HuGE Literature Finder
Records 1-30
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Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study.
BMC cancer 2019 Aug 19 (1): 772. Casula Milena, Paliogiannis Panagiotis, Ayala Fabrizio, De Giorgi Vincenzo, Stanganelli Ignazio, Mandalà Mario, Colombino Maria, Manca Antonella, Sini Maria Cristina, Caracò Corrado, Ascierto Paolo Antonio, Satta Rosanna Rita, , Lissia Amelia, Cossu Antonio, Palmieri Giuseppe, |
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Multi-Modality Analysis Improves Survival Prediction in Enucleated Uveal Melanoma Patients.
Investigative ophthalmology & visual science 2019 Aug 60 (10): 3595-3605. Drabarek Wojtek, Yavuzyigitoglu Serdar, Obulkasim Askar, van Riet Job, Smit Kyra N, van Poppelen Natasha M, Vaarwater Jolanda, Brands Tom, Eussen Bert, Verdijk Robert M, Naus Nicole C, Mensink Hanneke W, Paridaens Dion, Boersma Eric, van de Werken Harmen J G, Kilic Emine, de Klein Annelies, |
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Multigene panel testing in unselected Israeli breast cancer cases: mutational spectrum and use of BRCA1/2 mutation prediction algorithms.
Breast cancer research and treatment 2019 Apr . Bernstein-Molho Rinat, Singer Amihood, Laitman Yael, Netzer Iris, Zalmanoviz Shelley, Friedman Eit |
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Germline large deletion of BAP1 and decreased expression in non-tumor choroid in uveal melanoma patients with high risk for inherited cancer.
Genes, chromosomes & cancer 2019 Mar . Boru Getachew, Grosel Timothy W, Pilarski Robert, Stautberg Meredith, Massengill James B, Jeter Joanne, Singh Arun, Marino Meghan J, McElroy Joseph P, Davidorf Frederick H, Cebulla Colleen M, Abdel-Rahman Mohamed |
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Clonal architectures predict clinical outcome in clear cell renal cell carcinoma.
Nature communications 2019 03 10 (1): 1245. Huang Yi, Wang Jiayin, Jia Peilin, Li Xiangchun, Pei Guangsheng, Wang Changxi, Fang Xiaodong, Zhao Zhongming, Cai Zhiming, Yi Xin, Wu Song, Zhang Baife |
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Molecular and immunohistochemical analyses of uveal melanoma patient cohort.
Melanoma research 2019 06 29 (3): 248-253. Sarubi Helena C, Pereira Núbia B, Gomes Carolina C, Gomez Ricardo S, Carmo Ana C M, Melo Flavia M, Bastos-Rodrigues Luciana, Pedrosa Moisés S, Friedman Eitan, De Marco Lu |
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Frequency of Germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 Aug JCO2018785204. Panou Vasiliki, Gadiraju Meghana, Wolin Arthur, Weipert Caroline M, Skarda Emily, Husain Aliya N, Patel Jyoti D, Rose Buerkley, Zhang Shannon R, Weatherly Madison, Nelakuditi Viswateja, Knight Johnson Amy, Helgeson Maria, Fischer David, Desai Arpita, Sulai Nanna, Ritterhouse Lauren, Røe Oluf D, Turaga Kiran K, Huo Dezheng, Segal Jeremy, Kadri Sabah, Li Zejuan, Kindler Hedy L, Churpek Jane |
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Analysis of the Exome Aggregation Consortium (ExAC) database suggests that the BAP1-tumor predisposition syndrome is underreported in cancer patients.
Genes, chromosomes & cancer 2018 May . Massengill James B, Sample Klarke M, Pilarski Robert, McElroy Joseph, Davidorf Frederick H, Cebulla Colleen M, Abdel-Rahman Mohamed |
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Histomorphologic spectrum of germline-related and sporadic BAP-1 Inactivated Melanocytic Tumors.
