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Linghan GAO |
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Ph.D., Assistant Professor, Deputy Principal Investigator
B.S. (1992-1996) Harbin Normal University
M.S. (1998-2001) Harbin Medical University
Ph.D. (2001-2005) Harbin Medical University
Post-doc (2005-2007) Shanghai Jiaotong University
Email: gaolh@sjtu.edu.cn |
INTRODUCTION:
Dr Gao¨s research works have been sponsored by NSFC and Shanghai Natural Science Foundation.
RESEARCH INTERESTS:
Gene mapping and cloning of monogenetic diseases, including bone diseases, eye diseases, skin diseases, neuromuscular diseases, nephropathy, etc., as well as functional studies of the disease-causing genes.
REPRESENTATIVE PUBLICATIONS:
Gu Z, Zhao P, He G, Wan C, Ma G, Yu L, Zhang J, Feng G, He L, Gao L*. An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigree. Molecular Vision. 2011 Dec 17:3200-07. Gu Z, Ji B, Wan C, He G, Zhang J, Zhang M, Feng G, He L, Gao L*. A splice site mutation in CRYBA1/A3 causing autosomal dominant posterior polar cataract in a Chinese pedigree. Mol Vis. 2010; 16:154-60. Ji B#, La Y#, Gao L#, Zhu H, Tian N, Zhang M, Yang Y, Zhao X, Tang R, Ma G, Zhou J, Meng J, Ma J, Zhang Z, Li H, Feng G, Wang Y, He L*, Wan C*. A comparative proteomics analysis of rat mitochondria from the cerebral cortex and hippocampus in response to antipsychotic medications. J Proteome Res. 2009; 8(7):3633-41. Cui X#, Gao L#, Jin Y, Zhang Y, Bai J, Feng G, Gao W, Liu P, He L*, Fu S*. The E233del mutation in BFSP2 causes a progressive autosomal dominant cataract in a Chinese family. Mol Vis. 2007; 13:2023-2029. Zhang L#, Gao L#, Li Z, Qin W, Gao W, Cui X, Feng G, Fu S, He L, Liu P*. Progressive sutural cataract associated with a BFSP2 mutation in a Chinese family. Mol Vis. 2006; 12: 1626-1631. Gao L#, Qin W#, Cui H#, Feng G, Liu P, Gao W, Ma L, Li P, He L, Fu S*. A Novel Locus of Coralliform Cataract Mapped to Chromosome 2p24-pter. Journal of Human Genetics. 2005; 50(6):305-310.
# Contributed equally to the paper * Corresponding author
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