Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population

被引:0
|
作者
Celia M Pereda
Fabienne Lesueur
Maroulio Pertesi
Nivonirina Robinot
Juan J Lence-Anta
Silvia Turcios
Milagros Velasco
Mae Chappe
Idalmis Infante
Marlene Bustillo
Anabel García
Enora Clero
Constance Xhaard
Yan Ren
Stéphane Maillard
Francesca Damiola
Carole Rubino
Sirced Salazar
Regla Rodriguez
Rosa M Ortiz
Florent de Vathaire
机构
[1] Institute of Oncology and Radiobiology,The French National Institute of Health and Medical Research (Inserm), U900
[2] Institut Curie,Genetic Cancer Susceptibility
[3] Mines ParisTech,The French National Institute of Health and Medical Research (Inserm), Centre for Research in Epidemiology and Population Health (CESP), U1018
[4] International Agency for Research on Cancer (IARC),CRCL, CNRS UMR5286, the French National Institute of Health and Medical Research (Inserm) U1052
[5] National Institute of Endocrinology,undefined
[6] Cuban Health Public Ministry,undefined
[7] Radiation Epidemiology Group,undefined
[8] Paris-Sud University,undefined
[9] Institut Gustave Roussy (IGR),undefined
[10] Centre Léon Bérard,undefined
来源
BMC Genetics | / 16卷
关键词
Differentiated thyroid carcinoma; Cuba; Genetic susceptibility; ATM; FOXE1; NKX2-1; Polymorphism;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 27 条
  • [21] Association Between Potentially Functional Variants in chr5q14 and the Risk of Cervical Cancer in a Chinese Population
    Liu, Yuqing
    Mei, Ling
    Chen, Yueyue
    Zhang, Xiaoli
    Wei, Dongmei
    Cui, Tao
    Zhang, Yueting
    Wang, Tao
    Niu, Xiaoyu
    REPRODUCTIVE SCIENCES, 2023, 30 (01) : 301 - 308
  • [22] Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population
    Wang, Yu-Long
    Feng, Shou-Hao
    Guo, Shi-Cheng
    Wei, Wen-Jun
    Li, Duan-Shu
    Wang, Yu
    Wang, Xiaofeng
    Wang, Zhuo-Ying
    Ma, Yan-Yun
    Jin, Li
    Ji, Qing-Hai
    Wang, Jiu-Cun
    JOURNAL OF MEDICAL GENETICS, 2013, 50 (10) : 689 - 695
  • [23] Common and rare copy number variants at chromosomes 3q13, 12p12 and 14q11 are associated with sporadic colorectal cancer risk
    Cheah, P.
    Thean, L.
    Low, Y.
    Lo, M.
    Teo, Y.
    Koh, W.
    Yuan, J.
    Chew, M.
    Tang, C.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 766 - 766
  • [24] Assessment of Association between Common Variants at 17q12 and Prostate Cancer Risk-Evidence from Serbian Population and Meta-Analysis
    Nikolic, Zorana Z.
    Brankovic, Ana S.
    Savic-Pavicevic, Dusanka L. J.
    Prekovic, Stefan M.
    Vukotic, Vinka D.
    Cerovic, Snezana J.
    Filipovic, Natasa N.
    Tomovic, Sasa M.
    Romac, Stanka P.
    Brajuskovic, Goran N.
    CTS-CLINICAL AND TRANSLATIONAL SCIENCE, 2014, 7 (04): : 307 - 313
  • [25] Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
    Antoniou, Antonis C.
    Kuchenbaecker, Karoline B.
    Soucy, Penny
    Beesley, Jonathan
    Chen, Xiaoqing
    McGuffog, Lesley
    Lee, Andrew
    Barrowdale, Daniel
    Healey, Sue
    Sinilnikova, Olga M.
    Caligo, Maria A.
