HuGE Literature Finder
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Records 1-100
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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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The genetic landscape of anaplastic pleomorphic xanthoastrocytoma.
Brain pathology (Zurich, Switzerland) 2019 Jan 29 (1): 85-96. Phillips Joanna J, Gong Henry, Chen Katharine, Joseph Nancy M, van Ziffle Jessica, Bastian Boris C, Grenert James P, Kline Cassie N, Mueller Sabine, Banerjee Anuradha, Nicolaides Theodore, Gupta Nalin, Berger Mitchel S, Lee Han S, Pekmezci Melike, Tihan Tarik, Bollen Andrew W, Perry Arie, Shieh Joseph T C, Solomon David |
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CDKN2A germline mutations are not associated with poor survival in an Italian cohort of melanoma patients.
Journal of the American Academy of Dermatology 2018 Sep . Dalmasso Bruna, Pastorino Lorenza, Ciccarese Giulia, Andreotti Virginia, Grillo Federica, Mastracci Luca, Spagnolo Francesco, Ballestrero Alberto, Queirolo Paola, Bruno William, Ghiorzo Pao |
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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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Targeted next-generation sequencing of 50 cancer-related genes in Japanese patients with oral squamous cell carcinoma.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2018 Sep 40 (9): 1010428318800180. Nakagaki Takafumi, Tamura Miyuki, Kobashi Kenta, Omori Akina, Koyama Ryota, Idogawa Masashi, Ogi Kazuhiro, Hiratsuka Hiroyoshi, Tokino Takashi, Sasaki Yasus |
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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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Mutation allele frequency threshold does not affect prognostic analysis using next-generation sequencing in oral squamous cell carcinoma.
BMC cancer 2018 Jul 18 (1): 758. Ma Jie, Fu Yong, Tu Yao-Yao, Liu Ying, Tan Yi-Ran, Ju Wu-Tong, Pickering Curtis R, Myers Jeffrey N, Zhang Zhi-Yuan, Zhong Lai-Pi |
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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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The genetic landscape of ganglioglioma.
Acta neuropathologica communications 2018 Jun 6 (1): 47. Pekmezci Melike, Villanueva-Meyer Javier E, Goode Benjamin, Van Ziffle Jessica, Onodera Courtney, Grenert James P, Bastian Boris C, Chamyan Gabriel, Maher Ossama M, Khatib Ziad, Kleinschmidt-DeMasters Bette K, Samuel David, Mueller Sabine, Banerjee Anuradha, Clarke Jennifer L, Cooney Tabitha, Torkildson Joseph, Gupta Nalin, Theodosopoulos Philip, Chang Edward F, Berger Mitchel, Bollen Andrew W, Perry Arie, Tihan Tarik, Solomon David |
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Association between long non-coding RNA polymorphisms and cancer risk: a meta-analysis.
Bioscience reports 2018 May . Huang Xin, Zhang Weiyue, Shao Zeng |
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Associations between skin rash, treatment outcome, and single nucleotide polymorphisms in head and neck cancer patients receiving the EGFR-inhibitor zalutumumab: results from the DAHANCA 19 trial.
Acta oncologica (Stockholm, Sweden) 2018 May 1-6. Brøndum Line, Alsner Jan, Sørensen Brita Singers, Maare Christian, Johansen Jørgen, Primdahl Hanne, Evensen Jan Folkvard, Kristensen Claus Andrup, Andersen Lisbeth Juhler, Overgaard Jens, Eriksen Jesper Gr |
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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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Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes.
International journal of hematology 2018 May . Tomoyasu Chihiro, Imamura Toshihiko, Tomii Toshihiro, Yano Mio, Asai Daisuke, Goto Hiroaki, Shimada Akira, Sanada Masashi, Iwamoto Shotaro, Takita Junko, Minegishi Masayoshi, Inukai Takeshi, Sugita Kanji, Hosoi Haji |
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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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Genomic landscape and prognostic analysis of mantle cell lymphoma.
Cancer gene therapy 2018 May . Yang Ping, Zhang Weilong, Wang Jing, Liu Yuanyuan, An Ran, Jing Hongm |
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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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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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Simultaneous detection of ABL1 mutation and IKZF1 deletion in Philadelphia chromosome-positive acute lymphoblastic leukemia using a customized target enrichment system panel.