Journal of the American Academy of Dermatology 2018 May . Garfield Erin M, Walton Kara E, Quan Victor L, VandenBoom Timothy, Zhang Bin, Kong Betty Y, Isales Maria Cristina, Panah Elnaz, Kim Gene, Gerami Pedr |
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The loss of BAP1 protein expression predicts poor prognosis in patients with nonmetastatic clear cell renal cell carcinoma with inferior vena cava tumor thrombosis.
Urologic oncology 2018 May . Oka Suguru, Inoshita Naoko, Miura Yuji, Oki Ryosuke, Miyama Yu, Nagamoto Shoichi, Ogawa Kohei, Sakaguchi Kazushige, Kondoh Chihiro, Kurosawa Kazuhiro, Urakami Shinji, Takano Toshimi, Okaneya Toshika |
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A mutational signature associated with alcohol consumption and prognostically significantly mutated driver genes in esophageal squamous cell carcinoma.
Annals of oncology : official journal of the European Society for Medical Oncology 2018 Jan . Li X C, Wang M Y, Yang M, Dai H J, Zhang B F, Wang W, Chu X L, Wang X, Zheng H, Niu R F, Zhang W, Chen K |
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Genetic Background of Iris Melanomas and Iris Melanocytic Tumors of Uncertain Malignant Potential.
Ophthalmology 2018 Jan . van Poppelen Natasha M, Vaarwater Jolanda, Mudhar Hardeep S, Sisley Karen, Rennie Ian G, Rundle Paul, Brands Tom, van den Bosch Quincy C C, Mensink Hanneke W, de Klein Annelies, Kiliç Emine, Verdijk Robert |
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Genomically annotated risk model for advanced renal-cell carcinoma: a retrospective cohort study.
The Lancet. Oncology 2018 12 19 (12): 1688-1698. Voss Martin H, Reising Albert, Cheng Yuan, Patel Parul, Marker Mahtab, Kuo Fengshen, Chan Timothy A, Choueiri Toni K, Hsieh James J, Hakimi A Ari, Motzer Robert |
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Common, germline genetic variations in the novel tumor suppressor BAP1 and risk of developing different types of cancer.
Oncotarget 2017 Sep 8 (43): 74936-74946. Lin Moubin, Zhang Liren, Hildebrandt Michelle A T, Huang Maosheng, Wu Xifeng, Ye Yuanqi |
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Frequent GNAQ, GNA11, and EIF1AX Mutations in Iris Melanoma.
Investigative ophthalmology & visual science 2017 Jul 58 (9): 3464-3470. Scholz Simone L, Möller Inga, Reis Henning, Süßkind Daniela, van de Nes Johannes A P, Leonardelli Sonia, Schilling Bastian, Livingstone Elisabeth, Schimming Tobias, Paschen Annette, Sucker Antje, Murali Rajmohan, Steuhl Klaus-Peter, Schadendorf Dirk, Westekemper Henrike, Griewank Klaus |
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Genomic Biomarkers of a Randomized Trial Comparing First-line Everolimus and Sunitinib in Patients with Metastatic Renal Cell Carcinoma.
European urology 2016 Oct . Hsieh James J, Chen David, Wang Patricia I, Marker Mahtab, Redzematovic Almedina, Chen Ying-Bei, Selcuklu S Duygu, Weinhold Nils, Bouvier Nancy, Huberman Kety H, Bhanot Umesh, Chevinsky Michael S, Patel Parul, Pinciroli Patrizia, Won Helen H, You Daoqi, Viale Agnes, Lee William, Hakimi A Ari, Berger Michael F, Socci Nicholas D, Cheng Emily H, Knox Jennifer, Voss Martin H, Voi Maurizio, Motzer Robert |
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Germline BAP1 Alterations in Familial Uveal Melanoma.
Genes, chromosomes & cancer 2016 Oct . Rai Karan, Pilarski Robert, Boru Getachew, Rehman Muneeb, Saqr Ahmad H, Massengill James B, Singh Arun, Marino Meghan J, Davidorf Frederick H, Cebulla Colleen M, Abdel-Rahman Moham |
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Molecular analysis of aggressive renal cell carcinoma with unclassified histology reveals distinct subsets.
