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    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.

    Show item 1 to 25 of 35  
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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
    Journal article
    Chris Mungall, Julie McMurry, Sebastian Köhler 0001, James P. Balhoff, Charles D. Borromeo, Matthew H. Brush, Seth Carbon, Tom Conlin, Nathan Dunn, Mark Engelstad, Erin Foster, Jean-Philippe Gourdine, Julius O. B. Jacobsen, Dan Keith, Bryan Laraway, Suzanna Lewis, Jeremy NguyenXuan, Kent Shefchek, Nicole Vasilevsky, Zhou Yuan, Nicole L. Washington, Harry Hochheiser, Tudor Groza, Damian Smedley, Peter N. Robinson, Melissa Haendel.
    The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.
    Nucleic Acids Research 2017, Volume 45 (0) 2017
    Journal article
    Tobias Penzkofer, Marten Jäger, Marek Figlerowicz, Richard Badge, Stefan Mundlos, Peter N. Robinson, Tomasz Zemojtel.
    L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomes.
    Nucleic Acids Research 2017, Volume 45 (0) 2017
    Journal article
    Sebastian Köhler 0001, Nicole Vasilevsky, Mark Engelstad, Erin Foster, Julie McMurry, Ségolène Aymé, Gareth Baynam, Susan M. Bello, Cornelius F. Boerkoel, Kym M. Boycott, Michael Brudno, Orion J. Buske, Patrick F. Chinnery, Valentina Cipriani, Laureen E. Connell, Hugh J. S. Dawkins, Laura E. DeMare, Andrew Devereau, Bert B. A. de Vries, Helen V. Firth, Kathleen Freson, Daniel Greene, Ada Hamosh, Ingo Helbig, Courtney Hum, Johanna Jähn, Roger James, Roland Krause, Stanley J. F. Laulederkind, Hanns Lochmüller, Gholson J. Lyon, Soichi Ogishima, Annie Olry, Willem Ouwehand, Nikolas Pontikos, Ana Rath, Franz Schaefer, Richard H. Scott, Michael Segal, Panagiotis I. Sergouniotis, Richard Sever, Cynthia L. Smith, Volker Straub, Rachel Thompson, Catherine Turner, Ernest Turro, Marijcke W. M. Veltman, Tom Vulliamy, Jing Yu, Julie von Ziegenweidt, Andreas Zankl, Stephan Züchner, Tomasz Zemojtel, Julius O. B. Jacobsen, Tudor Groza, Damian Smedley, Chris Mungall, Melissa Haendel, Peter N. Robinson.
    The Human Phenotype Ontology in 2017.
    Nucleic Acids Research 2017, Volume 45 (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
    Nicole Vasilevsky, Mark Engelstad, Erin Foster, Chris Mungall, Peter N. Robinson, Sebastian Köhler 0001, Melissa Haendel.
    Enhancing the Human Phenotype Ontology for Use by the Layperson.
    Proceedings of the Joint International Conference on Biological Ontology and BioCreative, Corvallis, Oregon, United States, August 1-4, 2016. 2016 (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
    Conference paper
    Sebastian Köhler 0001, Sandra C. Doelken, Chris Mungall, Sebastian Bauer, Helen V. Firth, Isabelle Bailleul-Forestier, Graeme C. M. Black, Danielle L. Brown, Michael Brudno, Jennifer Campbell, David R. FitzPatrick, Janan T. Eppig, Andrew P. Jackson, Kathleen Freson, Marta Gîrdea, Ingo Helbig, Jane A. Hurst, Johanna Jähn, Laird G. Jackson, Anne M. Kelly, David H. Ledbetter, Sahar Mansour, Christa L. Martin, Celia Moss, Andrew Mumford, Willem Ouwehand, Soo-Mi Park, Erin Rooney Riggs, Richard H. Scott, Sanjay Sisodiya, Steven Van Vooren, Ronald J. Wapner, Andrew O. M. Wilkie, Caroline F. Wright, Anneke T. Vulto-van Silfhout, Nicole de Leeuw, Bert B. A. de Vries, Nicole L. Washington, Cynthia L. Smith, Monte Westerfield, Paul N. Schofield, Barbara J. Ruef, Georgios V. Gkoutos, Melissa Haendel, Damian Smedley, Suzanna Lewis, Peter N. Robinson.