International journal of laboratory hematology 2018 Mar . Aoe M, Ishida H, Matsubara T, Karakawa S, Kawaguchi H, Fujiwara K, Kanamitsu K, Washio K, Okada K, Shibakura M, Shimada |
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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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Frequency of Somatic TP53 Mutations in Combination with Known Pathogenic Mutations in Colon Adenocarcinoma, Non-Small Cell Lung Carcinoma, and Gliomas as Identified by Next-Generation Sequencing.
Neoplasia (New York, N.Y.) 2018 Feb 20 (3): 256-262. Shajani-Yi Zahra, de Abreu Francine B, Peterson Jason D, Tsongalis Gregory |
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The landscape of genetic alterations in ameloblastomas relates to clinical features.
Virchows Archiv : an international journal of pathology 2018 Feb . Gültekin Sibel Elif, Aziz Reem, Heydt Carina, Sengüven Burcu, Zöller Joachim, Safi Ali Farid, Kreppel Matthias, Buettner Reinha |
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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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Genomic CDKN2A/2B deletions in adult Ph+ ALL are adverse despite allogeneic stem cell transplantation.
Blood 2018 Jan . Pfeifer Heike, Raum Katharina, Markovic Sandra, Nowak Verena, Fey Stephanie, Obländer Julia, Pressler Jovita, Böhm Verena, Brüggemann Monika, Wunderle Lydia, Hüttmann Andreas, Wäsch Ralph, Beck Joachim, Stelljes Matthias, Viardot Andreas, Lang Fabian, Hoelzer Dieter, Hofmann Wolf-Karsten, Serve Hubert, Weiss Christel, Goekbuget Nicola, Ottmann Oliver G, Nowak Dani |
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[Genetic basis of pediatric T-cell acute lymphoblastic leukemia and its clinical impact].
[Rinsho ketsueki] The Japanese journal of clinical hematology 2018 59 (7): 953-959. Takita Jun |
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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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Comprehensive analysis of cancers of unknown primary for the biomarkers of response to immune checkpoint blockade therapy.
European journal of cancer (Oxford, England : 1990) 2018 05 94 179-186. Gatalica Zoran, Xiu Joanne, Swensen Jeff, Vranic Sem |
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Genomic analysis of head and neck cancer cases from two high incidence regions.
PloS one 2018 13 (1): e0191701. Perdomo Sandra, Anantharaman Devasena, Foll Matthieu, Abedi-Ardekani Behnoush, Durand Geoffroy, Reis Rosa Luciana Albina, Holmila Reetta, Le Calvez-Kelm Florence, Tajara Eloiza H, Wünsch-Filho Victor, Levi José Eduardo, Vilensky Marta, Polesel Jerry, Holcatova Ivana, Simonato Lorenzo, Canova Cristina, Lagiou Pagona, McKay James D, Brennan Pa |
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The 9p21 locus as a potential therapeutic target and prognostic marker in colorectal cancer.
Pharmacogenomics 2018 04 19 (5): 463-474. Bahrami Afsane, Hassanian Seyed Mahdi, Khazaei Majid, Gharib Masoumeh, Rahmani Mahsa, Fiuji Hamid, Jazayeri Mir Hadi, Moetamani-Ahmadi Mehrdad, Ferns Gordon A, Avan Am |
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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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Role of CDKN2A/p16 expression in the prognostication of oral squamous cell carcinoma.
Oral oncology 2017 Oct 73 27-35. Padhi Swati Shree, Roy Souvick, Kar Madhabananda, Saha Arka, Roy Shomereeta, Adhya Amit, Baisakh Manas, Banerjee Birendrana |
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Spectrum of genetic mutations in de novo PUNLMP of the urinary bladder.
Virchows Archiv : an international journal of pathology 2017 Jun . Rodriguez Pena Maria Del Carmen, Tregnago Aline C, Eich Marie-Lisa, Springer Simeon, Wang Yuxuan, Taheri Diana, Ertoy Dilek, Fujita Kazutoshi, Bezerra Stephania M, Cunha Isabela W, Raspollini Maria Rosaria, Yu Lijia, Bivalacqua Trinity J, Papadopoulos Nickolas, Kinzler Kenneth W, Vogelstein Bert, Netto George |
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Endoscopic and Molecular Characterization of Colorectal Sessile Serrated Adenoma/polyps with Cytological Dysplasia.
