HuGE Literature Finder
Records 1-30
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Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study.
BMC cancer 2019 Aug 19 (1): 772. Casula Milena, Paliogiannis Panagiotis, Ayala Fabrizio, De Giorgi Vincenzo, Stanganelli Ignazio, Mandalà Mario, Colombino Maria, Manca Antonella, Sini Maria Cristina, Caracò Corrado, Ascierto Paolo Antonio, Satta Rosanna Rita, , Lissia Amelia, Cossu Antonio, Palmieri Giuseppe, |
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Common Type 2 Diabetes Genetic Risk Variants Improve the Prediction of Gestational Diabetes.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2019 Jul . Dziedziejko Violetta, Safranow Krzysztof, Tarnowski Maciej, Pawlik Andrz |
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Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriers.
Familial cancer 2019 Jun . Christodoulou E, Visser M, Potjer T P, van der Stoep N, Rodríguez-Girondo M, van Doorn R, Gruis |
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Identification of CDKN2A variants in breast cancer patients in Pakistan.
Genes & genetic systems 2019 Jun . Khan Ranjha, Aftab Ayesha, Tabassum Sobia, Hussain Hafiz Muhammad Jafar, Hameed Abdul, Mahmood Humera, Munir Faiza, Bukhari Ihtish |
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Blood-based analysis of type-2 diabetes mellitus susceptibility genes identifies specific transcript variants with deregulated expression and association with disease risk.
Scientific reports 2019 Feb 9 (1): 1512. Christodoulou Maria-Ioanna, Avgeris Margaritis, Kokkinopoulou Ioanna, Maratou Eirini, Mitrou Panayota, Kontos Christos K, Pappas Efthimios, Boutati Eleni, Scorilas Andreas, Fragoulis Emmanuel |
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Functional Genetic Single-Nucleotide Polymorphisms (SNPs) in Cyclin-Dependent Kinase Inhibitor 2A/B (CDKN2A/B) Locus Are Associated with Risk and Prognosis of Osteosarcoma in Chinese Populations.
Medical science monitor : international medical journal of experimental and clinical research 2019 Feb 25 1307-1313. Zhang Huahui, Mao Jian-S, Hu Wei |
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Risk Factors of Subsequent Primary Melanomas in Austria.
JAMA dermatology 2019 Feb 155 (2): 188-195. Müller Christoph, Wendt Judith, Rauscher Sabine, Sunder-Plassmann Raute, Richtig Erika, Fae Ingrid, Fischer Gottfried, Okamoto Ichi |
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Genetic polymorphisms of diabetes-related genes, their interaction with diabetes status, and breast cancer incidence and mortality: The Long Island Breast Cancer Study Project.
Molecular carcinogenesis 2019 03 58 (3): 436-446. Parada Humberto, Cleveland Rebecca J, North Kari E, Stevens June, Teitelbaum Susan L, Neugut Alfred I, Santella Regina M, Martinez Maria E, Gammon Marilie |
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Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers.
Archives of dermatological research 2018 Sep . Gironi Laura Cristina, Colombo Enrico, Pasini Barbara, Giorgione Roberto, Farinelli Pamela, Zottarelli Francesca, Esposto Elia, Zavattaro Elisa, Allara Elias, Ogliara Paola, Betti Marta, Dianzani Irma, Savoia Pao |
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Association of Breast and Ovarian Cancers With Predisposition Genes Identified by Large-Scale Sequencing.
JAMA oncology 2018 Aug . Lu Hsiao-Mei, Li Shuwei, Black Mary Helen, Lee Shela, Hoiness Robert, Wu Sitao, Mu Wenbo, Huether Robert, Chen Jefferey, Sridhar Srijani, Tian Yuan, McFarland Rachel, Dolinsky Jill, Tippin Davis Brigette, Mexal Sharon, Dunlop Charles, Elliott Aar |
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Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
Breast cancer research : BCR 2018 Aug 20 (1): 87. Penkert Judith, Schmidt Gunnar, Hofmann Winfried, Schubert Stephanie, Schieck Maximilian, Auber Bernd, Ripperger Tim, Hackmann Karl, Sturm Marc, Prokisch Holger, Hille-Betz Ursula, Mark Dorothea, Illig Thomas, Schlegelberger Brigitte, Steinemann Dor |
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Frequency of Germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 Aug JCO2018785204. Panou Vasiliki, Gadiraju Meghana, Wolin Arthur, Weipert Caroline M, Skarda Emily, Husain Aliya N, Patel Jyoti D, Rose Buerkley, Zhang Shannon R, Weatherly Madison, Nelakuditi Viswateja, Knight Johnson Amy, Helgeson Maria, Fischer David, Desai Arpita, Sulai Nanna, Ritterhouse Lauren, Røe Oluf D, Turaga Kiran K, Huo Dezheng, Segal Jeremy, Kadri Sabah, Li Zejuan, Kindler Hedy L, Churpek Jane |
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FTO, GCKR, CDKAL1 and CDKN2A/B gene polymorphisms and the risk of gestational diabetes mellitus: a meta-analysis.
Archives of gynecology and obstetrics 2018 Aug . Guo Fang, Long Wei, Zhou Wenbai, Zhang Bin, Liu Jianbing, Yu B |
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Germline cancer susceptibility gene variants, somatic second hits, and survival outcomes in patients with resected pancreatic cancer.
