Publications:

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Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.

Nature Communications

Shi, Jianxin J; Shiraishi, Kouya K; Choi, Jiyeon J; Matsuo, Keitaro K; Chen, Tzu-Yu TY; Dai, Juncheng J; Hung, Rayjean J RJ; Chen, Kexin K; Shu, Xiao-Ou XO; Kim, Young Tae YT; Landi, Maria Teresa MT; Lin, Dongxin D; Zheng, Wei W; Yin, Zhihua Z; Zhou, Baosen B; Song, Bao B; Wang, Jiucun J; Seow, Wei Jie WJ; Song, Lei L; Chang, I-Shou IS; Hu, Wei W; Chien, Li-Hsin LH; Cai, Qiuyin Q; Hong, Yun-Chul YC; Kim, Hee Nam HN; Wu, Yi-Long YL; Wong, Maria Pik MP; Richardson, Brian Douglas BD; Funderburk, Karen M KM; Li, Shilan S; Zhang, Tongwu T; Breeze, Charles C; Wang, Zhaoming Z; Blechter, Batel B; Bassig, Bryan A BA; Kim, Jin Hee JH; Albanes, Demetrius D; Wong, Jason Y Y JYY; Shin, Min-Ho MH; Chung, Lap Ping LP; Yang, Yang Y; An, She-Juan SJ; Zheng, Hong H; Yatabe, Yasushi Y; Zhang, Xu-Chao XC; Kim, Young-Chul YC; Caporaso, Neil E NE; Chang, Jiang J; Ho, James Chung Man JCM; Kubo, Michiaki M; Daigo, Yataro Y; Song, Minsun M; Momozawa, Yukihide Y; Kamatani, Yoichiro Y; Kobayashi, Masashi M; Okubo, Kenichi K; Honda, Takayuki T; Hosgood, Dean H DH; Kunitoh, Hideo H; Patel, Harsh H; Watanabe, Shun-Ichi SI; Miyagi, Yohei Y; Nakayama, Haruhiko H; Matsumoto, Shingo S; Horinouchi, Hidehito H; Tsuboi, Masahiro M; Hamamoto, Ryuji R; Goto, Koichi K; Ohe, Yuichiro Y; Takahashi, Atsushi A; Goto, Akiteru A; Minamiya, Yoshihiro Y; Hara, Megumi M; Nishida, Yuichiro Y; Takeuchi, Kenji K; Wakai, Kenji K; Matsuda, Koichi K; Murakami, Yoshinori Y; Shimizu, Kimihiro K; Suzuki, Hiroyuki H; Saito, Motonobu M; Ohtaki, Yoichi Y; Tanaka, Kazumi K; Wu, Tangchun T; Wei, Fusheng F; Dai, Hongji H; Machiela, Mitchell J MJ; Su, Jian J; Kim, Yeul Hong YH; Oh, In-Jae IJ; Lee, Victor Ho Fun VHF; Chang, Gee-Chen GC; Tsai, Ying-Huang YH; Chen, Kuan-Yu KY; Huang, Ming-Shyan MS; Su, Wu-Chou WC; Chen, Yuh-Min YM; Seow, Adeline A; Park, Jae Yong JY; Kweon, Sun-Seog SS; Chen, Kun-Chieh KC; Gao, Yu-Tang YT; Qian, Biyun B; Wu, Chen C; Lu, Daru D; Liu, Jianjun J; Schwartz, Ann G AG; Houlston, Richard R; Spitz, Margaret R MR; Gorlov, Ivan P IP; Wu, Xifeng X; Yang, Ping P; Lam, Stephen S; Tardon, Adonina A; Chen, Chu C; Bojesen, Stig E SE; Johansson, Mattias M; Risch, Angela A; Bickeböller, Heike H; Ji, Bu-Tian BT; Wichmann, H-Erich HE; Christiani, David C DC; Rennert, Gadi G; Arnold, Susanne S; Brennan, Paul P; McKay, James J; Field, John K JK; Shete, Sanjay S SS; Le Marchand, Loic L; Liu, Geoffrey G; Andrew, Angeline A; Kiemeney, Lambertus A LA; Zienolddiny-Narui, Shan S; Grankvist, Kjell K; Johansson, Mikael M; Cox, Angela A; Taylor, Fiona F; Yuan, Jian-Min JM; Lazarus, Philip P; Schabath, Matthew B MB; Aldrich, Melinda C MC; Jeon, Hyo-Sung HS; Jiang, Shih Sheng SS; Sung, Jae Sook JS; Chen, Chung-Hsing CH; Hsiao, Chin-Fu CF; Jung, Yoo Jin YJ; Guo, Huan H; Hu, Zhibin Z; Burdett, Laurie L; Yeager, Meredith M; Hutchinson, Amy A; Hicks, Belynda B; Liu, Jia J; Zhu, Bin B; Berndt, Sonja I SI; Wu, Wei W; Wang, Junwen J; Li, Yuqing Y; Choi, Jin Eun JE; Park, Kyong Hwa KH; Sung, Sook Whan SW; Liu, Li L; Kang, Chang Hyun CH; Wang, Wen-Chang WC; Xu, Jun J; Guan, Peng P; Tan, Wen W; Yu, Chong-Jen CJ; Yang, Gong G; Sihoe, Alan Dart Loon ADL; Chen, Ying Y; Choi, Yi Young YY; Kim, Jun Suk JS; Yoon, Ho-Il HI; Park, In Kyu IK; Xu, Ping P; He, Qincheng Q; Wang, Chih-Liang CL; Hung, Hsiao-Han HH; Vermeulen, Roel C H RCH; Cheng, Iona I; Wu, Junjie J; Lim, Wei-Yen WY; Tsai, Fang-Yu FY; Chan, John K C JKC; Li, Jihua J; Chen, Hongyan H; Lin, Hsien-Chih HC; Jin, Li L; Liu, Jie J; Sawada, Norie N; Yamaji, Taiki T; Wyatt, Kathleen K; Li, Shengchao A SA; Ma, Hongxia H; Zhu, Meng M; Wang, Zhehai Z; Cheng, Sensen S; Li, Xuelian X; Ren, Yangwu Y; Chao, Ann A; Iwasaki, Motoki M; Zhu, Junjie J; Jiang, Gening G; Fei, Ke K; Wu, Guoping G; Chen, Chih-Yi CY; Chen, Chien-Jen CJ; Yang, Pan-Chyr PC; Yu, Jinming J; Stevens, Victoria L VL; Fraumeni, Joseph F JF; Chatterjee, Nilanjan N; Gorlova, Olga Y OY; Hsiung, Chao Agnes CA; Amos, Christopher I CI; Shen, Hongbing H; Chanock, Stephen J SJ; Rothman, Nathaniel N; Kohno, Takashi T; Lan, Qing Q