    The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
    Nucleic Acids Research 2014, Volume 42 (0) 2014
    Conference paper
    Aaron J. Masino, Elizabeth T. Dechene, Matthew C. Dulik, Alisha Wilkens, Nancy B. Spinner, Ian D. Krantz, Jeffrey W. Pennington, Peter N. Robinson, Peter S. White.
    Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology.
    BMC Bioinformatics 2014, Volume 15 (0) 2014
    Conference paper
    Damian Smedley, Sebastian Köhler 0001, Johanna Christina Czeschik, Joanna S. Amberger, Carol A. Bocchini, Ada Hamosh, Julian Veldboer, Tomasz Zemojtel, Peter N. Robinson.
    Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases.
    Bioinformatics 2014, Volume 30 (0) 2014
    Conference paper
    Sebastian Köhler 0001, Sandra C. Doelken, Chris Mungall, Sebastian Bauer, Helen V. Firth, Isabelle Bailleul-Forestier, Graeme C. M. Black, Danielle L. Brown, Michael Brudno, Jennifer Campbell, David R. FitzPatrick, Janan T. Eppig, Andrew P. Jackson, Kathleen Freson, Marta Gîrdea, Ingo Helbig, Jane A. Hurst, Johanna Jähn, Laird G. Jackson, Anne M. Kelly, David H. Ledbetter, Sahar Mansour, Christa L. Martin, Celia Moss, Andrew Mumford, Willem Ouwehand, Soo-Mi Park, Erin Rooney Riggs, Richard H. Scott, Sanjay Sisodiya, Steven Van Vooren, Ronald J. Wapner, Andrew O. M. Wilkie, Caroline F. Wright, Anneke T. Vulto-van Silfhout, Nicole de Leeuw, Bert B. A. de Vries, Nicole L. Washington, Cynthia L. Smith, Monte Westerfield, Paul N. Schofield, Barbara J. Ruef, Georgios V. Gkoutos, Melissa Haendel, Damian Smedley, Suzanna Lewis, Peter N. Robinson.
    The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
    Nucleic Acids Research 2014, Volume 42 (0) 2014
    Conference paper
    Julien Grosjean, Tayeb Merabti, Lina Fatima Soualmia, Catherine Letord, Jean Charlet, Peter N. Robinson, Stéfan Jacques Darmoni.
    Integrating the Human Phenotype Ontology into HeTOP Terminology-Ontology Server.
    MEDINFO 2013 - Proceedings of the 14th World Congress on Medical and Health Informatics, 20-13 August 2013, Copenhagen, Denmark 2013 (0) 2013
    Conference paper
    Damian Smedley, Anika Oellrich, Sebastian Köhler 0001, Barbara J. Ruef, Monte Westerfield, Peter N. Robinson, Suzanna Lewis, Chris Mungall.
    PhenoDigm: analyzing curated annotations to associate animal models with human diseases.
    Database 2013, Volume 2013 (0) 2013
    Conference paper
    Sebastian Bauer, Sebastian Köhler 0001, Marcel H. Schulz, Peter N. Robinson.
    Bayesian ontology querying for accurate and noise-tolerant semantic searches.
    Bioinformatics 2012, Volume 28 (0) 2012
    Journal article
    Maria Taboada, Diego Martínez Hernández, Belén Pilo, Adriano Jiménez-Escrig, Peter N. Robinson, María Jesús Sobrido.
    Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of cerebrotendinous xanthomatosis.
    BMC Med. Inf. Decision Making 2012, Volume 12 (0) 2012
    Conference paper
    Christian Rödelsperger, Peter Krawitz, Sebastian Bauer, Jochen Hecht, Abigail W. Bigham, Michael Bamshad, Birgit Jonske de Condor, Michal R. Schweiger, Peter N. Robinson.
    Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders.
    Bioinformatics 2011, Volume 27 (0) 2011
    Conference paper
    Sebastian Bauer, Peter N. Robinson, Julien Gagneur.
    Model-based gene set analysis for Bioconductor.
    Bioinformatics 2011, Volume 27 (0) 2011
    Conference paper
    Sebastian Köhler 0001, Sebastian Bauer, Chris Mungall, Gabriele Carletti, Cynthia L. Smith, Paul Schofield, Georgios V. Gkoutos, Peter N. Robinson.
    Improving ontologies by automatic reasoning and evaluation of logical definitions.
    BMC Bioinformatics 2011, Volume 12 (0) 2011
    Show item 1 to 25 of 35  

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