Naren Prahalada Rao

This study uses whole exome sequencing in families with multiple affected individuals to identify rare variants in genes associated with both Mendelian and complex neuropsychiatric syndromes.

This study determines the minimum sample size needed for multisite harmonization using structural brain MRI features and shows how sample size requirements increase with site variability.

The paper analyzes whole exome sequencing data from individuals with severe mental illness to identify genes under positive selection and their biological functions.

This study shows that stimulus-induced gamma oscillations in EEG are reliable across test-retest intervals in healthy elderly, suggesting their potential as a biomarker for early AD diagnosis and subject identification.

The paper develops and validates age-specific Indian brain templates and atlases for spatial normalization of MRI data across ages 6-60 years.

The paper examines the relationship between adverse childhood experiences (ACEs) and the age of onset of psychiatric diagnoses in individuals from families with multiple affected members.

This study examines gamma oscillations in elderly humans and finds age-related decreases in power and center frequency, but not alpha power, suggesting potential biomarkers for cognitive decline.

The paper develops a database of coding variations from the Indian population to aid in understanding genotype-phenotype correlations and disease mechanisms.