Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 39 Records) |
| Query Trace: Neoplasms and SDHB[original query] |
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| Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. JAMA oncology 2015 Apr 1 (1): 23-32. Hansford Samantha, Kaurah Pardeep, Li-Chang Hector, Woo Michelle, Senz Janine, Pinheiro Hugo, Schrader Kasmintan A, Schaeffer David F, Shumansky Karey, Zogopoulos George, Santos Teresa Almeida, Claro Isabel, Carvalho Joana, Nielsen Cydney, Padilla Sarah, Lum Amy, Talhouk Aline, Baker-Lange Katie, Richardson Sue, Lewis Ivy, Lindor Noralane M, Pennell Erin, MacMillan Andree, Fernandez Bridget, Keller Gisella, Lynch Henry, Shah Sohrab P, Guilford Parry, Gallinger Steven, Corso Giovanni, Roviello Franco, Caldas Carlos, Oliveira Carla, Pharoah Paul D P, Huntsman David |
| Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis. International journal of endocrinology 2015 2015 138573. Luchetti Andrea, Walsh Diana, Rodger Fay, Clark Graeme, Martin Tom, Irving Richard, Sanna Mario, Yao Masahiro, Robledo Mercedes, Neumann Hartmut P H, Woodward Emma R, Latif Farida, Abbs Stephen, Martin Howard, Maher Eamonn |
| Familiar Papillary Thyroid Carcinoma in a Large Brazilian Family Is Not Associated with Succinate Dehydrogenase Defects. European thyroid journal 2016 Jul 5 (2): 94-9. Accordi Elen Dias, Xekouki Paraskevi, Azevedo Bruna, de Alexandre Rodrigo Bertollo, Frasson Carla, Gantzel Siliane Marie, Papadakis Georgios Z, Angelousi Anna, Stratakis Constantine A, Sotomaior Vanessa Santos, Faucz Fabio |
| Molecular cytology genotyping of primary and metastatic GI stromal tumors by using a custom two-gene targeted next-generation sequencing panel with therapeutic intent. Gastrointestinal endoscopy 2016 Apr . Gleeson Ferga C, Kerr Sarah E, Kipp Benjamin R, Voss Jesse S, Minot Douglas M, Tu Zheng Jin, Henry Michael R, Vasmatzis George, Cheville John C, Lazaridis Konstantinos N, Levy Michael |
| Clinical management of pheochromocytoma and paraganglioma in Singapore: missed opportunities for genetic testing. Molecular genetics & genomic medicine 2017 9 5 (5): 602-607. Chew Winston Hong Wern, Courtney Eliza, Lim Kok Hing, Li Shao Tzu, Chen Yanni, Tan Min Han, Chung Alexander, Khoo Joan, Loh Amos, Soh Shui Yen, Iyer Prasad, Loh Lih Ming, Ngeow Joan |
| Bayesian approach to determining penetrance of pathogenic SDH variants. Journal of medical genetics 2018 Sep . Benn Diana E, Zhu Ying, Andrews Katrina A, Wilding Mathilda, Duncan Emma L, Dwight Trisha, Tothill Richard W, Burgess John, Crook Ashley, Gill Anthony J, Hicks Rodney J, Kim Edward, Luxford Catherine, Marfan Helen, Richardson Anne Louise, Robinson Bruce, Schlosberg Arran, Susman Rachel, Tacon Lyndal, Trainer Alison, Tucker Katherine, Maher Eamonn R, Field Michael, Clifton-Bligh Roderick |
| Prevalence of Germline Mutations in Cancer Susceptibility Genes in Patients With Advanced Renal Cell Carcinoma. JAMA oncology 2018 7 4 (9): 1228-1235. Carlo Maria I, Mukherjee Semanti, Mandelker Diana, Vijai Joseph, Kemel Yelena, Zhang Liying, Knezevic Andrea, Patil Sujata, Ceyhan-Birsoy Ozge, Huang Kuo-Cheng, Redzematovic Almedina, Coskey Devyn T, Stewart Carolyn, Pradhan Nisha, Arnold Angela G, Hakimi A Ari, Chen Ying-Bei, Coleman Jonathan A, Hyman David M, Ladanyi Marc, Cadoo Karen A, Walsh Michael F, Stadler Zsofia K, Lee Chung-Han, Feldman Darren R, Voss Martin H, Robson Mark, Motzer Robert J, Offit Kenne |
| Telomerase Activation and ATRX Mutations Are Independent Risk Factors for Metastatic Pheochromocytoma and Paraganglioma. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 10 25 (2): 760-770. Job Sylvie, Draskovic Irena, Burnichon Nelly, Buffet Alexandre, Cros Jérôme, Lépine Charles, Venisse Annabelle, Robidel Estelle, Verkarre Virginie, Meatchi Tchao, Sibony Mathilde, Amar Laurence, Bertherat Jérôme, de Reyniès Aurélien, Londoño-Vallejo Arturo, Favier Judith, Castro-Vega Luis Jaime, Gimenez-Roqueplo Anne-Pau |
