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M. Kamate · SciRah

Researcher profile · Semantic Scholar

M. Kamate

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M. Kamate — researcher profile on SciRah

h-index: 19
Works: 154
Citations: 1,246

Most-cited papers

Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes
M. Quadri, M. Kamate, Suvasini Sharma, S. Olgiati +11 more
2015Movement Disorders63 citations
Semantic Scholar
Neuronal ceroid lipofuscinosis type-11 in an adolescent.
M. Kamate, M. Detroja, V. Hattiholi
2019Brain & development (Tokyo. 1979)39 citations
Semantic Scholar
Acute Leukoencephalopathy with Restricted Diffusion
M. Kamate
2018Indian Journal of Critical Care Medicine39 citations Open access
Semantic Scholar
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing
K. Kumar, G. Wali, M. Kamate, Gautam Wali +8 more
2016Neurogenetics36 citations Open access
Semantic Scholar
Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients
A. Ganapathy, A. Mishra, M. Soni, Priyanka Kumar +38 more
2019Journal of Neurology35 citations
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
Recurrent and novel GLB1 mutations in India.
Abdul Mueed Bidchol, A. Dalal, Rakesh Trivedi, A. Shukla +26 more
2015Gene26 citations
Semantic Scholar
Effect of Maternal Docosahexaenoic Acid (DHA) Supplementation on Offspring Neurodevelopment at 12 Months in India: A Randomized Controlled Trial
S. Khandelwal, D. Kondal, M. Chaudhry, K. Patil +10 more
2020Nutrients24 citations Open access
Semantic Scholar
Lysosomal storage disorders in Indian children with neuroregression attending a genetic center
J. Sheth, M. Mistri, Riddhi Bhavsar, F. Sheth +3 more
2015Indian Pediatrics21 citations
Semantic Scholar
Spectrum of ARSA variations in Asian Indian patients with Arylsulfatase A deficient metachromatic leukodystrophy
D. Narayanan, D. Matta, N. Gupta, M. Kabra +8 more
2019Journal of Human Genetics20 citations
Semantic Scholar
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children
Divyani Garg, S. Yoganathan, U. Shamim, K. Mankad +24 more
2022Movement Disorders Clinical Practice18 citations Open access
Semantic Scholar
The Effectiveness of a Computer Game-Based Rehabilitation Platform for Children With Cerebral Palsy: Protocol for a Randomized Clinical Trial
A. Kanitkar, T. Szturm, S. Parmar, D. Gandhi +8 more
2017JMIR Research Protocols18 citations Open access
Semantic Scholar
Clinical and Genetic Spectrum of 104 Indian families with Central Nervous System White Matter Abnormalities
P. Kaur, Michelle C. Do Rosario, M. Hebbar, Suvasini Sharma +28 more
2021Clinical Genetics17 citations Open access
Semantic Scholar
Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual development
Ann-Charlotte Thuresson, G. Van Buggenhout, F. Sheth, M. Kamate +3 more
2017Clinical Genetics17 citations Open access
Semantic Scholar
Batten disease: biochemical and molecular characterization revealing novel PPT1 and TPP1 gene mutations in Indian patients
J. Sheth, M. Mistri, Riddhi Bhavsar, Dhairya Pancholi +9 more
2018BMC Neurology16 citations Open access
Semantic Scholar
Neuronal Ceroid Lipofuscinoses in Children
M. Kamate, Narendra Reddy, M. Detroja, V. Hattiholi
2021Annals of Indian Academy of Neurology14 citations Open access
Semantic Scholar
ADCY5-related dyskinesia
M. Kamate, Nishant Mittal
2018Neurology India14 citations
Semantic Scholar
Management of Neurocysticercosis in Children: Association of Child Neurology Consensus Guidelines
N. Sankhyan, R. Kadwa, M. Kamate, Lakshminarayanan Kannan +4 more
2021Indian Pediatrics13 citations
Semantic Scholar
Acute Leucoencephalopathy with Restricted Diffusion in Children – A case series
M. Kamate, M. Detroja, V. Hattiholi
2021Neurology India12 citations
Semantic Scholar
The impact of DocosaHexaenoic Acid supplementation during pregnancy and lactation on Neurodevelopment of the offspring in India (DHANI): trial protocol
S. Khandelwal, M. K. Swamy, K. Patil, D. Kondal +14 more
2018BMC Pediatrics12 citations Open access
Semantic Scholar
Safety of lacosamide in children with refractory partial epilepsy
Ismail Pasha, M. Kamate, D. Suresh
2015Saudi Pharmaceutical Journal11 citations Open access
Semantic Scholar
Familial hypomagnesemia with secondary hypocalcemia mimicking neurodegenerative disorder
M. Kamate, Neha Singh, S. Patil
2015Indian Pediatrics11 citations
Semantic Scholar
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1
P. Tamhankar, L. Vasudevan, P. Kondurkar, Sarfaraj Niazi +14 more
2020Journal of Pediatric Genetics10 citations Open access
Semantic Scholar
Clinico-Investigative Profile of Hereditary Spastic Paraplegia in Children
M. Kamate, M. Detroja
2019Annals of Indian Academy of Neurology10 citations Open access
Semantic Scholar
Single Lysis‐Salting Out Method of Genomic DNA Extraction From Dried Blood Spots
Muntaj Shaik, Devaraju Kuramkote Shivanna, M. Kamate, Vedamurthy Ab +1 more
2016Journal of clinical laboratory analysis (Print)10 citations Open access
Semantic Scholar
Disorders of Tetrahydrobiopterin Metabolism: Experience from South India
