Impaired Structural Motor Connectome in Amyotrophic Lateral Sclerosis

by Verstraete, Esther, Veldink, Jan H., Mandl, Rene C. W., van den Berg, Leonard H., van den Heuvel, Martijn P.
Published 2011

Associated autoimmune diseases in patients with multifocal motor neuropathy and their family members

by Cats, Elisabeth A., Bertens, Anne Suzanne, Veldink, Jan H., van den Berg, Leonard H., van der Pol, W. Ludo
Published 2011

Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner

by de Jong, Simone, Chepelev, Iouri, Janson, Esther, Strengman, Eric, van den Berg, Leonard H, Veldink, Jan H, Ophoff, Roel A
Published 2012

Widespread structural brain involvement in ALS is not limited to the C9orf72 repeat expansion

by Westeneng, Henk-Jan, Walhout, Renée, Straathof, Milou, Schmidt, Ruben, Hendrikse, Jeroen, Veldink, Jan H, van den Heuvel, Martijn P, van den Berg, Leonard H
Published 2016

Whole Blood Gene Expression Profiles of Patients with a Past Aneurysmal Subarachnoid Hemorrhage

by van ’t Hof, Femke N. G., Ruigrok, Ynte M., Medic, Jelena, Sanjabi, Bahram, van der Vlies, Pieter, Rinkel, Gabriel J. E., Veldink, Jan H.
Published 2015

Correlation Between Structural and Functional Connectivity Impairment in Amyotrophic Lateral Sclerosis

by Schmidt, Ruben, Verstraete, Esther, de Reus, Marcel A, Veldink, Jan H, van den Berg, Leonard H, van den Heuvel, Martijn P
Published 2014

Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects

by van Eijk, Kristel R, de Jong, Simone, Boks, Marco PM, Langeveld, Terry, Colas, Fabrice, Veldink, Jan H, de Kovel, Carolien GF, Janson, Esther, Strengman, Eric, Langfelder, Peter, Kahn, René S, van den Berg, Leonard H, Horvath, Steve, Ophoff, Roel A
Published 2012

Characterization of FUS Mutations in Amyotrophic Lateral Sclerosis Using RNA-Seq

by van Blitterswijk, Marka, Wang, Eric T., Friedman, Brad A., Keagle, Pamela J., Lowe, Patrick, Leclerc, Ashley Lyn, van den Berg, Leonard H., Housman, David E., Veldink, Jan H., Landers, John E.
Published 2013

Genetic Overlap between Apparently Sporadic Motor Neuron Diseases

by van Blitterswijk, Marka, Vlam, Lotte, van Es, Michael A., van der Pol, W-Ludo, Hennekam, Eric A. M., Dooijes, Dennis, Schelhaas, Helenius J., van der Kooi, Anneke J., de Visser, Marianne, Veldink, Jan H., van den Berg, Leonard H.
Published 2012

C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits

by Koppers, Max, Blokhuis, Anna M., Westeneng, Henk‐Jan, Terpstra, Margo L., Zundel, Caroline A. C., Vieira de Sá, Renata, Schellevis, Raymond D., Waite, Adrian J., Blake, Derek J., Veldink, Jan H., van den Berg, Leonard H., Pasterkamp, R. Jeroen
Published 2015

Full ablation of C9orf72 in mice causes immune system-related pathology and neoplastic events but no motor neuron defects

by Sudria-Lopez, Emma, Koppers, Max, de Wit, Marina, van der Meer, Christiaan, Westeneng, Henk-Jan, Zundel, Caroline A. C., Youssef, Sameh A., Harkema, Liesbeth, de Bruin, Alain, Veldink, Jan H., van den Berg, Leonard H., Pasterkamp, R. Jeroen
Published 2016

Unraveling the Regulatory Mechanisms Underlying Tissue-Dependent Genetic Variation of Gene Expression

by Fu, Jingyuan, Wolfs, Marcel G. M., Deelen, Patrick, Westra, Harm-Jan, Fehrmann, Rudolf S. N., te Meerman, Gerard J., Buurman, Wim A., Rensen, Sander S. M., Groen, Harry J. M., Weersma, Rinse K., van den Berg, Leonard H., Veldink, Jan, Ophoff, Roel A., Snieder, Harold, van Heel, David, Jansen, Ritsert C., Hofker, Marten H., Wijmenga, Cisca, Franke, Lude
Published 2012

DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts

by Zhernakova, Daria V., de Klerk, Eleonora, Westra, Harm-Jan, Mastrokolias, Anastasios, Amini, Shoaib, Ariyurek, Yavuz, Jansen, Rick, Penninx, Brenda W., Hottenga, Jouke J., Willemsen, Gonneke, de Geus, Eco J., Boomsma, Dorret I., Veldink, Jan H., van den Berg, Leonard H., Wijmenga, Cisca, den Dunnen, Johan T., van Ommen, Gert-Jan B., 't Hoen, Peter A. C., Franke, Lude
Published 2013

Correction: DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts

by Zhernakova, Daria V., de Klerk, Eleonora, Westra, Harm-Jan, Mastrokolias, Anastasios, Amini, Shoaib, Ariyurek, Yavuz, Jansen, Rick, Penninx, Brenda W., Hottenga, Jouke J., Willemsen, Gonneke, de Geus, Eco J., Boomsma, Dorret I., Veldink, Jan H., van den Berg, Leonard H., Wijmenga, Cisca, den Dunnen, Johan T., van Ommen, Gert-Jan B., 't Hoen, Peter A. C., Franke, Lude
Published 2013

Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

by Gaastra, Benjamin, Shatunov, Aleksey, Pulit, Sara, Jones, Ashley R., Sproviero, William, Gillett, Alexandra, Chen, Zhongbo, Kirby, Janine, Fogh, Isabella, Powell, John F., Leigh, P. Nigel, Morrison, Karen E., Shaw, Pamela J., Shaw, Christopher E., van den Berg, Leonard H., Veldink, Jan H., Lewis, Cathryn M., Al-Chalabi, Ammar
Published 2016

Complement activity is associated with disease severity in multifocal motor neuropathy

by Vlam, Lotte, Cats, Elisabeth A., Harschnitz, Oliver, Jansen, Marc D., Piepers, Sanne, Veldink, Jan Herman, Franssen, Hessel, Stork, Abraham C.J., Heezius, Erik, Rooijakkers, Suzan H.M., Herpers, Bjorn L., van Strijp, Jos A., van den Berg, Leonard H., van der Pol, W. Ludo
Published 2015

Genomic signals of migration and continuity in Britain before the Anglo-Saxons

by Martiniano, Rui, Caffell, Anwen, Holst, Malin, Hunter-Mann, Kurt, Montgomery, Janet, Müldner, Gundula, McLaughlin, Russell L., Teasdale, Matthew D., van Rheenen, Wouter, Veldink, Jan H., van den Berg, Leonard H., Hardiman, Orla, Carroll, Maureen, Roskams, Steve, Oxley, John, Morgan, Colleen, Thomas, Mark G., Barnes, Ian, McDonnell, Christine, Collins, Matthew J., Bradley, Daniel G.
Published 2016

Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways

by Blokhuis, Anna M., Koppers, Max, Groen, Ewout J. N., van den Heuvel, Dianne M. A., Dini Modigliani, Stefano, Anink, Jasper J., Fumoto, Katsumi, van Diggelen, Femke, Snelting, Anne, Sodaar, Peter, Verheijen, Bert M., Demmers, Jeroen A. A., Veldink, Jan H., Aronica, Eleonora, Bozzoni, Irene, den Hertog, Jeroen, van den Berg, Leonard H., Pasterkamp, R. Jeroen
Published 2016

Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA

by Fehrmann, Rudolf S. N., Jansen, Ritsert C., Veldink, Jan H., Westra, Harm-Jan, Arends, Danny, Bonder, Marc Jan, Fu, Jingyuan, Deelen, Patrick, Groen, Harry J. M., Smolonska, Asia, Weersma, Rinse K., Hofstra, Robert M. W., Buurman, Wim A., Rensen, Sander, Wolfs, Marcel G. M., Platteel, Mathieu, Zhernakova, Alexandra, Elbers, Clara C., Festen, Eleanora M., Trynka, Gosia, Hofker, Marten H., Saris, Christiaan G. J., Ophoff, Roel A., van den Berg, Leonard H., van Heel, David A., Wijmenga, Cisca, te Meerman, Gerard J., Franke, Lude
Published 2011

Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS

by Diekstra, Frank P., Saris, Christiaan G. J., van Rheenen, Wouter, Franke, Lude, Jansen, Ritsert C., van Es, Michael A., van Vught, Paul W. J., Blauw, Hylke M., Groen, Ewout J. N., Horvath, Steve, Estrada, Karol, Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, Andre G., Robberecht, Wim, Andersen, Peter M., Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E., Brown, Robert H., Shatunov, Aleksey, Shaw, Christopher E., Leigh, P. Nigel, Al-Chalabi, Ammar, Ophoff, Roel A., van den Berg, Leonard H., Veldink, Jan H.
Published 2012