Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: Neoplasms and RTEL1[original query] |
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Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
![]() Nature genetics 2009 Aug 41 (8): 905-8. Wrensch Margaret, Jenkins Robert B, Chang Jeffrey S, Yeh Ru-Fang, Xiao Yuanyuan, Decker Paul A, Ballman Karla V, Berger Mitchel, Buckner Jan C, Chang Susan, Giannini Caterina, Halder Chandralekha, Kollmeyer Thomas M, Kosel Matthew L, LaChance Daniel H, McCoy Lucie, O'Neill Brian P, Patoka Joe, Pico Alexander R, Prados Michael, Quesenberry Charles, Rice Terri, Rynearson Amanda L, Smirnov Ivan, Tihan Tarik, Wiemels Joe, Yang Ping, Wiencke John |
Cancer susceptibility variants and the risk of adult glioma in a US case-control study. Journal of neuro-oncology 2011 1 104 (2): 535-42. Egan Kathleen M, Thompson Reid C, Nabors L B, Olson Jeffrey J, Brat Daniel J, Larocca Renato V, Brem Steven, Moots Paul L, Madden Melissa H, Browning James E, Ann Chen |
Known glioma risk loci are associated with glioma with a family history of brain tumours -- a case-control gene association study. International journal of cancer. Journal international du cancer 2013 May 132 (10): 2464-8. Melin Beatrice, Dahlin Anna M, Andersson Ulrika, Wang Zhaoming, Henriksson Roger, Hallmans Göran, Bondy Melissa L, Johansen Christoffer, Feychting Maria, Ahlbom Anders, Kitahara Cari M, Wang Sophia S, Ruder Avima M, Carreón Tania, Butler Mary Ann, Inskip Peter D, Purdue Mark, Hsing Ann W, Mechanic Leah, Gillanders Elizabeth, Yeager Meredith, Linet Martha, Chanock Stephen J, Hartge Patricia, Rajaraman Preet |
A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk.
![]() Human molecular genetics 2013 Dec 22 (24): 5056-64. Pooley Karen A, Bojesen Stig E, Weischer Maren, Nielsen Sune F, Thompson Deborah, Amin Al Olama Ali, Michailidou Kyriaki, Tyrer Jonathan P, Benlloch Sara, Brown Judith, Audley Tina, Luben Robert, Khaw K-T, Neal David E, Hamdy Freddie C, Donovan Jenny L, Kote-Jarai Zsofia, Baynes Caroline, Shah Mitul, Bolla Manjeet K, Wang Qin, Dennis Joe, Dicks Ed, Yang Rongxi, Rudolph Anja, Schildkraut Joellen, Chang-Claude Jenny, Burwinkel Barbara, Chenevix-Trench Georgia, Pharoah Paul D P, Berchuck Andrew, Eeles Rosalind A, Easton Douglas F, Dunning Alison M, Nordestgaard Børge |
Identification of seven loci affecting mean telomere length and their association with disease.
