A digital platform to support communication and organization in the general practice: Evaluation of healthcare usage and costs using claims data of a health insurer von Willemsen, R F, Aardoom, J J, van der Galiën, O P, van de Vijver, S, Chavannes, N H, Versluis, A

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Patient and healthcare provider perspectives on a digital first general practice: mixed-method study von Versluis, A, Willemsen, R F, Chavannes, N H, Aardoom, J J

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Clinical spectrum of ataxia-telangiectasia in adulthood von VERHAGEN, M. M. M, ABDO, W. F, BROEKS, A, LAST, J. I, VAN'T VEER, L. J, TIJSSEN, M. A. J, DUBOIS, A. M. I, KREMER, H. P. H, WEEMAES, C. M. R, TAYLOR, A. M. R, VAN DEUREN, M, WILLEMSEN, M. A. A. P, HOGERVORST, F. B. L, SMEETS, D. F. C. M, HIEL, J. A. P, BRUNT, E. R, VAN RIJN, M. A, KRAKAUER, D. Majoor, OLDENBURG, R. A

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Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability von Lelieveld, Stefan H, Reijnders, Margot R F, Pfundt, Rolph, Yntema, Helger G, Kamsteeg, Erik-Jan, de Vries, Petra, de Vries, Bert B A, Willemsen, Marjolein H, Kleefstra, Tjitske, Löhner, Katharina, Vreeburg, Maaike, Stevens, Servi J C, van der Burgt, Ineke, Bongers, Ernie M H F, Stegmann, Alexander P A, Rump, Patrick, Rinne, Tuula, Nelen, Marcel R, Veltman, Joris A, Vissers, Lisenka E L M, Brunner, Han G, Gilissen, Christian

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Targeted optical fluorescence imaging: a meta-narrative review and future perspectives von Schouw, H. M., Huisman, L. A., Janssen, Y. F., Slart, R. H. J. A., Borra, R. J. H., Willemsen, A. T. M., Brouwers, A. H., van Dijl, J. M., Dierckx, R. A., van Dam, G. M., Szymanski, W., Boersma, H. H., Kruijff, S.

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Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID von van Bon, B W M, Coe, B P, Bernier, R, Green, C, Gerdts, J, Witherspoon, K, Kleefstra, T, Willemsen, M H, Kumar, R, Bosco, P, Fichera, M, Li, D, Amaral, D, Cristofoli, F, Peeters, H, Haan, E, Romano, C, Mefford, H C, Scheffer, I, Gecz, J, de Vries, B B A, Eichler, E E

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Construction of a strawberry breeding core collection to capture and exploit genetic variation von Koorevaar, T, Willemsen, J H, Visser, R G F, Arens, P, Maliepaard, C

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Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study von de Mol, C. L., Wong, Y. Y. M., van Pelt, E. D., Ketelslegers, I. A., Bakker, D. P., Boon, M., Braun, K. P. J., van Dijk, K. G. J., Eikelenboom, M. J., Engelen, M., Geleijns, K., Haaxma, C. A., Niermeijer, J. M. F., Niks, E. H., Peeters, E. A. J., Peeters-Scholte, C. M. P. C. D., Poll-The, B. T., Portier, R. P., de Rijk-van Andel, J. F., Samijn, J. P. A., Schippers, H. M., Snoeck, I. N., Stroink, H., Vermeulen, R. J., Verrips, A., Visscher, F., Vles, J. S. H., Willemsen, M. A. A. P., Catsman-Berrevoets, C. E., Hintzen, R. Q., Neuteboom, R. F.

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[11 C]-PK11195 PET: Quantification of neuroinflammation and a monitor of anti-inflammatory treatment in Parkinson's disease? von Bartels, A.L, Willemsen, A.T.M, Doorduin, J, de Vries, E.F.J, Dierckx, R.A, Leenders, K.L

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Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis von Willemsen, Michèl A., Verbeek, Marcel M., Kamsteeg, Erik-Jan, de Rijk-van Andel, Johanneke F., Aeby, Alec, Blau, Nenad, Burlina, Alberto, Donati, Maria A., Geurtz, Ben, Grattan-Smith, Padraic J., Haeussler, Martin, Hoffmann, Georg F., Jung, Hans, de Klerk, Johannis B., van der Knaap, Marjo S., Kok, Fernando, Leuzzi, Vincenzo, de Lonlay, Pascale, Megarbane, Andre, Monaghan, Hugh, Renier, Willy O., Rondot, Pierre, Ryan, Monique M., Seeger, Jürgen, Smeitink, Jan A., Steenbergen-Spanjers, Gerry C., Wassmer, Evangeline, Weschke, Bernhard, Wijburg, Frits A., Wilcken, Bridget, Zafeiriou, Dimitrios I., Wevers, Ron A.

