Jeroen van Rooij
0000-0001-9754-073X
3 papers found
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Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Reduced penetrance of pathogenic ACMG variants in a deeply phenotyped cohort study and evaluation of ClinVar classification over time
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
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