Concepedia

Author

Melissa Haendel

Oregon Health & Science UniversityORCID

Also Known As

Adam SL Graefe, Alden Huang, Alexander, G. Caleb, Amanda P. Haddock, Andrea L. Gropman, Bennett T.D., Bradford, Yvonne, Brannock, M. Daniel, Bretaudeau, Anthony, Catherine A Groden

606

Publications

23.6K

Citations

75

H-Index

246

Concepts

All Affiliations

Oregon Health & Science UniversityLawrence Berkeley National LaboratoryUniversity of Colorado Anschutz Medical CampusJackson LaboratoryJohns Hopkins University
MH

About

Melissa Haendel is an author at Oregon Health & Science University specializing in medicine, genetics, and bioinformatics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Engineering

21

31

3.3K

2

Arts

1

1

48

3

Education

1

1

68

4

Health Sciences

1

1

71

5

Humanities

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20

Melissa Haendel

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183

Publications

19.2K

Citations

68

H-Index

YearCitations

The Human Phenotype Ontology in 2021

Sebastian Köhler, Michael Gargano, Nicolas Matentzoglu,

Nucleic Acids Research

2020

1.2K

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

Sebastian Köhler, Sandra C. Doelken, Chris Mungall,

Nucleic Acids Research

2013

834

Development of a Definition of Postacute Sequelae of SARS-CoV-2 Infection

Tanayott Thaweethai, Sarah E. Jolley, Elizabeth W. Karlson,

JAMA

2023

792

Uberon, an integrative multi-species anatomy ontology

Chris Mungall, Carlo Torniai, Georgios V. Gkoutos,

Genome biology

2012

756

Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources

Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky,

Nucleic Acids Research

2018

711

The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment

Melissa Haendel, Christopher G. Chute, Tellen D. Bennett,

Journal of the American Medical Informatics Association

2020

569

The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species

Chris Mungall, Julie A. McMurry, Sebastian Köhler,

Nucleic Acids Research

2016

480

The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery

Anthony Philippakis, Danielle R. Azzariti, Sergi Beltrán,

Human Mutation

2015

468

Next-generation diagnostics and disease-gene discovery with the Exomiser

Damian Smedley, Julius O.B. Jacobsen, Marten Jäger,

Nature Protocols

2015

435

The Ontology for Biomedical Investigations

Anita Bandrowski, Ryan R. Brinkman, Mathias Brochhausen,

PLoS ONE

2016

367

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