HuGE Literature Finder
Records 1-30
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Clinical Impact of Somatic Variants in Homologous Recombination Repair-Related Genes in Ovarian High-Grade Serous Carcinoma.
Cancer research and treatment : official journal of Korean Cancer Association 2020 Jan . Choi Min Chul, Hwang Sohyun, Kim Sewha, Jung Sang Geun, Park Hyun, Joo Won Duk, Song Seung Hun, Lee Chan, Kim Tae-Heon, Kang Haeyoun, An Hee Ju |
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Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma.
Genetics in medicine : official journal of the American College of Medical Genetics 2019 Dec . Nassar Amin H, Abou Alaiwi Sarah, AlDubayan Saud H, Moore Nicholas, Mouw Kent W, Kwiatkowski David J, Choueiri Toni K, Curran Catherine, Berchuck Jacob E, Harshman Lauren C, Nuzzo Pier V, Chanza Nieves Martinez, Van Allen Eliezer, Esplin Edward D, Yang Shan, Callis Thomas, Garber Judy E, Rana Huma Q, Sonpavde Gu |
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Molecular classification of endometrial carcinoma applied to endometrial biopsy specimens: Towards early personalized patient management.
Gynecologic oncology 2019 Jun . Abdulfatah Eman, Wakeling Erin, Sakr Sharif, Al-Obaidy Khaleel, Bandyopadhyay Sudeshna, Morris Robert, Feldman Gerald, Ali-Fehmi Rou |
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Microsatellite Instability Occurs in a Subset of Follicular Thyroid Cancers.
Thyroid : official journal of the American Thyroid Association 2019 Feb . Genutis Luke K, Tomsic Jerneja, Bundschuh Ralf, Brock Pamela, Williams Michelle D, Roychowdhury Sameek, Reeser Julie W, Frankel Wendy L, Alsomali Mohammed, Routbort Mark J, Broaddus Russell R, Wakely Paul E, Phay John E, Walker Christopher J, de la Chapelle Albe |
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Mutational profiles of persistent/recurrent laryngeal squamous cell carcinoma.
Head & neck 2019 Feb 41 (2): 423-428. Smith Joshua D, Birkeland Andrew C, Rosko Andrew J, Hoesli Rebecca C, Foltin Susan K, Swiecicki Paul, Mierzwa Michelle, Chinn Steven B, Shuman Andrew G, Malloy Kelly M, Casper Keith A, McLean Scott A, Wolf Gregory T, Bradford Carol R, Prince Mark E, Brenner John Chad, Spector Matthew |
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Rs2303428 of MSH2 Is Associated with Hepatocellular Carcinoma Prognosis in a Chinese Population.
DNA and cell biology 2018 Jun . Zhu Xiaonian, Wang Zhigang, Qiu Xiaoqiang, Wang Weiwei, Bei Chunhua, Tan Chao, Qin Linyuan, Ren Yuan, Tan Shengk |
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Polymorphisms in DNA mismatch repair pathway genes predict toxicity and response to cisplatin chemoradiation in head and neck squamous cell carcinoma patients.
Oncotarget 2018 07 9 (51): 29538-29547. Nogueira Guilherme Augusto Silva, Costa Ericka Francislaine Dias, Lopes-Aguiar Leisa, Lima Tathiane Regine Penna, Visacri Marília Berlofa, Pincinato Eder Carvalho, Lourenço Gustavo Jacob, Calonga Luciane, Mariano Fernanda Viviane, Altemani Albina Messias de Almeida Milani, Altemani João Maurício Carrasco, Moriel Patrícia, Chone Carlos Takahiro, Ramos Celso Dario, Lima Carmen Silvia Pass |
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Clinicopathologic and Molecular Characteristics of Synchronous Colorectal Carcinoma With Mismatch Repair Deficiency.
The American journal of surgical pathology 2017 Sep . Nakano Kayoko, Yamamoto Hidetaka, Fujiwara Minako, Koga Yutaka, Tsuruta Shinichi, Ihara Eikichi, Oki Eiji, Nakamura Masafumi, Ogawa Yoshihiro, Oda Yoshin |
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Single-Nucleotide Polymorphisms of the MSH2 and MLH1 Genes, Potential Molecular Markers for Susceptibility to the Development of Basal Cell Carcinoma in the Brazilian Population.
Pathology oncology research : POR 2017 Jun . da Silva Calixto Poliane, Lopes Otávio Sérgio, Dos Santos Maia Mayara, Herrero Sylvia Satomi Takeno, Longui Carlos Alberto, Melo Cynthia Germoglio Farias, de Carvalho Filho Ivan Rodrigues, Soares Leonardo Ferreira, de Medeiros Arnaldo Correia, Delatorre Plínio, Khayat André Salim, Burbano Rommel Rodriguez, Lima Eleonidas Mou |
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High-risk epithelial ovarian cancer patients for hereditary ovarian cancer.