Publication Date: 2023-05-26

Variant appearance in text: rs13167280

PubMed Link: 37236969

Variant Present in the following documents:

• Main text
• 41467_2023_Article_38196.pdf

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Cumulative Evidence for Relationships Between Multiple Variants in the TERT and CLPTM1L Region and Risk of Cancer and Non-Cancer Disease.

Frontiers In Oncology

Tian, Jie J; Wang, Yan Y; Dong, Yingxian Y; Chang, Junke J; Wu, Yongming Y; Chang, Shuai S; Che, Guowei G

Publication Date: 2022

Variant appearance in text: rs13167280

PubMed Link: 35847915

Variant Present in the following documents:

• Main text
• DataSheet_1.pdf
• fonc-12-946039.pdf
• DataSheet_3.pdf

View BVdb publication page

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Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis.

Nature Genetics

Kar, Siddhartha P SP; Quiros, Pedro M PM; Gu, Muxin M; Jiang, Tao T; Mitchell, Jonathan J; Langdon, Ryan R; Iyer, Vivek V; Barcena, Clea C; Vijayabaskar, M S MS; Fabre, Margarete A MA; Carter, Paul P; Petrovski, Slavé S; Burgess, Stephen S; Vassiliou, George S GS

Publication Date: 2022-08

Variant appearance in text: rs13167280

PubMed Link: 35835912

Variant Present in the following documents:

• Main text
• 41588_2022_Article_1121.pdf

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Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study.

