Lawrence T. Reiter
Affiliations: | University of Tennessee Health Science Center, Memphis, TN, United States |
Area:
human disease models, autism, siezureGoogle:
"Lawrence Reiter"Parents
Sign in to add mentor| James Lupski | grad student | Baylor College of Medicine | ||
| (Genomic Disorders) | ||||
| Ethan Bier | post-doc | 1999-2005 | UCSD | |
Collaborators
Sign in to add collaborator| Janis O'Donnell | collaborator | University of Alabama | ||
| Seymour Benzer | collaborator | 1988-1991 | Caltech | |
| (Worked in his wife's laboratory (Carol Miller) and collaborated on a fly antibody project.) | ||||
BETA: Related publications
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Publications
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| Victor AK, Donaldson M, Johnson D, et al. (2021) Molecular Changes in Prader-Willi Syndrome Neurons Reveals Clues About Increased Autism Susceptibility. Frontiers in Molecular Neuroscience. 14: 747855 |
| Chen H, Victor AK, Klein J, et al. (2020) Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production. Jci Insight. 5 |
| Saravanapandian V, Frohlich J, Hipp JF, et al. (2020) Properties of beta oscillations in Dup15q syndrome. Journal of Neurodevelopmental Disorders. 12: 22 |
| Roy B, Han J, Hope KA, et al. (2020) An Unbiased Drug Screen for Seizure Suppressors in Duplication 15q Syndrome Reveals 5-HT and Dopamine Pathway Activation as Potential Therapies. Biological Psychiatry |
| Hope KA, Johnson D, Miller PW, et al. (2020) Transcriptomic and proteomic profiling of glial versus neuronal Dube3a overexpression reveals common molecular changes in gliopathic epilepsies. Neurobiology of Disease. 104879 |
| DiStefano C, Wilson RB, Hyde C, et al. (2019) Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials. American Journal of Medical Genetics. Part A |
| Hope KA, Flatten D, Cavitch P, et al. (2019) The Drosophila Gene Modulates Autism-Like Behaviors. Frontiers in Genetics. 10: 574 |
| Frohlich J, Reiter LT, Saravanapandian V, et al. (2019) Mechanisms underlying the EEG biomarker in Dup15q syndrome. Molecular Autism. 10: 29 |
| Hope KA, McGinn A, Reiter LT. (2019) A genome-wide enhancer/suppressor screen for Dube3a interacting genes in Drosophila melanogaster. Scientific Reports. 9: 2382 |
| Toro C, Hori RT, Malicdan MCV, et al. (2018) A recurrent de novo missense mutation in UBTF causes developmental neuroregression. Human Molecular Genetics |