| Emerging behavioral and neuroimaging biomarkers for early and accurate characterization of autism spectrum disorders: a systematic review CS Hiremath, KJV Sagar, BK Yamini, AS Girimaji, R Kumar, SL Sravanti, ... Translational Psychiatry 11 (1), 42, 2021 | 95 | 2021 |
| Systemic inflammatory syndrome in COVID-19–SISCoV study: systematic review and meta-analysis D Dhar, T Dey, MM Samim, H Padmanabha, A Chatterjee, P Naznin, ... Pediatric Research 91 (6), 1334-1349, 2022 | 57 | 2022 |
| Home-based sensory interventions in children with autism spectrum disorder: a randomized controlled trial H Padmanabha, P Singhi, JK Sahu, P Malhi The Indian Journal of Pediatrics 86 (1), 18-25, 2019 | 40 | 2019 |
| Clinical profile and treatment outcomes of hypermanganesemia with dystonia 1 and 2 among 27 Indian children D Garg, S Yoganathan, U Shamim, K Mankad, P Gulati, V Bonifati, A Botre, ... Movement Disorders Clinical Practice 9 (7), 886-899, 2022 | 25 | 2022 |
| Comprehensive immunoprofiling of neurodevelopmental disorders suggests three distinct classes based on increased neurogenesis, Th-1 polarization or IL-1 signaling N Sreenivas, M Maes, H Padmanabha, A Dharmendra, P Chakkera, ... Brain, Behavior, and Immunity 115, 505-516, 2024 | 20 | 2024 |
| COLQ-related congenital myasthenic syndrome and response to salbutamol therapy H Padmanabha, AG Saini, N Sankhyan, P Singhi Journal of Clinical Neuromuscular Disease 18 (3), 162-163, 2017 | 19 | 2017 |
| N-methyl-D-aspartate encephalitis our experience with diagnostic dilemmas, clinical features, and outcome SR Chandra, H Padmanabha, N Koti, KK Vyasaraj, P Mailankody, AR Pai Journal of Pediatric Neurosciences 13 (4), 423-428, 2018 | 17 | 2018 |
| Subacute sclerosing panencephalitis presenting as acute cerebellar ataxia and brain stem hyperintensities AG Saini, N Sankhyan, H Padmanabh, JK Sahu, S Vyas, P Singhi European Journal of Paediatric Neurology 20 (3), 435-438, 2016 | 17 | 2016 |
| A rare case of ataxia-telangiectasia-like disorder with MRE11 mutation RR Mahale, N Reddy, P Mathuranth, P Mailankody, H Padmanabha, ... Journal of pediatric neurosciences 15 (3), 283-285, 2020 | 16 | 2020 |
| Hereditary Sensory Polyneuropathy, Pain Insensitivity and Global Developmental Delay due to Novel Mutation in PRDM12 Gene AG Saini, H Padmanabh, JK Sahu, I Kurth, M Voigt, P Singhi The Indian Journal of Pediatrics 84 (4), 332-333, 2017 | 16 | 2017 |
| Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort K Polavarapu, B Sunitha, A Töpf, V Preethish-Kumar, R Thompson, ... Brain 147 (1), 281-296, 2024 | 15 | 2024 |
| Altered cerebellar lobular volumes correlate with clinical deficits in siblings and children with ASD: evidence from toddlers M Kumar, C Hiremath, SK Khokhar, E Bansal, KJV Sagar, H Padmanabha, ... Journal of Translational Medicine 21 (1), 246, 2023 | 14 | 2023 |
| Association of Child Neurology (AOCN) consensus statement on the diagnosis and management of febrile seizures JS Kaushik, V Sondhi, S Yoganathan, R Dubey, S Sharma, KP Vinayan, ... Indian Pediatrics 59 (4), 300-306, 2022 | 14 | 2022 |
| Syndrome of X linked intellectual disability, epilepsy, progressive brain atrophy and large head associated with SLC9A6 mutation H Padmanabha, AG Saini, JK Sahu, P Singhi Case Reports 2017, bcr-2017-222050, 2017 | 14 | 2017 |
| SEPN1-related Rigid Spine Muscular Dystrophy AG Saini, H Padmanabha, S Kumar, N Sankhyan, P Singhi The Indian Journal of Pediatrics 85 (11), 1033-1034, 2018 | 13 | 2018 |
| Recurrent facial palsy and electrophysiological findings in oligosymptomatic Melkersson Rosenthal syndrome AG Saini, N Sankhyan, H Padmanabh, A Das, P Singhi The Indian Journal of Pediatrics 83 (10), 1188-1190, 2016 | 13 | 2016 |
| Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C M Bardhan, RM Anjanappa, K Polavarapu, V Preethish-Kumar, S Vengalil, ... neurogenetics 23 (3), 187-202, 2022 | 12 | 2022 |
| Pediatric neurobrucellosis: a systematic review with case report D Dhar, RS Jaipuriar, MS Mondal, SP Shunmugakani, S Nagarathna, ... Journal of Tropical Pediatrics 69 (1), fmad004, 2023 | 11 | 2023 |
| Genotype–phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India S Nashi, K Polavarapu, M Bardhan, RM Anjanappa, V Preethish-Kumar, ... neurogenetics 24 (1), 43-53, 2023 | 10 | 2023 |
| Hereditary sensory and autonomic neuropathy: A case series of six children R Suthar, IK Sharawat, K Eggermann, H Padmanabha, AG Saini, B Bharti, ... Neurology India 70 (1), 231-237, 2022 | 10 | 2022 |
