Emma Roisin Woodward (Emma R Woodward)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 32

Top Venues

Journal of medical genetics

European journal of human genetics : EJHG

Cancers

Human mutation

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

Publications

Emma Roisin Woodward, Fiona Lalloo, Claire Forde, Sarah Pugh, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Anthony Howell, Sacha J Howell, Ashu Gandhi, D Gareth Evans
Germline testing of BRCA1 , BRCA2 , PALB2 and CHEK2 c.1100delC in 1514 triple negative familial and isolated breast cancers from a single centre, with extended testing of ATM , RAD51C and RAD51D in over 400. Journal of medical genetics 61 (4) (2024)
Marianne Geilswijk, Maurizio Genuardi, Emma Roisin Woodward, Katie Nightingale, Jazzmin Huber, Mia Gebauer Madsen, Dieke Liekelema-van der Heij, Ian Lisseman, Jenny Marlé-Ballangé, Cormac McCarthy, Fred H Menko, R Jeroen A van Moorselaar, Elzbieta Radzikowska, Stéphane Richard, Neil Rajan, Mette Sommerlund, Maria T A Wetscherek, Nataliya Di Donato, Eamonn R Maher, Joan Brunet
ERN GENTURIS clinical practice guidelines for the diagnosis, surveillance and management of people with Birt-Hogg-Dubé syndrome. European journal of human genetics : EJHG (2024)
Emma Roisin Woodward, Fiona Lalloo, Claire Forde, Sarah Pugh, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Anthony Howell, Sacha J Howell, Ashu Gandhi, D Gareth Evans
Germline testing of BRCA1 , BRCA2 , PALB2 and CHEK2 c.1100delC in 1514 triple negative familial and isolated breast cancers from a single centre, with extended testing of ATM , RAD51C and RAD51D in over 400. Journal of medical genetics 61 (4) (2024)
Melissa R Perrino, Anirban Das, Sarah R Scollon, Sarah G Mitchell, Mary-Louise C Greer, Marielle E Yohe, Jordan R Hansford, Jennifer M Kalish, Kris Ann P Schultz, Suzanne P MacFarland, Wendy K Kohlmann, Philip J Lupo, Kara N Maxwell, Stefan M Pfister, Rosanna Weksberg, Orli Michaeli, Marjolijn C J Jongmans, Gail E Tomlinson, Jack J Brzezinski, Uri Tabori, Gina M Ney, Karen W Gripp, Andrea M Gross, Brigitte C Widemann, Douglas R Stewart, Emma Roisin Woodward, Christian Peter Kratz
Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies. Clinical cancer research : an official journal of the American Association for Cancer Research (2024)
Nicola Flaum, Emma J Crosbie, Emma Roisin Woodward, Fiona Lalloo, Robert Morgan, Neil Ryan, Dafydd Gareth Evans
MSH2 is the very young onset ovarian cancer predisposition gene, not BRCA1 . Journal of medical genetics (2023)
Dafydd Gareth Evans, Elaine F Harkness, Emma Roisin Woodward
TP53 c.455C>T p.(Pro152Leu) pathogenic variant is a lower risk allele with attenuated risks of breast cancer and sarcoma. Journal of medical genetics (2023)
Emma Roisin Woodward, Fiona Lalloo, Claire Forde, Sarah Pugh, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Anthony Howell, Sacha J Howell, Ashu Gandhi, D Gareth Evans
Germline testing of BRCA1 , BRCA2 , PALB2 and CHEK2 c.1100delC in 1514 triple negative familial and isolated breast cancers from a single centre, with extended testing of ATM , RAD51C and RAD51D in over 400. Journal of medical genetics (2023)
Dafydd Gareth Evans, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Ashu Gandhi, Sacha J Howell, Anthony Howell, Claire Forde, Fiona Lalloo, William G Newman, Miriam Jane Smith, Emma Roisin Woodward
Detection of pathogenic variants in breast cancer susceptibility genes in bilateral breast cancer. 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)