Genetics in medicine : official journal of the American College of Medical Genetics 2018 Jul . Yurgelun Matthew B, Chittenden Anu B, Morales-Oyarvide Vicente, Rubinson Douglas A, Dunne Richard F, Kozak Margaret M, Qian Zhi Rong, Welch Marisa W, Brais Lauren K, Da Silva Annacarolina, Bui Justin L, Yuan Chen, Li Tingting, Li Wanwan, Masuda Atsuhiro, Gu Mancang, Bullock Andrea J, Chang Daniel T, Clancy Thomas E, Linehan David C, Findeis-Hosey Jennifer J, Doyle Leona A, Thorner Aaron R, Ducar Matthew D, Wollison Bruce M, Khalaf Natalia, Perez Kimberly, Syngal Sapna, Aguirre Andrew J, Hahn William C, Meyerson Matthew L, Fuchs Charles S, Ogino Shuji, Hornick Jason L, Hezel Aram F, Koong Albert C, Nowak Jonathan A, Wolpin Brian |
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High growth rate of pancreatic ductal adenocarcinoma in CDKN2A-p16-Leiden mutation carriers.
Cancer prevention research (Philadelphia, Pa.) 2018 Jul . Ibrahim Isaura S, Wasser Martin N J M, Wu Yinghui, Inderson Akin, De Vos Tot Nederveen Cappel Wouter H, Morreau Hans, Hes Frederik J, Veenendaal Roeland A, Putter Hein, Feshtali Shirin, van Mil Anneke M, Gruis Nelleke A, Tollenaar Robert A E M, Bergman Wilma, Bonsing Bert A, Vasen Hans F |
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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 |
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LncRNA ANRIL Expression and ANRIL Gene Polymorphisms Contribute to the Risk of Ischemic Stroke in the Chinese Han Population.
Cellular and molecular neurobiology 2018 Jun . Yang Jialei, Gu Lian, Guo Xiaojing, Huang Jiao, Chen Zhaoxia, Huang Guifeng, Kang Yiwen, Zhang Xiaoting, Long Jianxiong, Su |
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CDKN2A/CDK4 Status in Greek Patients with Familial Melanoma and Association with Clinico-epidemiological Parameters.
Acta dermato-venereologica 2018 May . Karagianni Fani, Njauw Ching-Ni, Kypreou Katerina P, Stergiopoulou Aravela, Plaka Michaela, Polydorou Dorothea, Chasapi Vasiliki, Pappas Leon, Stratigos Ioannis, Champsas Gregory, Panagiotou Peter, Gogas Helen, Evangelou Evangelos, Tsao Hensin, Stratigos Alexander, Stefanaki Ire |
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Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland.
Cancer research and treatment : official journal of Korean Cancer Association 2018 May . D?bniak Tadeusz, Scott Rodney J, Lea Rodney A, Górski Bohdan, Masoj? Bart?omiej, Cybulski Cezary, Kram Andrzej, Maleszka Romuald, Gromowski Tomasz, Paszkowska-Szczur Katarzyna, Kashyap Aniruddh, Lener Marcin R, Mali?ska Karolina, Rogo?a Emilia, Murawa Dawid, Rudnicka Helena, Deptu?a Jakub, Lubi?ski J |
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Investigating the Feasibility of Targeted Next-Generation Sequencing to Guide the Treatment of Head and Neck Squamous Cell Carcinoma.
Cancer research and treatment : official journal of Korean Cancer Association 2018 May . Lim Sun Min, Cho Sang Hee, Hwang In Gyu, Choi Jae Woo, Chang Hyun, Ahn Myung-Ju, Park Keon Uk, Kim Ji-Won, Ko Yoon Ho, Ahn Hee Kyung, Cho Byoung Chul, Nam Byung-Ho, Chun Sang Hoon, Hong Ji Hyung, Kwon Jung Hye, Choi Jong Gwon, Kang Eun Joo, Yun Tak, Lee Keun-Wook, Kim Joo-Hang, Kim Jin Soo, Lee Hyun Woo, Kim Min Kyoung, Jung Dongmin, Kim Ji Eun, Keam Bhumsuk, Yun Hwan Jung, Kim Sangwoo, Kim Hye Ry |
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Single nucleotide polymorphisms in long noncoding RNA, ANRIL, are not associated with severe periodontitis but with adverse cardiovascular events among patients with cardiovascular disease.
Journal of periodontal research 2018 May . Schulz S, Seitter L, Werdan K, Hofmann B, Schaller H-G, Schlitt A, Reichert |
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The ANRIL Genetic Variants and Their Interactions with Environmental Risk Factors on Atherothrombotic Stroke in a Han Chinese Population.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2018 May . Xiong Li, Liu Wei, Gao Li, Mu Qiwen, Liu Xindong, Feng Yuhuan, Tang Zhi, Tang Huanyu, Liu H |
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Association of the independent polymorphisms in CDKN2A with susceptibility of acute lymphoblastic leukemia.
Bioscience reports 2018 Apr . Zhou Xueyan, Liao Fei, Zhang Junlong, Qin Yun, Xu Heng, Ding Zhenyu, Zhang Yan, Zhang Fe |
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Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q.
European journal of human genetics : EJHG 2018 Apr . Potrony Miriam, Puig-Butille Joan Anton, Farnham James M, Giménez-Xavier Pol, Badenas Celia, Tell-Martí Gemma, Aguilera Paula, Carrera Cristina, Malvehy Josep, Teerlink Craig C, Puig Susa |
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GWAS implicated risk variants in different genes contribute additively to increase the risk of coronary artery disease (CAD) in the Pakistani subjects.
Lipids in health and disease 2018 Apr 17 (1): 89. Shahid Saleem Ullah, Shabana N A, Rehman Abdul, Humphries Ste |
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Variants of CDKAL1 rs7754840 (G/C) and CDKN2A/2B rs10811661 (C/T) with gestational diabetes: insignificant association.
BMC research notes 2018 Mar 11 (1): 181. Noury Amr El, Azmy Osama, Alsharnoubi Jehan, Salama Sameh, Okasha Ahmed, Gouda Wea |
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CDKN2A/B
T2D GWAS Risk-SNPs Impact Locus Gene Expression and Proliferation in Human Islets.
