Zobrazeno 1 - 10
of 33
pro vyhledávání: '"BOCHUM, Sylvia"'
Publikováno v:
Studies in Health Technology & Informatics; 2024, Vol. 317, p105-114, 10p
Publikováno v:
In Journal of Biomedical Informatics April 2016 60:385-394
Autor:
Sigle, Stefan, Kaufmes, Kevin, Werner, Patrick, Bochum, Sylvia, Martens, Uwe, Fegeler, Christian
Publikováno v:
66. Jahrestagung der Deutschen Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie e. V. (GMDS), 12. Jahreskongress der Technologie-und Methodenplattform für die vernetzte medizinische Forschung e.V. (TMF); 20210926-20210930; sine loco [digital]; DOCAbstr. 48 /20210924/
Introduction: Revision of annotated data generated by a broad genomic panel (>500 genes) within oncological precision medicine exceeds the resources of a single expert [ref:1] and requires clinical decision support [ref:2]. In order to provide person
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70323765d4b4a06586872ca7fc106209
http://www.egms.de/en/meetings/gmds2021/21gmds054.shtml
http://www.egms.de/en/meetings/gmds2021/21gmds054.shtml
Autor:
Bailey-Wilson Joan E, Childs Erica J, Cropp Cheryl D, Schaid Daniel J, Xu Jianfeng, Camp Nicola J, Cannon-Albright Lisa A, Farnham James M, George Asha, Powell Isaac, Carpten John D, Giles Graham G, Hopper John L, Severi Gianluca, English Dallas R, Foulkes William D, Mæhle Lovise, Møller Pål, Eeles Rosalind, Easton Douglas, Guy Michelle, Edwards Steve, Badzioch Michael D, Whittemore Alice S, Oakley-Girvan Ingrid, Hsieh Chih-Lin, Dimitrov Latchezar, Stanford Janet L, Karyadi Danielle M, Deutsch Kerry, McIntosh Laura, Ostrander Elaine A, Wiley Kathleen E, Isaacs Sarah D, Walsh Patrick C, Thibodeau Stephen N, McDonnell Shannon K, Hebbring Scott, Lange Ethan M, Cooney Kathleen A, Tammela Teuvo LJ, Schleutker Johanna, Maier Christiane, Bochum Sylvia, Hoegel Josef, Grönberg Henrik, Wiklund Fredrik, Emanuelsson Monica, Cancel-Tassin Geraldine, Valeri Antoine, Cussenot Olivier, Isaacs William B
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 46 (2012)
Abstract Background Genetic variants are likely to contribute to a portion of prostate cancer risk. Full elucidation of the genetic etiology of prostate cancer is difficult because of incomplete penetrance and genetic and phenotypic heterogeneity. Cu
Externí odkaz:
https://doaj.org/article/ce263c9f82cb4988ac4dd3b4b9593d1c
Publikováno v:
Studies in Health Technology & Informatics; 2021, Issue 278, p150-155, 6p, 1 Diagram, 1 Chart, 1 Graph
Akademický článek
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Publikováno v:
Deutsche Krebsgesellschaft. Forum; Oct2018, Vol. 33 Issue 5, p322-328, 7p
Autor:
Bailey-Wilson, Joan E, Childs, Erica J, Cropp, Cheryl D, Schaid, Daniel J, Xu, Jianfeng, Camp, Nicola J, Cannon-Albright, Lisa A, Farnham, James M, George, Asha, Powell, Isaac, Carpten, John D, Giles, Graham G, Hopper, John L, Severi, Gianluca, English, Dallas R, Foulkes, William D, Mæhle, Lovise, Møller, Pål, Eeles, Rosalind, Easton, Douglas, Guy, Michelle, Edwards, Steve, Badzioch, Michael D, Whittemore, Alice S, Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Dimitrov, Latchezar, Stanford, Janet L, Karyadi, Danielle M, Deutsch, Kerry, McIntosh, Laura, Ostrander, Elaine A, Wiley, Kathleen E, Isaacs, Sarah D, Walsh, Patrick C, Thibodeau, Stephen N, McDonnell, Shannon K, Hebbring, Scott, Lange, Ethan M, Cooney, Kathleen A, Tammela, Teuvo LJ, Schleutker, Johanna, Maier, Christiane, Bochum, Sylvia, Hoegel, Josef, Grönberg, Henrik, Wiklund, Fredrik, Emanuelsson, Monica, Cancel-Tassin, Geraldine, Valeri, Antoine, Cussenot, Olivier, Isaacs, William B, International Consortium for Prostate Cancer Genetics
BACKGROUND: Genetic variants are likely to contribute to a portion of prostate cancer risk. Full elucidation of the genetic etiology of prostate cancer is difficult because of incomplete penetrance and genetic and phenotypic heterogeneity. Current ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______109::8e0bbd6ba352484756cb7f86d1749dc5
http://www.dspace.cam.ac.uk/handle/1810/243936
http://www.dspace.cam.ac.uk/handle/1810/243936
Akademický článek
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Publikováno v:
In Data in Brief June 2016 7:654-657