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dr. W. (Wouter) van Rheenen

dr. W. (Wouter) van Rheenen

Assistant Professor

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Research Output (64)

Amyotrophic lateral sclerosis is not linked to multiple sclerosis in a population based study

van Doormaal P.T.C., Gallo A., van Rheenen W., Veldink J.H., van Es M.A., van den Berg L.H. 2013, In: Journal of Neurology, Neurosurgery and Psychiatry. 84 , p. 940-941 2 p.

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis

van Rheenen W., Diekstra F.P., van Doormaal P.T.C., Seelen M., Kenna K., McLaughlin R.L., Shatunov A., Czell D., van Es M.A., van Vught P.W.J., van Damme P., Smith B., Waibel S., Schelhaas H.J., van der Kooi A.J., de Visser M., Weber M, Robberecht W., Hardiman O., Shaw C.E., Morrison K.E., Al-Chalabi A., Andersen P.M., Ludolph A.C., Veldink J.H., van den Berg L.H. 2013, In: Neurobiology of Aging. 34 , p. 1517e 5-1517e 7 3 p.

Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3

Koppers M., Groen E.J.N., van Vught P.W.J., van Rheenen W., Witteveen E, van Es M.A., Pasterkamp R.J., van den Berg L.H., Veldink J.H. 2013, In: Neurobiology of Aging. 34 , p. 1518e5-1518e7 3 p.

UNC13A is a modifier of survival in amyotrophic lateral sclerosis

Diekstra F.P., van Vught P.W.J., van Rheenen W., Koppers M., Pasterkamp R.J., van Es M.A., Schelhaas H.J., Visser M.C., Robberecht W., van Damme P., Andersen P.M., van den Berg L.H., Veldink J.H. 2012, In: Neurobiology of Aging. 33 , p. 630.e3-8 6 p.

Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS

Diekstra F.P., Saris C.G.J., van Rheenen W., Franke L., Jansen R.C., van Es M.A., van Vught P.W.J., Blauw H.M., Groen E.J.N., Horvath S., Estrada K., Rivadeneira F., Hofman A., Uitterlinden A.G., Robberecht W., Andersen P.M., Melki J., Meininger V., Hardiman O., Landers J.E., Brown R.H. Jr., Shatunov A., Shaw C.E., Leigh P.N., Al-Chalabi A., Ophoff R.A., van den Berg L.H., Veldink J.H. 2012, In: PLoS ONE [E]. 7 , p. e35333 1 p.

VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient

van Blitterswijk M.M., van Es M.A., Koppers M., van Rheenen W., Medic J., Schelhaas H.J., van der Kooi A.J., Visser M.C., Veldink J.H., van den Berg L.H. 2012, In: Neurobiology of Aging. 33 , p. e1-e4 4 p.

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis

Groen E.J.N., van Rheenen W., Koppers M., van Doormaal P.T.C., Vlam L., Diekstra F.P., Dooijes D., Pasterkamp R.J., van den Berg L.H., Veldink J.H. 2012, In: Neurobiology of Aging. 33 3 p.

UBQLN2 in familial amyotrophic lateral sclerosis in The Netherlands

van Doormaal P.T.C., van Rheenen W., van Blitterswijk M.M., Schellevis R., Schelhaas H.J., de Visser M., van der Kooi A.J., Veldink J.H., van den Berg L.H. 2012, In: Neurobiology of Aging. 33 , p. 2233e7-2233e8 2 p.

SMN1 gene duplications are associated with sporadic ALS

Blauw H.M., Barnes C.P., van Vught P.W.J., van Rheenen W., Verheul M., Cuppen E.P.J.G., Veldink J.H., van den Berg L.H. 2012, In: Neurology. 78 , p. 776-780 5 p.

Evidence for an oligogenic basis of amyotrophic lateral sclerosis

Van Blitterswijk Marka, Van Es Michael A., Hennekam Eric A M, Dooijes Dennis, Van Rheenen Wouter, Medic Jelena, Bourque Pierre R., Schelhaas Helenius J., Van der Kooi Anneke J., De Visser Marianne, De Bakker Paul I W, Veldink Jan H., van den Berg Leonard H. 2012, In: Human Molecular Genetics. 21 , p. 3776-3784 9 p.

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