Lista de obras - Julie A. McMurry - Dominio Público Uruguay

A Census of Disease Ontologies

artículo científico publicado en 2018

A Measure of Open Data: A Metric and Analysis of Reusable Data Practices in Biomedical Data Resources

scholarly article published 16 March 2018

A Simple Standard for Sharing Ontological Mappings (SSSOM)

artículo científico publicado en 2022

A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease

artículo científico publicado en 2016

A call to cellular & humoral arms: enlisting cognate T cell help to develop broad-spectrum vaccines against influenza A.

artículo científico publicado en 2007

A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer

artículo científico publicado en 2020

Activation of natural regulatory T cells by IgG Fc-derived peptide "Tregitopes"

artículo científico publicado en 2008

An analysis and metric of reusable data licensing practices for biomedical resources

Analyzing Mycobacterium tuberculosis proteomes for candidate vaccine epitopes

artículo científico publicado en 2004

Biolink Model: A Universal Schema for Knowledge Graphs in Clinical, Biomedical, and Translational Science ⬇️

artículo científico publicado en 2022

Characterizing Long COVID: Deep Phenotype of a Complex Condition

artículo científico publicado en 2021

Developing an epitope-driven tuberculosis (TB) vaccine

artículo científico publicado en 2005

Diversity of Francisella tularensis Schu4 antigens recognized by T lymphocytes after natural infections in humans: Identification of candidate epitopes for inclusion in a rationally designed tularemia vaccine

artículo científico publicado en 2007

Encoding Clinical Data with the Human Phenotype Ontology for Computational Differential Diagnostics

scientific article published on 01 September 2019

Epitope-based vaccination against pneumonic tularemia

artículo científico publicado en 2009

Epitope-driven TB vaccine development: a streamlined approach using immuno-informatics, ELISpot assays, and HLA transgenic mice

artículo científico publicado en 2007

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

article by Sebastian Köhler et al published 8 January 2019 in Nucleic Acids Research

Expression Atlas update--a database of gene and transcript expression from microarray- and sequencing-based functional genomics experiments

artículo científico publicado en 2014

How many rare diseases are there?

artículo científico publicado en 2020

Identification of genome-derived vaccine candidates conserved between human and mouse-adapted strains of H. pylori

artículo científico publicado en 2008

Identification of immunogenic HLA-B7 "Achilles' heel" epitopes within highly conserved regions of HIV

artículo científico publicado en 2007

Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data

artículo científico publicado en 2017

Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data

artículo científico publicado en 2017

Immuno-informatics: Mining genomes for vaccine components

artículo científico publicado en 2002

Immunogenicity Screening Usingin Silico Methods: Correlation between T-Cell Epitope Content and Clinical Immunogenicity of Monoclonal Antibodies

article

In silico-accelerated identification of conserved and immunogenic variola/vaccinia T-cell epitopes.

artículo científico publicado en 2009

Interpretable Clinical Genomics with a Likelihood Ratio Paradigm

scientific article published on 29 July 2020

Interpretable Clinical Genomics with a Likelihood Ratio Paradigm

scholarly article published 28 January 2020

Interpretable prioritization of splice variants in diagnostic next-generation sequencing

artículo científico publicado en 2021

Mycobacterium tuberculosis

scholarly article published 2009

NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study

artículo científico publicado en 2022

Navigating the Phenotype Frontier: The Monarch Initiative

artículo científico publicado en 2016

Navigating the phenotype frontier: The Monarch Initiative

Novel function of complement C3d as an autologous helper T-cell target

artículo científico publicado en 2008

Ontology Development Kit: a toolkit for building, maintaining, and standardising biomedical ontologies

preprint published on 06 July 2022

Plain-language medical vocabulary for precision diagnosis.

artículo científico publicado en 2018

Prediction of immunogenicity: in silico paradigms, ex vivo and in vivo correlates

artículo científico publicado en 2008

Progress towards a genome-derived, epitope-driven vaccine for latent TB infection

scientific article published on October 2007

Representing glycophenotypes: semantic unification of glycobiology resources for disease discovery

scientific article published on 01 January 2019

Sharing Clinical and Genomic Data on Cancer - The Need for Global Solutions

artículo científico publicado en 2017

Sleep and circadian informatics data harmonization: a workshop report from the Sleep Research Society and Sleep Research Network

artículo científico publicado en 2022

The Human Phenotype Ontology in 2017

artículo científico publicado en 2016

The Human Phenotype Ontology in 2021

artículo científico publicado en 2020

The Human Phenotype Ontology in 2024: phenotypes around the world

artículo científico publicado en 2023

The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species

artículo científico publicado en 2020

The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species

The Monarch Initiative: Insights across species reveal human disease mechanisms

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

artículo científico publicado en 2017

The Ontology of Biological Attributes (OBA) - Computational Traits for the Life Sciences

