Vineet Arora

Highly motivated Postdoctoral Researcher, conducts research on animal models for studying cellular and molecular mechanisms of neurodevelopmental disorders. Documented publication record in neuroscience peer-reviewed literature especially related to Autism spectral disorders. Ph.D in Neuroscience (Kainate receptors neurobiology) with effective verbal and written communication skills to deliver excellent presentations and prepare written reports.

Presentations at the meetings

• ECNP Congress, Barcelona (October 2018)

• Gordon research conference on synaptic transmission in Waterville valley, NH, USA (August 2018)

• FENS 2018, Berlin (July 2018)

• Gordon Research Seminar on Fragile X and Autism Spectral Disorders in Lucca (Braga) Italy

• ENCODS 2017, Benidorm (Spain),

• 17 National Congress of the Spanish Society of Neuroscience, Alicante

• BYNS 2017 - Barcelona Young Neuroscientists Symposium, Barcelona (Spain),

• ECNP Workshop on Neuropsychopharmacology for Junior Scientists in Europe, Nice, France




Publications




Endogenous Syngap1 alpha splice forms promote cognitive function and seizure protection. eLife 2022;11:e75707

Murat Kilinc, Vineet Arora, Thomas K Creson, Camilo Rojas, Aliza A Le, Julie Lauterborn, Brent Wilkinson, Nicolas Hartel, Nicholas Graham, Adrian Reich, Gemma Gou, Yoichi Araki, Àlex Bayés, Marcelo Coba, Gary Lynch, Courtney A Miller, Gavin Rumbaugh




SYNGAP1 Controls the Maturation of Dendrites, Synaptic Function, and Network Activity in Developing Human Neurons. Journal of Neuroscience 4 September 2020, JN-RM-1367- 20; DOI: 10.1523/JNEUROSCI.1367-20.2020

Nerea Llamosas, Vineet Arora, Ridhima Vij, Murat Kilinc, Lukasz Bijoch, Camilo Rojas, Adrian Reich, Ba nuPriya Sridharan, Erik Willems, David R. Piper, Louis Scampavia, Timothy P. Spicer, Courtney A. Miller, J. Lloyd Holder, Gavin Rumbaugh




Increased Grik4 Gene Dosage Causes Imbalanced Circuit Output and Human Disease-Related Behaviors. Cell Reports, Volume 23, Issue 13, 3827 – 3838




Arora V., Pecoraro V., Aller M., Román C., Paternain A., Lerma J. (June 2018)




A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance. BMC Neurology, 14, 118. Engeholm, M., Sekler, J., Schöndorf, D. C., Arora, V., Schittenhelm, J., Biskup, Gasser, T. (June 2014).