| Association of birth during the COVID-19 pandemic with neurodevelopmental status at 6 months in infants with and without in utero exposure to maternal SARS-CoV-2 infection LC Shuffrey, MR Firestein, MH Kyle, A Fields, C Alcántara, D Amso, ... JAMA pediatrics 176 (6), e215563-e215563, 2022 | 211 | 2022 |
| Neurologic manifestations in an infant with COVID-19 R Dugue, KC Cay-Martínez, KT Thakur, JA Garcia, LV Chauhan, ... Neurology 94 (24), 1100-1102, 2020 | 163 | 2020 |
| Vascular endothelial growth factors A and C are induced in the SVZ following neonatal hypoxia–ischemia and exert different effects on neonatal glial progenitors JM Bain, L Moore, Z Ren, S Simonishvili, SW Levison Translational stroke research 4 (2), 158-170, 2013 | 83 | 2013 |
| Variants in HNRNPH2 on the X chromosome are associated with a neurodevelopmental disorder in females JM Bain, MT Cho, A Telegrafi, A Wilson, S Brooks, C Botti, G Gowans, ... The American Journal of Human Genetics 99 (3), 728-734, 2016 | 69 | 2016 |
| TGFß1 stimulates the over-production of white matter astrocytes from precursors of the “brain marrow” in a rodent model of neonatal encephalopathy JM Bain, A Ziegler, Z Yang, SW Levison, E Sen PLoS One 5 (3), e9567, 2010 | 65 | 2010 |
| Encephalopathy and bilateral thalamic lesions in a child with MIS-C associated with COVID-19 D Abel, MY Shen, Z Abid, C Hennigan, A Boneparth, EH Miller, ... Neurology 95 (16), 745-748, 2020 | 61 | 2020 |
| Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (MELAS): a case report and critical reappraisal of treatment options RH Fryer, JM Bain, C Darryl Pediatric neurology 56, 59-61, 2016 | 56 | 2016 |
| Phenotype of GABA-transaminase deficiency MK Koenig, R Hodgeman, JJ Riviello, W Chung, J Bain, CA Chiriboga, ... Neurology 88 (20), 1919-1924, 2017 | 55 | 2017 |
| How has DSM-5 affected autism diagnosis? A 5-year follow-up systematic literature review and meta-analysis KM Kulage, J Goldberg, J Usseglio, D Romero, JM Bain, AM Smaldone Journal of autism and developmental disorders 50, 2102-2127, 2020 | 44 | 2020 |
| Prevalence of seizures in pediatric extracorporeal membrane oxygenation patients as measured by continuous electroencephalography S Okochi, A Shakoor, S Barton, AR Zenilman, C Street, S Streltsova, ... Pediatric Critical Care Medicine 19 (12), 1162-1167, 2018 | 41 | 2018 |
| Assessing autonomic dysfunction symptoms in children: a pilot study X Ming, JM Bain, D Smith, M Brimacombe, G Gold von-Simson, ... Journal of Child Neurology 26 (4), 420-427, 2011 | 39 | 2011 |
| Genetic testing in individuals with cerebral palsy HJ May, JA Fasheun, JM Bain, EH Baugh, LE Bier, A Revah‐Politi, ... Developmental Medicine & Child Neurology 63 (12), 1448-1455, 2021 | 30 | 2021 |
| Inpatient neurology consultations during the onset of the SARS-CoV-2 New York City pandemic: a single center case series S Radmard, SE Epstein, HJ Roeder, AJ Michalak, SD Shapiro, A Boehme, ... Frontiers in neurology 11, 805, 2020 | 25 | 2020 |
| Assessment of neurodevelopment in infants with and without exposure to asymptomatic or mild maternal SARS-CoV-2 infection during pregnancy MR Firestein, LC Shuffrey, Y Hu, M Kyle, M Hussain, C Bianco, V Hott, ... JAMA Network Open 6 (4), e237396-e237396, 2023 | 23 | 2023 |
| Cerebrospinal analysis in patients with COVID-19 EH Miller, VS Namale, C Kim, R Dugue, G Waldrop, P Ciryam, AM Chong, ... Open forum infectious diseases 7 (11), ofaa501, 2020 | 23 | 2020 |
| PDGF-responsive progenitors persist in the subventricular zone across the lifespan L Moore, JM Bain, JM Loh, SW Levison ASN neuro 6 (2), AN20120041, 2013 | 23 | 2013 |
| Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder JM Bain, O Thornburg, C Pan, D Rome-Martin, L Boyle, X Fan, ... Neurology: Genetics 7 (1), e551, 2021 | 20 | 2021 |
| Call-Fleming syndrome: headache in a 16-year-old girl J Bain, D Segal, R Amin, D Monoky, SJ Thompson Pediatric Neurology 49 (2), 130-133. e1, 2013 | 20 | 2013 |
| Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition EE Palmer, M Pusch, A Picollo, C Forwood, MH Nguyen, V Suckow, ... Molecular psychiatry 28 (2), 668-697, 2023 | 17 | 2023 |
| CERT1 mutations perturb human development by disrupting sphingolipid homeostasis C Gehin, MA Lone, W Lee, L Capolupo, S Ho, AM Adeyemi, EH Gerkes, ... The Journal of clinical investigation 133 (10), 2023 | 16 | 2023 |
