Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

被引：0

作者：

Julius Gudmundsson

Patrick Sulem

Daniel F Gudbjartsson

Jon G Jonasson

Asgeir Sigurdsson

Jon T Bergthorsson

Huiling He

Thorarinn Blondal

Frank Geller

Margret Jakobsdottir

Droplaug N Magnusdottir

Sigurborg Matthiasdottir

Simon N Stacey

Oskar B Skarphedinsson

Hafdis Helgadottir

Wei Li

Rebecca Nagy

Esperanza Aguillo

Eduardo Faure

Enrique Prats

Berta Saez

Mariano Martinez

Gudmundur I Eyjolfsson

Unnur S Bjornsdottir

Hilma Holm

Kristleifur Kristjansson

Michael L Frigge

Hoskuldur Kristvinsson

Jeffrey R Gulcher

Thorvaldur Jonsson

Thorunn Rafnar

Hannes Hjartarsson

Jose I Mayordomo

Albert de la Chapelle

Jon Hrafnkelsson

Unnur Thorsteinsdottir

Augustine Kong

Kari Stefansson

机构：

[1] deCODE genetics,Department of Pathology

[2] Sturlugata 8,Division of Endocrinology

[3] Landspitali-University Hospital Hringbraut,Division of Nuclear Medicine

[4] Faculty of Medicine,Division of Surgery

[5] University of Iceland,Department of Internal Medicine, Division of Cardiology

[6] The Icelandic Cancer Registry,Department of Surgery

[7] Human Cancer Genetics Program,H&N Surgery Department

[8] Comprehensive Cancer Center,Division of Medical Oncology

[9] The Ohio State University,Department of Oncology

[10] University Hospital,undefined

[11] University Hospital,undefined

[12] The Health Science Institute,undefined

[13] Nanotechnology Institute of Aragon,undefined

[14] University Hospital,undefined

[15] The Laboratory in Mjodd,undefined

[16] Emory University School of Medicine,undefined

[17] Landspitali-University Hospital Hringbraut,undefined

[18] ORL,undefined

[19] Landspitali-University Hospital Fossvogi,undefined

[20] Lozano Blesa University Hospital,undefined

[21] University of Zaragoza,undefined

[22] Landspitali-University Hospital Hringbraut,undefined

来源：

Nature Genetics | 2009年 / 41卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Julius Gudmundsson and colleagues report the association of two SNPs on chromosomes 9 and 14 with thyroid cancer in European populations. The variants are near FOXE1 and NKX2-1, both good biological candidates, and individuals who are homozygous for both risk variants have a 5.7-fold greater risk of thyroid cancer.

引用

页码：460 / 464

页数：4

共 35 条

[31] Common genetic variants (rs4779584 and rs10318) at 15q13.3 contributes to colorectal adenoma and colorectal cancer susceptibility: evidence based on 22 studies
Tu, Lin
Yan, Bin
Peng, Zhiyong
MOLECULAR GENETICS AND GENOMICS, 2015, 290 (03) : 901 - 912
[32] 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
[33] 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)
[34] 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
[35] 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

← 1 2 3 4 →