PC1 phenotype
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (19)
Papers in which this entity is mentioned.
- Virtual Ontogeny of Cortical Growth Preceding Mental Illness. (2022)
- DNA methylation in relation to gestational age and brain dysmaturation in preterm infants. (2022)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- Exposure to ethanol leads to midfacial hypoplasia in a zebrafish model of FASD via indirect interactions with the Shh pathway. (2021)
- An enriched biosignature of gut microbiota-dependent metabolites characterizes maternal plasma in a mouse model of fetal alcohol spectrum disorder. (2021)
- Neuronal ApoE upregulates MHC-I expression to drive selective neurodegeneration in Alzheimer's disease. (2021)
- Cannabis Teratology Explains Current Patterns of Coloradan Congenital Defects: The Contribution of Increased Cannabinoid Exposure to Rising Teratological Trends. (2019)
- The Immune Landscape of Cancer. (2018)
- Genome-wide association analysis identifies common variants influencing infant brain volumes. (2017)
- Combined soft and skeletal tissue modelling of normal and dysmorphic midface postnatal development. (2016)
- Epigenomic profiling of preterm infants reveals DNA methylation differences at sites associated with neural function. (2016)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- An anatomically comprehensive atlas of the adult human brain transcriptome. (2012)
- Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. (2012)
- Implication of European-derived adiposity loci in African Americans. (2012)
- The face signature of fibrodysplasia ossificans progressiva. (2012)
- A genome-wide association study of neuroticism in a population-based sample. (2010)
- Analysis and application of European genetic substructure using 300 K SNP information. (2008)
Merged raw entities (2)
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 |
|---|---|---|---|
| pc1 | phenotype | 17 | 30 |
| principal component 1 | phenotype | 2 | 2 |