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Publications by Shiqiang Li
Novel Truncation Mutations in MYRF Cause Autosomal Dominant High Hyperopia Mapped to 11p12–q13.3
Human Genetics
Genetics
Unique Variants inOPN1LWCause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
GSK-3β Phosphorylation-Dependent Degradation of ZNF281 by β-TrCP2 Suppresses Colorectal Cancer Progression
Oncotarget
Oncology
Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients
PLoS ONE
Multidisciplinary
Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients With Leber Congenital Amaurosis
PLoS ONE
Multidisciplinary
GPR143 Mutations in Chinese Patients With Ocular Albinism Type 1
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Microphthalmia, Late Onset Keratitis, and Iris Coloboma/Aniridia in a Family With a novelPAX6mutation
Ophthalmic Genetics
Child Health
Ophthalmology
Pediatrics
Perinatology
Genetics
Microwave-Assisted Synthesis of Semiconductor Nanomaterials for Energy Storage
Current Nanoscience
Pharmaceutical Science
Nanoscience
Bioengineering
Medicine
Biotechnology
Nanotechnology
Biomedical Engineering
High Myopia Is Not Associated With the SNPs in theTGIF, Lumican,TGFB1, andHGFGenes
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Confirmation of a Genetic Locus for X-Linked Recessive High Myopia Outside MYP1
Journal of Human Genetics
Genetics
