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NAR Genomics and Bioinformatics|March 10, 2022
Generation and network analysis of an RNA-seq transcriptional atlas for the ratKim M Summers, Stephen J Bush, Chunlei Wu, et al.Molecular Genetics and Metabolism|July 3, 2010
Molecular genetics of long QT syndromeNilesh J Bokil, John M Baisden, Dorothy J Radford, et al.Frontiers in Genetics|May 13, 2020
Disease Severity-Associated Gene Expression in Canine Myxomatous Mitral Valve Disease Is Dominated by TGFβ SignalingGreg R Markby, Vicky E Macrae, Kim M Summers, et al.Veterinary Sciences|October 24, 2017
Comparative Transcriptomic Profiling and Gene Expression for Myxomatous Mitral Valve Disease in the Dog and HumanGreg R Markby, Kim M Summers, Vicky E MacRae, et al.Molecular Vision|November 8, 2008
Anterior segment mesenchymal dysgenesis in a large Australian family is associated with the recurrent 17 bp duplication in PITX3Kim M Summers, Stephen J Withers, Glen A Gole, et al.Canine Genetics and Epidemiology|September 25, 2015
The challenges of pedigree dog health: approaches to combating inherited diseaseLindsay L Farrell, Jeffrey J Schoenebeck, Pamela Wiener, et al.European Journal of Human Genetics : EJHG|June 17, 2010
Co-expression of FBN1 with mesenchyme-specific genes in mouse cell lines: implications for phenotypic variability in Marfan syndromeKim M Summers, Sobia Raza, Erik van Nimwegen, et al.Genomics|March 10, 2010
Functional clustering and lineage markers: insights into cellular differentiation and gene function from large-scale microarray studies of purified primary cell populationsDavid A Hume, Kim M Summers, Sobia Raza, et al.Neurogenetics|February 13, 2017
Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and diseaseSarah M Carpanini, Thomas M Wishart, Thomas H Gillingwater, et al.Journal of Leukocyte Biology|July 23, 2019
Phenotypic impacts of CSF1R deficiencies in humans and model organismsDavid A Hume, Melanie Caruso, Michelle Ferrari-Cestari, et al.Pageof 9