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.

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.

(2023) , Nucleic Acids Res , 51 , D1038-D1045


PMID: 36305825

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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.

(2023) , BMC Biol , 21 , 22



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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.

(2023) , Mamm Genome , 34 , 180-199



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Mendelian gene identification through mouse embryo viability screening

Cacheiro, P., Westerberg, C. H., Mager, J., Dickinson, M. E., Nutter, L. M. J., Muñoz-Fuentes, V., Hsu, C. W., Van den Veyver, I. B., Flenniken, A. M., McKerlie, C., Murray, S. A., Teboul, L., Heaney, J. D., Lloyd, K. C. K., Lanoue, L., Braun, R. E., White, J. K., Creighton, A. K., Laurin, V., Guo, R., Qu, D., Wells, S., Cleak, J., Bunton-Stasyshyn, R., Stewart, M., Harrisson, J., Mason, J., Haseli Mashhadi, H., Parkinson, H., Mallon, A. M., Smedley, D.

(2022) , Genome Med , 14 , 119



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Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

Spielmann, S, Miller, G., Oprea, T.I., et al.

(2022) , Nat Cardiovasc Res , 1 , 157-173


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