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Hans F. A. Vasen

leiden university

110H指数
607论文数
4.9W被引数
收录论文 198
发表时间
Germline variants in patients from the Iranian hereditary colorectal cancer registry来自伊朗遗传性结直肠癌登记处的患者中的生殖系变异
err2025-04-13
err0
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errGoshayeshi, Lena; Hoorang, Saeed; Hoseini, Benyamin; Abbaszadegan, Mohammad Reza; Afrazeh, Maryam; Alimardani, Maliheh; Maghool, Fatemeh; Shademan, Milad; Zahedi, Morteza; Zeinalian, Mehrdad; Alborzi, Foroogh; Keramati, Mohammad Reza; Torshizian, Ashkan; Vosoghinia, Hassan; Rajabzadeh, Farnood; Bary, Alireza; Bahar, Massih; Javadmanesh, Ali; Sorouri-Khorashad, Jamshid; Emami, Mohammad Hassan; Daryani, Nasser Ebrahimi; Vasen, Hans F. A.; Goshayeshi, Ladan; Dehghani, Hesam
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Surveillance for Pancreatic Cancer in High-Risk Individuals Leads to Improved Outcomes: A Propensity Score-Matched Analysis
err2023-06-01
err30
errOAAI
errKlatte, Derk C. F.; Boekestijn, Bas; Onnekink, Anke M.; Dekker, Friedo W.; van der Geest, Lydia G.; Wasser, Martin N. J. M.; Feshtali, Shirin; Luelmo, Saskia A. C.; Morreau, Hans; Potjer, Thomas P.; Inderson, Akin; Boonstra, Jurjen J.; Vasen, Hans F. A.; van Hooft, Jeanin E.; Bonsing, Bert A.; van Leerdam, Monique E.
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Cost-effectiveness of pancreas surveillance: The CDKN2A-p16-Leiden cohort
err2023-02-13
err10
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errIbrahim, Isaura S.; Vasen, Hans F. A.; Wasser, Martin N. J. M.; Feshtali, Shirin; Bonsing, Bert A.; Morreau, Hans; Inderson, Akin; Cappel, Wouter H. de Vos Tot Nederveen H.; van den Hout, Wilbert B.
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High yield of surveillance in patients diagnosed with constitutional mismatch repair deficiency
err2022-11-21
err10
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errGhorbanoghli, Zeinab; van Kouwen, Mariette; Versluys, Birgitta; Bonnet, Delphine; Devalck, Christine; Tinat, Julie; Januszkiewicz-Lewandowska, Danuta; Costas, Consuelo Calvino; Cottereau, Edouard; Hardwick, James C. H.; Wimmer, Katharina; Brugieres, Laurence; Colas, Chrystelle; Vasen, Hans F. A.
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Colonoscopic-Assisted Laparoscopic Wedge Resection for Colonic Lesions A Prospective Multicenter Cohort Study (LIMERIC-Study)
err2022-02-17
err15
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errLeicher, Laura W.; Huisman, Jelle F.; van Grevenstein, Wilhelmina M. U.; Didden, Paul; Backes, Yara; Offerhaus, G. Johan A.; Lacle, Miangela M.; Moll, Freek C. P.; Geesing, Joost M. J.; Smakman, Niels; Droste, Jochim S. Terhaar Sive; Verdaasdonk, Emiel G. G.; ter Borg, Frank; Talsma, A. Koen; Erkelens, G. Willemien; van der Zaag, Edwin S.; Schrauwen, Ruud W. M.; van Wely, Bob J.; Schot, Ingrid; Vermaas, Maarten; van Bergeijk, Jeroen D.; Sietses, Colin; Hazen, Wouter L.; Wasowicz, Dareczka K.; Ramsoekh, Dewkoemar; Tuynman, Jurriaan B.; Alderlieste, Yasser A.; Renger, Rutger-Jan; Oort, Frank A.; Bilgen, Ernst Jan Spillenaar; Vleggaar, Frank P.; Vasen, Hans F. A.; Cappel, Wouter H. de Vos tot Nederveen; Moons, Leon M. G.; van Westreenen, Henderik L.
