PC2 phenotype

Aliases

principal component 2

No related entities found.

Mentioned in (15)

Papers in which this entity is mentioned.

• Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA. (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)
• The Immune Landscape of Cancer. (2018)
• Harmonization of cortical thickness measurements across scanners and sites. (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)
• The face signature of fibrodysplasia ossificans progressiva. (2012)
• 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.