Dafydd Gareth Evans, Siva Sithambaram, Elke Maria van Veen, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Helen Byers, Jamie M Ellingford, Ashu Gandhi, Sacha J Howell, Anthony Howell, Claire Forde, Fiona Lalloo, William G Newman, Miriam Jane Smith, Emma Roisin Woodward
Differential involvement of germline pathogenic variants in breast cancer genes between DCIS and low-grade invasive cancers. Journal of medical genetics (2022)
Alexander J Thompson, Yousef M Alwan, Vijay A C Ramani, Dafydd Gareth Evans, Eamonn R Maher, Emma Roisin Woodward
Cost-effectiveness model of renal cell carcinoma (RCC) surveillance in hereditary leiomyomatosis and renal cell carcinoma (HLRCC). Journal of medical genetics (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)
Emma Roisin Woodward, Stefan Meyer
Fanconi Anaemia, Childhood Cancer and the BRCA Genes. Genes 12 (10) (2021)
Dafydd Gareth Evans, Elke Maria van Veen, Emma Roisin Woodward, Elaine F Harkness, Jamie M Ellingford, Naomi L Bowers, Andrew J Wallace, Sacha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam Jane Smith
Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability. Cancers 13 (16) (2021)
Sarah Bennett, Elizabeth Alexander, Harry Fraser, Naomi Bowers, Andrew Wallace, Emma Roisin Woodward, Fiona Lalloo, Anne Marie Quinn, Shuwen Huang, Helene Schlecht, Dafydd Gareth Evans
Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives. European journal of human genetics : EJHG 29 (5) (2021)
Dafydd Gareth Evans, Fiona Lalloo, Neil Aj Ryan, Naomi Bowers, Kate Green, Emma Roisin Woodward, Tara Clancy, James Bolton, Rhona J McVey, Andrew J Wallace, Katy Newton, James Hill, Raymond McMahon, Emma J Crosbie
Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers. Journal of medical genetics (2021)
Hugh Furness, Louay Salfity, Johanna Devereux, Dorothy Halliday, Helen Hanson, Deborah M Ruddy, null Uk Vhl Study Group, Neha Shah, George Sultana, Emma Roisin Woodward, Richard N Sandford, Katie M Snape, Eamonn R Maher
Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel-Lindau Disease. Genes 12 (9) (2021)
Ruta Marcinkute, Emma Roisin Woodward, Ashu Gandhi, Sacha Howell, Emma J Crosbie, Julie Wissely, James Harvey, Lindsay Highton, John Murphy, Cathrine Holland, Richard Edmondson, Richard Clayton, Lester Barr, Elaine F Harkness, Anthony Howell, Fiona Lalloo, Dafydd Gareth Evans
Uptake and efficacy of bilateral risk reducing surgery in unaffected female BRCA1 and BRCA2 carriers. Journal of medical genetics (2021)
Dafydd Gareth Evans, Elke Maria van Veen, Helen J Byers, Sarah J Evans, George Joseph Burghel, Emma Roisin Woodward, Elaine F Harkness, Diana M Eccles, Stephanie L Greville-Haygate, Jamie M Ellingford, Naomi L Bowers, Marta Pereira, Andrew J Wallace, Sasha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam Jane Smith
High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer. Journal of medical genetics (2021)
Emma Roisin Woodward, Kate Green, George J Burghel, Michael Bulman, Tara Clancy, Fiona Lalloo, Helene Schlecht, Andrew J Wallace, Dafydd Gareth Evans
30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes. European journal of human genetics : EJHG (2021)
Emma Roisin Woodward, Elke M van Veen, Claire Forde, Elaine F Harkness, Helen J Byers, Jamie M Ellingford, George J Burghel, Helene Schlech, Naomi L Bowers, Andrew J Wallace, Sacha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam J Smith, D Gareth Evans
Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer. Genetics in medicine : official journal of the American College of Medical Genetics 23 (10) (2021)
Mikey B Lebrett, Emma J Crosbie, Miriam Jane Smith, Emma Roisin Woodward, Dafydd Gareth Evans, Philip A J Crosbie
Targeting lung cancer screening to individuals at greatest risk: the role of genetic factors. Journal of medical genetics 58 (4) (2021)
Emma J Crosbie, Neil A J Ryan, Rhona J McVey, Fiona Lalloo, Naomi Bowers, Kate Green, Emma Roisin Woodward, Tara Clancy, James Bolton, Andrew J Wallace, Raymond F McMahon, Dafydd Gareth Evans
Assessment of mismatch repair deficiency in ovarian cancer. Journal of medical genetics 58 (10) (2020)
Mariona Terradas, Pilar Mur, Sami Belhadj, Emma Roisin Woodward, George Joseph Burghel, Pau M Muñoz-Torres, Isabel Quintana, Matilde Navarro, Joan Brunet, Conxi Lazaro Garcia, Marta Pineda, Victor Moreno, Gabriel Capellá Munar, Dafydd Gareth Evans, Laura Valle
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut 70 (6) (2020)
Michael T Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lidia Feliubadaló, Cora M Aalfs, Simona Agata, Kristiina Aittomäki, Elisa Alducci, María Concepción Alonso-Cerezo, Norbert Arnold, Bernd Auber, Rachel Austin, Jacopo Azzollini, Judith Balmaña, Elena Barbieri, Claus R Bartram, Ana Blanco, Britta Blümcke, Sandra Bonache, Bernardo Bonanni, Åke Borg, Beatrice Bortesi, Joan Brunet, Carla Bruzzone, Karolin Bucksch, Giulia Cagnoli, Trinidad Caldés, Almuth Caliebe, Maria A Caligo, Mariarosaria Calvello, Gabriele L Capone, Sandrine M Caputo, Ileana Carnevali, Estela Carrasco, Virginie Caux-Moncoutier, Pietro Cavalli, Giulia Cini, Edward M Clarke, Paola Concolino, Elisa J Cops, Laura Cortesi, Fergus J Couch, Esther Darder, Miguel de la Hoya, Michael Dean, Irmgard Debatin, Jesús Del Valle, Capucine Delnatte, Nicolas Derive, Orland Diez, Nina Ditsch, Susan M Domchek, Véronique Dutrannoy, Diana M Eccles, Hans Ehrencrona, Ute Enders, D Gareth Evans, Chantal Farra, Ulrike Faust, Ute Felbor, Irene Feroce, Miriam Fine, William D Foulkes, Henrique C R Galvao, Gaetana Gambino, Andrea Gehrig, Francesca Gensini, Anne-Marie Gerdes, Aldo Germani, Jutta Giesecke, Viviana Gismondi, Carolina Gómez, Encarna B Gómez Garcia, Sara González, Elia Grau, Sabine Grill, Eva Gross, Aliana Guerrieri-Gonzaga, Marine Guillaud-Bataille, Sara Gutiérrez-Enríquez, Thomas Haaf, Karl Hackmann, Thomas V O Hansen, Marion Harris, Jan Hauke, Tilman Heinrich, Heide Hellebrand, Karen N Herold, Ellen Honisch, Judit Horvath, Claude Houdayer, Verena Hübbel, Silvia Iglesias, Angel Izquierdo, Paul A James, Linda A M Janssen, Udo Jeschke, Silke Kaulfuß, Katharina Keupp, Marion Kiechle, Alexandra Kölbl, Sophie Krieger, Torben A Kruse, Anders Kvist, Fiona Lalloo, Mirjam Larsen, Vanessa L Lattimore, Charlotte Lautrup, Susanne Ledig, Elena Leinert, Alexandra L Lewis, Joanna Lim, Markus Loeffler, Adrià López-Fernández, Emanuela Lucci-Cordisco, Nicolai Maass, Siranoush Manoukian, Monica Marabelli, Laura Matricardi, Alfons Meindl, Rodrigo D Michelli, Setareh Moghadasi, Alejandro Moles-Fernández, Marco Montagna, Gemma Montalban, Alvaro N Monteiro, Eva Montes, Luigi Mori, Lidia Moserle, Clemens R Müller, Christoph Mundhenke, Nadia Naldi, Katherine L Nathanson, Matilde Navarro, Heli Nevanlinna, Cassandra B Nichols, Dieter Niederacher, Henriette R Nielsen, Kai-Ren Ong, Nicholas Pachter, Edenir I Palmero, Laura Papi, Inge Sokilde Pedersen, Bernard Peissel, Pedro Perez-Segura, Katharina