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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
err2021-06-28
err13
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errDominguez-Valentin, Mev; Plazzer, John-Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capella, Gabriel; Balaguer, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, Dafydd Gareth; Burn, John; Greenblatt, Marc; Cappel, Wouter H. de Vos Tot Nederveen; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Alvarez, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans F. A.; Perne, Claudia; Buettner, Reinhard; Goergens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Doeberitz, Magnus von Knebel; Loeffler, Markus; Rahner, Nils; Weitz, Juergen; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sanchez, Ariadna; Serra-Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Pavicic, Walter Hernan; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Peltomaki, Paivi; Hopper, John L.; Win, Aung Ko; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rodland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Moslein, Gabriela; Seppala, Toni T.; Moller, Pal
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A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants
err2021-05-31
err8
errOAAI
errWiik, Mariann Unhjem; Evans, Tiffany-Jane; Belhadj, Sami; Bolton, Katherine A.; Dymerska, Dagmara; Jagmohan-Changur, Shantie; Capella, Gabriel; Kurzawski, Grzegorz; Wijnen, Juul T.; Valle, Laura; Vasen, Hans F. A.; Lubinski, Jan; Scott, Rodney J.; Talseth-Palmer, Bente A.
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Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
err2021-05-01
err14
errOAAI
errSeppala, Toni T.; Dominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia M.; 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, Marta; Navarro, Matilde; Vida, Joan B.; Kariv, Revital; Rosner, Guy; Pinero, Tamara A.; Pavicic, Walter; Kalfayan, Pablo; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; Cappel, Wouter H. de Vos Tot Nederveen; Della Valle, Adriana; Lopez-Koestner, Francisco; Alvarez, Karin; Buettner, Reinhard; Goergens, Heike; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Doeberitz, Magnus von Knebel; Loeffler, Markus; Redler, Silke; Weitz, Jurgen; Pylvaenaeinen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Hopper, John L.; Win, Aung K.; Lindor, Noralane M.; Gallinger, Steven; Marchand, Loic Le; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Wadt, Karin A. W.; Mourits, Marian J. E.; Ketabi, Zohreh; Denton, Oliver G.; Rodland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Moeslein, Gabriela; Rokkones, Erik; Sampson, Julian R.; Evans, D. G.; Moller, Pal
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Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
err2021-04-01
err25
errOAAI
errDominguez-Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Nakken, Sigve; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; 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, Marta; Navarro, Matilde; Brunet Vidal, Joan; Kariv, Revital; Rosner, Guy; Alejandra Pinero, Tamara; Laura Gonzalez, Maria; Kalfayan, Pablo; Ryan, Neil; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; Cappel, Wouter H. de Vos tot Nederveen; Della Valle, Adriana; Lopez-Koestner, Francisco; Alvarez, Karin; Buettner, Reinhard; Goergens, Heike; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; Doeberitz, Magnus von Knebel; Loeffler, Markus; Rahner, Nils; Weitz, Jurgen; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Lepisto, Anna; Auranen, Annika; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rodland, Einar Andreas; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Moeslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppala, Toni T.; Moller, Pal
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Duodenal Adenomas and Cancer in MUTYH-associated Polyposis: An International Cohort Study
err2021-02-01
err21
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errThomas, Laura E.; Hurley, Joanna J.; Sanchez, Angel Alonso; Aznarez, M. Rosario; Backman, Ann-Sofie; Bjork, Jan; Capella, Gabriel; Clark, Susan K.; Colas, Chrystelle; Dekker, Evelien; Dolwani, Sunil; Ghorbanoghli, Zeinab; Gonn, Mark; Romero, S. Gonzalez; Hes, Frederik J.; Jundi, Hala; Kelland, Sarah; Latchford, Andrew R.; Brito, Helena Leon; Lynch, Patrick M.; Meuser, Elena; Mork, Maureen E.; Mort, Matthew; Garcia, M. Navarro; Nielsen, Maartje; Parc, Yann; Ricci, Maria T.; Saurin, Jean-Christophe; van der Tuin, Karin; Vasen, Hans; Vilar, Eduardo; Vinet, Olivier; Vitellaro, Marco; Walton, Sarah-Jane; West, Hannah D.; Sampson, Julian R.
