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PLoS ONE, ISSN 1932-6203, 2016, Volume 11, Issue 6
BACKGROUND AND AIMS: Lynch Syndrome (LS) is caused by pathogenic germline variants in one of the mismatch repair (MMR) genes. However, up to 60% of... 
Journal Article
by Antoniou, Antonis C and Wang, Xianshu and Fredericksen, Zachary S and McGuffog, Lesley and Tarrell, Robert and Sinilnikova, Olga M and Healey, Sue and Morrison, Jonathan and Kartsonaki, Christiana and Lesnick, Timothy and Ghoussaini, Maya and Barrowdale, Daniel and Peock, Susan and Cook, Margaret and Oliver, Clare and Frost, Debra and Eccles, Diana and Evans, D. Gareth and Eeles, Ros and Izatt, Louise and Chu, Carol and Douglas, Fiona and Paterson, Joan and Stoppa-Lyonnet, Dominique and Houdayer, Claude and Mazoyer, Sylvie and Giraud, Sophie and Lasset, Christine and Remenieras, Auey and Caron, Olivier and Hardouin, Agnès and Berthet, Pascaline and Hogervorst, Frans B. L and Rookus, Matti A and Jager, Agnes and van den Ouweland, Ans and Hoogerbrugge, Nicoline and van der Luijt, Rob B and Meijers-Heijboer, Hanne and Gómez García, Encarna B and Devilee, Peter and Vreeswijk, Maaike P. G and Lubinski, Jan and Jakubowska, Anna and Gronwald, Jacek and Huzarski, Tomasz and Byrski, Tomasz and Górski, Bohdan and Cybulski, Cezary and Spurdle, Amanda B and Holland, Helene and Goldgar, David E and John, Esther M and Hopper, John L and Southey, Melissa and Buys, Sauna S and Daly, Mary B and Terry, Mary-Beth and Schmutzler, Rita K and Wappenschmidt, Barbara and Engel, Christoph and Meindl, Alfons and Preisler-Adams, Sabine and Arnold, Norbert and Niederacher, Dieter and Sutter, Christian and Domchek, Susan M and Nathanson, Katherine L and Rebbeck, Timothy and Blum, Joanne L and Piedmonte, Marion and Roiguez, Gustavo C and Wakeley, Katie and Boggess, John F and Basil, Jack and Blank, Stephanie V and Friedman, Eitan and Kaufman, Bella and Laitman, Yael and Milgrom, Roni and Anulis, Irene L and Glendon, Gord and Ozcelik, Hilmi and Kirchhoff, Tomas and Vijai, Joseph and Gaudet, Mia M and Altshuler, David and Guiducci, Candace and Loman, Niklas and Harbst, Katja and Rantala, Johanna and Ehrencrona, Hans and Gerdes, Anne-Marie and Thomassen, Mads and Sunde, Lone and Peterlongo, Paolo and Manoukian, Siranoush and Bonanni, Bernardo and Viel, Alessana and Radice, Paolo and ... and KConFab and EMBRACE and GEMO Study Collaborators and GENICA and MOD SQUAD and HEBON and SWE-BRCA and kConFab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature genetics, ISSN 1061-4036, 2010, Volume 42, Issue 10, pp. 885 - 892
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2011, Volume 12, Issue 1, pp. 49 - 55
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 07/2016, Volume 24, Issue 7, pp. 1089 - 1092
Journal Article
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 05/2012, Volume 18, Issue 10, pp. 2828 - 2837
Journal Article
European journal of human genetics, ISSN 1018-4813, 2017, Volume 25, Issue 11, pp. 1246 - 1252
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2016, Volume 11, Issue 6, p. e0157381
Journal Article
Gastroenterology, ISSN 0016-5085, 2015, Volume 149, Issue 4, pp. 897 - 906.e19
Background & Aims Germline mutations in the cadherin 1, type 1, E-cadherin gene ( CDH1 ) cause a predisposition to gastric cancer. We evaluated the ability of... 
Gastroenterology and Hepatology | Genetic Risk Factor | Stomach | LBC | Carcinogenesis | VARIANTS | GENE CDH1 | GUIDELINES | RISK | E-CADHERIN MUTATIONS | FAMILY-HISTORY | IDENTIFICATION | BREAST-CANCER | EARLY-ONSET | GASTROENTEROLOGY & HEPATOLOGY | CARCINOMA | Predictive Value of Tests | Carcinoma, Lobular - pathology | Neoplastic Syndromes, Hereditary - pathology | Prognosis | Humans | Middle Aged | Male | Stomach Neoplasms - pathology | Carcinoma, Lobular - mortality | Neoplastic Syndromes, Hereditary - mortality | Breast Neoplasms - therapy | Young Adult | Netherlands | Carcinoma, Lobular - therapy | Carcinoma, Lobular - genetics | Time Factors | DNA Mutational Analysis | Germ-Line Mutation | Adult | Female | Neoplastic Syndromes, Hereditary - genetics | Retrospective Studies | Cadherins - genetics | Stomach Neoplasms - genetics | Genetic Predisposition to Disease | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Stomach Neoplasms - therapy | Survival Rate | Heredity | Phenotype | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Pedigree | Neoplastic Syndromes, Hereditary - therapy | Breast Neoplasms - mortality | Aged | Stomach Neoplasms - mortality | Care and treatment | Gene mutations | Patient outcomes | Medical genetics | Medical tests | Diagnosis | Stomach cancer | Cancer | Index Medicus | Abridged Index Medicus
Journal Article