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Exosome-mediated transmission of hepatitis C virus between human hepatoma Huh7.5 cells von Ramakrishnaiah, Vedashree, Thumann, Christine, Fofana, Isabel, Habersetzer, Francois, Pan, Qiuwei, de Ruiter, Petra E., Willemsen, Rob, Demmers, Jeroen A. A., Raj, Victor Stalin, Jenster, Guido, Kwekkeboom, Jaap, Tilanus, Hugo W., Haagmans, Bart L., Baumert, Thomas F., van der Laan, Luc J. W.

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Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder von Koemans, Tom S, Kleefstra, Tjitske, Chubak, Melissa C, Stone, Max H, Reijnders, Margot R F, de Munnik, Sonja, Willemsen, Marjolein H, Fenckova, Michaela, Stumpel, Connie T R M, Bok, Levinus A, Sifuentes Saenz, Margarita, Byerly, Kyna A, Baughn, Linda B, Stegmann, Alexander P A, Pfundt, Rolph, Zhou, Huiqing, van Bokhoven, Hans, Schenck, Annette, Kramer, Jamie M

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Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study von Ketelslegers, I. A., Catsman-Berrevoets, C. E., Neuteboom, R. F., Boon, M., van Dijk, K. G. J., Eikelenboom, M. J., Gooskens, R. H. J. M., Niks, E. H., Overweg-Plandsoen, W. C. G., Peeters, E. A. J., Peeters-Scholte, C. M. P. C. D., Poll-The, B. T., de Rijk-van Andel, J. F., Samijn, J. P. A., Snoeck, I. N., Stroink, H., Vermeulen, R. J., Verrips, A., Vles, J. S. H., Willemsen, M. A. A. P., Rodrigues Pereira, R., Hintzen, R. Q.

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Ataxia-telangiectasia: Immunodeficiency and survival von van Os, Nienke J.H, Jansen, Anne F.M, van Deuren, Marcel, Haraldsson, Asgeir, van Driel, Nieke T.M, Etzioni, Amos, van der Flier, Michiel, Haaxma, Charlotte A, Morio, Tomohiro, Rawat, Amit, Schoenaker, Michiel H.D, Soresina, Annarosa, Taylor, Alexander M.R, van de Warrenburg, Bart P.C, Weemaes, Corry M.R, Roeleveld, Nel, Willemsen, Michèl A.A.P

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Polygenic dissection of major depression clinical heterogeneity von Milaneschi, Y, Lamers, F, Peyrot, W J, Abdellaoui, A, Willemsen, G, Hottenga, J-J, Jansen, R, Mbarek, H, Dehghan, A, Lu, C, Boomsma, D I, Penninx, B W J H

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Nicotinamide Riboside Improves Ataxia Scores and Immunoglobulin Levels in Ataxia Telangiectasia von Veenhuis, Stefanie J.G., Os, Nienke J.H., Janssen, Anjo J.W.M., Gerven, Marjo H.J.C., Coene, Karlien L.M., Engelke, Udo. F.H., Wevers, Ron A., Tinnevelt, Gerjen H., Heine, Rob, Warrenburg, Bart P.C., Weemaes, Corry M.R., Roeleveld, Nel, Willemsen, Michèl A.A.P.

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Contrast-enhancement influences skeletal muscle density, but not skeletal muscle mass, measurements on computed tomography von van Vugt, Jeroen L.A., Coebergh van den Braak, Robert R.J., Schippers, Henk J.W., Veen, Kevin M., Levolger, Stef, de Bruin, Ron W.F., Koek, Marcel, Niessen, Wiro J., IJzermans, Jan N.M., Willemsen, François E.J.A.

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Poor replication of candidate genes for major depressive disorder using genome-wide association data von Bosker, F J, Hartman, C A, Nolte, I M, Prins, B P, Terpstra, P, Posthuma, D, van Veen, T, Willemsen, G, DeRijk, R H, de Geus, E J, Hoogendijk, W J, Sullivan, P F, Penninx, B W, Boomsma, D I, Snieder, H, Nolen, W A

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A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP von Helsmoortel, Céline, Vulto-van Silfhout, Anneke T, Coe, Bradley P, Vandeweyer, Geert, Rooms, Liesbeth, van den Ende, Jenneke, Schuurs-Hoeijmakers, Janneke H M, Marcelis, Carlo L, Willemsen, Marjolein H, Vissers, Lisenka E L M, Yntema, Helger G, Bakshi, Madhura, Wilson, Meredith, Witherspoon, Kali T, Malmgren, Helena, Nordgren, Ann, Annerén, Göran, Fichera, Marco, Bosco, Paolo, Romano, Corrado, de Vries, Bert B A, Kleefstra, Tjitske, Kooy, R Frank, Eichler, Evan E, Van der Aa, Nathalie

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Gene expression in major depressive disorder von Jansen, R, Penninx, B W J H, Madar, V, Xia, K, Milaneschi, Y, Hottenga, J J, Hammerschlag, A R, Beekman, A, van der Wee, N, Smit, J H, Brooks, A I, Tischfield, J, Posthuma, D, Schoevers, R, van Grootheest, G, Willemsen, G, de Geus, E J, Boomsma, D I, Wright, F A, Zou, F, Sun, W, Sullivan, P F

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