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Human Genetics|March 17, 2023
Nuclear speckleopathies: developmental disorders caused by variants in genes encoding nuclear speckle proteinsKelly E Regan-Fendt, Kosuke IzumiAMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|August 18, 2017
Integrative network and transcriptomics-based approach predicts genotype- specific drug combinations for melanomaKelly E Regan, Philip R O Payne, Fuhai LiNPJ Systems Biology and Applications|March 2, 2019
Synergy from gene expression and network mining (SynGeNet) method predicts synergistic drug combinations for diverse melanoma genomic subtypesKelly E Regan-Fendt, Jielin Xu, Mallory DiVincenzo, et al.Journal of the American Medical Informatics Association : JAMIA|January 29, 2013
Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseasesYounghee Lee, Haiquan Li, Jianrong Li, et al.American Journal of Medical Genetics. Part A|May 22, 2023
Retrospective identification of patients with SRRM2-related neurodevelopmental disorder in a single tertiary children's hospitalKelly E Regan-Fendt, Alyssa L Rippert, Livija Medne, et al.Oncotargets and Therapy|October 13, 2016
MicroRNA profiling of patient plasma for clinical trials using bioinformatics and biostatistical approachesJoseph Markowitz, Zachary Abrams, Naduparambil K Jacob, et al.Pageof 1