Nature communications 2016 Oct 7 13131. Chen Ying-Bei, Xu Jianing, Skanderup Anders Jacobsen, Dong Yiyu, Brannon A Rose, Wang Lu, Won Helen H, Wang Patricia I, Nanjangud Gouri J, Jungbluth Achim A, Li Wei, Ojeda Virginia, Hakimi A Ari, Voss Martin H, Schultz Nikolaus, Motzer Robert J, Russo Paul, Cheng Emily H, Giancotti Filippo G, Lee William, Berger Michael F, Tickoo Satish K, Reuter Victor E, Hsieh James |
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Whole Exome Sequencing Identifies TSC1/TSC2 Biallelic Loss as the Primary and Sufficient Driver Event for Renal Angiomyolipoma Development.
PLoS genetics 2016 Aug 12 (8): e1006242. Giannikou Krinio, Malinowska Izabela A, Pugh Trevor J, Yan Rachel, Tseng Yuen-Yi, Oh Coyin, Kim Jaegil, Tyburczy Magdalena E, Chekaluk Yvonne, Liu Yang, Alesi Nicola, Finlay Geraldine A, Wu Chin-Lee, Signoretti Sabina, Meyerson Matthew, Getz Gad, Boehm Jesse S, Henske Elizabeth P, Kwiatkowski David |
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Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease.
Neurobiology of aging 2016 Jul . Lubbe S J, Escott-Price V, Brice A, Gasser T, Pittman A M, Bras J, Hardy J, Heutink P, Wood N M, Singleton A B, Grosset D G, Carroll C B, Law M H, Demenais F, Iles M M, , Bishop D T, Newton-Bishop J, Williams N M, Morris H R, |
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Risk of second primary cancers after malignant mesothelioma and vice versa.
Cancer letters 2016 May 379 (1): 94-99. Chen Tianhui, Kharazmi Elham, Lou Jianlin, Zhang Xing, Sundquist Kristina, Hemminki Ka |
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Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new era.
Critical reviews in oncology/hematology 2016 Apr 100 190-208. Pillai Suja, Gopalan Vinod, Smith Robert A, Lam Alfred K |
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BAP1 Germline Mutations in Finnish Patients with Uveal Melanoma.
Ophthalmology 2016 Feb . Turunen Joni A, Markkinen Salla, Wilska Rosi, Saarinen Silva, Raivio Virpi, Täll Martin, Lehesjoki Anna-Elina, Kivelä Tero |
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Genomic characterization of sarcomatoid transformation in clear cell renal cell carcinoma.
Proceedings of the National Academy of Sciences of the United States of America 2016 Feb . Bi Mark, Zhao Siming, Said Jonathan W, Merino Maria J, Adeniran Adebowale J, Xie Zuoquan, Nawaf Cayce B, Choi Jaehyuk, Belldegrun Arie S, Pantuck Allan J, Kluger Harriet M, Bilgüvar Kaya, Lifton Richard P, Shuch Bri |
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Cholangiocarcinoma Heterogeneity Revealed by Multigene Mutational Profiling: Clinical and Prognostic Relevance in Surgically Resected Patients.
Annals of surgical oncology 2015 Dec . Ruzzenente Andrea, Fassan Matteo, Conci Simone, Simbolo Michele, Lawlor Rita T, Pedrazzani Corrado, Capelli Paola, D'Onofrio Mirko, Iacono Calogero, Scarpa Aldo, Guglielmi Alfre |
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Germline BAP1 mutational landscape of asbestos-exposed malignant mesothelioma patients with family history of cancer.
Cancer research 2015 Dec . Ohar Jill A, Cheung Mitchell, Talarchek Jacqueline, Howard Suzanne E, Howard Timothy D, Hesdorffer Mary, Peng Hongzhuang, Rauscher Frank J, Testa Joseph |
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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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Metastatic disease in uveal melanoma: importance of a genetic profile?
Melanoma research 2015 Oct 25 (5): 447-9. Van Beek Jackelien G M, Koopmans Anna E, Vaarwater Jolanda, Verdijk Rob M, de Klein Annelies, Naus Nicole C, Kiliç Emi |
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Clinical Characteristics of Uveal Melanoma in Patients With Germline BAP1 Mutations.
