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H. Padmanabha · SciRah

Researcher profile · Semantic Scholar

H. Padmanabha

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H. Padmanabha — researcher profile on SciRah

h-index: 9
Works: 127
Citations: 477

Most-cited papers

Emerging behavioral and neuroimaging biomarkers for early and accurate characterization of autism spectrum disorders: a systematic review
Chandrakanta S. Hiremath, K. Sagar, B. Yamini, Akhila S. Girimaji +10 more
2021Translational Psychiatry68 citations Open access
Semantic Scholar
Systemic inflammatory syndrome in COVID-19–SISCoV study: systematic review and meta-analysis
D. Dhar, T. Dey, M. Samim, H. Padmanabha +9 more
2021Pediatric Research33 citations Open access
Semantic Scholar
Comprehensive immunoprofiling of neurodevelopmental disorders suggests three distinct classes based on increased neurogenesis, Th-1 polarization or IL-1 signaling.
N. Sreenivas, Michael Maes, H. Padmanabha, Apoorva Dharmendra +8 more
2023Brain, behavior, and immunity22 citations Open access
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
DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: A novel phenotype.
S. Ray, H. Padmanabha, R. Mahale, P. Mailankody +1 more
2021Parkinsonism & Related Disorders14 citations
Semantic Scholar
Altered cerebellar lobular volumes correlate with clinical deficits in siblings and children with ASD: evidence from toddlers
Manoj Kumar, Chandrakanta S. Hiremath, S. Khokhar, Eshita Bansal +9 more
2023Journal of Translational Medicine9 citations Open access
Semantic Scholar
Hereditary Sensory and Autonomic Neuropathy: A Case Series of Six Children
Renu Suthar, I. Sharawat, K. Eggermann, H. Padmanabha +5 more
2022Neurology India9 citations
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 levodopa responsive parkinsonism in PPP2R5D mutation.
R. Mahale, G. Arunachal, Deepak Chadha, H. Padmanabha +2 more
2024Parkinsonism & Related Disorders8 citations
Semantic Scholar
Parental KAP and its Relation with the Quality of Life in Children with Epilepsy
Sanitha Sadanandan, A. U. Shreedevi, H. Padmanabha
2023Annals of Indian Academy of Neurology8 citations Open access
Semantic Scholar
Pediatric neurobrucellosis: a systematic review with case report.
D. Dhar, Ravi Shekhar Jaipuriar, M. Mondal, Siva Prakash Shunmugakani +6 more
2022Journal of Tropical Pediatrics8 citations
Semantic Scholar
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation
R. Mahale, G. Arunachal, Jyothi Gautam, D. Dutta +4 more
2021Annals of Indian Academy of Neurology8 citations Open access
Semantic Scholar
Episodic ataxia in child with 16p11.2 deletion including PRRT2.
H. Padmanabha, K. Raghavendra, G. Arunachal, A. Nagaraj +5 more
2023Parkinsonism & Related Disorders7 citations Open access
Semantic Scholar
Genotype–phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India
S. Nashi, K. Polavarapu, M. Bardhan, R. Anjanappa +20 more
2022Neurogenetics7 citations
Semantic Scholar
COASY Protein-Associated Neurodegeneration: Report from India
R. Mahale, Raviprakash Singh, Pavankumar Katragadda, H. Padmanabha
2023Annals of Indian Academy of Neurology6 citations Open access
Semantic Scholar
DYT30 due to VPS16 Mutation: An Etiology of Childhood-Onset Generalized Dystonia
Sridhar Shashi, S. Nashi, G. Arunachal, N. Venkatachalam +7 more
2023Annals of Indian Academy of Neurology6 citations Open access
Semantic Scholar
MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO)
Dipti Baskar, S. Vengalil, S. Nashi, M. Bardhan +8 more
2023Journal of Neuromuscular Diseases6 citations Open access
Semantic Scholar
Clinico-investigational profile, relapse predictors and outcomes of pediatric patients with anti-myelin oligodendrocyte associated disorders: An experience from tertiary centre.
D. Dhar, Subhajit Roy, R. Kenchaiah, M. Mondal +11 more
2025Multiple Sclerosis and Related Disorders5 citations
Semantic Scholar
Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvement.
S. Sridhar, S. Nashi, K. Kulanthaivelu, S. Vengalil +18 more
2024Neuromuscular Disorders5 citations
Semantic Scholar
Genetic spectrum of neuronal ceroid lipofuscinosis & its genotype-phenotype correlation -A single centre experience of 56 cases.
Sangeeth Thuppanattumadam Ananthasubramanian, H. Padmanabha, C. Ravindranadh, Raghavendra Kenchiah +16 more
2024Journal of Neurological Sciences5 citations
Semantic Scholar
Cerebral Sparganosis – An Unusual Parasitic Infection Mimicking Cerebral Tuberculosis: Isolation of a Live Plerocercoid Larva of Spirometra mansoni
Abhishek Rathore, H. Padmanabha, R. Mahale, Ankit Arora +11 more
2024Annals of Indian Academy of Neurology5 citations Open access
Semantic Scholar
Neuro-Bechet’s disease: a case series from India
R. Mahale, S. Kamath, C. M. Ravindranadh, H. Padmanabha +2 more
2022The Egyptian Journal of Neurology Psychiatry and Neurosurgery5 citations Open access
Semantic Scholar
CSF1R-related disorder: A clinical, imaging and genetic profile review
R. Mahale, H. Padmanabha, P. Mailankody
2025Neurological Sciences4 citations
Semantic Scholar
Targeted metabolomics in children with autism spectrum disorder with and without developmental regression
Chakkera Priyanka, R. Christopher, M. Nagappa, J. Kommu +9 more
2025Metabolic brain disease4 citations
Semantic Scholar
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from India
T. Chawla, S. Nashi, Dipti Baskar, K. Polavarapu +13 more
2024Neurogenetics4 citations
Semantic Scholar
Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India
G. Harikrishna, H. Padmanabha, K. Polavarapu, R. Anjanappa +12 more
2024Journal of Neuromuscular Diseases4 citations Open access
Semantic Scholar
Clinical, imaging and genetic profile of twenty-four patients with pantothenate kinase-associated neurodegeneration (PKAN)- A single centre study from India.
N. Sriram, V. Holla, R. Kumari, N. Kamble +10 more
2023Parkinsonism & Related Disorders4 citations
Semantic Scholar
Longitudinally Extensive Transverse Myelitis with Optic Neuritis Related to Profound Biotinidase Deficiency: NMOSD Mimic!
N. A. Ravikumar, D. Dhar, R. Mahale, A. Reddy +7 more
2023Annals of Indian Academy of Neurology4 citations Open access
Semantic Scholar
Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy
R. Mahale, Ravi Tiwari, G. Arunachal, H. Padmanabha +1 more
2021Acta Neurologica Belgica4 citations
Semantic Scholar
Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene
R. Mahale, J. Gautham, P. Mailankody, H. Padmanabha +1 more
2021Acta Neurologica Belgica4 citations
Semantic Scholar
A Novel Mutation in KMT2B Gene Causing Childhood-onset Generalized Dystonia with Expanded Phenotype from India
H. Padmanabha, A. Awati, K. Thomas, Gosala R. K. Sarma
2021Neurology India4 citations Open access
Semantic Scholar
Cerebral abscesses due to Pseudallescheria boydii mycoses: a diagnostic and therapeutic conundrum
H. Padmanabha, N. Chandrashekar, Dhaval P. Shukla, M. Pooja +1 more
2024Acta Neurologica Belgica3 citations
Semantic Scholar
ANCA-associated Vasculitic Neuropathy Following Anti-SARS-CoV-2 Vaccination: An Epiphenomenon or Causal Association?
Shreyashi Jha, A. Hema, H. Padmanabha, A. Mahadevan +3 more
2023Annals of Indian Academy of Neurology3 citations Open access
Semantic Scholar
Childhood-Onset Generalized Dystonia Due to NDUFA9 Gene Mutation: An Expansion of Mutations Causing Leigh’s Syndrome
Raviprakash Singh, H. Padmanabha, Gautam Arunachal, P. Mailankody +1 more
2023Annals of Indian Academy of Neurology3 citations Open access
