BCM-HGSC | Yumei Li, Ph.D. | page 4

Assistant Professor, Department of Molecular and Human Genetics

Contact information

Publications

2014

Wang F, Wang Y, Zhang B, Zhao L, Lyubasyuk V, Wang K, et al.. A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2014;55(11):7159-64.

Haelterman NA, Jiang L, Li Y, Bayat V, Sandoval H, Ugur B, et al.. Large-scale identification of chemically induced mutations in Drosophila melanogaster. Genome Res. 2014;24(10):1707-18.

Wang F, Wang H, Tuan H-F, Nguyen DH, Sun V, Keser V, et al.. Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements. Hum Genet. 2014;133(3):331-45.

Wang F, Li H, Xu M, Li H, Zhao L, Yang L, et al.. A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2014;56(1):150-5.

2013

Wang X, Wang H, Sun V, Tuan H-F, Keser V, Wang K, et al.. Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing. J Med Genet. 2013;50(10):674-88.

Fu Q, Wang F, Wang H, Xu F, Zaneveld JE, Ren H, et al.. Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2013;54(6):4158-66.

2011

Daines B, Wang H, Wang L, Li Y, Han Y, Emmert D, et al.. The Drosophila melanogaster transcriptome by paired-end RNA sequencing. Genome Res. 2011;21(2):315-24.

2010

Wang H, Chattopadhyay A, Li Z, Daines B, Li Y, Gao C, et al.. Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing. Genome Res. 2010;20(7):981-8.

2009

Wang H, Hollander AI den, Moayedi Y, Abulimiti A, Li Y, Collin RWJ, et al.. Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. Am J Hum Genet. 2009;84(3):380-7.

Li Y, Wang H, Peng J, Gibbs RA, Lewis RAlan, Lupski JR, et al.. Mutation survey of known LCA genes and loci in the Saudi Arabian population. Invest Ophthalmol Vis Sci. 2009;50(3):1336-43.

Daines B, Wang H, Li Y, Han Y, Gibbs RA, Chen R. High-throughput multiplex sequencing to discover copy number variants in Drosophila. Genetics. 2009;182(4):935-41.

2006

Ostrin EJ, Li Y, Hoffman K, Liu J, Wang K, Zhang L, et al.. Genome-wide identification of direct targets of the Drosophila retinal determination protein Eyeless. Genome Res. 2006;16(4):466-76.