학술논문
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'학술논문'
에서 검색결과 9건 | 목록
1~20
Academic Journal
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)
Academic Journal
Mev Dominguez-Valentin; Toni T. Seppälä; Julian R. Sampson; Finlay Macrae; Ingrid Winship; D. Gareth Evans; Rodney J. Scott; John Burn; Gabriela Möslein; Inge Bernstein; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; Anna Lepistö; Annika Lindblom; John-Paul Plazzer; Douglas Tjandra; Huw Thomas; Kate Green; Fiona Lalloo; Emma J. Crosbie; James Hill; Gabriel Capella; Marta Pineda; Matilde Navarro; Joan Brunet Vidal; Karina Rønlund; Randi Thyregaard Nielsen; Mette Yilmaz; Louise Laurberg Elvang; Lior Katz; Maartje Nielsen; Sanne W. ten Broeke; Sigve Nakken; Eivind Hovig; Lone Sunde; Matthias Kloor; Magnus v Knebel Doeberitz; Aysel Ahadova; Noralane Lindor; Verena Steinke-Lange; Elke Holinski-Feder; Jukka-Pekka Mecklin; Pål Møller
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-6 (2019)
Academic Journal
Aysel Ahadova; Toni T. Seppälä; Christoph Engel; Richard Gallon; John Burn; Elke Holinski‐Feder; Verena Steinke‐Lange; Gabriela Möslein; Maartje Nielsen; Sanne W. ten Broeke; Luigi Laghi; Mev Dominguez‐Valentin; Gabriel Capella; Finlay Macrae; Rodney Scott; Robert Hüneburg; Jacob Nattermann; Michael Hoffmeister; Hermann Brenner; Hendrik Bläker; Magnus von Knebel Doeberitz; Julian R. Sampson; Hans Vasen; Jukka‐Pekka Mecklin; Pål Møller; Matthias Kloor
Dipòsit Digital de la UB
Universidad de Barcelona
Articles publicats en revistes (Ciències Clíniques)
Universidad de Barcelona
Articles publicats en revistes (Ciències Clíniques)
Academic Journal
Sanne W. ten Broeke; Mar Rodríguez-Girondo; Manon Suerink; Stefan Aretz; Inge Bernstein; Gabriel Capellá; Christoph Engel; Encarna B. Gomez-Garcia; Liselot P. van Hest; Magnus von Knebel Doeberitz; Kristina Lagerstedt-Robinson; Tom G.W. Letteboer; Pal Moller; Theo A. van Os; Marta Pineda; Nils Rahner; Maran J.W. Olderode-Berends; Jenny von Salomé; Hans K. Schackert; Liesbeth Spruijt; Verena Steinke-Lange; Anja Wagner; Carli M.J. Tops; Maartje Nielsen
Ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Møller, P, van Os, T A M, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salomé, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, 'The apparent genetic anticipation in PMS2-associated Lynch syndrome families is explained by birth cohort effect', Cancer Epidemiology, Biomarkers & Prevention, vol. 28, no. 6, pp. 1010-1014. https://doi.org/10.1158/1055-9965.EPI-18-0576
ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Moller, P, van Os, T A, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salome, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, 'The apparent genetic anticipation in PMS2-associated lynch syndrome families is explained by birth-cohort effect', Cancer Epidemiology Biomarkers and Prevention, vol. 28, no. 6, pp. 1010-1014. https://doi.org/10.1158/1055-9965.EPI-18-0576
Cancer Epidemiology, Biomarkers & Prevention, 28, 6, pp. 1010-1014
ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Moller, P, van Os, T A, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salome, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, 'The apparent genetic anticipation in PMS2-associated lynch syndrome families is explained by birth-cohort effect', Cancer Epidemiology Biomarkers and Prevention, vol. 28, no. 6, pp. 1010-1014. https://doi.org/10.1158/1055-9965.EPI-18-0576
