Relative power and sample size analysis on gene expression profiling data von Iterson, M. van, Hoen, P.A.C. 't, Pedotti, P, Hooiveld, G.J.E.J, Dunnen, J.T. den, Ommen, G.J.B. van, Boer, J.M, Menezes, R.X

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F03 Whole blood SAGE digital gene expression profiling from Huntington's disease patients von Mastrokolias, A, van Duijn, E, van der Mast, RC, van Ommen, GJB, Den Dunnen, JT, 't Hoen, PAC, van Roon-Mom, WMC

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Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles von Bruder, Carl E.G., Piotrowski, Arkadiusz, Gijsbers, Antoinet A.C.J., Andersson, Robin, Erickson, Stephen, Diaz de Ståhl, Teresita, Menzel, Uwe, Sandgren, Johanna, von Tell, Desiree, Poplawski, Andrzej, Crowley, Michael, Crasto, Chiquito, Partridge, E. Christopher, Tiwari, Hemant, Allison, David B., Komorowski, Jan, van Ommen, Gert-Jan B., Boomsma, Dorret I., Pedersen, Nancy L., den Dunnen, Johan T., Wirdefeldt, Karin, Dumanski, Jan P.

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BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres von van Ommen, Gert-Jan B, Törnwall, Outi, Bréchot, Christian, Dagher, Georges, Galli, Joakim, Hveem, Kristian, Landegren, Ulf, Luchinat, Claudio, Metspalu, Andres, Nilsson, Cecilia, Solesvik, Ove V, Perola, Markus, Litton, Jan-Eric, Zatloukal, Kurt

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Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD) von Nadarajah, V.D, van Putten, M, Chaouch, A, Garrood, P, Straub, V, Lochmüller, H, Ginjaar, H.B, Aartsma-Rus, A.M, van Ommen, G.J.B, den Dunnen, J.T, t Hoen, P.A.C

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Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications von DEN DUNNEN, J. T, GROOTSCHOLTEN, P. M, BAKKER, E, BLONDEN, L. A. J, GINJAAR, H. B, WAPENAAR, M. C, VAN PAASSEN, H. M. B, VAN BROECKHOVEN, C, PEARSON, P. L, VAN OMMEN, G. J. B

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Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease von Roelfsema, Jeroen H., White, Stefan J., Ariyürek, Yavuz, Bartholdi, Deborah, Niedrist, Dunja, Papadia, Francesco, Bacino, Carlos A., den Dunnen, Johan T., van Ommen, Gert-Jan B., Breuning, Martijn H., Hennekam, Raoul C., Peters, Dorien J.M.

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Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy von van der Maarel, Silvère M, van Overveld, Petra G M, Lemmers, Richard J F L, Sandkuijl, Lodewijk A, Enthoven, Leo, Winokur, Sara T, Bakels, Floor, Padberg, George W, van Ommen, Gert-Jan B, Frants, Rune R

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Frequency of new copy number variation in humans von van Ommen, Gert-Jan B

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Advances in Duchenne muscular dystrophy gene therapy von van Deutekom, Judith C. T, van Ommen, Gert-Jan B

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Therapeutic antisense-induced exon skipping in cultured muscle cells from six different DMD patients von Aartsma-Rus, Annemieke, Janson, Anneke A.M., Kaman, Wendy E., Bremmer-Bout, Mattie, den Dunnen, Johan T., Baas, Frank, van Ommen, Gert-Jan B., van Deutekom, Judith C.T.

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Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere von van der Maarel, Silvère M, Lemmers, Richard J.L.F, de Kievit, Peggy, Sandkuijl, Lodewijk, Padberg, George W, van Ommen, Gert-Jan B, Frants, Rune R

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 von Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Oefner, P J, Hoffman, S M, Lamerdin, J E, Mohrenweiser, H W, Bulman, D E, Ferrari, M, Haan, J, Lindhout, D, van Ommen, G J, Hofker, M H, Ferrari, M D, Frants, R R

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Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells von van Deutekom, J C, Bremmer-Bout, M, Janson, A A, Ginjaar, I B, Baas, F, den Dunnen, J T, van Ommen, G J

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FcγRI (CD64) Contributes Substantially to Severity of Arthritis, Hypersensitivity Responses, and Protection from Bacterial Infection von Ioan-Facsinay, A, de Kimpe, S.J, Hellwig, S.M.M, van Lent, P.L, Hofhuis, F.M.A, van Ojik, H.H, Sedlik, C, da Silveira, S.A, Gerber, J, de Jong, Y.F, Roozendaal, R, Aarden, L.A, van den Berg, W.B, Saito, T, Mosser, D, Amigorena, S, Izui, S, van Ommen, G-J.B, van Vugt, M, van de Winkel, J.G.J, Verbeek, J.S

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Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization von White, Stefan, Kalf, Margot, Liu, Qiang, Villerius, Michel, Engelsma, Dieuwke, Kriek, Marjolein, Vollebregt, Ellen, Bakker, Bert, van Ommen, Gert-Jan B., Breuning, Martijn H., den Dunnen, Johan T.

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Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells von Aartsma-Rus, A, Kaman, W E, Bremmer-Bout, M, Janson, A A M, den Dunnen, J T, van Ommen, G-J B, van Deutekom, J C T

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Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers von Demant, Peter, Ruivenkamp, Claudia A.L, van Wezel, Tom, Zanon, Carlo, Stassen, Alphons P.M, Vlcek, Cestmir, Csikós, Tamás, Klous, Anita M, Tripodis, Nikos, Perrakis, Anastassis, Boerrigter, Lucie, Groot, Peter C, Lindeman, Jan, Mooi, Wolter J, Meijjer, Gerrit A, Scholten, Gert, Dauwerse, Hans, Paces, Vaclav, van Zandwijk, Nico, van Ommen, Gert Jan B

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Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling von Turk, R, Sterrenburg, E, de Meijer, E J, van Ommen, G-J B, den Dunnen, J T, 't Hoen, P A C

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The PWWP domain: a potential protein–protein interaction domain in nuclear proteins influencing differentiation? von Stec, Ingrid, Nagl, Sylvia B., van Ommen, Gert-Jan B., den Dunnen, Johan T.

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