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JAMA Neurology|August 19, 2014
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxiaBrent L Fogel, Hane Lee, Joshua L Deignan, et al.
Frontiers in Cell and Developmental Biology|September 4, 2023
Elucidation of bioinformatic-guided high-prospect drug repositioning candidates for DMD via Swanson linking of target-focused latent knowledge from text-mined categorical metadataJ Wes Ulm, Florian Barthélémy, Stanley F Nelson
BMC Bioinformatics|January 8, 2011
SeqWare Query Engine: storing and searching sequence data in the cloudBrian D O'Connor, Barry Merriman, Stanley F Nelson
Frontiers in Cardiovascular Medicine|January 24, 2022
Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in TSFM Gene Causing Juvenile Hypertrophic CardiomyopathyJamie O Yang, Hapet Shaybekyan, Yan Zhao, et al.
Nature Reviews. Neuroscience|September 21, 2004
DNA-microarray analysis of brain cancer: molecular classification for therapyPaul S Mischel, Timothy F Cloughesy, Stanley F Nelson
Cancer Biology & Therapy|July 25, 2003
Molecular analysis of glioblastoma: pathway profiling and its implications for patient therapyPaul S Mischel, Stanley F Nelson, Timothy F Cloughesy
NPJ Genomic Medicine|September 5, 2017
Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformationXiaoyan Ge, Henry Gong, Kevin Dumas, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Validation and Detection of Exon Skipping Boosters in DMD Patient Cell Models and mdx MouseFlorian Barthelemy, Dereck Wang, Stanley F Nelson, et al.
Nature|November 26, 2010
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulationRamin Nazarian, Hubing Shi, Qi Wang, et al.
BMC Cancer|February 6, 2013
Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemiaVivian Y Chang, Giuseppe Basso, Kathleen M Sakamoto, et al.
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