JAMA ophthalmology 2015 Aug 133 (8): 881-7. Gupta Mrinali P, Lane Anne Marie, DeAngelis Margaret M, Mayne Katie, Crabtree Margaux, Gragoudas Evangelos S, Kim Ivana |
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Radiogenomics of clear cell renal cell carcinoma: preliminary findings of The Cancer Genome Atlas-Renal Cell Carcinoma (TCGA-RCC) Imaging Research Group.
Abdominal imaging 2015 Aug 40 (6): 1684-92. Shinagare Atul B, Vikram Raghu, Jaffe Carl, Akin Oguz, Kirby Justin, Huang Erich, Freymann John, Sainani Nisha I, Sadow Cheryl A, Bathala Tharakeswara K, Rubin Daniel L, Oto Aytekin, Heller Matthew T, Surabhi Venkateswar R, Katabathina Venkat, Silverman Stuart |
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Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma.
Gene 2015 May 563 (1): 103-5. Sneddon Sophie, Leon Justine S, Dick Ian M, Cadby Gemma, Olsen Nola, Brims Fraser, Allcock Richard J N, Moses Eric K, Melton Phillip E, de Klerk Nicholas, Musk A W Bill, Robinson Bruce W S, Creaney Jenet |
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Genomic analyses reveal mutational signatures and frequently altered genes in esophageal squamous cell carcinoma.
American journal of human genetics 2015 Apr 96 (4): 597-611. Zhang Ling, Zhou Yong, Cheng Caixia, Cui Heyang, Cheng Le, Kong Pengzhou, Wang Jiaqian, Li Yin, Chen Wenliang, Song Bin, Wang Fang, Jia Zhiwu, Li Lin, Li Yaoping, Yang Bin, Liu Jing, Shi Ruyi, Bi Yanghui, Zhang Yanyan, Wang Juan, Zhao Zhenxiang, Hu Xiaoling, Yang Jie, Li Hongyi, Gao Zhibo, Chen Gang, Huang Xuanlin, Yang Xukui, Wan Shengqing, Chen Chao, Li Bin, Tan Yongkai, Chen Longyun, He Minghui, Xie Sha, Li Xiangchun, Zhuang Xuehan, Wang Mengyao, Xia Zhi, Luo Longhai, Ma Jie, Dong Bing, Zhao Jiuzhou, Song Yongmei, Ou Yunwei, Li Enming, Xu Liyan, Wang Jinfen, Xi Yanfeng, Li Guodong, Xu Enwei, Liang Jianfang, Yang Xiaofeng, Guo Jiansheng, Chen Xing, Zhang Yanbo, Li Qingshan, Liu Lixin, Li Yingrui, Zhang Xiuqing, Yang Huanming, Lin Dongxin, Cheng Xiaolong, Guo Yongjun, Wang Jun, Zhan Qimin, Cui Yongpi |
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High Incidence of Somatic BAP1 alterations in sporadic malignant mesothelioma.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2015 Apr 10 (4): 565-76. Nasu Masaki, Emi Mitsuru, Pastorino Sandra, Tanji Mika, Powers Amy, Luk Hugh, Baumann Francine, Zhang Yu-An, Gazdar Adi, Kanodia Shreya, Tiirikainen Maarit, Flores Erin, Gaudino Giovanni, Becich Michael J, Pass Harvey I, Yang Haining, Carbone Miche |
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Prevalence of Germline BAP1, CDKN2A, and CDK4 Mutations in an Australian Population-Based Sample of Cutaneous Melanoma Cases.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2015 Apr 18 (2): 126-33. Aoude Lauren G, Gartside Michael, Johansson Peter, Palmer Jane M, Symmons Judith, Martin Nicholas G, Montgomery Grant W, Hayward Nicholas |
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Targeted next-generation sequencing of cancer genes in advanced stage malignant pleural mesothelioma: a retrospective study.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2015 Mar 10 (3): 492-9. Lo Iacono Marco, Monica Valentina, Righi Luisella, Grosso Federica, Libener Roberta, Vatrano Simona, Bironzo Paolo, Novello Silvia, Musmeci Loredana, Volante Marco, Papotti Mauro, Scagliotti Giorgio |
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Whole-genome copy-number analysis identifies new leads for chromosomal aberrations involved in the oncogenesis and metastastic behavior of uveal melanomas.
