HuGE Literature Finder
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| 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 |
| 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 |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome. Journal of the National Cancer Institute 2013 Feb . Win AK, Lindor NM, Winship I, Tucker KM, Buchanan DD, Young JP, Rosty C, Leggett B, Giles GG, Goldblatt J, Macrae FA, Parry S, Kalady MF, Baron JA, Ahnen DJ, Marchand LL, Gallinger S, Haile RW, Newcomb PA, Hopper JL, Jenkins MA |
| Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Mar 30 (9): 958-64. Win Aung Ko, Young Joanne P, Lindor Noralane M, Tucker Katherine M, Ahnen Dennis J, Young Graeme P, Buchanan Daniel D, Clendenning Mark, Giles Graham G, Winship Ingrid, Macrae Finlay A, Goldblatt Jack, Southey Melissa C, Arnold Julie, Thibodeau Stephen N, Gunawardena Shanaka R, Bapat Bharati, Baron John A, Casey Graham, Gallinger Steven, Le Marchand Loïc, Newcomb Polly A, Haile Robert W, Hopper John L, Jenkins Mark |
| Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers. Obstetrics and gynecology 2011 Apr 117 (4): 899-905. Win Aung Ko, Dowty James G, Antill Yoland C, English Dallas R, Baron John A, Young Joanne P, Giles Graham G, Southey Melissa C, Winship Ingrid, Lipton Lara, Parry Susan, Thibodeau Stephen N, Haile Robert W, Gallinger Steven, Le Marchand Loïc, Lindor Noralane M, Newcomb Polly A, Hopper John L, Jenkins Mark |
| PMS2 involvement in patients suspected of Lynch syndrome. Genes, chromosomes & cancer 2009 Apr 48 (4): 322-9. Niessen Renée C, Kleibeuker Jan H, Westers Helga, Jager Paul O J, Rozeveld Dennie, Bos Krista K, Boersma-van Ek Wytske, Hollema Harry, Sijmons Rolf H, Hofstra Robert M |
| High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers. Familial cancer 2009 8 (2): 145-51. Grindedal Eli Marie, Blanco Ignacio, Stormorken Astrid, Maehle Lovise, Clark Neal, González Sara, Capella Gabriel, Vasen Hans, Burn John, Møller P |
| The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations. Gastroenterology 2008 Aug 135 (2): 419-28. Senter Leigha, Clendenning Mark, Sotamaa Kaisa, Hampel Heather, Green Jane, Potter John D, Lindblom Annika, Lagerstedt Kristina, Thibodeau Stephen N, Lindor Noralane M, Young Joanne, Winship Ingrid, Dowty James G, White Darren M, Hopper John L, Baglietto Laura, Jenkins Mark A, de la Chapelle Albe |
| Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications. Evidence report/technology assessment 2007 May (150): 1-180. Bonis Peter A, Trikalinos Thomas A, Chung Mei, Chew Priscilla, Ip Stanley, DeVine Deirdre A, Lau Jose |
| Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer research 2006 Aug 66 (15): 7810-7. Hampel Heather, Frankel Wendy, Panescu Jenny, Lockman Janet, Sotamaa Kaisa, Fix Daniel, Comeras Ilene, La Jeunesse Jennifer, Nakagawa Hidewaki, Westman Judith A, Prior Thomas W, Clendenning Mark, Penzone Pamela, Lombardi Janet, Dunn Patti, Cohn David E, Copeland Larry, Eaton Lynne, Fowler Jeffrey, Lewandowski George, Vaccarello Luis, Bell Jeffrey, Reid Gary, de la Chapelle Albe |
| Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain. International journal of cancer. Journal international du cancer 2002 Apr 98 (5): 774-9. Caldes Trinidad, Godino Javier, de la Hoya Miguel, Garcia Carbonero Iciar, Perez Segura Pedro, Eng Charis, Benito Manuel, Diaz-Rubio Eduar |
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- Page last updated:Jun 28, 2022
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