Candace T. Myers, Ph.D.
Affiliations: | 2013 | Molecular & Cellular Biology | University of Arizona, Tucson, AZ |
Area:
Molecular Biology, Human DevelopmentGoogle:
"Candace Myers"Parents
Sign in to add mentor| Paul A. Krieg | grad student | 2013 | University of Arizona | |
| (Origins and development of the embryonic vascular system in Xenopus.) | ||||
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Publications
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| Carvill GL, Helbig KL, Myers CT, et al. (2020) Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy. Human Mutation |
| Scheffer IE, Boysen KE, Schneider AL, et al. (2019) BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures. Developmental Medicine and Child Neurology |
| Bar C, Barcia G, Jennesson M, et al. (2019) Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. Human Mutation |
| Salpietro V, Dixon CL, Guo H, et al. (2019) AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature Communications. 10: 3094 |
| Bisulli F, Licchetta L, Baldassari S, et al. (2019) SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus. Epileptic Disorders : International Epilepsy Journal With Videotape |
| Pippucci T, Licchetta L, Baldassari S, et al. (2019) Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies. Annals of Clinical and Translational Neurology. 6: 475-485 |
| Vlaskamp DRM, Shaw BJ, Burgess R, et al. (2018) encephalopathy: A distinctive generalized developmental and epileptic encephalopathy. Neurology |
| Gregor A, Sadleir LG, Asadollahi R, et al. (2018) De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. American Journal of Human Genetics |
| Di Donato N, Timms AE, Aldinger KA, et al. (2018) Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Johannesen KM, Gardella E, Linnankivi T, et al. (2018) Defining the phenotypic spectrum of SLC6A1 mutations. Epilepsia |