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Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 16, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypesHeike Kollmus, Helmut Fuchs, Christoph Lengger, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2009
Systemic first-line phenotypingValérie Gailus-Durner, Helmut Fuchs, Thure Adler, et al.
Behavioural Brain Research|October 3, 2017
Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse ClinicHelmut Fuchs, Juan Antonio Aguilar-Pimentel, Oana V Amarie, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Plos One|June 16, 2012
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemJohn F Staropoli, Larissa Haliw, Sunita Biswas, et al.
EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
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.
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