학술논문
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'학술논문'
에서 검색결과 287건 | 목록
1~20
Academic Journal
Vlaming, M.; Ausems, M.G.; Schijven, G.; Oort, I.M. van; Kets, C.M.; Komdeur, F.L.; Kolk, L.E. van der; Oldenburg, R.A.; Sijmons, R.H.; Kiemeney, L.A.L.M.; Bleiker, E.M.
Fam Cancer
Familial Cancer, 23, 2, pp. 165-175
Familial Cancer, 23, 2, pp. 165-175
Academic Journal
Alimohamed, M.Z.; Johansson, L.F.; Posafalvi, A.; Boven, L.G.; Dijk, K.K. van; Walters, L.; Vos, Y.J.; Westers, H.; Hoedemaekers, Y.M.; Sinke, R.J.; Sijmons, R.H.; Sikkema-Raddatz, B.; Jongbloed, J.D.; Zwaag, Paul A. van der
International Journal of Cardiology, 332, pp. 99-104
Academic Journal
Seppala, T.T.; Dominguez-Valentin, M.; Crosbie, E.J.; Engel, C.; Aretz, S.; Macrae, F.; Winship, I.; Capella, G.; Thomas, H.; Hovig, E.; Nielsen, M.; Sijmons, R.H.; Bertario, L.; Bonanni, B.; Tibiletti, M.G.; Cavestro, G.M.; Mints, M.; Gluck, N.; Katz, L.; Heinimann, K.; Vaccaro, C.A.; Green, K.; Lalloo, F.; Hill, J.; Schmiegel, W.; Vangala, D.; Perne, C.; Strauss, H.G.; Tecklenburg, J.; Holinski-Feder, E.; Steinke-Lange, V.; Mecklin, J.P.; Plazzer, J.P.; Pineda, M.; Navarro, M.; Vida, J.B.; Kariv, R.; Rosner, G.; Pinero, T.A.; Pavicic, W.; Kalfayan, P.; Broeke, S.W. ten; Jenkins, M.A.; Sunde, L.; Bernstein, I.; Burn, J.; Greenblatt, M.; Cappel, W.H.D.T.N.; Valle, A. della; Lopez-Koestner, F.; Alvarez, K.; Buttner, R.; Gorgens, H.; Morak, M.; Holzapfel, S.; Huneburg, R.; Doeberitz, M.V.; Loeffler, M.; Redler, S.; Weitz, J.; Pylvanainen, K.; Renkonen-Sinisalo, L.; Lepisto, A.; Hopper, J.L.; Win, A.K.; Lindor, N.M.; Gallinger, S.; Marchand, L.L.; Newcomb, P.A.; Figueiredo, J.C.; Thibodeau, S.N.; Therkildsen, C.; Wadt, K.A.W.; Mourits, M.J.E.; Ketabi, Z.; Denton, O.G.; Rodland, E.A.; Vasen, H.; Neffa, F.; Esperon, P.; Tjandra, D.; Moslein, G.; Rokkones, E.; Sampson, J.R.; Evans, D.G.; Moller, P.