Diabetes 2018 Feb . Kong Yahui, Sharma Rohit B, Ly Socheata, Stamateris Rachel E, Jesdale William M, Alonso Laura |
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Characteristics of Familial Melanoma in Valencia, Spain, Based on the Presence of CDKN2A Mutations and MC1R Variants.
Acta dermato-venereologica 2018 Feb . Huerta Claudia, Garcia-Casado Zaida, Bañuls José, Moragon Manuel, Oliver Vicente, Unamuno Blanca, Requena Celia, Kumar Rajiv, Nagore Eduar |
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Genetic variants identified from GWAS for predisposition to type 2 diabetes predict sulfonylurea drug response.
Current molecular medicine 2018 Feb . Phani N M, Vohra M, Adhikari P, Nagri S K, Shashikiran U, D'Souza S C, Kalluri P R R, Satyamoorthy K, Rai P |
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APOL1, CDKN2A/CDKN2B, and HDAC9 polymorphisms and small vessel ischemic stroke.
Acta neurologica Scandinavica 2018 Jan 137 (1): 133-141. Akinyemi R, Tiwari H K, Arnett D K, Ovbiagele B, Irvin M R, Wahab K, Sarfo F, Srinivasasainagendra V, Adeoye A, Perry R T, Akpalu A, Jenkins C, Arulogun O, Gebregziabher M, Owolabi L, Obiako R, Sanya E, Komolafe M, Fawale M, Adebayo P, Osaigbovo G, Sunmonu T, Olowoyo P, Chukwuonye I, Obiabo Y, Onoja A, Akinyemi J, Ogbole G, Melikam S, Saulson R, Owolabi M, |
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Comprehensive genomic profiling of head and neck squamous cell carcinoma reveals FGFR1 amplifications and tumour genomic alterations burden as prognostic biomarkers of survival.
European journal of cancer (Oxford, England : 1990) 2018 Jan 91 47-55. Dubot C, Bernard V, Sablin M P, Vacher S, Chemlali W, Schnitzler A, Pierron G, Ait Rais K, Bessoltane N, Jeannot E, Klijanienko J, Mariani O, Jouffroy T, Calugaru V, Hoffmann C, Lesnik M, Badois N, Berger F, Le Tourneau C, Kamal M, Bieche |
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Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese.
Scientific reports 2018 Jan 8 (1): 789. Urayama Kevin Y, Takagi Masatoshi, Kawaguchi Takahisa, Matsuo Keitaro, Tanaka Yoichi, Ayukawa Yoko, Arakawa Yuki, Hasegawa Daisuke, Yuza Yuki, Kaneko Takashi, Noguchi Yasushi, Taneyama Yuichi, Ota Setsuo, Inukai Takeshi, Yanagimachi Masakatsu, Keino Dai, Koike Kazutoshi, Toyama Daisuke, Nakazawa Yozo, Kurosawa Hidemitsu, Nakamura Kozue, Moriwaki Koichi, Goto Hiroaki, Sekinaka Yujin, Morita Daisuke, Kato Motohiro, Takita Junko, Tanaka Toshihiro, Inazawa Johji, Koh Katsuyoshi, Ishida Yasushi, Ohara Akira, Mizutani Shuki, Matsuda Fumihiko, Manabe Atsus |
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Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
JAMA 2018 06 319 (23): 2401-2409. Hu Chunling, Hart Steven N, Polley Eric C, Gnanaolivu Rohan, Shimelis Hermela, Lee Kun Y, Lilyquist Jenna, Na Jie, Moore Raymond, Antwi Samuel O, Bamlet William R, Chaffee Kari G, DiCarlo John, Wu Zhong, Samara Raed, Kasi Pashtoon M, McWilliams Robert R, Petersen Gloria M, Couch Fergus |
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Phenocopies in melanoma-prone families with germ-line CDKN2A mutations.
Genetics in medicine : official journal of the American College of Medical Genetics 2017 Dec . Helgadottir Hildur, Olsson Håkan, Tucker Margaret A, Yang Xiaohong R, Höiom Veronica, Goldstein Alisa |
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A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations.
International journal of molecular sciences 2017 Nov 18 (11): . Zanon-Moreno Vicente, Ortega-Azorin Carolina, Asensio-Marquez Eva M, Garcia-Medina Jose J, Pinazo-Duran Maria D, Coltell Oscar, Ordovas Jose M, Corella Dolor |
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Association of p16 (CDKN2A) polymorphisms with the development of HPV16-related precancerous lesions and cervical cancer in the Greek population.
Journal of medical virology 2017 Nov . Tsakogiannis D, Moschonas G D, Bella E, Kyriakopoulou Z, Amoutzias G D, Dimitriou T G, Kottaridi C, Markoulatos |
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Cancer risks and survival in patients with multiple primary melanomas: Association with family history of melanoma and germline CDKN2A mutation status.
Journal of the American Academy of Dermatology 2017 Aug . Helgadottir Hildur, Tuominen Rainer, Olsson Håkan, Hansson Johan, Höiom Veroni |
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Contributions of IKZF1, DDC, CDKN2A, CEBPE, and LMO1 Gene Polymorphisms to Acute Lymphoblastic Leukemia in a Yemeni Population.
Genetic testing and molecular biomarkers 2017 Aug . Al-Absi Boshra, Razif Muhammad F M, Noor Suzita M, Saif-Ali Riyadh, Aqlan Mohammed, Salem Sameer D, Ahmed Radwan H, Muniandy Sekar |
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Interleukin-6 (IL-6) rs1800796 and cyclin dependent kinase inhibitor (CDKN2A/CDKN2B) rs2383207 are associated with ischemic stroke in indigenous West African Men.
