Ricardo E. Dolmetsch
Affiliations: | Stanford University, Palo Alto, CA |
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"Ricardo Dolmetsch"Mean distance: 13.71 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Richard S. Lewis | grad student | 1991-1997 | Stanford |
| Michael E. Greenberg | post-doc | Harvard Medical School |
Children
Sign in to add trainee| Jocelyn Krey | grad student | Stanford | |
| Georgia Panagiotakos | grad student | 2007- | Stanford Medical School |
| Jacob S. Brenner | grad student | 2007 | Stanford |
| Natalia Gomez-Ospina | grad student | 2002-2008 | Stanford |
| Eric Green | grad student | 2003-2009 | Harvard University MGH |
| Sergiu P. Pasca | post-doc | Stanford Medical School | |
| Masayuki Yazawa | post-doc | 2003-2009 | Columbia |
| Alex Shcheglovitov | post-doc | 2009-2014 | Stanford |
| Jason S. Bant | post-doc | 2013-2014 | Stanford School of Medicine |
| Rong Mao | research scientist | 2010- | Stanford |
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Publications
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| Kostic M, Raymond JJ, Freyre CAC, et al. (2023) Patient Brain Organoids Identify a Link between the 16p11.2 Copy Number Variant and the Gene. Acs Chemical Neuroscience |
| Cable J, Purcell RH, Robinson E, et al. (2021) Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report. Annals of the New York Academy of Sciences |
| Roth JG, Muench KL, Asokan A, et al. (2020) 16p11.2 microdeletion imparts transcriptional alterations in human iPSC-derived models of early neural development. Elife. 9 |
| Khan TA, Revah O, Gordon A, et al. (2020) Neuronal defects in a human cellular model of 22q11.2 deletion syndrome. Nature Medicine |
| Panagiotakos G, Haveles C, Arjun A, et al. (2019) Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy Syndrome. Elife. 8 |
| Sanders SJ, Sahin M, Hostyk J, et al. (2019) A framework for the investigation of rare genetic disorders in neuropsychiatry. Nature Medicine |
| Sun Y, Dolmetsch RE. (2019) Investigating the Therapeutic Mechanism of Cannabidiol in a Human Induced Pluripotent Stem Call (iPSC)-Based Cellular Model of Dravet Syndrome. Cold Spring Harbor Symposia On Quantitative Biology |
| Ihry RJ, Salick MR, Ho DJ, et al. (2019) Genome-Scale CRISPR Screens Identify Human Pluripotency-Specific Genes. Cell Reports. 27: 616-630.e6 |
| Panagiotakos G, Haveles C, Arjun A, et al. (2019) Author response: Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome Elife |
| Sun Y, Paşca SP, Portmann T, et al. (2016) A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients. Elife. 5 |