson
Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice. British journal of cancer 130 (12) (2024)
Catherine Huntley, Bethany Torr, Grace L Kavanaugh, Angela George, Helen Hanson, Katie M Snape, John Broggio, Louise Glasgow, Marc Tischkowitz, Dafydd Gareth Evans, Antonis C Antoniou, Clare Turnbull
Breast cancer risk assessment for prescription of menopausal hormone therapy in women with a family history of breast cancer: an epidemiological modelling study. The British journal of general practice : the journal of the Royal College of General Practitioners (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)
Olga Tsoulaki, Marc Tischkowitz, Antonis C Antoniou, Hannah Musgrave, Gillian Rea, Ashu Gandhi, Karina Cox, Tracey Irvine, Sue Holcombe, Diana Eccles, Clare Turnbull, Ramsey Cutress, null null, Stephanie Archer, Helen Hanson
Joint ABS-UKCGG-CanGene-CanVar consensus regarding the use of CanRisk in clinical practice. British journal of cancer 130 (12) (2024)
Sophie Allen, Lucy Loong, Alice Garrett, Bethany Torr, Miranda Durkie, James Drummond, Alison Callaway, Rachel Robinson, George Joseph Burghel, Helen Hanson, Joanne Field, Trudi McDevitt, Terri P McVeigh, Tina Bedenham, Christopher Bowles, Kirsty Bradshaw, Claire Brooks, Samantha Butler, Juan Carlos Del Rey Jimenez, Lorraine Hawkes, Victoria Stinton, Suzanne MacMahon, Martina Owens, Sheila Palmer-Smith, Kenneth Smith, James Tellez, Mikel Valganon-Petrizan, Erik Waskiewicz, Michael Yau, Diana M Eccles, Marc Tischkowitz, Shilpi Goel, Fiona McRonald, Antonis C Antoniou, Eva Morris, Steven Hardy, Catherine Huntley
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of medical genetics 61 (4) (2024)
Anne G Lincoln, Sally C Benton, Carolyn Piggott, Shama Riaz Sheikh, Andrew D Beggs, Leah Buckley, Bianca DeSouza, James E East, Pete Sanders, Michael Lim, Donal Sheehan, Katie Snape, Helen Hanson, John R Greenaway, John Burn, David Nylander, Menna Hawkins, Fiona Lalloo, Kate Green, Thomas J Lee, Julie Walker, Gillian Matthews, Terry Rutherford, Peter D Sasieni, Kevin J Monahan
Risk-stratified faecal immunochemical testing (FIT) for urgent colonoscopy in Lynch syndrome during the COVID-19 pandemic. BJS open 7 (5) (2023)
Sophie Allen, Lucy Loong, Alice Garrett, Bethany Torr, Miranda Durkie, James Drummond, Alison Callaway, Rachel Robinson, George Joseph Burghel, Helen Hanson, Joanne Field, Trudi McDevitt, Terri P McVeigh, Tina Bedenham, Christopher Bowles, Kirsty Bradshaw, Claire Brooks, Samantha Butler, Juan Carlos Del Rey Jimenez, Lorraine Hawkes, Victoria Stinton, Suzanne MacMahon, Martina Owens, Sheila Palmer-Smith, Kenneth Smith, James Tellez, Mikel Valganon-Petrizan, Erik Waskiewicz, Michael Yau, Diana M Eccles, Marc Tischkowitz, Shilpi Goel, Fiona McRonald, Antonis C Antoniou, Eva Morris, Steven Hardy, Catherine Huntley
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of medical genetics (2023)
Fiona Lalloo, Anju Kulkarni, Cindy Chau, Maartje Nielsen, Michael Sheaff, Jeremy Steele, Remco van Doorn, Karin Wadt, Monica Hamill, Bethany Torr, Marc Tischkowitz, null null, Helen Hanson
Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome. European journal of human genetics : EJHG (2023)
Sophie Allen, Lucy Loong, Alice Garrett, Bethany Torr, Miranda Durkie, James Drummond, Alison Callaway, Rachel Robinson, George Joseph Burghel, Helen Hanson, Joanne Field, Trudi McDevitt, Terri P McVeigh, Tina Bedenham, Christopher Bowles, Kirsty Bradshaw, Claire Brooks, Samantha Butler, Juan Carlos Del Rey Jimenez, Lorraine Hawkes, Victoria Stinton, Suzanne MacMahon, Martina Owens, Sheila Palmer-Smith, Kenneth Smith, James Tellez, Mikel Valganon-Petrizan, Erik Waskiewicz, Michael Yau, Diana M Eccles, Marc Tischkowitz, Shilpi Goel, Fiona McRonald, Antonis C Antoniou, Eva Morris, Steven Hardy, Catherine Huntley
Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey. Journal of medical genetics (2023)
Helen Hanson, Miranda Durkie, Fiona Lalloo, Louise Izatt, Terri P McVeigh, Jackie A Cook, Carole Brewer, James Drummond, Samantha Butler, Treena Cranston, Ruth Casey, Tricia Tan, Daniel Morganstein, Diana M Eccles, Marc Tischkowitz, Clare Turnbull, Emma Roisin Woodward, Eamonn R Maher, null null