Eur J Cancer
Dipòsit Digital de la UB
Universidad de Barcelona
Articles publicats en revistes (Ciències Clíniques)
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Hovig, E, Nielsen, M,Sijmons , R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J P, Plazzer, J P, Pineda, M, Navarro, M, Vida, J B, Kariv, R, Rosner, G, Piñero, T A, Pavicic, W, Kalfayan, P, ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Redler, S, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Hopper, J L, Win, A K, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Therkildsen, C, Wadt, K A W, Mourits, M J E, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Rokkones, E, Sampson, J R, Evans, D G & Møller, P 2021, 'Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report', European Journal of Cancer, vol. 148, pp. 124-133. https://doi.org/10.1016/j.ejca.2021.02.022
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Hovig, E, Nielsen, M,Sijmons , R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J P, Plazzer, J P, Pineda, M, Navarro, M, Vida, J B, Kariv, R, Rosner, G, Piñero, T A, Pavicic, W, Kalfayan, P, ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Redler, S, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Hopper, J L, Win, A K, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Therkildsen, C, Wadt, K A W, Mourits, M J E, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Rokkones, E, Sampson, J R, Evans, D G & Møller, P 2021, ' Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report ', European Journal of Cancer, vol. 148, pp. 124-133 . https://doi.org/10.1016/j.ejca.2021.02.022
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Hovig, E, Nielsen, M,Sijmons , R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H-G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J-P, Plazzer, J-P, Pineda, M, Navarro, M, Vida, J B, Kariv, R, Rosner, G, Piñero, T A, Pavicic, W, Kalfayan, P, Ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos Tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Redler, S, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Hopper, J L, Win, A K, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Therkildsen, C, Wadt, K A W, Mourits, M J E, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Rokkones, E, Sampson, J R, Evans, D G & Møller, P 2021, 'Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report', European Journal of Cancer, vol. 148, pp. 124-133. https://doi.org/10.1016/j.ejca.2021.02.022
Dipòsit Digital de la UB
Universidad de Barcelona
Articles publicats en revistes (Ciències Clíniques)
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Hovig, E, Nielsen, M,
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Hovig, E, Nielsen, M,
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Hovig, E, Nielsen, M,
Academic Journal
Dominguez-Valentin, M.; Crosbie, E.J.; Engel, C.; Aretz, S.; Macrae, F.; Winship, I.; Capella, G.; Thomas, H.; Nakken, S.; Hovig, E.; Nielsen, M.; Sijmons, R.H.; Bertario, L.; Bonanni, B.; Tibiletti, M.G.; Cavestro, G.M.; Mints, M.; Gluck, N.; Katz, L.; Heinimann, K.; Vaccaro, C.A.; Green, K.; Lalloo, F.; Hill, J.; Schmiegel, W.; Vangala, D.; Perne, C.; Strauss, H.G.; Tecklenburg, J.; Holinski-Feder, E.; Steinke-Lange, V.; Mecklin, J.P.; Plazzer, J.P.; Pineda, M.; Navarro, M.; Vidal, J.B.; Kariv, R.; Rosner, G.; Pinero, T.A.; Gonzalez, M.L.; Kalfayan, P.; Ryan, N.; Broeke, S.W. ten; Jenkins, M.A.; Sunde, L.; Bernstein, I.; Burn, J.; Greenblatt, M.; Cappel, W.H.D.T.N.; Valle, A. della; Lopez-Koestner, F.; Alvarez, K.; Buttner, R.; Gorgens, H.; Morak, M.; Holzapfel, S.; Huneburg, R.; Doeberitz, M.V.; Loeffler, M.; Rahner, N.; Weitz, J.; Pylvanainen, K.; Renkonen-Sinisalo, L.; Lepisto, A.; Auranen, A.; Hopper, J.L.; Win, A.K.; Haile, R.W.; Lindor, N.M.; Gallinger, S.; Marchand, L. le; Newcomb, P.A.; Figueiredo, J.C.; Thibodeau, S.N.; Therkildsen, C.; Okkels, H.; Ketabi, Z.; Denton, O.G.; Rodland, E.A.; Vasen, H.; Neffa, F.; Esperon, P.; Tjandra, D.; Moslein, G.; Sampson, J.R.; Evans, D.G.; Seppala, T.T.; Moller, P.
