Rachayata Dharmat
Affiliations: | Molecular and Huaman Genetics | Baylor College of Medicine, Houston, TX |
Area:
Genetics of Visual disfunction, photoreceptor sensory ciliopathy, Single cell sequencingWebsite:
https://www.bcm.edu/people/view/rachayata-dharmat/b170d6d3-ffed-11e2-be68-080027880ca6Google:
"Rachayata Dharmat"Mean distance: (not calculated yet)
Collaborators
Sign in to add collaborator| Graeme Mardon | collaborator | Baylor College of Medicine | |
| Theodore G. Wensel | collaborator | Baylor College of Medicine |
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Publications
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| 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 |
| 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 |
| Dharmat R, Eblimit A, Robichaux MA, et al. (2018) SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium. The Journal of Cell Biology |
| Yu B, Egbejimi A, Dharmat R, et al. (2018) Phagocytosed photoreceptor outer segments activate mTORC1 in the retinal pigment epithelium. Science Signaling. 11 |
| Dharmat R, Liu W, Ge Z, et al. (2017) IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration. Investigative Ophthalmology & Visual Science. 58: 2483-2490 |
| Xu M, Xie YA, Abouzeid H, et al. (2017) Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies. American Journal of Human Genetics |
| Soens ZT, Li Y, Zhao L, et al. (2016) Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1. Genetics in Medicine : Official Journal of the American College of Medical Genetics |