Phenotype ontologies and cross-species analysis for translational research
about
The Human Phenotype Ontology: Semantic Unification of Common and Rare DiseaseCapturing phenotypes for precision medicineMechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome RearrangementsPhenotype-driven strategies for exome prioritization of human Mendelian disease genes.Disease insights through cross-species phenotype comparisonsThe Human Phenotype Ontology in 2017Applications of comparative evolution to human disease geneticsPrediction of Genetic Interactions Using Machine Learning and Network PropertiesClinical interpretation of CNVs with cross-species phenotype dataPhenoMiner: from text to a database of phenotypes associated with OMIM diseases.Use of model organism and disease databases to support matchmaking for human disease gene discovery.Deletions of chromosomal regulatory boundaries are associated with congenital disease.Limbform: a functional ontology-based database of limb regeneration experiments.Finding our way through phenotypes.Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeGene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disorders.The differential view of genotype-phenotype relationships.Application of linear mixed models to study genetic stability of height and body mass index across countries and timeWhat to compare and how: Comparative transcriptomics for Evo-Devo.The digital revolution in phenotyping.The failure of anxiolytic therapies in early clinical trials: what needs to be done.The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease.Using the phenoscape knowledgebase to relate genetic perturbations to phenotypic evolution.Best behaviour? Ontologies and the formal description of animal behaviour.PhenomeExpress: a refined network analysis of expression datasets by inclusion of known disease phenotypes.The genomic birthday paradox: how much is enough?A new synonym-substitution method to enrich the human phenotype ontology.Haploinsufficiency predictions without study bias.Diverse type 2 diabetes genetic risk factors functionally converge in a phenotype-focused gene network.
P2860
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P2860
Phenotype ontologies and cross-species analysis for translational research
description
2014 nî lūn-bûn
@nan
2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Phenotype ontologies and cross-species analysis for translational research
@ast
Phenotype ontologies and cross-species analysis for translational research
@en
type
label
Phenotype ontologies and cross-species analysis for translational research
@ast
Phenotype ontologies and cross-species analysis for translational research
@en
prefLabel
Phenotype ontologies and cross-species analysis for translational research
@ast
Phenotype ontologies and cross-species analysis for translational research
@en
P2860
P1433
P1476
Phenotype ontologies and cross-species analysis for translational research
@en
P2093
Caleb Webber
P2860
P304
P356
10.1371/JOURNAL.PGEN.1004268
P577
2014-04-01T00:00:00Z
2014-04-03T00:00:00Z