De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Anju Shukla, Shrikiran Aroor et al.|European Journal of Human Genetics|2023Cited by 18
Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90Dhanya Lakshmi Narayanan, Anju Shukla, Purvi Majethia et al.|European Journal of Medical Genetics|2021Cited by 15
Second report of SHMT2 related neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalitiesPurvi Majethia, Anju Shukla, Vivekananda Bhat 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, Namanpreet Kaur et al.|Clinical Genetics|2024Cited by 7
Further evidence of muscle involvement in neurodevelopmental disorder with epilepsy, spasticity, and brain atrophyPurvi Majethia, Anju Shukla, Michelle C. do Rosario et al.|Annals of Human Genetics|2021Cited by 6