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Verfasst von:Milne, Roger L. [VerfasserIn]   i
 Lorenzo Bermejo, Justo [VerfasserIn]   i
 Burwinkel, Barbara [VerfasserIn]   i
 Frank, Bernd [VerfasserIn]   i
 Heil, Jörg [VerfasserIn]   i
 Chang-Claude, Jenny [VerfasserIn]   i
 Hamann, Ute [VerfasserIn]   i
Titel:7q21-rs6964587 and breast cancer risk
Titelzusatz:an extended case-control study by the Breast Cancer Association Consortium
Verf.angabe:Roger L. Milne, Justo Lorenzo-Bermejo, Barbara Burwinkel, Núria Malats, Jose Ignacio Arias, M. Pilar Zamora, Javier Benítez, Manjeet K. Humphreys, Montserrat García-Closas, Stephen J. Chanock, Jolanta Lissowska, Mark E. Sherman, Arto Mannermaa, Vesa Kataja, Veli-Matti Kosma, Heli Nevanlinna, Tuomas Heikkinen, Kristiina Aittomäki, Carl Blomqvist, Hoda Anton-Culver, Argyrios Ziogas, Peter Devilee, Christie J. van Asperen, Rob A.E.M. Tollenaar, Caroline Seynaeve, Per Hall, Kamila Czene, Jianjun Liu, Astrid K. Irwanto, Daehee Kang, Keun-Young Yoo, Dong-Young Noh, Fergus J. Couch, Janet E. Olson, Xianshu Wang, Zachary Fredericksen, Børge G. Nordestgaard, Stig E. Bojesen, Henrik Flyger, Sara Margolin, Annika Lindblom, Peter A. Fasching, Ruediger Schulz-Wendtland, Arif B. Ekici, Matthias W. Beckmann, Shan Wang-Gohrke, Chen-Yang Shen, Jyh-Cherng Yu, Huan-Ming Hsu, Pei-Ei Wu, Graham G. Giles, Gianluca Severi, Laura Baglietto, Dallas R. English, Angela Cox, Ian Brock, Graeme Elliott, Malcolm W. R. Reed, Jonathan Beesley, Xiaoqing Chen, kConFab Investigators, Aocs Group, Olivia Fletcher, Lorna Gibson, Isabel dos Santos Silva, Julian Peto, Bernd Frank, Joerg Heil, Alfons Meindl, Jenny Chang-Claude, Rebecca Hein, Alina Vrieling, Dieter Flesch-Janys, Melissa C. Southey, Letitia Smith, Carmel Apicella, John L. Hopper, Alison M. Dunning, Karen A. Pooley, Paul D.P. Pharoah, Ute Hamann, Beate Pesch, Yon-Dschun Ko, The GENICA Network, Douglas F. Easton, Georgia Chenevix-Trench
E-Jahr:2011
Jahr:September 19, 2011
Umfang:5 S.
Fussnoten:Gesehen am 07.09.2022
Titel Quelle:Enthalten in: Journal of medical genetics
Ort Quelle:London : BMJ Publishing Group, 1964
Jahr Quelle:2011
Band/Heft Quelle:48(2011), 10, Seite 698-702
ISSN Quelle:1468-6244
Abstract:Background: Using the Breast Cancer Association Consortium, the authors previously reported that the single nucleotide polymorphism 7q21-rs6964587 (AKAP9-M463I) is associated with breast cancer risk. The authors have now assessed this association more comprehensively using 16 independent case-control studies. - Methods: The authors genotyped 14 843 invasive case patients and 19 852 control subjects with white European ancestry and 2595 invasive case patients and 2192 control subjects with Asian ancestry. ORs were estimated by logistic regression, adjusted for study. Heterogeneity in ORs was assessed by fitting interaction terms or by subclassifying case patients and applying polytomous logistic regression. - Results: For white European women, the minor T allele of 7q21-rs6964587 was associated with breast cancer risk under a recessive model (OR 1.07, 95% CI 1.00 to 1.13, p=0.04). Results were inconclusive for Asian women. From a combined analysis of 24 154 case patients and 33 376 control subjects of white European ancestry from the present and previous series, the best-fitting model was recessive, with an estimated OR of 1.08 (95% CI 1.03 to 1.13, p=0.001). The OR was greater at younger ages (p trend=0.01). - Conclusion: This may be the first common susceptibility allele for breast cancer to be identified with a recessive mode of inheritance.
DOI:doi:10.1136/jmedgenet-2011-100303
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1136/jmedgenet-2011-100303
 Volltext: https://jmg.bmj.com/content/48/10/698
 DOI: https://doi.org/10.1136/jmedgenet-2011-100303
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Breast neoplasms
 cancer: breast
 epidemiology
 genetic epidemiology
 genetic predisposition to disease
 molecular epidemiology
 other oncology
K10plus-PPN:1815960868
Verknüpfungen:→ Zeitschrift

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