Related references
Note: Only part of the references are listed.The Comparative Toxicogenomics Database: update 2013
Allan Peter Davis et al.
NUCLEIC ACIDS RESEARCH (2013)
Discovering disease-disease associations by fusing systems-level molecular data
Marinka Zitnik et al.
SCIENTIFIC REPORTS (2013)
Information Flow in Interaction Networks II: Channels, Path Lengths, and Potentials
Aleksandar Stojmirovic et al.
JOURNAL OF COMPUTATIONAL BIOLOGY (2012)
Disease Ontology: a backbone for disease semantic integration
Lynn Marie Schriml et al.
NUCLEIC ACIDS RESEARCH (2012)
MEDIC: a practical disease vocabulary used at the Comparative Toxicogenomics Database
Allan Peter Davis et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2012)
Viral Perturbations of Host Networks Reflect Disease Etiology
Natali Gulbahce et al.
PLOS COMPUTATIONAL BIOLOGY (2012)
The expanded human disease network combining protein-protein interaction information
Xuehong Zhang et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
A New Face and New Challenges for Online Mendelian Inheritance in Man (OMIM®)
Joanna Amberger et al.
HUMAN MUTATION (2011)
Identification of ADAMTS18 as a gene mutated in Knobloch syndrome
Mohammed A. Aldahmesh et al.
JOURNAL OF MEDICAL GENETICS (2011)
Network medicine: a network-based approach to human disease
Albert-Laszlo Barabasi et al.
NATURE REVIEWS GENETICS (2011)
Neural Systems Governed by Nicotinic Acetylcholine Receptors: Emerging Hypotheses
Julie M. Miwa et al.
NEURON (2011)
Gene-Disease Network Analysis Reveals Functional Modules in Mendelian, Complex and Environmental Diseases
Anna Bauer-Mehren et al.
PLOS ONE (2011)
ppiTrim: constructing non-redundant and up-to-date interactomes
Aleksandar Stojmirovic et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2011)
Robust and accurate data enrichment statistics via distribution function of sum of weights
Aleksandar Stojmirovic et al.
BIOINFORMATICS (2010)
Genome-wide inferring gene-phenotype relationship by walking on the heterogeneous network
Yongjin Li et al.
BIOINFORMATICS (2010)
Network-Based Elucidation of Human Disease Similarities Reveals Common Functional Modules Enriched for Pluripotent Drug Targets
Silpa Suthram et al.
PLOS COMPUTATIONAL BIOLOGY (2010)
Myopathy and Polyneuropathy in an Adolescent With the Kyphoscoliotic Type of Ehlers-Danlos Syndrome
N. C. Voermans et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
A Dynamic Network Approach for the Study of Human Phenotypes
Cesar A. Hidalgo et al.
PLOS COMPUTATIONAL BIOLOGY (2009)
Genome-wide prioritization of disease genes and identification of disease-disease associations from an integrated human functional linkage network
Bolan Linghu et al.
GENOME BIOLOGY (2009)
iRefIndex: A consolidated protein interaction database with provenance
Sabry Razick et al.
BMC BIOINFORMATICS (2008)
The implications of human metabolic network topology for disease comorbidity
D. -S. Lee et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Information flow in interaction networks
Aleksandar Stojmircivic et al.
JOURNAL OF COMPUTATIONAL BIOLOGY (2007)
Weighted network modules
Illes J. Farkas et al.
NEW JOURNAL OF PHYSICS (2007)
The human disease network
Kwang-Il Goh et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Activating mutations in the ABCC8 gene in neonatal diabetes mellitus
Andrey P. Babenko et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production
Orchidee Filipe-Santos et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2006)
A text-mining analysis of the human phenome
MA van Driel et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Uncovering the overlapping community structure of complex networks in nature and society
G Palla et al.
NATURE (2005)
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q
C Toomes et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating
M Bienengraeber et al.
NATURE GENETICS (2004)
Human nuclear factor κB essential modulator mutation can result in immunodeficiency without ectodermal dysplasia
JS Orange et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2004)
Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone- shaped epiphyses in hands and hips
J Hellemans et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Pathways and consequences:: Hedgehog signaling in human disease
JL Mullor et al.
TRENDS IN CELL BIOLOGY (2002)
High bone density due to a mutation in LDL-receptor-related protein 5
LM Boyden et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development
YQ Gong et al.
CELL (2001)
Technical milestone - Medical subject headings used to search the biomedical literature
MH Coletti et al.
JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION (2001)
KEGG: Kyoto Encyclopedia of Genes and Genomes
M Kanehisa et al.
NUCLEIC ACIDS RESEARCH (2000)