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Mouse Genome Database (MGD)-2018: knowledgebase for the laboratory mouse
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00335-012-9414-2openalex-snapshot
The diversity outbred mouse population
inferredcites →https://doi.org/10.1007/s00335-012-9421-3openalex-snapshot
The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data
inferredcites →https://doi.org/10.1007/s00335-012-9422-2openalex-snapshot
The mammalian gene function resource: the international knockout mouse consortium
inferredcites →https://doi.org/10.1007/s00335-015-9573-zopenalex-snapshot
MouseMine: a new data warehouse for MGI
inferredcites →https://doi.org/10.1007/s00335-015-9576-9openalex-snapshot
The Disease Ontology: fostering interoperability between biological and clinical human disease-related data
inferredcites →https://doi.org/10.1007/s00335-015-9598-3openalex-snapshot
Beyond knockouts: the International Knockout Mouse Consortium delivers modular and evolving tools for investigating mammalian genes
inferredcites →https://doi.org/10.1007/s00335-015-9599-2openalex-snapshot
A mouse informatics platform for phenotypic and translational discovery
inferredcites →https://doi.org/10.1007/s00335-015-9600-0openalex-snapshot
The International Mouse Strain Resource (IMSR): cataloging worldwide mouse and ES cell line resources
inferredcites →https://doi.org/10.1016/j.bcmd.2012.09.004openalex-snapshot
ENU mutagenesis identifies the first mouse mutants reproducing human β-thalassemia at the genomic level
inferredcites →https://doi.org/10.1038/nature14269openalex-snapshot
Global genetic analysis in mice unveils central role for cilia in congenital heart disease
inferredcites →https://doi.org/10.1093/cercor/bht209openalex-snapshot
A Forward Genetic Screen in Mice Identifies Mutants with Abnormal Cortical Patterning
inferredcites →https://doi.org/10.1093/nar/gku1179openalex-snapshot
Gene Ontology Consortium: going forward
inferredcites →https://doi.org/10.1093/nar/gku1205openalex-snapshot
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
inferredcites →https://doi.org/10.1093/nar/gku967openalex-snapshot
The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease
inferredcites →https://doi.org/10.1093/nar/gku987openalex-snapshot
Mouse Tumor Biology (MTB): a database of mouse models for human cancer
inferredcites →https://doi.org/10.1093/nar/gkw1039openalex-snapshot
The Human Phenotype Ontology in 2017
inferredcites →https://doi.org/10.1093/nar/gkw1040openalex-snapshot
Mouse Genome Database (MGD)-2017: community knowledge resource for the laboratory mouse
inferredcites →https://doi.org/10.1093/nar/gkw1073openalex-snapshot
The mouse Gene Expression Database (GXD): 2017 update
inferredcites →https://doi.org/10.1186/gb-2013-14-9-r96openalex-snapshot
An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouse
inferredcites →https://doi.org/10.1242/dmm.011957openalex-snapshot
Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice
inferredcites →https://doi.org/10.1534/genetics.111.138032openalex-snapshot
Ten Years of the Collaborative Cross
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The role of epigenetic modifications in neurodevelopmental disorders: A systematic review
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Biallelic TMEM72 Variants in Patients with a Nephronophthisis-Like Phenotype
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An Evolutionary Based Strategy for Predicting Rational Mutations in G Protein-Coupled Receptors
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Genome-wide association analysis reveals QTL and candidate mutations involved in white spotting in cattle
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A unified nomenclature for vertebrate olfactory receptors
inferred← citeshttps://doi.org/10.1186/s12864-020-07016-9openalex-snapshot
Expression profiling of WD40 family genes including DDB1- and CUL4- associated factor (DCAF) genes in mice and human suggests important regulatory roles in testicular development and spermatogenesis
inferred← citeshttps://doi.org/10.1186/s12864-020-6496-1openalex-snapshot
Functional and population genetic features of copy number variations in two dairy cattle populations
inferred← citeshttps://doi.org/10.1186/s12864-020-6583-3openalex-snapshot
Expert curation of the human and mouse olfactory receptor gene repertoires identifies conserved coding regions split across two exons
inferred← citeshttps://doi.org/10.1186/s12915-020-00826-zopenalex-snapshot
Large-scale discovery of male reproductive tract-specific genes through analysis of RNA-seq datasets