Genet Med
Articles publicats en revistes (Ciències Clíniques)
Dipòsit Digital de la UB
instname
Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Nakken, S, Hovig, E, Nielsen, M,Sijmons , R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J P, Plazzer, J P, Pineda, M, Navarro, M, Vidal, J B, Kariv, R, Rosner, G, Piñero, T A, Gonzalez, M L, Kalfayan, P, Ryan, N, ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Auranen, A, 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, Therkildsen, C, Okkels, H, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Sampson, J R, Evans, D G, Seppälä, T T & Møller, P 2021, 'Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report', Genetics in Medicine, vol. 23, no. 4, pp. 705–712. https://doi.org/10.1038/s41436-020-01029-1
Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Nakken, S, Hovig, E, Nielsen, M,Sijmons , R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauss, H-G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J-P, Plazzer, J-P, Pineda, M, Navarro, M, Brunet Vidal, J, Kariv, R, Rosner, G, Alejandra Pinero, T, Laura Gonzalez, M, Kalfayan, P, Ryan, N, Ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, Cappel, W H D V T N, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Buettner, R, Goergens, H, Morak, M, Holzapfel, S, Hueneburg, R, Doeberitz, M V K, Loeffler, M, Rahner, N, Weitz, J, Pylvanainen, K, Renkonen-Sinisalo, L, Lepisto, A, Auranen, A, 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, Therkildsen, C, Okkels, H, Ketabi, Z, Denton, O G, Rodland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Moeslein, G, Sampson, J R, Evans, D G, Seppala, T T & Moller, P 2021, 'Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report', Genetics in Medicine, vol. 23, no. 4, pp. 705-712. https://doi.org/10.1038/s41436-020-01029-1
Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Nakken, S, Hovig, E, Nielsen, M,Sijmons , R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H-G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J-P, Plazzer, J-P, Pineda, M, Navarro, M, Vidal, J B, Kariv, R, Rosner, G, Piñero, T A, Kalfayan, P, Ryan, N, Ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos Tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Auranen, A, 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, Therkildsen, C, Okkels, H, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Sampson, J R, Evans, D G, Seppälä, T T & Møller, P 2020, 'Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report', Genetics in medicine : official journal of the American College of Medical Genetics. https://doi.org/10.1038/s41436-020-01029-1
Articles publicats en revistes (Ciències Clíniques)
Dipòsit Digital de la UB
instname
Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Nakken, S, Hovig, E, Nielsen, M,
Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Nakken, S, Hovig, E, Nielsen, M,
Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Nakken, S, Hovig, E, Nielsen, M,
Academic Journal
Drost, M.; Tiersma, Y.; Thompson, B.A.; Frederiksen, J.H.; Keijzers, G.; Glubb, D.; Kathe, S.; Osinga, J.; Westers, H.; Pappas, L.; Boucher, K.M.; Molenkamp, S.; Zonneveld, J.B.; Asperen, C.J. van; Goldgar, D.E.; Wallace, S.S.; Sijmons, R.H.; Spurdle, A.B.; Rasmussen, L.J.; Greenblatt, M.S.; Wind, N. de; Tavtigian, S.V.
Genetics in Medicine. 21:1486-1496
Academic Journal
Woolderink, J.M. ; De Bock, G.H. ; de Hullu, J.A. ; Hollema, H. ; Zweemer, R.P. ; Slangen, B.F.M. ; Gaarenstroom, K.N. ; van Beurden, M. ; van Doorn, H.C. ; Sijmons, R.H. ; Vasen, H.F.A. ; Mourits, M.J.E.
In Gynecologic Oncology August 2018 150(2):324-330
Academic Journal
Weren, R.D.A.; van der Post, R.S.; Vogelaar, I.P.; van Krieken, J.H.J.M.; Spruijt, L.; Lubinski, J.; Jakubowska, A.; Teodorczyk, U.; Aalfs, C.M.; van Hest, L.P.; de Oliveira, C.; Kamping, E.J.; Schackert, H.K.; Ranzani, G.N.; Garcia, E.B.; Hes, F.J.; Holinski-Feder, E.; Genuardi, M.; Ausems, M.G.E.M.; Sijmons, R.H.; Wagner, A.; van der Kolk, L.E.; Cats, A.; Bjornevoll, I.; Hoogerbrugge, N.; Ligtenberg, M.J.L.
