Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Counseling and MUTYH[original query] |
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Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas. Human mutation 2004 Oct 24 (4): 353-4. Isidro Glória, Laranjeira Francisco, Pires Ana, Leite Júlio, Regateiro Fernando, Castro e Sousa F, Soares José, Castro Clara, Giria João, Brito Maria J, Medeira Ana, Teixeira Ricardo, Morna Henrique, Gaspar Isabel, Marinho Carla, Jorge Rosa, Brehm António, Ramos J Silva, Boavida Maria Gui |
Germline susceptibility to colorectal cancer due to base-excision repair gene defects. American journal of human genetics 2005 Jul 77 (1): 112-9. Farrington Susan M, Tenesa Albert, Barnetson Rebecca, Wiltshire Alice, Prendergast James, Porteous Mary, Campbell Harry, Dunlop Malcolm |
Analysis of MUTYH genotypes and colorectal phenotypes in patients With MUTYH-associated polyposis. Gastroenterology 2009 Feb 136 (2): 471-6. Nielsen Maartje, Joerink-van de Beld Mirjam C, Jones Natalie, Vogt Stefanie, Tops Carli M, Vasen Hans F A, Sampson Julian R, Aretz Stefan, Hes Frederik |
Clinical implications of the colorectal cancer risk associated with MUTYH mutation. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009 Aug 27 (24): 3975-80. Lubbe Steven J, Di Bernardo Maria Chiara, Chandler Ian P, Houlston Richard |
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 |
Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2015 Feb 33 (5): 426-32. Chubb Daniel, Broderick Peter, Frampton Matthew, Kinnersley Ben, Sherborne Amy, Penegar Steven, Lloyd Amy, Ma Yussanne P, Dobbins Sara E, Houlston Richard |
Type 1 serrated polyposis represents a predominantly female disease with a high prevalence of dysplastic serrated adenomas, without germline mutation in MUTYH, APC, and PTEN genes. United European gastroenterology journal 2016 Apr 4 (2): 305-13. Petronio Marco, Pinson Stephane, Walter Thomas, Joly Marie-Odile, Hervieu Valerie, Forestier Julien, Saurin Jean-Christop |
Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort. Scientific reports 2017 May 7 (1): 2214. Khan Nikhat, Lipsa Anuja, Arunachal Gautham, Ramadwar Mukta, Sarin Raj |
Insight into genetic susceptibility to male breast cancer by multigene panel testing: Results from a multicenter study in Italy. International journal of cancer 2019 1 145 (2): 390-400. Rizzolo Piera, Zelli Veronica, Silvestri Valentina, Valentini Virginia, Zanna Ines, Bianchi Simonetta, Masala Giovanna, Spinelli Alessandro Mauro, Tibiletti Maria Grazia, Russo Antonio, Varesco Liliana, Giannini Giuseppe, Capalbo Carlo, Calistri Daniele, Cortesi Laura, Viel Alessandra, Bonanni Bernardo, Azzollini Jacopo, Manoukian Siranoush, Montagna Marco, Peterlongo Paolo, Radice Paolo, Palli Domenico, Ottini Lau |
Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer. Genes, chromosomes & cancer 2020 7 59 (12): 697-701. Schubert Stephanie A, Ruano Dina, Tiersma Yvonne, Drost Mark, de Wind Niels, Nielsen Maartje, van Hest Liselotte P, Morreau Hans, de Miranda Noel F C C, van Wezel T |
Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer. Frontiers in oncology 2021 11 637431. Zeng Bing, Huang Peide, Du Peina, Sun Xiaohui, Huang Xuanlin, Fang Xiaodong, Li L |
Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients. Medeniyet medical journal 2022 6 37 (2): 150-158. Arslan Ates Esra, Turkyilmaz Ayberk, Alavanda Ceren, Yildirim Ozlem, Guney Ahmet Ilt |
Breast and Ovarian Cancer Penetrance Estimates Derived From Germline Multiple-Gene Sequencing Results in Women. JCO precision oncology 2022 2 1 1-12. Kurian Allison W, Hughes Elisha, Handorf Elizabeth A, Gutin Alexander, Allen Brian, Hartman Anne-Renee, Hall Michael |
An updated counseling framework for moderate-penetrance colorectal cancer susceptibility genes. Genetics in medicine : official journal of the American College of Medical Genetics 2022 10 24 (12): 2587-2590. Breen Kelsey E, Katona Bryson W, Catchings Amanda, Ranganathan Megha, Marcell Vanessa, Latham Alicia, Yurgelun Matthew B, Stadler Zsofia |
Molecular characteristics of young-onset colorectal cancer in Vietnamese patients. Asia-Pacific journal of clinical oncology 2022 Jan . Do Minh Duc, Nguyen Thinh Huu, Le Khuong Thai, Le Linh Hoang Gia, Nguyen Bac Hoang, Le Kien Trung, Doan Thao Phuong Thi, Ho Chuong Quoc, Nguyen Hoai-Nghia, Tran Tuan Diep, Vu Hoang A |
Completion of Genetic Testing and Incidence of Pathogenic Germline Mutation among Patients with Early-Onset Colorectal Cancer: A Single Institution Analysis. Cancers 2023 7 15 (14): . Michael H Storandt, Kara R Rogen, Anushka Iyyangar, Rylie R Schnell, Jessica L Mitchell, Joleen M Hubbard, Frank A Sinicrope, Aminah Jatoi, Amit Mahipal, Qian Shi, Zhaohui J |
Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling. Mutation research 2023 7 827 111831. Zeynep Özdemir, Ezgi Çevik, Ömür Berna Çakmak Öksüzo?lu, Mutlu Do?an, Öztürk Ate?, Ece Esin, ?rem Bilgetekin, Umut Demirci, Ça?lar Köseo?lu, Alper Topal, Nuri Karadurmu?, Haktan Ba??? Erdem, Taha Bah |
New pathogenic germline variants identified in mesothelioma. Lung cancer (Amsterdam, Netherlands) 2023 3 179 107172. Belcaid Laila, Bertelsen Birgitte, Wadt Karin, Tuxen Ida, Spanggaard Iben, Højgaard Martin, Benn Sørensen Jens, Ravn Jesper, Lassen Ulrik, Cilius Nielsen Finn, Rohrberg Kristoffer, Westmose Yde Christi |
High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variants. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2023 2 . Reznick Levi Gili, Goldberg Yael, Segev Hanna, Maza Itay, Gorelik Yuri, Laish Ido, Levi Zohar, Kedar Inbal, Naftali Nathan Sonia, Sharon Swartzman Nitzan, Abu Freha Naim, Paritsky Maya, Rennert Gad, Baris Feldman Hagit, Paperna Tamar, Weiss Karin, Half Elizabeth |
Breast cancers in monoallelic MUTYH germline mutation carriers have clinicopathological features overlapping with those in BRCA1 germline mutation carriers. Breast cancer research and treatment 2023 12 . Aysenur Keske, Paul Weisman, Monica Ospina-Romero, Prachi Raut, Kelcy Smith-Simmer, Anna L Zakas, Christopher Flynn, Jin |
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- Page last updated:Apr 22, 2024
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