![]() Nature genetics 2013 Apr 45 (4): 422-7, 427e1-2. Codd Veryan, Nelson Christopher P, Albrecht Eva, Mangino Massimo, Deelen Joris, Buxton Jessica L, Hottenga Jouke Jan, Fischer Krista, Esko Tõnu, Surakka Ida, Broer Linda, Nyholt Dale R, Mateo Leach Irene, Salo Perttu, Hägg Sara, Matthews Mary K, Palmen Jutta, Norata Giuseppe D, O'Reilly Paul F, Saleheen Danish, Amin Najaf, Balmforth Anthony J, Beekman Marian, de Boer Rudolf A, Böhringer Stefan, Braund Peter S, Burton Paul R, de Craen Anton J M, Denniff Matthew, Dong Yanbin, Douroudis Konstantinos, Dubinina Elena, Eriksson Johan G, Garlaschelli Katia, Guo Dehuang, Hartikainen Anna-Liisa, Henders Anjali K, Houwing-Duistermaat Jeanine J, Kananen Laura, Karssen Lennart C, Kettunen Johannes, Klopp Norman, Lagou Vasiliki, van Leeuwen Elisabeth M, Madden Pamela A, Mägi Reedik, Magnusson Patrik K E, Männistö Satu, McCarthy Mark I, Medland Sarah E, Mihailov Evelin, Montgomery Grant W, Oostra Ben A, Palotie Aarno, Peters Annette, Pollard Helen, Pouta Anneli, Prokopenko Inga, Ripatti Samuli, Salomaa Veikko, Suchiman H Eka D, Valdes Ana M, Verweij Niek, Viñuela Ana, Wang Xiaoling, Wichmann H-Erich, Widen Elisabeth, Willemsen Gonneke, Wright Margaret J, Xia Kai, Xiao Xiangjun, van Veldhuisen Dirk J, Catapano Alberico L, Tobin Martin D, Hall Alistair S, Blakemore Alexandra I F, van Gilst Wiek H, Zhu Haidong, Consortium Cardiogram, Erdmann Jeanette, Reilly Muredach P, Kathiresan Sekar, Schunkert Heribert, Talmud Philippa J, Pedersen Nancy L, Perola Markus, Ouwehand Willem, Kaprio Jaakko, Martin Nicholas G, van Duijn Cornelia M, Hovatta Iiris, Gieger Christian, Metspalu Andres, Boomsma Dorret I, Jarvelin Marjo-Riitta, Slagboom P Eline, Thompson John R, Spector Tim D, van der Harst Pim, Samani Nilesh |
Telomere length and risk of glioma. Cancer epidemiology 2013 Dec 37 (6): 935-8. Walcott Farzana, Rajaraman Preetha, Gadalla Shahinaz M, Inskip Peter D, Purdue Mark P, Albanes Demetrius, Orr Esther, De Vivo Immaculata, Savage Sharon |
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.
![]() Nature genetics 2014 Jul 46 (7): 731-5. Walsh Kyle M, Codd Veryan, Smirnov Ivan V, Rice Terri, Decker Paul A, Hansen Helen M, Kollmeyer Thomas, Kosel Matthew L, Molinaro Annette M, McCoy Lucie S, Bracci Paige M, Cabriga Belinda S, Pekmezci Melike, Zheng Shichun, Wiemels Joseph L, Pico Alexander R, Tihan Tarik, Berger Mitchell S, Chang Susan M, Prados Michael D, Lachance Daniel H, O'Neill Brian Patrick, Sicotte Hugues, Eckel-Passow Jeanette E, , van der Harst Pim, Wiencke John K, Samani Nilesh J, Jenkins Robert B, Wrensch Margaret |
Investigation of established genetic risk variants for glioma in prediagnostic samples from a population-based nested case-control study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015 May 24 (5): 810-6. Wibom Carl, Späth Florentin, Dahlin Anna M, Langseth Hilde, Hovig Eivind, Rajaraman Preetha, Johannesen Tom Børge, Andersson Ulrika, Melin Beatri |
The RTEL1 rs6010620 polymorphism and glioma risk: a meta-analysis based on 12 case-control studies. Asian Pacific journal of cancer prevention : APJCP 2014 15 (23): 10175-9. Du Shu-Li, Geng Ting-Ting, Feng Tian, Chen Cui-Ping, Jin Tian-Bo, Chen Ch |