J Med Genet
Weren, R D A, van der Post, R S, Vogelaar, I P, Han van Krieken, J, Spruijt, L, Lubinski, J, Jakubowska, A, Teodorczyk, U, Aalfs, C M, van Hest, L P, Oliveira, C, Kamping, E J, Schackert, H K, Ranzani, G N, García, E B G M, Hes, F J, Holinski-Feder, E, Genuardi, M, Ausems, M G E M,Sijmons , R H, Wagner, A, van der Kolk, L E, Cats, A, Bjørnevoll, I, Hoogerbrugge, N & Ligtenberg, M J L 2018, 'Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility', Journal of Medical Genetics, vol. 55, no. 10, pp. 669-674. https://doi.org/10.1136/jmedgenet-2017-104962
Journal of Medical Genetics, 55, 10, pp. 669-674
Weren, R D A, van der Post, R S, Vogelaar, I P, Han van Krieken, J, Spruijt, L, Lubinski, J, Jakubowska, A, Teodorczyk, U, Aalfs, C M, van Hest, L P, Oliveira, C, Kamping, E J, Schackert, H K, Ranzani, G N, García, E B G M, Hes, F J, Holinski-Feder, E, Genuardi, M, Ausems, M G E M,
Journal of Medical Genetics, 55, 10, pp. 669-674
Academic Journal
Vogelaar, I.P.; van der Post, R.S.; van Krieken, J.H.; Spruijt, L.; van Zelst-Stams, W.A.G.; Kets, C.M.; Lubinski, J.; Jakubowska, A.; Teodorczyk, U.; Aalfs, C.M.; van Hest, L.P.; Pinheiro, H.; de Oliveira, C.; Jhangiani, S.N.; Muzny, D.M.; Gibbs, R.A.; Lupski, J.R.; de Ligt, J.; Vissers, L.E.L.M.; Hoischen, A.; Gilissen, C.; van de Vorst, J.M.; Goeman, J.J.; Schackert, H.K.; Ranzani, G.N.; Molinaro, V.; Garcia, E.B.; Hes, F.J.; Holinski-Feder, E.; Genuardi, M.; Ausems, M.; Sijmons, R.H.; Wagner, A.; van der Kolk, L.E.; Bjornevoll, I.; Hoberg-Vetti, H.; Geurts van Kessel, A.H.M.; Kuiper, R.P.; Ligtenberg, M.J.L.; Hoogerbrugge, N.
Eur J Hum Genet
Vogelaar, I P, Van Der Post, R S, Van Krieken, J H J M, Spruijt, L, Van Zelst-Stams, W A G, Kets, C M, Lubinski, J, Jakubowska, A, Teodorczyk, U, Aalfs, C M, Van Hest, L P, Pinheiro, H, Oliveira, C, Jhangiani, S N, Muzny, D M, Gibbs, R A, Lupski, J R, De Ligt, J, Vissers, L E L M, Hoischen, A, Gilissen, C, Van De Vorst, M, Goeman, J J, Schackert, H K, Ranzani, G N, Molinaro, V, García, E B G, Hes, F J, Holinski-Feder, E, Genuardi, M, Ausems, M G E M,Sijmons , R H, Wagner, A, Van Der Kolk, L E, Bjørnevoll, I, Høberg-Vetti, H, Van Kessel, A G, Kuiper, R P, Ligtenberg, M J L & Hoogerbrugge, N 2017, 'Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing', European Journal of Human Genetics, vol. 25, no. 11, pp. 1246-1252. https://doi.org/10.1038/ejhg.2017.138
European Journal of Human Genetics, 25, 11, pp. 1246-1252
Vogelaar, I P, Van Der Post, R S, Van Krieken, J H J M, Spruijt, L, Van Zelst-Stams, W A G, Kets, C M, Lubinski, J, Jakubowska, A, Teodorczyk, U, Aalfs, C M, Van Hest, L P, Pinheiro, H, Oliveira, C, Jhangiani, S N, Muzny, D M, Gibbs, R A, Lupski, J R, De Ligt, J, Vissers, L E L M, Hoischen, A, Gilissen, C, Van De Vorst, M, Goeman, J J, Schackert, H K, Ranzani, G N, Molinaro, V, García, E B G, Hes, F J, Holinski-Feder, E, Genuardi, M, Ausems, M G E M,
European Journal of Human Genetics, 25, 11, pp. 1246-1252
Academic Journal
