Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Lesley, Andrews"'
Autor:
Martin B Delatycki, Chris Jacobs, Bettina Meiser, Ian G Campbell, Lesley Andrews, Paul A James, Alison Trainer, AGNES BANKIER, Kristine Barlow-Stewart, Jane Tiller, Nicole E Cousens, Simone Rowley, Sakshi Mahale, Rajneesh Kaur, Leslie Burnett, Suzanne Neil
Publikováno v:
BMJ Open, Vol 11, Iss 6 (2021)
Introduction People of Ashkenazi Jewish (AJ) ancestry are more likely than unselected populations to have a BRCA1/2 pathogenic variant, which cause a significantly increased risk of breast, ovarian and prostate cancer. Three specific BRCA1/2 pathogen
Externí odkaz:
https://doaj.org/article/c13502b3150143889118fe9f14053fbc
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-11 (2017)
Abstract Background Endometrial, ovarian and breast cancers are paradigms for global health disparity. Women living in the developing world continue to present in later stages of disease and have fewer options for treatment than those in developed co
Externí odkaz:
https://doaj.org/article/de756df75ba0416595079b6f695c5f5b
Autor:
Amber L. Johns, Skye H. McKay, Jeremy L. Humphris, Mark Pinese, Lorraine A. Chantrill, R. Scott Mead, Katherine Tucker, Lesley Andrews, Annabel Goodwin, Conrad Leonard, Hilda A. High, Katia Nones, Ann-Marie Patch, Neil D. Merrett, Nick Pavlakis, Karin S. Kassahn, Jaswinder S. Samra, David K. Miller, David K. Chang, Marina Pajic, Australian Pancreatic Cancer Genome Initiative, John V. Pearson, Sean M. Grimmond, Nicola Waddell, Nikolajs Zeps, Anthony J. Gill, Andrew V. Biankin
Publikováno v:
Genome Medicine, Vol 9, Iss 1, Pp 1-9 (2017)
Abstract Background The return of research results (RoR) remains a complex and well-debated issue. Despite the debate, actual data related to the experience of giving individual results back, and the impact these results may have on clinical care and
Externí odkaz:
https://doaj.org/article/2890c395e52345e4baee26649c8cae4b
Autor:
Rachel, Delahunty, Linh, Nguyen, Stuart, Craig, Belinda, Creighton, Dinuka, Ariyaratne, Dale W, Garsed, Elizabeth, Christie, Sian, Fereday, Lesley, Andrews, Alexandra, Lewis, Sharne, Limb, Ahwan, Pandey, Joy, Hendley, Nadia, Traficante, Natalia, Carvajal, Amanda B, Spurdle, Bryony, Thompson, Michael T, Parsons, Victoria, Beshay, Mila, Volcheck, Timothy, Semple, Richard, Lupat, Kenneth, Doig, Jiaan, Yu, Xiao Qing, Chen, Anna, Marsh, Christopher, Love, Sanela, Bilic, Maria, Beilin, Cassandra B, Nichols, Christina, Greer, Yeh Chen, Lee, Susan, Gerty, Lynette, Gill, Emma, Newton, Julie, Howard, Rachel, Williams, Christie, Norris, Andrew N, Stephens, Erin, Tutty, Courtney, Smyth, Shona, O'Connell, Thomas, Jobling, Colin J R, Stewart, Adeline, Tan, Stephen B, Fox, Nicholas, Pachter, Jason, Li, Jason, Ellul, Gisela, Mir Arnau, Mary-Anne, Young, Louisa, Gordon, Laura, Forrest, Marion, Harris, Karen, Livingstone, Jane, Hill, Georgia, Chenevix-Trench, Paul A, Cohen, Penelope M, Webb, Michael, Friedlander, Paul, James, David, Bowtell, Kathryn, Alsop
Publikováno v:
Journal of Clinical Oncology. 40:2036-2047
PURPOSE Tubo-ovarian cancer (TOC) is a sentinel cancer for BRCA1 and BRCA2 pathogenic variants (PVs). Identification of a PV in the first member of a family at increased genetic risk (the proband) provides opportunities for cancer prevention in other
Autor:
