Borut Peterlin

发表

Cross-border Italy-Slovenia biomedical research: Are we ready for horizon 2020? Conference proceedings with an analysis of innovation management and knowledge transfer potential for a smart specialization strategy

Sabina Passamonti, Rado Pišot, Tamara Lah Turnšek, 2014 .

Supporting Discovery in Medicine by Association Rule Mining of Bibliographic Databases

Saso Dzeroski, Borut Peterlin, Dimitar Hristovski, 2000, PKDD.

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge

Daniel Nilsson, Peter Szolovits, Karen Eilbeck, 2014, Genome Biology.

Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service

Borut Peterlin, Dimitar Hristovski, Irena Vrecar, 2017, Journal of Medical Systems.

PEDIA: prioritization of exome data by image analysis

Borut Peterlin, Sebastian Köhler, Na Zhu, 2018, Genetics in Medicine.

PEDIA: Prioritization of Exome Data by Image Analysis

Borut Peterlin, Sebastian Köhler, Na Zhu, 2018 .

Semantic Relations for Interpreting DNA Microarray Data

Borut Peterlin, Thomas C. Rindflesch, Dimitar Hristovski, 2009, AMIA.

Towards using Literature-based Discovery for Interpretation of Next Generation Sequencing Results

Borut Peterlin, Dimitar Hristovski, Andrej Kastrin, 2018, AMIA.

Using literature-based discovery to identify novel therapeutic approaches.

Borut Peterlin, Thomas C. Rindflesch, Dimitar Hristovski, 2013, Cardiovascular & hematological agents in medicinal chemistry.

Using data mining and OLAP to discover patterns in a database of patients with Y-chromosome deletions

Saso Dzeroski, Borut Peterlin, Dimitar Hristovski, 2000, AMIA.

Exploiting Semantic Relations for Literature-Based Discovery

Carol Friedman, Borut Peterlin, Thomas C. Rindflesch, 2006, AMIA.

Combining Semantic Relations and DNA Microarray Data for Novel Hypotheses Generation

Borut Peterlin, Thomas C. Rindflesch, Dimitar Hristovski, 2009, BioLINK@ISMB/ECCB.

Literature Based Discovery Support System and Its Application to Disease Gene Identification

Saso Dzeroski, Borut Peterlin, Dimitar Hristovski, 2007, Computational Discovery of Scientific Knowledge.

Supporting Discovery in Medicine by Association Rule Mining in Medline and UMLS

Saso Dzeroski, Borut Peterlin, Dimitar Hristovski, 2001, MedInfo.

Rasch-based high-dimensionality data reduction and class prediction with applications to microarray gene expression data

Borut Peterlin, Andrej Kastrin, B. Peterlin, 2010, Expert Syst. Appl..

Chi-square-based Scoring Function for Categorization of MEDLINE Citations

Borut Peterlin, Dimitar Hristovski, Andrej Kastrin, 2010, Methods of Information in Medicine.

Using literature-based discovery to identify disease candidate genes

Joyce A. Mitchell, Borut Peterlin, Susanne M. Humphrey, 2005, Int. J. Medical Informatics.

Improving Literature Based Discovery Support by Genetic Knowledge Integration

Joyce A. Mitchell, Borut Peterlin, Susanne M. Humphrey, 2003, MIE.

Positional integratomic approach in identification of genomic candidate regions for Parkinson's disease

Borut Peterlin, Ales Maver, B. Peterlin, 2011, Bioinform..

Integration of Data from Omic Studies with the Literature-Based Discovery towards Identification of Novel Treatments for Neovascularization in Diabetic Retinopathy

Borut Peterlin, Thomas C. Rindflesch, Dimitar Hristovski, 2013, BioMed research international.

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)

Borut Peterlin, David E Barton, Jayne Y Hehir-Kwa, 2013, European Journal of Human Genetics.

Association of Vascular Endothelial Growth Factor Gene Polymorphism with Myocardial Infarction in Patients with Type 2 Diabetes

Borut Peterlin, B. Peterlin, J. Osredkar, 2007, Cardiology.

Identifying candidate genes for Parkinson's disease by integrative genomics method.

Borut Peterlin, Amela Karic, Rifet Terzic, 2011, Biochemia medica.

Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21

Borut Peterlin, Aleš Maver, Luca Lovrečić, 2013, PloS one.

Mutations in SCN3A cause early infantile epileptic encephalopathy

Ethan M. Goldberg, Borut Peterlin, Livija Medne, 2018, Annals of neurology.