Moller, P.; Seppala, T.T.; Bernstein, I.; Holinski-Feder, E.; Sala, P.; Evans, D.G.; Lindblom, A.; Macrae, F.; Blanco, I.; Sijmons, R.H.; Jeffries, J.; Vasen, H.F.A.; Burn, J.; Nakken, S.; Hovig, E.; Rodland, E.A.; Tharmaratnam, K.; Cappel, W.H.D.T.N.; Hill, J.; Wijnen, J.T.; Jenkins, M.A.; Green, K.; Lalloo, F.; Sunde, L.; Mints, M.; Bertario, L.; Pineda, M.; Navarro, M.; Morak, M.; Renkonen-Sinisalo, L.; Valentin, M.D.; Frayling, I.M.; Plazzer, J.P.; Pylvanainen, K.; Genuardi, M.; Mecklin, J.P.; Moeslein, G.; Sampson, J.R.; Capella, G.; Collaboration Mallorca Grp
Gut
Dipòsit Digital de la UB
Universidad de Barcelona
Articles publicats en revistes (Ciències Clíniques)
instname
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Gareth Evans, D, Lindblom, A, Macrae, F, Blanco, I,Sijmons , R H, Jeffries, J, Vasen, H F A, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J T, Jenkins, M A, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Valentin, M D, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Möslein, G, Sampson, J R, Capellá, G & Mallorca Group 2018, 'Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age : a report from the Prospective Lynch Syndrome Database', Gut, vol. 67, no. 7, pp. 1306–1316. https://doi.org/10.1136/gutjnl-2017-314057
Moller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, D, Lindblom, A, Macrae, F, Blanco, I,Sijmons , R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Dominguez Valentin, M, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Möslein, G, Sampson, J & Capella, G 2017, 'Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age; a report from the Prospective Lynch Syndrome Database', Gut. https://doi.org/10.1136/gutjnl-2017-314057
Møller, P, Seppälä, T T, Bernstein, I, Holinski-Feder, E, Sala, P, Gareth Evans, D, Lindblom, A, Macrae, F, Blanco, I,Sijmons , R H, Jeffries, J, Vasen, H F A, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J T, Jenkins, M A, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Valentin, M D, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Moeslein, G, Sampson, J R, Capella, G & Mallorca Group 2018, 'Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age : a report from the Prospective Lynch Syndrome Database', Gut, vol. 67, no. 7, pp. 1306-1316. https://doi.org/10.1136/gutjnl-2017-314057
Dipòsit Digital de la UB
Universidad de Barcelona
Articles publicats en revistes (Ciències Clíniques)
instname
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Gareth Evans, D, Lindblom, A, Macrae, F, Blanco, I,
Moller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, D, Lindblom, A, Macrae, F, Blanco, I,
Møller, P, Seppälä, T T, Bernstein, I, Holinski-Feder, E, Sala, P, Gareth Evans, D, Lindblom, A, Macrae, F, Blanco, I,
Academic Journal
Ghorbanoghli, Z.; Nieuwenhuis, M.H.; Houwing-Duistermaat, J.J.; Jagmohan-Changur, S.; Hes, F.J.; Tops, C.M.; Wagner, A.; Aalfs, C.M.; Verhoef, S.; Garcia, E.B.G.; Sijmons, R.H.; Menko, F.H.; Letteboer, T.G.; Hoogerbrugge, N.; Wezel, T. van; Vasen, H.F.A.; Wijnen, J.T.
Fam Cancer
Familial Cancer, 15, 4, pp. 563-70
Familial Cancer, 15, 4, pp. 563-70
Academic Journal
Lammens, C.R.M.; Bleiker, E.M.A.; Verhoef, S.; Hes, F.J.; Ausems, M.G.E.M.; Majoor-Krakauer, D.; Sijmons, R.H.; Luijt, R.B. van der; Ouweland, A.M.W. van den; Os, T. van; Hoogerbrugge, N.; Garcia, E.B.G.; Dommering, C.J.; Gundy, C.M.; Aaronson, N.K.
