Consortium Papers
Publications detailing the collaborative efforts of the MLC with international consortia involved in the targeted construction and phenotyping of mutant mouse lines, as well as the archiving and distribution of mouse disease models and disease gene discovery. These include the IMPC, EUMODIC and INFRAFRONTIER.
Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)
Ellwanger, K., Brill, J. A., de Boer, E., Efthymiou, S., Elgersma, Y., Icmat, M., Lecoquierre, F., Lobato, A. G., Morleo, M., Ori, M., Schaffer, A. E., Vitobello, A., Wells, S., Yalcin, B., Zhai, R. G., Sturm, M., Zurek, B., Graessner, H., Bermejo-Sánchez, E., Evangelista, T., Hoogerbrugge, N., Nigro, V., Schüle, R., Verloes, A., Brunner, H., Campeau, P. M., Lasko, P., Riess, O.
Improving laboratory animal genetic reporting: LAG-R guidelines
Teboul, L., Amos-Landgraf, J., Benavides, F. J., Birling, M. C., Brown, S. D. M., Bryda, E., Bunton-Stasyshyn, R., Chin, H. J., Crispo, M., Delerue, F., Dobbie, M., Franklin, C. L., Fuchtbauer, E. M., Gao, X., Golzio, C., Haffner, R., Hérault, Y., Hrabe de Angelis, M., Lloyd, K. C. K., Magnuson, T. R., Montoliu, L., Murray, S. A., Nam, K. H., Nutter, L. M. J., Pailhoux, E., Pardo Manuel de Villena, F., Peterson, K., Reinholdt, L., Sedlacek, R., Seong, J. K., Shiroishi, T., Smith, C., Takeo, T., Tinsley, L., Vilotte, J. L., Warming, S., Wells, S., Whitelaw, C. B., Yoshiki, A., Asian Mouse Mutagenesis Resource Assocation, CELPHEDIA infrastructure, INFRAFRONTIER consortium, International Mammalian Genome Society, International Mouse Phenotyping Consortium, International Society for Transgenic Technologies, Mutant Mouse Resource and Research Centers, Phenomics Australia, RRRC- Rat Resource and Research Center, Pavlovic, G.
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease
Groza, T., Gomez, F. L., Mashhadi, H. H., Muñoz-Fuentes, V., Gunes, O., Wilson, R., Cacheiro, P., Frost, A., Keskivali-Bond, P., Vardal, B., McCoy, A., Cheng, T. K., Santos, L., Wells, S., Smedley, D., Mallon, A. M., Parkinson, H.
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
Chee, J. M., Lanoue, L., Clary, D., Higgins, K., Bower, L., Flenniken, A., Guo, R., Adams, D. J., Bosch, F., Braun, R. E., Brown, S. D. M., Chin, H. G., Dickinson, M. E., Hsu, C. W., Dobbie, M., Gao, X., Galande, S., Grobler, A., Heaney, J. D., Herault, Y., de Angelis, M. H., Mammano, F., Nutter, L. M. J., Parkinson, H., Qin, C., Shiroishi, T., Sedlacek, R., Seong, J. K., Xu, Y., Brooks, B., McKerlie, C., Lloyd, K. C. K., Westerberg, H., Moshiri, A.
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice
Oestereicher, M. A., Wotton, J. M., Ayabe, S., Bou About, G., Cheng, T. K., Choi, J. H., Clary, D., Dew, E. M., Elfertak, L., Guimond, A., Haseli Mashhadi, H., Heaney, J. D., Kelsey, L., Keskivali-Bond, P., Lopez Gomez, F., Marschall, S., McFarland, M., Meziane, H., Munoz Fuentes, V., Nam, K. H., Nichtová, Z., Pimm, D., Bower, L., Prochazka, J., Rozman, J., Santos, L., Stewart, M., Tanaka, N., Ward, C. S., Willett, A. M. E., Wilson, R., Braun, R. E., Dickinson, M. E., Flenniken, A. M., Herault, Y., Lloyd, K. C. K., Mallon, A. M., McKerlie, C., Murray, S. A., Nutter, L. M. J., Sedlacek, R., Seong, J. K., Sorg, T., Tamura, M., Wells, S., Schneltzer, E., Fuchs, H., Gailus-Durner, V., Hrabe de Angelis, M., White, J. K., Spielmann, N.