부산대학교 도서관

Wang, H. H.; Kats-Ugurlu, G.; Sijmons, R. H.; Kluiver, J. L.; Commandeur-Jan, S. Z.; Noordzij, W.; van Etten, B.; Plukker, J. T. M.; Hospers, G. A. P.; Knapen, D. G.

Virchows Archiv: European Journal of Pathology. :1-5

Sijmons, Daniel; Islas Rios, Heber; Turner, Benjamin R.; Wanicek, Emma; Holien, Jessica K.; Walduck, Anna K.; Ramsland, Paul A.

Biomolecules. October, 2025, Vol. 15 Issue 10,.

Vos, JR; Giepmans, L; Roehl, C; Geverink, N; Hoogerbrugge, N; Ligtenberg, M; Kets, M; Sijmons, R; Evans, G; Woodward, E

FAMILIAL CANCER. 18(2):281-284

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Lennart F. Johansson; Hendrik A. de Weerd; Eddy N. de Boer; Freerk van Dijk; Gerard J. te Meerman; Rolf H. Sijmons; Birgit Sikkema-Raddatz; Morris A. Swertz

BMC Bioinformatics, Vol 19, Iss 1, Pp 1-5 (2018)

Moller, P; Seppala, T; Bernstein, I; Holinski-Feder, E; Sala, P; Evans, DG; Lindblom, A; Macrae, F; Blanco, I; Sijmons, R

GUT. 66(3):464-472

Moller, P; Seppala, T; Bernstein, I; Holinski-Feder, E; Sala, P; Evans, DG; Lindblom, A; Macrae, F; Blanco, I; Sijmons, R

GUT. 66(9):1657-1664

Bokkers, K.; Bleiker, E. M.A.; Aalfs, C. M.; van Dalen, T.; Velthuizen, M. E.; Duijveman, P.; Sijmons, R. H.; Koole, W.; Schoenmaeckers, E. J.P.; Ausems, M. G.E.M.

Ann Surg Oncol

Pal Møller; Toni T. Seppälä; Aysel Ahadova; Emma J. Crosbie; Elke Holinski-Feder; Rodney Scott; Saskia Haupt; Gabriela Möslein; Ingrid Winship; Sanne W. Bajwa-ten Broeke; Kelly E. Kohut; Neil Ryan; Peter Bauerfeind; Laura E. Thomas; D. Gareth Evans; Stefan Aretz; Rolf H. Sijmons; Elizabeth Half; Karl Heinimann; Karoline Horisberger; Kevin Monahan; Christoph Engel; Giulia Martina Cavestro; Robert Fruscio; Naim Abu-Freha; Levi Zohar; Luigi Laghi; Lucio Bertario; Bernardo Bonanni; Maria Grazia Tibiletti; Leonardo S. Lino-Silva; Carlos Vaccaro; Adriana Della Valle; Benedito Mauro Rossi; Leandro Apolinário da Silva; Ivana Lucia de Oliveira Nascimento; Norma Teresa Rossi; Tadeusz Dębniak; Jukka-Pekka Mecklin; Inge Bernstein; Annika Lindblom; Lone Sunde; Sigve Nakken; Vincent Heuveline; John Burn; Eivind Hovig; Matthias Kloor; Julian R. Sampson; Mev Dominguez-Valentin; On behalf of the Prospective Lynch Syndrome Database (www.plsd.eu) and The European Hereditary Tumour Group (www.ehtg.org)

Hereditary Cancer in Clinical Practice, Vol 21, Iss 1, Pp 1-12 (2023)

Frebourg, T.; Bajalica Lagercrantz, S.; Oliveira, C.; Magenheim, R.; Evans, D. G.; Hoogerbrugge, N.; Ligtenberg, M.; Kets, M.; Oostenbrink, R.; Sijmons, R.; Evans, G.; Woodward, E.; Tischkowitz, M.; Maher, E.; Ferner, R. E.; Aretz, S.; Spier, I.; Steinke-Lange, V.; Holinski-Feder, E.; Schröck, E.; Houdayer, C.; Colas, C.; Wolkenstein, P.; Bours, Vincent; Legius, E.; Poppe, B.; Claes, K.; de Putter, R.; Guillermo, I. B.; Capella, G.; Vidal, J. B.; Lázaro, C.; Balmaña, J.; Hernandez, H. S.; Teixeira, M.; Bajalica-Lagercrantz, S.; Tham, E.; Lubinski, J.; Ertmanska, K.; Melegh, B.; Krajc, M.; Blatnik, A.; Peltonen, S.; Hietala, M.; The European Reference Network GENTURIS