Lammens, C R M, Bleiker, E M A, Verhoef, S, Hes, F J, Ausems, M G E M, Majoor-Krakauer, D, Sijmons , RH, van der Luijt, R B, van den Ouweland, A M W, Van Os, T, Hoogerbrugge, N, Garcia, E B G, Dommering, C J, Gundy, C & Aaronson, N K 2010, 'Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distress', Clinical Genetics, vol. 77, no. 5, pp. 483-491. https://doi.org/10.1111/j.1399-0004.2009.01333.x
Clinical Genetics, 77, 5, pp. 483-91
Clinical Genetics, 77, 5, pp. 483-91
Academic Journal
Broeke, S.W. ten; Brohet, R.M.; Tops, C.M.; Klift, H.M. van der; Velthuizen, M.E.; Bernstein, I.; Munar, G.C.; Garcia, E.G.; Hoogerbrugge, N.; Letteboer, T.G.W.; Menko, F.H.; Lindblom, A.; Mensenkamp, A.R.; Moller, P.; Os, T.A. van; Rahner, N.; Redeker, B.J.W.; Sijmons, R.H.; Spruijt, L.; Suerink, M.; Vos, Y.J.; Wagner, A.; Hes, F.J.; Vasen, H.F.; Nielsen, M.; Wijnen, J.T.
Ten Broeke, S W, Brohet, R M, Tops, C M, van der Klift, H M, Velthuizen, M E, Bernstein, I, Capellá Munar, G, Gomez Garcia, E, Hoogerbrugge, N, Letteboer, T G W, Menko, F H, Lindblom, A, Mensenkamp, A R, Moller, P, van Os, T A, Rahner, N, Redeker, B J W, Sijmons , R H, Spruijt, L, Suerink, M, Vos, Y J, Wagner, A, Hes, F J, Vasen, H F, Nielsen, M & Wijnen, J T 2015, 'Lynch Syndrome Caused by Germline PMS2 Mutations : Delineating the Cancer Risk', Journal of Clinical Oncology, vol. 33, no. 4, pp. 319-325. https://doi.org/10.1200/JCO.2014.57.8088
ten Broeke, S W, Brohet, R M, Tops, C M, van der Klift, H M, Velthuizen, M E, Bernstein, I, Munar, G C, Garcia, E G, Hoogerbrugge, N, Letteboer, T G W, Menko, F H, Lindblom, A, Mensenkamp, A R, Moller, P, Os, T A, Rahner, N, Redeker, B J W,Sijmons , R H, Spruijt, L, Suerink, M, Vos, Y J, Wagner, A, Hes, F J, Vasen, HF, Nielsen, M & Wijnen, J T 2015, 'Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk', Journal of Clinical Oncology, vol. 33, no. 4, pp. 319-325. https://doi.org/10.1200/JCO.2014.57.8088
Journal of Clinical Oncology, 33, 4, pp. 319-25
ten Broeke, S W, Brohet, R M, Tops, C M, van der Klift, H M, Velthuizen, M E, Bernstein, I, Munar, G C, Garcia, E G, Hoogerbrugge, N, Letteboer, T G W, Menko, F H, Lindblom, A, Mensenkamp, A R, Moller, P, Os, T A, Rahner, N, Redeker, B J W,
Journal of Clinical Oncology, 33, 4, pp. 319-25
Academic Journal
de Geus, E.; Aalfs, C.M.; Menko, F.H.; Sijmons, R.H.; Verdam, M.G.E.; de Haes, H.C.J.M.; Smets, E.M.A.
