Divya Matta
15PUBLICATIONS
34CO-AUTHORS
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Publications (15)
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|Oct 29, 2024
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population.Namanpreet Kaur, Michelle C do Rosario, Purvi Majethia
|Feb 20, 2024
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications.Purvi Majethia, Namanpreet Kaur, Selinda Mascarenhas
|Dec 19, 2023
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.Shruti Pande, Purvi Majethia, Karthik Nair
|Nov 29, 2023
A novel homozygous variant in PMVK is associated with enhanced IL1β secretion and a hyper-IgD syndrome-like phenotype.Amit Jairaman, Vaishnavi Ashok Badiger, Spoorthy Raj
|Jun 20, 2023
Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B-related BAFopathy.Shruti Pande, Selinda Mascarenhas, Aishwarya Venkatraman
|Feb 24, 2022
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.Chiara Klöckner, J Pedro Fernández-Murray, Mahtab Tavasoli
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Frequent Collaborators
10 joint publications
Anju Shukla
8 joint publications
Katta Mohan Girisha
2 joint publications
Siddaramappa J Patil
2 joint publications
Purvi Majethia
2 joint publications
Sheela Nampoothiri
2 joint publications
Vivekananda Bhat
2 joint publications
Shruti Pande
1 joint publications
Aneek Das Bhowmik
1 joint publications
Gandham Sl Bhavani
1 joint publications
Chiara Klöckner