Gut

Buch, Stephan S; Innes, Hamish H; Lutz, Philipp Ludwig PL; Nischalke, Hans Dieter HD; Marquardt, Jens U JU; Fischer, Janett J; Weiss, Karl Heinz KH; Rosendahl, Jonas J; Marot, Astrid A; Krawczyk, Marcin M; Casper, Markus M; Lammert, Frank F; Eyer, Florian F; Vogel, Arndt A; Marhenke, Silke S; von Felden, Johann J; Sharma, Rohini R; Atkinson, Stephen Rahul SR; McQuillin, Andrew A; Nattermann, Jacob J; Schafmayer, Clemens C; Franke, Andre A; Strassburg, Christian C; Rietschel, Marcella M; Altmann, Heidi H; Sulk, Stefan S; Thangapandi, Veera Raghavan VR; Brosch, Mario M; Lackner, Carolin C; Stauber, Rudolf E RE; Canbay, Ali A; Link, Alexander A; Reiberger, Thomas T; Mandorfer, Mattias M; Semmler, Georg G; Scheiner, Bernhard B; Datz, Christian C; Romeo, Stefano S; Ginanni Corradini, Stefano S; Irving, William Lucien WL; Morling, Joanne R JR; Guha, Indra Neil IN; Barnes, Eleanor E; Ansari, M Azim MA; Quistrebert, Jocelyn J; Valenti, Luca L; Müller, Sascha A SA; Morgan, Marsha Yvonne MY; Dufour, Jean-François JF; Trebicka, Jonel J; Berg, Thomas T; Deltenre, Pierre P; Mueller, Sebastian S; Hampe, Jochen J; Stickel, Felix F

Publication Date: 2022-07-04

Variant appearance in text: rs13167280

PubMed Link: 35788059

Variant Present in the following documents:

• gutjnl-2022-327196supp001.pdf

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The Genetic Makeup of Myeloproliferative Neoplasms: Role of Germline Variants in Defining Disease Risk, Phenotypic Diversity and Outcome.

Cells

Masselli, Elena E; Pozzi, Giulia G; Carubbi, Cecilia C; Vitale, Marco M

Publication Date: 2021-09-29

Variant appearance in text: rs13167280

PubMed Link: 34685575

Variant Present in the following documents:

• Main text

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Germline mutations among Polish patients with acute myeloid leukemia.

Hereditary Cancer In Clinical Practice

Bąk, Aneta A; Skonieczka, Katarzyna K; Jaśkowiec, Anna A; Junkiert-Czarnecka, Anna A; Heise, Marta M; Pilarska-Deltow, Maria M; Potoczek, Stanisław S; Czyżewska, Maria M; Haus, Olga O

Publication Date: 2021-10-12

Variant appearance in text: rs13167280

PubMed Link: 34641967

Variant Present in the following documents:

• Main text
• 13053_2021_Article_200.pdf

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics

Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F

Publication Date: 2021

Variant appearance in text: TERT: 1770-24C>T; rs13167280

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Germline risk of clonal haematopoiesis.

Nature Reviews. Genetics

Silver, Alexander J AJ; Bick, Alexander G AG; Savona, Michael R MR

Publication Date: 2021-09

Variant appearance in text: rs13167280

PubMed Link: 33986496

Variant Present in the following documents:

• Main text

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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology

Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA

Publication Date: 2021

Variant appearance in text: rs13167280

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes.

