Published in Nat Genet on July 27, 2015
High-throughput discovery of novel developmental phenotypes. Nature (2016) 1.10
Epigenetic germline inheritance of diet-induced obesity and insulin resistance. Nat Genet (2016) 0.96
Genetic Background Limits Generalizability of Genotype-Phenotype Relationships. Neuron (2016) 0.90
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat Genet (2017) 0.89
Beyond knockouts: the International Knockout Mouse Consortium delivers modular and evolving tools for investigating mammalian genes. Mamm Genome (2015) 0.82
A staging system for correct phenotype interpretation of mouse embryos harvested on embryonic day 14 (E14.5). J Anat (2017) 0.77
Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population. Genome Res (2016) 0.76
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations. G3 (Bethesda) (2016) 0.75
Integrating Genomic Data Sets for Knowledge Discovery: An Informed Approach to Management of Captive Endangered Species. Int J Genomics (2016) 0.75
Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction. BMC Cell Biol (2016) 0.75
The flora phenotype ontology (FLOPO): tool for integrating morphological traits and phenotypes of vascular plants. J Biomed Semantics (2016) 0.75
Rapid phenotyping of knockout mice to identify genetic determinants of bone strength. J Endocrinol (2016) 0.75
INFRAFRONTIER: a European resource for studying the functional basis of human disease. Mamm Genome (2016) 0.75
Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC. Dis Model Mech (2016) 0.75
Scaling up phenotyping studies. Nat Biotechnol (2015) 0.75
Genetic differential calculus. Nat Genet (2015) 0.75
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors. Nat Nanotechnol (2016) 0.75
Addressing reproducibility in single-laboratory phenotyping experiments. Nat Methods (2017) 0.75
From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health. Am J Hum Genet (2017) 0.75
Systematic screening for skin, hair, and nail abnormalities in a large-scale knockout mouse program. PLoS One (2017) 0.75
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nat Commun (2017) 0.75
Do Gametes Woo? Evidence for Their Nonrandom Union at Fertilization. Genetics (2017) 0.75
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis. Nat Genet (2017) 0.75
Measuring inconsistency in meta-analyses. BMJ (2003) 128.20
A conditional knockout resource for the genome-wide study of mouse gene function. Nature (2011) 9.93
Mendelian Inheritance in Man and its online version, OMIM. Am J Hum Genet (2007) 9.61
Ensembl 2015. Nucleic Acids Res (2014) 8.30
Characterising and predicting haploinsufficiency in the human genome. PLoS Genet (2010) 4.85
Agouti C57BL/6N embryonic stem cells for mouse genetic resources. Nat Methods (2009) 3.68
The pleiotropic structure of the genotype-phenotype map: the evolvability of complex organisms. Nat Rev Genet (2011) 3.57
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes. Cell (2013) 3.47
Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users. Hum Mutat (2012) 3.17
Understanding mammalian genetic systems: the challenge of phenotyping in the mouse. PLoS Genet (2006) 3.14
Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium. Dis Model Mech (2012) 2.73
EuroPhenome: a repository for high-throughput mouse phenotyping data. Nucleic Acids Res (2009) 2.72
EMPReSS: standardized phenotype screens for functional annotation of the mouse genome. Nat Genet (2005) 2.71
The Mouse Genome Database: integration of and access to knowledge about the laboratory mouse. Nucleic Acids Res (2013) 2.68
PhenomeNET: a whole-phenome approach to disease gene discovery. Nucleic Acids Res (2011) 2.67
EuroPhenome and EMPReSS: online mouse phenotyping resource. Nucleic Acids Res (2007) 2.54
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data. Nucleic Acids Res (2013) 2.20
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol (2013) 2.04
Introducing the German Mouse Clinic: open access platform for standardized phenotyping. Nat Methods (2005) 1.93
Rapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strength. PLoS Genet (2012) 1.64
The functional annotation of mammalian genomes: the challenge of phenotyping. Annu Rev Genet (2009) 1.54
GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies. Eur J Hum Genet (2013) 1.52
Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia. PLoS One (2012) 0.96
Functionally enigmatic genes: a case study of the brain ignorome. PLoS One (2014) 0.96
Laboratory mouse models for the human genome-wide associations. PLoS One (2010) 0.90
Applying the ARRIVE Guidelines to an In Vivo Database. PLoS Biol (2015) 0.89
Orthopaedic literature and MeSH. Clin Orthop Relat Res (2010) 0.89
EuroPhenome: a repository for high-throughput mouse phenotyping data. Nucleic Acids Res (2009) 2.72
High-throughput mouse phenotyping. Methods (2010) 0.94
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat Genet (2017) 0.89
Comparative visualization of genotype-phenotype relationships. Nat Methods (2015) 0.78
Lysosome-associated membrane glycoprotein 1 predicts fratricide amongst T cell receptor transgenic CD8+ T cells directed against tumor-associated antigens. Oncotarget (2016) 0.77
CIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes Infection. PLoS One (2016) 0.75
Genome-to-genome analysis highlights the effect of the human innate and adaptive immune systems on the hepatitis C virus. Nat Genet (2017) 0.75
Orthotopic T-cell receptor replacement in primary human T cells using CRISPR-Cas9-mediated homology-directed repair. STAR Protoc (2021) 0.75
Comparing two sequential Monte Carlo samplers for exact and approximate Bayesian inference on biological models. J R Soc Interface (2017) 0.75