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 mutations in Thai patients with nonmucinous epithelial ovarian cancer. World journal of clinical oncology 2019 Nov 10 (11): 358-368. Manchana Tarinee, Phowthongkum Prasit, Teerapakpinyo Chinacho |
| Lynch syndrome-related non-endometrioid endometrial cancer: analysis of outcomes. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2019 Nov . Bogani Giorgio, Tibiletti Maria Grazia, Ricci Maria Teresa, Carnevali Ileana, Liberale Viola, Paolini Biagio, Milione Massimo, Vitellaro Marco, Murgia Ferdinando, Chiappa Valentina, Ditto Antonino, Ghezzi Fabio, Raspagliesi Frances |
| 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 |
| Targeted Next-Generation Sequencing of MLH1, MSH2, and MSH6 Genes in Patients with Endometrial Carcinoma under 50 Years of Age Balkan medical journal 2019 01 36 (1): 37-42. Özdemir Taha Resid, Alan Murat, Sanci Muzaffer, Koç Alt |
| Prevalence of Lynch syndrome in unselected patients with endometrial or ovarian cancer. Archives of gynecology and obstetrics 2016 Nov 294 (6): 1299-1303. Kast Karin, Dobberschütz Catharina, Sadowski Carolin Eva, Pistorius Steffen, Wimberger Pauli |
| 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, |
| Genetic alterations in endometrial cancer by targeted next-generation sequencing. Experimental and molecular pathology 2015 Nov . Chang Ya-Sian, Huang Hsien-Da, Yeh Kun-Tu, Chang Jan-Gow |
| Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition. Human genetics 2015 Mar 134 (3): 269-78. Moir-Meyer Gemma L, Pearson John F, Lose Felicity, , Scott Rodney J, McEvoy Mark, Attia John, Holliday Elizabeth G, , , Pharoah Paul D, Dunning Alison M, Thompson Deborah J, Easton Douglas F, Spurdle Amanda B, Walker Logan |
| 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 |
| Excess of extracolonic non-endometrial multiple primary cancers in MSH2 germline mutation carriers over MLH1. Journal of surgical oncology 2013 Dec 108 (7): 433-7. Lin-Hurtubise Kevin M, Yheulon Christopher G, Gagliano Ronald A, Lynch Henry |
| 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 |
| The spectrum of urological malignancy in Lynch syndrome. Familial cancer 2013 Mar 12 (1): 57-63. Barrow P J, Ingham S, O'Hara C, Green K, McIntyre I, Lalloo F, Hill J, Evans D |
| 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 |
| Cancer risks for MLH1 and MSH2 mutation carriers. Human mutation 2012 Dec . Dowty JG, Win AK, Buchanan DD, Lindor NM, Macrae FA, Clendenning M, Antill YC, Thibodeau SN, Casey G, Gallinger S, Le Marchand L, Newcomb PA, Haile RW, Young GP, James PA, Giles GG, Gunawardena SR, Leggett BA, Gattas M, Boussioutas A, Ahnen DJ, Baron JA, Parry S, Goldblatt J, Young JP, Hopper JL, Jenkins MA |
| Risks of less common cancers in proven mutation carriers with lynch syndrome. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Oct . Engel C, Loeffler M, Steinke V, Rahner N, Holinski-Feder E, Dietmaier W, Schackert HK, Goergens H, von Knebel Doeberitz M, Goecke TO, Schmiegel W, Buettner R, Moeslein G, Letteboer TG, García EG, Hes FJ, Hoogerbrugge N, Menko FH, van Os TA, Sijmons RH, Wagner A, Kluijt I, Propping P, Vasen HF |
| Simplified identification of Lynch syndrome: a prospective, multicenter study. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2012 Jun 44 (6): 515-22. Bonnet Delphine, Selves Janick, Toulas Christine, Danjoux Marie, Duffas Jean Pierre, Portier Guillaume, Kirzin Sylvain, Ghouti Laurent, Carrère Nicolas, Suc Bertrand, Alric Laurent, Barange Karl, Buscail Louis, Chaubard Thierry, Imani Kamran, Guimbaud Rosi |
| 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 |
| Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA 2011 Jun 305 (22): 2304-10. Bonadona Valérie, Bonaïti Bernard, Olschwang Sylviane, Grandjouan Sophie, Huiart Laetitia, Longy Michel, Guimbaud Rosine, Buecher Bruno, Bignon Yves-Jean, Caron Olivier, Colas Chrystelle, Noguès Catherine, Lejeune-Dumoulin Sophie, Olivier-Faivre Laurence, Polycarpe-Osaer Florence, Nguyen Tan Dat, Desseigne Françoise, Saurin Jean-Christophe, Berthet Pascaline, Leroux Dominique, Duffour Jacqueline, Manouvrier Sylvie, Frébourg Thierry, Sobol Hagay, Lasset Christine, Bonaïti-Pellié Catherine, |
| 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 |
| Endometrial cancer and genetic variation in PTEN, PIK3CA, AKT1, MLH1, and MSH2 within a population-based case-control study. Gynecologic oncology 2011 Feb 120 (2): 167-73. Lacey James V, Yang Hannah, Gaudet Mia M, Dunning Alison, Lissowska Jolanta, Sherman Mark E, Peplonska Beata, Brinton Louise A, Healey Catherine S, Ahmed Shahana, Pharoah Paul, Easton Douglas, Chanock Stephen, Garcia-Closas Montserr |
| 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 |
| Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome. Gastroenterology 2009 Nov 137 (5): 1621-7. Stoffel Elena, Mukherjee Bhramar, Raymond Victoria M, Tayob Nabihah, Kastrinos Fay, Sparr Jennifer, Wang Fei, Bandipalliam Prathap, Syngal Sapna, Gruber Stephen |
| 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 |
| Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Aug 17 (8): 2044-51. Kastrinos Fay, Stoffel Elena M, Balmaña Judith, Steyerberg Ewout W, Mercado Rowena, Syngal Sap |
| Risk of gynecologic cancers in Danish hereditary non-polyposis colorectal cancer families. Acta obstetricia et gynecologica Scandinavica 2008 87 (11): 1129-35. Boilesen Astrid Elisabeth Bruun, Bisgaard Marie Luise, Bernstein In |
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- Page last updated:Aug 10, 2022
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