Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Counseling and APC[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 |
| 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 |
| CTNNB1 genotyping and APC screening in pediatric desmoid tumors: a proposed algorithm. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 15 (5): 361-7. Wang Wei-Lien, Nero Christopher, Pappo Alberto, Lev Dina, Lazar Alexander J, López-Terrada Dolor |
| 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 |
| Clinicopathological features of familial adenomatous polyposis in Korean patients. World journal of gastroenterology 2016 May 22 (17): 4380-8. Jung Sung Min, Yoon Yong Sik, Lim Seok-Byeong, Yu Chang Sik, Kim Jin Che |
| 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 |
| Value of a molecular screening program to support clinical trial enrollment in Asian cancer patients: The Integrated Molecular Analysis of Cancer (IMAC) Study. International journal of cancer 2018 05 142 (9): 1890-1900. Heong Valerie, Syn Nicholas L, Lee Xiao Wen, Sapari Nur Sabrina, Koh Xue Qing, Adam Isa Zul Fazreen, Sy Lim Joey, Lim Diana, Pang Brendan, Thian Yee Liang, Ng Lai Kuan, Wong Andrea L, Soo Ross Andrew, Yong Wei Peng, Chee Cheng Ean, Lee Soo-Chin, Goh Boon-Cher, Soong Richie, Tan David S |
| 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 |
| Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. JAMA oncology 2020 Mar . Mirabello Lisa, Zhu Bin, Koster Roelof, Karlins Eric, Dean Michael, Yeager Meredith, Gianferante Matthew, Spector Logan G, Morton Lindsay M, Karyadi Danielle, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Song Lei, Pankratz Nathan, Pinheiro Maisa, Gastier-Foster Julie M, Gorlick Richard, de Toledo Silvia Regina Caminada, Petrilli Antonio S, Patino-Garcia Ana, Lecanda Fernando, Gutierrez-Jimeno Miriam, Serra Massimo, Hattinger Claudia, Picci Piero, Scotlandi Katia, Flanagan Adrienne M, Tirabosco Roberto, Amary Maria Fernanda, Kurucu Nilgün, Ilhan Inci Ergurhan, Ballinger Mandy L, Thomas David M, Barkauskas Donald A, Mejia-Baltodano Gerardo, Valverde Patricia, Hicks Belynda D, Zhu Bin, Wang Mingyi, Hutchinson Amy A, Tucker Margaret, Sampson Joshua, Landi Maria T, Freedman Neal D, Gapstur Susan, Carter Brian, Hoover Robert N, Chanock Stephen J, Savage Sharon |
| 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 |
| Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report. Molecular biology reports 2022 2 49 (5): 3823-3837. Khider Feriel, Cherbal Farid, Boumehdi Asma-Lamia, Layaida Karim, Mahfouf Hassen, Zebboudj Ferhat, Maaoui Mustap |
| 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 |
| 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 |
| Evaluation of genetic alterations in hereditary cancer susceptibility genes in the Ashkenazi Jewish women community of Mexico. Frontiers in genetics 2023 2 14 1094260. Díaz-Velásquez Clara Estela, Gitler Rina, Antoniano Adriana, Kershenovich Sefchovich Ronny, De La Cruz-Montoya Aldo Hugo, Martínez-Gregorio Héctor, Rojas-Jiménez Ernesto Arturo, Cortez Cardoso Penha Ricardo, Terrazas Luis Ignacio, Wegman-Ostrosky Talia, Levi-Lahad Ephrat, Zabaleta Jovanny, Perdomo Sandra, Vaca-Paniagua Feli |
| Identification of Germline Variants in Patients with Hereditary Cancer Syndromes in Northeast Mexico. Genes 2023 2 14 (2): . Pérez-Ibave Diana Cristina, Garza-Rodríguez María Lourdes, Noriega-Iriondo María Fernanda, Flores-Moreno Sonia María, González-Geroniz Manuel Ismael, Espinoza-Velazco Absalon, Castruita-Ávila Ana Lilia, Alcorta-Núñez Fernando, Zayas-Villanueva Omar Alejandro, González-Guerrero Juan Francisco, Alcorta-Garza Adelina, Vidal-Gutiérrez Oscar, Burciaga-Flores Carlos Horac |
| Prevalence of Potentially Pathogenic Germline Variants Among Adult Patients in the Philippines With Solid Malignancies Who Underwent Tumor Genomic Profiling. JCO global oncology 2024 6 10 e2400019. Paula Isabel Franco, Jose Jasper Andal, Daphne Chua Ang, Frances Victoria Q |
| Targeted genotyping for recurring variants in cancer susceptibility genes in non-Ashkenazi Jewish patients with breast cancer diagnosed ?50 years. Cancer 2024 4 . Rinat Bernstein-Molho, Narmeen Abu Shhada, Yael Laitman, Iris Netzer, Shelley Shoval, Eitan Friedm |
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