Related references
Note: Only part of the references are listed.A Framework for Identifying Genotypic Information from Clinical Records: Exploiting Integrated Ontology Structures to Transfer Annotations between ICD Codes and Gene Ontologies
Seyedsasan Hashemikhabir et al.
IEEE-ACM TRANSACTIONS ON COMPUTATIONAL BIOLOGY AND BIOINFORMATICS (2018)
Defining Glioblastoma Resectability Through the Wisdom of the Crowd: A Proof-of-Principle Study
Adam M. Sonabend et al.
NEUROSURGERY (2017)
The UCSC Genome Browser database: 2016 update
Matthew L. Speir et al.
NUCLEIC ACIDS RESEARCH (2016)
ClinVar: public archive of interpretations of clinically relevant variants
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2016)
VarElect: the phenotype-based variation prioritizer of the GeneCards Suite
Gil Stelzer et al.
BMC GENOMICS (2016)
Next generation sequencing: implications in personalized medicine and pharmacogenomics
Bahareh Rabbani et al.
MOLECULAR BIOSYSTEMS (2016)
GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data
Shani Ben-Ari Fuchs et al.
OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY (2016)
Mouse Genome Informatics (MGI): reflecting on 25 years
Janan T. Eppig et al.
MAMMALIAN GENOME (2015)
DISEASES: Text mining and data integration of disease-gene associations
Sune Pletscher-Frankild et al.
METHODS (2015)
PathCards: multi-source consolidation of human biological pathways
Frida Belinky et al.
Database-The Journal of Biological Databases and Curation (2015)
Database of RNA binding protein expression and disease dynamics (READ DB)
Seyedsasan Hashemikhabir et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2015)
DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes
Janet Pinero et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2015)
COSMIC: exploring the world's knowledge of somatic mutations in human cancer
Simon A. Forbes et al.
NUCLEIC ACIDS RESEARCH (2015)
Disease Ontology 2015 update: an expanded and updated database of human diseases for linking biomedical knowledge through disease data
Warren A. Kibbe et al.
NUCLEIC ACIDS RESEARCH (2015)
Gene Ontology Consortium: going forward
J. A. Blake et al.
NUCLEIC ACIDS RESEARCH (2015)
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
Joanna S. Amberger et al.
NUCLEIC ACIDS RESEARCH (2015)
The Comparative Toxicogenomics Database's 10th year anniversary: update 2015
Allan Peter Davis et al.
NUCLEIC ACIDS RESEARCH (2015)
Genetic Variations and Diseases in UniProtKB/Swiss-Prot: The Ins and Outs of Expert Manual Curation
Maria Livia Famiglietti et al.
HUMAN MUTATION (2014)
Next Generation Sequencing and the Future of Genetic Diagnosis
Katja Lohmann et al.
NEUROTHERAPEUTICS (2014)
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
Sebastian Koehler et al.
NUCLEIC ACIDS RESEARCH (2014)
Human symptoms-disease network
XueZhong Zhou et al.
NATURE COMMUNICATIONS (2014)
Addiction and reward-related genes show altered expression in the postpartum nucleus accumbens
Changjiu Zhao et al.
FRONTIERS IN BEHAVIORAL NEUROSCIENCE (2014)
An innovative portal for rare genetic diseases research: The semantic Diseasecard
Pedro Lopes et al.
JOURNAL OF BIOMEDICAL INFORMATICS (2013)
The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency
Wendy S. Rubinstein et al.
NUCLEIC ACIDS RESEARCH (2013)
LifeMap Discovery™ : The Embryonic Development, Stem Cells, and Regenerative Medicine Research Portal
Ron Edgar et al.
PLOS ONE (2013)
Orphanet and its consortium: where to find expert-validated information on rare diseases
S. Maiella et al.
REVUE NEUROLOGIQUE (2013)
MalaCards: an integrated compendium for diseases and their annotation
Noa Rappaport et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2013)
An overview of MetaMap: historical perspective and recent advances
Alan R. Aronson et al.
JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION (2010)
GeneCards Version 3: the human gene integrator
Marilyn Safran et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2010)
GeneDecks: Paralog Hunting and Gene-Set Distillation with GeneCards Annotation
Gil Stelzer et al.
OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY (2009)
A Dynamic Network Approach for the Study of Human Phenotypes
Cesar A. Hidalgo et al.
PLOS COMPUTATIONAL BIOLOGY (2009)
Share Paper