inferred← citeshttps://doi.org/10.1186/s12915-025-02279-8openalex-snapshot
Multi-dimensional annotation of porcine variants using genomic and epigenomic features in pigs
inferred← citeshttps://doi.org/10.1186/s13041-020-00706-1openalex-snapshot
Identification of FMRP target mRNAs in the developmental brain: FMRP might coordinate Ras/MAPK, Wnt/β-catenin, and mTOR signaling during corticogenesis
inferred← citeshttps://doi.org/10.1186/s13046-020-01673-0openalex-snapshot
CREB5 promotes invasiveness and metastasis in colorectal cancer by directly activating MET
inferred← citeshttps://doi.org/10.1186/s13059-018-1490-5openalex-snapshot
A comparative study of endoderm differentiation in humans and chimpanzees
inferred← citeshttps://doi.org/10.1186/s13073-020-00738-1openalex-snapshot
EM-mosaic detects mosaic point mutations that contribute to congenital heart disease
inferred← citeshttps://doi.org/10.1186/s13100-019-0157-4openalex-snapshot
Mouse germ line mutations due to retrotransposon insertions
inferred← citeshttps://doi.org/10.1186/s40246-019-0232-4openalex-snapshot
Three miRNAs cooperate with host genes involved in human cardiovascular disease
inferred← citeshttps://doi.org/10.1186/s40959-025-00349-yopenalex-snapshot
Unraveling the genetic blueprint of doxorubicin-induced cardiotoxicity through systems genetics approaches
inferred← citeshttps://doi.org/10.1242/dmm.042317openalex-snapshot
Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility
inferred← citeshttps://doi.org/10.1242/dmm.047225openalex-snapshot
Hearing impairment due to Mir183/96/182 mutations suggests both loss-of-function and gain-of-function effects
inferred← citeshttps://doi.org/10.1242/jcs.243519openalex-snapshot
Squaring the EMC – how promoting membrane protein biogenesis impacts cellular functions and organismal homeostasis
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1006790openalex-snapshot
Apollo: Democratizing genome annotation
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007879openalex-snapshot
An interaction-based model for neuropsychiatric features of copy-number variants
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008855openalex-snapshot
Estimation of non-null SNP effect size distributions enables the detection of enriched genes underlying complex traits
inferred← citeshttps://doi.org/10.1371/journal.pone.0214526openalex-snapshot
Bacterial translocation in acute lymphocytic leukemia
inferred← citeshttps://doi.org/10.1371/journal.pone.0221402openalex-snapshot
Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model
inferred← citeshttps://doi.org/10.14806/ej.26.a.953openalex-snapshot
In silico characterisation of the gene repertoires of immunoglobulins and T cell receptors of the various inbred laboratory strains of Mus musculus
inferred← citeshttps://doi.org/10.14814/phy2.14251openalex-snapshot
Sex effects of dietary protein source and acid load on renal and bone status in the Pah enu2 mouse model of phenylketonuria
inferred← citeshttps://doi.org/10.1515/hsz-2019-0149openalex-snapshot
The microtubule skeleton and the evolution of neuronal complexity in vertebrates
inferred← citeshttps://doi.org/10.1515/jib-2018-0069openalex-snapshot
A Survey of Gene Prioritization Tools for Mendelian and Complex Human Diseases
inferred← citeshttps://doi.org/10.1530/joe-23-0341openalex-snapshot
Interplay between caveolin-1 and mineralocorticoid receptor in cardiometabolic disease
inferred← citeshttps://doi.org/10.1534/g3.119.400729openalex-snapshot
Regeneration Rosetta: An Interactive Web Application To Explore Regeneration-Associated Gene Expression and Chromatin Accessibility
inferred← citeshttps://doi.org/10.15835/buasvmcn-agr:5171openalex-snapshot
Old Principles – New Methods in the Volatile Oils Approach
inferred← citeshttps://doi.org/10.18174/566496openalex-snapshot
Structural variants in the bovine genome
inferred← citeshttps://doi.org/10.2174/0929867325666180530100332openalex-snapshot
Computational Drug Repurposing: Current Trends
inferred← citeshttps://doi.org/10.3384/diss.diva-152259openalex-snapshot
Identification of candidate genes involved in Mercury Toxicokinetics and Mercury Induced Autoimmunity
inferred← citeshttps://doi.org/10.3389/fbioe.2020.00035openalex-snapshot
Dynamic Alternative Splicing During Mouse Preimplantation Embryo Development
inferred← citeshttps://doi.org/10.3389/fcell.2020.00061openalex-snapshot
Toward Development of the Male Pill: A Decade of Potential Non-hormonal Contraceptive Targets
inferred← citeshttps://doi.org/10.3389/fcvm.2023.1089963openalex-snapshot