Telomere structure and maintenance gene variants and risk of five cancer types. International journal of cancer 2016 Dec 139 (12): 2655-2670. Karami Sara, Han Younghun, Pande Mala, Cheng Iona, Rudd James, Pierce Brandon L, Nutter Ellen L, Schumacher Fredrick R, Kote-Jarai Zsofia, Lindstrom Sara, Witte John S, Fang Shenying, Han Jiali, Kraft Peter, Hunter David J, Song Fengju, Hung Rayjean J, McKay James, Gruber Stephen B, Chanock Stephen J, Risch Angela, Shen Hongbing, Haiman Christopher A, Boardman Lisa, Ulrich Cornelia M, Casey Graham, Peters Ulrike, Amin Al Olama Ali, Berchuck Andrew, Berndt Sonja I, Bezieau Stephane, Brennan Paul, Brenner Hermann, Brinton Louise, Caporaso Neil, Chan Andrew T, Chang-Claude Jenny, Christiani David C, Cunningham Julie M, Easton Douglas, Eeles Rosalind A, Eisen Timothy, Gala Manish, Gallinger Steven J, Gayther Simon A, Goode Ellen L, Grönberg Henrik, Henderson Brian E, Houlston Richard, Joshi Amit D, Küry Sébastien, Landi Mari T, Le Marchand Loic, Muir Kenneth, Newcomb Polly A, Permuth-Wey Jenny, Pharoah Paul, Phelan Catherine, Potter John D, Ramus Susan J, Risch Harvey, Schildkraut Joellen, Slattery Martha L, Song Honglin, Wentzensen Nicolas, White Emily, Wiklund Fredrik, Zanke Brent W, Sellers Thomas A, Zheng Wei, Chatterjee Nilanjan, Amos Christopher I, Doherty Jennifer A, |
Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers. Carcinogenesis 2016 Jun 37 (6): 576-82. Walsh Kyle M, Whitehead Todd P, de Smith Adam J, Smirnov Ivan V, Park Minsun, Endicott Alyson A, Francis Stephen S, Codd Veryan, , Samani Nilesh J, Metayer Catherine, Wiemels Joseph |
Genetic Variation Associated with Longer Telomere Length Increases Risk of Chronic Lymphocytic Leukemia. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016 May . Ojha Juhi, Codd Veryan, Nelson Christopher P, Samani Nilesh J, Smirnov Ivan V, Madsen Nils R, Hansen Helen M, de Smith Adam J, Bracci Paige M, Wiencke John K, Wrensch Margaret R, Wiemels Joseph L, Walsh Kyle |
Mutational analysis of FANCJ helicase. Methods (San Diego, Calif.) 2016 Apr . Guo Manhong, Vidhyasagar Venkatasubramanian, Talwar Tanu, Kariem Ahmad, Wu Yulia |
RTEL1 polymorphisms are associated with lung cancer risk in the Chinese Han population. Oncotarget 2016 Oct 7 (43): 70475-70480. Yan Shouchun, Xia Ridong, Jin Tianbo, Ren Hui, Yang Hua, Li Jing, Yan Mengdan, Zhu Yuanyuan, Chen Mingw |
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
![]() Nature genetics 2017 Jun . McKay James D, Hung Rayjean J, Han Younghun, Zong Xuchen, Carreras-Torres Robert, Christiani David C, Caporaso Neil E, Johansson Mattias, Xiao Xiangjun, Li Yafang, Byun Jinyoung, Dunning Alison, Pooley Karen A, Qian David C, Ji Xuemei, Liu Geoffrey, Timofeeva Maria N, Bojesen Stig E, Wu Xifeng, Le Marchand Loic, Albanes Demetrios, Bickeböller Heike, Aldrich Melinda C, Bush William S, Tardon Adonina, Rennert Gad, Teare M Dawn, Field John K, Kiemeney Lambertus A, Lazarus Philip, Haugen Aage, Lam Stephen, Schabath Matthew B, Andrew Angeline S, Shen Hongbing, Hong Yun-Chul, Yuan Jian-Min, Bertazzi Pier Alberto, Pesatori Angela C, Ye Yuanqing, Diao Nancy, Su Li, Zhang Ruyang, Brhane Yonathan, Leighl Natasha, Johansen Jakob S, Mellemgaard Anders, Saliba Walid, Haiman Christopher A, Wilkens Lynne R, Fernandez-Somoano