| 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 | 58 | 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 | 54 | 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, 18-25, 2019 | 29 | 2019 |
| 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 | 18 | 2017 |
| 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 | 16 | 2016 |
| 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, 332-333, 2017 | 15 | 2017 |
| 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 | 14 | 2022 |
| SEPN1-related Rigid Spine Muscular Dystrophy AG Saini, H Padmanabha, S Kumar, N Sankhyan, P Singhi The Indian Journal of Pediatrics 85, 1033-1034, 2018 | 12 | 2018 |
| 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 | 12 | 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, 1188-1190, 2016 | 12 | 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 | 10 | 2020 |
| 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 | 10 | 2017 |
| DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: a novel phenotype S Ray, H Padmanabha, R Mahale, P Mailankody, G Arunachal Parkinsonism & Related Disorders 89, 1-3, 2021 | 8 | 2021 |
| 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 | 7 | 2022 |
| 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 | 7 | 2022 |
| Disorders of tetrahydrobiopterin metabolism: Experience from south India S Ray, H Padmanabha, VK Gowda, R Mahale, R Christopher, ... Metabolic Brain Disease 37 (3), 743-760, 2022 | 7 | 2022 |
| 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 | 7 | 2022 |
| Long-term seroprotection rates following second dose of measles as MMR vaccine at 15 months in Indian children P Hansashree, S Verma, A Rawat, N Sankhyan, B Bharti Indian Pediatrics 55, 405-407, 2018 | 7 | 2018 |
| 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 | 6 | 2023 |
| Stiffness, facial dysmorphism, and skeletal abnormalities: Schwartz-Jampel syndrome 1A H Padmanabha, R Suthar, N Sankhyan, P Singhi The Journal of Pediatrics 200, 286-286. e1, 2018 | 6 | 2018 |
