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1. Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence

Author

S M Ashiqul Islam, Irina I. Abnizova, James McKay, Yudou He, Estelle Chanudet, Behnoush Abedi-Ardekani, Dariush Nasrollahzadeh, Michael Eden, Alisa M. Goldstein, Jon W. Teague, Blandina T. Mmbaga, Nan Hu, Karl Smith-Byrne, Sandra Perdomo, Jingwei Wang, Christine Carreira, Jean-Yves Scoazec, Rebecca C. Fitzgerald, Luis Felipe Ribeiro, Michael R. Stratton, Samad Gharavi, Sergey Senkin, Erik N Bergstrom, Hiva Saffar, Sarah Moody, Sheila Coelho Soares-Lima, Pauline E Bucciarelli, Stefano Serra, Ghislaine Scelo, Charles Dzamalala, Valerie McCormack, Reza Malekzadeh, Hossein Poustchi, Valerie Gaborieau, Lia S Campos, Joshua R. Atkins, Paul Brennan, Emily Thomas, David T. Jones, Paul Richman, Farid Azmoudeh-Ardalan, Masoud Sotoudeh, Ahmadreza Niavarani, Tatsuhiro Shibata, Calli Latimer, Stephen Fitzgerald, Ludmil B Alexandrov, Ricardo Cortez Cardoso Penha, Abdolreza Fazel, Laura Humphreys, Azhar Khandekar, Arash Nikmanesh, and Diana Menya

Subjects
Adult, Male, APOBEC, China, Esophageal Neoplasms, Apolipoprotein B, Iran, Biology, medicine.disease_cause, Genome, Esophageal squamous cell carcinoma, Germline, 03 medical and health sciences, 0302 clinical medicine, Epidemiology of cancer, Genetics, medicine, Humans, APOBEC Deaminases, Aged, 030304 developmental biology, Aged, 80 and over, 0303 health sciences, Mutation, Whole Genome Sequencing, Aldehyde Dehydrogenase, Mitochondrial, Incidence, Incidence (epidemiology), Middle Aged, United Kingdom, digestive system diseases, 3. Good health, 030220 oncology & carcinogenesis, biology.protein, Cancer research, Female, Esophageal Squamous Cell Carcinoma, Tumor Suppressor Protein p53, Brazil
Abstract

Esophageal squamous cell carcinoma (ESCC) shows remarkable variation in incidence that is not fully explained by known lifestyle and environmental risk factors. It has been speculated that an unknown exogenous exposure(s) could be responsible. Here we combine the fields of mutational signature analysis with cancer epidemiology to study 552 ESCC genomes from eight countries with varying incidence rates. Mutational profiles were similar across all countries studied. Associations between specific mutational signatures and ESCC risk factors were identified for tobacco, alcohol, opium and germline variants, with modest impacts on mutation burden. We find no evidence of a mutational signature indicative of an exogenous exposure capable of explaining differences in ESCC incidence. Apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-like (APOBEC)-associated mutational signatures single-base substitution (SBS)2 and SBS13 were present in 88% and 91% of cases, respectively, and accounted for 25% of the mutation burden on average, indicating that APOBEC activation is a crucial step in ESCC tumor development.

Published
2021
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2. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