Journal of the neurological sciences 2017 Aug 379 229-235. Akinyemi Rufus, Arnett Donna K, Tiwari Hemant K, Ovbiagele Bruce, Sarfo Fred, Srinivasasainagendra Vinodh, Irvin Marguerite Ryan, Adeoye Abiodun, Perry Rodney T, Akpalu Albert, Jenkins Carolyn, Owolabi Lukman, Obiako Reginald, Wahab Kolawole, Sanya Emmanuel, Komolafe Morenikeji, Fawale Michael, Adebayo Philip, Osaigbovo Godwin, Sunmonu Taofiki, Olowoyo Paul, Chukwuonye Innocent, Obiabo Yahaya, Akpa Onoja, Melikam Sylvia, Saulson Raelle, Kalaria Raj, Ogunniyi Adesola, Owolabi Mayowa, |
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Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
Journal of cardiovascular translational research 2017 Jun . Pignataro Piero, Pezone Lucia, Di Gioia Giuseppe, Franco Danilo, Iaccarino Guido, Iolascon Achille, Ciccarelli Michele, Capasso Mar |
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Genomic Profiling of Small-Bowel Adenocarcinoma.
JAMA oncology 2017 Jun . Schrock Alexa B, Devoe Craig E, McWilliams Robert, Sun James, Aparicio Thomas, Stephens Philip J, Ross Jeffrey S, Wilson Richard, Miller Vincent A, Ali Siraj M, Overman Michael |
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The research on association of copy number variation in chromosome 9p21 region with atherothrombotic stroke in the Han Chinese population.
Journal of the neurological sciences 2017 Jun 377 88-94. Liu Hua, Yang Min, Wang Xiaoming, Ji Yifei, Zhao Jin, Liu Wei, Zheng Ji |
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"Desert" gene (Chr9p21) variants as novel markers for coronary artery disease.
Anatolian journal of cardiology 2017 May . Shendy Heba A, Hassanein Sally I, Gad Mohamed |
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p16 gene silencing along with p53 single-nucleotide polymorphism and risk of esophageal cancer in Northeast India.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2017 May 39 (5): 1010428317698384. Das Mandakini, Sharma Santanu Kumar, Sekhon Gaganpreet Singh, Mahanta Jagadish, Phukan Rup Kumar, Jalan Bimal Kum |
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A genetic variant in CDKN2A/B gene is associated with the increased risk of breast cancer.
Journal of clinical laboratory analysis 2017 Mar . ShahidSales Soodabeh, Mehramiz Mehraneh, Ghasemi Faezeh, Aledavood Amir, Shamsi Mehri, Hassanian Seyed Mahdi, Ghayour-Mobarhan Majid, Avan Am |
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CDKN2A and MC1R variants found in Cypriot patients diagnosed with cutaneous melanoma.
Journal of genetics 2017 Mar 96 (1): 155-160. Koulermou Georgia, Shammas Christos, Vassiliou Andreas, Kyriakides Tassos C, Costi Constantina, Neocleous Vassos, Phylactou Leonidas A, Pantelidou Mar |
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Genetic alterations in seborrheic keratoses.
Oncotarget 2017 Mar . Heidenreich Barbara, Denisova Evygenia, Rachakonda Sivaramakrishna, Sanmartin Onofre, Dereani Timo, Hosen Ismail, Nagore Eduardo, Kumar Raj |
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The effects of CDKN2A rs3731249, rs11515, and rs3088440 polymorphisms on cancer risk.
Cellular and molecular biology (Noisy-le-Grand, France) 2017 Mar 63 (3): 40-44. Dong Y, Wang X, Yang Y-W, Liu Y |
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CDC123/CAMK1D gene rs12779790 polymorphism and rs10811661 polymorphism upstream of the CDKN2A/2B gene in women with gestational diabetes.
Journal of perinatology : official journal of the California Perinatal Association 2017 Jan . Tarnowski M, Malinowski D, Safranow K, Dziedziejko V, Pawlik |
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Variants in ANRIL gene correlated with its expression contribute to myocardial infarction risk.
Oncotarget 2017 Jan . Cheng Jie, Cai Meng-Yun, Chen Yu-Ning, Li Zhi-Cheng, Tang Sai-Sai, Yang Xi-Li, Chen Can, Liu Xinguang, Xiong Xing-Do |
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Interaction between a variant of CDKN2A/B-gene with lifestyle factors in determining dyslipidemia and estimated cardiovascular risk: A step toward personalized nutrition.
Clinical nutrition (Edinburgh, Scotland) 2016 Dec . Mehramiz Mehrane, Ghasemi Faeze, Esmaily Habibollah, Tayefi Maryam, Hassanian Seyed Mahdi, Sadeghzade Mahsa, Sadabadi Fatemeh, Moohebati Mohsen, Azarpazhooh Mahmoud Reza, Parizadeh Seyed Mohammad Reza, Heidari-Bakavoli Alireza, Safarian Mohammad, Nematy Mohsen, Ebrahimi Mahmoud, Ryzhikov Mikhail, Ferns Gordon A, Ghayour-Mobarhan Majid, Avan Am |
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Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes.
Acta diabetologica 2016 Dec 53 (6): 915-923. Chidambaram Manickam, Liju Samuel, Saboo Banshi, Sathyavani Kumpatla, Viswanathan Vijay, Pankratz Nathan, Gross Myron, Mohan Viswanathan, Radha Venkates |
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.
Leukemia 2016 Nov . Vijayakrishnan J, Kumar R, Henrion M Y R, Moorman A V, Rachakonda P S, Hosen I, da Silva Filho M I, Holroyd A, Dobbins S E, Koehler R, Thomsen H, Irving J A, Allan J M, Lightfoot T, Roman E, Kinsey S E, Sheridan E, Thompson P D, Hoffmann P, Nöthen M M, Heilmann-Heimbach S, Jöckel K H, Greaves M, Harrison C J, Bartram C R, Schrappe M, Stanulla M, Hemminki K, Houlston R |
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ANRIL rs2383207 polymorphism and coronary artery disease (CAD) risk: a meta-analysis with observational studies.
