Browsing by Author Steinke Lange, Verena

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Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)
1-Oct-2022Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortiumMøller, Pål; Seppälä, Toni T.; Dowty, James G.; Haupt, Saskia; Dominguez Valentin, Mev; Sunde, Lone; Bernstein, Inge; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capellá, G. (Gabriel); Chen Shtoyerman, Rakefet; Heuveline, Vincent; Senter, Leigha; Rasmussen, Lene J.; Ward, Robyn; Parry, Susan; Evans, D. Gareth; Sampson, Julian R.; Moslein, Gabriela; Bonanni, Bernardo; Lindblom, Annika; Dębniak, Tadeusz; John, Thomas; Hopper, John L.; Gallinger, Steven; Figueiredo, Jane; Ten Broeke, Sanne W.; Van Overeem Hansen, Thomas; Caldés, Trinidad; Yamaguchi, Tatsuro; Barca Tierno, Verónica; Gluck, Nathan; Garre, Pilar; Kennelly, Rory; Cavestro, Giulia Martina; Dueñas, Nuria; Greenblatt, Marc; Weitz, Jürgen; Pineda, Marta; Lino Silva, Leonardo S.; Redler, Silke; Nakken, Sigve; Kalfayan, Pablo; Burn, John; Büttner, Reinhard; Brunet, Joan; Green, Kate; Sheth, Harsh; Rossi, Benedito Mauro; Stakelum, Aine; Portenkirchner, Carmen; Lalloo, Fiona; Newton, Katie; Torrezan, Giovana Tardin; Martin, Claudia; Kloor, Matthias; The European Hereditary Tumour Group (ehtg) And The International Mismatch Repair Consortium (imrc); Bertario, Lucio; Crosbie, Emma J.; Mints, Miriam; Tjandra, Douglas; Neffa, Florencia; Perne, Claudia; Esperon, Patricia; Winship, Ingrid; Latchford, Andrew; Kariv, Revital; Macrae, Finlay; Guillén Ponce, Carmen; Rosner, Guy; Levi, Zohar; Tibiletti, Maria Grazia; Pavicic, Walter Hernán; Plazzer, John Paul; Sijmons, Rolf; Backman, Ann Sofie; De Vargas, Aída Falcón; Vangala, Deepak; Lautrup, Charlotte K.; Laghi, Luigi; Valle, Adriana Della; Abu Freha, Naim; Winter, Des; Bohorquez, Mabel; Horisberger, Karoline; Heinimann, Karl; Half, Elizabeth; Lopez Köstner, Francisco; Alvarez Valenzuela, Karin; Van Hest, Liselotte P.; Scott, Rodney J.; Ligtenberg, Marjolijn J. L.; Katz, Lior; Da Silva, Leandro Apolinário; Zahary, Mohd N.; Laish, Ido; Rossi, Norma Teresa; Morrison, Patrick J.; Vainer, Elez; Nascimento, Ivana; Steinke Lange, Verena; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Thomas, Huw; Zaránd, Attila; Poplawski, Nicola; Aronson, Melyssa; Kohonen Corish, Maija R. J.; Lee, Grant; Mecklin, Jukka Pekka; Pylvänäinen, Kirsi; Schmiegel, Wolff; Hüneburg, Robert; Gerdes, Anne Marie; Snyder, Carrie; Renkonen Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Therkildsen, Christina; Lindberg, Lars Joachim; Lindor, Noralane; Thorlacius Ussing, Ole; Stoffel, Elena; Newcomb, Polly A.; Von Knebel Doeberitz, Magnus; Palmero, Edenir; Thibodeau, Stephen N.; Loeffler, Markus; Amor, David; Hoogerbrugge, Nicoline; Rahner, Nils; Duijkers, Floor; Hall, Michael J.; Buchanan, Daniel D.; Le Marchand, Loïc; Win, Aung Ko; Hovig, Eivind; Hampel, Heather; Williams, Heinric; Ricciardiello, Luigi; Southey, Melissa; Samadder, N. Jewel; James, Paul; Okkels, Henrik; Lubiński, Jan; Reece, Jeanette; Ngeow, Joanne; Bassaneze, Thiago; Guillem, Jose G.; Ahadova, Aysel; Arnold, Julie; Pai, Rish; Jenkins, Mark A.; Wadt, Karin; Ankathil, Ravindran; Holinski Feder, Elke; Monahan, Kevin