Gastrointestinal endoscopy 2017 May . Tanaka Yoshihito, Yamano Hiro-O, Yamamoto Eiichiro, Matushita Hiro-O, Aoki Hironori, Yoshikawa Kenjiro, Takagi Ryo, Harada Eiji, Nakaoka Michiko, Yoshida Yuko, Eizuka Makoto, Sugai Tamotsu, Suzuki Hiromu, Nakase Hiros |
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Clinical significance of recurrent copy number aberrations in B-lineage acute lymphoblastic leukaemia without recurrent fusion genes across age cohorts.
British journal of haematology 2017 Apr . Messina Monica, Chiaretti Sabina, Fedullo Anna Lucia, Piciocchi Alfonso, Puzzolo Maria Cristina, Lauretti Alessia, Gianfelici Valentina, Apicella Valerio, Fazi Paola, Te Kronnie Geertruy, Testi Anna Maria, Vitale Antonella, Guarini Anna, Foà Rob |
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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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Influence of MTHFR Genetic Background on p16 and MGMT Methylation in Oral Squamous Cell Cancer.
International journal of molecular sciences 2017 Mar 18 (4): . Ferlazzo Nadia, Currò Monica, Zinellu Angelo, Caccamo Daniela, Isola Gaetano, Ventura Valeria, Carru Ciriaco, Matarese Giovanni, Ientile Riccar |
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Polymorphism in ANRIL is associated with relapse in patients with multiple myeloma after autologous stem cell transplant.
Molecular carcinogenesis 2017 Feb . Poi Ming J, Li Junan, Sborov Douglas W, VanGundy Zachary, Cho Yu Kyoung, Lamprecht Misty, Pichiorri Flavia, Phelps Mitch A, Hofmeister Craig |
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Utility of Assessing the Number of Mutated KRAS, CDKN2A, TP53, and SMAD4 Genes Using a Targeted Deep Sequencing Assay as a Prognostic Biomarker for Pancreatic Cancer.
Pancreas 2017 Jan . Hayashi Hideyuki, Kohno Takashi, Ueno Hideki, Hiraoka Nobuyoshi, Kondo Shunsuke, Saito Motonobu, Shimada Yoko, Ichikawa Hitoshi, Kato Mamoru, Shibata Tatsuhiro, Morizane Chigusa, Sakamoto Yasunari, Shimada Kazuaki, Komatsu Yoshito, Sakamoto Naoya, Okusaka Taku |
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Prognostic value of ALDH2 polymorphism for patients with oropharyngeal cancer in a Japanese population.
PloS one 2017 12 (12): e0187992. Shinomiya Hirotaka, Shinomiya Hitomi, Kubo Mie, Saito Yuki, Yoshida Masafumi, Ando Mizuo, Teshima Masanori, Otsuki Naoki, Kiyota Naomi, Sasaki Ryohei, Nibu Ken-Ic |
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Coexistence of p16/CDKN2A homozygous deletions and activating EGFR mutations in lung adenocarcinoma patients signifies a poor response to EGFR-TKIs.
Lung cancer (Amsterdam, Netherlands) 2016 Dec 102 101-107. Jiang Juhong, Gu Yingying, Liu Jing, Wu Ruibin, Fu Lin, Zhao Jin, Guan Yub |
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Receptor tyrosine kinase amplification is predictive of distant metastasis in patients with oral squamous cell carcinoma.
Cancer science 2016 Nov . Oikawa Yu, Morita Kei-Ichi, Kayamori Kou, Tanimoto Kousuke, Sakamoto Kei, Katoh Hiroto, Ishikawa Shumpei, Inazawa Johji, Harada Hiroyu |
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Prognostic significance of non-HPV16 genotypes in oropharyngeal squamous cell carcinoma.
Oral oncology 2016 Oct 61 98-103. Mazul Angela L, Rodriguez-Ormaza Nidia, Taylor James M, Desai Dipan D, Brennan Paul, Anantharaman Devasena, Gheit Tarik, Tommasino Massimo, Abedi-Ardekani Behnoush, Olshan Andrew F, Zevallos Jose |
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Spatio-temporal mutation profiles of case-matched colorectal carcinomas and their metastases reveal unique de novo mutations in metachronous lung metastases by targeted next generation sequencing.