Eur J Hum Genet
European Journal of Human Genetics, 28, 10, pp. 1379-86
EUROPEAN JOURNAL OF HUMAN GENETICS

Stępień, Beata; Early, Bryan R.; Grauvogel, Julia; Preble, Keith A.; Truskolaski, Szymon

European Journal on Criminal Policy and Research, 30, 2, 301-326

Pål Møller; Toni Seppälä; James G. Dowty; Saskia Haupt; Mev Dominguez-Valentin; Lone Sunde; Inge Bernstein; Christoph Engel; Stefan Aretz; Maartje Nielsen; Gabriel Capella; Dafydd Gareth Evans; John Burn; Elke Holinski-Feder; Lucio Bertario; Bernardo Bonanni; Annika Lindblom; Zohar Levi; Finlay Macrae; Ingrid Winship; John-Paul Plazzer; Rolf Sijmons; Luigi Laghi; Adriana Della Valle; Karl Heinimann; Elizabeth Half; Francisco Lopez-Koestner; Karin Alvarez-Valenzuela; Rodney J. Scott; Lior Katz; Ido Laish; Elez Vainer; Carlos Alberto Vaccaro; Dirce Maria Carraro; Nathan Gluck; Naim Abu-Freha; Aine Stakelum; Rory Kennelly; Des Winter; Benedito Mauro Rossi; Marc Greenblatt; Mabel Bohorquez; Harsh Sheth; Maria Grazia Tibiletti; Leonardo S. Lino-Silva; Karoline Horisberger; Carmen Portenkirchner; Ivana Nascimento; Norma Teresa Rossi; Leandro Apolinário da Silva; Huw Thomas; Attila Zaránd; Jukka-Pekka Mecklin; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; Anna Lepisto; Päivi Peltomäki; Christina Therkildsen; Lars Joachim Lindberg; Ole Thorlacius-Ussing; Magnus von Knebel Doeberitz; Markus Loeffler; Nils Rahner; Verena Steinke-Lange; Wolff Schmiegel; Deepak Vangala; Claudia Perne; Robert Hüneburg; Aída Falcón de Vargas; Andrew Latchford; Anne-Marie Gerdes; Ann-Sofie Backman; Carmen Guillén-Ponce; Carrie Snyder; Charlotte K. Lautrup; David Amor; Edenir Palmero; Elena Stoffel; Floor Duijkers; Michael J. Hall; Heather Hampel; Heinric Williams; Henrik Okkels; Jan Lubiński; Jeanette Reece; Joanne Ngeow; Jose G. Guillem; Julie Arnold; Karin Wadt; Kevin Monahan; Leigha Senter; Lene J. Rasmussen; Liselotte P. van Hest; Luigi Ricciardiello; Maija R. J. Kohonen-Corish; Marjolijn J. L. Ligtenberg; Melissa Southey; Melyssa Aronson; Mohd N. Zahary; N. Jewel Samadder; Nicola Poplawski; Nicoline Hoogerbrugge; Patrick J. Morrison; Paul James; Grant Lee; Rakefet Chen-Shtoyerman; Ravindran Ankathil; Rish Pai; Robyn Ward; Susan Parry; Tadeusz Dębniak; Thomas John; Thomas van Overeem Hansen; Trinidad Caldés; Tatsuro Yamaguchi; Verónica Barca-Tierno; Pilar Garre; Giulia Martina Cavestro; Jürgen Weitz; Silke Redler; Reinhard Büttner; Vincent Heuveline; John L. Hopper; Aung Ko Win; Noralane Lindor; Steven Gallinger; Loïc Le Marchand; Polly A. Newcomb; Jane Figueiredo; Daniel D. Buchanan; Stephen N. Thibodeau; Sanne W. ten Broeke; Eivind Hovig; Sigve Nakken; Marta Pineda; Nuria Dueñas; Joan Brunet; Kate Green; Fiona Lalloo; Katie Newton; Emma J. Crosbie; Miriam Mints; Douglas Tjandra; Florencia Neffa; Patricia Esperon; Revital Kariv; Guy Rosner; Walter Hernán Pavicic; Pablo Kalfayan; Giovana Tardin Torrezan; Thiago Bassaneze; Claudia Martin; Gabriela Moslein; Aysel Ahadova; Matthias Kloor; Julian R. Sampson; Mark A. Jenkins; The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC)

Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-11 (2022)

Tischkowitz, M.; Colas, C.; Pouwels, S.; Hoogerbrugge, N.; Bisseling, T.; Bubien, V.; Caux, F.; Chabbert-Buffet, N.; Da Mota Gomes, S.; Gotthardt, M.; Kets, M.; Lachlan, K. L.; Links, T. P.; Longy, M.; Mann, R.; Kool, L. S.; Semple, R. K.; Stock, I.; Vos, J.; Ligtenberg, M.; Oostenbrink, R.; Sijmons, R.; Evans, G.; Woodward, E.; Maher, E.; Ferner, R. E.; Aretz, S.; Spier, I.; Steinke-Lange, V.; Holinski-Feder, E.; Schröck, E.; Frebourg, T.; Houdayer, C.; Wolkenstein, P.; Bours, Vincent; Legius, E.; Poppe, B.; Claes, K.; de Putter, R.; Guillermo, I. B.; Capella, G.; Vidal, J. B.; Lázaro, C.; Balmaña, J.; Hernandez, H. S.; Oliveira, C.; Teixeira, M.; Bajalica-Lagercrantz, S.; Tham, E.; Lubinski, J.; Ertmanska, K.; Melegh, B.; Krajc, M.; Blatnik, A.; Peltonen, S.; Hietala, M.; PHTS Guideline Development Group; The European Reference Network GENTURIS

Eur J Hum Genet
European Journal of Human Genetics, 28, 10, pp. 1387-1393
Semple, R K 2020, ' Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome ', European Journal of Human Genetics . https://doi.org/10.1038/s41431-020-0651-7
EUROPEAN JOURNAL OF HUMAN GENETICS

Alexander A.J. Grüter, MD; Julie M.L. Sijmons, MD; Usha K. Coblijn, MD, PhD; Boudewijn R. Toorenvliet, MD, PhD; Pieter J. Tanis, MD, PhD; Jurriaan B. Tuynman, MD, PhD

Annals of Surgery Open, Vol 4, Iss 4, p e343 (2023)

Alimohamed MZ; Department of Biochemistry and Molecular Biology, School of Biomedical Sciences, Muhimbili University of Health and Allied Sciences, Dar es salaam, Tanzania. mzahir89@gmail.com.; Tanzania Human Genetics Organization, Dar es salaam, Tanzania. mzahir89@gmail.com.; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands. mzahir89@gmail.com.; Kiula A; Department of Biochemistry and Molecular Biology, School of Biomedical Sciences, Muhimbili University of Health and Allied Sciences, Dar es salaam, Tanzania.; Fundikira L; Directorate of Clinical Support Services, Jakaya Kikwete Cardiac Institute, Dar es Salaam, Tanzania.; Letara N; Directorate of Clinical Support Services, Jakaya Kikwete Cardiac Institute, Dar es Salaam, Tanzania.; Mayala H; Directorate of Clinical Support Services, Jakaya Kikwete Cardiac Institute, Dar es Salaam, Tanzania.; Sijmons R; Department of Biochemistry and Molecular Biology, School of Biomedical Sciences, Muhimbili University of Health and Allied Sciences, Dar es salaam, Tanzania.; Tanzania Human Genetics Organization, Dar es salaam, Tanzania.; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.; Jongbloed JDH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.; Hershberger RE; Divisions of Human Genetics and Cardiovascular Medicine in the Department of Internal Medicine and the Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH, USA.; Williams SM; Departments of Population and Quantitative Health Sciences and Genetics and Genome Sciences Cleveland Institute for Computational Biology, Case Western Reserve University, Cleveland, OH, USA.; Asselbergs FW; Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.; Institute of Health Informatics, University College London, London, UK.; National Institute for Health Research, University College London Hospitals, Biomedical Research Centre, University College London, London, UK.; Chillo P; Directorate of Clinical Support Services, Jakaya Kikwete Cardiac Institute, Dar es Salaam, Tanzania.; Department of Internal Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Publisher: Nature Portfolio Country of Publication: England NLM ID: 9918250414506676 Publication Model: Electronic Cited Medium: Internet ISSN: 2730-664X (Electronic) Linking ISSN: 2730664X NLM ISO Abbreviation: Commun Med (Lond) Subsets: PubMed not MEDLINE

