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Ashitha, S. N. and Ramachandra, N. B. (2020) Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders. Neuroscience, 438. pp. 25-40. ISSN 1873-7544
Ashitha, S. N. and Avinash, M. V. and Ramachandra, N. B. (2017) Whole exome sequencing of discordant diseases in Monozygotic twins with Down syndrome reveals mutations for Congenital Heart Defect and epileptic seizures. Meta Gene, 12. 134 - 137. ISSN 2214-5400
