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 · 229 citations · Full text

Life Sciences, Genetics, Immunology +13

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

Life Sciences, Genetics, Hematology +13

Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis

Melanie J. Percy, Philip Beer, Gavin Campbell et al. · Blood · 2008 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases

Celeste Bento, Melanie J. Percy, Betty Gardie et al. · Human Mutation · 2013 · 125 citations · Full text

Life Sciences, Genetics, Hematology +17

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 · 104 citations · Full text

Natural Sciences, Biophysics, Cell Biology +17