Author

Vesa Kataja, Aida Karina Dieffenbach, Chia-Ni Hsiung, Catherine S. Healey, Gie Hooi Tan, Soo Hwang Teo, Domenico Palli, Frederik Marme, Katri Pylkäs, Roger L. Milne, Jaana M. Hartikainen, Gord Glendon, Susan L. Slager, Chen-Yang Shen, Fredrick R. Schumacher, Daniel F. Schmidt, Suleeporn Sangrajrang, Kee Seng Chia, Lorna Gibson, Pascal Guénel, Alice S. Whittemore, Jenny Chang-Claude, Yu Tang Gao, Hidemi Ito, Simon S. Cross, Sofia Khan, Marie Sanchez, Daniel Vincent, Daniel Herrero, Nicola Miller, Antoinette Hollestelle, Caroline M. Seynaeve, Christopher A. Haiman, Hermann Brenner, Kay-Tee Khaw, Loris Bernard, Habibul Ahsan, Melissa C. Southey, David Van Den Berg, Martha J. Shrubsole, Daniel O. Stram, William Blot, Mel Maranian, Robert Winqvist, Keitaro Matsuo, John W. M. Martens, Heli Nevanlinna, Mia M. Gaudet, Anna Jakubowska, Christine D. Berg, Paul D.P. Pharoah, Jacques Simard, Manjeet K. Bolla, Dieter Flesch-Janys, Mark S. Goldberg, Paul Brennan, Ching Wan Chan, Sune F. Nielsen, Sara Lindström, Mitul Shah, Matthias W. Beckmann, Craig Luccarini, Jonathan Beesley, Kyriaki Michailidou, Paolo Peterlongo, Marc J. Gunter, Anna González-Neira, Ji Yeob Choi, Per Hall, Sarah Stewart-Brown, Keith Humphreys, Hui Cai, Kathleen E. Malone, Elinor J. Sawyer, Louise A. Brinton, Marjanka K. Schmidt, Xiao-Ou Shu, Barbara Perkins, Lotte Maxild Mortensen, Chiu-Chen Tseng, Hanne Meijers-Heijboer, Minouk J. Schoemaker, Keun-Young Yoo, Julia A. Knight, Alan Ashworth, Stig E. Bojesen, Kamila Czene, Artitaya Lophatananon, Graham G. Giles, S. Ahmed, Kazuo Tajima, Douglas F. Easton, Maria Kabisch, Arja Jukkola-Vuorinen, Wei Lu, Peter A. Fasching, Irene L. Andrulis, Clare Turnbull, Caroline Baynes, Christine B. Ambrosone, Jan Lubinski, Muriel A. Adank, A. Meindl, Taru A. Muranen, Siranoush Manoukian, Susan M. Gapstur, Natalia Bogdanova, Alexander Hein, Annika Lindblom, Nazneen Rahman, Annegien Broeks, Lothar Haeberle, Federico Canzian, G Pita, Ming-Feng Hou, Hiroji Iwata, Drakoulis Yannoukakos, Diana Torres, Vessela N. Kristensen, Peter Devilee, Qiuyin Cai, Christi J Asperen, John L. Hopper, Diether Lambrechts, Michael Lush, Hans Wildiers, Joe Dennis, Sandra L. Halverson, Carl Blomqvist, Erik Van Limbergen, Malin Sund, Daehee Kang, Grethe I. Grenaker Alnæs, Marilie D. Gammon, Ursula Eilber, Ian Tomlinson, Thérèse Truong, Amanda E. Toland, Anna Marie Mulligan, Kirsimari Aaltonen, Olivia Fletcher, Jonine D. Figueroa, Angela Cox, Pei Ei Wu, Maartje J. Hooning, Catriona McLean, Georgia Chenevix-Trench, Pornthep Siriwanarangsan, Malcolm W.R. Reed, Emily Hallberg, Sara Margolin, Volker Arndt, Montserrat Garcia-Closas, Francois Bacot, Rita K. Schmutzler, Julian Peto, David J. Hunter, Thomas Brüning, Katarzyna Jaworska, Christof Sohn, Børge G. Nordestgaard, Enes Makalic, Hatef Darabi, Barbara Burwinkel, Petra P.H. Peeters, J. Margriet Collée, Rongxi Yang, Robert N. Hoover, Eiliv Lund, Fergus J. Couch, Ute Hamann, Jirong Long, Wei Zheng, Sabine Behrens, Giske Ursin, Muhammad G. Kibriya, Claire Mulot, Laure Dossus, Helen Tsimiklis, Tomasz Huzarski, Peter Kraft, Anja Rudolph, Arto Mannermaa, Alison M. Dunning, Lisa B. Signorello, Valerie Gaborieau, Kenneth Muir, Anthony J. Swerdlow, Javier Benitez, Judith S. Brand, Sander Canisius, Hoda Anton-Culver, Veli-Matti Kosma, Thilo Dörk, Sten Cornelissen, Christa Stegmaier, Cheng Har Yip, Brian E. Henderson, Harald Surowy, Jingmei Li, Nur Aishah Taib, W. Ryan Diver, Carmel Apicella, Janet E. Olson, Kristiina Aittomäki, Celine M. Vachon, Regina M. Santella, Dimitrios Trichopoulos, Jianjun Liu, Nick Orr, Martine Dumont, Christian Sutter, Sue K. Park, Mikael Hartman, Susan L. Neuhausen, Hui Miao, M. Pilar Zamora, Anna H. Wu, Rob B. van der Luijt, Isabel dos-Santos-Silva, Graham Casey, Henrik Flyger, M. Rosario Alonso, Nuria Álvarez, Michael J. Kerin, Loic Le Marchand, Jose Ignacio Arias Perez, Mikael Eriksson, Esther M. John, Quinten Waisfisz, Qin Wang, Daniel C. Tessier, Paolo Radice, Robert A.E.M. Tollenaar, James McKay, Silje Nord, Hiltrud Brauch, José María Huerta, Stephen J. Chanock, Mervi Grip, Patrick Neven, Senno Verhoef, Clinical Genetics, Obstetrics & Gynecology, Medical Oncology, Cardiothoracic Surgery, Dennis, Joe [0000-0003-4591-1214], Wang, Jean [0000-0002-9139-0627], Khaw, Kay-Tee [0000-0002-8802-2903], Pharoah, Paul [0000-0001-8494-732X], Dunning, Alison [0000-0001-6651-7166], Easton, Douglas [0000-0003-2444-3247], Apollo - University of Cambridge Repository, Human genetics, and CCA - Oncogenesis

