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1.
Hölter, S.M. ; Garrett, L. ; Bludau, S.* & Amunts, K.*: Digital tools of analysis and data integration facilitate synergy between mouse and human brain research and enable translation. Mamm. Genome, DOI: 10.1007/s00335-024-10072-1 (2024)
2.
Ali Khan, A. et al.: INFRAFRONTIER: Mouse model resources for modelling human diseases. Mamm. Genome 34, 408-417 (2023)
3.
Bukas, C. et al.: Echo2Pheno: A deep-learning application to uncover echocardiographic phenotypes in conscious mice. Mamm. Genome 34, 200-215 (2023)
4.
da Silva Buttkus, P. et al.: Knockout mouse models as a resource for the study of rare diseases. Mamm. Genome 34, 244-261 (2023)
5.
Kottmann, P.* et al.: EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease. Mamm. Genome 34, 285-297 (2023)
6.
Lindovsky, J.* et al.: A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice. Mamm. Genome 34, 107-122 (2023)
7.
Oestereicher, M.A. et al.: Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice. Mamm. Genome 34, 180-199 (2023)
8.
Rozman, J.* ; Yang, Z.* & Spielmann, N.: Introduction to Mammalian Genome special issue: Cardiovascular disease in the Mammalian Genome. Mamm. Genome 34, 105-106 (2023)
9.
Garrett, L. et al.: A rationale for considering heart/brain axis control in neuropsychiatric disease. Mamm. Genome 34, 331-350 (2022)
10.
Spielmann, N. et al.: Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction. Mamm. Genome 34, 229-243 (2022)
11.
Biagosch, C. et al.: A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse. Mamm. Genome 32, 332-349 (2021)
12.
Ehlich, H.* et al.: INFRAFRONTIER quality principles in systemic phenotyping. Mamm. Genome, DOI: 10.1007/s00335-021-09892-2 (2021)
13.
Beckers, J. ; Teperino, R. ; Hérault, Y.* & Hrabě de Angelis, M.: Introduction to mammalian genome special issue: Epigenetics. Mamm. Genome, DOI: 10.1007/s00335-020-09843-3 (2020)
14.
Kamies, R. & Martinez Jimenez, C.P.: Advances of single-cell genomics and epigenomics in human disease: Where are we now? Mamm. Genome 31, 170-180 (2020)
15.
Kaspar, D. ; Hastreiter, S. ; Irmler, M. ; Hrabě de Angelis, M. & Beckers, J.: Nutrition and its role in epigenetic inheritance of obesity and diabetes across generations. Mamm. Genome 31, 119–133 (2020)
16.
Kollmus, H.* et al.: A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes. Mamm. Genome 31, 30-48 (2020)
17.
Ruberte, J.* et al.: PATHBIO: An international training program for precision mouse phenotyping. Mamm. Genome 31, 49-53 (2020)
18.
Tomar, A. & Teperino, R.: Genetic control of non-genetic inheritance in mammals: state-of-the-art and perspectives. Mamm. Genome 31, 146–156 (2020)
19.
Danner, E.* et al.: Control of gene editing by manipulation of DNA repair mechanisms. Mamm. Genome 28, 262-274 (2017)
20.
Diener, S. et al.: Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia. Mamm. Genome 27, 111-121 (2016)
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