HuGE Literature Finder
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Records 1-100
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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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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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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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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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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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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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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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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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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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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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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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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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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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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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Benefit of Surveillance for Pancreatic Cancer in High-Risk Individuals: Outcome of Long-Term Prospective Follow-Up Studies From Three European Expert Centers.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 Apr . Vasen Hans, Ibrahim Isaura, Ponce Carmen Guillen, Slater Emily P, Matthäi Elvira, Carrato Alfredo, Earl Julie, Robbers Kristin, van Mil Anneke M, Potjer Thomas, Bonsing Bert A, de Vos Tot Nederveen Cappel Wouter H, Bergman Wilma, Wasser Martin, Morreau Hans, Klöppel Günter, Schicker Christoph, Steinkamp Martin, Figiel Jens, Esposito Irene, Mocci Evelina, Vazquez-Sequeiros Enrique, Sanjuanbenito Alfonso, Muñoz-Beltran Maria, Montans José, Langer Peter, Fendrich Volker, Bartsch Detlef |
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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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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.
Familial cancer 2015 Oct . Harland Mark, Petljak Mia, Robles-Espinoza Carla Daniela, Ding Zhihao, Gruis Nelleke A, van Doorn Remco, Pooley Karen A, Dunning Alison M, Aoude Lauren G, Wadt Karin A W, Gerdes Anne-Marie, Brown Kevin M, Hayward Nicholas K, Newton-Bishop Julia A, Adams David J, Bishop D Timot |
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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 |
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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A comparison of type 2 diabetes risk allele load between African Americans and European Americans.
Human genetics 2014 Dec 133 (12): 1487-95. Keaton Jacob M, Cooke Bailey Jessica N, Palmer Nicholette D, Freedman Barry I, Langefeld Carl D, Ng Maggie C Y, Bowden Donald |
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Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers.
Carcinogenesis 2014 Dec 35 (12): 2698-705. Li Wen-Qing, Pfeiffer Ruth M, Hyland Paula L, Shi Jianxin, Gu Fangyi, Wang Zhaoming, Bhattacharjee Samsiddhi, Luo Jun, Xiong Xiaoqin, Yeager Meredith, Deng Xiang, Hu Nan, Taylor Philip R, Albanes Demetrius, Caporaso Neil E, Gapstur Susan M, Amundadottir Laufey, Chanock Stephen J, Chatterjee Nilanjan, Landi Maria Teresa, Tucker Margaret A, Goldstein Alisa M, Yang Xiaohong |
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Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.
Familial cancer 2014 Dec 13 (4): 645-9. de Ávila Alexandre Leon Ribeiro, Krepischi Ana Cristina Victorino, Moredo Luciana Facure, Aguiar Talita Ferreira Marques, da Silva Felipe Carneiro, de Sá Bianca Costa Soares, de Nóbrega Amanda França, Achatz Maria Isabel Waddington, Duprat João Pedreira, Landman Gilles, Carraro Dirce Mar |
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Polymorphisms of cell cycle control genes influence the development of sporadic medullary thyroid carcinoma.
European journal of endocrinology / European Federation of Endocrine Societies 2014 Dec 171 (6): 761-7. Barbieri R B, Bufalo N E, Secolin R, Assumpção L V M, Maciel R M B, Cerutti J M, Ward L |
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Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling.
Journal of the American Academy of Dermatology 2014 Nov 71 (5): 888-95. Potrony Miriam, Puig-Butillé Joan Anton, Aguilera Paula, Badenas Celia, Carrera Cristina, Malvehy Josep, Puig Susa |
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High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
Journal of medical genetics 2014 Aug 51 (8): 545-52. Helgadottir Hildur, Höiom Veronica, Jönsson Göran, Tuominen Rainer, Ingvar Christian, Borg Ake, Olsson Håkan, Hansson Joh |
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Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia.
American journal of hematology 2014 Jul 89 (7): 721-5. Walsh Kyle M, de Smith Adam J, Welch Tara C, Smirnov Ivan, Cunningham Marc J, Ma Xiaomei, Chokkalingam Anand P, Dahl Gary V, Roberts William, Barcellos Lisa F, Buffler Patricia A, Metayer Catherine, Wiemels Joseph |
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Genotype analysis in Hungarian patients with multiple primary melanoma.
