Lista de obras - Nicole Vasilevsky - Dominio Público Uruguay

A Simple Standard for Ontological Mappings 2022: Updates of data model and outlook ⬇️

Conference paper

A Simple Standard for Sharing Ontological Mappings (SSSOM)

artículo científico publicado en 2022

An open source knowledge graph ecosystem for the life sciences

artículo científico publicado en 2024

BOSC 2022: the first hybrid and 23rd annual Bioinformatics Open Source Conference

artículo científico publicado en 2022

Characterizing Long COVID: Deep Phenotype of a Complex Condition

artículo científico publicado en 2021

Community Approaches for Integrating Environmental Exposures into Human Models of Disease

artículo científico publicado en 2020

Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.

artículo científico publicado en 2015

Conference report: Biocuration 2021 Virtual Conference

artículo científico publicado en 2022

Curriculum Development of a Research Laboratory Methodology Course for Complementary and Integrative Medicine Students.

artículo científico publicado en 2015

Dealing with data: a case study on information and data management literacy

artículo científico publicado en 2012

Disease insights through cross-species phenotype comparisons

artículo científico publicado en 2015

Effect of impact factor and discipline on journal data sharing policies

Effects of Hydrastis Canadensis, Commiphora Habessinica, Phytolacca Americana, and Echinacea Purpurea on Bacterial Growth

artículo científico publicado en 2020

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

scientific article published on 01 September 2019

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

Extension of Roles in the ChEBI Ontology

artículo científico publicado en 2020

Gold-standard ontology-based anatomical annotation in the CRAFT Corpus

article

Guidelines for reporting single-cell RNA-seq experiments

artículo científico publicado en 2020

How many rare diseases are there?

artículo científico publicado en 2020

Is authorship sufficient for today's collaborative research? A call for contributor roles

artículo científico publicado en 2020

Mondo: Unifying diseases for the world, by the world

Navigating the Phenotype Frontier: The Monarch Initiative

artículo científico publicado en 2016

Navigating the phenotype frontier: The Monarch Initiative

OBO Foundry in 2021: operationalizing open data principles to evaluate ontologies

artículo científico publicado en 2021

OX40 engagement stabilizes Mxd4 and Mnt protein levels in antigen-stimulated T cells leading to an increase in cell survival

artículo científico publicado en 2011

On the reproducibility of science: unique identification of research resources in the biomedical literature

artículo científico publicado en 2013

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

preprint published on 06 July 2022

Ontology based molecular signatures for immune cell types via gene expression analysis

artículo científico publicado en 2013

Overview of the interactive task in BioCreative V

artículo científico publicado en 2016

Plain-language medical vocabulary for precision diagnosis.

artículo científico publicado en 2018

Registered report: A chromatin-mediated reversible drug-tolerant state in cancer cell subpopulations

artículo científico publicado en 2016

Representing glycophenotypes: semantic unification of glycobiology resources for disease discovery

scientific article published on 01 January 2019

Reproducibility and conflicts in immune epitope data

artículo científico publicado en 2015

Reproducible and reusable research: Are journal data sharing policies meeting the mark?

artículo científico publicado en 2016

Reproducible and reusable research: are journal data sharing policies meeting the mark?

artículo científico publicado en 2017

Research resources: curating the new eagle-i discovery system ⬇️

artículo científico publicado en 2012

Semantic Integration of Clinical Laboratory Tests from Electronic Health Records for Deep Phenotyping and Biomarker Discovery: Supplementary materials

article

Semantic integration of clinical laboratory tests from electronic health records for deep phenotyping and biomarker discovery

article

Significantly different clinical phenotypes associated with mutations in synthesis and transamidase+remodeling glycosylphosphatidylinositol (GPI)-anchor biosynthesis genes

artículo científico publicado en 2020

TMOD-19. GABRIELLA MILLER KIDS FIRST DATA RESOURCE CENTER: LARGE-SCALE HARMONIZED CLINICAL AND GENOMIC DATA PLATFORM TO SUPPORT CHILDHOOD CANCER AND STRUCTURAL BIRTH DEFECT RESEARCH

artículo científico publicado en 2019

Teaching data science fundamentals through realistic synthetic clinical cardiovascular data

scholarly article published 12 December 2017

The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability

artículo científico publicado en 2016

The First National Institutes of Health Institutional Training Program in Emergency Care Research: Productivity and Outcomes

