PuSH - Publication Server of Helmholtz Zentrum München

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1.
Rozman, J. et al.: Identification of genetic elements in metabolism by high-throughput mouse phenotyping.   Nat. Commun. 9:288 (2018)
2.
Bowl, M.R.* et al.: A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nat. Commun. 8:886 (2017)
3.
Dickinson, M.E.* et al.: Corrigendum: High-throughput discovery of novel developmental phenotypes. Nature 551, 398 (2017)
4.
Meehan, T.F.* et al.: Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat. Genet. 49, 1231-1238 (2017)
5.
Dickinson, M.E.* et al.: High-throughput discovery of novel developmental phenotypes. Nature 537, 508-514 (2016)
6.
Hrabě de Angelis, M. et al.: Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat. Genet. 47, 969-978 (2015)
7.
Karp, N.A.* et al.: Applying the ARRIVE guidelines to an in vivo database. PLoS Biol. 13:e1002151 (2015)
8.
Simon, M.M.* et al.: A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 14:R82 (2013)
9.
Bradley, A.* et al.: The mammalian gene function resource: The International Knockout Mouse Consortium. Mamm. Genome 23, 580-586 (2012)
10.
Wilkinson, P.* et al.: EMMA - mouse mutant resources for the international scientific community. Nucleic Acids Res. 38, D570-D576 (2010)