Fatemeh Ghorbani; Mohamed Z. Alimohamed; Juliana F. Vilacha; Krista K. Van Dijk; Jelkje De Boer-Bergsma; Michiel R. Fokkens; Henny Lemmink; Rolf H. Sijmons; Birgit Sikkema-Raddatz; Matthew R. Groves; Corien C. Verschuuren-Bemelmans; Dineke S. Verbeek; Cleo C. Van Diemen; Helga Westers

Frontiers in Genetics, Vol 13 (2022)

Møller, P.; Seppälä, T.; Dowty, J.G.; Haupt, S.; Dominguez-Valentin, M.; Sunde, L.; Bernstein, I.; Engel, C.; Aretz, S.; Nielsen, M.; Capella, G.; Evans, D.G.; Burn, J.; Holinski-Feder, E.; Bertario, L.; Bonanni, B.; Lindblom, A.; Levi, Z.; Macrae, F.; Winship, I.; Plazzer, J.P.; Sijmons, R.; Laghi, L.; Valle, A.D.; Heinimann, K.; Half, E.; Lopez-Koestner, F.; Alvarez-Valenzuela, K.; Scott, R.J.; Katz, L.; Laish, I.; Vainer, E.; Vaccaro, C.A.; Carraro, D.M.; Gluck, N.; Abu-Freha, N.; Stakelum, A.; Kennelly, R.; Winter, D.; Rossi, B.M.; Greenblatt, M.; Bohorquez, M.; Sheth, H.; Tibiletti, M.G.; Lino-Silva, L.S.; Horisberger, K.; Portenkirchner, C.; Nascimento, I.; Rossi, N.T.; da Silva, L.A.; Thomas, H; Zaránd, A.; Mecklin, J.P.; Pylvänäinen, K.; Renkonen-Sinisalo, L.; Lepisto, A.; Peltomäki, P.; Therkildsen, C.; Lindberg, L.J.; Thorlacius-Ussing, O.; von Knebel Doeberitz, M.; Loeffler, M.; Rahner, N.; Steinke-Lange, V.; Schmiegel, W.; Vangala, D.; Perne, C.; Hüneburg, R.; de Vargas, A.F.; Latchford, A.; Gerdes, A.M.; Backman, A.S.; Guillén-Ponce, C.; Snyder, C.; Lautrup, C.K.; Amor, D.; Palmero, E.; Stoffel, E.; Duijkers, F.; Hall, M.J.; Hampel, H.; Williams, H.; Okkels, H.; Lubiński, J.; Reece, J.; Ngeow, J.; Guillem, J.G.; Arnold, J.; Wadt, K.; Monahan, K.; Senter, L.; Rasmussen, L.J.; van Hest, L.P.; Ricciardiello, L.; Kohonen-Corish, M.R.J.; Ligtenberg, M.J.L.; Southey, M.; Aronson, M.; Zahary, M.N.; Samadder, N.J.; Hoogerbrugge, N.; Sampson, J.R.; Jenkins, M.A.

