Ricardo E. Dolmetsch

Affiliations: 
Stanford University, Palo Alto, CA 
Google:
"Ricardo Dolmetsch"
Mean distance: 13.71 (cluster 11)
 
SNBCP
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
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
Bidinosti M, Botta P, Krüttner S, et al. (2016) CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency. Science (New York, N.Y.)
Sun Y, Paşca SP, Portmann T, et al. (2016) Author response: A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients Elife
See more...