S. Ray, H. Padmanabha, V. Gowda, R. Mahale +11 more
2021Metabolic brain disease9 citations Open access
Semantic Scholar
Early-onset phenotype of bi-allelic GRN mutations.
C. Neuray, Tipu Sultan, J. R. Alvi, M. França +15 more
2020Brain : a journal of neurology9 citations Open access
Semantic Scholar
Prevalence of Hypocalcemia in Seizures in Infancy
M. Kamate, K. Sharma, V. Patil
2018Indian Journal of Pediatrics9 citations
Semantic Scholar
Antenatal presentation and supratentorial brain abnormalities in a child with Poretti-Boltshauser syndrome.
M. Kamate, N. Goudar, V. Hattiholi
2021Brain & development (Tokyo. 1979)8 citations
Semantic Scholar
CAD Deficiency-Another Treatable Early Infantile Epileptic Encephalopathy.
M. Kamate, S. Patil
2020Pediatric Neurology7 citations
Semantic Scholar
Is Expanded Newborn Screening Adequate to Detect Indian Biochemical Low Excretor Phenotype Patients of Glutaric Aciduria Type I?
Muntaj Shaik, Kruthika-Vinod T. P., M. Kamate, Vedamurthy A. B.
2019Indian Journal of Pediatrics7 citations
Semantic Scholar
Effect of kangaroo mother care on neurodevelopmental outcome of low birth weight babies: a one-year randomized control trial
Prathiba N. Doddabasappa, N. Mahantshetti, M. Kamate, E. Adarsh
20187 citations Open access
Semantic Scholar
Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India
Harsh Sheth, Aadhira Nair, Riddhi Bhavsar, M. Kamate +38 more
2024Human Genomics6 citations Open access
Semantic Scholar
Genetic Screening of Selected Disease-Causing Mutations in Glutaryl-CoA Dehydrogenase Gene among Indian Patients with Glutaric Aciduria Type I
Kruthika-Vinod Tp, S. Muntaj, K. Devaraju, M. Kamate +1 more
2017Journal of Pediatric Genetics6 citations Open access
Semantic Scholar
The Genomic Landscape of Wilson Disease in a Pan India Disease Cohort and Population‐Scale Data
Mukesh Kumar, Srishti Sharma, Sanjay Pandey, Geetha Mammayil +36 more
2024Movement Disorders Clinical Practice5 citations Open access
Semantic Scholar
Venom-Induced Reversible Leukoencephalopathy: A Novel Cause of Toxic Acute Leukoencephalopathy With Restricted Diffusion.
M. Kamate, Thanuja Basavanagowda, V. Hattiholi
2023Pediatric Neurology5 citations
Semantic Scholar
Which is the Most Common Physiologic Type of Cerebral Palsy?
M. Kamate, M. Detroja
2022Neurology India5 citations Open access
Semantic Scholar
Identification of novel variants in a large cohort of children with Tay–Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India
M. Mistri, S. Mehta, Dhaval I Solanki, M. Kamate +8 more
2019Journal of Human Genetics5 citations
Semantic Scholar
Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India
J. Sheth, M. Mistri, Lakshmi Mahadevan, S. Mehta +3 more
2018BMC Medical Genetics5 citations Open access
Semantic Scholar
Effect of Risperidone on the Motor and Functional Disability in Children With Choreoathetoid Cerebral Palsy.
M. Kamate, Nishant Mittal, Deepa C. Metgud
2018Pediatric Neurology5 citations
Semantic Scholar
Neonatal Rotaviral Encephalitis
M. Kamate, S. Naik, Shankar Torse, V. Hattiholi
2017Indian Journal of Pediatrics5 citations
Semantic Scholar
Spongy White Matter: A Novel Neuroimaging Finding in Canavan Disease.
M. Kamate, Vinayak Kabate, Mukul Malhotra
2016Pediatric Neurology5 citations
Semantic Scholar
Perinatal Infections: An Important Etiological Risk Factor for Mineralizing Angiopathy
M. Kamate, N. A. Reddy, M. Detroja
2020Indian Journal of Pediatrics4 citations
Semantic Scholar
Isolated and Asymmetric Basal Ganglia Involvement in Early Subacute Sclerosing Panencephalitis
M. Kamate, M. Detroja
2019Annals of Indian Academy of Neurology4 citations Open access
Semantic Scholar
Subacute Sclerosing Panencephalitis: A Disease Not to be Forgotten.
M. Kamate, M. Detroja
2018Indian Pediatrics4 citations
Semantic Scholar
Attention-deficit hyperactivity disorder in children with idiopathic epilepsy: A cross-sectional study
J. Philip, N. Patil, M. Kamate
20164 citations Open access
Semantic Scholar
Macroamylasemia: A benign cause for high serum amylase
J. Agarwal, G. Deepika, A. Razak, N. Nagesh +10 more
2015Indian Pediatrics4 citations
Semantic Scholar
Neurological Manifestations of Mumps
M. Kamate, Gayatri R. Pawar
2025Indian Pediatrics3 citations
Semantic Scholar
Role of Antiplatelet Therapy in Pediatric Stroke with Mineralizing Angiopathy
M. Kamate, N. Goudar, M. Detroja
2021Indian Journal of Pediatrics3 citations Open access
Semantic Scholar
Mitochondrial DNA Depletion Syndrome: Mimicker for Hereditary Tyrosinemia
M. Kamate, Saurabh Singh
2020Indian Journal of Pediatrics3 citations Open access
Semantic Scholar

Frequent co-authors

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M. Detroja×10
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F. Sheth×8
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V. Hattiholi×7
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Chaitanya A. Datar×4

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Riddhi Bhavsar — researcher profile on SciRah

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