Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: Endometrial Neoplasms and PMS2[original query] |
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Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations. Gastroenterology 2014 Dec 147 (6): 1308-1316.e1. Haraldsdottir Sigurdis, Hampel Heather, Tomsic Jerneja, Frankel Wendy L, Pearlman Rachel, de la Chapelle Albert, Pritchard Colin |
Risk of secondary malignancy (including breast) in patients with mismatch-repair protein deficiency. The American journal of surgical pathology 2014 Nov 38 (11): 1494-500. Clay Michael R, Allison Kimberly H, Folkins Ann K, Longacre Teri |
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2015 Feb 33 (4): 319-25. ten Broeke Sanne W, Brohet Richard M, Tops Carli M, van der Klift Heleen M, Velthuizen Mary E, Bernstein Inge, Capellá Munar Gabriel, Gomez Garcia Encarna, Hoogerbrugge Nicoline, Letteboer Tom G W, Menko Fred H, Lindblom Annika, Mensenkamp Arjen R, Moller Pal, van Os Theo A, Rahner Nils, Redeker Bert J W, Sijmons Rolf H, Spruijt Liesbeth, Suerink Manon, Vos Yvonne J, Wagner Anja, Hes Frederik J, Vasen Hans F, Nielsen Maartje, Wijnen Juul |
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Jun . Suerink Manon, van der Klift Heleen M, Ten Broeke Sanne W, Dekkers Olaf M, Bernstein Inge, Capellá Munar Gabriel, Gomez Garcia Encarna, Hoogerbrugge Nicoline, Letteboer Tom G W, Menko Fred H, Lindblom Annika, Mensenkamp Arjen, Moller Pal, van Os Theo A, Rahner Nils, Redeker Bert J W, Olderode Maran, Spruijt Liesbeth, Vos Yvonne J, Wagner Anja, Morreau Hans, Hes Frederik J, Vasen Hans F A, Tops Carli M, Wijnen Juul T, Nielsen Maart |
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database. Gut 2015 Dec . Møller Pål, Seppälä Toni, Bernstein Inge, Holinski-Feder Elke, Sala Paola, Evans D Gareth, Lindblom Annika, Macrae Finlay, Blanco Ignacio, Sijmons Rolf, Jeffries Jacqueline, Vasen Hans, Burn John, Nakken Sigve, Hovig Eivind, Rødland Einar Andreas, Tharmaratnam Kukatharmini, de Vos Tot Nederveen Cappel Wouter H, Hill James, Wijnen Juul, Green Kate, Lalloo Fiona, Sunde Lone, Mints Miriam, Bertario Lucio, Pineda Marta, Navarro Matilde, Morak Monika, Renkonen-Sinisalo Laura, Frayling Ian M, Plazzer John-Paul, Pylvanainen Kirsi, Sampson Julian R, Capella Gabriel, Mecklin Jukka-Pekka, Möslein Gabriela, |
Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies. JAMA oncology 2017 8 3 (12): 1702-1706. Ryan Neil A J, Morris Julie, Green Kate, Lalloo Fiona, Woodward Emma R, Hill James, Crosbie Emma J, Evans D Gare |
Phenotypic Heterogeneity by Germline Mismatch Repair Gene Defect in Lynch Syndrome Patients. Acta medica portuguesa 2017 1 29 (10): 587-596. Hernâni-Eusébio Jorge, Barbosa Elisabe |
A novel MLH1 mutation in a Japanese family with Lynch syndrome associated with small bowel cancer. Human genome variation 2018 8 5 13. Akizawa Yoshika, Yamamoto Toshiyuki, Tamura Kazuo, Kanno Toshiyuki, Takahashi Nobuko, Ohki Takeshi, Omori Teppei, Tokushige Katsutoshi, Yamamoto Masakazu, Saito Kayo |
Cancer Risks for PMS2-Associated Lynch Syndrome. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 8 36 (29): 2961-2968. Ten Broeke Sanne W, van der Klift Heleen M, Tops Carli M J, Aretz Stefan, Bernstein Inge, Buchanan Daniel D, de la Chapelle Albert, Capella Gabriel, Clendenning Mark, Engel Christoph, Gallinger Steven, Gomez Garcia Encarna, Figueiredo Jane C, Haile Robert, Hampel Heather L, Hopper John L, Hoogerbrugge Nicoline, von Knebel Doeberitz Magnus, Le Marchand Loic, Letteboer Tom G W, Jenkins Mark A, Lindblom Annika, Lindor Noralane M, Mensenkamp Arjen R, Møller Pål, Newcomb Polly A, van Os Theo A M, Pearlman Rachel, Pineda Marta, Rahner Nils, Redeker Egbert J W, Olderode-Berends Maran J W, Rosty Christophe, Schackert Hans K, Scott Rodney, Senter Leigha, Spruijt Liesbeth, Steinke-Lange Verena, Suerink Manon, Thibodeau Stephen, Vos Yvonne J, Wagner Anja, Winship Ingrid, Hes Frederik J, Vasen Hans F A, Wijnen Juul T, Nielsen Maartje, Win Aung |
