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Publications by Vinodh Narayanan
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
American Journal of Human Genetics
Genetics
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
American Journal of Human Genetics
Genetics
Biallelic VARS Variants Cause Developmental Encephalopathy With Microcephaly That Is Recapitulated in Vars Knockout Zebrafish
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
Delineating the GRIN1 Phenotypic Spectrum
Neurology
Neurology
A Gain-Of-Function Mutation in theGRIK2gene Causes Neurodevelopmental Deficits
Neurology: Genetics
Neurology
Genetics
Simultaneous Recordings of Ocular Microtremor and Microsaccades With a Piezoelectric Sensor and a Video-Oculography System
PeerJ
Genetics
Molecular Biology
Biochemistry
Biological Sciences
Medicine
Agricultural
Neuroscience
Evidence for Population Variation in TSC1 and TSC2 Gene Expression
BMC Medical Genetics
Genetics
