Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Milita Zaheed"'
Autor:
Jonathan Baber, Shuai Li, Melissa Green, Emma Rath, Tuong L. Nguyen, Thomas Ludwig, Piyushkumar Mundra, Mandy Ballinger, Isabelle Ray coquard, Milita Zaheed, Shyamsundar Ravishankar, Michelle Haber, Coonoor Chandrasekar
Publikováno v:
Science. 379:253-260
Cancer genetics has to date focused on epithelial malignancies, identifying multiple histotype-specific pathways underlying cancer susceptibility. Sarcomas are rare malignancies predominantly derived from embryonic mesoderm. To identify pathways spec
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:
Danielle Klingberg, Janene Dalrymple, Milita Zaheed, Craig R. Lewis, Tom John, Chee Khoon Lee
Publikováno v:
Journal of Clinical Oncology. 40:9131-9131
9131 Background: Next generation sequencing (NGS) is used widely to identify somatic oncogenic driver mutations in aNSCLC to guide treatment. Comprehensive profiling has led to identification of multiple gene mutations of unclear significance, includ
Publikováno v:
Journal of Thoracic Oncology. 13:e62-e64
Publikováno v:
Journal of Clinical Oncology. 38:1524-1524
1524 Background: Sarcomas are rare heterogenous cancers affecting a predominantly younger population. The most recognised autosomal dominant contributor being pathogenic TP53 variants associated with Li Fraumeni Syndrome (LFS). When referred, patient
Sequencing of anthracyclines and taxanes in neoadjuvant and adjuvant therapy for early breast cancer
Publikováno v:
The Cochrane Library
Background Anthracyclines and taxanes are chemotherapeutic agents widely used in a sequential regimen in the adjuvant and neoadjuvant treatment of early breast cancer to reduce the risk of cancer recurrence. Standard practice is to administer anthrac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c364d3dc2578ec1b6b068a9307b1f5b0
https://europepmc.org/articles/PMC6486143/
https://europepmc.org/articles/PMC6486143/