Experimental dermatology 2014 May 23 (5): 361-4. Hatvani Zsófia, Brodszky Valentin, Mazán Mercédesz, Pintér Dóra, Hársing Judit, Tóth Veronika, Somlai Beáta, Kárpáti Sarol |
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Association of CDKN2A polymorphisms with the severity of cervical neoplasia in a Brazilian population.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2014 Mar 19 (2): 121-7. Vargas-Torres Sandra Liliana, Portari Elyzabeth Avvad, Klumb Evandro Mendes, Guillobel Heloisa Carneiro da Rocha, de Camargo Maria José, Russomano Fábio Bastos, Macedo Jacyara Maria Bri |
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Gender-dependent associations of CDKN2A/2B, KCNJ11, POLI, SLC30A8, and TCF7L2 variants with type 2 diabetes in (North African) Tunisian Arabs.
Diabetes research and clinical practice 2014 Mar 103 (3): e40-3. Turki Amira, Al-Zaben Ghadeer S, Khirallah Moncef, Marmouch Hela, Mahjoub Touhami, Almawi Wassim |
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Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families.
The Journal of investigative dermatology 2014 Feb 134 (2): 481-7. Liang Xueying, Pfeiffer Ruth M, Li Wen-Qing, Brossard Myriam, Burke Laura S, Wheeler William, Calista Donato, Fargnoli Maria Concetta, Ghiorzo Paola, Peris Ketty, Bianchi-Scarra Giovanna, Chaudru Valerie, Zelenika Diana, Maeder Dennis, Burdette Laurie, Yeager Meredith, Chanock Stephen, Landi Maria Teresa, Demenais Florence, Tucker Margaret A, Goldstein Alisa M, Yang Xiaohong |
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Comprehensive genomic profiling of relapsed and metastatic adenoid cystic carcinomas by next-generation sequencing reveals potential new routes to targeted therapies.
The American journal of surgical pathology 2014 Feb 38 (2): 235-8. Ross Jeffrey S, Wang Kai, Rand Janna V, Sheehan Christine E, Jennings Timothy A, Al-Rohil Rami N, Otto Geoff A, Curran John C, Palmer Gary, Downing Sean R, Yelensky Roman, Lipson Doron, Balasubramanian Sohail, Garcia Lazaro, Mahoney Kristen, Ali Siraj M, Miller Vincent A, Stephens Philip |
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Genetic gains and losses in oral squamous cell carcinoma: impact on clinical management.
Cellular oncology (Dordrecht) 2014 Feb 37 (1): 29-39. Ribeiro Ilda Patrícia, Marques Francisco, Caramelo Francisco, Pereira João, Patrício Miguel, Prazeres Hugo, Ferrão José, Julião Maria José, Castelo-Branco Miguel, de Melo Joana Barbosa, Baptista Isabel Poiares, Carreira Isabel Marqu |
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Genetic variants for type 2 diabetes and new-onset cancer in Chinese with type 2 diabetes.
Diabetes research and clinical practice 2014 Feb 103 (2): 328-37. Ma R C W, So W Y, Tam C H T, Luk A O, Ho J S K, Wang Y, Lam V K, Lee H M, Kong A P, Tong P C, Xu G, Chow C C, Ng M C, Yang X L, Chan J |
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A replication study and a meta-analysis of the association between the CDKN2A rs1333049 polymorphism and coronary heart disease.
Journal of atherosclerosis and thrombosis 2014 21 (11): 1109-20. Lian Jiangfang, Ba Yanna, Dai Dongjun, Chen Zhikui, Lou Yumei, Jiang Qingjun, Zhao Ruochi, Sun Liqin, Huang Xiaoyan, Yang Xi, Ye Ming, Wang Ying, Mao Haiyan, Guan Haiwang, Xu Limin, Guo Jian, Fang Peiliang, Li Junxin, Ye Huadan, Chen Xiaoliang, Peng Ping, Zhou Jianqing, Duan Shiw |
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Analysis and comparison of somatic mutations in paired primary and recurrent epithelial ovarian cancer samples.
PloS one 2014 9 (6): e99451. Kim Yong-Man, Lee Shin-Wha, Chun Sung-Min, Kim Dae-Yeon, Kim Jong-Hyeok, Kim Kyu-Rae, Kim Young-Tak, Nam Joo-Hyun, van Hummelen Paul, MacConaill Laura E, Hahn William C, Jang Se J |
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Associations between the CDKN2A/B, ADTRP and PDGFD polymorphisms and the development of coronary atherosclerosis in Japanese patients.
Journal of atherosclerosis and thrombosis 2014 21 (7): 680-90. Dechamethakun Sariya, Ikeda Shinobu, Arai Tomio, Sato Noriko, Sawabe Motoji, Muramatsu Masaa |
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Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population.
Scientific reports 2014 4 5115. Vishal Mansi, Sharma Anchal, Kaurani Lalit, Chakraborty Subhadip, Ray Jharna, Sen Abhijit, Mukhopadhyay Arijit, Ray Kun |
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Genetic association study with metabolic syndrome and metabolic-related traits in a cross-sectional sample and a 10-year longitudinal sample of chinese elderly population.
