Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

PhenoHM: human-mouse comparative phenome-genome server.

Nucleic acids research - 1 Jul 2010

Sardana Divya, Vasa Suresh, Vepachedu Nishanth, Chen Jing, Gudivada Ranga Chandra, Aronow Bruce J, Jegga Anil G

Abstract excerpt

PhenoHM is a human-mouse comparative phenome-genome server that facilitates cross-species identification of genes associated with orthologous phenotypes (http://phenome.cchmc.org; full open access, login not required). Combining and extrapolating the knowledge about the roles of individual gene functions in the determination of phenotype across multiple organisms improves our understanding of gene function in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cataract
Share to Disease
Share to Gene Regulatory Networks

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome

Share to Internet

Share to Software

Share to Vocabulary, Controlled

Source

Open in PubMed Open full text

Identifiers

PMID: 20507906
DOI: 10.1093/nar/gkq472
PMCID: PMC2896149

Genes

MPO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PhenoHM: human-mouse comparative phenome-genome server.PMID 20507906Read ↗

Expanding and refining the Mammalian Phenotype Ontology to enhance disease model discovery.Semantic proximity Read ↗

Computational identification of disease models through cross-species phenotype comparison.Semantic proximity Read ↗

PhenoGO: an integrated resource for the multiscale mining of clinical and biological data.Semantic proximity Read ↗

Disease insights through cross-species phenotype comparisons.Semantic proximity Read ↗

Phenotype ontologies for mouse and man: bridging the semantic gap.Semantic proximity Read ↗

The mammalian phenotype ontology: enabling robust annotation and comparative analysis.Semantic proximity Read ↗

Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information.Semantic proximity Read ↗

Contribution of model organism phenotypes to the computational identification of human disease genes.Semantic proximity Read ↗

New approaches to the representation and analysis of phenotype knowledge in human diseases and their animal models.Semantic proximity Read ↗

The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data.Semantic proximity Read ↗

The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information.Semantic proximity Read ↗

Investigating gene function and human disease through data on the IMPC portalSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.