Nature

Bick, Alexander G AG; Weinstock, Joshua S JS; Nandakumar, Satish K SK; Fulco, Charles P CP; Bao, Erik L EL; Zekavat, Seyedeh M SM; Szeto, Mindy D MD; Liao, Xiaotian X; Leventhal, Matthew J MJ; Nasser, Joseph J; Chang, Kyle K; Laurie, Cecelia C; Burugula, Bala Bharathi BB; Gibson, Christopher J CJ; Lin, Amy E AE; Taub, Margaret A MA; Aguet, Francois F; Ardlie, Kristin K; Mitchell, Braxton D BD; Barnes, Kathleen C KC; Moscati, Arden A; Fornage, Myriam M; Redline, Susan S; Psaty, Bruce M BM; Silverman, Edwin K EK; Weiss, Scott T ST; Palmer, Nicholette D ND; Vasan, Ramachandran S RS; Burchard, Esteban G EG; Kardia, Sharon L R SLR; He, Jiang J; Kaplan, Robert C RC; Smith, Nicholas L NL; Arnett, Donna K DK; Schwartz, David A DA; Correa, Adolfo A; de Andrade, Mariza M; Guo, Xiuqing X; Konkle, Barbara A BA; Custer, Brian B; Peralta, Juan M JM; Gui, Hongsheng H; Meyers, Deborah A DA; McGarvey, Stephen T ST; Chen, Ida Yii-Der IY; Shoemaker, M Benjamin MB; Peyser, Patricia A PA; Broome, Jai G JG; Gogarten, Stephanie M SM; Wang, Fei Fei FF; Wong, Quenna Q; Montasser, May E ME; Daya, Michelle M; Kenny, Eimear E EE; North, Kari E KE; Launer, Lenore J LJ; Cade, Brian E BE; Bis, Joshua C JC; Cho, Michael H MH; Lasky-Su, Jessica J; Bowden, Donald W DW; Cupples, L Adrienne LA; Mak, Angel C Y ACY; Becker, Lewis C LC; Smith, Jennifer A JA; Kelly, Tanika N TN; Aslibekyan, Stella S; Heckbert, Susan R SR; Tiwari, Hemant K HK; Yang, Ivana V IV; Heit, John A JA; Lubitz, Steven A SA; Johnsen, Jill M JM; Curran, Joanne E JE; Wenzel, Sally E SE; Weeks, Daniel E DE; Rao, Dabeeru C DC; Darbar, Dawood D; Moon, Jee-Young JY; Tracy, Russell P RP; Buth, Erin J EJ; Rafaels, Nicholas N; Loos, Ruth J F RJF; Durda, Peter P; Liu, Yongmei Y; Hou, Lifang L; Lee, Jiwon J; Kachroo, Priyadarshini P; Freedman, Barry I BI; Levy, Daniel D; Bielak, Lawrence F LF; Hixson, James E JE; Floyd, James S JS; Whitsel, Eric A EA; Ellinor, Patrick T PT; Irvin, Marguerite R MR; Fingerlin, Tasha E TE; Raffield, Laura M LM; Armasu, Sebastian M SM; Wheeler, Marsha M MM; Sabino, Ester C EC; Blangero, John J; Williams, L Keoki LK; Levy, Bruce D BD; Sheu, Wayne Huey-Herng WH; Roden, Dan M DM; Boerwinkle, Eric E; Manson, JoAnn E JE; Mathias, Rasika A RA; Desai, Pinkal P; Taylor, Kent D KD; Johnson, Andrew D AD; , ; Auer, Paul L PL; Kooperberg, Charles C; Laurie, Cathy C CC; Blackwell, Thomas W TW; Smith, Albert V AV; Zhao, Hongyu H; Lange, Ethan E; Lange, Leslie L; Rich, Stephen S SS; Rotter, Jerome I JI; Wilson, James G JG; Scheet, Paul P; Kitzman, Jacob O JO; Lander, Eric S ES; Engreitz, Jesse M JM; Ebert, Benjamin L BL; Reiner, Alexander P AP; Jaiswal, Siddhartha S; Abecasis, Gonçalo G; Sankaran, Vijay G VG; Kathiresan, Sekar S; Natarajan, Pradeep P

Publication Date: 2020-10

Variant appearance in text: rs13167280

PubMed Link: 33057201

Variant Present in the following documents:

• Main text
• nihms-1609346.pdf

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Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.

Acta Neuropathologica Communications

Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C

Publication Date: 2019-08-30

Variant appearance in text: rs13167280

PubMed Link: 31470906

Variant Present in the following documents:

• 40478_2019_793_MOESM1_ESM.xlsx, sheet 2

View BVdb publication page

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Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.

