Sakkubai Naidu
Kennedy Krieger Institute(US)Johns Hopkins University(US)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, RNA regulation and disease, Autism Spectrum Disorder Research, Peroxisome Proliferator-Activated Receptors, Metabolism and Genetic Disorders
Most-Cited Works
- → Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter(2001)416 cited
- → Lysosomal glycogen storage disease with normal acid maltase(1981)403 cited
- → Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter(2001)382 cited
- → Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls(1999)345 cited
- Alexander disease: diagnosis with MR imaging.(2001)
- → Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus(2012)286 cited
- → Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease