Published in Wiley Interdiscip Rev Syst Biol Med on August 15, 2012
High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes. Bone Res (2014) 0.98
High-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice. Mamm Genome (2013) 0.90
Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach. Transgenic Res (2015) 0.76
A large and persistent carbon sink in the world's forests. Science (2011) 17.84
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes. Cell (2013) 3.47
The mammalian gene function resource: the International Knockout Mouse Consortium. Mamm Genome (2012) 2.65
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project. Mamm Genome (2012) 2.12
The evolution of the DLK1-DIO3 imprinted domain in mammals. PLoS Biol (2008) 2.05
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol (2013) 2.04
Rapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strength. PLoS Genet (2012) 1.64
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement. Nat Genet (2012) 1.34
Histopathology reveals correlative and unique phenotypes in a high-throughput mouse phenotyping screen. Dis Model Mech (2014) 1.30
Divalent cation transport and susceptibility to infectious and autoimmune disease: continuation of the Ity/Lsh/Bcg/Nramp1/Slc11a1 gene story. Immunol Lett (2003) 1.29
Fenton chemistry and oxidative stress mediate the toxicity of the beta-amyloid peptide in a Drosophila model of Alzheimer's disease. Eur J Neurosci (2009) 1.23
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice. Proc Natl Acad Sci U S A (2006) 1.22
The role of sphingosine-1-phosphate transporter Spns2 in immune system function. J Immunol (2012) 1.20
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins. J Gen Virol (2009) 1.16
Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome. Am J Hum Genet (2012) 1.13
Slc11a1, formerly Nramp1, is expressed in dendritic cells and influences major histocompatibility complex class II expression and antigen-presenting cell function. Infect Immun (2007) 1.11
Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome. PLoS Genet (2012) 1.06
The mouse genetics toolkit: revealing function and mechanism. Genome Biol (2011) 1.05
In vivo analysis of proteomes and interactomes using Parallel Affinity Capture (iPAC) coupled to mass spectrometry. Mol Cell Proteomics (2011) 1.05
Optimising experimental design for high-throughput phenotyping in mice: a case study. Mamm Genome (2010) 0.98
Molecular characterization of mutant mouse strains generated from the EUCOMM/KOMP-CSD ES cell resource. Mamm Genome (2013) 0.96
Recommendations on bioanalytical method stability implications of co-administered and co-formulated drugs by Global CRO Council for Bioanalysis (GCC). Bioanalysis (2012) 0.94
Impaired tissue growth is mediated by checkpoint kinase 1 (CHK1) in the integrated stress response. J Cell Sci (2010) 0.92
Mcph1-deficient mice reveal a role for MCPH1 in otitis media. PLoS One (2013) 0.90
High-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice. Mamm Genome (2013) 0.90
Recommendations on: internal standard criteria, stability, incurred sample reanalysis and recent 483s by the Global CRO Council for Bioanalysis. Bioanalysis (2011) 0.89
The fallacy of ratio correction to address confounding factors. Lab Anim (2012) 0.86
Influence of Slc11a1 (formerly Nramp1) on DSS-induced colitis in mice. J Leukoc Biol (2008) 0.84
Experimental and husbandry procedures as potential modifiers of the results of phenotyping tests. Physiol Behav (2012) 0.82
Candidate gene association study of solute carrier family 11a members 1 (SLC11A1) and 2 (SLC11A2) genes in Alzheimer's disease. Neurosci Lett (2005) 0.81
Modeling partial monosomy for human chromosome 21q11.2-q21.1 reveals haploinsufficient genes influencing behavior and fat deposition. PLoS One (2012) 0.80
Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase. Transgenic Res (2013) 0.79
Generation of the Sotos syndrome deletion in mice. Mamm Genome (2012) 0.79
Genomic analysis of a novel spontaneous albino C57BL/6N mouse strain. Genesis (2013) 0.78
2013 White Paper on recent issues in bioanalysis: 'hybrid'--the best of LBA and LCMS. Bioanalysis (2013) 0.78
Recommendations on the interpretation of the new European Medicines Agency Guideline on Bioanalytical Method Validation by Global CRO Council for Bioanalysis (GCC). Bioanalysis (2012) 0.78
Efficacy of plasma phospholipid removal during sample preparation and subsequent retention under typical UHPLC conditions. Bioanalysis (2012) 0.78
The Bangladesh Risk of Acute Vascular Events (BRAVE) Study: objectives and design. Eur J Epidemiol (2015) 0.77
Comparative analysis of two slc11 (Nramp) loci in Takifugu rubripes. DNA Cell Biol (2004) 0.76
Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1. Mamm Genome (2012) 0.75
7th GCC Insights: incurred samples use; fit-for-purpose validation, solution stability, electronic laboratory notebook and hyperlipidemic matrix testing. Bioanalysis (2014) 0.75
Conference report: the 3rd Global CRO Council for Bioanalysis at the International Reid Bioanalytical Forum. Bioanalysis (2011) 0.75
Recommendations on ISR in multi analyte assays, QA/bioanalytical consultants and GCP by Global CRO Council for Bioanalysis (GCC). Bioanalysis (2012) 0.75
Recommendations on incurred sample stability (ISS) by GCC. Bioanalysis (2014) 0.75