Sexual differences in onset of disease and response to exercise in a transgenic model of ALS von Veldink, J.H., Bär, P.R., Joosten, E.A.J., Otten, M., Wokke, J.H.J., van den Berg, L.H.

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Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS von VELDINK, J. H, VAN DEN BERG, L. H, COBBEN, J. M, STULP, R. P, DE JONG, J. M. B. V, VOGELS, O. J, BAAS, F, WOKKE, J. H. J, SCHEFFER, H

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Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2 von VAN DAMME, P, VELDINK, J. H, VAN BLITTERSWIJK, M, CORVELEYN, A, VAN VUGHT, P. W. J, THIJS, V, DUBOIS, B, MATTHIJS, G, VAN DEN BERG, L. H, ROBBERECHT, W

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Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy von CATS, E. A, VAN DER POL, W.-L, WOKKE, J. H, VELDINK, J. H, VAN DEN BERG, L. H, PIEPERS, S, FRANSSEN, H, JACOBS, B. C, VAN DEN BERG-VOS, R. M, KUKS, J. B, VAN DOORN, P. A, VAN ENGELEN, B. G, VERSCHUUREN, J. J

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Zinc amplifies mSOD1-mediated toxicity in a transgenic mouse model of amyotrophic lateral sclerosis von Groeneveld, G.J., de Leeuw van Weenen, J., van Muiswinkel, F.L., Veldman, H., Veldink, J.H., Wokke, J.H.J., Bär, P.R., van den Berg, L.H.

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SMN1 gene duplications are associated with sporadic ALS von BLAUW, H. M, BARNES, C. P, VAN VUGHT, P. W. J, VAN RHEENEN, W, CUPPEN, E, VERHEUL, M, VELDINK, J. H, VAN DEN BERG, L. H

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Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis von Veldink, J H, Kalmijn, S, Groeneveld, G-J, Wunderink, W, Koster, A, de Vries, J H M, van der Luyt, J, Wokke, J H J, Van den Berg, L H

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Family history of neurodegenerative and vascular diseases in ALS: A population-based study von HUISMAN, M. H. B, DE JONG, S. W, VERWIJS, M. C, SCHELHAAS, H. J, VAN DER KOOI, A. J, DE VISSER, M, VELDINK, J. H, VAN DEN BERG, L. H

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CHCHD10 variants in amyotrophic lateral sclerosis: Where is the evidence? von Tazelaar, G.H.P, van Rheenen, W, Pulit, S.L, van der Spek, R.A.A, Dekker, A.M, Moisse, M, McLaughlin, R.L, Sproviero, W, Kenna, K.P, Kooyman, M, van Doormaal, P.T.C, van Eijk, K.E, Middelkoop, B.M, Schellevis, R.D, Brands, W.J, Al-Chalabi, A, Morrison, K.E, Shaw, P.J, Shaw, C.E, Newhouse, S.E, van Es, M.A, Basak, A.N, Akçimen, F, Kocoglu, C, Tunca, C, Povedano, M, Mora, J.S, Glass, J.D, Van Damme, P, Robberecht, W, HardimanMD, O, Landers, J.E, van den Berg, L.H, Veldink, J.H

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GENOME-WIDE ASSOCIATION STUDY AND META-ANALYSIS IDENTIFY DISEASE SUSCEPTIBILITY LOCI ASSOCIATED WITH TRANSPOSITION OF THE GREAT ARTERIES von Tadros, R., Milosavljevic, D., Lahrouchi, N., Tjong, F.V., Beekman, L., Veldink, J.H., Lodder, E.M., Goodship, J.A., Cordell, H.J., Tanck, M.W., Keavney, B.D., Mulder, B.J., Postma, A.V., Bezzina, C.R.

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GENOME-WIDE ASSOCIATION STUDY AND META-ANALYSIS IDENTIFY DISEASE SUSCEPTIBILITY LOCI ASSOCIATED WITH TRANSPOSITION OF THE GREAT ARTERIES von Tadros, R, Milosavljevic, D, Lahrouchi, N, Tjong, F.V, Beekman, L, Veldink, J.H, Lodder, E.M, Goodship, J.A, Cordell, H.J, Tanck, M.W, Keavney, B.D, Mulder, B.J, Postma, A.V, Bezzina, C.R

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Lifetime occupation, education, smoking, and risk of ALS von Sutedja, N.A, Veldink, J.H, Fischer, K, Kromhout, H, Wokke, J.H.J, Huisman, M.H.B, Heederik, D.J.J, van den Berg, L.H

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Lipid-induced transcriptomic changes in blood link to lipid metabolism and allergic response von Dekkers, K.F., Slieker, R.C., Ioan-Facsinay, A., Iterson, M. van, Ikram, M.A., Greevenbroek, M.M.J. van, Veldink, J.H., Franke, L., Boomsma, D.I., Slagboom, P.E., Jukema, J.W., Heijmans, B.T.

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Inter- and intraindividual variability of riluzole serum concentrations in patients with ALS von Groeneveld, G.J, van Kan, H.J.M, Sastre Toraño, J, Veldink, J.H, Guchelaar, H.-J, Wokke, J.H.J, van den Berg, L.H

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Mutations in the tail and rod domains of the neurofilament heavy‐chain gene increase the risk of ALS von Marriott, H, Spargo, T.P, Al Khleifat, A, Andersen, P.M, Başak, N.A, Cooper‐Knock, J, Corcia, P, Couratier, P, de Carvalho, M, Drory, V, Gotkine, M, Landers, J.E, McLaughlin, R, Pardina, J.S.M, Morrison, K.E, Pinto, S, Shaw, C.E, Shaw, P.J, Silani, V, Ticozzi, N, van Damme, P, van den Berg, L.H, Vourc'h, P, Weber, M, Veldink, J.H, Dobson, R.J, Schwab, P, Al‐Chalabi, A, Iacoangeli, A

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Advances in the genetic classification of amyotrophic lateral sclerosis von Cooper-Knock, J, Harvey, C, Zhang, S, Moll, T, Timpanaro, I.S, Kenna, K.P, Iacoangeli, A, Veldink, J.H

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Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis von Harvey, C, Weinreich, M, Lee, J.A.K, Shaw, A.C, Ferraiuolo, L, Mortiboys, H, Zhang, S, Hop, P.J, Zwamborn, R.A.J, van Eijk, K, Julian, T.H, Moll, T, Iacoangeli, A, Al Khleifat, A, Quinn, J.P, Pfaff, A.L, Kõks, S, Poulton, J, Battle, S.L, Arking, D.E, Snyder, M.P, Veldink, J.H, Kenna, K.P, Shaw, P.J, Cooper-Knock, J

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Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression von Jonkman, T.H., Dekkers, K.F., Slieker, R.C., Grant, C.D., Ikram, M.A., Greevenbroek, M.M.J. van, Franke, L., Veldink, J.H., Boomsma, D.I., Slagboom, P.E., Consortium, B.I.O.S., Heijmans, B.T.

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Crossreactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies von Hop, P.J, Zwamborn, R.A.J., Veldink, J.H.

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pjhop/DNAmCrosshyb: hg38 and hg19 bisulfite-converted genomes (R .rds files) von Hop, P.J., Zwamborn, R.A.J., Veldink, J.H.

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