Melanoma research 2015 Mar . van Engen-van Grunsven Adriana C H, Baar Marjolein P, Pfundt Rolph, Rijntjes Jos, Küsters-Vandevelde Heidi V N, Delbecq Ann-Laure, Keunen Jan E, Klevering Jeroen B, Wesseling Pieter, Blokx Willeke A M, Groenen Patricia J T |
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Mesothelioma patients with germline BAP1 mutations have 7-fold improved long-term survival.
Carcinogenesis 2015 Jan 36 (1): 76-81. Baumann Francine, Flores Erin, Napolitano Andrea, Kanodia Shreya, Taioli Emanuela, Pass Harvey, Yang Haining, Carbone Miche |
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Prevalence of BRCA-1 associated protein 1 germline mutation in sporadic malignant pleural mesothelioma cases.
Lung cancer (Amsterdam, Netherlands) 2015 Jan 87 (1): 77-9. Rusch Andreas, Ziltener Gabriela, Nackaerts Kristiaan, Weder Walter, Stahel Rolf A, Felley-Bosco Emanue |
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Whole-exome sequencing reveals frequent genetic alterations in BAP1, NF2, CDKN2A, and CUL1 in malignant pleural mesothelioma.
Cancer research 2015 Jan 75 (2): 264-9. Guo Guangwu, Chmielecki Juliann, Goparaju Chandra, Heguy Adriana, Dolgalev Igor, Carbone Michele, Seepo Sara, Meyerson Matthew, Pass Harvey |
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Gender Specific Mutation Incidence and Survival Associations in Clear Cell Renal Cell Carcinoma (CCRCC).
PloS one 2015 10 (10): e0140257. Ricketts Christopher J, Linehan W Marst |
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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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Patterns and functional implications of rare germline variants across 12 cancer types.
Nature communications 2015 6 10086. Lu Charles, Xie Mingchao, Wendl Michael C, Wang Jiayin, McLellan Michael D, Leiserson Mark D M, Huang Kuan-Lin, Wyczalkowski Matthew A, Jayasinghe Reyka, Banerjee Tapahsama, Ning Jie, Tripathi Piyush, Zhang Qunyuan, Niu Beifang, Ye Kai, Schmidt Heather K, Fulton Robert S, McMichael Joshua F, Batra Prag, Kandoth Cyriac, Bharadwaj Maheetha, Koboldt Daniel C, Miller Christopher A, Kanchi Krishna L, Eldred James M, Larson David E, Welch John S, You Ming, Ozenberger Bradley A, Govindan Ramaswamy, Walter Matthew J, Ellis Matthew J, Mardis Elaine R, Graubert Timothy A, Dipersio John F, Ley Timothy J, Wilson Richard K, Goodfellow Paul J, Raphael Benjamin J, Chen Feng, Johnson Kimberly J, Parvin Jeffrey D, Ding |
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Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity.
