congenital anomalies phenotype

Aliases

congenital anomaly

Related entities (1)

Mentioned in (27)

Papers in which this entity is mentioned.

• Neonatal mortality prediction with routinely collected data: a machine learning approach. (2021)
• Relationship of prenatal maternal obesity and diabetes to offspring neurodevelopmental and psychiatric disorders: a narrative review. (2020)
• Cannabis Teratology Explains Current Patterns of Coloradan Congenital Defects: The Contribution of Increased Cannabinoid Exposure to Rising Teratological Trends. (2019)
• Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE. (2018)
• Chromosome 19 microRNAs exert antiviral activity independent from type III interferon signaling. (2018)
• Identification of novel candidate disease genes from de novo exonic copy number variants. (2017)
• The gestational foundation of sex differences in development and vulnerability. (2017)
• Human Brain Abnormalities Associated With Prenatal Alcohol Exposure and Fetal Alcohol Spectrum Disorder. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• Structural brain anomalies in healthy adolescents in the NCANDA cohort: relation to neuropsychological test performance, sex, and ethnicity. (2017)
• Association between alcohol consumption during pregnancy and risks of congenital heart defects in offspring: meta-analysis of epidemiological observational studies. (2016)
• Fetal exposure to maternal depressive symptoms is associated with cortical thickness in late childhood. (2015)
• Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis. (2015)
• Passive smoking in the etiology of non-syndromic orofacial clefts: a systematic review and meta-analysis. (2015)
• A comparison of the prevalence of prenatal alcohol exposure obtained via maternal self-reports versus meconium testing: a systematic literature review and meta-analysis. (2014)
• Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013)
• Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. (2012)
• CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
• Teratogenic effects of thalidomide: molecular mechanisms. (2011)
• Infant brain atlases from neonates to 1- and 2-year-olds. (2011)
• Significant differences in global genomic DNA methylation by gender and race/ethnicity in peripheral blood. (2011)
• Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. (2011)
• Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions. (2011)
• Interaction between GSTM1/GSTT1 polymorphism and blood mercury on birth weight. (2010)
• Effects of prenatal multimicronutrient supplementation on pregnancy outcomes: a meta-analysis. (2009)
• Developmental origins of health and disease: environmental exposures. (2009)
• Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis. (2005)

Merged raw entities (2)

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