The journal of obstetrics and gynaecology research 2017 Feb . Chirasophon Seksit, Manchana Tarinee, Teerapakpinyo Chinacho |
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Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2016 Nov 29 (11): 1381-1389. Ring Kari L, Bruegl Amanda S, Allen Brian A, Elkin Eric P, Singh Nanda, Hartman Anne-Renee, Daniels Molly S, Broaddus Russell |
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Contribution of rare germline copy number variations and common susceptibility loci in Lynch Syndrome patients negative for mutations in the mismatch repair genes.
International journal of cancer. Journal international du cancer 2015 Dec . Villacis Rolando A R, Miranda Priscila M, Gomy Israel, Santos Erika M M, Carraro Dirce M, Achatz Maria I, Rossi Benedito M, Rogatto Silvia |
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Inherited Mutations in Women With Ovarian Carcinoma.
JAMA oncology 2015 Dec 1-9. Norquist Barbara M, Harrell Maria I, Brady Mark F, Walsh Tom, Lee Ming K, Gulsuner Suleyman, Bernards Sarah S, Casadei Silvia, Yi Qian, Burger Robert A, Chan John K, Davidson Susan A, Mannel Robert S, DiSilvestro Paul A, Lankes Heather A, Ramirez Nilsa C, King Mary Claire, Swisher Elizabeth M, Birrer Michael |
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Mutational landscape of MCPyV-positive and MCPyV-negative merkel cell carcinomas with implications for immunotherapy.
Oncotarget 2015 Dec . Goh Gerald, Walradt Trent, Markarov Vladimir, Blom Astrid, Riaz Nadeem, Doumani Ryan, Stafstrom Krista, Moshiri Ata, Yelistratova Lola, Levinsohn Jonathan, Chan Timothy A, Nghiem Paul, Lifton Richard P, Choi Jaehy |
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Association between genetic polymorphisms in DNA mismatch repair-related genes with risk and prognosis of head and neck squamous cell carcinoma.
International journal of cancer. Journal international du cancer 2015 Aug 137 (4): 810-8. Nogueira Guilherme Augusto Silva, Lourenço Gustavo Jacob, Oliveira Camila Borges Martins, Marson Fernando Augusto Lima, Lopes-Aguiar Leisa, Costa Ericka Francislaine Dias, Lima Tathiane Regine Penna, Liutti Vitor Teixeira, Leal Frederico, Santos Vivian Castro Antunes, Rinck-Junior José Augusto, Lima Carmen Silvia Pass |
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Microsatellite instability in gallbladder carcinoma.
Virchows Archiv : an international journal of pathology 2015 Apr 466 (4): 393-402. Moy Andrea P, Shahid Mohammad, Ferrone Cristina R, Borger Darrell R, Zhu Andrew X, Ting David, Deshpande Vikr |
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KRAS and BRAF gene mutations and DNA mismatch repair status in Chinese colorectal carcinoma patients.
World journal of gastroenterology : WJG 2015 Feb 21 (5): 1595-605. Ye Ju-Xiang, Liu Yan, Qin Yun, Zhong Hao-Hao, Yi Wei-Ning, Shi Xue-Yi |
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BRAFV600E immunohistochemistry in conjunction with mismatch repair status predicts survival in patients with colorectal cancer.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2014 May 27 (5): 644-50. Toon Christopher W, Chou Angela, DeSilva Keshani, Chan Joseph, Patterson Jillian, Clarkson Adele, Sioson Loretta, Jankova Lucy, Gill Anthony |
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Molecular and clinical characteristics of MSH6 germline variants detected in colorectal cancer patients.
Oncology reports 2013 Dec 30 (6): 2909-16. Terui Hiroko, Tachikawa Tetsuhiko, Kakuta Miho, Nishimura Yoji, Yatsuoka Toshimasa, Yamaguchi Kensei, Yura Kei, Akagi Kiwa |
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Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry.
Familial cancer 2013 Dec 12 (4): 719-40. Casey Murray Joseph, Bewtra Chhanda, Lynch Henry T, Snyder Carrie, Stacy Mark, Watson Patri |
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Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.
European urology 2013 Feb 63 (2): 379-85. Skeldon Sean C, Semotiuk Kara, Aronson Melyssa, Holter Spring, Gallinger Steven, Pollett Aaron, Kuk Cynthia, van Rhijn Bas, Bostrom Peter, Cohen Zane, Fleshner Neil E, Jewett Michael A, Hanna Sally, Shariat Shahrokh F, Van Der Kwast Theodorus H, Evans Andrew, Catto Jim, Bapat Bharati, Zlotta Alexandre |
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BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma.
Cancer 2013 Jan 119 (2): 332-8. Pennington Kathryn P, Walsh Tom, Lee Ming, Pennil Christopher, Novetsky Akiva P, Agnew Kathy J, Thornton Anne, Garcia Rochelle, Mutch David, King Mary-Claire, Goodfellow Paul, Swisher Elizabeth |
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Germline mutation analysis of MLH1 and MSH2 in Malaysian Lynch syndrome patients.
World journal of gastroenterology : WJG 2012 Feb 18 (8): 814-20. Zahary Mohd Nizam, Kaur Gurjeet, Abu Hassan Muhammad Radzi, Singh Harjinder, Naik Venkatesh R, Ankathil Ravindr |
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The rate of the predominant Jewish mutations in the BRCA1, BRCA2, MSH2 and MSH6 genes in unselected Jewish endometrial cancer patients.
Gynecologic oncology 2010 Dec 119 (3): 511-5. Barak Frida, Milgrom Roni, Laitman Yael, Gemer Ofer, Rabinovich Alex, Piura Benjamin, Anteby Eyal, Baruch Gilad Ben, Korach Jacob, Friedman Eit |
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Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.
Journal of medical genetics 2010 Jul 47 (7): 464-70. van der Post R S, Kiemeney L A, Ligtenberg M J L, Witjes J A, Hulsbergen-van de Kaa C A, Bodmer D, Schaap L, Kets C M, van Krieken J H J M, Hoogerbrugge |
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Cancer risk in MLH1, MSH2 and MSH6 mutation carriers; different risk profiles may influence clinical management.
Hereditary cancer in clinical practice 2009 7 (1): 17. Ramsoekh Dewkoemar, Wagner Anja, van Leerdam Monique E, Dooijes Dennis, Tops Carli Mj, Steyerberg Ewout W, Kuipers Ernst |
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Detection of mismatch repair gene germline mutation carrier among Chinese population with colorectal cancer.
BMC cancer 2008 8 (1): 44. Jin Hei-Ying, Liu Xiufang, Li Vicky Ka Ming, Ding Yijiang, Yang Bolin, Geng Jianxiang, Lai Rensheng, Ding Shuqing, Ni Min, Zhao Rongh |
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Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer.
International journal of cancer. Journal international du cancer 2007 Aug 121 (3): 555-8. Schafmayer Clemens, Buch Stephan, Egberts Jan Hendrik, Franke Andre, Brosch Mario, El Sharawy Abdou, Conring Mareike, Koschnick Maralde, Schwiedernoch Sven, Katalinic Alexander, Kremer Bernd, Fölsch Ulrich R, Krawczak Michael, Fändrich Fred, Schreiber Stefan, Tepel Jürgen, Hampe Joch |
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The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC).
Journal of medical genetics 2005 Oct 42 (10): 769-73. Krüger S, Bier A, Engel C, Mangold E, Pagenstecher C, von Knebel Doeberitz M, Holinski-Feder E, Moeslein G, Schulmann K, Plaschke J, Rüschoff J, Schackert H K, |
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Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study.
The Lancet. Oncology 2005 Aug 6 (8): 566-72. Krüger Stefan, Silber Ann-Sophie, Engel Christoph, Görgens Heike, Mangold Elisabeth, Pagenstecher Constanze, Holinski-Feder Elke, von Knebel Doeberitz Magnus, Moeslein Gabriela, Dietmaier Wolfgang, Stemmler Susanne, Friedl Waltraut, Rüschoff Josef, Schackert Hans K, |
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Clinical and genetic findings in an Ashkenazi Jewish population with colorectal neoplasms.
Cancer 2005 Aug 104 (4): 719-29. Zauber N Peter, Sabbath-Solitare Marlene, Marotta Stephen, Zauber Ann G, Foulkes William, Chan May, Turner Faye, Bishop D Timot |
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Identification of predictive factors for the occurrence of predisposing MLH1 and MSH2 germline mutations among Sardinian patients with colorectal carcinoma.
European journal of cancer (Oxford, England : 1990) 2005 May 41 (7): 1058-64. Colombino Maria, Cossu Antonio, Budroni Mario, Satta Maria P, Baldinu Paola, Casula Milena, Palomba Grazia, Pisano Marina, Sini Maria C, Deiana Angelo, Tanda Francesco, Palmieri Giusep |
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Prognostic relevance of MLH1 and MSH2 mutations in hereditary non-polyposis colorectal cancer patients.
Tumori 0 95 (6): 731-8. Russo Antonio, Sala Paola, Alberici Paola, Gazzoli Isabella, Radice Paolo, Montefusco Claudia, Torrini Margherita, Mareni Cristina, Fornasarig Mara, Santarosa Manuela, Viel Alessandra, Benatti Piero, Pedroni Monica, Pedroni Maurizio, de Leon Maurizio Ponz, Lucci-Cordisco Emanuela, Genuardi Maurizio, Messerini Luca, Stigliano Vittoria, Cama Alessandro, Curia Maria Cristina, de Lellis Laura, Signoroni Stefano, Pierotti Marco A, Bertario Luc |
- Page last reviewed:Oct 1, 2020
- Page last updated:Oct 14, 2020
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