Search Results - Sijmons, Rolf
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1
PMS2-associated Lynch syndrome: past, present and future by Andini, Katarina (Author) , Nielsen, Maartje (Author) , Suerink, Manon (Author) , Helderman, Noah C. (Author) , Koornstra, Jan Jacob (Author) , Ahadova, Aysel (Author) , Kloor, Matthias (Author) , Mourits, Marian J.E. (Author) , Kok, Klaas (Author) , Sijmons, Rolf H. (Author) , Bajwa-ten Broeke, Sanne W. (Author) ,
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2
Investigation of rare non-coding variants in familial multiple myeloma by Niazi, Yasmeen (Author) , Paramasivam, Nagarajan (Author) , Blocka, Joanna (Author) , Kumar, Abhishek (Author) , Huhn, Stefanie (Author) , Schlesner, Matthias (Author) , Weinhold, Niels (Author) , Sijmons, Rolf (Author) , De Jong, Mirjam (Author) , Durie, Brian (Author) , Goldschmidt, Hartmut (Author) , Hemminki, Kari (Author) , Försti, Asta (Author) ,
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Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement by Møller, Pål (Author) , Seppälä, Toni T. (Author) , Ahadova, Aysel (Author) , Crosbie, Emma J. (Author) , Holinski-Feder, Elke (Author) , Scott, Rod (Author) , Haupt, Saskia (Author) , Möslein, Gabriela (Author) , Winship, Ingrid (Author) , Ten Broeke, Sanne W. (Author) , Kohut, Kelly E. (Author) , Ryan, Neil (Author) , Bauerfeind, Peter (Author) , Thomas, Laura E. (Author) , Evans, D. Gareth (Author) , Aretz, Stefan (Author) , Sijmons, Rolf H. (Author) , Half, Elizabeth (Author) , Heinimann, Karl (Author) , Horisberger, Karoline (Author) , Monahan, Kevin (Author) , Engel, Christoph (Author) , Cavestro, Giulia Martina (Author) , Fruscio, Robert (Author) , Abu-Freha, Naim (Author) , Zohar, Levi (Author) , Laghi, Luigi (Author) , Bertario, Lucio (Author) , Bonanni, Bernardo (Author) , Tibiletti, Maria Grazia (Author) , Lino-Silva, Leonardo S. (Author) , Vaccaro, Carlos Alberto (Author) , Valle, Adriana Della (Author) , Rossi, Benedito Mauro (Author) , da Silva, Leandro Apolinário (Author) , de Oliveira Nascimento, Ivana Lucia (Author) , Rossi, Norma Teresa (Author) , Dębniak, Tadeusz (Author) , Mecklin, Jukka-Pekka (Author) , Bernstein, Inge (Author) , Lindblom, Annika (Author) , Sunde, Lone (Author) , Nakken, Sigve (Author) , Heuveline, Vincent (Author) , Burn, John (Author) , Hovig, Eivind (Author) , Kloor, Matthias (Author) , Sampson, Julian R. (Author) , Dominguez-Valentin, Mev (Author) ,
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A rare large duplication of MLH1 identified in Lynch syndrome by Kumar, Abhishek (Author) , Paramasivam, Nagarajan (Author) , Bandapalli, Obul Reddy (Author) , Schlesner, Matthias (Author) , Chen, Tianhui (Author) , Sijmons, Rolf (Author) , Dymerska, Dagmara (Author) , Golebiewska, Katarzyna (Author) , Kuswik, Magdalena (Author) , Lubinski, Jan (Author) , Hemminki, Kari (Author) , Försti, Asta (Author) ,
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Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report by Seppälä, Toni T. (Author) , Dominguez-Valentin, Mev (Author) , Crosbie, Emma J. (Author) , Engel, Christoph (Author) , Aretz, Stefan (Author) , Macrae, Finlay (Author) , Winship, Ingrid (Author) , Capella, Gabriel (Author) , Thomas, Huw (Author) , Hovig, Eivind (Author) , Nielsen, Maartje (Author) , Sijmons, Rolf H. (Author) , Bertario, Lucio (Author) , Bonanni, Bernardo (Author) , Tibiletti, Maria G. (Author) , Cavestro, Giulia M. (Author) , Mints, Miriam (Author) , Gluck, Nathan (Author) , Katz, Lior (Author) , Heinimann, Karl (Author) , Vaccaro, Carlos A. (Author) , Green, Kate (Author) , Lalloo, Fiona (Author) , Hill, James (Author) , Schmiegel, Wolff (Author) , Vangala, Deepak (Author) , Perne, Claudia (Author) , Strauß, Hans-Georg (Author) , Tecklenburg, Johanna (Author) , Holinski-Feder, Elke (Author) , Steinke-Lange, Verena (Author) , Mecklin, Jukka-Pekka (Author) , Plazzer, John-Paul (Author) , Pineda, Marta (Author) , Navarro, Matilde (Author) , Vida, Joan B. (Author) , Kariv, Revital (Author) , Rosner, Guy (Author) , Piñero, Tamara A. (Author) , Pavicic, Walter (Author) , Kalfayan, Pablo (Author) , Ten Broeke, Sanne W. (Author) , Jenkins, Mark A. (Author) , Sunde, Lone (Author) , Bernstein, Inge (Author) , Burn, John (Author) , Greenblatt, Marc (Author) , de Vos tot Nederveen Cappel, Wouter H. (Author) , Della Valle, Adriana (Author) , Lopez-Koestner, Francisco (Author) , Alvarez, Karin (Author) , Büttner, Reinhard (Author) , Görgens, Heike (Author) , Morak, Monika (Author) , Holzapfel, Stefanie (Author) , Hüneburg, Robert (Author) , Knebel Doeberitz, Magnus von (Author) , Loeffler, Markus (Author) , Redler, Silke (Author) , Weitz, Jürgen (Author) , Pylvänäinen, Kirsi (Author) , Renkonen-Sinisalo, Laura (Author) , Lepistö, Anna (Author) , Hopper, John L. (Author) , Win, Aung K. (Author) , Lindor, Noralane M. (Author) , Gallinger, Steven (Author) , Le Marchand, Loïc (Author) , Newcomb, Polly A. (Author) , Figueiredo, Jane C. (Author) , Thibodeau, Stephen N. (Author) , Therkildsen, Christina (Author) , Wadt, Karin A. W. (Author) , Mourits, Marian J. E. (Author) , Ketabi, Zohreh (Author) , Denton, Oliver G. (Author) , Rødland, Einar A. (Author) , Vasen, Hans (Author) , Neffa, Florencia (Author) , Esperon, Patricia (Author) , Tjandra, Douglas (Author) , Möslein, Gabriela (Author) , Rokkones, Erik (Author) , Sampson, Julian R. (Author) , Evans, D. G. (Author) , Møller, Pål (Author) ,
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No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2: a prospective Lynch Syndrome Database study by Dominguez-Valentin, Mev (Author) , Plazzer, John-Paul (Author) , Sampson, Julian R. (Author) , Engel, Christoph (Author) , Aretz, Stefan (Author) , Jenkins, Mark A. (Author) , Sunde, Lone (Author) , Bernstein, Inge (Author) , Capella, Gabriel (Author) , Balaguer, Francesc (Author) , Macrae, Finlay (Author) , Winship, Ingrid M. (Author) , Thomas, Huw (Author) , Evans, Dafydd Gareth (Author) , Burn, John (Author) , Greenblatt, Marc (Author) , de Vos tot Nederveen Cappel, Wouter H. (Author) , Sijmons, Rolf H. (Author) , Nielsen, Maartje (Author) , Bertario, Lucio (Author) , Bonanni, Bernardo (Author) , Tibiletti, Maria Grazia (Author) , Cavestro, Giulia Martina (Author) , Lindblom, Annika (Author) , Valle, Adriana Della (Author) , Lopez-Kostner, Francisco (Author) , Alvarez, Karin (Author) , Gluck, Nathan (Author) , Katz, Lior (Author) , Heinimann, Karl (Author) , Vaccaro, Carlos A. (Author) , Nakken, Sigve (Author) , Hovig, Eivind (Author) , Green, Kate (Author) , Lalloo, Fiona (Author) , Hill, James (Author) , Vasen, Hans F. A. (Author) , Perne, Claudia (Author) , Büttner, Reinhard (Author) , Görgens, Heike (Author) , Holinski-Feder, Elke (Author) , Morak, Monika (Author) , Holzapfel, Stefanie (Author) , Hüneburg, Robert (Author) , Knebel Doeberitz, Magnus von (Author) , Loeffler, Markus (Author) , Rahner, Nils (Author) , Weitz, Jürgen (Author) , Steinke-Lange, Verena (Author) , Schmiegel, Wolff (Author) , Vangala, Deepak (Author) , Crosbie, Emma J. (Author) , Pineda, Marta (Author) , Navarro, Matilde (Author) , Brunet, Joan (Author) , Moreira, Leticia (Author) , Sánchez, Ariadna (Author) , Serra-Burriel, Miquel (Author) , Mints, Miriam (Author) , Kariv, Revital (Author) , Rosner, Guy (Author) , Piñero, Tamara Alejandra (Author) , Pavicic, Walter Hernán (Author) , Kalfayan, Pablo (Author) , Broeke, Sanne W. ten (Author) , Mecklin, Jukka-Pekka (Author) , Pylvänäinen, Kirsi (Author) , Renkonen-Sinisalo, Laura (Author) , Lepistö, Anna (Author) , Peltomäki, Päivi (Author) , Hopper, John L. (Author) , Win, Aung Ko (Author) , Buchanan, Daniel D. (Author) , Lindor, Noralane M. (Author) , Gallinger, Steven (Author) , Marchand, Loïc Le (Author) , Newcomb, Polly A. (Author) , Figueiredo, Jane C. (Author) , Thibodeau, Stephen N. (Author) , Therkildsen, Christina (Author) , Hansen, Thomas V. O. (Author) , Lindberg, Lars (Author) , Rødland, Einar Andreas (Author) , Neffa, Florencia (Author) , Esperon, Patricia (Author) , Tjandra, Douglas (Author) , Möslein, Gabriela (Author) , Seppälä, Toni T. (Author) , Møller, Pål (Author) ,
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7
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report by Dominguez-Valentin, Mev (Author) , Crosbie, Emma J. (Author) , Engel, Christoph (Author) , Aretz, Stefan (Author) , Macrae, Finlay (Author) , Winship, Ingrid (Author) , Capellá, Gabriel (Author) , Thomas, Huw (Author) , Nakken, Sigve (Author) , Hovig, Eivind (Author) , Nielsen, Maartje (Author) , Sijmons, Rolf H. (Author) , Bertario, Lucio (Author) , Bonanni, Bernardo (Author) , Tibiletti, Maria Grazia (Author) , Cavestro, Giulia Martina (Author) , Mints, Miriam (Author) , Gluck, Nathan (Author) , Katz, Lior (Author) , Heinimann, Karl (Author) , Vaccaro, Carlos A. (Author) , Green, Kate (Author) , Lalloo, Fiona (Author) , Hill, James (Author) , Schmiegel, Wolff-Helmut (Author) , Vangala, Deepak (Author) , Perne, Claudia (Author) , Strauß, Hans-Georg (Author) , Tecklenburg, Johanna (Author) , Holinski-Feder, Elke (Author) , Steinke, Verena (Author) , Mecklin, Jukka-Pekka (Author) , Plazzer, John-Paul (Author) , Pineda, Marta (Author) , Navarro, Matilde (Author) , Vidal, Joan Brunet (Author) , Kariv, Revital (Author) , Rosner, Guy (Author) , Piñero, Tamara Alejandra (Author) , Gonzalez, María Laura (Author) , Kalfayan, Pablo (Author) , Ryan, Neil (Author) , Ten Broeke, Sanne W. (Author) , Jenkins, Mark A. (Author) , Sunde, Lone (Author) , Bernstein, Inge (Author) , Burn, John (Author) , Greenblatt, Marc (Author) , de Vos tot Nederveen Cappel, Wouter H. (Author) , Della Valle, Adriana (Author) , Lopez-Koestner, Francisco (Author) , Alvarez, Karin (Author) , Büttner, Reinhard (Author) , Görgens, Heike (Author) , Morak, Monika (Author) , Holzapfel, Stefanie (Author) , Hüneburg, Robert (Author) , Knebel Doeberitz, Magnus von (Author) , Loeffler, Markus (Author) , Rahner, Nils (Author) , Weitz, Jürgen (Author) , Pylvänäinen, Kirsi (Author) , Renkonen-Sinisalo, Laura (Author) , Lepistö, Anna (Author) , Auranen, Annika (Author) , Hopper, John L. (Author) , Win, Aung Ko (Author) , Haile, Robert W. (Author) , Lindor, Noralane M. (Author) , Gallinger, Steven (Author) , Le Marchand, Loïc (Author) , Newcomb, Polly A. (Author) , Figueiredo, Jane C. (Author) , Thibodeau, Stephen N. (Author) , Therkildsen, Christina (Author) , Okkels, Henrik (Author) , Ketabi, Zohreh (Author) , Denton, Oliver G. (Author) , Rødland, Einar Andreas (Author) , Vasen, Hans (Author) , Neffa, Florencia (Author) , Esperon, Patricia (Author) , Tjandra, Douglas (Author) , Möslein, Gabriela (Author) , Sampson, Julian R. (Author) , Evans, D. Gareth (Author) , Seppälä, Toni T. (Author) , Møller, Pål (Author) ,
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8
Cancer predisposition genes in cancer-free families by Zheng, Guoqiao (Author) , Catalano, Calogerina (Author) , Bandapalli, Obul Reddy (Author) , Paramasivam, Nagarajan (Author) , Chattopadhyay, Subhayan (Author) , Schlesner, Matthias (Author) , Sijmons, Rolf (Author) , Hemminki, Akseli (Author) , Dymerska, Dagmara (Author) , Lubinski, Jan (Author) , Hemminki, Kari (Author) , Försti, Asta (Author) ,
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Related Subjects
Lynch syndrome
<i>MLH1</i>
<i>MSH2</i>
Endometrial cancer
Genetic predisposition
Hysterectomy
MAPK pathway
Mismatch repair genes
Oophorectomy
Ovarian cancer
Risk-reducing surgery
Whole-genome sequencing
aberrant splicing
cancer incidence
familial multiple myeloma
high-risk genes
missense
non-coding genome
penetrance
polygenic risk
predisposing genes
random environment
truncating
whole-genome sequencing