Subjects
Breast Neoplasms, Single-nucleotide polymorphism, Genome-wide association study, Biology, Research Support, Polymorphism, Single Nucleotide, N.I.H, Cohort Studies, brca1, Breast cancer, Research Support, N.I.H., Extramural, Meta-Analysis as Topic, SDG 3 - Good Health and Well-being, common variants, Journal Article, estrogen, chek2-asterisk-1100delc, Genetics, medicine, Humans, Genetic Predisposition to Disease, 1000 Genomes Project, Non-U.S. Gov't, genotype imputation, risk, Genetic association, Research Support, Non-U.S. Gov't, Chromatin binding, Extramural, Cancer, Microarray Analysis, confer susceptibility, medicine.disease, 3. Good health, ovarian-cancer, Genetic Loci, Case-Control Studies, alleles, Female, Imputation (genetics), Genome-Wide Association Study, metaanalysis
Abstract

Genome-wide association studies (GWAS) and large-scale replication studies have identified common variants in 79 loci associated with breast cancer, explaining ∼14% of the familial risk of the disease. To identify new susceptibility loci, we performed a meta-analysis of 11 GWAS, comprising 15,748 breast cancer cases and 18,084 controls together with 46,785 cases and 42,892 controls from 41 studies genotyped on a 211,155-marker custom array (iCOGS). Analyses were restricted to women of European ancestry. We generated genotypes for more than 11 million SNPs by imputation using the 1000 Genomes Project reference panel, and we identified 15 new loci associated with breast cancer at P < 5 × 10(-8). Combining association analysis with ChIP-seq chromatin binding data in mammary cell lines and ChIA-PET chromatin interaction data from ENCODE, we identified likely target genes in two regions: SETBP1 at 18q12.3 and RNF115 and PDZK1 at 1q21.1. One association appears to be driven by an amino acid substitution encoded in EXO1. ispartof: Nature Genetics vol:47 issue:4 pages:373-80 ispartof: location:United States status: published

Published
2015
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3. Proceedings of the 7th Biannual International Symposium on Nasopharyngeal Carcinoma 2015

