Hugo J. Bellen
Affiliations: | Baylor College of Medicine, Houston, TX |
Area:
neural development, synaptic vesicle traffickingWebsite:
http://www.bcm.edu/genetics/?pmid=10582Google:
"Hugo Bellen"Bio:
http://flypush.imgen.bcm.tmc.edu/lab/index.html
Cross-listing: Neurotree - BCM Tree
Parents
Sign in to add mentor| John A. Kiger | grad student | 1983-1986 | UC Davis |
| Walter Gehring | post-doc | 1987-1989 | University of Basel |
Children
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BETA: Related publications
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Publications
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| Goodman LD, Ralhan I, Li X, et al. (2024) Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stress. Nature Neuroscience |
| Huang Y, Jay KL, Huang AY, et al. (2024) Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101218 |
| Mao D, Liu C, Wang L, et al. (2024) AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. Nejm Ai. 1 |
| Moulton MJ, Atala K, Zheng Y, et al. (2024) Dominant Missense Variants in SREBF2 are Associated with Complex Dermatological, Neurological, and Skeletal Abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101174 |
| Goodman LD, Moulton MJ, Lin G, et al. (2024) Does glial lipid dysregulation alter sleep in Alzheimer's and Parkinson's disease? Trends in Molecular Medicine |
| Liao JZ, Chung HL, Shih C, et al. (2024) Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila. Nature Communications. 15: 3326 |
| Park YJ, Lu TC, Jackson T, et al. (2024) Whole organism snRNA-seq reveals systemic peripheral changes in Alzheimer's Disease fly models. Biorxiv : the Preprint Server For Biology |
| Ma M, Ganapathi M, Zheng Y, et al. (2024) Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101125 |
| 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 |
| Vuocolo B, German RJ, Lalani SR, et al. (2024) Improving access to exome sequencing in a medically underserved population through the Texome Project. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101102 |