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Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortJoint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitisALS in Danish Registries: Heritability and links to psychiatric and cardiovascular disordersAssociations of autozygosity with a broad range of human phenotypesThe project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
P50
description
researcher (ORCID 0000-0002-5860-1533)
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wetenschapper
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name
Wouter van Rheenen
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Wouter van Rheenen
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type
label
Wouter van Rheenen
@en
Wouter van Rheenen
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prefLabel
Wouter van Rheenen
@en
Wouter van Rheenen
@nl
P31
P496
0000-0002-5860-1533