developmental disorders phenotype

Aliases

DD

Related entities (5)

Mentioned in (57)

Papers in which this entity is mentioned.

• Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• Subcortical volume in middle-aged adults with fetal alcohol spectrum disorders. (2024)
• mutations, genetic mosaicism and human disease. (2022)
• A methodological pipeline to generate an epigenetic marker of prenatal exposure to air pollution indicators. (2022)
• Placental genomic risk scores and early neurodevelopmental outcomes. (2021)
• Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
• Neurodevelopment in adolescents and adults with fetal alcohol spectrum disorders (FASD): A magnetic resonance region of interest analysis. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• Relationship of prenatal maternal obesity and diabetes to offspring neurodevelopmental and psychiatric disorders: a narrative review. (2020)
• De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
• Association Between Prenatal Exposure to Alcohol and Tobacco and Neonatal Brain Activity: Results From the Safe Passage Study. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. (2019)
• Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue. (2019)
• Epigenetic mechanisms in alcohol- and adversity-induced developmental origins of neurobehavioral functioning. (2018)
• The enduring impact of neurulation stage alcohol exposure: A combined behavioral and structural neuroimaging study in adult male and female C57BL/6J mice. (2018)
• Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. (2018)
• The gestational foundation of sex differences in development and vulnerability. (2017)
• Developmental Connectomics from Infancy through Early Childhood. (2017)
• Functional Connectivity of the Infant Human Brain: Plastic and Modifiable. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Gene-environment interactions in development and disease. (2017)
• Fetal Alcohol Spectrum Disorders: A Case Study. (2017)
• Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature. (2017)
• Single-Cell Profiling of an In Vitro Model of Human Interneuron Development Reveals Temporal Dynamics of Cell Type Production and Maturation. (2017)
• Fast and Accurate Genomic Analyses using Genome Graphs (2017)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• Annual research review: Growth connectomics--the organization and reorganization of brain networks during normal and abnormal development. (2015)
• Cortical maturation and myelination in healthy toddlers and young children. (2015)
• Computed tomography assessment of peripubertal craniofacial morphology in a sheep model of binge alcohol drinking in the first trimester. (2015)
• Pediatric neuroimaging using magnetic resonance imaging during non-sedated sleep. (2014)
• Gene expression signatures affected by alcohol-induced DNA methylomic deregulation in human embryonic stem cells. (2014)
• Intersubject variability of and genetic effects on the brain's functional connectivity during infancy. (2014)
• The use of near-infrared spectroscopy in the study of typical and atypical development. (2014)
• Prenatal ethanol exposure disrupts intraneocortical circuitry, cortical gene expression, and behavior in a mouse model of FASD. (2013)
• Distribution of disease-associated copy number variants across distinct disorders of cognitive development. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate. (2013)
• Suppression and epigenetic regulation of MiR-9 contributes to ethanol teratology: evidence from zebrafish and murine fetal neural stem cell models. (2013)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
• Measuring and comparing brain cortical surface area and other areal quantities. (2012)
• Resiliency in adolescents at high risk for substance abuse: flexible adaptation via subthalamic nucleus and linkage to drinking and drug use in early adulthood. (2012)
• Sex matters during adolescence: testosterone-related cortical thickness maturation differs between boys and girls. (2012)
• The quest for a neurobehavioral profile of heavy prenatal alcohol exposure. (2011)
• Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
• Beyond age and gender: relationships between cortical and subcortical brain volume and cognitive-motor abilities in school-age children. (2011)
• Fetal alcohol spectrum disorders: research challenges and opportunities. (2011)
• Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library. (2010)
• The development of gyrification in childhood and adolescence. (2010)
• Evaluating the validity of volume-based and surface-based brain image registration for developmental cognitive neuroscience studies in children 4 to 11 years of age. (2010)
• Associations between IQ, total and regional brain volumes, and demography in a large normative sample of healthy children and adolescents. (2010)
• Neurocognitive profile in children with fetal alcohol spectrum disorders. (2009)
• Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation. (2009)
• Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)
• A structural MRI study of human brain development from birth to 2 years. (2008)
• GitHub - im3sanger/dndscv: dN/dS methods to quantify selection in cancer and somatic evolution · GitHub

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