| Patterns of Mutation Enrichment in Metastatic Triple-Negative Breast Cancer. Clinical Medicine Insights. Oncology 2019 13 1179554919868482. Saravia César H, Flores Claudio, Schwarz Luis J, Bravo Leny, Zavaleta Jenny, Araujo Jhajaira, Neciosup Silvia, Pinto Joseph |
| Loss of BAP1 in Pheochromocytomas and Paragangliomas Seems Unrelated to Genetic Mutations. Endocrine pathology 2019 11 30 (4): 276-284. Maffeis Valeria, Cappellesso Rocco, Nicolè Lorenzo, Guzzardo Vincenza, Menin Chiara, Elefanti Lisa, Schiavi Francesca, Guido Maria, Fassina Ambrog |
| The Impact Of Succinate Dehydrogenase Gene (SDH) Mutations In Renal Cell Carcinoma (RCC): A Systematic Review. OncoTargets and therapy 2019 10 12 7929-7940. Aghamir Seyed Mohammad Kazem, Heshmat Ramin, Ebrahimi Mehdi, Ketabchi Seyed Ebrahim, Parichehreh Dizaji Somayeh, Khatami Fatem |
| Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients. Human genetics 2020 7 140 (2): 321-331. Horiuchi Yasue, Matsubayashi Hiroyuki, Kiyozumi Yoshimi, Nishimura Seiichiro, Higashigawa Satomi, Kado Nobuhiro, Nagashima Takeshi, Mizuguchi Maki, Ohnami Sumiko, Arai Makoto, Urakami Kenichi, Kusuhara Masatoshi, Yamaguchi K |
| High-Throughput Sequencing of Gastric Cancer Patients: Unravelling Genetic Predispositions Towards an Early-Onset Subtype. Cancers 2020 7 12 (7): . Machlowska Julita, Kapusta Przemys?aw, Baj Jacek, Morsink Folkert H M, Wo?kow Pawe?, Maciejewski Ryszard, Offerhaus G Johan A, Sitarz Robe |
| Ancestry-specific predisposing germline variants in cancer. Genome medicine 2020 5 12 (1): 51. Oak Ninad, Cherniack Andrew D, Mashl R Jay, , Hirsch Fred R, Ding Li, Beroukhim Rameen, Gümü? Zeynep H, Plon Sharon E, Huang Kuan-L |
| A long noncoding RNA-microRNA expression signature predicts metastatic signature in pheochromocytomas and paragangliomas. Endocrine 2021 9 75 (1): 244-253. Ghosal Suman, Zhu Boqun, Huynh Thanh-Truc, Meuter Leah, Jha Abhishek, Talvacchio Sara, Knue Marianne, Patel Mayank, Prodanov Tamara, Das Shaoli, Zeiger Martha A, Nilubol Naris, Shankavaram Uma T, Taieb David, Pacak Kar |
| LncRNA expression and SDHB mutations in pheochromocytomas and paragangliomas. Annals of diagnostic pathology 2021 8 55 151801. Li Huihua, Hardin Heather, Zaeem Misbah, Huang Wei, Hu Rong, Lloyd Ricardo |
| Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. JNCI cancer spectrum 2021 7 5 (2): . Kim Jung, Gianferante Matthew, Karyadi Danielle M, Hartley Stephen W, Frone Megan N, Luo Wen, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Dean Michael, Yeager Meredith, Zhu Bin, Song Lei, Sampson Joshua N, Yasui Yutaka, Leisenring Wendy M, Brodie Seth A, de Andrade Kelvin C, Fortes Fernanda P, Goldstein Alisa M, Khincha Payal P, Machiela Mitchell J, McMaster Mary L, Nickerson Michael L, Oba Leatrisse, Pemov Alexander, Pinheiro Maisa, Rotunno Melissa, Santiago Karina, Wegman-Ostrosky Talia, Diver W Ryan, Teras Lauren, Freedman Neal D, Hicks Belynda D, Zhu Bin, Wang Mingyi, Jones Kristine, Hutchinson Amy A, Dagnall Casey, Savage Sharon A, Tucker Margaret A, Chanock Stephen J, Morton Lindsay M, Stewart Douglas R, Mirabello Li |
| Mutation Profile of Aggressive Pheochromocytoma and Paraganglioma with Comparison of TCGA Data. Cancers 2021 May 13 (10): . Choi Yun Mi, Lim Jinyeong, Jeon Min Ji, Lee Yu-Mi, Sung Tae-Yon, Hong Eun-Gyoung, Lee Ji-Young, Jang Se Jin, Kim Won Gu, Song Dong Eun, Chun Sung-M |
| Pseudohypoxic pheochromocytomas and paragangliomas dominate in children. Pediatric blood & cancer 2021 3 68 (7): e28981. Redlich Antje, Pamporaki Christina, Lessel Lienhard, Frühwald Michael C, Vorwerk Peter, Kuhlen Michae |
| Case Report: Genetic Alterations Associated with the Progression of Carotid Paraganglioma. Current issues in molecular biology 2021 12 43 (3): 2266-2275. Pavlov Vladislav, Snezhkina Anastasiya, Kalinin Dmitry, Golovyuk Alexander, Kobelyatskaya Anastasiya, Bakhtogarimov Ildar, Volchenko Nadezhda, Krasnov George, Kudryavtseva An |