UK recommendations for SDHA germline genetic testing and surveillance in clinical practice. Journal of medical genetics (2022)
Sherly X Li, Valentina Silvestri, Goska Leslie, Timothy R Rebbeck, Susan L Neuhausen, John L Hopper, Henriette Roed Nielsen, Andrew J Lee, Xin Yang, Lesley McGuffog, Michael T Parsons, Irene L Andrulis, Norbert Arnold, Muriel Belotti, Åke Borg, Bruno Buecher, Saundra S Buys, Sandrine M Caputo, Wendy K Chung, Chrystelle Colas, Sarah V Colonna, Jackie Cook, Mary B Daly, Miguel de la Hoya, Antoine De Pauw, Hélène Delhomelle, Jacqueline Eason, Christoph Engel, D Gareth Evans, Ulrike Faust, Tanja N Fehm, Florentia Fostira, George Fountzilas, Megan N Frone, Vanesa Garcia-Barberan, Pilar Garre, Marion Gauthier-Villars, Andrea Gehrig, Gord Glendon, David E Goldgar, Lisa Golmard, Mark H Greene, Eric Hahnen, Ute Hamann, Helen Hanson, Tiara Hassan, Julia Hentschel, Judit Horvath, Louise Izatt, Ramunas Janavicius, Yue Jiao, Isabelle Durot, Beth Y Karlan, Sung-Won Kim, Irene Konstantopoulou, Ava Kwong, Anthony Laugé, Jong Won Lee, Fabienne Lesueur, Noura Mebirouk, Alfons Meindl, Emmanuelle Mouret-Fourme, Hannah Musgrave, Joanne Ngeow Yuen Yie, Dieter Niederacher, Sue K Park, Inge Sokilde Pedersen, Juliane Ramser, Susan J Ramus, Johanna Rantala, Muhammad Usman Rashid, Florian Reichl, Julia Ritter, Andreas Rump, Marta Santamariña, Claire Saule, Gunnar Schmidt, Rita K Schmutzler, Leigha Senter, Saba Shariff, Christian F Singer, Melissa C Southey, Dominique Stoppat-Lyonnet, Christian Sutter, Yen Tan, Soo-Hwang Teo, Mary Beth Terry, Mads Thomassen, Marc Tischkowitz, Amanda Ewart Toland, Diana Torres, Ana Vega, Sebastian A Wagner, Shan Wang-Gohrke, Barbara Wappenschmidt, Bernhard Heinrich Friedrich Weber, Drakoulis Yannoukakos, Amanda B Spurdle, Douglas F Easton, Georgia Chenevix-Trench, Laura Ottini, Antonis C Antoniou
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 40 (14) (2022)
Helen Hanson, Anjana Kulkarni, Lucy Loong, Grace Kavanaugh, Bethany Torr, Sophie Allen, Munaza Ahmed, Antonis C Antoniou, Ruth Cleaver, Tabib Dabir, Dafydd Gareth Evans, Ellen Golightly, Rosalyn Jewell, Kelly Kohut, Ranjit Manchanda, Alex Murray, Jennie Murray, Kai-Ren Ong, Adam N Rosenthal, Emma Roisin Woodward, Diana M Eccles, Catherine Huntley, Marc Tischkowitz, null null, Fiona Lalloo
UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variants in cancer predisposition genes: RAD51C , RAD51D , BRIP1 and PALB2 . Journal of medical genetics (2022)
Sue Philpott, Maria Raikou, Ranjit Manchanda, Michelle Lockley, Naveena Singh, Malcolm Scott, Dafydd Gareth Evans, Julian Adlard, Munaza Ahmed, Richard Edmondson, Emma Roisin Woodward, Athena Lamnisos, Janos Balega, Aarti Sharma, Louise Izatt, Anjana Kulkarni, Vishakha Tripathi, Joyce S Solomons, Kevin Hayes, Helen Hanson, Katie M Snape, Lucy Side, Steve Skates, Alistair McGuire, Adam N Rosenthal
The avoiding late diagnosis of ovarian cancer (ALDO) project; a pilot national surveillance programme for women with pathogenic germline variants in BRCA1 and BRCA2 . Journal of medical genetics (2022)
Faiza Gaba, Shivam Goyal, Dalya Marks, Dhivya Chandrasekaran, Olivia Evans, Sadiyah Robbani, Charlotte Tyson, Rosa Legood, Ertan Saridogan, W Glenn McCluggage, Helen Hanson, Naveena Singh, D Gareth Evans, Usha Menon, Ranjit Manchanda, null null
Surgical decision making in premenopausal BRCA carriers considering risk-reducing early salpingectomy or salpingo-oophorectomy: a qualitative study. Journal of medical genetics (2021)
Sarah Wedderburn, Stephanie Archer, Marc Tischkowitz, Helen Hanson, null null
Update: variable implementation of the 2018 UKCGG/UKGTN guidelines for breast cancer gene panel tests offered by UK genetics services. Journal of medical genetics 58 (8) (2021)
Helen Hanson, Angela F Brady, Gillian Crawford, Rosalind A Eeles, Sarah Gibson, Mette Jorgensen, Louise Izatt, Aslam Sohaib, Marc Tischkowitz, Dafydd Gareth Evans, null null
UKCGG Consensus Group guidelines for the management of patients with constitutional TP53 pathogenic variants. Journal of medical genetics (2020)

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Publication Activity (10 Years)

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Helen Hanson