de Geus, E, Aalfs, C M, Menko, F H, Sijmons , R H, Verdam, M G E, de Haes, H C J M & Smets, E M A 2015, 'Development of the Informing Relatives Inventory (IRI): Assessing Index Patients' Knowledge, Motivation and Self-Efficacy Regarding the Disclosure of Hereditary Cancer Risk Information to Relatives', International Journal of Behavioral Medicine, vol. 22, no. 4, pp. 551-560. https://doi.org/10.1007/s12529-014-9455-x
Academic Journal
Thompson, B.A.; Spurdle, A.B.; Plazzer, J.P.; Greenblatt, M.S.; Akagi, K.; Al-Mulla, F.; Bapat, B.V.; Bernstein, I.T.; Capellá, G.M.; Den Dunnen, J.T.; Du Sart, D.; Fabre, A.J.; Farrell, M.P.; Farrington, S.M.; Frayling, I.M.; Frébourg, T.H.; Goldgar, D.E.J.; Heinen, C.D.; Holinski-Feder, E.; Kohonen-Corish, M.R.J.; Robinson, K.L.; Leung, S.Y.; Martins, A.; Möller, P.; Morak, M.; Nyström, M.; Peltomäki, P.T.; Pineda, M.; Qi, M.; Ramesar, R.; Rasmussen, L.J.; Royer-Pokora, B.; Scott, R.J.; Sijmons, R.H.; Tavtigian, S.V.S.V.; Tops, C.M.J.; Weber, T.K.; Wijnen, J.T.H.; Woods, M.O.; Macrae, F.A.; Genuardi, M.; Castillejo, A.; Sexton, A.C.; Chan, A.K.W.; Viel, A.G.M.; Blanco, A.M.; French, A.J.; Laner, A.; Wagner, A.; Van Den Ouweland, A.M.W.; Mensenkamp, A.R.; Payá, A.; Betz, B.; Redeker, B.J.W.; Smith, B.G.; Espenschied, C.R.; Cummings, C.; Engel, C.; Fornes, C.; Valenzuela, C.; Alenda, C.; Buchanan, D.D.; Barana, D.; Konstantinova, D.V.; Cairns, D.; Glaser, E.; Silva, F.; Lalloo, F.I.; Crucianelli, F.; Hogervorst, F.B.L.; Casey, G.R.; Tomlinson, I.P.M.; Blanco, I.B.S.I.; Villar, I.L.; García-Planells, J.; Bigler, J.; Shia, J.; Martínez-López, J.J.; Gille, J.J.P.; Hopper, J.L.; Potter, J.D.; Soto, J.L.; Kantelinen, J.; Ellis, K.; Mann, K.; Varesco, L.; Zhang, L.; Marchand, L.L.; Marafie, M.J.; Nordling, Margareta, 1962; Tibiletti, M.G.; Kahan, M.A.; Ligtenberg, M.J.L.; Clendenning, M.; Jenkins, M.A.; Speevak, M.D.; Digweed, M.; Kloor, M.; Hitchins, M.P.; Myers, M.; Aronson, M.D.; Valentin, M.D.; Kutsche, M.; Parsons, M.T.; Walsh, M.D.; Kansikas, M.; Zahary, M.N.; Pedroni, M.; Heider, N.; Poplawski, N.K.; Rahner, N.; Lindor, N.M.; Sala, P.; Nan, P.; Propping, P.; Newcomb, P.; Sarin, R.; Haile, R.W.C.; Hofstra, R.M.W.; Ward, R.L.; Tricarico, R.; Bacares, R.; Young, S.; Chialina, S.G.; Kovalenko, S.P.; Gunawardena, S.R.; Moreno, S.; Ho, S.; Yuen, S.T.; Thibodeau, S.N.; Gallinger, S.S.; Burnett, T.S.; Teitsch, T.; Chan, T.L.; Smyrk, T.C.; Cranston, T.; Psofaki, V.; Steinke-Lange, V.; Barberá, V.M.
Nature Genetics. 46(2):107-115
Academic Journal
In Gynecologic Oncology November 2013 131(2):304-308
Academic Journal
Hes, F.J.; Ruano, D.; Nieuwenhuis, M.; Tops, C.M.; Schrumpf, M.; Nielsen, M.; Huijts, P.E.; Wijnen, J.T.; Wagner, A.; Garcia, E.B.; Sijmons, R.H.; Menko, F.H.; Letteboer, T.G.; Hoogerbrugge, N.; Harryvan, J.; Kampman, E.; Morreau, H.; Vasen, H.F.; van Wezel, T.