PloS one 2014 9 (6): e100548. Yang Jinghui, Liu Jianwei, Liu Jing, Li Wenyuan, Li Xiaoying, He Yao, Ye Li |
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Genetic variants associated with myocardial infarction and the risk factors in Chinese population.
PloS one 2014 9 (1): e86332. Wang Yongqin, Wang Lefeng, Liu Xin, Zhang Yongzhi, Yu Liping, Zhang Fan, Liu Lisheng, Cai Jun, Yang Xinchun, Wang Xing |
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Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.
BMC medical genetics 2014 15 (1): 55. Silva Felipe C, Lisboa Bianca Cg, Figueiredo Marcia Cp, Torrezan Giovana T, Santos Erika Mm, Krepischi Ana C, Rossi Benedito M, Achatz Maria I, Carraro Dirce |
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Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population.
BMC cardiovascular disorders 2014 14 170. Zhang Liu-wei, Li Jian-ping, Duan Fang-fang, Liu Zhi-ke, Zhan Si-yan, Hu Yong-hua, Jiang Jie, Zhang Yan, Huo Yong, Chen Da-fa |
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Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity.
Diabetes 2013 Dec . Dimas AS, Lagou V, Barker A, Knowles JW, Mägi R, Hivert MF, Benazzo A, Rybin D, Jackson AU, Stringham HM, Song C, Fischer-Rosinsky A, Boesgaard TW, Grarup N, Abbasi FA, Assimes TL, Hao K, Yang X, Lecoeur C, Barroso I, Bonnycastle LL, Böttcher Y, Bumpstead S, Chines PS, Erdos MR, Graessler J, Kovacs P, Morken MA, Narisu N, Payne F, Stancakova A, Swift AJ, Tönjes A, Bornstein SR, Cauchi S, Froguel P, Meyre D, Schwarz PE, Häring HU, Smith U, Boehnke M, Bergman RN, Collins FS, Mohlke KL, Tuomilehto J, Quertemous T, Lind L, Hansen T, Pedersen O, Walker M, Pfeiffer AF, Spranger J, Stumvoll M, Meigs JB, Wareham NJ, Kuusisto J, Laakso M, Langenberg C, Dupuis J, Watanabe RM, Florez JC, Ingelsson E, McCarthy MI, Prokopenko I |
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The relationship between five widely-evaluated variants in CDKN2A/B and CDKAL1 genes and the risk of type 2 diabetes: a meta-analysis.
Gene 2013 Dec 531 (2): 435-43. Peng Feng, Hu Dan, Gu Chaohao, Li Xiaobo, Li Yuqiong, Jia Nan, Chu Shaoli, Lin Jinxiu, Niu Wenqu |
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Trans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population.
Diabetologia 2013 Dec 56 (12): 2619-28. Kuo Jane Z, Sheu Wayne Huey-Herng, Assimes Themistocles L, Hung Yi-Jen, Absher Devin, Chiu Yen-Feng, Mak Jordan, Wang Jun-Sing, Kwon Soonil, Hsu Chih-Cheng, Goodarzi Mark O, Lee I-Te, Knowles Joshua W, Miller Brittany E, Lee Wen-Jane, Juang Jyh-Ming J, Wang Tzung-Dau, Guo Xiuqing, Taylor Kent D, Chuang Lee-Ming, Hsiung Chao A, Quertermous Thomas, Rotter Jerome I, Chen Yii-Der |
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Association between type 2 diabetes and rs10811661 polymorphism upstream of CDKN2A/B: a meta-analysis.
Acta diabetologica 2013 Oct 50 (5): 657-62. Li Hui, Tang Xiaojun, Liu Qin, Wang Ya |
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Genetic modifiers of cystic fibrosis-related diabetes.
Diabetes 2013 Oct 62 (10): 3627-35. Blackman Scott M, Commander Clayton W, Watson Christopher, Arcara Kristin M, Strug Lisa J, Stonebraker Jaclyn R, Wright Fred A, Rommens Johanna M, Sun Lei, Pace Rhonda G, Norris Sarah A, Durie Peter R, Drumm Mitchell L, Knowles Michael R, Cutting Garry |
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Surveillance of second-degree relatives from melanoma families with a CDKN2A germline mutation.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2013 Oct 22 (10): 1771-7. van der Rhee Jasper I, Boonk Stephanie E, Putter Hein, Cannegieter Suzanne C, Flinterman Linda E, Hes Frederik J, de Snoo Femke A, Mooi Wolter J, Gruis Nelleke A, Vasen Hans F A, Kukutsch Nicole A, Bergman Wil |
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Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia.