Cellular and molecular biology (Noisy-le-Grand, France) 2016 Oct 62 (12): 6-10. Wang P, Dong P, Yang |
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Wide spetcrum mutational analysis of metastatic renal cell cancer: a retrospective next generation sequencing approach.
Oncotarget 2016 Oct . Fiorentino Michelangelo, Gruppioni Elisa, Massari Francesco, Giunchi Francesca, Altimari Annalisa, Ciccarese Chiara, Bimbatti Davide, Scarpa Aldo, Iacovelli Roberto, Porta Camillo, Virinder Sarhadi, Tortora Giampaolo, Artibani Walter, Schiavina Riccardo, Ardizzoni Andrea, Brunelli Matteo, Knuutila Sakari, Martignoni Gui |
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Association of type 2 diabetes mellitus genes in polycystic ovary syndrome aetiology among women from southern India.
The Indian journal of medical research 2016 Sep 144 (3): 400-408. Reddy Battini Mohan, Kommoju Uma Jyothi, Dasgupta Shilpi, Rayabarapu Pranavcha |
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Low homozygous/high heterozygous deletion status by p16 FISH correlates with a better prognostic group than high homozygous deletion status in malignant pleural mesothelioma.
Lung cancer (Amsterdam, Netherlands) 2016 Sep 99 155-61. Hamasaki Makoto, Matsumoto Shinji, Abe Sousei, Hamatake Daisuke, Kamei Toshiaki, Hiroshima Kenzo, Kawahara Kunimitsu, Sato Ayuko, Tsujimura Tohru, Nakatani Yukio, Yoshida Yasuhiro, Iwasaki Akinori, Nabeshima Kazu |
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Molecular determination of the clonal relationships between multiple tumors in BRCA1/2-associated breast and/or ovarian cancer patients is clinically relevant.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 Sep . Geurts-Giele Willemina R R, van Verschuer Victorien M T, van Deurzen Carolien H M, van Diest Paul J, Pedrosa Rute M S M, Collée J Margriet, Koppert Linetta B, Seynaeve Caroline, Dinjens Winand N |
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Functional single nucleotide polymorphisms within the cyclin-dependent kinase inhibitor 2A/2B region affect pancreatic cancer risk.
Oncotarget 2016 Jul . Campa Daniele, Pastore Manuela, Gentiluomo Manuel, Talar-Wojnarowska Renata, Kupcinskas Juozas, Malecka-Panas Ewa, Neoptolemos John P, Niesen Willem, Vodicka Pavel, Delle Fave Gianfranco, Bas Bueno-de-Mesquita H, Gazouli Maria, Pacetti Paola, Di Leo Milena, Ito Hidemi, Klüter Harald, Soucek Pavel, Corbo Vincenzo, Yamao Kenji, Hosono Satoyo, Kaaks Rudolf, Vashist Yogesh, Gioffreda Domenica, Strobel Oliver, Shimizu Yasuhiro, Dijk Frederike, Andriulli Angelo, Ivanauskas Audrius, Bugert Peter, Tavano Francesca, Vodickova Ludmila, Federico Zambon Carlo, Lovecek Martin, Landi Stefano, Key Timothy J, Boggi Ugo, Pezzilli Raffaele, Jamroziak Krzysztof, Mohelnikova-Duchonova Beatrice, Mambrini Andrea, Bambi Franco, Busch Olivier, Pazienza Valerio, Valente Roberto, Theodoropoulos George E, Hackert Thilo, Capurso Gabriele, Martina Cavestro Giulia, Pasquali Claudio, Basso Daniela, Sperti Cosimo, Matsuo Keitaro, Büchler Markus, Khaw Kay-Tee, Izbicki Jakob, Costello Eithne, Katzke Verena, Michalski Christoph, Stepien Anna, Rizzato Cosmeri, Canzian Federi |
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Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF.
The British journal of dermatology 2016 Jul . Mangas C, Potrony M, Mainetti C, Bianchi E, Carrozza Merlani P, Mancarella Eberhardt A, Maspoli-Postizzi E, Marazza G, Marcollo-Pini A, Pelloni F, Sessa C, Simona B, Puig-Butillé J A, Badenas C, Puig |
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Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Human genetics 2016 Jul . Yang Xiaohong R, Rotunno Melissa, Xiao Yanzi, Ingvar Christian, Helgadottir Hildur, Pastorino Lorenza, van Doorn Remco, Bennett Hunter, Graham Cole, Sampson Joshua N, Malasky Michael, Vogt Aurelie, Zhu Bin, Bianchi-Scarra Giovanna, Bruno William, Queirolo Paola, Fornarini Giuseppe, Hansson Johan, Tuominen Rainer, Burdett Laurie, Hicks Belynda, Hutchinson Amy, Jones Kristine, Yeager Meredith, Chanock Stephen J, Landi Maria Teresa, Höiom Veronica, Olsson Håkan, Gruis Nelleke, Ghiorzo Paola, Tucker Margaret A, Goldstein Alisa |
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Rare germline copy number variations and disease susceptibility in familial melanoma.
