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Ranjith Kumar Manokaran

Observed names: Dr. Ranjith Kumar Manokaran, Ranjith Kumar Manokaran, Ranjith K Manokaran, Ranjith K. Manokaran, RanjithKumar Manokaran, Ranjithkumar Manokaran
Observed institutions: University of Toronto, Sri Ramachandra Institute of Higher Education and Research, Great Ormond Street Hospital, Hospital for Sick Children, Sri Ramachandra Medical Centre, Bai Jerbai Wadia Hospital for Children, Neurology, Inc, All India Institute of Medical Sciences
ORCID: 0000-0001-8774-7462
Observed ORCID: 0000-0001-8774-7462
OpenAlex ID: A5006091195
Development and validation of DSM-5 based diagnostic tool for children with Autism Spectrum Disorder
2019 · Sheffali Gulati, Jaya Shankar Kaushik, et al. · PLoS ONE · 42
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The 2022 International League Against Epilepsy Classification and Definition of Childhood Epilepsy Syndromes: An Update for Pediatricians
2024 · Ranjith Kumar Manokaran, Suvasini Sharma, et al. · Indian Pediatrics · 20
Sleep Abnormalities and Polysomnographic Profile in Children With Drug-resistant Epilepsy
2020 · Ranjith Kumar Manokaran, Manjari Tripathi, et al. · Seizure · 16
Favorable Response to “Memantine” in a Child with GRIN2B Epileptic Encephalopathy
2021 · Sathya Chidambaram, Ranjith Kumar Manokaran · Neuropediatrics · 13
KCTD7 ‐related progressive myoclonic epilepsy: Report of 42 cases and review of literature
2024 · Sangeetha Yoganathan, Robyn Whitney, et al. · Epilepsia · 12
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Clinical and molecular spectrum associated with Polymerase-γ related disorders
2022 · Ruchika Jha, Harshkumar Patel, et al. · Journal of Child Neurology · 12
Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy
2020 · Ranjith K. Manokaran, Sandeep Aggarwala, et al. · Muscle & Nerve · 10
Serum Magnesium Levels in Children With and Without Migraine: A Cross-Sectional Study
2022 · Rishab Bhurat, Sarala Premkumar, et al. · Indian Pediatrics · 8
Favorable response to classic ketogenic diet in a child with anti-GAD 65 antibody mediated super refractory status epilepticus
2022 · Deepika Sivathanu, Deepti Kewalramani, et al. · Epilepsy & Behavior Reports · 8
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Guillain–Barré Syndrome with Preserved Reflexes in a Child after COVID-19 Infection
2021 · Aparna Krishnakumar, Deepti Kewalramani, et al. · The Indian Journal of Pediatrics · 8
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Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Associated with Dengue Infection in a Child
2020 · Ranjith Kumar Manokaran, Harshavardhan Mahalingam, et al. · Journal of Tropical Pediatrics · 8
Stimulation-Induced Seizures in Children Undergoing Stereo-EEG Evaluation
2024 · Ranjith Kumar Manokaran, Ayako Ochi, et al. · Journal of Clinical Neurophysiology · 7
A case of carbonic anhydrase type VA deficiency presenting as West syndrome in an infant with a novel mutation in the CA-VA gene
2022 · Niranjani Mani Urmila, Deepti Kewalramani, et al. · Epilepsy & Behavior Reports · 6
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Gut–brain axis: role of probiotics in neurodevelopmental disorders including autism spectrum disorder
2021 · Ranjith Kumar Manokaran, Sheffali Gulati · Elsevier eBooks · 6
Phenytoin Induced Status Dystonicus: A Rare Manifestation of Phenytoin Toxicity in a Child with Autism Spectrum Disorder
2020 · D. Rajkumar, Ranjith Kumar Manokaran, et al. · The Indian Journal of Pediatrics · 5
Drug-resistant focal epilepsy in a girl with SETD5-related intellectual disability
2023 · Ranjith Kumar Manokaran, Ayako Ochi, et al. · Seizure · 4
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Primary Headache in Children Aged Between 6 and 18 Years—Causes and Associated Factors
2022 · Abdul Rahman Abul Hassan, Anita Palani, et al. · The Indian Journal of Pediatrics · 3
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An atypical presentation of Joubert syndrome due to a novel mutation in ZNF423 gene
2020 · RanjithKumar Manokaran, Deepika Sivathanu, et al. · Journal of Pediatric Neurosciences · 3
Distinct Facial Dysmorphisms in a Child with Renpenning Syndrome
2025 · Yathwin Kanagavel, Ranjith K Manokaran · Annals of Indian Academy of Neurology · 2
Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality
2024 · Ankit Sabharwal, Vishu Gupta, et al. · Mitochondrion · 2
Myoclonic Status Epilepticus in TBC1D24-Related Developmental/Epileptic Encephalopathy (DEE)
2023 · Ranjith Kumar Manokaran, Jaina Patel, et al. · Neuropediatrics · 2
Hypermanganesemia with Dystonia Type 2
2023 · B Madhubala, Harshavardhan Mahalingam, et al. · Neurology India · 2
Atypical presentation of rapid-onset dystonia–parkinsonism in a toddler with a novel mutation in the ATP1A3 gene
2021 · Aishwarya Ganesh, Samyuktha Sivakumar, et al. · BMJ Case Reports · 2
Treatable cause of refractory seizures in an infant with a novel mutation
2021 · RanjithKumar Manokaran, RuchiR Mittal, et al. · Journal of Pediatric Neurosciences · 2
Novel association of sensorineural hearing loss with childhood-onset neurodegeneration with brain atrophy (CONDBA): Expanding the phenotypic spectrum of UBTF-related disorders
2025 · M. Yathwin Kanagavel, Lokesh Saini, et al. · Clinical Neurology and Neurosurgery · 1
Works count: 75
Citation count: 208
H-index: 8
I10-index: 7
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