Brent L. Fogel, Ph.D.
Affiliations: | 2001 | Medical College of Wisconsin, Milwaukee, WI, United States |
Area:
Microbiology Biology, Molecular BiologyGoogle:
"Brent Fogel"Parents
Sign in to add mentorMark T. McNally | grad student | 2001 | Medical College of Wisconsin | |
(Identification of hnRNP H as a cellular protein which binds to the negative regulator of splicing element from Rous sarcoma virus and characterization of its role in viral RNA processing.) |
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Publications
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Ringman JM, Qiao Y, Garbin A, et al. (2020) Emotional detachment, gait ataxia, and cerebellar dysconnectivity associated with compound heterozygous mutations in the gene. Neurocase. 1-6 |
Burdekin ED, Fogel BL, Jeste SS, et al. (2020) The Neurodevelopmental and Motor Phenotype of SCA21 (ATX-TMEM240). Journal of Child Neurology. 883073820943488 |
McEachin ZT, Gendron TF, Raj N, et al. (2020) Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36. Neuron |
Xiao C, M Binkley E, Rexach J, et al. (2019) A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an mutation. Neurology. Genetics. 5: e357 |
Ngo KJ, Rexach JE, Lee H, et al. (2019) A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders. Human Mutation |
Lee H, Huang AY, Wang LK, et al. (2019) Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Rafehi H, Szmulewicz DJ, Bennett MF, et al. (2019) Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS. American Journal of Human Genetics |
Rexach J, Lee H, Martinez-Agosto JA, et al. (2019) Clinical application of next-generation sequencing to the practice of neurology. The Lancet. Neurology. 18: 492-503 |
Becherel OJ, Fogel BL, Zeitlin SI, et al. (2019) Disruption of Spermatogenesis and Infertility in Ataxia with Oculomotor Apraxia Type 2 (AOA2). Cerebellum (London, England) |
Ramos EM, Carecchio M, Lemos R, et al. (2018) Primary brain calcification: an international study reporting novel variants and associated phenotypes. European Journal of Human Genetics : Ejhg |