Grants per year
Personal profile
Education/Academic qualification
Biological Sciences, PhD, University of Maryland
… → 2015
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Dive into the research topics where Richard Scott Smith is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Grants
- 1 Active
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Role for Ion Conducting Proteins in Cortical Malformation Diseases
National Institute of Neurological Disorders and Stroke
3/1/23 → 2/28/26
Project: Research project
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Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants
Hojlo, M. A., Ghebrelul, M., Genetti, C. A., Smith, R., Rockowitz, S., Deaso, E., Beggs, A. H., Agrawal, P. B., Glahn, D. C., Gonzalez-Heydrich, J. & Brownstein, C. A., Apr 2023, In: Genes. 14, 4, 779.Research output: Contribution to journal › Article › peer-review
Open Access -
Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis
Qian, X., DeGennaro, E. M., Talukdar, M., Akula, S. K., Lai, A., Shao, D. D., Gonzalez, D., Marciano, J. H., Smith, R. S., Hylton, N. K., Yang, E., Bazan, J. F., Barrett, L., Yeh, R. C., Hill, R. S., Beck, S. G., Otani, A., Angad, J., Mitani, T., Posey, J. E., & 15 others, Oct 24 2022, In: Developmental Cell. 57, 20, p. 2381-2396.e13Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum Disorder
Brownstein, C. A., Douard, E., Mollon, J., Smith, R., Hojlo, M. A., Das, A., Goldman, M., Garvey, E., Cabral, K., Li, J., Bowen, J., Rao, A. S., Genetti, C., Carroll, D., Knowles, E. E. M., Deaso, E., Agrawal, P. B., Beggs, A. H., D'Angelo, E., Almasy, L., & 8 others, Nov 2022, In: American Journal of Psychiatry. 179, 11, p. 853-861 9 p.Research output: Contribution to journal › Article › peer-review
5 Scopus citations -
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro
Sundberg, M., Pinson, H., Smith, R. S., Winden, K. D., Venugopal, P., Tai, D. J. C., Gusella, J. F., Talkowski, M. E., Walsh, C. A., Tegmark, M. & Sahin, M., Dec 1 2021, In: Nature communications. 12, 1, 2897.Research output: Contribution to journal › Article › peer-review
Open Access24 Scopus citations -
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features
Shao, D. D., Straussberg, R., Ahmed, H., Khan, A., Tian, S., Hill, R. S., Smith, R. S., Majmundar, A. J., Ameziane, N., Neil, J. E., Yang, E., Al Tenaiji, A., Jamuar, S. S., Schlaeger, T. M., Al-Saffar, M., Hovel, I., Al-Shamsi, A., Basel-Salmon, L., Amir, A. Z., Rento, L. M., & 13 others, Jun 2021, In: Genetics in Medicine. 23, 6, p. 1158-1162 5 p.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations