congenital heart disease phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| de novo variant | risk_factor_for | congenital heart disease | — | 1 |
Mentioned in (35)
Papers in which this entity is mentioned.
- Cardiovascular and Metabolic Outcomes in Adults with Fetal Alcohol Spectrum Disorders: A Retrospective Cohort Study. (2026)
- 3D spatial organization of heterogeneous nkx2.5+ progenitors in the zebrafish heart field pre-patterns cardiovascular development. (2025)
- Nkx2.7 is a conserved regulator of craniofacial development. (2025)
- A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
- Atypical developmental trajectories of white matter microstructure in prenatal alcohol exposure: Preliminary evidence from neurite orientation dispersion and density imaging. (2023)
- GATA4/5/6 family transcription factors are conserved determinants of cardiac versus pharyngeal mesoderm fate. (2022)
- Alterations in Insulin Levels in Adults with Prenatal Alcohol Exposure. (2021)
- Maternal Obesity during Pregnancy is Associated with Lower Cortical Thickness in the Neonate Brain. (2021)
- Studying the Effect of Maternal Pregestational Diabetes on Fetal Neurodevelopment Using Magnetoencephalography. (2020)
- Best practices for variant calling in clinical sequencing. (2020)
- Epigenetic mechanisms in alcohol- and adversity-induced developmental origins of neurobehavioral functioning. (2018)
- Slit-Robo signalling in heart development. (2018)
- Human Brain Abnormalities Associated With Prenatal Alcohol Exposure and Fetal Alcohol Spectrum Disorder. (2017)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
- Association between alcohol consumption during pregnancy and risks of congenital heart defects in offspring: meta-analysis of epidemiological observational studies. (2016)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- Inhibition of histone H3K9 acetylation by anacardic acid can correct the over-expression of Gata4 in the hearts of fetal mice exposed to alcohol during pregnancy. (2014)
- Development of thalamocortical connectivity during infancy and its cognitive correlations. (2014)
- Longitudinal MRI reveals altered trajectory of brain development during childhood and adolescence in fetal alcohol spectrum disorders. (2013)
- Associations between maternal genotypes and metabolites implicated in congenital heart defects. (2012)
- Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
- How to measure cortical folding from MR images: a step-by-step tutorial to compute local gyrification index. (2012)
- Zebrafish as a model to study cardiac development and human cardiac disease. (2011)
- PDGF function in diverse neural crest cell populations. (2010)
- A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
- Normal development of brain circuits. (2010)
- Maternal folate-related gene environment interactions and congenital heart defects. (2010)
- Prevalence of congenital heart defects and persistent pulmonary hypertension of the neonate with Down syndrome. (2010)
- Reduced cortical folding in mental retardation. (2010)
- Developmental origins of health and disease: environmental exposures. (2009)
- Fetal alcohol spectrum disorders and their persisting sequelae in adult life. (2008)
- The power of comparative and developmental studies for mouse models of Down syndrome. (2007)
- Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique. (2004)
- Clinical Recognition of FAS: Difficulties of Detection and Diagnosis. (1994)
Merged raw entities (1)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| congenital heart disease | phenotype | 35 | 61 |