The Lancet. Respiratory Medicine

Dai, Juncheng J; Lv, Jun J; Zhu, Meng M; Wang, Yuzhuo Y; Qin, Na N; Ma, Hongxia H; He, Yong-Qiao YQ; Zhang, Ruoxin R; Tan, Wen W; Fan, Jingyi J; Wang, Tianpei T; Zheng, Hong H; Sun, Qi Q; Wang, Lijuan L; Huang, Mingtao M; Ge, Zijun Z; Yu, Canqing C; Guo, Yu Y; Wang, Tong-Min TM; Wang, Jie J; Xu, Lin L; Wu, Weibing W; Chen, Liang L; Bian, Zheng Z; Walters, Robin R; Millwood, Iona Y IY; Li, Xi-Zhao XZ; Wang, Xin X; Hung, Rayjean J RJ; Christiani, David C DC; Chen, Haiquan H; Wang, Mengyun M; Wang, Cheng C; Jiang, Yue Y; Chen, Kexin K; Chen, Zhengming Z; Jin, Guangfu G; Wu, Tangchun T; Lin, Dongxin D; Hu, Zhibin Z; Amos, Christopher I CI; Wu, Chen C; Wei, Qingyi Q; Jia, Wei-Hua WH; Li, Liming L; Shen, Hongbing H

Publication Date: 2019-10

Variant appearance in text: rs13167280

PubMed Link: 31326317

Variant Present in the following documents:

• Main text

View BVdb publication page

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Specific V-ATPase expression sub-classifies IDHwt lower-grade gliomas and impacts glioma growth in vivo.

Ebiomedicine

Terrasi, Andrea A; Bertolini, Irene I; Martelli, Cristina C; Gaudioso, Gabriella G; Di Cristofori, Andrea A; Storaci, Alessandra Maria AM; Formica, Miriam M; Bosari, Silvano S; Caroli, Manuela M; Ottobrini, Luisa L; Vaccari, Thomas T; Vaira, Valentina V

Publication Date: 2019-03

Variant appearance in text: rs13167280

PubMed Link: 30737087

Variant Present in the following documents:

• mmc1.xlsx, sheet 9

View BVdb publication page

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: TERT: 1770-24C>T; rs13167280

PubMed Link: 30319441

Variant Present in the following documents:

• Table_6.xlsx, sheet 1

View BVdb publication page

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Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers.

International Journal Of Epidemiology

Kachuri, Linda L; Saarela, Olli O; Bojesen, Stig Egil SE; Davey Smith, George G; Liu, Geoffrey G; Landi, Maria Teresa MT; Caporaso, Neil E NE; Christiani, David C DC; Johansson, Mattias M; Panico, Salvatore S; Overvad, Kim K; Trichopoulou, Antonia A; Vineis, Paolo P; Scelo, Ghislaine G; Zaridze, David D; Wu, Xifeng X; Albanes, Demetrius D; Diergaarde, Brenda B; Lagiou, Pagona P; Macfarlane, Gary J GJ; Aldrich, Melinda C MC; Tardón, Adonina A; Rennert, Gad G; Olshan, Andrew F AF; Weissler, Mark C MC; Chen, Chu C; Goodman, Gary E GE; Doherty, Jennifer A JA; Ness, Andrew R AR; Bickeböller, Heike H; Wichmann, H-Erich HE; Risch, Angela A; Field, John K JK; Teare, M Dawn MD; Kiemeney, Lambertus A LA; van der Heijden, Erik H F M EHFM; Carroll, June C JC; Haugen, Aage A; Zienolddiny, Shanbeh S; Skaug, Vidar V; Wünsch-Filho, Victor V; Tajara, Eloiza H EH; Ayoub Moysés, Raquel R; Daumas Nunes, Fabio F; Lam, Stephen S; Eluf-Neto, Jose J; Lacko, Martin M; Peters, Wilbert H M WHM; Le Marchand, Loïc L; Duell, Eric J EJ; Andrew, Angeline S AS; Franceschi, Silvia S; Schabath, Matthew B MB; Manjer, Jonas J; Arnold, Susanne S; Lazarus, Philip P; Mukeriya, Anush A; Swiatkowska, Beata B; Janout, Vladimir V; Holcatova, Ivana I; Stojsic, Jelena J; Mates, Dana D; Lissowska, Jolanta J; Boccia, Stefania S; Lesseur, Corina C; Zong, Xuchen X; McKay, James D JD; Brennan, Paul P; Amos, Christopher I CI; Hung, Rayjean J RJ

Publication Date: 2019-06-01

Variant appearance in text: rs13167280

PubMed Link: 30059977

Variant Present in the following documents:

• Main text

View BVdb publication page

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs13167280

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs13167280

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

View BVdb publication page

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Characterization of population-based variation and putative functional elements for the multiple-cancer susceptibility loci at 5p15.33.

