De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Anju Shukla, Sheela Nampoothiri et al.|European Journal of Human Genetics|2023Cited by 18
Second report of SHMT2 related neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalitiesPurvi Majethia, Anju Shukla, B.L. Yatheesha et al.|European Journal of Medical Genetics|2022Cited by 9
Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implicationsPurvi Majethia, Anju Shukla, Leslie Lewis et al.|Clinical Genetics|2024Cited by 7
Bi‐Allelic Splicing Variant, c.153‐<scp>2A</scp> > C in <scp><i>TOMM7</i></scp> Is Associated With Leigh SyndromeMayuri Yeole, Vivekananda Bhat, Katta M. Girisha et al.|American Journal of Medical Genetics Part A|2024Cited by 2
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian PopulationNamanpreet Kaur, Anju Shukla, Selinda Mascarenhas et al.|American Journal of Medical Genetics Part A|2024Cited by 2