| Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy JR Lemke, K Geider, KL Helbig, HO Heyne, H Schütz, J Hentschel, ... Neurology 86 (23), 2171-2178, 2016 | 188 | 2016 |
| A diffusion tensor imaging study of the cerebellar pathways in children with autism spectrum disorder L Sivaswamy, A Kumar, D Rajan, M Behen, O Muzik, D Chugani, ... Journal of child neurology 25 (10), 1223-1231, 2010 | 114 | 2010 |
| Autism and developmental disability caused by KCNQ3 gain‐of‐function variants TT Sands, F Miceli, G Lesca, AE Beck, LG Sadleir, DK Arrington, ... Annals of neurology 86 (2), 181-192, 2019 | 91 | 2019 |
| Adults with cerebral palsy require ongoing neurologic care: a systematic review SE Smith, M Gannotti, EA Hurvitz, FE Jensen, LE Krach, MC Kruer, ... Annals of neurology 89 (5), 860-871, 2021 | 43 | 2021 |
| Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder S Kour, DS Rajan, TR Fortuna, EN Anderson, C Ward, Y Lee, S Lee, ... Nature communications 12 (1), 2558, 2021 | 29 | 2021 |
| A case of de novo NAA10 mutation presenting with eyelid myoclonias (AKA Jeavons syndrome) V Valentine, Y Sogawa, D Rajan, D Ortiz Seizure 60, 120-122, 2018 | 14 | 2018 |
| Allen's Test C Puttarajappa, DS Rajan New England Journal of Medicine 363 (14), e20, 2010 | 14 | 2010 |
| Survival of a male patient harboring CASK Arg27Ter mutation to adolescence K Mukherjee, PA Patel, DS Rajan, LEW LaConte, S Srivastava Molecular Genetics & Genomic Medicine 8 (10), e1426, 2020 | 12 | 2020 |
| Autosomal recessive cerebellar atrophy and spastic ataxia in patients with pathogenic biallelic variants in GEMIN5 DS Rajan, S Kour, TR Fortuna, MA Cousin, SS Barnett, Z Niu, ... Frontiers in Cell and Developmental Biology 10, 783762, 2022 | 11 | 2022 |
| Optimization of friction stir welding process parameters using MCDM method B Singaravel, B Chakradhar, DS Rajan, AK Kumar Materials Today: Proceedings 76, 597-601, 2023 | 9 | 2023 |
| Functional and structural deficiencies of Gemin5 variants associated with neurological disorders R Francisco-Velilla, A Embarc-Buh, F del Caño-Ochoa, S Abellan, M Vilar, ... Life Science Alliance 5 (7), 2022 | 9 | 2022 |
| Imaging review of common and rare causes of stroke in children G Zuccoli, C Fitz, S Greene, SA Lindner, R Nardone, AS Khan, D Rajan, ... Topics in Magnetic Resonance Imaging 27 (6), 463-477, 2018 | 7 | 2018 |
| Nonaneurysmal subarachnoid hemorrhage in sickle cell disease: description of a case and a review of the literature G Zuccoli, R Nardone, D Rajan, AS Khan, DD Cummings The Neurologist 23 (4), 122-127, 2018 | 7 | 2018 |
| Olfactory bulb and olfactory tract abnormalities in acrocallosal syndrome and Greig cephalopolysyndactyly syndrome S Subramanian, D Soundara Rajan, J Gaesser, C Wen-Ya Lo, ... Pediatric radiology 49, 1368-1373, 2019 | 6 | 2019 |
| Longterm outcomes of patients receiving umbilical blood stem cell transplantation for MPS II M Escolar, M Poe, D Rajan, P Szabolcs Molecular Genetics and Metabolism 2 (108), S37-S38, 2013 | 6 | 2013 |
| Evolving therapies in neuronopathic LSDs: opportunities and challenges DS Rajan, ML Escolar Metabolic Brain Disease 37 (7), 2245-2256, 2022 | 5 | 2022 |
| SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration TR Fortuna, S Kour, AV Chimata, A Muiños-Bühl, EN Anderson, ... Acta Neuropathologica 146 (3), 477-498, 2023 | 3 | 2023 |
| Corpus callosum lipoma DS Rajan, A Popescu Neurology 78 (17), 1366-1366, 2012 | 3 | 2012 |
| Interim results of Transpher A, a multicenter, single-dose clinical trial of UX111 gene therapy for Sanfilippo syndrome type A (mucopolysaccharidosis IIIA) KM Flanigan, N Smith, ML Couce, D Rajan, K Truxal, KL McBride, ... Molecular Genetics and Metabolism 138 (2), 107101, 2023 | 2 | 2023 |
| A neurenteric cyst presenting as a brainstem tumor: imaging and clinical findings JD Ly, S Subramanian, S Greene, D Rajan, J Kofler, G Zuccoli Journal of Pediatric Neurology 16 (06), 404-407, 2018 | 2 | 2018 |