Author

IB Tan, Ellen T. Chang, Chien-Jen Chen, Wan-Lun Hsu, Yin-Chu Chien, Allan Hildesheim, James D. McKay, Valerie Gaborieau, Mohamed Arifin Bin Kaderi, Dewajani Purnomosari, Catherine Voegele, Florence LeCalvez-Kelm, Graham Byrnes, Paul Brennan, Beena Devi, L. Li, Y. Zhang, Y. Fan, K. Sun, Z. Du, H. Sun, A. T. Chan, S. W. Tsao, Y. X. Zeng, Q. Tao, Pierre Busson, Claire Lhuillier, Olivier Morales, Dhafer Mrizak, Aurore Gelin, Nikiforos Kapetanakis, Nadira Delhem, Sheila Mansouri, Jennifer Cao, Anup Vaidya, Lori Frappier, Lo Kwok Wai, Sui-Hong Chen, Jin-lin Du, Ming-Fang Ji, Qi-Hong Huang, Qing Liu, Su-Mei Cao, Denise L. Doolan, Anna Coghill, Jason Mulvenna, Carla Proietti, Lea Lekieffre, Jeffrey Bethony, and Allan Hildesheim, Renske Fles, Sagung Rai Indrasari, Camelia Herdini, Santi Martini, Atoillah Isfandiari, Achmad Rhomdoni, Marlinda Adham, Ika Mayangsari, Erik van Werkhoven, Maarten Wildeman, Bambang Hariwiyanto, Bambang Hermani, Widodo Ario Kentjono, Sofia Mubarika Haryana, Marjanka Schmidt, Brian O’Sullivan, Enis Ozyar, Anne W. M. Lee, Mu-Sheng Zeng, Xiaojiang Gao, Minzhong Tang, Pat Martin, Yi Zeng, Mary Carrington, Anna E. Coghill, Wei Bu, Hanh Nguyen, Kelly J. Yu, Pei-Jen Lou, Cheng-Ping Wang, Jeffrey I. Cohen, Ann D. King, Tseng-Cheng Chen, Ching-Yuan Lin, Yung-An Tsou, Yi-Shing Leu, Li-Jen Laio, Yen-Liang Chang, Chun-Hun Hua, Ming-Shiang Wu, Chu-Hsing Kate Hsiao, Jehn-Chuan Lee, Ming-Hsui Tsai, Skye Hung-Chun Cheng, Li-Jen Liao, Tsung-Lin Yang, Jenq-Yuh Ko, Josephine Mun Yee Ko, Wei Dai, Dora Kwong, Wai Tong Ng, Anne Lee, Roger Kai Cheong Ngan, Chun Chung Yau, Stewart Tung, Maria Li Lung, Mingfang Ji, Wei Sheng, Mun Hon Ng, Weimin Cheng, Xia Yu, Biaohua Wu, Kuangrong Wei, Jun Zhan, Yi Xin Zeng, Su Mei Cao, Ningshao Xia, Yong Yuan, Qian Cui, Miao Xu, Jin-Xin Bei, Yi-Xin Zeng, B Şahin, A Dizman, M Esassolak, A Saran İkizler, HC Yıldırım, M Çaloğlu, B Atalar, F Akman, C Demiroz, BM Atasoy, E Canyilmaz, S Igdem, G Ugurluer, T Kütük, M Akmansoy, E Ozyar, Kiattisa Sommat, Fu Qiang Wang, Li-Lian Kwok, Terence Tan, Kam Weng Fong, Yoke Lim Soong, Shie Lee Cheah, Joseph Wee, M Casanova, E Özyar, C Patte, D Orbach, A Ferrari, VF Cristine, H Errihani, J Pan, L Zhang, S Liji, K Grzegorzewski, L Gore, A Varan, Susanna Hilda Hutajulu, Guntara Khuzairi, Henry Kusumo, Mardiah Suci Hardianti, Kartika Widayati Taroeno-Hariadi, Ibnu Purwanto, Johan Kurnianda, Troy E. Messick, Kimberly Malecka, Lois Tolvinski, Samantha Soldan, Julianna Deakyne, Hui Song, Antonio van den Heuvel, Baiwei Gu, Joel Cassel, Mark McDonnell, Garry R. Smith, Venkata Velvadapu, Haiyan Bian, Yan Zhang, Marianne Carlsen, Shuai Chen, Alastair Donald, Christian Lemmen, Allen B. Reitz, Paul M. Lieberman, King Chi Chan, Lai Sheung Chan, Kwok Wai Lo, Timothy Tak Chun Yip, Michael Kahn, Nai Ki Mak, Fei-Fei Liu, Wafa Khaali, Juliette Thariat, Laurence Fantin, Flavia Spirito, Meriem Khyatti, El Khalil Ben Driss, Sylvain Olivero, Janet Maryanski, Alain Doglio, Mengxue Xia, Yunfei Xia, Hui Chang, Rachel Shaw, Pudji Rahaju, Sindhu Wisesa, Kartika Widayati Taroeno-Harijadi, Wigati Dhamiyati, Sang-Nee Tan, Sai-Peng Sim, Muhtarum Yusuf, Ahmad C. Romdhoni, Widodo Ario K, Fedik Abdul Rantam, null Sugiyanto, Lina Aryati, Fajar Adi-Kusumo, SY Bintoro, R. Oktriani, C. Herawati, A. Surono, Sofia M. Haryana, L. Zhong, B. B. Ma, M. Kalra, M. Ngo, S. Perna, A. Leen, N. Lapteva, C. M. Rooney, S. Gottschalk, Elida Mustikaningtyas, Sri Herawati, Achmad C. Romdhoni, Yarui Xu, Shengxiang Ge, Fugui Li, M. H. Ng, Louise SY Tan, Benjamin Wong, C. M. Lim, Fedik A. Rantam, Deasy Z. Madani, Nur Akbar, Agung Dinasti Permana, Jajah Fachiroh, Dwi Hartati, T. Baning Rahayudjati, Iswandi Darwis, Khoirul Anwar, Sri Retna Dwidanarti, Dominicus Wendhy Pramana, Diah Ari Safitri, Sri Retna Dwi Danarti, Suryo A Taroeno, I. Wijaya, A. Oehadian, D. Prasetya, Kelly J Yu, Sukri Rahman, Bestari J. Budiman, null Novialdi, null Rahmadona, Dewi Yuri Lestari, C. Yin, A. Foussadier, E. Blein, C. Chen, N. Bournet Ammour, M. Khiatti, S. Cao, Dewi Syafriyetti Soeis Marzaini, Baning Rahayujati, L. Gunawan, S. Mubarika Haryana, Michael Hartono, Umi Intansari, Dewi Kartikawati Paramita, Akmal Akbar, Benny Hermawan, Dewi K. Paramita, Gabriella Argy, Theodora Caroline Sihotang, Daniel Joko Wahyono, Purnomo Soeharso, Dwi Anita Suryandari, null Lisnawati, Zanil Musa, Maelinda Daker, Yeo Jiun Tzen, Norhasimah Bakar, Asma’ Saiyidatina Aishah Abdul Rahman, Munirah Ahmad, Yeo Tiong Chia, Alan Khoo Soo Beng, Widyandani Sasikirana, Tirta Wardana, Muhammad Radifar, Cita Herawati, and Agus Surono