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (vol 22, pg 15, 2020)
err2020-09-01
err4
errOAAI
errDominguez-Valentin, Mev; Sampson, Julian R.; Seppala, Toni T.; ten Broeke, Sanne W.; Plazzer, John-Paul; Nakken, Sigve; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capella, Gabriel; Balaguer, Francesc; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; Hovig, Eivind; de Vos tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Bertario, Lucio; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Gluck, Nathan; Katz, Lior H.; Heinimann, Karl; Vaccaro, Carlos A.; Buttner, Reinhard; Gorgens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Huneburg, Robert; Knebel Doeberitz, Magnus von; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Wadt, Karin; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Moreira, Leticia; Sanchez, Ariadna; Serra-Burriel, Miquel; Pineda, Marta; Navarro, Matilde; Blanco, Ignacio; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Denton, Oliver G.; Frayling, Ian M.; Rodland, Einar Andreas; Vasen, Hans; Mints, Miriam; Neffa, Florencia; Esperon, Patricia; Alvarez, Karin; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Gonzalez, Maria Laura; Kalfayan, Pablo; Tjandra, Douglas; Winship, Ingrid M.; Macrae, Finlay; Moslein, Gabriela; Mecklin, Jukka-Pekka; Nielsen, Maartje; Moller, Pal
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Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriers青少年息肉病综合征的疾病表达: 对221名欧洲患者队列的回顾性调查,并与473 SMAD4/BMPR1A致病变异携带者的文献队列进行比较
err2020-09-01
err46
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errBlatter, Robert; Tschupp, Benjamin; Aretz, Stefan; Bernstein, Inge; Colas, Chrystelle; Evans, D. Gareth; Genuardi, Maurizio; Hes, Frederik J.; Hueneburg, Robert; Jarvinen, Heikki; Lalloo, Fiona; Moeslein, Gabriela; Renkonen-Sinisalo, Laura; Resta, Nicoletta; Spier, Isabel; Varvara, Dora; Vasen, Hans; Latchford, Andrew R.; Heinimann, Karl
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Associations of Height With the Risks of Colorectal and Endometrial Cancer in Persons With Lynch Syndrome
err2020-08-17
err1
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errBrouwer, Jesca G. M.; Newcomb, Polly A.; Bisseling, Tanya M.; Figueiredo, Jane C.; Hopper, John L.; Jenkins, Mark A.; Koornstra, Jan J.; Lindor, Noralane M.; Vasen, Hans F. A.; Win, Aung K.; Kampman, Ellen; van Duijnhoven, Franzel J. B.
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The unnatural history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillanceLynch综合征结直肠癌的非自然病史: 结肠镜监测的经验教训
err2020-08-03
err67
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errAhadova, Aysel; Seppala, Toni T.; Engel, Christoph; Gallon, Richard; Burn, John; Holinski-Feder, Elke; Steinke-Lange, Verena; Moeslein, Gabriela; Nielsen, Maartje; ten Broeke, Sanne W.; Laghi, Luigi; Dominguez-Valentin, Mev; Capella, Gabriel; Macrae, Finlay; Scott, Rodney; Hueneburg, Robert; Nattermann, Jacob; Hoffmeister, Michael; Brenner, Hermann; Blaeker, Hendrik; Doeberitz, Magnus von Knebel; Sampson, Julian R.; Vasen, Hans; Mecklin, Jukka-Pekka; Moller, Pal; Kloor, Matthias
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Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants
err2020-06-01
err15
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errOverbeek, Kasper A.; Rodriguez-Girondo, Mar D. M.; Wagner, Anja; van der Stoep, Nienke; van den Akker, Peter C.; Oosterwijk, Jan C.; van Os, Theo A.; van der Kolk, Lizet E.; Vasen, Hans F. A.; Hes, Frederik J.; Cahen, Djuna L.; Bruno, Marco J.; Potjer, Thomas P.
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Psychological distress and quality of life following positive fecal occult blood testing in colorectal cancer screening
err2020-04-14
err15
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errVermeer, Nina C. A.; van der Valk, Maxime J. M.; Snijders, Heleen S.; Vasen, Hans F. A.; van der Hoop, Arthur Gerritsen; Guicherit, Onno R.; Liefers, Gerrit-Jan; van de Velde, Cornelis J. H.; Stiggelbout, Anne M.; Peeters, Koen C. M. J.