Nature communications 2015 6 6120. Fujimoto Akihiro, Furuta Mayuko, Shiraishi Yuichi, Gotoh Kunihito, Kawakami Yoshiiku, Arihiro Koji, Nakamura Toru, Ueno Masaki, Ariizumi Shun-ichi, Nguyen Ha Hai, Shigemizu Daichi, Abe Tetsuo, Boroevich Keith A, Nakano Kaoru, Sasaki Aya, Kitada Rina, Maejima Kazihiro, Yamamoto Yujiro, Tanaka Hiroko, Shibuya Tetsuo, Shibata Tatsuhiro, Ojima Hidenori, Shimada Kazuaki, Hayami Shinya, Shigekawa Yoshinobu, Aikata Hiroshi, Ohdan Hideki, Marubashi Shigeru, Yamada Terumasa, Kubo Michiaki, Hirano Satoshi, Ishikawa Osamu, Yamamoto Masakazu, Yamaue Hiroki, Chayama Kazuaki, Miyano Satoru, Tsunoda Tatsuhiko, Nakagawa Hidewa |
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Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2014 Oct 27 (10): 1321-30. Koopmans Anna E, Verdijk Robert M, Brouwer Rutger W W, van den Bosch Thierry P P, van den Berg Mike M P, Vaarwater Jolanda, Kockx Christel E M, Paridaens Dion, Naus Nicole C, Nellist Mark, van IJcken Wilfred F J, Kiliç Emine, de Klein Anneli |
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Concurrent alterations in TERT, KDM6A, and the BRCA pathway in bladder cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2014 Sep 20 (18): 4935-48. Nickerson Michael L, Dancik Garrett M, Im Kate M, Edwards Michael G, Turan Sevilay, Brown Joseph, Ruiz-Rodriguez Christina, Owens Charles, Costello James C, Guo Guangwu, Tsang Shirley X, Li Yingrui, Zhou Quan, Cai Zhiming, Moore Lee E, Lucia M Scott, Dean Michael, Theodorescu D |
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A specific missense mutation in GTF2I occurs at high frequency in thymic epithelial tumors.
Nature genetics 2014 Aug 46 (8): 844-9. Petrini Iacopo, Meltzer Paul S, Kim In-Kyu, Lucchi Marco, Park Kang-Seo, Fontanini Gabriella, Gao James, Zucali Paolo A, Calabrese Fiorella, Favaretto Adolfo, Rea Federico, Rodriguez-Canales Jaime, Walker Robert L, Pineda Marbin, Zhu Yuelin J, Lau Christopher, Killian Keith J, Bilke Sven, Voeller Donna, Dakshanamurthy Sivanesan, Wang Yisong, Giaccone Giusep |
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Chromosome 3 status combined with BAP1 and EIF1AX mutation profiles are associated with metastasis in uveal melanoma.
Investigative ophthalmology & visual science 2014 Aug 55 (8): 5160-7. Ewens Kathryn G, Kanetsky Peter A, Richards-Yutz Jennifer, Purrazzella Juliana, Shields Carol L, Ganguly Tapan, Ganguly Aru |
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Identification of novel therapeutic targets in the PI3K/AKT/mTOR pathway in hepatocellular carcinoma using targeted next generation sequencing.
Oncotarget 2014 May 5 (10): 3012-22. Janku Filip, Kaseb Ahmed O, Tsimberidou Apostolia M, Wolff Robert A, Kurzrock Razel |
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Multigene mutational profiling of cholangiocarcinomas identifies actionable molecular subgroups.
Oncotarget 2014 May 5 (9): 2839-52. Simbolo Michele, Fassan Matteo, Ruzzenente Andrea, Mafficini Andrea, Wood Laura D, Corbo Vincenzo, Melisi Davide, Malleo Giuseppe, Vicentini Caterina, Malpeli Giorgio, Antonello Davide, Sperandio Nicola, Capelli Paola, Tomezzoli Anna, Iacono Calogero, Lawlor Rita T, Bassi Claudio, Hruban Ralph H, Guglielmi Alfredo, Tortora Giampaolo, de Braud Filippo, Scarpa Al |
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BAP1 immunohistochemistry predicts outcomes in a multi-institutional cohort with clear cell renal cell carcinoma.
The Journal of urology 2014 Mar 191 (3): 603-10. Kapur Payal, Christie Alana, Raman Jay D, Then Matthew T, Nuhn Philipp, Buchner Alexander, Bastian Patrick, Seitz Christian, Shariat Shahrokh F, Bensalah Karim, Rioux-Leclercq Nathalie, Xie Xian-Jin, Lotan Yair, Margulis Vitaly, Brugarolas Jam |
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Whole-exome sequencing of pancreatic neoplasms with acinar differentiation.
