Rui Chen, PhD
Affiliations: | Molecular and human genetics | Baylor College of Medicine, Houston, TX | |
| Human genome sequencing center | Baylor College of Medicine, Houston, TX |
Area:
Genetics of visual impairment, Single cell sequencingWebsite:
https://sites.google.com/a/rchenlab.org/www/homeGoogle:
"Rui Chen"Mean distance: (not calculated yet)
Collaborators
Sign in to add collaborator| Lakshya Bajaj | collaborator | 2017-2018 | Baylor College of Medicine |
| Dany Roman | collaborator | 2015-2019 | Baylor College of Medicine |
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Publications
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| Go YM, Zhang J, Fernandes J, et al. (2020) MTOR-initiated metabolic switch and degeneration in the retinal pigment epithelium. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology |
| Bajaj L, Sharma J, di Ronza A, et al. (2020) A CLN6-CLN8 complex recruits lysosomal enzymes at the ER for Golgi transfer. The Journal of Clinical Investigation |
| Cherry TJ, Yang MG, Harmin DA, et al. (2020) Mapping the -regulatory architecture of the human retina reveals noncoding genetic variation in disease. Proceedings of the National Academy of Sciences of the United States of America |
| Devlin DJ, Agrawal-Zaneveld S, Nozawa K, et al. (2020) Knockout of mouse receptor accessory protein 6 (REEP6) leads to sperm function and morphology defects. Biology of Reproduction |
| Dharmat R, Kim S, Li Y, et al. (2020) Single-Cell Capture, RNA-seq, and Transcriptome Analysis from the Neural Retina. Methods in Molecular Biology (Clifton, N.J.). 2092: 159-186 |
| Liang Q, Dharmat R, Owen L, et al. (2019) Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profiling. Nature Communications. 10: 5743 |
| Shurygina MF, Parker MA, Schlechter CL, et al. (2019) A case report of two siblings with Alstrom syndrome without hearing loss associated with two new ALMS1 variants. Bmc Ophthalmology. 19: 246 |
| MacKay H, Scott CA, Duryea JD, et al. (2019) DNA methylation in AgRP neurons regulates voluntary exercise behavior in mice. Nature Communications. 10: 5364 |
| Fasham J, Arno G, Lin S, et al. (2019) Delineating the expanding phenotype associated with SCAPER gene mutation. American Journal of Medical Genetics. Part A |
| Kim S, Lowe A, Dharmat R, et al. (2019) Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids. Proceedings of the National Academy of Sciences of the United States of America |