| # | Title | Journal | Year | Citations |
|---|
| 1 | Gaze behavior and affect at 6 months: predicting clinical outcomes and language development in typically developing infants and infants at risk for autism | Developmental Science | 2009 | 296 |
| 2 | Preliminary Findings of a Telehealth Approach to Parent Training in Autism | Journal of Autism and Developmental Disorders | 2013 | 255 |
| 3 | The operation of pattern separation and pattern completion processes associated with different attributes or domains of memory | Neuroscience and Biobehavioral Reviews | 2013 | 218 |
| 4 | Can one hour per week of therapy lead to lasting changes in young children with autism? | Autism | 2009 | 196 |
| 5 | GABAB Receptor Agonist R-Baclofen Reverses Social Deficits and Reduces Repetitive Behavior in Two Mouse Models of Autism | Neuropsychopharmacology | 2015 | 187 |
| 6 | A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins | Molecular Psychiatry | 2007 | 184 |
| 7 | Modeling fragile X syndrome in the <i>Fmr1</i> knockout mouse | Intractable and Rare Diseases Research | 2014 | 183 |
| 8 | Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism | Biological Psychiatry | 2017 | 173 |
| 9 | Genome-wide detection of tandem DNA repeats that are expanded in autism | Nature | 2020 | 155 |
| 10 | Regulation of autism-relevant behaviors by cerebellar–prefrontal cortical circuits | Nature Neuroscience | 2020 | 149 |
| 11 | Connectivity Strength of Dissociable Striatal Tracts Predict Individual Differences in Temporal Discounting | Journal of Neuroscience | 2014 | 147 |
| 12 | Behavioral phenotypes of genetic mouse models of autism | Genes, Brain and Behavior | 2016 | 137 |
| 13 | Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism | Molecular Autism | 2017 | 135 |
| 14 | Updated report on tools to measure outcomes of clinical trials in fragile X syndrome | Journal of Neurodevelopmental Disorders | 2017 | 123 |
| 15 | Neuron numbers increase in the human amygdala from birth to adulthood, but not in autism | Proceedings of the National Academy of Sciences of the United States of America | 2018 | 123 |
| 16 | Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size | Molecular Psychiatry | 2020 | 122 |
| 17 | Long-term exposure to intranasal oxytocin in a mouse autism model | Translational Psychiatry | 2014 | 112 |
| 18 | Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism | Neurotherapeutics | 2015 | 108 |
| 19 | Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics | Current Topics in Behavioral Neurosciences | 2015 | 100 |
| 20 | Changing conceptualizations of regression: What prospective studies reveal about the onset of autism spectrum disorder | Neuroscience and Biobehavioral Reviews | 2019 | 94 |
| 21 | Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome | Nature Medicine | 2020 | 90 |
| 22 | Effectiveness of community‐based early intervention for children with autism spectrum disorder: a meta‐analysis | Journal of Child Psychology and Psychiatry and Allied Disciplines | 2019 | 89 |
| 23 | Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion | Molecular Psychiatry | 2021 | 87 |
| 24 | R-Baclofen Reverses Cognitive Deficits and Improves Social Interactions in Two Lines of 16p11.2 Deletion Mice | Neuropsychopharmacology | 2018 | 75 |
| 25 | The Scope and Nature of Reading Comprehension Impairments in School-Aged Children with Higher-Functioning Autism Spectrum Disorder | Journal of Autism and Developmental Disorders | 2017 | 64 |
| 26 | Working Memory in Attention Deficit/Hyperactivity Disorder is Characterized by a Lack of Specialization of Brain Function | PLoS ONE | 2011 | 62 |
| 27 | Onset patterns in autism: Variation across informants, methods, and timing | Autism Research | 2018 | 57 |
| 28 | Reconsidering animal models used to study autism spectrum disorder: Current state and optimizing future | Genes, Brain and Behavior | 2022 | 55 |
| 29 | The Very Early Autism Phenotype | Journal of Autism and Developmental Disorders | 2007 | 54 |
| 30 | 16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks | Learning and Memory | 2015 | 53 |
| 31 | Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome | Neurobiology of Learning and Memory | 2019 | 53 |
| 32 | Touchscreen learning deficits and normal social approach behavior in the Shank3B model of Phelan–McDermid Syndrome and autism | Neuroscience | 2017 | 52 |
| 33 | Clinical and Cognitive Characteristics Associated with Mathematics Problem Solving in Adolescents with Autism Spectrum Disorder | Autism Research | 2016 | 50 |
| 34 | Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study | Molecular Psychiatry | 2020 | 50 |
| 35 | Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome | Translational Psychiatry | 2020 | 50 |
| 36 | Anxiety, attention problems, hyperactivity, and the Aberrant Behavior Checklist in fragile X syndrome | American Journal of Medical Genetics, Part A | 2014 | 48 |
| 37 | Behavioral Phenotyping Assays for Genetic Mouse Models of Neurodevelopmental, Neurodegenerative, and Psychiatric Disorders | Annual Review of Animal Biosciences | 2017 | 46 |
| 38 | Evaluation of the neuroactive steroid ganaxolone on social and repetitive behaviors in the BTBR mouse model of autism | Psychopharmacology | 2016 | 43 |
| 39 | Methodological Considerations for Optimizing and Validating Behavioral Assays | Current Protocols in Mouse Biology | 2016 | 42 |
| 40 | Hypothesis‐driven investigations of diverse pharmacological targets in two mouse models of autism | Autism Research | 2019 | 42 |
| 41 | Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects | American Journal of Human Genetics | 2020 | 42 |
| 42 | SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function | Cell Reports | 2018 | 41 |
| 43 | Electrodermal and Behavioral Responses of Children With Autism Spectrum Disorders to Sensory and Repetitive Stimuli | Autism Research | 2014 | 40 |
| 44 | The development of cognitive control in children with chromosome 22q11.2 deletion syndrome | Frontiers in Psychology | 2014 | 39 |
| 45 | Anxiety disorders in fragile X premutation carriers: Preliminary characterization of probands and non-probands | Intractable and Rare Diseases Research | 2015 | 39 |
| 46 | Best Practices in Fragile X Syndrome Treatment Development | Brain Sciences | 2018 | 37 |
| 47 | Prevalence and Predictors of Anxiety Disorders in Adolescent and Adult Males with Autism Spectrum Disorder and Fragile X Syndrome | Journal of Autism and Developmental Disorders | 2019 | 36 |
| 48 | A Spoken-Language Intervention for School-Aged Boys With Fragile X Syndrome | American Journal on Intellectual and Developmental Disabilities | 2016 | 35 |
| 49 | Biobehavioral composite of social aspects of anxiety in young adults with fragile X syndrome contrasted to autism spectrum disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2018 | 34 |
| 50 | Receptive vocabulary analysis in Down syndrome | Research in Developmental Disabilities | 2016 | 32 |
