Photo of Melissa A. Haendel, Ph.D.

Melissa A. Haendel Ph.D.

  •      (503) 407-5970
    • Associate Professor of Medical Informatics and Clinical Epidemiology School of Medicine
    • Co-Director, OHSU Library Library
    • Director of the Ontology Development Group Library
    • Biomedical Informatics Graduate Program School of Medicine

Melissa is co-director of the OHSU Library and the director of the Ontology Development Group and an Associate Professor in the Library and the Department of Medical Informatics and Clinical Epidemiology.

Major Responsibilities

Interim Co-Director of the Library Director of the Ontology Development Research Laboratory within the OHSU Library and Department of Medical Informatics and Epidemiology

Principal investigator of: 

The Monarch Initiative
The NCATS Data Translator
PCORI "Realization of a Standard of Care for Rare Diseases Using Patient-Engaged Phenotyping”

Development of ontologies and data standards

End-user requirements and user interface design and testing

Science of Science

Promotion of research reproducibility

Development of open science policies and practices

Areas of interest

  • When not working, Melissa is usually planting, harvesting, cooking, or eating food.

Education

  • Ph.D., University of Wisconsin, Madison Wisconsin United States 1999
  • B.A., Reed College, Portland Oregon United States 1991

Publications

Selected publications

  • Vasilevsky NA, Brush MH, Paddock H, Ponting L, Tripathy SJ, LaRocca GM, Haendel MA. (2013) On the reproducibility of science: unique identification of research resources in the biomedical literature.PeerJ 1:e148      

  • Meehan TF, Vasilevsky NA, Mungall CJ, Dougall DS, Haendel MA, Blake JA, Diehl AD. (2013) Ontology based molecular signatures for immune cell types via gene expression analysis. BMC Bioinformatics. 2013 Aug 30;14(1):263.

  • Haendel MA, Chesler EJ. Lost and found in behavioral informatics. (2012) Int Rev Neurobiol. 2012;103:1-18. doi:10.1016/B978-0-12-388408-4.00001-0.     

  • Nicole Vasilevsky, Tenille Johnson, Karen Corday, Carlo Torniai, Matthew Brush, Erik Segerdell, Melanie Wilson, Chris Shaffer, David Robinson and Melissa Haendel (2012) Research resources: curating the new eagle-i discovery system. Database Vol. 2012, bar067.            

  • Torniai, C., Brush, M., Vasilevsky, N., Segerdell, E., Wison, M., Johnson, T., Corday, K., Shaffer, C., and Haendel, M. (2011) Developing an application ontology for biomedical resource annotation and retrieval: Challenges and lessons learned. International Conference on Biomedical Ontology 2011; July 26–30, 2011; Buffalo, NY.   

  • Mungall CJ, Anderson D, Bandrowski A, Canada B, Chatyr-Aryamontri A, Cheng K, Conn PM, Dolinski K, Ellisman M, Eppig J, Grethe JS, Kemnitz J, Iadonato S, Larson SD, Magness C, Martone ME, Tyers M, Torniai C, Troyanskaya O, Turner J, Westerfield M, Haendel MA. (2011) An ontology-based approach to linking model organisms and resources to human diseases. Poster presentation at: International Conference on Biomedical Ontology 2011; July 26–30, 2011; Buffalo, NY.        

  • Mitchell S, Torniai C, Lowe, B, Corson-Rikert J, Wilson M, Ahmed M, Chen S, Ding Y, Rejack N, Haendel MA. (2011) Aligning research resource and researcher representation: the eagle-i and VIVO use case. Poster presentation at: International Conference on Biomedical Ontology 2011; July 26–30, 2011; Buffalo, NY.

  • Brush MH, Vasilevsky N, Torniai C, Johnson T, Shaffer C, Haendel MA. (2011) Developing a reagent application ontology within the OBO Foundry Framework. Poster presentation at: International Conference on Biomedical Ontology 2011; July 26–30, 2011; Buffalo, NY.

  • Mungall, C.J., Gkoutos, G.V., Smith, C.L., Haendel, M.A., Lewis, S.E., and Ashburner, M. (2010) Integrating Phenotype Ontologies across Multiple Species. Genome Biol. 2010 Jan 8;11(1):R2.        

  • Washington, N.L.*, Haendel, M.A.*, Mungall, C.J., Ashburner, M., Westerfield, M., and Lewis, S.L. (2009) Linking human disease to animal models using ontology-based phenotype annotation. PLoS Biol. 2009 Nov;7(11):e1000247. Epub 2009 Nov 24.                                                                     *These authors contributed equally to this manuscript.       