Jane M Tiller, Nicole E Cousens, Rajneesh Kaur, Simone Rowley, Yi-An Ko, Sakshi Mahale, Agnes Bankier, Bettina Meiser, Kristine Barlow-Stewart, Leslie Burnett, Chris Jacobs, Paul James, Alison Trainer, Suzanne Neil, Ian G Campbell, Lesley Andrews, Martin Delatycki
Publikováno v:
Journal of Medical Genetics. 60:265-273
BackgroundAshkenazi Jewish (AJ) people have a higher incidence ofBRCA1/2pathogenic variants (PVs) than unselected populations. ThreeBRCA-Jewish founder mutations (B-JFMs) comprise >90% ofBRCA1/2PVs in AJ people. Personal/family cancer history-based t
Autor:
Anna Morra, Nasim Mavaddat, Taru A. Muranen, Thomas U. Ahearn, Jamie Allen, Irene L. Andrulis, Päivi Auvinen, Heiko Becher, Sabine Behrens, Carl Blomqvist, Stig E. Bojesen, Manjeet K. Bolla, Hiltrud Brauch, Nicola J. Camp, Sara Carvalho, Jose E. Castelao, Melissa H. Cessna, Jenny Chang-Claude, Georgia Chenevix-Trench, Kamila Czene, Brennan Decker, Joe Dennis, Thilo Dörk, Leila Dorling, Alison M. Dunning, Arif B. Ekici, Mikael Eriksson, D. Gareth Evans, Peter A. Fasching, Jonine D. Figueroa, Henrik Flyger, Manuela Gago-Dominguez, Montserrat García-Closas, Willemina R.R. Geurts-Giele, Graham G. Giles, Pascal Guénel, Melanie Gündert, Eric Hahnen, Per Hall, Ute Hamann, Patricia A. Harrington, Wei He, Päivi Heikkilä, Maartje J. Hooning, Reiner Hoppe, Anthony Howell, Keith Humphreys, Anna Jakubowska, Audrey Y. Jung, Renske Keeman, Vessela N. Kristensen, Jan Lubiński, Arto Mannermaa, Mehdi Manoochehri, Siranoush Manoukian, Sara Margolin, Dimitrios Mavroudis, Roger L. Milne, Anna Marie Mulligan, William G. Newman, Tjoung-Won Park-Simon, Paolo Peterlongo, Paul D.P. Pharoah, Valerie Rhenius, Emmanouil Saloustros, Elinor J. Sawyer, Rita K. Schmutzler, Mitul Shah, Amanda B. Spurdle, Ian Tomlinson, Thérèse Truong, Elke M. van Veen, Maaike P.G. Vreeswijk, Qin Wang, Camilla Wendt, Xiaohong R. Yang, Heli Nevanlinna, Peter Devilee, Douglas F. Easton, Marjanka K. Schmidt, Kristine K. Sahlberg, Anne-Lise Børresen-Dale, Inger Torhild Gram, Karina Standahl Olsen, Olav Engebråten, Bjørn Naume, Jürgen Geisler, null OSBREAC, Grethe I. Grenaker Alnæs, David Amor, Lesley Andrews, Yoland Antill, Rosemary Balleine, Jonathan Beesley, Ian Bennett, Michael Bogwitz, Leon Botes, Meagan Brennan, Melissa Brown, Michael Buckley, Jo Burke, Phyllis Butow, Liz Caldon, Ian Campbell, Michelle Cao, Anannya Chakrabarti, Deepa Chauhan, Manisha Chauhan, Alice Christian, Paul Cohen, Alison Colley, Ashley Crook, James Cui, Eliza Courtney, Margaret Cummings, Sarah-Jane Dawson, Anna DeFazio, Martin Delatycki, Rebecca Dickson, Joanne Dixon, Ted Edkins, Stacey Edwards, Gelareh Farshid, Andrew Fellows, Georgina Fenton, Michael Field, James Flanagan, Peter Fong, Laura Forrest, Stephen Fox, Juliet French, Michael Friedlander, Clara Gaff, Mike Gattas, Peter George, Sian Greening, Marion Harris, Stewart Hart, Nick Hayward, John Hopper, Cass Hoskins, Clare Hunt, Paul James, Mark Jenkins, Alexa Kidd, Judy Kirk, Jessica Koehler, James Kollias, Sunil Lakhani, Mitchell Lawrence, Jason Lee, Shuai Li, Geoff Lindeman, Lara Lipton, Liz Lobb, Sherene Loi, Graham Mann, Deborah Marsh, Sue Anne McLachlan, Bettina Meiser, Roger Milne, Sophie Nightingale, Shona O'Connell, Sarah O'Sullivan, David Gallego Ortega, Nick Pachter, Jia-Min Pang, Gargi Pathak, Briony Patterson, Amy Pearn, Kelly Phillips, Ellen Pieper, Susan Ramus, Edwina Rickard, Bridget Robinson, Mona Saleh, Anita Skandarajah, Elizabeth Salisbury, Christobel Saunders, Jodi Saunus, Rodney Scott, Clare Scott, Adrienne Sexton, Andrew Shelling, Peter Simpson, Melissa Southey, Amanda Spurdle, Jessica Taylor, Renea Taylor, Heather Thorne, Alison Trainer, Kathy Tucker, Jane Visvader, Logan Walker, Rachael Williams, Ingrid Winship, Mary Ann Young, Milita Zaheed
