Thomas A Ravenscroft, Ph.D.
Affiliations: | 2016-2021 | Baylor College of Medicine, Houston, TX | |
| 2021- | HHMI Janelia Farm Campus |
Area:
Drosophila NeurobiologyGoogle:
"Thomas Ravenscroft"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Rosa Rademakers | research assistant | 2012-2016 | Mayo Clinic Jacksonville |
| Hugo J. Bellen | grad student | 2016- | Baylor College of Medicine |
| Gerald M. Rubin | post-doc | 2021- | HHMI Janelia Farm Campus (FlyTree) |
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Publications
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| Ravenscroft TA, Jacobs A, Gu M, et al. (2023) The Voltage-Gated Sodium Channel in , Para, Localizes to Dendrites As Well As Axons in Mechanosensitive Chordotonal Neurons. Eneuro. 10 |
| Marcogliese PC, Dutta D, Ray SS, et al. (2022) Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling. Science Advances. 8: eabl5613 |
| Goodman LD, Cope H, Nil Z, et al. (2021) TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. American Journal of Human Genetics |
| Ravenscroft TA, Phillips JB, Fieg E, et al. (2021) Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| 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 |