Leukemia research 2013 Aug 37 (8): 928-35. La Starza Roberta, Lettieri Antonella, Pierini Valentina, Nofrini Valeria, Gorello Paolo, Songia Simona, Crescenzi Barbara, Te Kronnie Geertruy, Giordan Marco, Leszl Anna, Valsecchi Maria Grazia, Aversa Franco, Basso Giuseppe, Biondi Andrea, Conter Valentino, Cazzaniga Giovanni, Mecucci Cristi |
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Do CDKN2 p16 540 C>G, CDKN2 p16 580 C>T, and MDM2 SNP309 T>G gene variants act on colorectal cancer development or progression?
DNA and cell biology 2013 Jul 32 (7): 400-8. Tuna Gülay, Küçükhüseyin Ozlem, Ar?kan Soykan, Kaytan Sa?lam Esra, Güler Erkan, Cac?na Canan, Oztop Ozge, Turan Saime, Korkmaz Gurbet, Yayl?m Ilh |
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Analysis of Latvian familial melanoma patients shows novel variants in the noncoding regions of CDKN2A and that the CDK4 mutation R24H is a founder mutation.
Melanoma research 2013 Jun 23 (3): 221-6. Veinalde R?ta, Ozola Aija, Azarjana Krist?ne, Molven Anders, Akslen Lars A, Doni?a Simona, Proboka Guna, C?ma Ingr?da, Baginskis Ain?rs, Pjanova Da |
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Association study of genetic variants of 17 diabetes-related genes/loci and cardiovascular risk and diabetic nephropathy in the Chinese She population.
Journal of diabetes 2013 Jun 5 (2): 136-45. Chen Gang, Xu Yuan, Lin Yinghua, Lai Xiaolan, Yao Jin, Huang Baoying, Chen Zichun, Huang Huibin, Fu Xianguo, Lin Lixiang, Lai Shenghan, Wen Junpi |
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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 |
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Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.
Journal of the National Cancer Institute 2013 May 105 (10): 733-42. Xu Heng, Yang Wenjian, Perez-Andreu Virginia, Devidas Meenakshi, Fan Yiping, Cheng Cheng, Pei Deqing, Scheet Paul, Burchard Esteban González, Eng Celeste, Huntsman Scott, Torgerson Dara G, Dean Michael, Winick Naomi J, Martin Paul L, Camitta Bruce M, Bowman W Paul, Willman Cheryl L, Carroll William L, Mullighan Charles G, Bhojwani Deepa, Hunger Stephen P, Pui Ching-Hon, Evans William E, Relling Mary V, Loh Mignon L, Yang Jun |
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Significance of MDM2 and P14 ARF polymorphisms in susceptibility to differentiated thyroid carcinoma.
Surgery 2013 May 153 (5): 711-7. Zhang Fenghua, Xu Li, Wei Qingyi, Song Xicheng, Sturgis Erich M, Li Guoj |
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Association of single nucleotide polymorphisms on chromosome 9p21.3 with cardiovascular death in kidney transplant recipients.
Transplantation 2013 Apr 95 (7): 928-32. Melk Anette, Schildhorn Carolin, Hömme Meike, Knoch Miriam, Schmidt Bernhard M W, Serth Jürgen, Scherer Sabine, Döhler Bernd, Opelz Gerha |
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Clinical and genetic risk factors for type 2 diabetes at early or late post partum after gestational diabetes mellitus.
The Journal of clinical endocrinology and metabolism 2013 Apr 98 (4): E744-52. Kwak Soo Heon, Choi Sung Hee, Jung Hye Seung, Cho Young Min, Lim Soo, Cho Nam H, Kim Seong Yeon, Park Kyong Soo, Jang Hak |
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Analysis of 60 Reported Glioma Risk SNPs Replicates Published GWAS Findings but Fails to Replicate Associations From Published Candidate-Gene Studies.
Genetic epidemiology 2013 Feb 37 (2): 2. Walsh KM, Anderson E, Hansen HM, Decker PA, Kosel ML, Kollmeyer T, Rice T, Zheng S, Xiao Y, Chang JS, McCoy LS, Bracci PM, Wiemels JL, Pico AR, Smirnov I, Lachance DH, Sicotte H, Eckel-Passow JE, Wiencke JK, Jenkins RB, Wrensch MR |
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Genetic variations of patients with familial or multiple melanoma in Southern Brazil.
Journal of the European Academy of Dermatology and Venereology : JEADV 2013 Feb 27 (2): e179-85. Grazziotin T C, Rey M C W, Bica C G, Pinto L A, Bonamigo R R, Puig-Butille J A, Cuellar F, Puig |
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