De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Anju Shukla, Neethukrishna Kausthubham et al.|European Journal of Human Genetics|2023Cited by 18
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
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Report of a novel recurrent homozygous variant c.620A>T in three unrelated families with thiamine metabolism dysfunction syndrome 5 and review of literatureSelinda Mascarenhas, Anju Shukla, Karthik Vijay Nair et al.|Clinical Dysmorphology|2024Cited by 1
Author response for "Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications"Purvi Majethia, Anju Shukla, Leslie Lewis et al.|Unknown|2024Cited by 0