The Journal of investigative dermatology 2016 Jul . Shi Jianxin, Zhou Weiyin, Zhu Bin, Hyland Paula L, Bennett Hunter, Xiao Yanzi, Zhang Xijun, Burke Laura S, Song Lei, Hsu Chih Hao, Yan Chunhua, Chen Qingrong, Meerzaman Daoud, Dagnall Casey L, Burdette Laurie, Hicks Belynda, Freedman Neal D, Chanock Stephen J, Yeager Meredith, Tucker Margaret A, Goldstein Alisa M, Yang Xiaohong |
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Association of common susceptibility variants of pancreatic cancer in higher risk patients: A PACGENE study.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016 May . Childs Erica J, Chaffee Kari G, Gallinger Steven, Syngal Sapna, Schwartz Ann G, Cote Michele L, Bondy Melissa L, Hruban Ralph H, Chanock Stephen J, Hoover Robert N, Fuchs Charles S, Rider David N, Amundadottir Laufey T, Stolzenberg-Solomon Rachael, Wolpin Brian M, Risch Harvey A, Goggins Michael G, Petersen Gloria M, Klein Alison |
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Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma.
Journal of neuro-oncology 2016 May 127 (3): 483-92. Ghasimi Soma, Wibom Carl, Dahlin Anna M, Brännström Thomas, Golovleva Irina, Andersson Ulrika, Melin Beatri |
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Association of CDKAL1, CDKN2A/B & HHEX gene polymorphisms with type 2 diabetes mellitus in the population of Hyderabad, India.
The Indian journal of medical research 2016 Apr 143 (4): 455-63. Kommoju Uma Jyothi, Samy Subburaj Kadarkarai, Maruda Jayaraj, Irgam Kumuda, Kotla Jaya Prasad, Velaga Lakshmi, Reddy Battini Moh |
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Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence.
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Benefit of Surveillance for Pancreatic Cancer in High-Risk Individuals: Outcome of Long-Term Prospective Follow-Up Studies From Three European Expert Centers.
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Enhanced Megakaryopoiesis and Platelet Activity in Hypercholesterolemic, B6-Ldlr-/-,Cdkn2a-Deficient Mice.
Circulation. Cardiovascular genetics 2016 Apr . Wang Wei, Oh Seon, Koester Mark, Abramowicz Sandra, Wang Nan, Tall Alan R, Welch Carrie |
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Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.
Experimental and molecular pathology 2016 Apr 100 (3): 421-425. Muller Kristen E, Marotti Jonathan D, de Abreu Francine B, Peterson Jason D, Miller Todd W, Chamberlin Mary D, Tsongalis Gregory J, Tafe Laura |
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Epidemiology and genetic susceptibility of malignant melanoma in North Sardinia, Italy.
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2016 Mar . Cossu Antonio, Casula Milena, Cesaraccio Rosaria, Lissia Amelia, Colombino Maria, Sini Maria C, Budroni Mario, Tanda Francesco, Paliogiannis Panagiotis, Palmieri Giusep |
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A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
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Gene Polymorphism Association with Type 2 Diabetes and Related Gene-Gene and Gene-Environment Interactions in a Uyghur Population.
Medical science monitor : international medical journal of experimental and clinical research 2016 Feb 22 474-87. Xiao Shan, Zeng Xiaoyun, Fan Yong, Su Yinxia, Ma Qi, Zhu Jun, Yao H |
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Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population.
Gastroenterology 2016 05 150 (5): 1171-1182. Sawada Genta, Niida Atsushi, Uchi Ryutaro, Hirata Hidenari, Shimamura Teppei, Suzuki Yutaka, Shiraishi Yuichi, Chiba Kenichi, Imoto Seiya, Takahashi Yusuke, Iwaya Takeshi, Sudo Tomoya, Hayashi Tomoatsu, Takai Hiroki, Kawasaki Yoshihiro, Matsukawa Takashi, Eguchi Hidetoshi, Sugimachi Keishi, Tanaka Fumiaki, Suzuki Hiromichi, Yamamoto Ken, Ishii Hideshi, Shimizu Makiko, Yamazaki Hiroshi, Yamazaki Makoto, Tachimori Yuji, Kajiyama Yoshiaki, Natsugoe Shoji, Fujita Hiromasa, Mafune Kenichi, Tanaka Yoichi, Kelsell David P, Scott Claire A, Tsuji Shoji, Yachida Shinichi, Shibata Tatsuhiro, Sugano Sumio, Doki Yuichiro, Akiyama Tetsu, Aburatani Hiroyuki, Ogawa Seishi, Miyano Satoru, Mori Masaki, Mimori Kos |
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Replication and Relevance of Multiple Susceptibility Loci Discovered from Genome Wide Association Studies for Type 2 Diabetes in an Indian Population.
PloS one 2016 11 (6): e0157364. Phani Nagaraja M, Adhikari Prabha, Nagri Shivashankara K, D'Souza Sydney C, Satyamoorthy Kapaettu, Rai Padmalatha |
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Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study.
PloS one 2016 11 (4): e0152107. Sohani Zahra N, Anand Sonia S, Robiou-du-Pont Sebastien, Morrison Katherine M, McDonald Sarah D, Atkinson Stephanie A, Teo Koon K, Meyre Dav |
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Absence of germline CDKN2A mutation in Sicilian Patients with Familial Malignant Melanoma: could it be a population-specific genetic signature?
Cancer biology & therapy 2015 Dec 0. Di Lorenzo Sara, Fanale Daniele, Corradino Bartolo, Calo Valentina, Rinaldi Gaetana, Bazan Viviana, Giordano Antonio, Cordova Adriana, Russo Anton |
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Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations.
JAMA dermatology 2015 Dec 1-8. Potrony Miriam, Puig-Butille Joan Anton, Aguilera Paula, Badenas Celia, Tell-Marti Gemma, Carrera Cristina, Javier Del Pozo Luis, Conejo-Mir Julian, Malvehy Josep, Puig Susa |
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A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution.
Cancer research 2015 Nov 75 (22): 4884-94. Walsh Kyle M, de Smith Adam J, Hansen Helen M, Smirnov Ivan V, Gonseth Semira, Endicott Alyson A, Xiao Jianqiao, Rice Terri, Fu Cecilia H, McCoy Lucie S, Lachance Daniel H, Eckel-Passow Jeanette E, Wiencke John K, Jenkins Robert B, Wrensch Margaret R, Ma Xiaomei, Metayer Catherine, Wiemels Joseph |
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CDKN2a mutation-negative melanoma families have increased risk exclusively for skin cancers but not for other malignancies.
