Stavros Niarchos Foundation Center for Precision Psychiatry & Mental Health

Displaying 1 - 10 of 10CSV
Thakur, P., Lackinger, M., Diamantopoulou, A., Rao, S., Chen, Y., Khalizova, K., Ferng, A., Mazur, C., Kordasiewicz, H., Shprintzen, R. J., Markx, S., Xu, B., & Gogos, J. A. (2025). An antisense oligonucleotide-based strategy to ameliorate cognitive dysfunction in the 22q11.2 Deletion Syndrome. ELife, 13. CLOCKSS. https://doi.org/10.7554/elife.103328
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Kowanda, M., Smith, R. S., Lundy, J., Kentros, C., Kleinman, E., Walsh, L. K., Schratt, G., Taylor, C., & Chung, W. (2024). P612: Improvement of variant reclassification in genetic neurodevelopmental conditions: Simons Searchlight research registry. Genetics in Medicine Open, 2, 101518. https://doi.org/10.1016/j.gimo.2024.101518
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Kowanda, M., Calakos, K., Snyder, L. G., Kentros, C., Bain, J., Srivastava, S., Sands, T., Schratt, G., Taylor, C., & Chung, W. (2024). P152: Seizure severity across neurogenetic conditions in Simons Searchlight*. Genetics in Medicine Open, 2, 101049. https://doi.org/10.1016/j.gimo.2024.101049
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Li, Y., Sun, Z., Zhu, H., Sun, Y., Shteyman, D. B., Markx, S., Leong, K. W., Xu, B., & Fu, B. M. (2023). Inhibition of Abl Kinase by Imatinib Can Rescue the Compromised Barrier Function of 22q11.2DS Patient-iPSC-Derived Blood–Brain Barriers. Cells, 12(3), 422. https://doi.org/10.3390/cells12030422
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Fenster, R., Ziegler, A., Kentros, C., Geltzeiler, A., Green Snyder, L., Brooks, E., & Chung, W. K. (2022). Characterization of phenotypic range in DYRK1A haploinsufficiency syndrome using standardized behavioral measures. American Journal of Medical Genetics Part A, 188(7), 1954–1963. Portico. https://doi.org/10.1002/ajmg.a.62721
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Kahen, A., Kavus, H., Geltzeiler, A., Kentros, C., Taylor, C., Brooks, E., Green Snyder, L., & Chung, W. (2021). Neurodevelopmental phenotypes associated with pathogenic variants in SLC6A1. Journal of Medical Genetics, 59(6), 536–543. https://doi.org/10.1136/jmedgenet-2021-107694
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de Jong, J. O., Llapashtica, C., Genestine, M., Strauss, K., Provenzano, F., Sun, Y., Zhu, H., Cortese, G. P., Brundu, F., Brigatti, K. W., Corneo, B., Migliori, B., Tomer, R., Kushner, S. A., Kellendonk, C., Javitch, J. A., Xu, B., & Markx, S. (2021). Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder. Nature Communications, 12(1). https://doi.org/10.1038/s41467-021-24358-4
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Li, Y., Xia, Y., Zhu, H., Luu, E., Huang, G., Sun, Y., Sun, K., Markx, S., Leong, K. W., Xu, B., & Fu, B. M. (2021). Investigation of Neurodevelopmental Deficits of 22 q11.2 Deletion Syndrome with a Patient-iPSC-Derived Blood–Brain Barrier Model. Cells, 10(10), 2576. https://doi.org/10.3390/cells10102576
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Kowanda, M., Cartner, L., Kentros, C., Geltzeiler, A. R., Singer, K. E., Weaver, W. C., Lehman, C. D., Smith, S., Smith, R. S., Walsh, L. K., Diehl, K., Nagpal, N., Brooks, E., Mebane, C. M., Wilson, A. L., Marvin, A. R., White, L. C., Law, J. K., Jensen, W., … Chung, W. K. (2021). Availability of Services and Caregiver Burden: Supporting Individuals With Neurogenetic Conditions During the COVID-19 Pandemic. Journal of Child Neurology, 36(9), 760–767. https://doi.org/10.1177/08830738211001209
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