Racial differences in endometrial cancer molecular portraits in The Cancer Genome Atlas. Oncotarget 2018 Mar 9 (24): 17093-17103. Guttery David S, Blighe Kevin, Polymeros Konstantinos, Symonds R Paul, Macip Salvador, Moss Esther |
A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families. Hereditary cancer in clinical practice 2018 11 16 16. Karimi Masoud, von Salomé Jenny, Aravidis Christos, Silander Gustav, Askmalm Marie Stenmark, Henriksson Isabelle, Gebre-Medhin Samuel, Frödin Jan-Erik, Björck Erik, Lagerstedt-Robinson Kristina, Lindblom Annika, Tham Em |
Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 10 37 (4): 286-295. Latham Alicia, Srinivasan Preethi, Kemel Yelena, Shia Jinru, Bandlamudi Chaitanya, Mandelker Diana, Middha Sumit, Hechtman Jaclyn, Zehir Ahmet, Dubard-Gault Marianne, Tran Christina, Stewart Carolyn, Sheehan Margaret, Penson Alexander, DeLair Deborah, Yaeger Rona, Vijai Joseph, Mukherjee Semanti, Galle Jesse, Dickson Mark A, Janjigian Yelena, O'Reilly Eileen M, Segal Neil, Saltz Leonard B, Reidy-Lagunes Diane, Varghese Anna M, Bajorin Dean, Carlo Maria I, Cadoo Karen, Walsh Michael F, Weiser Martin, Aguilar Julio Garcia, Klimstra David S, Diaz Luis A, Baselga Jose, Zhang Liying, Ladanyi Marc, Hyman David M, Solit David B, Robson Mark E, Taylor Barry S, Offit Kenneth, Berger Michael F, Stadler Zsofia |
Evaluation of universal immunohistochemical screening of sebaceous neoplasms in a service setting. Clinical and experimental dermatology 2018 1 43 (4): 410-415. Schon K, Rytina E, Drummond J, Simmonds J, Abbs S, Sandford R, Tischkowitz |
Germline mismatch repair gene variants analyzed by universal sequencing in Japanese cancer patients. Cancer medicine 2019 Aug . Kiyozumi Yoshimi, Matsubayashi Hiroyuki, Horiuchi Yasue, Higashigawa Satomi, Oishi Takuma, Abe Masato, Ohnami Sumiko, Urakami Kenichi, Nagashima Takeshi, Kusuhara Masatoshi, Miyake Hidehiko, Yamaguchi K |
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 |
Screening for hereditary cancers in patients with endometrial cancer reveals a high frequency of germline mutations in cancer predisposition genes. International journal of cancer 2019 5 145 (5): 1290-1298. Tian Wenjuan, Bi Rui, Ren Yulan, He Hongsheng, Shi Shanfu, Shan Boer, Yang Wentao, Wang Qing, Wang Huayi |
Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach. Gynecologic oncology 2020 Jul . Rosa Reginaldo Cruz Alves, Santis Jessica Oliveira, Teixeira Lorena Alves, Molfetta Greice Andreotti, Dos Santos Jennifer Thalita Targino, Ribeiro Vanessa Dos Santos, Chahud Fernando, Ribeiro-Silva Alfredo, Brunaldi Mariângela Ottoboni, Silva Wilson Araújo, Ferraz Victor Evangelista de Far |
Mismatch Repair Deficiency in Ovarian Carcinoma: Frequency, Causes, and Consequences. The American journal of surgical pathology 2020 4 44 (5): 649-656. Leskela Susanna, Romero Ignacio, Cristobal Eva, Pérez-Mies Belén, Rosa-Rosa Juan M, Gutierrez-Pecharroman Ana, Caniego-Casas Tamara, Santón Almudena, Ojeda Belén, López-Reig Raquel, Palacios-Berraquero María L, García Ángel, Ibarra Javier, Hakim Sofía, Guarch Rosa, López-Guerrero José A, Poveda Andrés, Palacios Jo |
DACH1 mutation frequency in endometrial cancer is associated with high tumor mutation burden. PloS one 2020 12 15 (12): e0244558. Riggs McKayla J, Lin Nan, Wang Chi, Piecoro Dava W, Miller Rachel W, Hampton Oliver A, Rao Mahadev, Ueland Frederick R, Kolesar Jill |