International journal of cancer. Journal international du cancer 2015 Nov 137 (9): 2220-6. Helgadottir Hildur, Höiom Veronica, Tuominen Rainer, Jönsson Göran, Månsson-Brahme Eva, Olsson Håkan, Hansson Joh |
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Association study of the miRNA-binding site polymorphisms of CDKN2A/B genes with gestational diabetes mellitus susceptibility.
Acta diabetologica 2015 Oct 52 (5): 951-8. Wang Xiaojing, Li Wei, Ma Liangkun, Gao Jinsong, Liu Juntao, Ping Fan, Nie M |
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Germline TERT promoter mutations are rare in familial melanoma.
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Novel CDKN2A mutations in Austrian melanoma patients.
Melanoma research 2015 Oct 25 (5): 412-20. Burgstaller-Muehlbacher Sebastian, Marko Martha, Müller Christoph, Wendt Judith, Pehamberger Hubert, Okamoto Ichi |
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Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.
Nature genetics 2015 Aug 47 (8): 911-6. Childs Erica J, Mocci Evelina, Campa Daniele, Bracci Paige M, Gallinger Steven, Goggins Michael, Li Donghui, Neale Rachel E, Olson Sara H, Scelo Ghislaine, Amundadottir Laufey T, Bamlet William R, Bijlsma Maarten F, Blackford Amanda, Borges Michael, Brennan Paul, Brenner Hermann, Bueno-de-Mesquita H Bas, Canzian Federico, Capurso Gabriele, Cavestro Giulia M, Chaffee Kari G, Chanock Stephen J, Cleary Sean P, Cotterchio Michelle, Foretova Lenka, Fuchs Charles, Funel Niccola, Gazouli Maria, Hassan Manal, Herman Joseph M, Holcatova Ivana, Holly Elizabeth A, Hoover Robert N, Hung Rayjean J, Janout Vladimir, Key Timothy J, Kupcinskas Juozas, Kurtz Robert C, Landi Stefano, Lu Lingeng, Malecka-Panas Ewa, Mambrini Andrea, Mohelnikova-Duchonova Beatrice, Neoptolemos John P, Oberg Ann L, Orlow Irene, Pasquali Claudio, Pezzilli Raffaele, Rizzato Cosmeri, Saldia Amethyst, Scarpa Aldo, Stolzenberg-Solomon Rachael Z, Strobel Oliver, Tavano Francesca, Vashist Yogesh K, Vodicka Pavel, Wolpin Brian M, Yu Herbert, Petersen Gloria M, Risch Harvey A, Klein Alison |
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Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.
Stroke; a journal of cerebral circulation 2015 Aug 46 (8): 2063-8. Carty Cara L, Keene Keith L, Cheng Yu-Ching, Meschia James F, Chen Wei-Min, Nalls Mike, Bis Joshua C, Kittner Steven J, Rich Stephen S, Tajuddin Salman, Zonderman Alan B, Evans Michele K, Langefeld Carl D, Gottesman Rebecca, Mosley Thomas H, Shahar Eyal, Woo Daniel, Yaffe Kristine, Liu Yongmei, Sale Michèle M, Dichgans Martin, Malik Rainer, Longstreth W T, Mitchell Braxton D, Psaty Bruce M, Kooperberg Charles, Reiner Alexander, Worrall Bradford B, Fornage Myriam, |
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Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
Genetics in medicine : official journal of the American College of Medical Genetics 2015 Aug 17 (8): 630-8. Maxwell Kara N, Wubbenhorst Bradley, D'Andrea Kurt, Garman Bradley, Long Jessica M, Powers Jacquelyn, Rathbun Katherine, Stopfer Jill E, Zhu Jiajun, Bradbury Angela R, Simon Michael S, DeMichele Angela, Domchek Susan M, Nathanson Katherine |
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BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study.
Genetics in medicine : official journal of the American College of Medical Genetics 2015 Jul 17 (7): 569-77. Zhen David B, Rabe Kari G, Gallinger Steven, Syngal Sapna, Schwartz Ann G, Goggins Michael G, Hruban Ralph H, Cote Michele L, McWilliams Robert R, Roberts Nicholas J, Cannon-Albright Lisa A, Li Donghui, Moyes Kelsey, Wenstrup Richard J, Hartman Anne-Renee, Seminara Daniela, Klein Alison P, Petersen Gloria |
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Diabetes susceptibility in Mayas: Evidence for the involvement of polymorphisms in HHEX, HNF4?, KCNJ11, PPAR?, CDKN2A/2B, SLC30A8, CDC123/CAMK1D, TCF7L2, ABCA1 and SLC16A11 genes.
Gene 2015 Jul 565 (1): 68-75. Lara-Riegos J C, Ortiz-López M G, Peña-Espinoza B I, Montúfar-Robles I, Peña-Rico M A, Sánchez-Pozos K, Granados-Silvestre M A, Menjivar |
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Distribution and Effects of CDKN2 p16 540 C>G and 580 C>T, and MDM2 SNP309 T>G Polymorphisms in Patients with Primary Brain Tumors.
Anticancer research 2015 Jul 35 (7): 3933-42. Kafadar Ali, Küçükhüseyin Özlem, Turan Saime, Yenilmez Ezgi Nurdan, Tunoglu Servet, Zeybek Umit, Kaynar Mehmet Yasar, Kemerdere Rahsan, Yaylim Ilh |
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Ultra-deep targeted sequencing of advanced oral squamous cell carcinoma identifies a mutation-based prognostic gene signature.
