New models for human disease from the International Mouse Phenotyping Consortium

P Cacheiro, MA Haendel, D Smedley - Mammalian Genome, 2019 - Springer
Abstract The International Mouse Phenotyping Consortium (IMPC) continues to expand the
catalogue of mammalian gene function by conducting genome and phenome-wide …

Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium

SDM Brown, MW Moore - Disease models & mechanisms, 2012 - journals.biologists.com
Nearly 10 years after the completion of the human genome project, and the report of a
complete sequence of the mouse genome, it is salutary to reflect that we remain remarkably …

Mouse genetic and phenotypic resources for human genetics

PN Schofield, R Hoehndorf, GV Gkoutos - Human mutation, 2012 - Wiley Online Library
The use of model organisms to provide information on gene function has proved to be a
powerful approach to our understanding of both human disease and fundamental …

High-throughput mouse phenomics for characterizing mammalian gene function

SDM Brown, CC Holmes, AM Mallon… - Nature Reviews …, 2018 - nature.com
We are entering a new era of mouse phenomics, driven by large-scale and economical
generation of mouse mutants coupled with increasingly sophisticated and comprehensive …

The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data

G Koscielny, G Yaikhom, V Iyer, TF Meehan… - Nucleic acids …, 2014 - academic.oup.com
Abstract The International Mouse Phenotyping Consortium (IMPC) web portal (http://www.
mousephenotype. org) provides the biomedical community with a unified point of access to …

The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease

T Groza, FL Gomez, HH Mashhadi… - Nucleic acids …, 2023 - academic.oup.com
Abstract The International Mouse Phenotyping Consortium (IMPC; https://www.
mousephenotype. org/) web portal makes available curated, integrated and analysed …

Disease insights through cross-species phenotype comparisons

MA Haendel, N Vasilevsky, M Brush, HS Hochheiser… - Mammalian …, 2015 - Springer
New sequencing technologies have ushered in a new era for diagnosis and discovery of
new causative mutations for rare diseases. However, the sheer numbers of candidate …

The future of model organisms in human disease research

TJ Aitman, C Boone, GA Churchill… - Nature Reviews …, 2011 - nature.com
Abstract Model organisms have played a huge part in the history of studies of human genetic
disease, both in identifying disease genes and characterizing their normal and abnormal …

Mouse large-scale phenotyping initiatives: Overview of the European mouse disease clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics …

A Ayadi, MC Birling, J Bottomley, J Bussell, H Fuchs… - Mammalian …, 2012 - Springer
Two large-scale phenotyping efforts, the European Mouse Disease Clinic (EUMODIC) and
the Wellcome Trust Sanger Institute Mouse Genetics Project (SANGER-MGP), started during …

Mouse-based phenogenomics for modelling human disease

J Rossant, C McKerlie - Trends in molecular medicine, 2001 - cell.com
The powerful and wide-ranging genetic tools available in the laboratory mouse make it the
major experimental model for studying mammalian gene function in vivo and modelling …