Katherine Roche
Affiliations: | National Institute of Neurological Disorders and Stroke, Bethesda, MD, United States |
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"Katherine Roche"Mean distance: 14.14 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Richard L. Huganir | grad student | 1992-1996 | Johns Hopkins Medical School |
| Robert J. Wenthold | post-doc | NIDCD |
Children
Sign in to add trainee| Tina T. Tang | grad student | 2005-2009 | NINDS |
| Stephaine A. McNeil | grad student | 2012 | Johns Hopkins |
| Bo-Shiun Chen | post-doc | NINDS | |
| Chul Hoon Kim | post-doc | Brown, NINDS | |
| Natalie F. Shanks | post-doc | NINDS | |
| Chan-Ying zheng | post-doc | 2010- | NIH |
| Shuxi Liu | post-doc | 2012- | NINDS |
BETA: Related publications
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Publications
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| Tian C, Paskus JD, Fingleton E, et al. (2021) Autism Spectrum Disorder/Intellectual Disability-associated mutations in Trio disrupt Neuroligin 1-mediated synaptogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Yong XLH, Zhang L, Yang L, et al. (2021) Regulation of NMDA receptor trafficking and gating by activity-dependent CaMKIIα phosphorylation of the GluN2A subunit. Cell Reports. 36: 109338 |
| May HJ, Jeong J, Revah-Politi A, et al. (2021) Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Fingleton E, Li Y, Roche KW. (2021) Advances in Proteomics Allow Insights Into Neuronal Proteomes. Frontiers in Molecular Neuroscience. 14: 647451 |
| Vieira MM, Jeong J, Roche KW. (2021) The role of NMDA receptor and neuroligin rare variants in synaptic dysfunction underlying neurodevelopmental disorders. Current Opinion in Neurobiology. 69: 93-104 |
| Jeong J, Li Y, Roche KW. (2021) CaMKII Phosphorylation Regulates Synaptic Enrichment of Shank3. Eneuro |
| Kats DJ, Roche KJ, Skotko BG. (2020) Epileptic spasms in individuals with Down syndrome: A review of the current literature. Epilepsia Open. 5: 344-353 |
| Mota Vieira M, Nguyen TA, Wu K, et al. (2020) An Epilepsy-Associated GRIN2A Rare Variant Disrupts CaMKIIα Phosphorylation of GluN2A and NMDA Receptor Trafficking. Cell Reports. 32: 108104 |
| Nguyen TA, Lehr AW, Roche KW. (2020) Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics. Frontiers in Synaptic Neuroscience. 12: 33 |
| Paskus JD, Herring BE, Roche KW. (2020) Kalirin and Trio: RhoGEFs in Synaptic Transmission, Plasticity, and Complex Brain Disorders. Trends in Neurosciences. 43: 505-518 |