The case for open science: rare diseases

artículo científico publicado en 2020

The landscape of nutri-informatics: a review of current resources and challenges for integrative nutrition research

Tularemia vaccines - an overview

artículo científico publicado en 2007

Uniform Resolution of Compact Identifiers for Biomedical Data

preprint

Uniform resolution of compact identifiers for biomedical data.

artículo científico publicado en 2018

Unifying the Identification of Biomedical Entities with the Bioregistry ⬇️

preprint published on 10 July 2022

Unifying the identification of biomedical entities with the Bioregistry ⬇️

artículo científico publicado en 2022

Lista de obras de Julie A. McMurry

A Census of Disease Ontologies

A Measure of Open Data: A Metric and Analysis of Reusable Data Practices in Biomedical Data Resources

A Simple Standard for Sharing Ontological Mappings (SSSOM)

A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease

A call to cellular & humoral arms: enlisting cognate T cell help to develop broad-spectrum vaccines against influenza A.

A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer

Activation of natural regulatory T cells by IgG Fc-derived peptide "Tregitopes"

An analysis and metric of reusable data licensing practices for biomedical resources

Analyzing Mycobacterium tuberculosis proteomes for candidate vaccine epitopes

Biolink Model: A Universal Schema for Knowledge Graphs in Clinical, Biomedical, and Translational Science ⬇️

Characterizing Long COVID: Deep Phenotype of a Complex Condition

Developing an epitope-driven tuberculosis (TB) vaccine

Diversity of Francisella tularensis Schu4 antigens recognized by T lymphocytes after natural infections in humans: Identification of candidate epitopes for inclusion in a rationally designed tularemia vaccine

Encoding Clinical Data with the Human Phenotype Ontology for Computational Differential Diagnostics

Epitope-based vaccination against pneumonic tularemia

Epitope-driven TB vaccine development: a streamlined approach using immuno-informatics, ELISpot assays, and HLA transgenic mice

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

Expression Atlas update--a database of gene and transcript expression from microarray- and sequencing-based functional genomics experiments

How many rare diseases are there?

Identification of genome-derived vaccine candidates conserved between human and mouse-adapted strains of H. pylori

Identification of immunogenic HLA-B7 "Achilles' heel" epitopes within highly conserved regions of HIV

Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data

Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data

Immuno-informatics: Mining genomes for vaccine components

Immunogenicity Screening Usingin Silico Methods: Correlation between T-Cell Epitope Content and Clinical Immunogenicity of Monoclonal Antibodies

In silico-accelerated identification of conserved and immunogenic variola/vaccinia T-cell epitopes.

Interpretable Clinical Genomics with a Likelihood Ratio Paradigm

Interpretable Clinical Genomics with a Likelihood Ratio Paradigm

Interpretable prioritization of splice variants in diagnostic next-generation sequencing

Mycobacterium tuberculosis

NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study

Navigating the Phenotype Frontier: The Monarch Initiative

Navigating the phenotype frontier: The Monarch Initiative

Novel function of complement C3d as an autologous helper T-cell target

Ontology Development Kit: a toolkit for building, maintaining, and standardising biomedical ontologies

Plain-language medical vocabulary for precision diagnosis.

Prediction of immunogenicity: in silico paradigms, ex vivo and in vivo correlates

Progress towards a genome-derived, epitope-driven vaccine for latent TB infection

Representing glycophenotypes: semantic unification of glycobiology resources for disease discovery

Sharing Clinical and Genomic Data on Cancer - The Need for Global Solutions

Sleep and circadian informatics data harmonization: a workshop report from the Sleep Research Society and Sleep Research Network

The Human Phenotype Ontology in 2017

The Human Phenotype Ontology in 2021

The Human Phenotype Ontology in 2024: phenotypes around the world

The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species

The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species

The Monarch Initiative: Insights across species reveal human disease mechanisms

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

The Ontology of Biological Attributes (OBA) - Computational Traits for the Life Sciences

The case for open science: rare diseases

The landscape of nutri-informatics: a review of current resources and challenges for integrative nutrition research

Tularemia vaccines - an overview

Uniform Resolution of Compact Identifiers for Biomedical Data

Uniform resolution of compact identifiers for biomedical data.

Unifying the Identification of Biomedical Entities with the Bioregistry ⬇️

Unifying the identification of biomedical entities with the Bioregistry ⬇️