Subjects
0301 basic medicine, Pathology, medicine.medical_specialty, business.industry, General Medicine, medicine.disease, medicine.disease_cause, Epstein–Barr virus, Virology, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Nasopharyngeal carcinoma, 030220 oncology & carcinogenesis, medicine, business, Epstein–Barr virus infection
Published
2016
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4. Genome-wide association study identifies novel breast cancer susceptibility loci

Author

Keun-Young Yoo, Sara Wedrén, Margaret R. E. McCredie, Jonathan J. Morrison, Per Hall, Beata Peplonska, Natalia Bogdanova, Robert Luben, Diana Eccles, Nazneen Rahman, Dennis G. Ballinger, Louise A. Brinton, Bruce H. Alexander, Janet E. Olson, C K Axelsson, Loic Le Marchand, Georgia Chenevix-Trench, Paul Brennan, Laurence K. Kolonel, David Cox, Peter Devilee, Nichola Johnson, Yen-Ling Low, Hui-Chun Wang, Angela Cox, Hanne Meijers-Heijboer, Pei-Ei Wu, Michele M. Doody, Alison M. Dunning, Vesa Kataja, Julian Peto, Susan E. Hankinson, Roger L. Milne, Fernando Rivadeneira, Børge G. Nordestgaard, Daehee Kang, Sheila Seal, Melissa C. Southey, Michael R. Stratton, David J. Hunter, Rob A. E. M. Tollenaar, Heli Nevanlinna, Christopher A. Haiman, Sei Hyun Ahn, Karen A. Pooley, Ans M.W. van den Ouweland, Valerie Gaborieau, Malcolm W.R. Reed, Catherine S. Healey, Amanda B. Spurdle, Chris Schroen, Jaana M. Hartikainen, Jolanta Lissowska, Bruce A.J. Ponder, Jonathan Beesley, Paul D.P. Pharoah, Douglas F. Easton, Gordon MacPherson, André G. Uitterlinden, Hiltrud Brauch, Arto Mannermaa, Jianjun Liu, Christina Justenhoven, Catharina E. Jacobi, Montserrat Garcia-Closas, Yon-Dschun Ko, Do¨rk Do¨rk, Richard Bowman, Rainer Fagerholm, Ian W. Brock, Nicholas J. Wareham, Jinghui Zhang, Dong-Young Noh, Xiaoqing Chen, Graham G. Giles, Brian E. Henderson, David G. Cox, D. Gareth Evans, Javier Benitez, kConFab, Veli-Matti Kosma, Fabrice Odefrey, Gloria Ribas, Helen I. Field, Ellen L. Goode, Fergus J. Couch, Kerstin B. Meyer, Stig E. Bojesen, Ute Hamann, John L. Hopper, Alice J. Sigurdson, Chen-Yang Shen, Suleeporn Sangrajrang, H Eerola, Shahana Ahmed, Jan G. M. Klijn, Jeffery P. Struewing, Stephen J. Chanock, Peter Schu¨rmann, Anna González-Neira, Deborah J. Thompson, Nicholas E. Day, Olivia Fletcher, Clinical Genetics, Medical Oncology, Internal Medicine, and Human Genetics

