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1.
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)
2.
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
3.
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)
4.
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)
5.
Simon, M.M.* et al.: A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 14:R82 (2013)
6.
Ayadi, A.* et al.: Mouse large-scale phenotyping initiatives: Overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute mouse genetics project. Mamm. Genome 23, 600-610 (2012)
7.
Hancock, J.M. et al.: Integration of mouse phenome data resources. Mamm. Genome 18, 157-163 (2007)