Shenzhao Lu
Affiliations: | Baylor College of Medicine, Houston, TX |
Area:
neuroscience, human genetics, precision medicineGoogle:
"Shenzhao Lu"Mean distance: (not calculated yet)
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Publications
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| Pan X, Tao AM, Lu S, et al. (2024) De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. American Journal of Human Genetics |
| Ma M, Zheng Y, Lu S, et al. (2024) variants in are associated with hearing impairment, ocular pathology, and cardiac defects. Medrxiv : the Preprint Server For Health Sciences |
| Pan X, Alvarez AN, Ma M, et al. (2023) Allelic strengths of encephalopathy-associated variants correlate between in vivo and in vitro assays. Elife. 12 |
| Pan X, Alvarez AN, Ma M, et al. (2023) Allelic strengths of encephalopathy-associated variants correlate between and assays. Medrxiv : the Preprint Server For Health Sciences |
| Guichard A, Lu S, Kanca O, et al. (2023) A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins. Cell Reports. 42: 112842 |
| Chung HL, Ye Q, Park YJ, et al. (2023) Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation. Cell Metabolism |
| Pan X, Dutta D, Lu S, et al. (2023) Sphingolipids in neurodegenerative diseases. Frontiers in Neuroscience. 17: 1137893 |
| Huang Y, Lemire G, Briere LC, et al. (2022) The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. American Journal of Human Genetics. 109: 2092 |
| Ma M, Zhang X, Zheng Y, et al. (2022) The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. Human Molecular Genetics |
| Lu S, Ma M, Mao X, et al. (2022) De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement. American Journal of Human Genetics. 109: 1932-1943 |