Thomas A Ravenscroft, Ph.D.

2016-2021 Baylor College of Medicine, Houston, TX 
 2021- HHMI Janelia Farm Campus 
Drosophila Neurobiology
"Thomas Ravenscroft"
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Rosa Rademakers research assistant 2012-2016 Mayo Clinic Jacksonville
Hugo J. Bellen grad student 2016- Baylor
Gerald M. Rubin post-doc 2021- HHMI Janelia Farm Campus (FlyTree)
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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
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
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