Melissa Haendel

Affiliations: 
Medical Informatics & Clinical Epidemiology Oregon Health and Science University, Portland, OR 
Area:
informatics
Website:
http://www.ohsu.edu/xd/education/library/about/staff-directory/melissa-haendel.cfm
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"Melissa Haendel"
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Parents

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Gary Lyons grad student 1993-1999 UW Madison
Judith Eisen post-doc 2000-2002 University of Oregon
George Bailey post-doc 2002-2004 Oregon State
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Publications

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Vestito L, Jacobsen JOB, Walker S, et al. (2024) Efficient reinterpretation of rare disease cases using Exomiser. Npj Genomic Medicine. 9: 65
Danis D, Bamshad MJ, Bridges Y, et al. (2024) A corpus of GA4GH phenopackets: case-level phenotyping for genomic diagnostics and discovery. Hgg Advances. 100371
Matentzoglu N, Bello SM, Stefancsik R, et al. (2024) The Unified Phenotype Ontology (uPheno): A framework for cross-species integrative phenomics. Biorxiv : the Preprint Server For Biology
Danis D, Bamshad MJ, Bridges Y, et al. (2024) A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery. Medrxiv : the Preprint Server For Health Sciences
Putman TE, Schaper K, Matentzoglu N, et al. (2023) The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species. Nucleic Acids Research
Gargano MA, Matentzoglu N, Coleman B, et al. (2023) The Human Phenotype Ontology in 2024: phenotypes around the world. Nucleic Acids Research
Danis D, Jacobsen JOB, Wagner AH, et al. (2023) Phenopacket-tools: Building and validating GA4GH Phenopackets. Plos One. 18: e0285433
Stefancsik R, Balhoff JP, Balk MA, et al. (2023) The Ontology of Biological Attributes (OBA)-computational traits for the life sciences. Mammalian Genome : Official Journal of the International Mammalian Genome Society
Stefancsik R, Balhoff JP, Balk MA, et al. (2023) The Ontology of Biological Attributes (OBA) - Computational Traits for the Life Sciences. Biorxiv : the Preprint Server For Biology
Thaxton C, Goldstein J, DiStefano M, et al. (2022) Lumping versus splitting: How to approach defining a disease to enable accurate genomic curation. Cell Genomics. 2
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