De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from IndiaShruti Pande, Anju Shukla, Jeevan Kumar et al.|European Journal of Human Genetics|2023Cited by 18
<i>RTN2</i> deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticityReza Maroofian, Henry Houlden, Payam Sarraf et al.|Brain|2024Cited by 8
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
Biallelic <i>EPB41L3</i> variants underlie a developmental disorder with seizures and myelination defectsElizabeth A. Werren, Anju Shukla, Guillermo Rodríguez Bey et al.|Brain|2024Cited by 3
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian PopulationNamanpreet Kaur, Anju Shukla, Michelle C. do Rosario et al.|American Journal of Medical Genetics Part A|2024Cited by 2