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Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome
err2020-04-01
err61
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errEngel, Christoph; Ahadova, Aysel; Seppala, Toni T.; Aretz, Stefan; Bigirwamungu-Bargeman, Marloes; Blaeker, Hendrik; Bucksch, Karolin; Buettner, Reinhard; Cappel, Wouter T. De Vos Tot Nederveen; Endris, Volker; Holinski-Feder, Elke; Holzapfel, Stefanie; Hueneburg, Robert; Jacobs, Maarten A. J. M.; Koornstra, Jan J.; Langers, Alexandra M.; Lepisto, Anna; Morak, Monika; Moeslein, Gabriela; Peltomaeki, Paivi; Pylvaenaeinen, Kirsi; Rahner, Nils; Renkonen-Sinisalo, Laura; Schulmann, Karsten; Steinke-Lange, Verena; Stenzinger, Albrecht; Strassburg, Christian P.; van de Meeberg, Paul C.; van Kouwen, Mariette; van Leerdam, Monique; Vangala, Deepak B.; Vecht, Juda; Verhulst, Marie-Louise; Doeberitz, Magnus von Knebel; Weitz, Juergen; Zachariae, Silke; Loeffler, Markus; Mecklin, Jukka-Pekka; Kloor, Matthias; Vasen, Hans F.
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database6350致病性错配修复变异体携带者的基因、年龄和性别的癌症风险: 来自前瞻性Lynch综合征数据库的发现
err2020-01-01
err409
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errDominguez-Valentin, Mev; Sampson, Julian R.; Seppala, Toni T.; ten Broeke, Sanne W.; Plazzer, John-Paul; Nakken, Sigve; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capella, Gabriel; Balaguer, Francesc; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; Hovig, Eivind; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Bertario, Lucio; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez-Kostner, Francisco; Gluck, Nathan; Katz, Lior H.; Heinimann, Karl; Vaccaro, Carlos A.; Buettner, Reinhard; Goergens, Heike; Holinski-Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Pylvanainen, Kirsi; Renkonen-Sinisalo, Laura; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loic; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Wadt, Karin; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Moreira, Leticia; Sanchez, Ariadna; Serra-Burriel, Miquel; Pineda, Marta; Navarro, Matilde; Blanco, Ignacio; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Denton, Oliver G.; Frayling, Ian M.; Rodland, Einar Andreas; Vasen, Hans; Mints, Miriam; Neffa, Florencia; Esperon, Patricia; Alvarez, Karin; Kariv, Revital; Rosner, Guy; Pinero, Tamara Alejandra; Gonzalez, Maria Laura; Kalfayan, Pablo; Tjandra, Douglas; Winship, Ingrid M.; Macrae, Finlay; Moeslein, Gabriela; Mecklin, Jukka-Pekka; Nielsen, Maartje; Moller, Pal
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An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome
err2019-12-01
err13
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errSuerink, Manon; Rodriguez-Girondo, Mar; van der Klift, Heleen M.; Colas, Chrystelle; Brugieres, Laurence; Lavoine, Noemie; Jongmans, Marjolijn; Capella Munar, Gabriel; Evans, D. Gareth; Farrell, Michael P.; Genuardi, Maurizio; Goldberg, Yael; Gomez-Garcia, Encarna; Heinimann, Karl; Hoell, Jessica, I; Aretz, Stefan; Jasperson, Kory W.; Kedar, Inbal; Modi, Mitul B.; Nikolaev, Sergey; van Os, Theo A. M.; Ripperger, Tim; Rueda, Daniel; Senter, Leigha; Sjursen, Wenche; Sunde, Lone; Therkildsen, Christina; Tibiletti, Maria G.; Trainer, Alison H.; Vos, Yvonne J.; Wagner, Anja; Winship, Ingrid; Wimmer, Katharina; Zimmermann, Stefanie Y.; Vasen, Hans F.; van Asperen, Christi J.; Houwing-Duistermaat, Jeanine J.; ten Broeke, Sanne W.; Nielsen, Maartje
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