Subjects
Genotype, MAP Kinase Kinase Kinase 1, Breast Neoplasms, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, SDG 3 - Good Health and Well-being, Genetic variation, Odds Ratio, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, Receptor, Fibroblast Growth Factor, Type 2, Alleles, Asia, Southeastern, 030304 developmental biology, Genetics, 0303 health sciences, Multidisciplinary, Genome, Human, Microfilament Proteins, Australia, High Mobility Group Proteins, Cancer, medicine.disease, 3. Good health, Europe, TOX3, Case-Control Studies, 030220 oncology & carcinogenesis, North America, Trans-Activators, Female, Apoptosis Regulatory Proteins, Receptors, Progesterone
Abstract

Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to the disease. Known susceptibility genes account for less than 25% of the familial risk of breast cancer, and the residual genetic variance is likely to be due to variants conferring more moderate risks. To identify further susceptibility alleles, we conducted a two-stage genome-wide association study in 4,398 breast cancer cases and 4,316 controls, followed by a third stage in which 30 single nucleotide polymorphisms (SNPs) were tested for confirmation in 21,860 cases and 22,578 controls from 22 studies. We used 227,876 SNPs that were estimated to correlate with 77% of known common SNPs in Europeans at r2 > 0.5. SNPs in five novel independent loci exhibited strong and consistent evidence of association with breast cancer (P

Published
2007
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5. Erratum: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

Author

Mari Nelis, Neil E. Caporaso, Tõnu Vooder, H. Bas Bueno-de-Mesquita, Ben Kinnersley, Frank Skorpen, Stephen J. Chanock, Mattias Johansson, Gary E. Goodman, Athena Matakidou, Kay-Tee Khaw, Amy Lloyd, Dana Mates, Neonilia Szeszenia-Dabrowska, Elisabete Weiderpass, Maiken Elvestad Gabrielsen, Paul Brennan, David C. Christiani, Maria Teresa Landi, Susan M. Gapstur, Yuanqing Ye, Andres Metspalu, Hendrik Dienemann, Nilanjan Chatterjee, Margaret R. Spitz, Younghun Han, Christopher I. Amos, James McKay, Manon Delahaye-Sourdeix, Lars J. Vatten, William Wheeler, Eleonora Fabianova, Daniel Chubb, Simone Benhamou, T. Eisen, Peter Rudnai, Chu Chen, Ghislaine Scelo, Antonio Agudo, Paolo Vineis, Marcin Lener, Mikael Johansson, Angela Risch, Maria Timofeeva, Mark Lathrop, Li Su, Yongyue Wei, Victoria L. Stevens, Peter Broderick, Maxime Vallée, Inger Njølstad, Rayjean J. Hung, David Zaridze, Thorunn Rafnar, Vladimir Janout, Yufei Wang, Jian Gu, Hans E. Krokan, Marc Henrion, Lenka Foretova, Kari Stefansson, Gudmar Thorleifsson, Demetrius Albanes, Patrick Sulem, Geoffrey Liu, Rudolf Kaaks, Marina Laplana, Jan Lubinski, Xuchen Zong, Vladimir Bencko, Elio Riboli, Zhaoming Wang, Françoise Clavel-Chapelon, Albert Rosenberger, Dimitrios Trichopoulos, Valerie Gaborieau, Florence Le Calvez-Kelm, Anne Tjønneland, Wei V. Chen, Jolanta Lissowska, Kristjan Välk, Richard S. Houlston, and Xifeng Wu

Subjects
0301 basic medicine, Oncology, medicine.medical_specialty, Biology, Affect (psychology), medicine.disease, 3. Good health, 03 medical and health sciences, 030104 developmental biology, Internal medicine, Genetics, medicine, Lung cancer, CHEK2
Abstract

Nat. Genet. 46, 736–741 (2014); published online 1 June 2014; corrected after print 23 January 2017 In the version of this article initially published, the name of author Florence Le Calvez-Kelm appeared incorrectly as Florence LeCalvez-Kelm. The error has been corrected in the HTML and PDF versionsof the article.

Published
2017
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