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Deepika Jain · SciRah

Researcher profile · Semantic Scholar

Deepika Jain

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Deepika Jain — researcher profile on SciRah

h-index: 4
Works: 9
Citations: 79

Most-cited papers

Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test
F. Sheth, J. Shah, Deepika Jain, Siddharth M. Shah +14 more
2023BMC Neurology33 citations Open access
Semantic Scholar
Burden of rare genetic disorders in India: twenty-two years’ experience of a tertiary centre
J. Sheth, Aadhira Nair, F. Sheth, Manali Ajagekar +47 more
2024Orphanet Journal of Rare Diseases27 citations Open access
Semantic Scholar
Adaptive behavior and its differences between children with autism spectrum disorder and social communication disorder
Deepika Jain, Kawaljit Singh Multani, Anjaliba Dodiya, Urva Benani +1 more
2025Autism10 citations
Semantic Scholar
Late infantile form of multiple sulfatase deficiency with a novel missense variant in the SUMF1 gene: case report and review
J. Sheth, Siddharth M. Shah, Chaitanya A. Datar, K. Bhatt +6 more
2023BMC Pediatrics4 citations Open access
Semantic Scholar
Identification of LRFN1 as a novel synaptopathy gene in a child with autism
J. Shah, Deepika Jain, J. Sheth, F. Sheth +2 more
2025Discover Neuroscience2 citations Open access
Semantic Scholar
A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report
F. Sheth, J. Shah, Ketan Patel, D. Patel +3 more
2023BMC Neurology2 citations Open access
Semantic Scholar
Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India
J. Shah, Debasrija Mondal, Deepika Jain, Priti Mhatre +9 more
2025BMC Medical Genomics1 citations Open access
Semantic Scholar
Raga-music intervention in verbal autistic children: A randomized controlled pilot study
Mihika Desai, Jagruti Bandhiya, Jyoti Nakum, Deepika Jain +4 more
2025The Neuroscience Chronicles0 citations Open access
Semantic Scholar
Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report
H. Sheth, Sunil S. Trivedi, T. Liehr, K. Patel +3 more
2020BMC Medical Genomics0 citations Open access
Semantic Scholar

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