Rowdy Meijer

Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

Kornelia Neveling, Lilian A. Martinez-Carrera, Irmgard Hölker et al. · The American Journal of Human Genetics · 2013 · 173 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +6

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

Sascha Vermeer, Rowdy Meijer, Benjamin J. Pijl et al. · Neurogenetics · 2008 · 147 citations · Full text

Neurological Disorder, Genetics, Genetic Epidemiology +18

Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia

Sascha Vermeer, Alexander Hoischen, Rowdy Meijer et al. · The American Journal of Human Genetics · 2010 · 147 citations · Full text

Autosomal-recessive Cerebellar Ataxia, Mendelian Disorder, Neurogenomics +7

<i><scp>RYR</scp>1</i>‐related myopathies: a wide spectrum of phenotypes throughout life

Marc Snoeck, Baziel G.M. van Engelen, Benno Küsters et al. · European Journal of Neurology · 2015 · 138 citations

Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene–disease associations and unanticipated rare disorders

Bart P.C. van de Warrenburg, Meyke Schouten, Susanne T. de Bot et al. · European Journal of Human Genetics · 2016 · 114 citations · Full text