Publications

  • "MARRVEL : Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome." American Journal of Human Genetics  In: , Vol. 100, No. 6, 01.06.2017, p. 843-853.
  • "Bedside Back to Bench : Building Bridges between Basic and Clinical Genomic Research." Cell  In: , Vol. 169, No. 1, 23.03.2017, p. 6-12.
  • "A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3." American Journal of Human Genetics  In: , Vol. 100, No. 1, 05.01.2017, p. 128-137.
  • "The Monarch Initiative : An integrative data and analytic platform connecting phenotypes to genotypes across species." Nucleic Acids Research In: , Vol. 45, No. D1, 01.01.2017, p. D712-D722.
  • "The human phenotype ontology in 2017." Nucleic Acids Research In: , Vol. 45, No. D1, 01.01.2017, p. D865-D876.
  • "Reproducible and reusable research : Are journal data sharing policies meeting the mark?" PeerJ In: , Vol. 2017, No. 4, e3208, 2017.
  • "Tools for exploring mouse models of human disease." Drug Discovery Today: Disease Models  In: , 2017.
  • "Navigating the phenotype frontier : The monarch initiative." Genetics In: , Vol. 203, No. 4, 01.08.2016, p. 1491-1495.
  • "Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency." Genetics in Medicine  In: , Vol. 18, No. 6, 01.06.2016, p. 608-617.
  • "A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease." American Journal of Human Genetics In: , 04.04.2016.
  • "The Ontology for Biomedical Investigations." PLoS One  In: , Vol. 11, No. 4, e0154556, 01.04.2016.
  • "Reproducibility and conflicts in immune epitope data." Immunology  In: , Vol. 147, No. 3, 01.03.2016, p. 349-354.
  • "Proceedings of a Sickle Cell Disease Ontology workshop - Towards the first comprehensive ontology for Sickle Cell Disease." Applied and Translational Genomics  In: , 01.03.2016.
  • "Muscle logic : New knowledge resource for anatomy enables comprehensive searches of the literature on the feeding muscles of mammals." PLoS One In: , Vol. 11, No. 2, e0149102, 01.02.2016.
  • "The Resource Identification Initiative : A cultural shift in publishing." Journal of Comparative Neurology  In: , Vol. 524, No. 1, 01.01.2016, p. 8-22.
  • "The Resource Identification Initiative : A cultural shift in publishing." Brain and Behavior  In: , Vol. 6, No. 1, 01.01.2016, p. 1-14.
  • "Laying a community-based foundation for data-driven semantic standards in environmental health sciences." Environmental Health Perspectives  In: , Vol. 124, No. 8, 2016, p. 1136-1140.
  • "The health care and life sciences community profile for dataset descriptions." PeerJ  In: , Vol. 2016, No. 8, e2331, 2016.
  • "Innovative approaches to combining genotype, phenotype, epigenetic, and exposure data for precision diagnostics."  Pacific Symposium on Biocomputing 2016, PSB 2016. World Scientific Publishing Co. Pte Ltd, 2016. p. 93-95.
  • "The cell ontology 2016 : Enhanced content, modularization, and ontology interoperability." Journal of Animal Science and Biotechnology In: , Vol. 7, No. 1, 44, 2016.
  • "Enhancing SciENcv through semantic research profile integration with the VIVO-ISF ontology." CEUR Workshop Proceedings  In: , Vol. 1747, 2016.
  • "Gold-standard ontology-based annotation of concepts in biomedical text in the CRAFT corpus : Updates and extensions." CEUR Workshop Proceedings  In: , Vol. 1747, 2016.
  • "Building a molecular glyco-phenotype ontology to decipher undiagnosed diseases." CEUR Workshop Proceedings In: , Vol. 1747, 2016.
  • "SEPIO : A semantic model for the integration and analysis of scientific evidence." CEUR Workshop Proceedings  In: , Vol. 1747, 2016.
  • "Enhancing the human phenotype ontology for use by the layperson." CEUR Workshop Proceedings  In: , Vol. 1747, 2016.
  • "Next-generation diagnostics and disease-gene discovery with the Exomiser." Nature Protocols In: , Vol. 10, No. 12, 01.12.2015, p. 2004-2015.
  • "The Resource Identification Initiative : A Cultural Shift in Publishing." Neuroinformatics  In: , 20.11.2015, p. 1-14.
  • "Use of Model Organism and Disease Databases to Support Matchmaking for Human Disease Gene Discovery." Human Mutation In: , Vol. 36, No. 10, 01.10.2015, p. 979-984.
  • "PhenomeCentral : A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases." Human Mutation  In: , Vol. 36, No. 10, 01.10.2015, p. 931-940.
  • "The Matchmaker Exchange : A Platform for Rare Disease Gene Discovery." Human Mutation In: , Vol. 36, No. 10, 01.10.2015, p. 915-921.

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