M. Malhotra

A novel abnormality annotation database for COVID-19 affected frontal lung X-rays

S. Chaudhury, A. Malhotra, R. Singh, 2021, medRxiv.

Clinico-radiological phenotyping and diagnostic pathways in childhood neurometabolic disorders—a practical introductory guide

F. D’Arco, K. Mankad, O. Carney, 2021, Translational pediatrics.

Eye signs in a child with ROBO3 gene mutation

S. Danda, S. Yoganathan, M. Thomas, 2022, Indian journal of ophthalmology.

Co‐occurrence of Aicardi–Goutières syndrome type 6 and dyschromatosis symmetrica hereditaria due to compound heterozygous pathogenic variants in ADAR1: a case series from India

S. Danda, B. Koshy, R. George, 2020, Clinical and experimental dermatology.