Maria van Genderen
Bartiméus(NL)
Publications by Year
Research Areas
Retinal Development and Disorders, Ophthalmology and Visual Impairment Studies, Retinal Diseases and Treatments, Photoreceptor and optogenetics research, Tactile and Sensory Interactions
Most-Cited Works
- → GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness(2012)159 cited
- → Mutations inGRM6Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram(2005)150 cited
- → Changes in causes of low vision between 1988 and 2009 in a Dutch population of children(2011)88 cited
- → Diagnosing Cerebral Visual Impairment in Children with Good Visual Acuity(2012)87 cited
- → Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome(2018)43 cited
- → Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry(2021)33 cited
- → The key role of electrophysiology in the diagnosis of visually impaired children(2006)27 cited
- → Altered organization of the visual cortex in FHONDA syndrome(2018)24 cited
- → Characteristics of childhood uveitis leading to visual impairment and blindness in the Netherlands(2014)24 cited
- → The conclusions of Clemson et al concerning valproic acid are premature(2010)23 cited