Consensus conferences as participatory policy analysis, a methodological contribution to the social management of technology von Mayer, I.S., Geurts, J.L.

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NTHL1 and MUTYH polyposis syndromes: two sides of the same coin? von Weren, Robbert DA, Ligtenberg, Marjolijn JL, Geurts van Kessel, Ad, De Voer, Richarda M, Hoogerbrugge, Nicoline, Kuiper, Roland P

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Effect of high compared with low dairy intake on blood pressure in overweight middle-aged adults: results of a randomized crossover intervention study von Rietsema, Susan, Eelderink, Coby, Joustra, Monica L, van Vliet, Iris MY, van Londen, Marco, Corpeleijn, Eva, Singh-Povel, Cecile M, Geurts, Jan MW, Kootstra-Ros, Jenny E, Westerhuis, Ralf, Navis, Gerjan, Bakker, Stephan JL

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The evolution of precision oncology: The ongoing impact of the Drug Rediscovery Protocol (DRUP) von Haj Mohammad, Soemeya F, Timmer, Hans J L, Zeverijn, Laurien J, Geurts, Birgit S, Spiekman, Ilse A C, Verkerk, Karlijn, Verbeek, Florentine A J, Verheul, Henk M W, Voest, Emile E, Gelderblom, Hans

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Diagnostic accuracy of cross-sectional and endoscopic imaging in ampullary tumours: systematic review von de Wilde, Anouk J, de Jong, Evelien J M, Gurusamy, Kurinchi S, Abu Hilal, Mohammad, Besselink, Marc G, Dewulf, Maxime J L, Geurts, Sandra M E, Neumann, Ulf P, Olde Damink, Steven W M, Poley, Jan-Werner, Tjan-Heijnen, Vivianne C G, de Vos-Geelen, Judith, Wiltberger, Georg, Coolsen, Mariëlle M E, Bouwense, Stefan A W

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The effect of high compared with low dairy consumption on glucose metabolism, insulin sensitivity, and metabolic flexibility in overweight adults: a randomized crossover trial von Eelderink, Coby, Rietsema, Susan, van Vliet, Iris M Y, Loef, Larissa C, Boer, Theo, Koehorst, Martijn, Nolte, Ilja M, Westerhuis, Ralf, Singh-Povel, Cécile M, Geurts, Jan M W, Corpeleijn, Eva, Bakker, Stephan J L

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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 von van Kessel, Ad Geurts, Hoenselaar, Eveline, Voorendt, Marsha, Kuiper, Roland P, Lee, Tracy Y H, Hendriks-Cornelissen, Sandra J B, Yuen, Siu Tsan, van Krieken, J Han J M, Leung, Suet Yi, Hoogerbrugge, Nicoline, Chan, Tsun Leung, Bodmer, Danielle, Ligtenberg, Marjolijn J L, Goossens, Monique, Hebeda, Konnie M, Tsui, Wai Yin, Brunner, Han G, Kong, Chi Kwan

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Mixed methods evaluation of a self-management group programme for patients with neuromuscular disease and chronic fatigue von Veenhuizen, Yvonne, Satink, Ton, Graff, Maud JL, Geurts, Alexander CH, Groothuis, Jan T, van Engelen, Baziel GM, Nijhuis-van der Sanden, Maria WG, Cup, Edith HC

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Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility von de Voer, Richarda M, Hahn, Marc-Manuel, Weren, Robbert D A, Mensenkamp, Arjen R, Gilissen, Christian, van Zelst-Stams, Wendy A, Spruijt, Liesbeth, Kets, C Marleen, Zhang, Junxiao, Venselaar, Hanka, Vreede, Lilian, Schubert, Nil, Tychon, Marloes, Derks, Ronny, Schackert, Hans K, Geurts van Kessel, Ad, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J L, Kuiper, Roland P

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Executive functions in trauma-exposed youth: a meta-analysis von Op den Kelder, Rosanne, Van den Akker, Alithe L., Geurts, Hilde M., Lindauer, Ramón J. L., Overbeek, Geertjan