Ana, Fernandez-Tardon Guillermo, van der Heijden Henricus F M, Kim Jin Hee, Dai Juncheng, Hu Zhibin, Davies Michael P A, Marcus Michael W, Brunnström Hans, Manjer Jonas, Melander Olle, Muller David C, Overvad Kim, Trichopoulou Antonia, Tumino Rosario, Doherty Jennifer A, Barnett Matt P, Chen Chu, Goodman Gary E, Cox Angela, Taylor Fiona, Woll Penella, Brüske Irene, Wichmann H-Erich, Manz Judith, Muley Thomas R, Risch Angela, Rosenberger Albert, Grankvist Kjell, Johansson Mikael, Shepherd Frances A, Tsao Ming-Sound, Arnold Susanne M, Haura Eric B, Bolca Ciprian, Holcatova Ivana, Janout Vladimir, Kontic Milica, Lissowska Jolanta, Mukeria Anush, Ognjanovic Simona, Orlowski Tadeusz M, Scelo Ghislaine, Swiatkowska Beata, Zaridze David, Bakke Per, Skaug Vidar, Zienolddiny Shanbeh, Duell Eric J, Butler Lesley M, Koh Woon-Puay, Gao Yu-Tang, Houlston Richard S, McLaughlin John, Stevens Victoria L, Joubert Philippe, Lamontagne Maxime, Nickle David C, Obeidat Ma'en, Timens Wim, Zhu Bin, Song Lei, Kachuri Linda, Artigas María Soler, Tobin Martin D, Wain Louise V, , Rafnar Thorunn, Thorgeirsson Thorgeir E, Reginsson Gunnar W, Stefansson Kari, Hancock Dana B, Bierut Laura J, Spitz Margaret R, Gaddis Nathan C, Lutz Sharon M, Gu Fangyi, Johnson Eric O, Kamal Ahsan, Pikielny Claudio, Zhu Dakai, Lindströem Sara, Jiang Xia, Tyndale Rachel F, Chenevix-Trench Georgia, Beesley Jonathan, Bossé Yohan, Chanock Stephen, Brennan Paul, Landi Maria Teresa, Amos Christopher |
Genome-wide association study of familial lung cancer.
![]() Carcinogenesis 2018 Jun . Byun Jinyoung, Schwartz Ann G, Lusk Christine, Wenzlaff Angela S, de Andrade Mariza, Mandal Diptasri, Gaba Colette, Yang Ping, You Ming, Kupert Elena Y, Anderson Marshall W, Han Younghun, Li Yafang, Qian David, Stilp Adrienne, Laurie Cathy, Nelson Sarah, Zheng Wenying, Hung Rayjean J, Gaborieau Valerie, Mckay James, Brennan Paul, Caporaso Neil E, Landi Maria Teresa, Wu Xifeng, McLaughlin John R, Brhane Yonathan, Bossé Yohan, Pinney Susan M, Bailey-Wilson Joan E, Amos Christopher |
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing. International journal of cancer 2018 Oct . Girard Elodie, Eon-Marchais Séverine, Olaso Robert, Renault Anne-Laure, Damiola Francesca, Dondon Marie-Gabrielle, Barjhoux Laure, Goidin Didier, Meyer Vincent, Le Gal Dorothée, Beauvallet Juana, Mebirouk Noura, Lonjou Christine, Coignard Juliette, Marcou Morgane, Cavaciuti Eve, Baulard Céline, Bihoreau Marie-Thérèse, Cohen-Haguenauer Odile, Leroux Dominique, Penet Clotilde, Fert-Ferrer Sandra, Colas Chrystelle, Frebourg Thierry, Eisinger François, Adenis Claude, Fajac Anne, Gladieff Laurence, Tinat Julie, Floquet Anne, Chiesa Jean, Giraud Sophie, Mortemousque Isabelle, Soubrier Florent, Audebert-Bellanger Séverine, Limacher Jean-Marc, Lasset Christine, Lejeune-Dumoulin Sophie, Dreyfus Hélène, Bignon Yves-Jean, Longy Michel, Pujol Pascal, Venat-Bouvet Laurence, Bonadona Valérie, Berthet Pascaline, Luporsi Elisabeth, Maugard Christine M, Noguès Catherine, Delnatte Capucine, Fricker Jean-Pierre, Gesta Paul, Faivre Laurence, Lortholary Alain, Buecher Bruno, Caron Olivier, Gauthier-Villars Marion, Coupier Isabelle, Servant Nicolas, Boland Anne, Mazoyer Sylvie, Deleuze Jean-François, Stoppa-Lyonnet Dominique, Andrieu Nadine, Lesueur Fabien |
