MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search

VarElect: the phenotype-based variation prioritizer of the GeneCards Suite

(2016) Gil Stelzer et al.   BMC GENOMICS

Next generation sequencing: implications in personalized medicine and pharmacogenomics

(2016) Bahareh Rabbani et al.   Molecular BioSystems

Defining Glioblastoma Resectability Through the Wisdom of the Crowd

(2016) Adam M. Sonabend et al.   NEUROSURGERY

GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data

(2016) Shani Ben-Ari Fuchs et al.   OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY

A framework for identifying genotypic information from clinical records: exploiting integrated ontology structures to transfer annotations between ICD codes and Gene Ontologies

(2015) Seyedsasan Hashemikhabir et al.   IEEE-ACM Transactions on Computational Biology and Bioinformatics

Mouse Genome Informatics (MGI): reflecting on 25 years

(2015) Janan T. Eppig et al.   MAMMALIAN GENOME

DISEASES: Text mining and data integration of disease–gene associations

(2015) Sune Pletscher-Frankild et al.   METHODS

The UCSC Genome Browser database: 2016 update

(2015) Matthew L. Speir et al.   NUCLEIC ACIDS RESEARCH

ClinVar: public archive of interpretations of clinically relevant variants

(2015) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

PathCards: multi-source consolidation of human biological pathways

(2015) Frida Belinky et al.   Database-The Journal of Biological Databases and Curation

Database of RNA binding protein expression and disease dynamics (READ DB)

(2015) Seyedsasan Hashemikhabir et al.   Database-The Journal of Biological Databases and Curation

DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes

(2015) J. Pinero et al.   Database-The Journal of Biological Databases and Curation

Genetic Variations and Diseases in UniProtKB/Swiss-Prot: The Ins and Outs of Expert Manual Curation

(2014) Maria Livia Famiglietti et al.   HUMAN MUTATION

An overview of MetaMap: historical perspective and recent advances

(2014) Alan R Aronson et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

Next Generation Sequencing and the Future of Genetic Diagnosis

(2014) Katja Lohmann et al.   Neurotherapeutics

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

(2014) Simon A. Forbes et al.   NUCLEIC ACIDS RESEARCH

Disease Ontology 2015 update: an expanded and updated database of human diseases for linking biomedical knowledge through disease data

(2014) Warren A. Kibbe et al.   NUCLEIC ACIDS RESEARCH

Gene Ontology Consortium: going forward

(2014)   NUCLEIC ACIDS RESEARCH

OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders

(2014) Joanna S. Amberger et al.   NUCLEIC ACIDS RESEARCH

The Comparative Toxicogenomics Database's 10th year anniversary: update 2015

(2014) Allan Peter Davis et al.   NUCLEIC ACIDS RESEARCH

Human symptoms–disease network

(2014) XueZhong Zhou et al.   Nature Communications

Addiction and reward-related genes show altered expression in the postpartum nucleus accumbens

(2014) Changjiu Zhao et al.   Frontiers in Behavioral Neuroscience

An innovative portal for rare genetic diseases research: The semantic Diseasecard

(2013) Pedro Lopes et al.   JOURNAL OF BIOMEDICAL INFORMATICS

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

(2013) Sebastian Köhler et al.   NUCLEIC ACIDS RESEARCH

LifeMap Discovery™: The Embryonic Development, Stem Cells, and Regenerative Medicine Research Portal

(2013) Ron Edgar et al.   PLoS One

Orphanet et son réseau : où trouver une information validée sur les maladies rares

(2013) S. Maiella et al.   REVUE NEUROLOGIQUE

MalaCards: an integrated compendium for diseases and their annotation

(2013) Noa Rappaport et al.   Database-The Journal of Biological Databases and Curation

The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency

(2012) Wendy S. Rubinstein et al.   NUCLEIC ACIDS RESEARCH

GeneCards Version 3: the human gene integrator

(2010) M. Safran et al.   Database-The Journal of Biological Databases and Curation

GeneDecks: Paralog Hunting and Gene-Set Distillation with GeneCards Annotation

(2009) Gil Stelzer et al.   OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY

A Dynamic Network Approach for the Study of Human Phenotypes

(2009) César A. Hidalgo et al.   PLoS Computational Biology