Hes, F J, Ruano, D, Nieuwenhuis, M, Tops, C M, Schrumpf, M, Nielsen, M, Huijts, P E A, Wijnen, J T, Wagner, A, Garcia, E B G, Sijmons , R H, Menko, F H, Letteboer, T G W, Hoogerbrugge, N, Harryvan, J, Kampman, E, Morreau, H, Vasen, H F A & van Wezel, T 2014, 'Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis', Journal of Medical Genetics, vol. 51, no. 1, pp. 55-60. https://doi.org/10.1136/jmedgenet-2013-102000
Journal of Medical Genetics, 51, 1, pp. 55-60
Journal of Medical Genetics, 51, 1, pp. 55-60
Academic Journal
Sikkema-Raddatz, B.; Johansson, L.F.; de Boer, E.N.; Almomani, R.; Boven, L.G.; van den Berg, M.P.; van Spaendonck-Zwarts, K.Y.; van Tintelen, J.P.; Sijmons, R.H.; Jongbloed, J.D.H.; Sinke, R.J.
Human Mutation. 34:1035-1042
Academic Journal
Plazzer, J.P.; Sijmons, R.H.; Woods, M.O.; Peltomaki, P.; Thompson, B.; Dunnen, J.T. den; Macrae, F.
Familial Cancer. 12:175-180
Academic Journal
Vasen, H.F.A.; Blanco, I.; Aktan-Collan, K.; Gopie, J.P.; Alonso, A.; Aretz, S.; Bernstein, I.; Bertario, L.; Burn, J.; Capella, G.; Colas, C.; Engel, C.; Frayling, I.M.; Genuardi, M.; Heinimann, K.; Hes, F.J.; Hodgson, S.V.; Karagiannis, J.A.; Lalloo, F.; Lindblom, A.; Mecklin, J.P.; Moller, P.; Myrhoj, T.; Nagengast, F.M.; Parc, Y.; Leon, M.P. de; Renkonen-Sinisalo, L.; Sampson, J.R.; Stormorken, A.; Sijmons, R.H.; Tejpar, S.; Thomas, H.J.W.; Rahner, N.; Wijnen, J.T.; Jarvinen, H.J.; Moslein, G.; Mallorca Grp
Gut
Gut, 62, 6, pp. 812-23
Gut, 62, 6, pp. 812-23
Academic Journal
Engel, C.; Loeffler, M.; Steinke, V.; Rahner, N.; Holinski-Feder, E.; Dietmaier, W.; Schackert, H.K.; Goergens, H.; von Knebel Doeberitz, M.; Goecke, T.O.; Schmiegel, W.; Buettner, R.; Moeslein, G.; Letteboer, T.G.; Garcia, E.G.; Hes, F.J.; Hoogerbrugge, N.; Menko, F.H.; van Os, T.A.; Sijmons, R.H.; Wagner, A.; Kluijt, I.; Propping, P.; Vasen, H.F.
Engel, C, Loeffler, M, Steinke, V, Rahner, N, Holinski-Feder, E, Dietmaier, W, Schackert, H K, Goergens, H, Doeberitz, M V, Goecke, T O, Schmiegel, W, Buettner, R, Moeslein, G, Letteboer, T G W, Garcia, E G, Hes, F J, Hoogerbrugge, N, Menko, F H, van Os, T A M, Sijmons , RH, Wagner, A, Kluijt, I, Propping, P & Vasen, H F A 2012, 'Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome', Journal of Clinical Oncology, vol. 30, no. 35, pp. 4409-4415. https://doi.org/10.1200/JCO.2012.43.2278
Journal of Clinical Oncology, 30, 35, pp. 4409-15
Journal of Clinical Oncology, 30, 35, pp. 4409-15
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