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Publications by Xueshan Xiao

Novel Truncation Mutations in MYRF Cause Autosomal Dominant High Hyperopia Mapped to 11p12–q13.3

Human Genetics
Genetics
2019English

Unique Variants inOPN1LWCause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2015English

Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients

PLoS ONE
Multidisciplinary
2011English

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients With Leber Congenital Amaurosis

PLoS ONE
Multidisciplinary
2011English

Microphthalmia, Late Onset Keratitis, and Iris Coloboma/Aniridia in a Family With a novelPAX6mutation

Ophthalmic Genetics
Child HealthOphthalmologyPediatricsPerinatologyGenetics
2011English

Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2

American Journal of Human Genetics
Genetics
2004English

High Myopia Is Not Associated With the SNPs in theTGIF, Lumican,TGFB1, andHGFGenes

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2009English

Confirmation of a Genetic Locus for X-Linked Recessive High Myopia Outside MYP1

Journal of Human Genetics
Genetics
2007English

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