| Papillary Thyroid Cancer and a TERT Promotor Mutation-positive Paraganglioma in a Patient With a Germline SDHB Mutation. Journal of the Endocrine Society 2022 6 6 (7): bvac076. Alzahrani Ali S, Alswailem Meshael, Murugan Avaniyapuram Kannan, Alghamdi Balgees, Al-Hindi Hin |
| Genomic and Metabolic Hallmarks of SDH- and FH-deficient Renal Cell Carcinomas. European urology focus 2022 3 8 (5): 1278-1288. Yoo Angela, Tang Cerise, Zucker Mark, Fitzgerald Kelly, DiNatale Renzo G, Rappold Phillip M, Weiss Kate, Freeman Benjamin, Lee Chung-Han, Schultz Nikolaus, Motzer Robert, Russo Paul, Coleman Jonathan, Reuter Victor E, Chen Ying-Bei, Carlo Maria I, Gill Anthony J, Kotecha Ritesh R, Ari Hakimi A, Reznik |
| Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disorders. Journal of medical genetics 2022 11 . Carrasco Estela, López-Fernández Adrià, Codina-Sola Marta, Valenzuela Irene, Cueto-González A M, Villacampa Guillermo, Navarro Victor, Torres-Esquius Sara, Palau Dolors, Cruellas Mara, Torres Maite, Perez-Dueñas Belen, Abulí Anna, Diez Orland, Sábado-Álvarez Constantino, García-Arumí Elena, Tizzano Eduardo F, Moreno Lucas, Balmaña Judi |
| TNM Staging and Overall Survival in Patients with Pheochromocytoma and Sympathetic Paraganglioma. The Journal of clinical endocrinology and metabolism 2022 11 . Jimenez Camilo, Ma Junsheng, Roman Gonzalez Alejandro, Varghese Jeena, Zhang Miao, Perrier Nancy, Habra Mouhammed Amir, Graham Paul, Waguespack Steven |
| Prevalence of germline mutations in cancer susceptibility genes in Chinese patients with renal cell carcinoma. Translational andrology and urology 2023 3 12 (2): 308-319. Feng Huayi, Cao Shouqing, Ouyang Qing, Li Huaikang, Li Xiubin, Chen Ke, Zhang Xiangyi, Huang Yan, Zhang Xu, Ma X |
| SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas. Frontiers in genetics 2023 1 13 999329. Manotas María Carolina, Rivera Ana Lucía, Gómez Ana Milena, Abisambra Patricia, Guevara Gonzalo, Medina Vilma, Tapiero Sandra, Huertas Antonio, Riaño-Moreno Julián, Mejía Juan Carlos, Gonzalez-Clavijo Angélica María, Tapiero-García Mireya, Cuéllar-Cuéllar Andrés Arturo, Fierro-Maya Luis Felipe, Sanabria-Salas María Caroli |
| Expanded genetic testing of GIST patients identifies high proportion of non-syndromic patients with germline alterations. NPJ precision oncology 2023 1 7 (1): 1. Mandelker Diana, Marra Antonio, Mehta Nikita, Selenica Pier, Yelskaya Zarina, Yang Ciyu, Somar Joshua, Mehine Miika, Misyura Maksym, Basturk Olca, Latham Alicia, Carlo Maria, Walsh Michael, Stadler Zsofia K, Offit Kenneth, Bandlamudi Chaitanya, Hameed Meera, Chi Ping, Reis-Filho Jorge S, Ceyhan-Birsoy Oz |
| Personalized management for phaeochromocytomas and paragangliomas in Latin America: A genetic perspective. Best practice & research. Clinical endocrinology & metabolism 2024 9 101922. Felipe Freitas-Castro, Madson Q Almei |
| The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory. Cancer genomics & proteomics 2024 8 21 (5): 448-463. Nikolaos Tsoulos, Konstantinos Agiannitopoulos, Kevisa Potska, Anastasia Katseli, Christina Ntogka, Georgia Pepe, Dimitra Bouzarelou, Athanasios Papathanasiou, Dimitrios Grigoriadis, Georgios N Tsaousis, Helen Gogas, Theodore Troupis, Konstantinos Papazisis, Ioannis Natsiopoulos, Vassileios Venizelos, Kyriakos Amarantidis, Stylianos Giassas, Christos Papadimitriou, Elena Fountzilas, Maroulio Stathoulopoulou, Anna Koumarianou, Grigorios Xepapadakis, Alexandru Blidaru, Daniela Zob, Oana Voinea, Mustafa Özdo?an, Mahmut Çerkez Ergören, Alinta Hegmane, Eirini Papadopoulou, George Nasioulas, Christos Markopoul |
| Molecular and clinicopathological features of KIT/PDGFRA wild-type gastrointestinal stromal tumors. Cancer science 2024 1 . Toshirou Nishida, Yoichi Naito, Tsuyoshi Takahashi, Takuro Saito, Shigeo Hisamori, Dai Manaka, Katsuhiro Ogawa, Seiichi Hirota, Hitoshi Ichika |
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