The Journal of pathology 2014 Mar 232 (4): 428-35. Jiao Yuchen, Yonescu Raluca, Offerhaus G Johan A, Klimstra David S, Maitra Anirban, Eshleman James R, Herman James G, Poh Weijie, Pelosof Lorraine, Wolfgang Christopher L, Vogelstein Bert, Kinzler Kenneth W, Hruban Ralph H, Papadopoulos Nickolas, Wood Laura |
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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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Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter in a single case of uveal melanoma.
British journal of cancer 2014 Feb 110 (4): 1058-65. Dono M, Angelini G, Cecconi M, Amaro A, Esposito A I, Mirisola V, Maric I, Lanza F, Nasciuti F, Viaggi S, Gualco M, Bandelloni R, Truini M, Coviello D A, Zupo S, Mosci C, Pfeffer |
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Radiogenomics of clear cell renal cell carcinoma: associations between CT imaging features and mutations.
Radiology 2014 Feb 270 (2): 464-71. Karlo Christoph A, Di Paolo Pier Luigi, Chaim Joshua, Hakimi A Ari, Ostrovnaya Irina, Russo Paul, Hricak Hedvig, Motzer Robert, Hsieh James J, Akin Og |
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Clinical and pathological impact of VHL, PBRM1, BAP1, SETD2, KDM6A, and JARID1c in clear cell renal cell carcinoma.
Genes, chromosomes & cancer 2014 Jan 53 (1): 38-51. Gossage Lucy, Murtaza Muhammed, Slatter Andrew F, Lichtenstein Conrad P, Warren Anne, Haynes Beverley, Marass Francesco, Roberts Ian, Shanahan Susan J, Claas Andreas, Dunham Andrew, May Andrew P, Rosenfeld Nitzan, Forshew Tim, Eisen T |
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Mutation profiling in cholangiocarcinoma: prognostic and therapeutic implications.
PloS one 2014 9 (12): e115383. Churi Chaitanya R, Shroff Rachna, Wang Ying, Rashid Asif, Kang HyunSeon C, Weatherly Jacqueline, Zuo Mingxin, Zinner Ralph, Hong David, Meric-Bernstam Funda, Janku Filip, Crane Christopher H, Mishra Lopa, Vauthey Jean-Nicholas, Wolff Robert A, Mills Gordon, Javle Mili |
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Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers.
Nature genetics 2013 Dec 45 (12): 1474-8. Chan-On Waraporn, Nairismägi Maarja-Liisa, Ong Choon Kiat, Lim Weng Khong, Dima Simona, Pairojkul Chawalit, Lim Kiat Hon, McPherson John R, Cutcutache Ioana, Heng Hong Lee, Ooi London, Chung Alexander, Chow Pierce, Cheow Peng Chung, Lee Ser Yee, Choo Su Pin, Tan Iain Bee Huat, Duda Dan, Nastase Anca, Myint Swe Swe, Wong Bernice Huimin, Gan Anna, Rajasegaran Vikneswari, Ng Cedric Chuan Young, Nagarajan Sanjanaa, Jusakul Apinya, Zhang Shenli, Vohra Priya, Yu Willie, Huang DaChuan, Sithithaworn Paiboon, Yongvanit Puangrat, Wongkham Sopit, Khuntikeo Narong, Bhudhisawasdi Vajaraphongsa, Popescu Irinel, Rozen Steven G, Tan Patrick, Teh Bin Te |
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Clinical characteristics of patients with malignant pleural mesothelioma harboring somatic BAP1 mutations.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2013 Nov 8 (11): 1430-3. Zauderer Marjorie G, Bott Matthew, McMillan Robert, Sima Camelia S, Rusch Valerie, Krug Lee M, Ladanyi Ma |
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A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma.
Molecular cancer research : MCR 2013 Sep 11 (9): 1061-71. Farley Megan N, Schmidt Laura S, Mester Jessica L, Peña-Llopis Samuel, Pavia-Jimenez Andrea, Christie Alana, Vocke Cathy D, Ricketts Christopher J, Peterson James, Middelton Lindsay, Kinch Lisa, Grishin Nick, Merino Maria J, Metwalli Adam R, Xing Chao, Xie Xian-Jin, Dahia Patricia L M, Eng Charis, Linehan W Marston, Brugarolas Jam |
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Adverse outcomes in clear cell renal cell carcinoma with mutations of 3p21 epigenetic regulators BAP1 and SETD2: a report by MSKCC and the KIRC TCGA research network.
