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Journal of Biomedical Informatics|February 18, 2014
Identifying scientific artefacts in biomedical literature: the Evidence Based Medicine use caseHamed Hassanzadeh, Tudor Groza, Jane HunterBMC Bioinformatics|October 16, 2012
Supervised segmentation of phenotype descriptions for the human skeletal phenome using hybrid methodsTudor Groza, Jane Hunter, Andreas ZanklPlos One|February 15, 2013
Mining skeletal phenotype descriptions from scientific literatureTudor Groza, Jane Hunter, Andreas ZanklBMC Bioinformatics|March 28, 2012
The Bone Dysplasia Ontology: integrating genotype and phenotype information in the skeletal dysplasia domainTudor Groza, Jane Hunter, Andreas ZanklBiomedical Informatics Insights|May 7, 2013
Recognizing scientific artifacts in biomedical literatureTudor Groza, Hamed Hassanzadeh, Jane HunterGenome Biology|October 2, 2013
Toward knowledge support for analysis and interpretation of complex traitsNigel Collier, Anika Oellrich, Tudor GrozaBiomedical Informatics Insights|February 27, 2013
Decomposing phenotype descriptions for the human skeletal phenomeTudor Groza, Jane Hunter, Andreas ZanklJournal of Biomedical Semantics|June 3, 2015
Concept selection for phenotypes and diseases using learn to rankNigel Collier, Anika Oellrich, Tudor GrozaAmerican Journal of Medical Genetics. Part A|August 29, 2018
Silver Russel syndrome in an aboriginal patient from AustraliaCathryn Poulton, Dimitar Azmanov, Vanessa Atkinson, et al.Clinical Dysmorphology|June 9, 2006
A case of 3q29 microdeletion with novel features and a review of cytogenetically visible terminal 3q deletionsGareth Baynam, Jack Goldblatt, Sharron TownshendPageof 23