| Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics | Journal of Clinical Investigation | 2012 | 203 |
| FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States | Genome Medicine | 2012 | 198 |
| Autism symptoms and internalizing psychopathology in girls and boys with autism spectrum disorders | Journal of Autism and Developmental Disorders | 2012 | 176 |
| Increased rate of amygdala growth in children aged 2 to 4 years with autism spectrum disorders: a longitudinal study | Archives of General Psychiatry | 2012 | 139 |
| AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome | Genetics in Medicine | 2012 | 126 |
| Signaling defects in iPSC-derived fragile X premutation neurons | Human Molecular Genetics | 2012 | 116 |
| Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS | Genes, Brain and Behavior | 2012 | 104 |
| Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation | Human Molecular Genetics | 2012 | 87 |
| Verbal ability, social stress, and anxiety in children with autistic disorder | Autism | 2012 | 68 |
| Effects of sampling context on spontaneous expressive language in males with fragile X syndrome or Down syndrome | Journal of Speech, Language, and Hearing Research | 2012 | 66 |
| Role of DNMT3B in the regulation of early neural and neural crest specifiers | Epigenetics | 2012 | 63 |
| Treatment of neurodevelopmental disorders in adulthood | Journal of Neuroscience | 2012 | 48 |
| Unstable mutations in the FMR1 gene and the phenotypes | Advances in Experimental Medicine and Biology | 2012 | 47 |
| Postnatal development of the amygdala: A stereological study in macaque monkeys | Journal of Comparative Neurology | 2012 | 46 |
| Neuronal populations in the basolateral nuclei of the amygdala are differentially increased in humans compared with apes: a stereological study | Journal of Comparative Neurology | 2012 | 40 |
| Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS) | American Journal of Medical Genetics, Part A | 2012 | 38 |
| Joint attention, social-cognition, and recognition memory in adults | Frontiers in Human Neuroscience | 2012 | 35 |
| Microglial KCa3.1 Channels as a Potential Therapeutic Target for Alzheimer's Disease | International Journal of Alzheimer's Disease | 2012 | 34 |
| Daytime secretion of salivary cortisol and alpha-amylase in preschool-aged children with autism and typically developing children | Journal of Autism and Developmental Disorders | 2012 | 32 |
| Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study | Clinical Chemistry | 2012 | 32 |
| Ischemic transient neurological events identified by immune response to cerebral ischemia | Stroke | 2012 | 32 |
| Feasibility, reliability, and clinical validity of the Test of Attentional Performance for Children (KiTAP) in Fragile X syndrome (FXS) | Journal of Neurodevelopmental Disorders | 2012 | 31 |
| Newborn, carrier, and early childhood screening recommendations for fragile X | Pediatrics | 2012 | 31 |
| Language development in school-age girls with fragile X syndrome | Journal of Intellectual Disability Research | 2012 | 23 |
| Atypical developmental trajectory of functionally significant cortical areas in children with chromosome 22q11.2 deletion syndrome | Human Brain Mapping | 2012 | 23 |