Publikováno v:
American Journal of Human Genetics
Morra, A, Mavaddat, N, Muranen, T A, Ahearn, T U, Allen, J, Andrulis, I L, Auvinen, P, Becher, H, Behrens, S, Blomqvist, C, Bojesen, S E, Bolla, M K, Brauch, H, Camp, N J, Carvalho, S, Castelao, J E, Cessna, M H, Chang-Claude, J, Chenevix-Trench, G, Czene, K, Decker, B, Dennis, J, Dörk, T, Dorling, L, Dunning, A M, Ekici, A B, Eriksson, M, Evans, D G, Fasching, P A, Figueroa, J D, Flyger, H, Gago-Dominguez, M, García-Closas, M, Geurts-Giele, W R R, Giles, G G, Guénel, P, Gündert, M, Hahnen, E, Hall, P, Hamann, U, Harrington, P A, He, W, Heikkilä, P, Hooning, M J, Hoppe, R, Howell, A, Humphreys, K, Jakubowska, A, Jung, A Y, Keeman, R, Kristensen, V N, Lubiński, J, Mannermaa, A, Manoochehri, M, Manoukian, S, Margolin, S, Mavroudis, D, Milne, R L, Mulligan, A M, Newman, W G, Park-Simon, T-W, Peterlongo, P, Pharoah, P D P, Rhenius, V, Saloustros, E, Sawyer, E J, Schmutzler, R K, Shah, M, Spurdle, A B, Tomlinson, I, Truong, T, van Veen, E M, Vreeswijk, M P G, Wang, Q, Wendt, C, Yang, X R, Nevanlinna, H & Devilee, P & Easton, D F & Schmidt, M K 2023, ' The impact of coding germline variants on contralateral breast cancer risk and survival ', American Journal of Human Genetics, vol. 110, no. 3, pp. 475-486 . https://doi.org/10.1016/j.ajhg.2023.02.003
Morra, A, Mavaddat, N, Muranen, T A, Ahearn, T U, Allen, J, Andrulis, I L, Auvinen, P, Becher, H, Behrens, S, Blomqvist, C, Bojesen, S E, Bolla, M K, Brauch, H, Camp, N J, Carvalho, S, Castelao, J E, Cessna, M H, Chang-Claude, J, Chenevix-Trench, G, Czene, K, Decker, B, Dennis, J, Dörk, T, Dorling, L, Dunning, A M, Ekici, A B, Eriksson, M, Evans, D G, Fasching, P A, Figueroa, J D, Flyger, H, Gago-Dominguez, M, García-Closas, M, Geurts-Giele, W R R, Giles, G G, Guénel, P, Gündert, M, Hahnen, E, Hall, P, Hamann, U, Harrington, P A, He, W, Heikkilä, P, Hooning, M J, Hoppe, R, Howell, A, Humphreys, K, Jakubowska, A, Jung, A Y, Keeman, R, Kristensen, V N, Lubiński, J, Mannermaa, A, Manoochehri, M, Manoukian, S, Margolin, S, Mavroudis, D, Milne, R L, Mulligan, A M, Newman, W G, Park-Simon, T-W, Peterlongo, P, Pharoah, P D P, Rhenius, V, Saloustros, E, Sawyer, E J, Schmutzler, R K, Shah, M, Spurdle, A B, Tomlinson, I, Truong, T, van Veen, E M, Vreeswijk, M P G, Wang, Q, Wendt, C, Yang, X R, Nevanlinna, H & Devilee, P & Easton, D F & Schmidt, M K 2023, ' The impact of coding germline variants on contralateral breast cancer risk and survival ', American Journal of Human Genetics, vol. 110, no. 3, pp. 475-486 . https://doi.org/10.1016/j.ajhg.2023.02.003
Evidence linking coding germline variants in breast cancer (BC)-susceptibility genes other than BRCA1, BRCA2, and CHEK2 with contralateral breast cancer (CBC) risk and breast cancer-specific survival (BCSS) is scarce. The aim of this study was to ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3606211c9deba682d78e97c763520f8
https://hdl.handle.net/11250/3079721
https://hdl.handle.net/11250/3079721
Autor:
