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BMC Medical Genomics|June 8, 2017
N-of-1-pathways MixEnrich: advancing precision medicine via single-subject analysis in discovering dynamic changes of transcriptomesQike Li, A Grant Schissler, Vincent Gardeux, et al.BMC Medical Genomics|June 8, 2017
Identification of epigenetic interactions between miRNA and DNA methylation associated with gene expression as potential prognostic markers in bladder cancerManu Shivakumar, Younghee Lee, Lisa Bang, et al.BMC Medical Genomics|March 12, 2010
mspecLINE: bridging knowledge of human disease with the proteomeJeremy Handcock, Eric W Deutsch, John BoyleBMC Medical Genomics|December 2, 2009
DNA microarray profiling of genes differentially regulated by the histone deacetylase inhibitors vorinostat and LBH589 in colon cancer cell linesMelissa J LaBonte, Peter M Wilson, William Fazzone, et al.BMC Medical Genomics|May 4, 2017
Post-operative atrial fibrillation examined using whole-genome RNA sequencing in human left atrial tissueMartin I Sigurdsson, Louis Saddic, Mahyar Heydarpour, et al.BMC Medical Genomics|May 4, 2017
Diet and exercise changes following direct-to-consumer personal genomic testingDaiva Elena Nielsen, Deanna Alexis Carere, Catharine Wang, et al.BMC Medical Genomics|May 27, 2017
CVE: an R package for interactive variant prioritisation in precision oncologyAndreas Mock, Suzanne Murphy, James Morris, et al.BMC Medical Genomics|March 18, 2010
Molecular sampling of prostate cancer: a dilemma for predicting disease progressionAndrea Sboner, Francesca Demichelis, Stefano Calza, et al.BMC Medical Genomics|July 11, 2018
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patientsRubén Cabanillas, Marta Diñeiro, Guadalupe A Cifuentes, et al.BMC Medical Genomics|November 19, 2008
Pathways affected by asbestos exposure in normal and tumour tissue of lung cancer patientsSalla Ruosaari, Tuija Hienonen-Kempas, Anne Puustinen, et al.Pageof 278