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Biological Procedures Online|May 8, 2003
A fluorescence microscopy method for quantifying levels of prostaglandin endoperoxide H synthase-1 and CD-41 in MEG-01 cellsDouglas J Franks, Cameron Mroske, Odette Laneuville
Human Gene Therapy Methods|May 23, 2012
A capillary electrophoresis sequencing method for the identification of mutations in the inverted terminal repeats of adeno-associated virusCameron Mroske, Hector Rivera, Taihra Ul-Hasan, et al.
American Journal of Medical Genetics. Part A|January 30, 2016
CLTC as a clinically novel gene associated with multiple malformations and developmental delayJoseph DeMari, Cameron Mroske, Sha Tang, et al.
Nature|January 30, 2004
TNF ligands: is TALL-1 a trimer or a virus-like cluster?Eugene A Zhukovsky, Jie-Oh Lee, Michael Villegas, et al.
Analytical Biochemistry|July 10, 2007
Toward a fluorescent single-strand conformation polymorphism technique that detects all mutations: F-DOVAM-SCameron Mroske, John Muci, Jicheng Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2016
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsyKatherine L Helbig, Kelly D Farwell Hagman, Deepali N Shinde, et al.
Journal of Pediatric Hematology/Oncology|August 21, 2020
Pediatric Myelodysplastic Syndrome With Germline RRAS Mutation: Expanding the Phenotype of RASopathiesDaniel S Catts, Cameron Mroske, Rebecca O Clark, et al.
BMC Medical Genetics|November 7, 2015
Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalitiesCameron Mroske, Kristen Rasmussen, Deepali N Shinde, et al.
Human Mutation|October 15, 2015
Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue DiseaseAlessandra Capuano, Francesco Bucciotti, Kelly D Farwell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseasesKelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, et al.
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