Cardiac copper content and its relationship with heart physiology: Insights based on quantitative genetic and functional analyses using BXD family mice
inferred← citeshttps://doi.org/10.3389/fendo.2019.00277openalex-snapshot
Mouse Models and Online Resources for Functional Analysis of Osteoporosis Genome-Wide Association Studies
inferred← citeshttps://doi.org/10.3389/fgene.2021.674295openalex-snapshot
Strategies to Uplift Novel Mendelian Gene Discovery for Improved Clinical Outcomes
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00405openalex-snapshot
Transcriptomic Analysis of Monocyte-Derived Non-Phagocytic Macrophages Favors a Role in Limiting Tissue Repair and Fibrosis
inferred← citeshttps://doi.org/10.3389/fmicb.2019.00355openalex-snapshot
Metabolic Regulators Nampt and Sirt6 Serially Participate in the Macrophage Interferon Antiviral Cascade
inferred← citeshttps://doi.org/10.3389/fnagi.2026.1737003openalex-snapshot
Identification of CTHRC1 as a novel candidate for neurodevelopmental disorders
inferred← citeshttps://doi.org/10.3389/fnins.2018.00706openalex-snapshot
Comparing Adult Hippocampal Neurogenesis Across Species: Translating Time to Predict the Tempo in Humans
inferred← citeshttps://doi.org/10.3389/fonc.2018.00268openalex-snapshot
Transgenic Mouse Models in Cancer Research
inferred← citeshttps://doi.org/10.3389/fvets.2022.832633openalex-snapshot
Runs of Homozygosity Uncover Potential Functional-Altering Mutation Associated With Body Weight and Length in Two Duroc Pig Lines
inferred← citeshttps://doi.org/10.3390/cancers11101510openalex-snapshot
Validation of Hepatocellular Carcinoma Experimental Models for TGF-β Promoting Tumor Progression
inferred← citeshttps://doi.org/10.3390/cells14161240openalex-snapshot
CREB5 Promotes the Proliferation of Neural Stem/Progenitor Cells in the Rat Subventricular Zone via the Regulation of NFIX Expression
inferred← citeshttps://doi.org/10.3390/cells8060629openalex-snapshot
mTOR Signaling Pathway Regulates Sperm Quality in Older Men
inferred← citeshttps://doi.org/10.3390/cells9020351openalex-snapshot
A20 Promotes Ripoptosome Formation and TNF-Induced Apoptosis via cIAPs Regulation and NIK Stabilization in Keratinocytes
inferred← citeshttps://doi.org/10.3390/genes11040460openalex-snapshot
An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data
inferred← citeshttps://doi.org/10.3390/genes11080943openalex-snapshot
Distinct Alteration of Gene Expression Programs in the Small Intestine of Male and Female Mice in Response to Ablation of Intestinal Fabp Genes
inferred← citeshttps://doi.org/10.3390/genes11101148openalex-snapshot
Multiple Isolated Transcription Factors Act as Switches and Contribute to Species Uniqueness
inferred← citeshttps://doi.org/10.3390/genes13091667openalex-snapshot
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
inferred← citeshttps://doi.org/10.3390/genes15010053openalex-snapshot
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach
inferred← citeshttps://doi.org/10.3390/genes16050605openalex-snapshot
Systems Genetics Reveals the Gene Regulatory Mechanisms of Arrb2 in the Development of Autism Spectrum Disorders
inferred← citeshttps://doi.org/10.3390/genes16101139openalex-snapshot
Atad1 Is a Potential Candidate Gene for Prepulse Inhibition
inferred← citeshttps://doi.org/10.3390/ijms20030617openalex-snapshot
Mechanisms of Developmental Toxicity of Dioxins and Related Compounds
inferred← citeshttps://doi.org/10.3390/ijms23179720openalex-snapshot
Massive Loss of Transcription Factors Promotes the Initial Diversification of Placental Mammals
inferred← citeshttps://doi.org/10.3390/ijms241814293openalex-snapshot
The Mechanisms and Efficacy of Photobiomodulation Therapy for Arthritis: A Comprehensive Review
inferred← citeshttps://doi.org/10.3390/jcdd10090393openalex-snapshot
Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways
inferred← citeshttps://doi.org/10.3410/f.734885428.793557347openalex-snapshot
Faculty Opinions recommendation of Standing genetic variation as the predominant source for adaptation of a songbird.
inferred← citeshttps://doi.org/10.3410/f.736054359.793562930openalex-snapshot
Faculty Opinions recommendation of Nrf2 activation promotes lung cancer metastasis by inhibiting the degradation of bach1.
inferred← citeshttps://doi.org/10.3892/ije.2021.9openalex-snapshot
TFBSPred: A functional transcription factor binding site prediction webtool for humans and mice
inferred← citeshttps://doi.org/10.3892/mmr.2018.9477openalex-snapshot
Network analysis of membranous glomerulonephritis based on metabolomics data
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