Semantic Scholar
Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence
R. Mahale, Arun Gokul Pon, M. Sandeep, H. Padmanabha +2 more
2022Annals of Indian Academy of Neurology3 citations Open access
Semantic Scholar
Clinical, Biochemical, Radiological, and Genetic Profile of Patients with Homocysteine Remethylation Pathway Defect and Spastic Paraplegia
H. Padmanabha, R. Mahale, Rita Christopher, G. Arunachal +10 more
2021Annals of Indian Academy of Neurology3 citations Open access
Semantic Scholar
CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!
N. Sriram, H. Padmanabha, S. Chandra, R. Mahale +7 more
2021Annals of Indian Academy of Neurology3 citations Open access
Semantic Scholar
Clinical spectrum of pediatric drug refractory epilepsy secondary to parieto-occipital gliosis.
S. Ray, R. Kenchaiah, A. Asranna, H. Padmanabha +6 more
2021Epilepsy Research3 citations
Semantic Scholar
ADCY5-Related Dyskinesia: A Genetic Cause of Early-Onset Chorea-Report of Two Cases and a Novel Mutation
H. Padmanabha, S. Ray, R. Mahale, G. Arunachal +3 more
2021Annals of Indian Academy of Neurology3 citations Open access
Semantic Scholar
Adult-Onset PLA2G6-Associated Neurodegeneration (PLAN): A Clinical, Imaging and Genetic Profile Review
R. Mahale, H. Padmanabha, P. Mailankody
2025Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques2 citations
Semantic Scholar
Retinitis pigmentosa in DJ1- associated early-onset Parkinson's disease: A phenotypic expansion.
R. Mahale, Deepak Chadha, H. Padmanabha, S. Nashi
2024Parkinsonism & Related Disorders2 citations
Semantic Scholar
Rare Encephalitis-Like Presentation of a Pediatric Patient with Dual Positive Aquaporin-4 and Myelin Oligodendrocyte Antibodies: A Case Report with Review of Literature
D. Dhar, Anita Mahadevan, A. Nagaraj, R. Mahale +5 more
2023Annals of Indian Academy of Neurology2 citations Open access
Semantic Scholar
Hereditary Spastic Paraplegia due to LYST Gene Mutation: A Novel Causative Gene
R. Mahale, Gautam Arunachal, Raviprakash Singh, H. Padmanabha +1 more
2023Annals of Indian Academy of Neurology2 citations Open access
Semantic Scholar
Collagen XII-Related Myopathy: An Emerging Spectrum of Extracellular Matrix-Related Myopathy
H. Padmanabha, G. Arunachal, Pratik Kishore, P. Sharma +5 more
2023Neurology India2 citations Open access
Semantic Scholar
Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype
R. Mahale, H. Padmanabha, P. Mailankody, Mathuranath S. Pavagada
2023Acta Neurologica Belgica2 citations
Semantic Scholar
Vascular Parkinsonism with Dystonia in Moyamoya Disease: An Expansion of Movement Disorder Phenomenology
R. Mahale, Rohin Dubbal, H. Padmanabha, P. Mailankody
2022Annals of Indian Academy of Neurology2 citations Open access
Semantic Scholar
Kennedy's Disease: A Second Genetically Confirmed Report from India
Rutul Shah, R. Mahale, H. Padmanabha, P. Mailankody
2021Annals of Indian Academy of Neurology2 citations Open access
Semantic Scholar
Pseudo-neonatal Adrenoleukodystrophy: A Rare Peroxisomal Disorder
Cheshta Arora, H. Padmanabha, Rita Christopher, R. Mahale +5 more
2021Annals of Indian Academy of Neurology2 citations Open access
Semantic Scholar
Upbeat Nystagmus in Late Onset Cerebellar Ataxia: Think of Anti-Glutamate Decarboxylase 65 Antibody-Associated Cerebellar Ataxia
R. Mahale, D. Dutta, J. Kovoor, P. Mailankody +2 more
2021Annals of Indian Academy of Neurology2 citations Open access
Semantic Scholar
KCTD7-related progressive myoclonic epilepsy: Clinical and genetic characterization of six Indian patients and review of literature.
T. A. Sangeeth, L. Viswanathan, H. Padmanabha, Akshaya Janardhanan +6 more
2026Seizure1 citations
Semantic Scholar

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