Cancer Epidemiology, Biomarkers & Prevention, 28, 6, pp. 1010-1014
Academic Journal
Sanne W. ten Broeke; Heleen M. van der Klift; Carli M.J. Tops; Stefan Aretz; Inge Bernstein; Daniel D. Buchanan; Albert de la Chapelle; Gabriel Capella; Mark Clendenning; Christoph Engel; Steven Gallinger; Encarna Gomez Garcia; Jane C. Figueiredo; Robert Haile; Heather L. Hampel; Liselotte van Hest; John L. Hopper; Nicoline Hoogerbrugge; Magnus von Knebel Doeberitz; Loic Le Marchand; Tom G.W. Letteboer; Mark A. Jenkins; Annika Lindblom; Noralane M. Lindor; Arjen R. Mensenkamp; Pål Møller; Polly A. Newcomb; Theo A.M. van Os; Rachel Pearlman; Marta Pineda; Nils Rahner; Egbert J.W. Redeker; Maran J.W. Olderode-Berends; Christophe Rosty; Hans K. Schackert; Rodney Scott; Leigha Senter; Liesbeth Spruijt; Verena Steinke-Lange; Manon Suerink; Stephen Thibodeau; Yvonne J. Vos; Anja Wagner; Ingrid Winship; Frederik J. Hes; Hans F.A. Vasen; Juul T. Wijnen; Maartje Nielsen; Aung Ko Win
Ten Broeke, S W, van der Klift, H M, Tops, C M J, Aretz, S, Bernstein, I, Buchanan, D D, de la Chapelle, A, Capella, G, Clendenning, M, Engel, C, Gallinger, S, Gomez Garcia, E, Figueiredo, J C, Haile, R, Hampel, H L, Hopper, J L, Hoogerbrugge, N, von Knebel Doeberitz, M, Le Marchand, L, Letteboer, T G W, Jenkins, M A, Lindblom, A, Lindor, N M, Mensenkamp, A R, Møller, P, Newcomb, P A, van Os, T A M, Pearlman, R, Pineda, M, Rahner, N, Redeker, E J W, Olderode-Berends, M J W, Rosty, C, Schackert, H K, Scott, R, Senter, L, Spruijt, L, Steinke-Lange, V, Suerink, M, Thibodeau, S, Vos, Y J, Wagner, A, Winship, I, Hes, F J, Vasen, H F A, Wijnen, J T, Nielsen, M & Win, A K 2018, 'Cancer Risks for PMS2-Associated Lynch Syndrome', Journal of clinical oncology : official journal of the American Society of Clinical Oncology, vol. 36, no. 29, pp. 2961-2968. https://doi.org/10.1200/JCO.2018.78.4777
Journal of Clinical Oncology, 36, 29, pp. 2961-2968
Journal of Clinical Oncology, 36, 29, pp. 2961-2968
Academic Journal
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
Articles publicats en revistes (Ciències Clíniques)
Dipòsit Digital de la UB
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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
Articles publicats en revistes (Ciències Clíniques)
Dipòsit Digital de la UB
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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
Academic Journal
Judith E. Grolleman; Richarda M. de Voer; Fadwa A. Elsayed; Maartje Nielsen; Robbert D. A. Weren; Claire Palles; Marjolijn J. L. Ligtenberg; Janet R. Vos; Sanne W. ten Broeke; Noel F. C. C. de Miranda; Renske A. Kuiper; Eveline J. Kamping; Erik A. M. Jansen; M. Elisa Vink-BBrger; Isabell Popp; Alois Lang; Isabel Spier; Robert HHneburg; Paul A. James; Na Li; Marija Staninova; Helen Lindsay; David Cockburn; Olivera Spasic-Boskovic; Mark Clendenning; Kevin Sweet; Gabriel Capelll; Wenche Sjursen; Hildegunn HHberg-Vetti; Marjolijn C. Jongmans; Kornelia Neveling; Ad Geurts van Kessel; Hans Morreau; Frederik J. Hes; Rolf H. Sijmons; Hans K. Schackert; Clara Ruiz-Ponte; Dagmara Dymerska; Jan Lubinski; Barbara Rivera; William D. Foulkes; Ian P. Tomlinson; Laura Valle; Daniel. D. Buchanan; Sue Kenwrick; Julian Adlard; Aleksandar J. Dimovski; Ian G. Campbell; Stefan Aretz; Detlev Schindler; Tom van Wezel; Nicoline Hoogerbrugge; Roland Kuiper
SSRN Electronic Journal.