Mev Dominguez-Valentin; Saskia Haupt; Toni T. Seppälä; Julian R. Sampson; Lone Sunde; Inge Bernstein; Mark A. Jenkins; Christoph Engel; Stefan Aretz; Maartje Nielsen; Gabriel Capella; Francesc Balaguer; Dafydd Gareth Evans; John Burn; Elke Holinski-Feder; Lucio Bertario; Bernardo Bonanni; Annika Lindblom; Zohar Levi; Finlay Macrae; Ingrid Winship; John-Paul Plazzer; Rolf Sijmons; Luigi Laghi; Adriana Della Valle; Karl Heinimann; Tadeusz Dębniak; Robert Fruscio; Francisco Lopez-Koestner; Karin Alvarez-Valenzuela; Lior H. Katz; Ido Laish; Elez Vainer; Carlos Vaccaro; Dirce Maria Carraro; Kevin Monahan; Elizabeth Half; Aine Stakelum; Des Winter; Rory Kennelly; Nathan Gluck; Harsh Sheth; Naim Abu-Freha; Marc Greenblatt; Benedito Mauro Rossi; Mabel Bohorquez; Giulia Martina Cavestro; Leonardo S. Lino-Silva; Karoline Horisberger; Maria Grazia Tibiletti; Ivana do Nascimento; Huw Thomas; Norma Teresa Rossi; Leandro Apolinário da Silva; Attila Zaránd; Juan Ruiz-Bañobre; Vincent Heuveline; Jukka-Pekka Mecklin; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; Anna Lepistö; Päivi Peltomäki; Christina Therkildsen; Mia Gebauer Madsen; Stefan Kobbelgaard Burgdorf; John L. Hopper; Aung Ko Win; Robert W. Haile; Noralane Lindor; Steven Gallinger; Loïc Le Marchand; Polly A. Newcomb; Jane Figueiredo; Daniel D. Buchanan; Stephen N. Thibodeau; Magnus von Knebel Doeberitz; Markus Loeffler; Nils Rahner; Evelin Schröck; Verena Steinke-Lange; Wolff Schmiegel; Deepak Vangala; Claudia Perne; Robert Hüneburg; Silke Redler; Reinhard Büttner; Jürgen Weitz; Marta Pineda; Nuria Duenas; Joan Brunet Vidal; Leticia Moreira; Ariadna Sánchez; Eivind Hovig; Sigve Nakken; Kate Green; Fiona Lalloo; James Hill; Emma Crosbie; Miriam Mints; Yael Goldberg; Douglas Tjandra; Sanne W. ten Broeke; Revital Kariv; Guy Rosner; Suresh H. Advani; Lidiya Thomas; Pankaj Shah; Mithun Shah; Florencia Neffa; Patricia Esperon; Walter Pavicic; Giovana Tardin Torrezan; Thiago Bassaneze; Claudia Alejandra Martin; Gabriela Moslein; Pål Moller