Molecular cancer 2016 Oct 15 (1): 63. Kovaleva Valentina, Geissler Anna-Lena, Lutz Lisa, Fritsch Ralph, Makowiec Frank, Wiesemann Sebastian, Hopt Ulrich T, Passlick Bernward, Werner Martin, Lassmann Sil |
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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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Biliary cancer: Utility of next-generation sequencing for clinical management.
Cancer 2016 Sep . Javle Milind, Bekaii-Saab Tanios, Jain Apurva, Wang Ying, Kelley Robin Katie, Wang Kai, Kang Hyunseon C, Catenacci Daniel, Ali Siraj, Krishnan Sunil, Ahn Daniel, Bocobo Andrea Grace, Zuo Mingxin, Kaseb Ahmed, Miller Vincent, Stephens Philip J, Meric-Bernstam Funda, Shroff Rachna, Ross Jeffr |
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Ki-67, p53, and p16 expression, and G691S RET polymorphism in desmoplastic melanoma (DM): A clinicopathologic analysis of predictors of outcome.
Journal of the American Academy of Dermatology 2016 Sep 75 (3): 595-602. Lawrence Nicholas F, Hammond Marc R, Frederick Dennie T, Su Yuhua, Dias-Santagata Dora, Deng April, Selim M Angelica, Mahalingam Meera, Flaherty Keith T, Hoang Mai |
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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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p16 upregulation is linked to poor prognosis in ERG negative prostate cancer.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2016 Sep 37 (9): 12655-12663. Burdelski Christoph, Dieckmann Tatsiana, Heumann Asmus, Hube-Magg Claudia, Kluth Martina, Beyer Burkhard, Steuber Thomas, Pompe Raisa, Graefen Markus, Simon Ronald, Minner Sarah, Tsourlakis Maria Christina, Koop Christina, Izbicki Jakob, Sauter Guido, Krech Till, Schlomm Thorsten, Wilczak Waldemar, Lebok Patri |
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Targeted next-generation sequencing identifies molecular subgroups in squamous cell carcinoma of the head and neck with distinct outcome after concurrent chemoradiation.
Annals of oncology : official journal of the European Society for Medical Oncology 2016 Sep . Tinhofer I, Stenzinger A, Eder T, Konschak R, Niehr F, Endris V, Distel L, Hautmann M G, Mandic R, Stromberger C, Weichert W, Budach |
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Two gene polymorphisms (rs4977756 and rs11515) in CDKN2A/B and glioma risk in South Indian population.
Meta gene 2016 Sep 9 215-8. Sibin M K, Dhananjaya I Bhat, Narasingarao K V L, Harshitha S M, Jeru-Manoj M, Chetan G |
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Next-generation sequencing survey of biliary tract cancer reveals the association between tumor somatic variants and chemotherapy resistance.
Cancer 2016 Aug . Ahn Daniel H, Javle Milind, Ahn Chul W, Jain Apurva, Mikhail Sameh, Noonan Anne M, Wu Christina, Shroff Rachna T, Chen James L, Bekaii-Saab Tani |
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A Proportion of Primary Squamous Cell Carcinomas of the Parotid Gland Harbor High Risk Human Papillomavirus.
Histopathology 2016 Jul . Xu Bin, Wang Lu, Borsu Laetitia, Ghossein Ronald, Katabi Nora, Ganly Ian, Dogan Snjeza |
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Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer.
Familial cancer 2016 Jul . Ibrahim Isaura S, Bonsing Bert A, Swijnenburg Rutger-Jan, Welling Lieke, Veenendaal Roeland A, Wasser Martin N J M, Morreau Hans, Inderson Akin, Vasen Hans F |
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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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Classification of TP53 mutations and HPV predict survival in advanced larynx cancer.
The Laryngoscope 2016 Jun . Scheel Adam, Bellile Emily, McHugh Jonathan B, Walline Heather M, Prince Mark E, Urba Susan, Wolf Gregory T, Eisbruch Avraham, Worden Francis, Carey Thomas E, Bradford Car |
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KRAS, BRAF oncogene mutations and tissue specific promoter hypermethylation of tumor suppressor SFRP2, DAPK1, MGMT, HIC1 and p16 genes in colorectal cancer patients.
