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prof. dr. J.H. (Jan) Veldink

prof. dr. J.H. (Jan) Veldink

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Research Output (298)

RNA-Sequencing Highlights Inflammation and Impaired Integrity of the Vascular Wall in Brain Arteriovenous Malformations

Hauer Allard J, Kleinloog Rachel, Giuliani Fabrizio, Rinkel Gabriël J E, de Kort Gerard A, Berkelbach van der Sprenkel Jan Willem, van der Zwan Albert, Gosselaar Peter H, van Rijen Peter C, de Boer-Bergsma Jelkje J, Deelen Patrick, Swertz Morris A, De Muynck Louis, Van Damme Philip, Veldink Jan H, Ruigrok Ynte M, Klijn Catharina J M 1 Jan 2020, In: Stroke. 51 , p. 268-274 7 p.

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

Tazelaar Gijs H P, Boeynaems Steven, De Decker Mathias, van Vugt Joke J F A, Kool Lindy, Goedee H Stephan, McLaughlin Russell L, Sproviero William, Iacoangeli Alfredo, Moisse Matthieu, Jacquemyn Maarten, Daelemans Dirk, Dekker Annelot M, van der Spek Rick A, Westeneng Henk-Jan, Kenna Kevin P, Assialioui Abdelilah, Da Silva Nica, Povedano Mónica, Pardina Jesus S Mora, Hardiman Orla, Salachas François, Millecamps Stéphanie, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Morrison Karen E, Shaw Pamela J, Shaw Christopher E, Pasterkamp R Jeroen, Landers John E, Van Den Bosch Ludo, Robberecht Wim, Al-Chalabi Ammar, van den Berg Leonard H, Van Damme Philip, Veldink Jan H, van Es Michael A, 2020, In: Brain communications. 2 , p. 1-13

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (vol 52, pg 1303, 2020):Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (Nature Genetics, (2020), 52, 12, (1303-1313), 10.1038/s41588-020-00725-7)

Bakker Mark K., van der Spek Rick A.A., van Rheenen Wouter, Morel Sandrine, Bourcier Romain, Hostettler Isabel C., Alg Varinder S., van Eijk Kristel R., Koido Masaru, Akiyama Masato, Terao Chikashi, Matsuda Koichi, Walters Robin G., Lin Kuang, Li Liming, Millwood Iona, Chen Zhengming, Rouleau Guy A., Zhou Sirui, Rannikmäe Kristiina, Sudlow Cathie L.M., Houlden Henry, van den Berg Leonard H., Dina Christian, Naggara Olivier, Gentric Jean Christophe, Shotar Eimad, Eugène François, Desal Hubert, Winsvold Bendik S., Børte Sigrid, Johnsen Marianne Bakke, Brumpton Ben M., Sandvei Marie Søfteland, Willer Cristen J., Hveem Kristian, Zwart John Anker, Verschuren W. M.Monique, Friedrich Christoph M., Hirsch Sven, Schilling Sabine, Dauvillier Jérôme, Martin Olivier, Bian Zheng, Chen Junshi, Klijn Catharina J.M., Rinkel Gabriel J.E., Lindgren Antti, Veldink Jan H., Ruigrok Ynte M., , , , , , , 2020, In: Nature Genetics. 53 , p. 254 1 p.

Distinctive pattern of temporal atrophy in patients with frontotemporal dementia and the I383V variant in TARDBP

Mol Merel O, Nijmeijer Sebastiaan W R, van Rooij Jeroen G J, van Spaendonk Resie M L, Pijnenburg Yolande A L, van der Lee Sven J, van Minkelen Rick, Donker Kaat Laura, Rozemuller Annemieke J M, Janse van Mantgem Mark R, van Rheenen Wouter, van Es Michael A, Veldink Jan H, Hennekam Frederic A M, Vernooij Meike, van Swieten John C, Cohn-Hokke Petra E, Seelaar Harro, Dopper Elise G P 2020, In: Journal of neurology, neurosurgery, and psychiatry. 92 , p. 787-789 3 p.

Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology

Reichenstein Irit, Eitan Chen, Diaz-Garcia Sandra, Haim Guy, Magen Iddo, Siany Aviad, Hoye Mariah L, Rivkin Natali, Olender Tsviya, Toth Beata, Ravid Revital, Mandelbaum Amitai D, Yanowski Eran, Liang Jing, Rymer Jeffrey K, Levy Rivka, Beck Gilad, Ainbinder Elena, Farhan Sali M K, Lennox Kimberly A, Bode Nicole M, Behlke Mark A, Möller Thomas, Saxena Smita, Moreno Cristiane A M, Costaguta Giancarlo, van Eijk Kristel R, Phatnani Hemali, Al-Chalabi Ammar, Başak A Nazli, van den Berg Leonard H, Hardiman Orla, Landers John E, Mora Jesus S, Morrison Karen E, Shaw Pamela J, Veldink Jan H, Pfaff Samuel L, Yizhar Ofer, Gross Christina, Brown Robert H, Ravits John M, Harms Matthew B, Miller Timothy M, Hornstein Eran 18 Dec 2019, In: Science Translational Medicine. 11 12 p.

WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

Nersisyan Lilit, Nikoghosyan Maria, Arakelyan Arsen, Francioli Laurent C., Menelaou Androniki, Pulit Sara L., Elbers Clara C., Kloosterman Wigard P., van Setten Jessica, Nijman Isaäc J., Renkens Ivo, de Bakker Paul I.W., van Dijk Freerk, Neerincx Pieter B.T., Deelen Patrick, Kanterakis Alexandros, Dijkstra Martijn, Byelas Heorhiy, van der Velde K. Joeri, Platteel Mathieu, Swertz Morris A., Wijmenga Cisca, Palamara Pier Francesco, Pe’er Itsik, Ye Kai, Ye Kai, Lameijer Eric Wubbo, Moed Matthijs H., Beekman Marian, de Craen Anton J.M., Suchiman H. Eka D., Slagboom P. Eline, Guryev Victor, Abdellaoui Abdel, Jan Hottenga Jouke, Kattenberg Mathijs, Willemsen Gonneke, Boomsma Dorret I., van Leeuwen Elisabeth M., Karssen Lennart C., Amin Najaf, Rivadeneira Fernando, Isaacs Aaron, Hofman Albert, Uitterlinden André G., van Duijn Cornelia M., van Oven Mannis, Kayser Manfred, Veldink Jan H., van den Berg Leonard H., 1 Dec 2019, In: Scientific Reports. 9

Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis

Dekker Annelot M, Diekstra Frank P, Pulit Sara L, Tazelaar Gijs H P, van der Spek Rick A, van Rheenen Wouter, van Eijk Kristel R, Calvo Andrea, Brunetti Maura, Damme Philip Van, Robberecht Wim, Hardiman Orla, McLaughlin Russell, Chiò Adriano, Sendtner Michael, Ludolph Albert C, Weishaupt Jochen H, Pardina Jesus S Mora, van den Berg Leonard H, Veldink Jan H 1 Dec 2019, In: Scientific Reports. 9

Associations of autozygosity with a broad range of human phenotypes

Clark David W et al. 1 Dec 2019, In: Nature Communications. 10

Coding and non-coding RNA abnormalities in bipolar disorder

Luykx Jurjen J., Giuliani Fabrizio, Giuliani Giuliano, Veldink Jan 1 Nov 2019, In: Genes. 10

Pharmacogenetic interactions in amyotrophic lateral sclerosis:a step closer to a cure?

van Eijk Ruben P A, Eijkemans Marinus J C, Nikolakopoulos Stavros, Jansen Marc D, Westeneng Henk-Jan, van Eijk Kristel R, van der Spek Rick A A, van Vugt Joke J F A, Piepers Sanne, Groeneveld Geert-Jan, Veldink Jan H, van den Berg Leonard H, van Es Michael A 17 Oct 2019, In: The Pharmacogenomics Journal. 20 , p. 220-226 7 p.

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