Pfeifer, Marta Pineda, Esther Pohl-Rescigno, Nicola K Poplawski, Berardino Porfirio, Anne S Quante, Juliane Ramser, Rui M Reis, Françoise Revillion, Kerstin Rhiem, Barbara Riboli, Julia Ritter, Daniela Rivera, Paula Rofes, Andreas Rump, Monica Salinas, Ana María Sánchez de Abajo, Gunnar Schmidt, Ulrike Schoenwiese, Jochen Seggewiß, Ares Solanes, Doris Steinemann, Mathias Stiller, Dominique Stoppa-Lyonnet, Kelly J Sullivan, Rachel Susman, Christian Sutter, Sean V Tavtigian, Soo H Teo, Alex Teulé, Mads Thomassen, Maria Grazia Tibiletti, Marc Tischkowitz, Silvia Tognazzo, Amanda Ewart Toland, Eva Tornero, Therese Törngren, Sara Torres-Esquius, Angela Toss, Alison H Trainer, Katherine M Tucker, Christi J van Asperen, Marion T van Mackelenbergh, Liliana Varesco, Gardenia Vargas-Parra, Raymonda Varon, Ana Vega, Ángela Velasco, Anne-Sophie Vesper, Alessandra Viel, Maaike P G Vreeswijk, Sebastian A Wagner, Anke Waha, Logan C Walker, Rhiannon J Walters, Shan Wang-Gohrke, Bernhard H F Weber, Wilko Weichert, Kerstin Wieland, Lisa Wiesmüller, Isabell Witzel, Achim Wöckel, Emma Roisin Woodward, Silke Zachariae, Valentina Zampiga, Christine Zeder-Göß, null null, Conxi Lázaro, Arcangela De Nicolo, Paolo Radice, Christoph Engel, Rita K Schmutzler, David E Goldgar, Amanda B Spurdle
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification. Human mutation 40 (9) (2020)
Zerin Hyder, Adele Fairclough, Mike Groom, Joan Getty, Elizabeth Alexander, Elke M van Veen, Guy Makin, Chitra Sethuraman, Vivian Tang, Dafydd Gareth Evans, Eamonn R Maher, Emma Roisin Woodward
Constitutional de novo deletion CNV encompassing REST predisposes to diffuse hyperplastic perilobar nephroblastomatosis (HPLN). Journal of medical genetics 58 (9) (2020)
Zerin Hyder, Elaine F Harkness, Emma Roisin Woodward, Naomi L Bowers, Marta Pereira, Andrew J Wallace, Sacha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam Jane Smith, Dafydd Gareth Evans
Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in BRCA1, BRCA2, and TP53 Genes in Women with Very Early-Onset (<36 Years) Breast Cancer. Cancers 12 (2) (2020)
Philip S Smith, Hannah West, James Whitworth, Bruce Castle, Francis H Sansbury, Anne Y Warren, Emma Roisin Woodward, Marc Tischkowitz, Eamonn R Maher
Pathogenic germline variants in patients with features of hereditary renal cell carcinoma: Evidence for further locus heterogeneity. Genes, chromosomes & cancer 60 (1) (2020)
Nicola Flaum, Robert D Morgan, George J Burghel, Michael Bulman, Andrew R Clamp, Jurjees Hasan, Claire L Mitchell, Doina Badea, Sarah Moon, Martin Hogg, Dennis Hadjiyiannakis, Tara Clancy, Helene Schlecht, Emma Roisin Woodward, Emma J Crosbie, Richard J Edmondson, Andrew J Wallace, Gordon C Jayson, Fiona I Lalloo, Elaine F Harkness, Dafydd Gareth Evans
Mainstreaming germline BRCA1/2 testing in non-mucinous epithelial ovarian cancer in the North West of England. European journal of human genetics : EJHG 28 (11) (2020)
Dafydd Gareth Evans, Emma Roisin Woodward, Svetlana Bajalica-Lagercrantz, Carla Oliveira, Thierry Frebourg
Germline TP53 Testing in Breast Cancers: Why, When and How? Cancers 12 (12) (2020)
D Gareth Evans, Clare Turnbull, Emma Roisin Woodward
Concern regarding classification of germline TP53 variants as likely pathogenic. Human mutation 40 (6) (2019)

Emma Roisin Woodward.css-eqlu8i{font-size:small;padding-left:4px;} (Emma R Woodward)

Publication Activity (10 Years)

Top Topics

Top Venues

Emma Roisin Woodward (Emma R Woodward)