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Publications by Qingjiong Zhang
Novel Truncation Mutations in MYRF Cause Autosomal Dominant High Hyperopia Mapped to 11p12–q13.3
Human Genetics
Genetics
Generation and Characterization of Induced Pluripotent Stem Cells and Retinal Organoids From a Leber’s Congenital Amaurosis Patient With Novel RPE65 Mutations
Frontiers in Molecular Neuroscience
Molecular Neuroscience
Molecular Biology
Cellular
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
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
High Myopia Is Not Associated With Single Nucleotide Polymorphisms in the COL2A1 Gene in the Chinese Population
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
Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
American Journal of Human Genetics
Genetics
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
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