1-Jan-2023Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk SyndromesGarcia Pelaez, José; Barbosa Matos, Rita; Lobo, Silvana; Dias, Alexandre; Garrido, Luzia; Castedo, Sérgio; Sousa, Sónia; Pinheiro, Hugo; Sousa, Liliana; Monteiro, Rita; Maqueda, Joaquin J.; Fernandes, Susana; Carneiro, Fátima; Pinto, Nádia; Lemos, Carolina; Pinto, Carla; Teixeira, Manuel R.; Aretz, Stefan; Bajalica Lagercrantz, Svetlana; Balmaña, Judith; Blatnik, Ana; Benusiglio, Patrick R.; Blanluet, Maud; Bours, Vincent; Brems, Hilde; Brunet, Joan; Calistri, Daniele; Capella, Gabriel; Carrera, Sergio; Colas, Chrystelle; Dahan, Karin; Putter, Robin de; Desseignés, Camille; Domínguez Garrido, Elena; Egas, Conceição; Evans, D. Gareth; Feret, Damien; Fewings, Eleanor; Fitzgerald, Rebecca C.; Coulet, Florence; Garcia Barcina, María; Genuardi, Maurizio; Golmard, Lisa; Hackmann, Karl; Hanson, Helen; Holinski Feder, Elke; Hüneburg, Robert; Krajc, Mateja; Lagerstedt Robinson, Kristina; Lázaro, Conxi; Ligtenberg, Marjolijn J. L.; Martínez Bouzas, Cristina; Merino, Sonia; Michils, Geneviève; Novaković, Srdjan; Patiño García, Ana; Ranzani, Guglielmina Nadia; Schröck, Evelin; Silva, Inês; Silveira, Catarina; Soto, José L.; Spier, Isabel; Steinke Lange, Verena; Tedaldi, Gianluca; Tejada, María isabel; Woodward, Emma R; Tischkowitz, Marc; Hoogerbrugge, Nicoline; Oliveira, Carla
28-Jun-2021No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyDominguez Valentin, Mev; Plazzer, John Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Valle, Adriana Della; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Serra Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Pavicic, Walter Hernán; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Hopper, John L.; Ko Win, Aung; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rødland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T.; Møller, Pål
14-Oct-2019Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportDominguez Valentin, Mev; Seppälä, Toni T.; Sampson, Julian R.; Macrae, Finlay; Winship, Ingrid; Evans, D. Gareth; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Pylvanainen, Kirsi; Renkonen Sinisalo, Laura; Lepisto, Anna; Lindblom, Annika; Plazzer, John-Paul; Tjandra, Douglas; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Ronlund, Karina; Nielsen, Randi Thyregaard; Yilmaz, Mette; Elvang, Louise Laurberg; Katz, Lior; Nielsen, Maartje; ten Broeke, Sanne W.; Nakken, Sigve; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Knebel Doeberitz, Magnus v; Ahadova, Aysel; Lindor, Noralane; Steinke Lange, Verena; Holinski Feder, Elke; Mecklin, Jukka-Pekka; Møller, Pål
15-Feb-2021The 'unnatural' history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillanceAhadova, Aysel; Seppälä, Toni T.; Engel, Christoph; Gallon, Richard; Burn, John; Holinski Feder, Elke; Steinke Lange, Verena; Möslein, Gabriela; Nielsen, Maartje; Ten Broeke, Sanne W.; Laghi, Luigi; Dominguez Valentin, Mev; Capellá, G. (Gabriel); Macrae, Finlay; Scott, Rodney; Hüneburg, Robert; Nattermann, Jacob; Hoffmeister, Michael; Brenner, Hermann; Bläker, Hendrik; von Knebel Doeberitz, Magnus; Sampson, Julian R.; Vasen, Hans; Mecklin, Jukka-Pekka; Møller, Pål; Kloor, Matthias
17-Mar-2021Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportSeppälä, Toni T.; Dominguez Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (Gabriel); Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans Georg; Tecklenburg, Johanna; Holinski Feder, Elke; Steinke Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John Paul; Pineda Riu, Marta; Navarro García, Matilde; Vida, Joan B.; Kariv, Revital; Rosner, Guy; Piñero, Tamara A.; Pavicic, Walter Hernán; Kalfayan, Pablo; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; De Vos Tot Nederveen Cappel, Wouter H.; Della Valle, Adriana; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Büttner, Reinhard; Görgens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; Von Knebel Doeberitz, Magnus; Loeffler, Markus; Redler, Silke; Weitz, Jürgen; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Hopper, John L.; Win, Aung K.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Wadt, Karin A.W.; Mourits, Marian J.E.; Ketabi, Zohreh; Denton, Oliver G.; Rødland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Rokkones, Erik; Evans, D. Gareth; Møller, Pål