Yoland Antill, Paul A. James, Judy Kirk, Uwe Dressel, Nicola K. Poplawski, Lucinda Salmon, Nicholas Pachter, Aimee L Davidson, Sharron Townshend, Michael Gattas, Emma Tudini, Gillian Mitchell, Helen Mar Fan, Rachel Susman, Katherine M. Tucker, Robyn L. Ward, Michael Field, Ashley Crook, Alison H. Trainer, Amanda B. Spurdle, Lesley Andrews, Rebecca Harris
Publikováno v:
Journal of Medical Genetics. 58:853-858
BackgroundThe strength of evidence supporting the validity of gene-disease relationships is variable. Hereditary cancer has the additional complexity of low or moderate penetrance for some confirmed disease-associated alleles.MethodsTo promote nation
Autor:
Stephan B. Dreyer, Rosie Upstill-Goddard, Assya Legrini, Andrew V. Biankin, Nigel B. Jamieson, David K. Chang, Sarah Allison, Dario Beraldi, Euan Cameron, Susanna L. Cooke, Richard Cunningham, Stephan Dreyer, Paul Grimwood, Shane Kelly, John Marshall, Brian McDade, Elizabeth A. Musgrove, Donna Ramsay, Lisa Evers, Selma Rebus, Lola Rahib, Bryan Serrels, Colin J. McKay, Paul Westwood, Nicola Williams, Fraser Duthie, William Shen, Antonio Pea, Amber L. Johns, Anthony J. Gill, Lorraine A. Chantrill, Paul Timpson, Angela Chou, Marina Pajic, Tanya Dwarte, David Herrmann, Claire Vennin, Thomas R. Cox, Brooke Pereira, Shona Ritchiee, Daniel A. Reed, Cecilia R. Chambers, Xanthe Metcalf, Max Nobis, Gloria Jeong, Lara Kenyon, Ruth J. Lyons, Nicola Waddell, John V. Pearson, Ann-Marie Patch, Katia Nones, Felicity Newell, Pamela Mukhopadhyay, Venkateswar Addala, Stephen Kazakoff, Oliver Holmes, Conrad Leonard, Scott Wood, Sean M. Grimmond, Oliver Hofmann, Jaswinder S. Samra, Nick Pavlakis, Jennifer Arena, Hilda A. High, Ray Asghari, Neil D. Merrett, Amitabha Das, Peter H. Cosman, Kasim Ismail, Alina Stoita, David Williams, Allan Spigellman, Duncan McLeod, Judy Kirk, James G. Kench, Peter Grimison, Charbel Sandroussi, Annabel Goodwin, R. Scott Mead, Katherine Tucker, Lesley Andrews, Michael Texler, Cindy Forrest, Mo Ballal, David Fletcher, Maria Beilin, Kynan Feeney, Krishna Epari, Sanjay Mukhedkar, Nikolajs Zeps, Nan Q. Nguyen, Andrew R. Ruszkiewicz, Chris Worthley, John Chen, Mark E. Brooke-Smith, Virginia Papangelis, Andrew D. Clouston, Andrew P. Barbour, Thomas J. O’Rourke, Jonathan W. Fawcett, Kellee Slater, Michael Hatzifotis, Peter Hodgkinson, Mehrdad Nikfarjam, James R. Eshleman, Ralph H. Hruban, Christopher L. Wolfgang, Aldo Scarpa, Rita T. Lawlor, Vincenzo Corbo, Claudio Bassi
Publikováno v:
Gastroenterology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee9df49d92ea32ac7a1cf88268d4685b
http://hdl.handle.net/11562/1056899
http://hdl.handle.net/11562/1056899
Publikováno v:
J Community Genet
Screening programmes for BRCA1/2 Jewish Founder mutations (JFM) in the Jewish community have been advocated internationally. Implementation of these programmes could decrease morbidity and mortality of BRCA1/2 JFM carriers through the uptake of cance
Autor:
Nicole E, Cousens, Jane, Tiller, Bettina, Meiser, Kristine, Barlow-Stewart, Simone, Rowley, Yi-An, Ko, Sakshi, Mahale, Ian G, Campbell, Rajneesh, Kaur, Agnes, Bankier, Leslie, Burnett, Chris, Jacobs, Paul A, James, Alison, Trainer, Suzanne, Neil, Martin B, Delatycki, Lesley, Andrews
Publikováno v:
BMJ Open
Introduction People of Ashkenazi Jewish (AJ) ancestry are more likely than unselected populations to have a BRCA1/2 pathogenic variant, which cause a significantly increased risk of breast, ovarian and prostate cancer. Three specific BRCA1/2 pathogen