Richard van Wijk

Mutations in the perforin gene can be linked to macrophage activation syndrome in patients with systemic onset juvenile idiopathic arthritis

Sebastiaan J. Vastert, Richard van Wijk, Leila Emma D’Urbano et al. · Lara D. Veeken · 2009 · 226 citations · Full text

A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies

Arjan Buijs, Pino J. Poddighe, Richard van Wijk et al. · Blood · 2001 · 132 citations · Full text

Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis

Melanie J. Percy, Philip Beer, Gavin Campbell et al. · Blood · 2008 · 127 citations · Full text

Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases

Celeste Bento, Melanie J. Percy, Betty Gardie et al. · Human Mutation · 2013 · 121 citations · Full text

Developmental Anomaly, Developmental Biology, Tissue Hypoxia +14

The fluid membrane determines mechanics of erythrocyte extracellular vesicles and is softened in hereditary spherocytosis

Daan Vorselen, Susan M. van Dommelen, Raya Sorkin et al. · Nature Communications · 2018 · 102 citations · Full text