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    Author information
    First name: Peter N.
    Last name: Robinson
    DBLP: 34/3156
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    Below you find the publications which have been written by this author.

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    Journal article
    Verena Heinrich, Tom Kamphans, Stefan Mundlos, Peter N. Robinson, Peter M. Krawitz.
    A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing data.
    Bioinformatics 2017, Volume 33 (0) 2017
    Conference paper
    Anika Oellrich, Nigel Collier, Tudor Groza, Dietrich Rebholz-Schuhmann, Nigam H. Shah, Olivier Bodenreider, Mary Regina Boland, Ivo I. Georgiev, Hongfang Liu, Kevin M. Livingston, Augustin Luna, Ann-Marie Mallon, Prashanti Manda, Peter N. Robinson, Gabriella Rustici, Michelle Simon, Liqin Wang, Rainer Winnenburg, Michel Dumontier.
    The digital revolution in phenotyping.
    Briefings in Bioinformatics 2016, Volume 17 (0) 2016
    Conference paper
    Giorgio Valentini, Sebastian Köhler 0001, Matteo Ré, Marco Notaro, Peter N. Robinson.
    Prediction of Human Gene - Phenotype Associations by Exploiting the Hierarchical Structure of the Human Phenotype Ontology.
    Bioinformatics and Biomedical Engineering - Third International Conference, IWBBIO 2015, Granada, Spain, April 15-17, 2015. Proceedings, Part I 2015 (0) 2015
    Conference paper
    Tudor Groza, Tania Tudorache, Peter N. Robinson, Andreas Zankl.
    Capturing domain knowledge from multiple sources: the rare bone disorders use case.
    J. Biomedical Semantics 2015, Volume 6 (0) 2015
    Conference paper
    Peter N. Robinson, Marco Frasca, Sebastian Köhler 0001, Marco Notaro, Matteo Ré, Giorgio Valentini.
    A Hierarchical Ensemble Method for DAG-Structured Taxonomies.
    Multiple Classifier Systems - 12th International Workshop, MCS 2015, Günzburg, Germany, June 29 - July 1, 2015, Proceedings 2015 (0) 2015
    Conference paper
    Léon Kuchenbecker, Mikalai Nienen, Jochen Hecht, Avidan U. Neumann, Nina Babel, Knut Reinert, Peter N. Robinson.
    IMSEQ - a fast and error aware approach to immunogenetic sequence analysis.
    Bioinformatics 2015, Volume 31 (0) 2015
    Conference paper
    Nigel Collier, Tudor Groza, Damian Smedley, Peter N. Robinson, Anika Oellrich, Dietrich Rebholz-Schuhmann.
    PhenoMiner: from text to a database of phenotypes associated with OMIM diseases.
    Database 2015, Volume 2015 (0) 2015
    Conference paper
    Na Zhu, Verena Heinrich, Thorsten Dickhaus, Jochen Hecht, Peter N. Robinson, Stefan Mundlos, Tom Kamphans, Peter M. Krawitz.
    Strategies to improve the performance of rare variant association studies by optimizing the selection of controls.
    Bioinformatics 2015, Volume 31 (0) 2015
    Conference paper
    Tudor Groza, Sebastian Köhler 0001, Sandra C. Doelken, Nigel Collier, Anika Oellrich, Damian Smedley, Francisco M. Couto, Gareth Baynam, Andreas Zankl, Peter N. Robinson.
    Automatic concept recognition using the Human Phenotype Ontology reference and test suite corpora.
    Database 2015, Volume 2015 (0) 2015
    Journal article
    Anika Oellrich, Sebastian Köhler 0001, Nicole L. Washington, Chris Mungall, Suzanna Lewis, Melissa Haendel, Peter N. Robinson, Damian Smedley.
    The influence of disease categories on gene candidate predictions from model organism phenotypes.
    J. Biomedical Semantics 2014, Volume 5 (0) 2014
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