Cancer biomarkers : section A of Disease markers 2016 Jun 17 (2): 133-43. Bagci Binnur, Sari Musa, Karadayi Kursat, Turan Mustafa, Ozdemir Ozturk, Bagci Gokh |
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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 genetic variants with tumor HPV16 status and survival in squamous cell carcinoma of the oropharynx.
Oral oncology 2016 May 56 78-83. Feng Yun, Li Yuncheng, Zhang Yang, Zheng Hongliang, Li Guoj |
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Characterization of leukemias with ETV6-ABL1 fusion.
Haematologica 2016 May . Zaliova Marketa, Moorman Anthony V, Cazzaniga Giovanni, Stanulla Martin, Harvey Richard C, Roberts Kathryn G, Heatley Sue L, Loh Mignon L, Konopleva Marina, Chen I-Ming, Zimmermannova Olga, Schwab Claire, Smith Owen, Mozziconacci Marie-Joelle, Chabannon Christian, Kim Myungshin, Falkenburg J H Frederik, Norton Alice, Marshall Karen, Haas Oskar A, Starkova Julia, Stuchly Jan, Hunger Stephen P, White Deborah, Mullighan Charles G, Willman Cheryl L, Stary Jan, Trka Jan, Zuna J |
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Coexistence of YWHAZ amplification predicts better prognosis in muscle-invasive bladder cancer with CDKN2A or TP53 loss.
Oncotarget 2016 May . Liu Shenghua, Wu Yishuo, Yang Tian, Feng Chenchen, Jiang Haow |
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Phenotypic characterization and clinical outcome in ampullary adenocarcinoma.
Journal of surgical oncology 2016 May . Asano Eisuke, Okano Keiichi, Oshima Minoru, Kagawa Seiko, Kushida Yoshio, Munekage Masaya, Hanazaki Kazuhiro, Watanabe Jota, Takada Yasutsugu, Ikemoto Tetsuya, Shimada Mitsuo, Suzuki Yasuyuki, |
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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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Collecting duct carcinoma of the kidney is associated with CDKN2A deletion and SLC family gene up-regulation.
Oncotarget 2016 Apr . Wang Jianmin, Papanicolau-Sengos Antonios, Chintala Sreenivasulu, Wei Lei, Liu Biao, Hu Qiang, Miles Kiersten Marie, Conroy Jeffrey M, Glenn Sean T, Costantini Manuela, Magi-Galluzzi Cristina, Signoretti Sabina, Choueiri Toni, Gallucci Michele, Sentinelli Steno, Fazio Vito M, Poeta Maria Luana, Liu Song, Morrison Carl, Pili Rober |
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Morphological and molecular approach to synchronous non-small cell lung carcinomas: impact on staging.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 Apr . Schneider Frank, Derrick Veronica, Davison Jon M, Strollo Diane, Incharoen Pimpin, Dacic San |
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Risk stratification of T-cell Acute Lymphoblastic Leukemia patients based on gene expression, mutations and copy number variation.
Leukemia research 2016 Apr 45 33-39. Mirji Gauri, Bhat Jaydeep, Kode Jyoti, Banavali Shripad, Sengar Manju, Khadke Prashant, Sait Osama, Chiplunkar Shubha |
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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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Two classes of intrahepatic cholangiocarcinoma defined by relative abundance of mutations and copy number alterations.
Oncotarget 2016 Mar . Kim Young-Ho, Hong Eun-Kyung, Kong Sun-Young, Han Sung-Sik, Kim Seoung-Hoon, Rhee Je-Keun, Hwang Soo-Kyung, Park Sang-Jae, Kim Tae-M |
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Association between the CpG island methylator phenotype and its prognostic significance in primary pulmonary adenocarcinoma.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2016 Feb . Koh Young Wha, Chun Sung-Min, Park Young-Soo, Song Joon Seon, Lee Geon Kook, Khang Shin Kwang, Jang Se J |
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Genetic differences between paediatric and adult Burkitt lymphomas.
British journal of haematology 2016 Feb . Havelange Violaine, Pepermans Xavier, Ameye Geneviève, Théate Ivan, Callet-Bauchu Evelyne, Barin Carole, Penther Dominique, Lippert Eric, Michaux Lucienne, Mugneret Francine, Dastugue Nicole, Raphaël Martine, Vikkula Miikka, Poirel Hélène |
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Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.