F1000Research

Mirabello, Lisa L; Chung, Charles C CC; Yeager, Meredith M; Savage, Sharon A SA

Publication Date: 2014

Variant appearance in text: rs13167280

PubMed Link: 26664699

Variant Present in the following documents:

• Main text
• f1000research-3-5532.pdf

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The TERT promoter SNP rs2853669 decreases E2F1 transcription factor binding and increases mortality and recurrence risks in liver cancer.

Oncotarget

Ko, Eunkyong E; Seo, Hyun-Wook HW; Jung, Eun Sun ES; Kim, Baek-hui BH; Jung, Guhung G

Publication Date: 2016-01-05

Variant appearance in text: rs13167280

PubMed Link: 26575952

Variant Present in the following documents:

• Main text

View BVdb publication page

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A screening-testing approach for detecting gene-environment interactions using sequential penalized and unpenalized multiple logistic regression.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing

Frost, H Robert HR; Andrew, Angeline S AS; Karagas, Margaret R MR; Moore, Jason H JH

Publication Date: 2015

Variant appearance in text: rs13167280

PubMed Link: 25592580

Variant Present in the following documents:

• Main text

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Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.

Acta Neuropathologica Communications

Shankar, Ganesh M GM; Taylor-Weiner, Amaro A; Lelic, Nina N; Jones, Robert T RT; Kim, James C JC; Francis, Joshua M JM; Abedalthagafi, Malak M; Borges, Lawrence F LF; Coumans, Jean-Valery JV; Curry, William T WT; Nahed, Brian V BV; Shin, John H JH; Paek, Sun Ha SH; Park, Sung-Hye SH; Stewart, Chip C; Lawrence, Michael S MS; Cibulskis, Kristian K; Thorner, Aaron R AR; Van Hummelen, Paul P; Stemmer-Rachamimov, Anat O AO; Batchelor, Tracy T TT; Carter, Scott L SL; Hoang, Mai P MP; Santagata, Sandro S; Louis, David N DN; Barker, Fred G FG; Meyerson, Matthew M; Getz, Gad G; Brastianos, Priscilla K PK; Cahill, Daniel P DP

Publication Date: 2014-12-24

Variant appearance in text: rs13167280

PubMed Link: 25589003

Variant Present in the following documents:

• 40478_2014_167_MOESM1_ESM.xlsx, sheet 6

View BVdb publication page

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Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis.

Journal Of The National Cancer Institute

Mocellin, Simone S; Verdi, Daunia D; Pooley, Karen A KA; Landi, Maria T MT; Egan, Kathleen M KM; Baird, Duncan M DM; Prescott, Jennifer J; De Vivo, Immaculata I; Nitti, Donato D

Publication Date: 2012-06-06

Variant appearance in text: rs13167280

PubMed Link: 22523397

Variant Present in the following documents:

• Main text

View BVdb publication page

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Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.

Journal Of Cancer Epidemiology

Van Dyke, Alison L AL; Cote, Michele L ML; Wenzlaff, Angela S AS; Abrams, Judith J; Land, Susan S; Iyer, Priyanka P; Schwartz, Ann G AG

Publication Date: 2009

Variant appearance in text: rs13167280

PubMed Link: 20445798

Variant Present in the following documents:

• Main text

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Bladder cancer SNP panel predicts susceptibility and survival.

Human Genetics

Andrew, Angeline S AS; Gui, Jiang J; Sanderson, Arthur C AC; Mason, Rebecca A RA; Morlock, Elaine V EV; Schned, Alan R AR; Kelsey, Karl T KT; Marsit, Carmen J CJ; Moore, Jason H JH; Karagas, Margaret R MR

Publication Date: 2009-06

Variant appearance in text: rs13167280

PubMed Link: 19252927

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variation in five genes important in telomere biology and risk for breast cancer.

British Journal Of Cancer

Savage, S A SA; Chanock, S J SJ; Lissowska, J J; Brinton, L A LA; Richesson, D D; Peplonska, B B; Bardin-Mikolajczak, A A; Zatonski, W W; Szeszenia-Dabrowska, N N; Garcia-Closas, M M

Publication Date: 2007-09-17

Variant appearance in text: rs13167280

PubMed Link: 17848914

Variant Present in the following documents:

• Main text
• 6603934a.pdf

View BVdb publication page

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