eClinicalMedicine
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instname
Dominguez-Valentin, M, Haupt, S, Seppälä, T T, Sampson, J R, Sunde, L, Bernstein, I, Jenkins, M A, Engel, C, Aretz, S, Nielsen, M, Capella, G, Balaguer, F, Evans, D G, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J-P, Sijmons, R, Laghi, L, Della Valle, A, Heinimann, K, Dębniak, T, Fruscio, R, Lopez-Koestner, F, Alvarez-Valenzuela, K, Katz, L H, Laish, I, Vainer, E, Vaccaro, C, Carraro, D M, Monahan, K, Half, E, Stakelum, A, Winter, D, Kennelly, R, Gluck, N, Sheth, H, Abu-Freha, N, Greenblatt, M, Rossi, B M, Bohorquez, M, Cavestro, G M, Lino-Silva, L S, Horisberger, K, Tibiletti, M G, Nascimento, I D, Thomas, H, Rossi, N T, Apolinário da Silva, L, Zaránd, A, Ruiz-Bañobre, J, Heuveline, V, Mecklin, J-P, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Peltomäki, P, Therkildsen, C, Madsen, M G, Burgdorf, S K, Hopper, J L, Win, A K, Haile, R W, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J, Buchanan, D D, Thibodeau, S N, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Schröck, E, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hüneburg, R, Redler, S, Büttner, R, Weitz, J, Pineda, M, Duenas, N, Vidal, J B, Moreira, L, Sánchez, A, Hovig, E, Nakken, S, Green, K, Lalloo, F, Hill, J, Crosbie, E, Mints, M, Goldberg, Y, Tjandra, D, Ten Broeke, S W, Kariv, R, Rosner, G, Advani, S H, Thomas, L, Shah, P, Shah, M, Neffa, F, Esperon, P, Pavicic, W, Torrezan, G T, Bassaneze, T, Martin, C A, Moslein, G & Moller, P 2023, 'Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database', EClinicalMedicine, vol. 58, 101909. https://doi.org/10.1016/j.eclinm.2023.101909
Dominguez-Valentin, M, Haupt, S, Seppälä, T T, Sampson, J R, Sunde, L, Bernstein, I, Jenkins, M A, Engel, C, Aretz, S, Nielsen, M, Capella, G, Balaguer, F, Evans, D G, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J P, Sijmons, R, Laghi, L, Della Valle, A, Heinimann, K, Dębniak, T, Fruscio, R, Lopez-Koestner, F, Alvarez-Valenzuela, K, Katz, L H, Laish, I, Vainer, E, Vaccaro, C, Carraro, D M, Monahan, K, Half, E, Stakelum, A, Winter, D, Kennelly, R, Gluck, N, Sheth, H, Abu-Freha, N, Greenblatt, M, Rossi, B M, Bohorquez, M, Cavestro, G M, Lino-Silva, L S, Horisberger, K, Tibiletti, M G, Nascimento, I D, Thomas, H, Rossi, N T, Apolinário da Silva, L, Zaránd, A, Ruiz-Bañobre, J, Heuveline, V, Mecklin, J P, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Peltomäki, P, Therkildsen, C, Madsen, M G, Burgdorf, S K, Hopper, J L, Win, A K, Haile, R W, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J, Buchanan, D D, Thibodeau, S N, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Schröck, E, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hüneburg, R, Redler, S, Büttner, R, Weitz, J, Pineda, M, Duenas, N, Vidal, J B, Moreira, L, Sánchez, A, Hovig, E, Nakken, S, Green, K, Lalloo, F, Hill, J, Crosbie, E, Mints, M, Goldberg, Y, Tjandra, D, ten Broeke, S W, Kariv, R, Rosner, G, Advani, S H, Thomas, L, Shah, P, Shah, M, Neffa, F, Esperon, P, Pavicic, W, Torrezan, G T, Bassaneze, T, Martin, C A, Moslein, G & Moller, P 2023, ' Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database ', EClinicalMedicine, vol. 58, 101909 . https://doi.org/10.1016/j.eclinm.2023.101909
Dominguez-Valentin, M, Haupt, S, Seppälä, T, Sampson, J R, Sunde, L, Bernstein, I, Jenkins, M A, Engel, C, Aretz, S, Nielsen, M, Capella, G, Balaguer, F, Evans, D G, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J-P, Sijmons, R, Laghi, L, Della Valle, A, Heinimann, K, Dębniak, T, Fruscio, R, Lopez-Koestner, F, Alvarez-Valenzuela, K, Katz, L H, Laish, I, Vainer, E, Vaccaro, C, Carraro, D M, Monahan, K, Half, E, Stakelum, A, Winter, D, Kennelly, R, Gluck, N, Sheth, H, Abu-Freha, N, Greenblatt, M, Rossi, B M, Bohorquez, M, Cavestro, G M, Lino-Silva, L S, Horisberger, K, Tibiletti, M G, Nascimento, I D, Rossi, N T, Apolinário da Silva, L, Zaránd, A, Ruiz-Bañobre, J, Heuveline, V, Mecklin, J-P, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Peltomäki, P, Therkildsen, C, Madsen, M G, Burgdorf, S K, Hopper, J L, Win, A K, Haile, R W, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J, Buchanan, D D, Thibodeau, S N, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Schröck, E, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hüneburg, R, Redler, S, Büttner, R, Weitz, J, Pineda, M, Duenas, N, Vidal, J B, Moreira, L, Sánchez, A, Hovig, E, Nakken, S, Green, K, Lalloo, F, Hill, J, Crosbie, E, Mints, M, Goldberg, Y, Tjandra, D, Ten Broeke, S W, Kariv, R, Rosner, G, Advani, S H, Thomas, L, Shah, P, Shah, M, Neffa, F, Esperon, P, Pavicic, W, Torrezan, G T, Bassaneze, T, Martin, C A, Moslein, G & Moller, P 2023, 'Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database', EClinicalMedicine, vol. 58, 101909. https://doi.org/10.1016/j.eclinm.2023.101909

Ahadova A; Witt J; Haupt S; Gallon R; Hüneburg R; Nattermann J; Ten Broeke S; Bohaumilitzky L; Hernandez-Sanchez A; Santibanez-Koref M; Jackson MS; Ahtiainen M; Pylvänäinen K; Andini K; Grolmusz VK; Möslein G; Dominguez-Valentin M; Møller P; Fürst D; Sijmons R; Borthwick GM; Burn J; Mecklin JP; Heuveline V; von Knebel Doeberitz M; Seppälä T; Kloor M

International Journal of Cancer. 152(10):2024-2031

L. F. Johansson; E. N. de Boer; H. A. de Weerd; F. van Dijk; M. G. Elferink; G. H. Schuring-Blom; R. F. Suijkerbuijk; R. J. Sinke; G. J. te Meerman; R. H. Sijmons; M. A. Swertz; B. Sikkema-Raddatz

Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)