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Methods (San Diego, Calif.)|August 17, 2010
Mouse phenotypingHelmut Fuchs, Valérie Gailus-Durner, Thure Adler, et al.G3 (Bethesda, Md.)|November 6, 2016
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic AlterationsHelmut Fuchs, Sibylle Sabrautzki, Gerhard K H Przemeck, et al.Cell|June 4, 2009
A humanized version of Foxp2 affects cortico-basal ganglia circuits in miceWolfgang Enard, Sabine Gehre, Kurt Hammerschmidt, et al.Nature Communications|November 12, 2022
Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J miceKan Xie, Helmut Fuchs, Enzo Scifo, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 29, 2012
Innovations in phenotyping of mouse models in the German Mouse ClinicHelmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, et al.Genome Biology|August 2, 2013
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strainsMichelle M Simon, Simon Greenaway, Jacqueline K White, et al.Plos Genetics|December 28, 2020
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral densityAnna L Swan, Christine Schütt, Jan Rozman, et al.Bioinformatics (Oxford, England)|October 9, 2019
Soft windowing application to improve analysis of high-throughput phenotyping dataHamed Haselimashhadi, Jeremy C Mason, Violeta Munoz-Fuentes, et al.American Journal of Human Genetics|July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth diseaseDaniel G Calame, Tianyu Guo, Chen Wang, et al.Nature Genetics|July 28, 2015
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinicsMartin Hrabě de Angelis, George Nicholson, Mohammed Selloum, et al.Pageof 10