Oncotarget 2015 Jul 6 (20): 18066-80. Chen Shu-Jen, Liu Hsuan, Liao Chun-Ta, Huang Po-Jung, Huang Yi, Hsu An, Tang Petrus, Chang Yu-Sun, Chen Hua-Chien, Yen Tzu-Ch |
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Disease-associated polymorphisms in 9p21 are not associated with extreme longevity.
Geriatrics & gerontology international 2015 Jun 15 (6): 797-803. Congrains Ada, Kamide Kei, Hirose Nobuyoshi, Arai Yasumichi, Oguro Ryousuke, Nakama Chikako, Imaizumi Yuki, Kawai Tatsuo, Kusunoki Hiroshi, Yamamoto Hiroko, Onishi-Takeya Miyuki, Takeya Yasushi, Yamamoto Koichi, Sugimoto Ken, Akasaka Hiroshi, Saitoh Shigeyuki, Miura Tetsuji, Awata Nobuhisa, Kato Norihiro, Katsuya Tomohiro, Ikebe Kazunori, Gondo Yasuyuki, Rakugi Hiro |
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Clinicopathological characteristics and mutation profiling in primary cutaneous melanoma.
The American Journal of dermatopathology 2015 May 37 (5): 389-97. Yaman Banu, Akalin Taner, Kandilo?lu Gül? |
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Genomic predictors of survival in patients with high-grade urothelial carcinoma of the bladder.
European urology 2015 Feb 67 (2): 198-201. Kim Philip H, Cha Eugene K, Sfakianos John P, Iyer Gopa, Zabor Emily C, Scott Sasinya N, Ostrovnaya Irina, Ramirez Ricardo, Sun Arony, Shah Ronak, Yee Alyssa M, Reuter Victor E, Bajorin Dean F, Rosenberg Jonathan E, Schultz Nikolaus, Berger Michael F, Al-Ahmadie Hikmat A, Solit David B, Bochner Bernard |
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Association Analysis of Genetic Variants with Type 2 Diabetes in a Mongolian Population in China.
Journal of diabetes research 2015 2015 613236. Bai Haihua, Liu Haiping, Suyalatu Suyalatu, Guo Xiaosen, Chu Shandan, Chen Ying, Lan Tianming, Borjigin Burenbatu, Orlov Yuriy L, Posukh Olga L, Yang Xiuqin, Guilan Guilan, Osipova Ludmila P, Wu Qizhu, Narisu Nari |
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Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study.
PloS one 2015 10 (1): e0116537. Qian Yun, Lu Feng, Dong Meihua, Lin Yudi, Li Huizhang, Dai Juncheng, Jin Guangfu, Hu Zhibin, Shen Hongbi |
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Gene Expression-Genotype Analysis Implicates GSDMA, GSDMB, and LRRC3C as Contributors to Inflammatory Bowel Disease Susceptibility.
BioMed research international 2015 2015 834805. Söderman Jan, Berglind Linda, Almer Sv |
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Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.
Nature communications 2015 6 7553. Xu Heng, Zhang Hui, Yang Wenjian, Yadav Rachita, Morrison Alanna C, Qian Maoxiang, Devidas Meenakshi, Liu Yu, Perez-Andreu Virginia, Zhao Xujie, Gastier-Foster Julie M, Lupo Philip J, Neale Geoff, Raetz Elizabeth, Larsen Eric, Bowman W Paul, Carroll William L, Winick Naomi, Williams Richard, Hansen Torben, Holm Jens-Christian, Mardis Elaine, Fulton Robert, Pui Ching-Hon, Zhang Jinghui, Mullighan Charles G, Evans William E, Hunger Stephen P, Gupta Ramneek, Schmiegelow Kjeld, Loh Mignon L, Relling Mary V, Yang Jun |
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Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.
PloS one 2015 10 (3): e0122662. Wadt Karin A W, Aoude Lauren G, Krogh Lotte, Sunde Lone, Bojesen Anders, Grønskov Karen, Wartacz Nine, Ek Jakob, Tolstrup-Andersen Morten, Klarskov-Andersen Mette, Borg Åke, Heegaard Steffen, Kiilgaard Jens F, Hansen Thomas V O, Klein Kerenaftali, Jönsson Göran, Drzewiecki Krzysztof T, Dunø Morten, Hayward Nicholas K, Gerdes Anne-Mar |
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The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A.
Scientific reports 2015 5 15065. Vijayakrishnan Jayaram, Henrion Marc, Moorman Anthony V, Fiege Bettina, Kumar Rajiv, Inacio da Silva Filho Miguel, Holroyd Amy, Koehler Rolf, Thomsen Hauke, Irving Julie A, Allan James M, Lightfoot Tracy, Roman Eve, Kinsey Sally E, Sheridan Eamonn, Thompson Pamela D, Hoffmann Per, Nöthen Markus M, Mühleisen Thomas W, Eisele Lewin, Bartram Claus R, Schrappe Martin, Greaves Mel, Hemminki Kari, Harrison Christine J, Stanulla Martin, Houlston Richard |
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TOX and CDKN2A/B Gene Polymorphisms Are Associated with Type 2 Diabetes in Han Chinese.
Scientific reports 2015 5 11900. Wei Fengjiang, Cai Chunyou, Feng Shuzhi, Lv Jia, Li Shen, Chang Baocheng, Zhang Hong, Shi Wentao, Han Hongling, Ling Chao, Yu Ping, Chen Yongjun, Sun Ning, Tian Jianli, Jiao Hongxiao, Yang Fuhua, Li Mingshan, Wang Yuhua, Zou Lei, Su Long, Li Jingbo, Li Ran, Qiu Huina, Shi Jingmin, Liu Shiying, Chang Mingqin, Lin Jingna, Chen Liming, Li Wei-Do |
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Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers.
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