Linking tissues to phenotypes using gene expression profiles

por Oellrich, Anika, Smedley, Damian
Publicado 2014

Toward knowledge support for analysis and interpretation of complex traits

por Collier, Nigel, Oellrich, Anika, Groza, Tudor
Publicado 2013

Linking gene expression to phenotypes via pathway information

por Papatheodorou, Irene, Oellrich, Anika, Smedley, Damian
Publicado 2015

Concept selection for phenotypes and diseases using learn to rank

por Collier, Nigel, Oellrich, Anika, Groza, Tudor
Publicado 2015

Interoperability between phenotype and anatomy ontologies

por Hoehndorf, Robert, Oellrich, Anika, Rebholz-Schuhmann, Dietrich
Publicado 2010

Automatically transforming pre- to post-composed phenotypes: EQ-lising HPO and MP

por Oellrich, Anika, Grabmüller, Christoph, Rebholz-Schuhmann, Dietrich
Publicado 2013

Using association rule mining to determine promising secondary phenotyping hypotheses

por Oellrich, Anika, Jacobsen, Julius, Papatheodorou, Irene, Smedley, Damian
Publicado 2014

Generation of Silver Standard Concept Annotations from Biomedical Texts with Special Relevance to Phenotypes

por Oellrich, Anika, Collier, Nigel, Smedley, Damian, Groza, Tudor
Publicado 2015

Improving Disease Gene Prioritization by Comparing the Semantic Similarity of Phenotypes in Mice with Those of Human Diseases

por Oellrich, Anika, Hoehndorf, Robert, Gkoutos, Georgios V., Rebholz-Schuhmann, Dietrich
Publicado 2012

Quantitative comparison of mapping methods between Human and Mammalian Phenotype Ontology

por Oellrich, Anika, Gkoutos, Georgios V, Hoehndorf, Robert, Rebholz-Schuhmann, Dietrich
Publicado 2012

Relations as patterns: bridging the gap between OBO and OWL

por Hoehndorf, Robert, Oellrich, Anika, Dumontier, Michel, Kelso, Janet, Rebholz-Schuhmann, Dietrich, Herre, Heinrich
Publicado 2010

PhenoMiner: from text to a database of phenotypes associated with OMIM diseases

por Collier, Nigel, Groza, Tudor, Smedley, Damian, Robinson, Peter N., Oellrich, Anika, Rebholz-Schuhmann, Dietrich
Publicado 2015

Interoperability between Biomedical Ontologies through Relation Expansion, Upper-Level Ontologies and Automatic Reasoning

por Hoehndorf, Robert, Dumontier, Michel, Oellrich, Anika, Rebholz-Schuhmann, Dietrich, Schofield, Paul N., Gkoutos, Georgios V.
Publicado 2011

Ontology design patterns to disambiguate relations between genes and gene products in GENIA

por Hoehndorf, Robert, Ngonga Ngomo, Axel-Cyrille, Pyysalo, Sampo, Ohta, Tomoko, Oellrich, Anika, Rebholz-Schuhmann, Dietrich
Publicado 2011

Reporting phenotypes in mouse models when considering body size as a potential confounder

por Oellrich, Anika, Meehan, Terrence F., Parkinson, Helen, Sarntivijai, Sirarat, White, Jacqueline K., Karp, Natasha A.
Publicado 2016

PhenoDigm: analyzing curated annotations to associate animal models with human diseases

por Smedley, Damian, Oellrich, Anika, Köhler, Sebastian, Ruef, Barbara, Westerfield, Monte, Robinson, Peter, Lewis, Suzanna, Mungall, Christopher
Publicado 2013

Learning to Recognize Phenotype Candidates in the Auto-Immune Literature Using SVM Re-Ranking

por Collier, Nigel, Tran, Mai-vu, Le, Hoang-quynh, Ha, Quang-Thuy, Oellrich, Anika, Rebholz-Schuhmann, Dietrich
Publicado 2013

The influence of disease categories on gene candidate predictions from model organism phenotypes

por Oellrich, Anika, Koehler, Sebastian, Washington, Nicole, Mungall, Chris, Lewis, Suzanna, Haendel, Melissa, Robinson, Peter N, Smedley, Damian
Publicado 2014

Thematic issue of the Second combined Bio-ontologies and Phenotypes Workshop

por Verspoor, Karin, Oellrich, Anika, Collier, Nigel, Groza, Tudor, Rocca-Serra, Philippe, Soldatova, Larisa, Dumontier, Michel, Shah, Nigam
Publicado 2016

Automated PDF highlighting to support faster curation of literature for Parkinson’s and Alzheimer’s disease

por Wu, Honghan, Oellrich, Anika, Girges, Christine, de Bono, Bernard, Hubbard, Tim J.P., Dobson, Richard J.B.
Publicado 2017