Utility of a custom designed next generation DNA sequencing gene panel to molecularly classify endometrial cancers according to The Cancer Genome Atlas subgroups. BMC medical genomics 2020 12 13 (1): 179. Miller Eirwen M, Patterson Nicole E, Gressel Gregory M, Karabakhtsian Rouzan G, Bejerano-Sagie Michal, Ravi Nivedita, Maslov Alexander, Quispe-Tintaya Wilber, Wang Tao, Lin Juan, Smith Harriet O, Goldberg Gary L, Kuo Dennis Y S, Montagna Cristi |
HNRNPCL1, PRAMEF1, CFAP74, and DFFB: Common Potential Biomarkers for Sporadic and Suspected Lynch Syndrome Endometrial Cancer. Cancer management and research 2020 12 11231-11241. Gao Yuan, Zhang Xiuping, Wang Tian, Zhang Ye, Wang Qingxuan, Hu Yuanji |
Analysis of 108 patients with endometrial carcinoma using the PROMISE classification and additional genetic analyses for MMR-D. Gynecologic oncology 2020 1 157 (1): 245-251. Timmerman S, Van Rompuy A S, Van Gorp T, Vanden Bempt I, Brems H, Van Nieuwenhuysen E, Han S N, Neven P, Victoor J, Laenen A, Vergote |
Case-case analysis addressing ascertainment bias for multigene panel testing implicates BRCA1 and PALB2 in endometrial cancer. Human mutation 2021 7 42 (10): 1265-1278. Johnatty Sharon E, Pesaran Tina, Dolinsky Jill, Yussuf Amal, LaDuca Holly, James Paul A, O'Mara Tracy A, Spurdle Amanda |
Lynch Syndrome in Thai Endometrial Cancer Patients. Asian Pacific journal of cancer prevention : APJCP 2021 5 22 (5): 1477-1483. Manchana Tarinee, Ariyasriwatana Chai, Triratanachat Surang, Phowthongkum Pras |
An effective algorithm to detect the possibility of being MSI phenotype in endometrial cancer given the BMI status and histological subtype: a statistical study. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2022 5 24 (9): 1809-1817. González Villa Isabel, González Dávila Enrique Francisco, Afonso Idaira Jael Expósito, Blanco Leynis Isabel Martínez, Ferrer Juan Francisco Loro, Galván Juan José Cabre |
The immunohistochemical molecular risk classification in endometrial cancer: A pragmatic and high-reproducibility method. Gynecologic oncology 2022 3 165 (3): 585-593. Perrone Emanuele, De Felice Francesca, Capasso Ilaria, Distefano Ettore, Lorusso Domenica, Nero Camilla, Arciuolo Damiano, Zannoni Gian Franco, Scambia Giovanni, Fanfani Frances |
Up-Front Multigene Panel Testing for Cancer Susceptibility in Patients With Newly Diagnosed Endometrial Cancer: A Multicenter Prospective Study. JCO precision oncology 2022 1 5 1588-1602. Levine Monica D, Pearlman Rachel, Hampel Heather, Cosgrove Casey, Cohn David, Chassen Alexis, Suarez Adrian, Barrington David A, McElroy Joseph P, Waggoner Steven, Nakayama John, Billingsley Caroline, Resnick Kim, Andrews Stephen, Singh Sareena, Jenison Eric, Clements Aine, Neff Robert, Goodfellow Paul J, |
Risk of Syndrome-Associated Cancers Among First-Degree Relatives of Patients With Pancreatic Ductal Adenocarcinoma With Pathogenic or Likely Pathogenic Germline Variants. JAMA oncology 2023 5 . Xuan Chen, Margaret A Meyer, Jennifer L Kemppainen, Masayasu Horibe, Shruti Chandra, Shounak Majumder, Gloria M Petersen, Kari G Ra |
Validation of Modaplex POLE mutation assay in endometrial carcinoma. Virchows Archiv : an international journal of pathology 2023 10 . Eduard Dorca, Ana Velasco, Mar Varela, Sonia Gatius, Sergio Villatoro, Neus Fullana, Dolors Cuevas, Marta Vaquero, Astrid Birnbaum, Karsten Neumann, Xavier Matias-Gu |
Characterization of a germline variant MSH6 c.4001G >?C in a Lynch syndrome family. Molecular genetics & genomic medicine 2023 1 11 (2): e2104. Yang Ciyu, Misyura Maksym, Kane Sarah, Rai Vikas, Latham Alicia, Zhang Liyi |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
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