Telomere length and aging-related outcomes in humans: A Mendelian randomization study in 261,000 older participants. Aging cell 2019 8 18 (6): e13017. Kuo Chia-Ling, Pilling Luke C, Kuchel George A, Ferrucci Luigi, Melzer Dav |
Genetic variants in RTEL1 influencing telomere length are associated with prostate cancer risk. Journal of Cancer 2019 10 (24): 6170-6174. Gu Cheng-Yuan, Jin Sheng-Ming, Qin Xiao-Jian, Zhu Yao, Bo Dai, Lin Guo-Wen, Shi Guo-Hai, Ye Ding-W |
Genetic analysis of the relation of telomere length-related gene (RTEL1) and coronary heart disease risk. Molecular genetics & genomic medicine 2019 1 7 (3): e550. Lu Shijuan, Zhong Jianghua, Wu Miao, Huang Kang, Zhou Yilei, Zhong Zanrui, Li Qiang, Zhou Hongh |
Genomic Methods Identify Homologous Recombination Deficiency in Pancreas Adenocarcinoma and Optimize Treatment Selection. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 May . Park Wungki, Chen Jiapeng, Chou Joanne F, Varghese Anna M, Yu Kenneth H, Wong Winston, Capanu Marinela, Balachandran Vinod, McIntyre Caitlin A, El Dika Imane, Khalil Danny N, Harding James J, Ghalehsari Nima, McKinnell Zoe, Chalasani Sree B, Makarov Vladimir, Selenica Pier, Pei Xin, Lecomte Nicolas, Kelsen David P, Abou-Alfa Ghassan K, Robson Mark E, Zhang Liying, Berger Michael F, Schultz Nikolaus, Chan Timothy A, Powell Simon N, Reis-Filho Jorge S, Iacobuzio-Donahue Christine A, Riaz Nadeem, O'Reilly Eileen |
Prevalence and spectrum of pathogenic germline variants in intestinal and pancreatobiliary type of ampullary cancer. Pathology, research and practice 2020 Dec 217 153309. Kumari Niraj, Singh Rajneesh K, Mishra Shravan K, L Raghvendra, Mohindra Samir, Krishnani Narend |
Next-generation sequencing analysis suggests varied multistep mutational pathogenesis for endocrine mucin-producing sweat gland carcinoma with comments on INSM1 and MUC2 suggesting a conjunctival origin. Journal of the American Academy of Dermatology 2021 1 86 (5): 1072-1079. Mathew Joseph G, Bowman Anita S, Saab Jad, Busam Klaus J, Nehal Kishwer, Pulitzer Melis |
A Large-Scale Exome-Wide Association Study Identifies Novel Germline Mutations in Lung Cancer. American journal of respiratory and critical care medicine 2023 5 . Sipeng Shen, Zaiming Li, Yunke Jiang, Weiwei Duan, Hongru Li, Sha Du, Manel Esteller, Hongbing Shen, Zhibin Hu, Yang Zhao, David C Christiani, Feng Ch |
Cross-cancer pleiotropic analysis identifies three novel genetic risk variants for colorectal cancer. Human molecular genetics 2023 3 . Sun Jing, Wang Lijuan, Zhou Xuan, Hu Lidan, Yuan Shuai, Bian Zilong, Chen Jie, Zhu Yingshuang, Farrington Susan M, Campbell Harry, Ding Kefeng, Zhang Dongfeng, Dunlop Malcolm G, Theodoratou Evropi, Li X |
High-throughput characterization of functional variants highlights heterogeneity and polygenicity underlying lung cancer susceptibility. American journal of human genetics 2024 6 . Erping Long, Harsh Patel, Alyxandra Golden, Michelle Antony, Jinhu Yin, Karen Funderburk, James Feng, Lei Song, Jason W Hoskins, Laufey T Amundadottir, Rayjean J Hung, Christopher I Amos, Jianxin Shi, Nathaniel Rothman, Qing Lan, , Jiyeon Ch |
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