WV
W van Rheenen
University Medical Center Utrecht, The University of Queensland, University Medical Center Utrecht, Brain Centre Rudolph Magnus
Research areas: Neuroscience · Cellular and Molecular Neuroscience · Amyotrophic Lateral Sclerosis Research · Hereditary Neurological Disorders · Genetic Associations and Epidemiology
0000-0002-5860-1533
Employment
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University of Queensland visiting researcher2017 - 2018
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Universitair Medisch Centrum Utrecht Resident2012 - Present
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Universitair Medisch Centrum Utrecht PhD student2010 - 2017
Education
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University Medical Center Utrecht Resident in Neurology2012 - Present
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University Medical Center Utrecht, Brain Centre Rudolph Magnus PhD in neurogenetics2010 - 2017
- 2004 - 2010
Projects & Funding
Projects & funding information is unavailable.
Publications (33)
- Sex-dependent DNA methylation in amyotrophic lateral sclerosis Save
- Tofersen treatment in respiratory onset amyotrophic lateral sclerosis and a variant of uncertain significance in SOD1; a case report Save
- The value of a family history to distinguish monogenic from polygenic amyotrophic lateral sclerosis Save
- Diagnostic Revision From Primary Lateral Sclerosis to Amyotrophic Lateral Sclerosis Save
- Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis Save
- A VAPB (P56S) mutation in a Dutch patient with familial motor neuron disease: a case report Save
- Reader Response: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype Save
- Dissecting epigenetic age acceleration in amyotrophic lateral sclerosis Save
- Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the Phenotype Save
- Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis Save
- Sex-specific risk loci and modifiedMEF2Cexpression in ALS Save
- Assessment of risk of ALS conferred by the GGGGCC hexanucleotide repeat expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion Save
- Association Between Serum Lipids and Survival in Patients With Amyotrophic Lateral Sclerosis Save
- Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia Save
- The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases Save
- Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology Save
- Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS Save
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology Save
- The Effect of SMN Gene Dosage on ALS Risk and Disease Severity Save
- Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways Save