article

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research

scientific article published on 21 November 2019

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 Human Phenotype Ontology: Semantic Unification of Common and Rare Disease

artículo científico publicado en 2015

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 Resource Identification Initiative: A Cultural Shift in Publishing

artículo científico publicado en 2016

The Resource Identification Initiative: A Cultural Shift in Publishing

artículo científico publicado en 2015

The Resource Identification Initiative: A cultural shift in publishing

artículo científico publicado en 2015

The Resource Identification Initiative: a cultural shift in publishing

artículo científico publicado en 2016

Lista de obras de Nicole Vasilevsky

A Simple Standard for Ontological Mappings 2022: Updates of data model and outlook ⬇️

A Simple Standard for Sharing Ontological Mappings (SSSOM)

An open source knowledge graph ecosystem for the life sciences

BOSC 2022: the first hybrid and 23rd annual Bioinformatics Open Source Conference

Characterizing Long COVID: Deep Phenotype of a Complex Condition

Community Approaches for Integrating Environmental Exposures into Human Models of Disease

Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.

Conference report: Biocuration 2021 Virtual Conference

Curriculum Development of a Research Laboratory Methodology Course for Complementary and Integrative Medicine Students.

Dealing with data: a case study on information and data management literacy

Disease insights through cross-species phenotype comparisons

Effect of impact factor and discipline on journal data sharing policies

Effects of Hydrastis Canadensis, Commiphora Habessinica, Phytolacca Americana, and Echinacea Purpurea on Bacterial Growth

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

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

Extension of Roles in the ChEBI Ontology

Gold-standard ontology-based anatomical annotation in the CRAFT Corpus

Guidelines for reporting single-cell RNA-seq experiments

How many rare diseases are there?

Is authorship sufficient for today's collaborative research? A call for contributor roles

Mondo: Unifying diseases for the world, by the world

Navigating the Phenotype Frontier: The Monarch Initiative

Navigating the phenotype frontier: The Monarch Initiative

OBO Foundry in 2021: operationalizing open data principles to evaluate ontologies

OX40 engagement stabilizes Mxd4 and Mnt protein levels in antigen-stimulated T cells leading to an increase in cell survival

On the reproducibility of science: unique identification of research resources in the biomedical literature

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

Ontology based molecular signatures for immune cell types via gene expression analysis

Overview of the interactive task in BioCreative V

Plain-language medical vocabulary for precision diagnosis.

Registered report: A chromatin-mediated reversible drug-tolerant state in cancer cell subpopulations

Representing glycophenotypes: semantic unification of glycobiology resources for disease discovery

Reproducibility and conflicts in immune epitope data

Reproducible and reusable research: Are journal data sharing policies meeting the mark?

Reproducible and reusable research: are journal data sharing policies meeting the mark?

Research resources: curating the new eagle-i discovery system ⬇️

Semantic Integration of Clinical Laboratory Tests from Electronic Health Records for Deep Phenotyping and Biomarker Discovery: Supplementary materials

Semantic integration of clinical laboratory tests from electronic health records for deep phenotyping and biomarker discovery

Significantly different clinical phenotypes associated with mutations in synthesis and transamidase+remodeling glycosylphosphatidylinositol (GPI)-anchor biosynthesis genes

TMOD-19. GABRIELLA MILLER KIDS FIRST DATA RESOURCE CENTER: LARGE-SCALE HARMONIZED CLINICAL AND GENOMIC DATA PLATFORM TO SUPPORT CHILDHOOD CANCER AND STRUCTURAL BIRTH DEFECT RESEARCH

Teaching data science fundamentals through realistic synthetic clinical cardiovascular data

The Cell Ontology 2016: enhanced content, modularization, and ontology interoperability

The First National Institutes of Health Institutional Training Program in Emergency Care Research: Productivity and Outcomes

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research

The Human Phenotype Ontology in 2017

The Human Phenotype Ontology in 2021

The Human Phenotype Ontology in 2024: phenotypes around the world

The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease

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 Resource Identification Initiative: A Cultural Shift in Publishing

The Resource Identification Initiative: A Cultural Shift in Publishing

The Resource Identification Initiative: A cultural shift in publishing

The Resource Identification Initiative: a cultural shift in publishing

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