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Wouter van Rheenen
Wouter van Rheenen
Fellow in Neuromuscular diseases, postdoc neurogenetics, UMC Utrecht, The Netherlands
Verified email at umcutrecht.nl
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Year
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
28082016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
5842016
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5702018
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
HJ Westeneng, TPA Debray, AE Visser, RPA van Eijk, JPK Rooney, ...
The Lancet Neurology 17 (5), 423-433, 2018
4202018
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
4082014
Evidence for an oligogenic basis of amyotrophic lateral sclerosis
M Van Blitterswijk, MA Van Es, EAM Hennekam, D Dooijes, ...
Human molecular genetics 21 (17), 3776-3784, 2012
4022012
Evidence for an oligogenic basis of amyotrophic lateral sclerosis
M Van Blitterswijk, MA Van Es, EAM Hennekam, D Dooijes, ...
Human molecular genetics 21 (17), 3776-3784, 2012
4022012
Genetic correlations of polygenic disease traits: from theory to practice
W Van Rheenen, WJ Peyrot, AJ Schork, SH Lee, NR Wray
Nature Reviews Genetics 20 (10), 567-581, 2019
3132019
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
2802016
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
2652021
Population genetic differentiation of height and body mass index across Europe
MR Robinson, G Hemani, C Medina-Gomez, M Mezzavilla, T Esko, ...
Nature genetics 47 (11), 1357-1362, 2015
2172015
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
MA Van Es, HJ Schelhaas, PWJ Van Vught, N Ticozzi, PM Andersen, ...
Annals of neurology 70 (6), 964-973, 2011
2112011
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
MK Bakker, RAA van der Spek, W van Rheenen, S Morel, R Bourcier, ...
Nature genetics 52 (12), 1303-1313, 2020
1762020
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
CM Lill, A Rengmark, L Pihlstrøm, I Fogh, A Shatunov, PM Sleiman, ...
Alzheimer's & Dementia 11 (12), 1407-1416, 2015
1742015
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
C Akimoto, AE Volk, M van Blitterswijk, M Van den Broeck, CS Leblond, ...
Journal of medical genetics 51 (6), 419-424, 2014
1402014
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
RL McLaughlin, D Schijven, W Van Rheenen, KR Van Eijk, M O’brien, ...
Nature communications 8 (1), 14774, 2017
1342017
UNC13A is a modifier of survival in amyotrophic lateral sclerosis
FP Diekstra, PWJ van Vught, W van Rheenen, M Koppers, RJ Pasterkamp, ...
Neurobiology of aging 33 (3), 630. e3-630. e8, 2012
1342012
Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases
W Van Rheenen, M Van Blitterswijk, MHB Huisman, L Vlam, ...
Neurology 79 (9), 878-882, 2012
1322012
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis
European Journal of Human Genetics 26 (10), 1537-1546, 2018
1292018
Genomic signals of migration and continuity in Britain before the Anglo-Saxons
R Martiniano, A Caffell, M Holst, K Hunter-Mann, J Montgomery, ...
Nature communications 7 (1), 10326, 2016
1232016
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