Academic Journal
Mev Dominguez-Valentin; Julian R. Sampson; Toni T. Seppälä; Sanne W. ten Broeke; John-Paul Plazzer; Sigve Nakken; Christoph Engel; Stefan Aretz; Mark A. Jenkins; Lone Sunde; Inge Bernstein; Gabriel Capella; Francesc Balaguer; Huw Thomas; D. Gareth Evans; John Burn; Marc Greenblatt; Eivind Hovig; Wouter H. de Vos tot Nederveen Cappel; Rolf H. Sijmons; Lucio Bertario; Maria Grazia Tibiletti; Giulia Martina Cavestro; Annika Lindblom; Adriana Della Valle; Francisco Lopez-Köstner; Nathan Gluck; Lior H. Katz; Karl Heinimann; Carlos A. Vaccaro; Reinhard Büttner; Heike Görgens; Elke Holinski-Feder; Monika Morak; Stefanie Holzapfel; Robert Hüneburg; Magnus von Knebel Doeberitz; Markus Loeffler; Nils Rahner; Hans K. Schackert; Verena Steinke-Lange; Wolff Schmiegel; Deepak Vangala; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; John L. Hopper; Aung Ko Win; Robert W. Haile; Noralane M. Lindor; Steven Gallinger; Loïc Le Marchand; Polly A. Newcomb; Jane C. Figueiredo; Stephen N. Thibodeau; Karin Wadt; Christina Therkildsen; Henrik Okkels; Zohreh Ketabi; Leticia Moreira; Ariadna Sánchez; Miquel Serra-Burriel; Marta Pineda; Matilde Navarro; Ignacio Blanco; Kate Green; Fiona Lalloo; Emma J. Crosbie; James Hill; Oliver G. Denton; Ian M. Frayling; Einar Andreas Rødland; Hans Vasen; Miriam Mints; Florencia Neffa; Patricia Esperon; Karin Alvarez; Revital Kariv; Guy Rosner; Tamara Alejandra Pinero; María Laura Gonzalez; Pablo Kalfayan; Douglas Tjandra; Ingrid M. Winship; Finlay Macrae; Gabriela Möslein; Jukka-Pekka Mecklin; Maartje Nielsen; Pål Møller
Genet Med
Articles publicats en revistes (Ciències Clíniques)
Dipòsit Digital de la UB
instname
Universidad de Barcelona
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J-P, Nielsen, M & Møller, P 2020, 'Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database', Genetics in Medicine, vol. 22, no. 1, pp. 15-25. https://doi.org/10.1038/s41436-019-0596-9
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M & Okkels, H 2020, 'Correction : Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database', Genetics in Medicine, vol. 22, no. 9. https://doi.org/10.1038/s41436-020-0892-4
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, ten Broeke, S W, Plazzer, J P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Evans, D G, Crosbie, E, Hill, J & et al. 2019, 'Cancer risks by gene, age and gender in 6,350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database', Genetics in Medicine. https://doi.org/10.1038/s41436-019-0596-9
Articles publicats en revistes (Ciències Clíniques)
Dipòsit Digital de la UB
instname
Universidad de Barcelona
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J-P, Nielsen, M & Møller, P 2020, 'Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database', Genetics in Medicine, vol. 22, no. 1, pp. 15-25. https://doi.org/10.1038/s41436-019-0596-9
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M & Okkels, H 2020, 'Correction : Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database', Genetics in Medicine, vol. 22, no. 9. https://doi.org/10.1038/s41436-020-0892-4
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, ten Broeke, S W, Plazzer, J P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Evans, D G, Crosbie, E, Hill, J & et al. 2019, 'Cancer risks by gene, age and gender in 6,350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database', Genetics in Medicine. https://doi.org/10.1038/s41436-019-0596-9
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