fragile X syndrome phenotype

Aliases

Fragile X

Related entities (4)

Mentioned in (53)

Papers in which this entity is mentioned.

• Regional hippocampal thinning and gyrification abnormalities and associated cognition in children with prenatal alcohol exposure. (2025)
• A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
• mutations, genetic mosaicism and human disease. (2022)
• Cotinine: Pharmacologically Active Metabolite of Nicotine and Neural Mechanisms for Its Actions. (2021)
• DNA methylation and brain structure and function across the life course: A systematic review. (2020)
• Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring. (2020)
• A review on neuroimaging studies of genetic and environmental influences on early brain development. (2019)
• Transient Potassium Channels: Therapeutic Targets for Brain Disorders. (2019)
• Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue. (2019)
• Hippocampal deficits in neurodevelopmental disorders. (2019)
• Cerebrospinal fluid and the early brain development of autism. (2018)
• Mental Illnesses-Associated Fxr1 and Its Negative Regulator Gsk3β Are Modulators of Anxiety and Glutamatergic Neurotransmission. (2018)
• Twin study confirms virtually identical prenatal alcohol exposures can lead to markedly different fetal alcohol spectrum disorder outcomes-fetal genetics influences fetal vulnerability. (2018)
• Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
• PI3K Signaling in Neurons: A Central Node for the Control of Multiple Functions. (2018)
• Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. (2018)
• Epigenetics studies of fetal alcohol spectrum disorder: where are we now? (2017)
• Effect of Neuroinflammation on Synaptic Organization and Function in the Developing Brain: Implications for Neurodevelopmental and Neurodegenerative Disorders. (2017)
• Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. (2016)
• Fetal Alcohol Spectrum Disorders: An Overview from the Glia Perspective. (2015)
• Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model. (2015)
• Lead exposure induces changes in 5-hydroxymethylcytosine clusters in CpG islands in human embryonic stem cells and umbilical cord blood. (2015)
• Parietal dysfunction during number processing in children with fetal alcohol spectrum disorders. (2015)
• ERBB4 polymorphism and family history of psychiatric disorders on age-related cortical changes in healthy children. (2015)
• Long Noncoding RNA-Directed Epigenetic Regulation of Gene Expression Is Associated With Anxiety-like Behavior in Mice. (2015)
• Genetics and genomics of psychiatric disease. (2015)
• Common DNA methylation alterations in multiple brain regions in autism. (2014)
• Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome. (2014)
• Cardiovascular and behavioral response to auditory stimuli in boys with fragile X syndrome. (2013)
• Early exposure to alcohol leads to permanent impairment of dendritic excitability in neocortical pyramidal neurons. (2012)
• Large-scale objective phenotyping of 3D facial morphology. (2012)
• Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
• Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. (2012)
• Plasma cytokine levels in children with autistic disorder and unrelated siblings. (2012)
• Facial phenotypes in subgroups of prepubertal boys with autism spectrum disorders are correlated with clinical phenotypes. (2011)
• Basal forebrain involvement in low-functioning autistic children: a voxel-based morphometry study. (2011)
• Brain growth across the life span in autism: age-specific changes in anatomical pathology. (2011)
• Normal development of brain circuits. (2010)
• The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. (2010)
• Population differences in dysmorphic features among children with fetal alcohol spectrum disorders. (2010)
• Reduced cortical folding in mental retardation. (2010)
• Differentiating prenatal exposure to methamphetamine and alcohol versus alcohol and not methamphetamine using tensor-based brain morphometry and discriminant analysis. (2010)
• A comprehensive volumetric analysis of the cerebellum in children and adolescents with autism spectrum disorder. (2009)
• Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts. (2009)
• Functional magnetic resonance imaging outcomes from a comprehensive magnetic resonance study of children with fetal alcohol spectrum disorders. (2009)
• The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA. (2009)
• Cerebellar vermal volumes and behavioral correlates in children with autism spectrum disorder. (2009)
• Characterization of white matter microstructure in fetal alcohol spectrum disorders. (2009)
• Three-dimensional brain growth abnormalities in childhood-onset schizophrenia visualized by using tensor-based morphometry. (2008)
• Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
• Impaired neural networks for approximate calculation in dyscalculic children: a functional MRI study. (2006)
• The long-term stability of new hippocampal place fields requires new protein synthesis. (2004)
• Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMR1 protein expression. (2002)

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