Jeevan Kumar

The E262K mutation in Lamin A links nuclear proteostasis imbalance to laminopathy‐associated premature aging

K. Girisha, S. Nampoothiri, A. Ranjan, 2022, Aging cell.

Subtelomeric rearrangements in Indian children with idiopathic intellectual disability/developmental delay: Frequency estimation & clinical correlation using fluorescence in situ hybridization (FISH)

S. Nampoothiri, Latha Ravichandran, S. Paul, 2016, The Indian journal of medical research.

Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association

T. Jayasudha, K. Gowrishankar, T. Vasanthi, 2011, Indian journal of human genetics.

De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.

K. Girisha, A. Shukla, S. Nampoothiri, 2023, European journal of human genetics : EJHG.