Thomas A Ravenscroft

Baylor College of Medicine, Houston, TX 
Drosophila Neurobiology
"Thomas Ravenscroft"
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Rosa Rademakers research assistant 2012-2016 Mayo Clinic Jacksonville
Hugo J. Bellen grad student 2016- Baylor
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Ravenscroft TA, Janssens J, Lee PT, et al. (2020) voltage-gated sodium channels are only expressed in active neurons and are localized to distal axonal initial segment-like domains. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Chung HL, Wangler MF, Marcogliese PC, et al. (2020) Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron
Ansar M, Chung HL, Al-Otaibi A, et al. (2019) Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature. American Journal of Human Genetics
Evers BM, Rodriguez-Navas C, Tesla RJ, et al. (2017) Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency. Cell Reports. 20: 2565-2574
Pottier C, Ravenscroft TA, Brown PH, et al. (2016) TYROBP genetic variants in early-onset Alzheimer's disease. Neurobiology of Aging
Ravenscroft TA, Pottier C, Murray ME, et al. (2016) The presenilin 1 p.Gly206Ala mutation is a frequent cause of early-onset Alzheimer's disease in Hispanics in Florida. American Journal of Neurodegenerative Disease. 5: 94-101
Pottier C, Ravenscroft TA, Sanchez-Contreras M, et al. (2016) Genetics of FTLD: Overview and what else we can expect from genetic studies. Journal of Neurochemistry
Rodriguez-Porcel F, Lowder L, Rademakers R, et al. (2016) Fulminant corticobasal degeneration: Agrypnia excitata in corticobasal syndrome. Neurology
Pottier C, Bieniek KF, Finch N, et al. (2015) Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease. Acta Neuropathologica. 130: 77-92
Kertesz A, Finger E, Murrell J, et al. (2015) Progressive supranuclear palsy in a family with TDP-43 pathology. Neurocase. 21: 178-84
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