Stephan J. Sanders, Ph.D/BMBS/MRCPCH
Affiliations: | Psychiatry | University of California, San Francisco, San Francisco, CA |
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Children
Sign in to add trainee| Donna M. Werling | post-doc | UCSF | |
| Joon Yong An | post-doc | 2015- | UCSF |
| Shan Dong | post-doc | 2015- | UCSF |
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Publications
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| Shin D, Kim CN, Ross J, et al. (2024) Thalamocortical organoids enable in vitro modeling of 22q11.2 microdeletion associated with neuropsychiatric disorders. Cell Stem Cell |
| Nelson AD, Catalfio AM, Gupta JP, et al. (2024) Physical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites. Neuron |
| Ljungdahl A, Kohani S, Page NF, et al. (2023) AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms. Biorxiv : the Preprint Server For Biology |
| Lagunas T, Plassmeyer SP, Fischer AD, et al. (2023) A Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of non-coding elements in vivo. Communications Biology. 6: 1151 |
| Lowther C, Valkanas E, Giordano JL, et al. (2023) Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies. American Journal of Human Genetics |
| Cioclu MC, Mosca I, Ambrosino P, et al. (2023) KCNT2-related disorders: phenotypes, functional and pharmacological properties. Annals of Neurology |
| Koesterich J, An JY, Inoue F, et al. (2023) Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays. International Journal of Molecular Sciences. 24 |
| Wigdor EM, Weiner DJ, Grove J, et al. (2022) The female protective effect against autism spectrum disorder. Cell Genomics. 2: 100134 |
| Parellada M, Andreu-Bernabeu Á, Burdeus M, et al. (2022) In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review. The American Journal of Psychiatry. appiajp21100992 |
| Fu JM, Satterstrom FK, Peng M, et al. (2022) Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics |