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dr. W. (Wouter) van Rheenen

dr. W. (Wouter) van Rheenen

Assistant Professor

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Research Output (64)

A reference panel of 64,976 haplotypes for genotype imputation

McCarthy Shane, Das Sayantan, Kretzschmar Warren, Delaneau Olivier, Wood Andrew R, Teumer Alexander, Kang Hyun Min, Fuchsberger Christian, Danecek Petr, Sharp Kevin, Luo Yang, Sidore Carlo, Kwong Alan, Timpson Nicholas, Koskinen Seppo, Vrieze Scott, Scott Laura J, Zhang He, Mahajan Anubha, Veldink Jan, Peters Ulrike, Pato Carlos, van Duijn Cornelia M, Gillies Christopher E, Gandin Ilaria, Mezzavilla Massimo, Gilly Arthur, Cocca Massimiliano, Traglia Michela, Angius Andrea, Barrett Jeffrey C, Boomsma Dorrett, Branham Kari, Breen Gerome, Brummett Chad M, Busonero Fabio, Campbell Harry, Chan Andrew, Chen Sai, Chew Emily, Collins Francis S, Corbin Laura J, Smith George Davey, Dedoussis George, Dorr Marcus, Farmaki Aliki-Eleni, Van den Berg Leonard H, Van Rheenen Wouter, de Bakker Paul I W, Dekker Annelot, 22 Aug 2016, In: Nature Genetics. 48 , p. 1279–1283

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Kenna Kevin P, van Doormaal Perry T C, Dekker Annelot M, Ticozzi Nicola, Kenna Brendan J, Diekstra Frank P, van Rheenen Wouter, van Eijk Kristel R, Jones Ashley R, Keagle Pamela, Shatunov Aleksey, Sproviero William, Smith Bradley N, van Es Michael A, Topp Simon D, Kenna Aoife, Miller Jack W, Fallini Claudia, Tiloca Cinzia, McLaughlin Russell L, Vance Caroline, Troakes Claire, Colombrita Claudia, Mora Gabriele, Calvo Andrea, Verde Federico, Al-Sarraj Safa, King Andrew, Calini Daniela, de Belleroche Jacqueline, Baas Frank, van der Kooi Anneke J, de Visser Marianne, Ten Asbroek Anneloor L M A, Sapp Peter C, McKenna-Yasek Diane, Polak Meraida, Asress Seneshaw, Muñoz-Blanco José Luis, Strom Tim M, Meitinger Thomas, Morrison Karen E, Lauria Giuseppe, Williams Kelly L, Leigh P Nigel, Nicholson Garth A, Blair Ian P, Leblond Claire S, van den Berg Leonard H, Veldink Jan H, 25 Jul 2016, In: Nature Genetics. 48 , p. 1037–1042

Autoantibody pathogenicity in a multifocal motor neuropathy induced pluripotent stem cell-derived model

Härschnitz Oliver, van den Berg Leonard H., Johansen Lill Eva, Jansen Marc D., Kling Sandra, Vieira de Sá Renata, Vlam Lotte, van Rheenen Wouter, Karst Henk, Wierenga Corette J., Pasterkamp R. Jeroen, van der Pol W. Ludo Jul 2016, In: Annals of Neurology. 80 , p. 71-88 18 p.

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis

Fogh Isabella, Lin Kuang, Tiloca Cinzia, Rooney James, Gellera Cinzia, Diekstra Frank P, Ratti Antonia, Shatunov Aleksey, van Es Michael A, Proitsi Petroula, Jones Ashley, Sproviero William, Chiò Adriano, McLaughlin Russell Lewis, Sorarù Gianni, Corrado Lucia, Stahl Daniel, Del Bo Roberto, Cereda Cristina, Castellotti Barbara, Glass Jonathan D, Newhouse Steven, Dobson Richard, Smith Bradley N, Topp Simon, van Rheenen Wouter, Meininger Vincent, Melki Judith, Morrison Karen E, Shaw Pamela J, Leigh P Nigel, Andersen Peter M, Comi Giacomo P, Ticozzi Nicola, Mazzini Letizia, D'Alfonso Sandra, Traynor Bryan J, Van Damme Philip, Robberecht Wim, Brown Robert H, Landers John E, Hardiman Orla, Lewis Cathryn M, van den Berg Leonard H, Shaw Christopher E, Veldink Jan H, Silani Vincenzo, Al-Chalabi Ammar, Powell John Jul 2016, In: JAMA Neurology. 73 , p. 812-820 9 p.

Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis

El Oussini Hajer, Bayer Hanna, Scekic-Zahirovic Jelena, Vercruysse Pauline, Sinniger Jérôme, Dirrig-Grosch Sylvie, Dieterlé Stéphane, Echaniz-Laguna Andoni, Larmet Yves, Müller Kathrin, Weishaupt Jochen H, Thal Dietmar R, van Rheenen Wouter, van Eijk Kristel, Lawson Roland, Monassier Laurent, Maroteaux Luc, Roumier Anne, Wong Philip C, van den Berg Leonard H, Ludolph Albert C, Veldink Jan H, Witting Anke, Dupuis Luc Mar 2016, In: Acta Neuropathologica. 131 , p. 465-480 16 p.

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

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 2016, In: Nature Communications [E]. 7 8 p.

Brain morphologic changes in asymptomatic C9orf72 repeat expansion carriers

Walhout Renée, Schmidt Ruben, Westeneng Henk-Jan, Verstraete Esther, Seelen Meinie, van Rheenen Wouter, de Reus Marcel A, van Es Michael A, Hendrikse J, Veldink Jan H, van den Heuvel Martijn P, van den Berg Leonard H 17 Nov 2015, In: Neurology. 85 , p. 1780-8 9 p.

Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers

Dekker Annelot M, Seelen Meinie, van Doormaal Perry T C, van Rheenen Wouter, Bothof Reinoud J P, van Riessen Tim, Brands William J, van der Kooi Anneke J, de Visser Marianne, Voermans Nicol C, Pasterkamp R Jeroen, Veldink Jan H, van den Berg Leonard H, van Es Michael A 2015, In: Neurobiology of Aging.

A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories

Akimoto C., Volk A., van Blitterswijk M.M., van den Broeck M., Leblond C.S., Lumbroso S., Camu W., Neitzel B., Onodera O., van Rheenen W., Pinto S., Weber M, Smith B., Proven M., Talbot K., Keagle P., Chesi A., Ratti A., van der Zee J., Alstermark H., Birve A., Calini D., Nordin A., Tradowsky D.C., Just W., Daoud H., Angerbauer S., Dejesus-Hernandez M., Konno T., Lloyd-Jani A., de Carvalho M., Mouzat K., Landers J.E., Veldink J.H., Silani V., Gitler A.D., Shaw C.E., Rouleau G.A., van den Berg L.H., van Broeckhoven C., Rademakers R., Andersen P.M., Kubisch C. 2014, In: Journal of Medical Genetics. 51 , p. 419-424 6 p.

Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

van Rheenen W., Diekstra F.P., van den Berg L.H., Veldink J.H. 2014, In: Brain. 13

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