Journal of the American Academy of Dermatology 2016 Feb 74 (2): 325-32. Bruno William, Pastorino Lorenza, Ghiorzo Paola, Andreotti Virginia, Martinuzzi Claudia, Menin Chiara, Elefanti Lisa, Stagni Camilla, Vecchiato Antonella, Rodolfo Monica, Maurichi Andrea, Manoukian Siranoush, De Giorgi Vincenzo, Savarese Imma, Gensini Francesca, Borgognoni Lorenzo, Testori Alessandro, Spadola Giuseppe, Mandalà Mario, Imberti Gianlorenzo, Savoia Paola, Astrua Chiara, Ronco Anna Maria, Farnetti Alessandra, Tibiletti Maria Grazia, Lombardo Maurizio, Palmieri Giuseppe, Ayala Fabrizio, Ascierto Paolo, Ghigliotti Giovanni, Muggianu Marisa, Spagnolo Francesco, Picasso Virginia, Tanda Enrica Teresa, Queirolo Paola, Bianchi-Scarrà Giovan |
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Characterization of high risk melanoma patients in Austria.
The British journal of dermatology 2016 Jan . Müller C, Wendt J, Rauscher S, Burgstaller-Muehlbacher S, Sunder-Plassmann R, Scheurecker C, Richtig E, Fae I, Fischer G, Pehamberger H, Okamoto |
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Human Papillomavirus 16 Infection and TP53 Mutation: Two Distinct Pathogeneses for Oropharyngeal Squamous Cell Carcinoma in an Eastern Chinese Population.
PloS one 2016 11 (10): e0164491. Wang Zhen, Xia Rong-Hui, Ye Dong-Xia, Li Jia |
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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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Analysis of somatic mutations in braf, CDKN2A/p16 and PI3KCA in patients with medullary thyroid carcinoma.
Molecular medicine reports 2015 Dec . Nascimento Fabrício P, Cardoso Mirian G, Lindsey Susan C, Kunii Ilda S, Valente Flávia O F, Kizys Marina M L, Delcelo Rosana, Camacho Cléber P, Maciel Rui M B, Dias-Da-Silva Magnus |
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Comprehensive genomic profiling of 295 cases of clinically advanced urothelial carcinoma of the urinary bladder reveals a high frequency of clinically relevant genomic alterations.
Cancer 2015 Dec . Ross Jeffrey S, Wang Kai, Khaira Depinder, Ali Siraj M, Fisher Huge A G, Mian Badar, Nazeer Tipu, Elvin Julia A, Palma Norma, Yelensky Roman, Lipson Doron, Miller Vincent A, Stephens Philip J, Subbiah Vivek, Pal Sumanta |
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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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Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.
The New England journal of medicine 2015 Nov . Linehan W Marston, Spellman Paul T, Ricketts Christopher J, Creighton Chad J, Fei Suzanne S, Davis Caleb, Wheeler David A, Murray Bradley A, Schmidt Laura, Vocke Cathy D, Peto Myron, Al Mamun Abu Amar M, Shinbrot Eve, Sethi Anurag, Brooks Samira, Rathmell W Kimryn, Brooks Angela N, Hoadley Katherine A, Robertson A Gordon, Brooks Denise, Bowlby Reanne, Sadeghi Sara, Shen Hui, Weisenberger Daniel J, Bootwalla Moiz, Baylin Stephen B, Laird Peter W, Cherniack Andrew D, Saksena Gordon, Haake Scott, Li Jun, Liang Han, Lu Yiling, Mills Gordon B, Akbani Rehan, Leiserson Mark D M, Raphael Benjamin J, Anur Pavana, Bottaro Donald, Albiges Laurence, Barnabas Nandita, Choueiri Toni K, Czerniak Bogdan, Godwin Andrew K, Hakimi A Ari, Ho Thai H, Hsieh James, Ittmann Michael, Kim William Y, Krishnan Bhavani, Merino Maria J, Shaw Kenna R Mills, Reuter Victor E, Reznik Ed, Shelley Carl S, Shuch Brian, Signoretti Sabina, Srinivasan Ramaprasad, Tamboli Pheroze, Thomas George, Tickoo Satish, Burnett Kenneth, Crain Daniel, Gardner Johanna, Lau Kevin, Mallery David, Morris Scott, Paulauskis Joseph D, Penny Robert J, Shelton Candace, Shelton W Troy, Sherman Mark, Thompson Eric, Yena Peggy, Avedon Melissa T, Bowen Jay, Gastier-Foster Julie M, Gerken Mark, Leraas Kristen M, Lichtenberg Tara M, Ramirez Nilsa C, Santos Tracie, Wise Lisa, Zmuda Erik, Demchok John A, Felau Ina, Hutter Carolyn M, Sheth Margi, Sofia Heidi J, Tarnuzzer Roy, Wang Zhining, Yang Liming, Zenklusen Jean C, Zhang Jiashan, Ayala Brenda, Baboud Julien, Chudamani Sudha, Liu Jia, Lolla Laxmi, Naresh Rashi, Pihl Todd, Sun Qiang, Wan Yunhu, Wu Ye, Ally Adrian, Balasundaram Miruna, Balu Saianand, Beroukhim Rameen, Bodenheimer Tom, Buhay Christian, Butterfield Yaron S N, Carlsen Rebecca, Carter Scott L, Chao Hsu, Chuah Eric, Clarke Amanda, Covington Kyle R, Dahdouli Mahmoud, Dewal Ninad, Dhalla Noreen, Doddapaneni Harsha V, Drummond Jennifer A, Gabriel Stacey B, Gibbs Richard A, Guin Ranabir, Hale Walker, Hawes Alicia, Hayes D Neil, Holt Robert A, Hoyle Alan P, Jefferys Stuart R, Jones Steven J M, Jones Corbin D, Kalra Divya, Kovar Christie, Lewis Lora, Li Jie, Ma Yussanne, Marra Marco A, Mayo Michael, Meng Shaowu, Meyerson Matthew, Mieczkowski Piotr A, Moore Richard A, Morton Donna, Mose Lisle E, Mungall Andrew J, Muzny Donna, Parker Joel S, Perou Charles M, Roach Jeffrey, Schein Jacqueline E, Schumacher Steven E, Shi Yan, Simons Janae V, Sipahimalani Payal, Skelly Tara, Soloway Matthew G, Sougnez Carrie, Tam Angela, Tan Donghui, Thiessen Nina, Veluvolu Umadevi, Wang Min, Wilkerson Matthew D, Wong Tina, Wu Junyuan, Xi Liu, Zhou Jane, Bedford Jason, Chen Fengju, Fu Yao, Gerstein Mark, Haussler David, Kasaian Katayoon, Lai Phillip, Ling Shiyun, Radenbaugh Amie, Van Den Berg David, Weinstein John N, Zhu Jingchun, Albert Monique, Alexopoulou Iakovina, Andersen Jeremiah J, Auman J Todd, Bartlett John, Bastacky Sheldon, Bergsten Julie, Blute Michael L, Boice Lori, Bollag Roni J, Boyd Jeff, Castle Erik, Chen Ying-Bei, Cheville John C, Curley Erin, Davies Benjamin, DeVolk April, Dhir Rajiv, Dike Laura, Eckman John, Engel Jay, Harr Jodi, Hrebinko Ronald, Huang Mei, Huelsenbeck-Dill Lori, Iacocca Mary, Jacobs Bruce, Lobis Michael, Maranchie Jodi K, McMeekin Scott, Myers Jerome, Nelson Joel, Parfitt Jeremy, Parwani Anil, Petrelli Nicholas, Rabeno Brenda, Roy Somak, Salner Andrew L, Slaton Joel, Stanton Melissa, Thompson R Houston, Thorne Leigh, Tucker Kelinda, Weinberger Paul M, Winemiller Cynthia, Zach Leigh Anne, Zuna Rosemary, |
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TERT promoter mutations and rs2853669 polymorphism: prognostic impact and interactions with common alterations in glioblastomas.
Journal of neuro-oncology 2015 Nov . Nencha Umberto, Rahimian Amithys, Giry Marine, Sechi Andrea, Mokhtari Karima, Polivka Marc, Schmitt Yohann, Di Stefano Anna-Luisa, Alentorn Agusti, Labussière Marianne, Sanson Ma |
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Biomarker-based prognostic stratification of young adult glioblastoma.
