Inge A. Meijer
University of Vienna(AT)Centre Hospitalier Universitaire Sainte-Justine(CA)Université de Montréal(CA)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Hereditary Neurological Disorders, Neurological disorders and treatments, Neurological diseases and metabolism, Mitochondrial Function and Pathology
Most-Cited Works
- → Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia(2006)192 cited
- → The genetic landscape of infantile spasms(2014)188 cited
- → A stop codon mutation in SCN9A causes lack of pain sensation(2007)184 cited
- → Recessive mutations in VPS13D cause childhood onset movement disorders(2018)128 cited
- → A Variant in XPNPEP2 Is Associated with Angioedema Induced by Angiotensin I–Converting Enzyme Inhibitors(2005)127 cited
- → An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred(2002)114 cited
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