Stephan J. Sanders, Ph.D/BMBS/MRCPCH
Affiliations: | Psychiatry | University of California, San Francisco, San Francisco, CA |
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"Stephan Sanders"Mean distance: 17.95 | S | N | B | C | P |
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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| Liu Z, Ypsilanti AR, Markenscoff-Papadimitriou E, et al. (2024) enhancers have distinct functions in controlling expression during cortical development. Proceedings of the National Academy of Sciences of the United States of America. 121: e2402368121 |
| Chardon FM, McDiarmid TA, Page NF, et al. (2024) Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements. Nature Communications. 15: 8209 |
| Chettle J, Louie RJ, Larner O, et al. (2024) LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder. Hgg Advances. 100345 |
| Chen Y, Dawes R, Kim HC, et al. (2024) De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature |
| Kim Y, Jeong M, Koh IG, et al. (2024) CWAS-Plus: estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. Briefings in Bioinformatics. 25 |
| Kissel LT, Pochareddy S, An JY, et al. (2024) Sex-Differential Gene Expression in Developing Human Cortex and Its Intersection With Autism Risk Pathways. Biological Psychiatry Global Open Science. 4: 100321 |
| Fazel Darbandi S, An JY, Lim K, et al. (2024) Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes. Cell Reports. 43: 114329 |
| Silva DB, Trinidad M, Ljungdahl A, et al. (2024) Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants. American Journal of Human Genetics |
| Kim Y, Jeong M, Koh IG, et al. (2024) CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data. Medrxiv : the Preprint Server For Health Sciences |
| Chen Y, Dawes R, Kim HC, et al. (2024) variants in the non-coding spliceosomal snRNA gene are a frequent cause of syndromic neurodevelopmental disorders. Medrxiv : the Preprint Server For Health Sciences |