Oncotarget 2015 Oct . Zhang Rui-Qi, Shi Zhifeng, Chen Hong, Chung Nellie Yuk-Fei, Yin Zi, Li Kay Ka-Wai, Chan Danny Tat-Ming, Poon Wai Sang, Wu Jinsong, Zhou Liangfu, Chan Aden Ka-Yin, Mao Ying, Ng Ho-Keu |
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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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Identification of germline genetic mutations in patients with pancreatic cancer.
Cancer 2015 Oct . Salo-Mullen Erin E, O'Reilly Eileen M, Kelsen David P, Ashraf Asad M, Lowery Maeve A, Yu Kenneth H, Reidy Diane L, Epstein Andrew S, Lincoln Anne, Saldia Amethyst, Jacobs Lauren M, Rau-Murthy Rohini, Zhang Liying, Kurtz Robert C, Saltz Leonard, Offit Kenneth, Robson Mark E, Stadler Zsofia |
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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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An Old Story Retold: Loss of G1 Control Defines A Distinct Genomic Subtype of Esophageal Squamous Cell Carcinoma.
Genomics, proteomics & bioinformatics 2015 Sep . Wang Qiyan, Bai Jian, Abliz Amir, Liu Ying, Gong Kenan, Li Jingjing, Shi Wenjie, Pan Yaqi, Liu Fangfang, Lai Shujuan, Yang Haijun, Lu Changdong, Zhang Lixin, Chen Wei, Xu Ruiping, Cai Hong, Ke Yang, Zeng Changqi |
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A clinicopathologic study of diencephalic pediatric low-grade gliomas with BRAF V600 mutation.
Acta neuropathologica 2015 Aug . Ho Cheng-Ying, Mobley Bret C, Gordish-Dressman Heather, VandenBussche Christopher J, Mason Gary E, Bornhorst Miriam, Esbenshade Adam J, Tehrani Mahtab, Orr Brent A, LaFrance Delecia R, Devaney Joseph M, Meltzer Beatrix W, Hofherr Sean E, Burger Peter C, Packer Roger J, Rodriguez Fausto |
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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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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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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Epidemiological features and prognostic parameters of multiple primary melanomas in CDKN2A-mutations patients.
Pigment cell & melanoma research 2015 Jul . De Giorgi Vincenzo, Savarese Imma, D'Errico Antonietta, Gori Alessia, Papi Federica, Colombino Maria, Sini Maria Cristina, Grazzini Marta, Stanganelli Ignazio, Rossari Susanna, Covarelli Paolo, Massi Daniela, Palmieri Giusep |
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Evaluation of Mutational Testing of Preneoplastic Barrett's Mucosa by Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Endoscopic Samples for Detection of Concurrent Dysplasia and Adenocarcinoma in Barrett's Esophagus.
The Journal of molecular diagnostics : JMD 2015 Jul 17 (4): 412-9. Del Portillo Armando, Lagana Stephen M, Yao Yuan, Uehara Takeshi, Jhala Nirag, Ganguly Tapan, Nagy Peter, Gutierrez Jorge, Luna Aesis, Abrams Julian, Liu Yang, Brand Randall, Sepulveda Jorge L, Falk Gary W, Sepulveda Antonia |
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Mutational dichotomy in desmoplastic malignant melanoma corroborated by multigene panel analysis.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2015 Jul 28 (7): 895-903. Jahn Stephan W, Kashofer Karl, Halbwedl Iris, Winter Gerlinde, El-Shabrawi-Caelen Laila, Mentzel Thomas, Hoefler Gerald, Liegl-Atzwanger Bernadet |
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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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Association of HPV with genetic and epigenetic alterations in colorectal adenocarcinoma from Indian population.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Jun 36 (6): 4661-70. Laskar Ruhina S, Talukdar Fazlur R, Choudhury Javed H, Singh Seram Anil, Kundu Sharbadeb, Dhar Bishal, Mondal Rosy, Ghosh Sankar Kum |
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Profiling of actionable gene alterations in ovarian cancer by targeted deep sequencing.
International journal of oncology 2015 Jun 46 (6): 2389-98. Takenaka Masataka, Saito Motonobu, Iwakawa Reika, Yanaihara Nozomu, Saito Misato, Kato Mamoru, Ichikawa Hitoshi, Shibata Tatsuhiro, Yokota Jun, Okamoto Aikou, Kohno Takas |
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