    Loman, Niklas
    Harbst, Katja
    Lindblom, Annika
    Arver, Brita
    Rosenquist, Richard
    Karlsson, Per
    Nathanson, Kate
    Domchek, Susan
    Rebbeck, Tim
    Jakubowska, Anna
    Lubinski, Jan
    Jaworska, Katarzyna
    Durda, Katarzyna
    Zlowowcka-Perlowska, Elzbieta
    Osorio, Ana
    Duran, Mercedes
    Andres, Raquel
    Benitez, Javier
    Hamann, Ute
    Hogervorst, Frans B.
    van Os, Theo A.
    Verhoef, Senno
    Meijers-Heijboer, Hanne E. J.
    Wijnen, Juul
    Garcia, Encarna B. Gomez
    Ligtenberg, Marjolijn J.
    Kriege, Mieke
    Collee, Margriet
    Ausems, Margreet G. E. M.
    Oosterwijk, Jan C.
    Peock, Susan
    Frost, Debra
    Ellis, Steve D.
    Platte, Radka
    Fineberg, Elena
    Evans, D. Gareth
    Lalloo, Fiona
    Jacobs, Chris
    Eeles, Ros
    BREAST CANCER RESEARCH, 2012, 14 (01)
  • [26] Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers
    Antonis C Antoniou
    Karoline B Kuchenbaecker
    Penny Soucy
    Jonathan Beesley
    Xiaoqing Chen
    Lesley McGuffog
    Andrew Lee
    Daniel Barrowdale
    Sue Healey
    Olga M Sinilnikova
    Maria A Caligo
    Niklas Loman
    Katja Harbst
    Annika Lindblom
    Brita Arver
    Richard Rosenquist
    Per Karlsson
    Kate Nathanson
    Susan Domchek
    Tim Rebbeck
    Anna Jakubowska
    Jan Lubinski
    Katarzyna Jaworska
    Katarzyna Durda
    Elżbieta Złowowcka-Perłowska
    Ana Osorio
    Mercedes Durán
    Raquel Andrés
    Javier Benítez
    Ute Hamann
    Frans B Hogervorst
    Theo A van Os
    Senno Verhoef
    Hanne EJ Meijers-Heijboer
    Juul Wijnen
    Encarna B Gómez Garcia
    Marjolijn J Ligtenberg
    Mieke Kriege
    J Margriet Collée
    Margreet GEM Ausems
    Jan C Oosterwijk
    Susan Peock
    Debra Frost
    Steve D Ellis
    Radka Platte
    Elena Fineberg
    D Gareth Evans
    Fiona Lalloo
    Chris Jacobs
    Ros Eeles
    Breast Cancer Research, 14
  • [27] Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium
    Figueroa, Jonine D.
    Garcia-Closas, Montserrat
    Humphreys, Manjeet
    Platte, Radka
    Hopper, John L.
    Southey, Melissa C.
    Apicella, Carmel
    Hammet, Fleur
    Schmidt, Marjanka K.
    Broeks, Annegien
    Tollenaar, Rob A. E. M.
    Van't Veer, Laura J.
    Fasching, Peter A.
    Beckmann, Matthias W.
    Ekici, Arif B.
    Strick, Reiner
    Peto, Julian
    Silva, Isabel dos Santos
    Fletcher, Olivia
    Johnson, Nichola
    Sawyer, Elinor
    Tomlinson, Ian
    Kerin, Michael
    Burwinkel, Barbara
    Marme, Federik
    Schneeweiss, Andreas
    Sohn, Christof
    Bojesen, Stig
    Flyger, Henrik
    Nordestgaard, Borge G.
    Benitez, Javier
    Milne, Roger L.
    Ignacio Arias, Jose
    Pilar Zamora, M.
    Brenner, Hermann
    Mueller, Heiko
    Arndt, Volker
    Rahman, Nazneen
    Turnbull, Clare
    Seal, Sheila
    Renwick, Anthony
    Brauch, Hiltrud
    Justenhoven, Christina
    Bruening, Thomas
    Chang-Claude, Jenny
    Hein, Rebecca
    Wang-Gohrke, Shan
    Doerk, Thilo
    Schuermann, Peter
    Bremer, Michael
    HUMAN MOLECULAR GENETICS, 2011, 20 (23) : 4693 - 4706