| # | Title | Journal | Year | Citations |
|---|
| 1 | Sensory and motor deficits in children with cerebral palsy born preterm correlate with diffusion tensor imaging abnormalities in thalamocortical pathways | Developmental Medicine and Child Neurology | 2009 | 276 |
| 2 | Cerebrospinal Fluid and Serum Markers of Inflammation in Autism | Pediatric Neurology | 2005 | 268 |
| 3 | Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics | 2012 | 234 |
| 4 | Clinical disorders of brain plasticity | Brain and Development | 2004 | 222 |
| 5 | Reduced cardiac parasympathetic activity in children with autism | Brain and Development | 2005 | 194 |
| 6 | Maternal antibrain antibodies in autism | Brain, Behavior, and Immunity | 2007 | 175 |
| 7 | Altered Connectivity and Action Model Formation in Autism Is Autism | Neuroscientist | 2011 | 132 |
| 8 | Behaviors Associated With Fever in Children With Autism Spectrum Disorders | Pediatrics | 2007 | 130 |
| 9 | Down syndrome and comorbid autism-spectrum disorder: Characterization using the aberrant behavior checklist | American Journal of Medical Genetics, Part A | 2005 | 127 |
| 10 | Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome | Neurologist | 2011 | 113 |
| 11 | Whittling Down the Wait Time | Pediatric Clinics of North America | 2016 | 111 |
| 12 | Fetal Mechanisms in Neurodevelopmental Disorders | Pediatric Neurology | 2008 | 104 |
| 13 | Management of children with holoprosencephaly | American Journal of Medical Genetics, Part C: Seminars in Medical Genetics | 2010 | 82 |
| 14 | β 2-Adrenergic Receptor Activation and Genetic Polymorphisms in Autism: Data from Dizygotic Twins | Journal of Child Neurology | 2005 | 78 |
| 15 | Survey of Aspirin Use in Sturge-Weber Syndrome | Journal of Child Neurology | 2011 | 70 |
| 16 | Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life | Clinical Genetics | 2015 | 59 |
| 17 | Central Hypothyroidism and Sturge-Weber Syndrome | Pediatric Neurology | 2008 | 49 |
| 18 | Conceptual, Regulatory and Strategic Imperatives in the Early Days of EEG-Based Biomarker Validation for Neurodevelopmental Disabilities | Frontiers in Integrative Neuroscience | 2019 | 48 |
| 19 | Brain plasticity in paediatric neurology | European Journal of Paediatric Neurology | 2003 | 46 |
| 20 | Plasma Serotonin in Autism | Pediatric Neurology | 2006 | 43 |
| 21 | Associations Between Psychiatric Comorbidities and Sleep Disturbances in Children With Attention-Deficit/Hyperactivity Disorder | Journal of Developmental and Behavioral Pediatrics | 2012 | 43 |
| 22 | β2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort | Molecular Psychiatry | 2007 | 41 |
| 23 | Variation in season of birth in singleton and multiple births concordant for autism spectrum disorders | Paediatric and Perinatal Epidemiology | 2008 | 41 |
| 24 | Use of quantitative EEG in infants with port-wine birthmark to assess for Sturge–Weber brain involvement | Clinical Neurophysiology | 2009 | 39 |
| 25 | COVID-19 Pandemic Health Disparities and Pediatric Health Care—The Promise of Telehealth | JAMA Pediatrics | 2021 | 38 |
| 26 | Epilepsy and Autism Severity: A Study of 6,975 Children | Autism Research | 2019 | 37 |
| 27 | Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy | European Journal of Human Genetics | 2016 | 36 |
| 28 | Sleep disturbance and neuropsychological function in young children with ADHD | Child Neuropsychology | 2016 | 35 |
| 29 | Comparative Outcomes in Children and Adults With Anti-N-Methyl-D-Aspartate (anti-NMDA) Receptor Encephalitis | Journal of Child Neurology | 2017 | 33 |
| 30 | Comparative quantitative clinical, neuroimaging, and functional profiles in children with acute flaccid myelitis at acute and convalescent stages of disease | Developmental Medicine and Child Neurology | 2019 | 33 |
| 31 | Neurobiology of Rett Syndrome | Journal of Child Neurology | 2003 | 32 |
| 32 | ST3GAL5-Related Disorders: A Deficiency in Ganglioside Metabolism and a Genetic Cause of Intellectual Disability and Choreoathetosis | Journal of Child Neurology | 2018 | 28 |
| 33 | Emerging Viral Infections and Their Impact on the Global Burden of Neurological Disease | Seminars in Neurology | 2018 | 28 |
| 34 | Autism traits in children and adolescents with Cornelia de Lange syndrome | American Journal of Medical Genetics, Part A | 2014 | 27 |
| 35 | Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H‐ABC) | American Journal of Medical Genetics, Part A | 2014 | 27 |
| 36 | Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype | Nature Communications | 2021 | 26 |
| 37 | Sirolimus Treatment in Sturge-Weber Syndrome | Pediatric Neurology | 2021 | 24 |
| 38 | Different effects of high- and low-dose phenobarbital on post-stroke seizure suppression and recovery in immature CD1 mice | Epilepsy Research | 2011 | 23 |
| 39 | Deletion 12p12 Involving SOX5 in Two Children With Developmental Delay and Dysmorphic Features | Pediatric Neurology | 2013 | 23 |
| 40 | Dynamics of functional and effective connectivity within human cortical motor control networks | Clinical Neurophysiology | 2015 | 23 |
| 41 | Translational challenges in advancing regenerative therapy for treating neurological disorders using nanotechnology | Advanced Drug Delivery Reviews | 2019 | 23 |
| 42 | Dyspraxia in ASD: Impaired coordination of movement elements | Autism Research | 2017 | 22 |
| 43 | Altered task‐related modulation of long‐range connectivity in children with autism | Autism Research | 2018 | 22 |
| 44 | MRI for neonatal encephalopathy in full-term infants | Lancet, The | 2003 | 21 |
| 45 | Neurodevelopmental Disabilities: Beyond the Diagnosis | Seminars in Pediatric Neurology | 2005 | 20 |
| 46 | Hypothesis: The Role of Sterols in Autism Spectrum Disorder | Autism Research & Treatment | 2011 | 20 |
| 47 | Genetic Counseling in Neurodevelopmental Disorders | Cold Spring Harbor Perspectives in Medicine | 2020 | 20 |
| 48 | The Impact of X-Chromosome Inactivation on Phenotypic Expression of X-Linked Neurodevelopmental Disorders | Brain Sciences | 2021 | 18 |
| 49 | Maintenance of relational information in working memory leads to suppression of the sensory cortex | Journal of Neurophysiology | 2014 | 17 |
| 50 | The Spectrum of Developmental Disability with Zika Exposure: What Is Known, What Is Unknown, and Implications for Clinicians | Journal of Developmental and Behavioral Pediatrics | 2019 | 17 |
