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

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

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Research Output (298)

Genetic analysis of ALS cases in the isolated island population of Malta

Borg Rebecca, Farrugia Wismayer Maia, Bonavia Karl, Farrugia Wismayer Andrew, Vella Malcolm, van Vugt Joke J F A, Kenna Brendan J, Kenna Kevin P, Vassallo Neville, Veldink Jan H, Cauchi Ruben J Apr 2021, In: European Journal of Human Genetics. 29 , p. 604-614 11 p.

The Effect of SMN Gene Dosage on ALS Risk and Disease Severity

Moisse Matthieu, Zwamborn Ramona A J, van Vugt Joke, van der Spek Rick, van Rheenen Wouter, Kenna Brendan, Van Eijk Kristel, Kenna Kevin, Corcia Philippe, Couratier Philippe, Vourc'h Patrick, Hardiman Orla, McLaughin Russell, Gotkine Marc, Drory Vivian, Ticozzi Nicola, Silani Vincenzo, de Carvalho Mamede, Mora Pardina Jesús S, Povedano Monica, Andersen Peter M, Weber Markus, Başak Nazli A, Chen Xiao, Eberle Michael A, Al-Chalabi Ammar, Shaw Chris, Shaw Pamela J, Morrison Karen E, Landers John E, Glass Jonathan D, Robberecht Wim, van Es Michael, van den Berg Leonard, Veldink Jan, Van Damme Philip, Apr 2021, In: Annals of Neurology. 89 , p. 686-697 12 p.

Erratum:Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene (Cell Reports (2020) 33(9), (S2211124720314455), (10.1016/j.celrep.2020.108456))

Cooper-Knock Johnathan, Zhang Sai, Kenna Kevin P, Moll Tobias, Franklin John P, Allen Samantha, Nezhad Helia Ghahremani, Iacoangeli Alfredo, Yacovzada Nancy Y, Eitan Chen, Hornstein Eran, Elhaik Eran, Celadova Petra, Bose Daniel, Farhan Sali, Fishilevich Simon, Lancet Doron, Morrison Karen E, Shaw Christopher E, Al-Chalabi Ammar, Veldink Jan H, Kirby Janine, Snyder Michael P, Shaw Pamela J, 2 Feb 2021, In: Cell Reports. 34

SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed

Iacoangeli Alfredo, Fogh Isabella, Selvackadunco Sashika, Topp Simon D, Shatunov Aleksey, van Rheenen Wouter, Al-Khleifat Ahmad, Opie-Martin Sarah, Ratti Antonia, Calvo Andrea, Van Damme Philip, Robberecht Wim, Chio Adriano, Dobson Richard J, Hardiman Orla, Shaw Christopher E, van den Berg Leonard H, Andersen Peter M, Smith Bradley N, Silani Vincenzo, Veldink Jan H, Breen Gerome, Troakes Claire, Al-Chalabi Ammar, Jones Ashley R, 2021, In: Brain communications. 3

Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

Nabais Marta F., Lin Tian, Benyamin Beben, Williams Kelly L., Garton Fleur C., Vinkhuyzen Anna A.E., Zhang Futao, Vallerga Costanza L., Restuadi Restuadi, Freydenzon Anna, Zwamborn Ramona A.J., Hop Paul J., Robinson Matthew R., Gratten Jacob, Visscher Peter M., Hannon Eilis, Mill Jonathan, Brown Matthew A., Laing Nigel G., Mather Karen A., Sachdev Perminder S., Ngo Shyuan T., Steyn Frederik J., Wallace Leanne, Henders Anjali K., Needham Merrilee, Veldink Jan H., Mathers Susan, Nicholson Garth, Rowe Dominic B., Henderson Robert D., McCombe Pamela A., Pamphlett Roger, Yang Jian, Blair Ian P., McRae Allan F., Wray Naomi R. 1 Dec 2020, In: npj Genomic Medicine. 5 , p. 1-9

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

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, Lin Kuang, Li Liming, Millwood Iona Y., 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., , , , , , , Dec 2020, In: Nature Genetics. 52 , p. 1303-1313 11 p.

Blood metal levels and amyotrophic lateral sclerosis risk:a prospective cohort

Peters Susan, Broberg Karin, Gallo Valentina, Levi Michael, Kippler Maria, Vineis Paolo, Veldink Jan, van den Berg Leonard, Middleton Lefkos, Travis Ruth C, Bergmann Manuela M, Palli Domenico, Grioni Sara, Tumino Rosario, Elbaz Alexis, Vlaar Tim, Mancini Francesca, Kühn Tilman, Katzke Verena, Agudo Antonio, Goñi Fernando, Gómez Jesús-Humberto, Rodríguez-Barranco Miguel, Merino Susana, Barricarte Aurelio, Trichopoulou Antonia, Jenab Mazda, Weiderpass Elisabete, Vermeulen Roel 17 Oct 2020, In: Annals of Neurology. 89 , p. 125-133 9 p.

Dutch population structure across space, time and GWAS design

Byrne Ross P, van Rheenen Wouter, van den Berg Leonard H, Veldink Jan H, McLaughlin Russell L, 11 Sep 2020, In: Nature Communications. 11 , p. 1-11

The distinct traits of the UNC13A polymorphism in amyotrophic lateral sclerosis

Tan Harold H G, Westeneng Henk-Jan, van der Burgh Hannelore K, van Es Michael A, Bakker Leonhard A, van Veenhuijzen Kevin, van Eijk Kristel R, van Eijk Ruben P A, Veldink Jan H, van den Berg Leonard H 6 Jul 2020, In: Annals of Neurology. 88 , p. 796-806 11 p.

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