Clinical cancer research : an official journal of the American Association for Cancer Research 2013 Jun 19 (12): 3259-67. Hakimi A Ari, Ostrovnaya Irina, Reva Boris, Schultz Nikolaus, Chen Ying-Bei, Gonen Mithat, Liu Han, Takeda Shugaku, Voss Martin H, Tickoo Satish K, Reuter Victor E, Russo Paul, Cheng Emily H, Sander Chris, Motzer Robert J, Hsieh James J, |
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Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma cases.
Pigment cell & melanoma research 2013 Mar 26 (2): 278-9. Aoude Lauren G, Vajdic Claire M, Kricker Anne, Armstrong Bruce, Hayward Nicholas |
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Effects on survival of BAP1 and PBRM1 mutations in sporadic clear-cell renal-cell carcinoma: a retrospective analysis with independent validation.
The Lancet. Oncology 2013 Feb 14 (2): 159-67. Kapur Payal, Peña-Llopis Samuel, Christie Alana, Zhrebker Leah, Pavía-Jiménez Andrea, Rathmell W Kimryn, Xie Xian-Jin, Brugarolas Jam |
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Clinical and Pathologic Impact of Select Chromatin-modulating Tumor Suppressors in Clear Cell Renal Cell Carcinoma.
European urology 2012 Sep . Hakimi AA, Chen YB, Wren J, Gonen M, Abdel-Wahab O, Heguy A, Liu H, Takeda S, Tickoo SK, Reuter VE, Voss MH, Motzer RJ, Coleman JA, Cheng EH, Russo P, Hsieh JJ |
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BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs.
Journal of translational medicine 2012 Aug 10 (1): 1. Carbone M, Korb Ferris L, Baumann F, Napolitano A, Lum CA, Flores EG, Gaudino G, Powers A, Bryant-Greenwood P, Krausz T, Hyjek E, Tate R, Friedberg J, Weigel T, Pass HI, Yang H |
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Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families.
PloS one 2012 7 (4): e35295. Njauw Ching-Ni Jenny, Kim Ivana, Piris Adriano, Gabree Michele, Taylor Michael, Lane Anne Marie, DeAngelis Margaret M, Gragoudas Evangelos, Duncan Lyn M, Tsao Hens |
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Pathway-based analysis of genetic susceptibility to cervical cancer in situ: HLA-DPB1 affects risk in Swedish women.
Genes and immunity 2011 Dec 12 (8): 605-14. Ivansson E L, Juko-Pecirep I, Erlich H A, Gyllensten U |
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Single nucleotide polymorphisms in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high-risk women.
International journal of cancer. Journal international du cancer 2010 Aug 127 (3): 589-97. Kontorovich Tair, Levy Asaf, Korostishevsky Michael, Nir Uri, Friedman Eit |
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Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants.
Cancer prevention research (Philadelphia, Pa.) 2009 Jul 2 (7): 617-24. Wu Xifeng, Spitz Margaret R, Lee J Jack, Lippman Scott M, Ye Yuanqing, Yang Hushan, Khuri Fadlo R, Kim Edward, Gu Jian, Lotan Reuben, Hong Waun |
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Genetic sequence variations of BRCA1-interacting genes AURKA, BAP1, BARD1 and DHX9 in French Canadian families with high risk of breast cancer.
Journal of human genetics 2009 Mar 54 (3): 152-61. Guénard Frédéric, Labrie Yvan, Ouellette Geneviève, Beauparlant Charles Joly, Durocher Francine, |
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Evaluating new candidate SNPs as low penetrance risk factors in sporadic breast cancer: a two-stage Spanish case-control study.
Gynecologic oncology 2009 Jan 112 (1): 210-4. Vega Ana, Salas Antonio, Milne Roger L, Carracedo Begoña, Ribas Gloria, Ruibal Alvaro, de León Antonio Cabrera, González-Hernández Ana, Benítez Javier, Carracedo Ang |
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