Yumei Li, Ph.D.

Assistant Professor, Department of Molecular and Human Genetics

Yumei Li, Ph.D.Contact information

yumeil@bcm.edu

 

 

 

 

 

Publications

2021
Qian X, Wang J, Wang M, Igelman AD, Jones KD, Li Y, et al.. Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases. Front Genet. 2021;12:647400.

2020
Li Y, Ren P, Dawson A, Vasquez HG, Ageedi W, Zhang C, et al.. Single-Cell Transcriptome Analysis Reveals Dynamic Cell Populations and Differential Gene Expression Patterns in Control and Aneurysmal Human Aortic Tissue. Circulation. 2020;142(14):1374-1388.

Luo W, Wang Y, Zhang L, Ren P, Zhang C, Li Y, et al.. Critical Role of Cytosolic DNA and Its Sensing Adaptor STING in Aortic Degeneration, Dissection, and Rupture. Circulation. 2020;141(1):42-66.

Dharmat R, Kim S, Li Y, Chen R. Single-Cell Capture, RNA-seq, and Transcriptome Analysis from the Neural Retina. Methods Mol Biol. 2020;2092:159-186.

2019
Zou X, Fu Q, Fang S, Li H, Ge Z, Yang L, et al.. PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY. Retina. 2019;39(10):2040-2052.

Kim S, Lowe A, Dharmat R, Lee S, Owen LA, Wang J, et al.. Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids. Proc Natl Acad Sci U S A. 2019;116(22):10824-10833.

Zaneveld SAgrawal, Eblimit A, Liang Q, Bertrand R, Wu N, Liu H, et al.. Gene Therapy Rescues Retinal Degeneration in Receptor Expression-Enhancing Protein 6 Mutant Mice. Hum Gene Ther. 2019;30(3):302-315.

Gunasekara CJ, C Scott A, Laritsky E, Baker MS, MacKay H, Duryea JD, et al.. A genomic atlas of systemic interindividual epigenetic variation in humans. Genome Biol. 2019;20(1):105.

Moshiri A, Chen R, Kim S, Harris RA, Li Y, Raveendran M, et al.. A nonhuman primate model of inherited retinal disease. J Clin Invest. 2019;129(2):863-874.

Liang Q, Dharmat R, Owen L, Shakoor A, Li Y, Kim S, et al.. Single-nuclei RNA-seq on human retinal tissue provides improved transcriptome profiling. Nat Commun. 2019;10(1):5743.

Shurygina MF, Parker MA, Schlechter CL, Chen R, Li Y, Weleber RG, et al.. A case report of two siblings with Alstrom syndrome without hearing loss associated with two new ALMS1 variants. BMC Ophthalmol. 2019;19(1):246.

2018
Yeung K, Wang F, Li Y, Wang K, Mardon G, Chen R. Integrative genomic analysis reveals novel regulatory mechanisms of eyeless during Drosophila eye development. Nucleic Acids Res. 2018;46(22):11743-11758.