Diffusion MRI-based cortical connectome reconstruction: dependency on tractography procedures and neuroanatomical characteristics von Sinke, Michel R. T., Otte, Willem M., Christiaens, Daan, Schmitt, Oliver, Leemans, Alexander, van der Toorn, Annette, Sarabdjitsingh, R. Angela, Joëls, Marian, Dijkhuizen, Rick M.

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Statistical power of clinical trials increased while effect size remained stable: an empirical analysis of 136,212 clinical trials between 1975 and 2014 von Lamberink, Herm J., Otte, Willem M., Sinke, Michel R.T., Lakens, Daniël, Glasziou, Paul P., Tijdink, Joeri K., Vinkers, Christiaan H.

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Bayesian exponential random graph modeling of whole-brain structural networks across lifespan von Sinke, Michel R.T., Dijkhuizen, Rick M., Caimo, Alberto, Stam, Cornelis J., Otte, Willem M.

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Re-emergence of acute myeloid leukemia in donor cells following allogeneic transplantation in a family with a germline DDX41 mutation von Berger, G, van den Berg, E, Sikkema-Raddatz, B, Abbott, K M, Sinke, R J, Bungener, L B, Mulder, A B, Vellenga, E

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Distinct structure-function relationships across cortical regions and connectivity scales in the rat brain von Straathof, Milou, Sinke, Michel R. T., Roelofs, Theresia J. M., Blezer, Erwin L. A., Sarabdjitsingh, R. Angela, van der Toorn, Annette, Schmitt, Oliver, Otte, Willem M., Dijkhuizen, Rick M.

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An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia von Jungerius, B J, Hoogendoorn, M L C, Bakker, S C, van't Slot, R, Bardoel, A F, Ophoff, R A, Wijmenga, C, Kahn, R S, Sinke, R J

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Imaging Markers for the Characterization of Gray and White Matter Changes from Acute to Chronic Stages after Experimental Traumatic Brain Injury von Sinke, Michel R. T., Otte, Willem M., Meerwaldt, Anu E., Franx, Bart A. A., Ali, Mohamed H. M., Rakib, Fazle, van der Toorn, Annette, van Heijningen, Caroline L., Smeele, Christel, Ahmed, Tariq, Blezer, Erwin L. A., Dijkhuizen, Rick M.

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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q von Bakker, S.C., Meulen, E. M. van der, Buitelaar, J.K., Sandkuijl, L.A., Pauls, D.L., Monsuur, A.J., Slot, R. van ‘t, Minderaa, R.B., Gunning, W.B., Pearson, P.L., Sinke, R.J.

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Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing von Baardman, R, Lemmink, H H, Yenamandra, V K, Commandeur-Jan, S Z, Viel, M, Kooi, K A, Diercks, G F H, Meijer, R, van Geel, M, Scheffer, H, Sinke, R J, Sikkema-Raddatz, B, Bolling, M C, van den Akker, P C

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Cardiomyopathy in patients with epidermolysis bullosa simplex with mutations in KLHL24 von Yenamandra, V.K., Akker, P.C., Lemmink, H.H., Jan, S.Z., Diercks, G.F.H., Vermeer, M., Berg, M.P., Meer, P., Pasmooij, A.M.G., Sinke, R.J., Jonkman, M.F., Bolling, M.C.

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“Duodenal Adenocarcinoma Giving Rise to Rectal Metastasis” a Rare Disease with an Extremely Rare Metastatic Pattern von Epskamp, Cynthia, van Eijck, C. H. J., Sinke, R. H. J. A., Hamberg, P.

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Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the Netherlands von Yuen, W.Y., Lemmink, H.H., van Dijk-Bos, K.K., Sinke, R.J., Jonkman, M.F.

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Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis von VAN DE WARRENBURG, B. P. C, SINKE, R. J, KNOERS, N. V. A. M, KREMER, H. P. H, VERSCHUUREN-BEMELMANS, C. C, SCHEFFER, H, BRUNT, E. R, IPPEL, P. F, MAAT-KIEVIT, J. A, DOOIJES, D, NOTERMANS, N. C, LINDHOUT, D

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Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing von Johansson, L. F., de Boer, E. N., de Weerd, H. A., van Dijk, F., Elferink, M. G., Schuring-Blom, G. H., Suijkerbuijk, R. F., Sinke, R. J., te Meerman, G. J., Sijmons, R. H., Swertz, M. A., Sikkema-Raddatz, B.

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ITGB4-associated non-Herlitz junctional epidermolysis bullosa: report of two new cases carrying two novel ITGB4 mutations von Yuen, W.Y., Sinke, R.J., Jonkman, M.F.

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Junctional epidermolysis bullosa of late onset explained by mutations in COL17A1 von Yuen, W.Y., Pas, H.H., Sinke, R.J., Jonkman, M.F.

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Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family von VAN DE WARRENBURG, B. P. C, VERBEEK, D. S, PIERSMA, S. J, HENNEKAM, F. A. M, PEARSON, P. L, KNOERS, N. V. A. M, KREMER, H. P. H, SINKE, R. J

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Association between an agouti-related protein gene polymorphism and anorexia nervosa von VINK, T, HINNEY, A, ADAN, R. A. H, VAN ELBURG, A. A, VAN GOOZEN, S. H. M, SANDKUIJL, L. A, SINKE, R. J, HERPERTZ-DAHLMANN, B-M, HEBEBRAND, J, REMSCHMIDT, H, VAN ENGELAND, H

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The association of alcohol intake with gamma-glutamyl transferase (GGT) levels: Evidence for correlated genetic effects von van Beek, Jenny H.D.A, de Moor, Marleen H.M, Geels, Lot M, Sinke, Michel R.T, de Geus, Eco J.C, Lubke, Gitta H, Kluft, Cornelis, Neuteboom, Jacoline, Vink, Jacqueline M, Willemsen, Gonneke, Boomsma, Dorret I

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Regulation of HDL-c levels via ABCA1 : A role for Lrp1 von Oldoni, F, van Capelleveen, J, Motazacker, M.M, Heeren, J, Sinke, R, Dallinga-Thie, G, Hui, D, Hovingh, K, Kuivenhoven, J.A

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