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Instruments for assessment of impairments and activity limitations in patients with hand conditions: A European Delphi study von van de Ven-Stevens, Lucelle A W, Graff, Maud J L, Selles, Ruud W, Schreuders, Ton A R, van der Linde, Harmen, Spauwen, Paul H, Geurts, Alexander C H

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A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer von Weren, Robbert D A, Ligtenberg, Marjolijn J L, Kets, C Marleen, de Voer, Richarda M, Verwiel, Eugène T P, Spruijt, Liesbeth, van Zelst-Stams, Wendy A G, Jongmans, Marjolijn C, Gilissen, Christian, Hehir-Kwa, Jayne Y, Hoischen, Alexander, Shendure, Jay, Boyle, Evan A, Kamping, Eveline J, Nagtegaal, Iris D, Tops, Bastiaan B J, Nagengast, Fokko M, Geurts van Kessel, Ad, van Krieken, J Han J M, Kuiper, Roland P, Hoogerbrugge, Nicoline

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Identification of candidate predisposing copy number variants in familial and early‐onset colorectal cancer patients von Venkatachalam, Ramprasath, Verwiel, Eugène T.P., Kamping, Eveline J., Hoenselaar, Eveline, Görgens, Heike, Schackert, Hans K., van Krieken, J. Han J.M., Ligtenberg, Marjolijn J.L., Hoogerbrugge, Nicoline, van Kessel, Ad Geurts, Kuiper, Roland P.

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Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer von de Voer, Richarda M., Hahn, Marc-Manuel, Mensenkamp, Arjen R., Hoischen, Alexander, Gilissen, Christian, Henkes, Arjen, Spruijt, Liesbeth, van Zelst-Stams, Wendy A., Marleen Kets, C., Verwiel, Eugene T., Nagtegaal, Iris D., Schackert, Hans K., van Kessel, Ad Geurts, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L., Kuiper, Roland P.

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Germline Mutations in the Spindle Assembly Checkpoint Genes BUB1 and BUB3 Are Risk Factors for Colorectal Cancer von de Voer, Richarda M, Geurts van Kessel, Ad, Weren, Robbert D.A, Ligtenberg, Marjolijn J.L, Smeets, Dominique, Fu, Lei, Vreede, Lilian, Kamping, Eveline J, Verwiel, Eugène T.P, Hahn, Marc–Manuel, Ariaans, Maayke, Spruijt, Liesbeth, van Essen, Ton, Houge, Gunnar, Schackert, Hans K, Sheng, Jian Q, Venselaar, Hanka, van Ravenswaaij–Arts, Conny M.A, van Krieken, J. Han J.M, Hoogerbrugge, Nicoline, Kuiper, Roland P

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Age-Dependent Effects of Methylphenidate on the Human Dopaminergic System in Young vs Adult Patients With Attention-Deficit/Hyperactivity Disorder: A Randomized Clinical Trial von Schrantee, Anouk, Tamminga, Hyke G. H, Bouziane, Cheima, Bottelier, Marco A, Bron, Esther E, Mutsaerts, Henk-Jan M. M, Zwinderman, Aeilko H, Groote, Inge R, Rombouts, Serge A. R. B, Lindauer, Ramon J. L, Klein, Stefan, Niessen, Wiro J, Opmeer, Brent C, Boer, Frits, Lucassen, Paul J, Andersen, Susan L, Geurts, Hilde M, Reneman, Liesbeth

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Germline copy number variation and cancer risk von Kuiper, Roland P, Ligtenberg, Marjolijn JL, Hoogerbrugge, Nicoline, Geurts van Kessel, Ad

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EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients von Ligtenberg, Marjolijn J. L., Kuiper, Roland P., Geurts van Kessel, Ad, Hoogerbrugge, Nicoline

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The genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery von Hahn, M. M., de Voer, R. M., Hoogerbrugge, N., Ligtenberg, M. J. L., Kuiper, R. P., van Kessel, A. Geurts

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Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis von van Wageningen, Thecla A., Gerrits, Emma, Brouwer, Nieske, Brevé, John J. P., Geurts, Jeroen J. G., Eggen, Bart J. L., Boddeke, H. W. G. M. (Erik), van Dam, Anne-Marie

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