Handong Dan
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Explore the profile of Handong Dan including associated specialties, affiliations and a list of published articles.
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15
Citations
79
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Recent Articles
11.
Application of targeted exome and whole-exome sequencing for Chinese families with Stargardt disease
Dan H, Huang X, Xing Y, Shen Y
Ann Hum Genet
. 2019 Nov;
84(2):177-184.
PMID: 31674661
Objective: The aim of this study was to investigate pathogenic variants and molecular etiologies of Stargardt disease (STGD) in a cohort of Chinese families. Materials And Methods: A cohort of...
12.
Dan H, Shen Y, Huang X, Zhou F, Xing Y
Curr Eye Res
. 2019 Jul;
44(12):1353-1359.
PMID: 31352839
: This study aimed to assess resting cerebral blood flow (CBF) changes in retinitis pigmentosa (RP) patients using a pseudo-continuous arterial spin labeling (pCASL) perfusion method.: Forty-nine RP patients and...
13.
Sun Y, Man J, Wan Y, Pan G, Du L, Li L, et al.
Sci Rep
. 2018 Aug;
8(1):11646.
PMID: 30076350
With the development of next generation sequencing, more and more common inherited diseases have been reported. However, accurate and convenient molecular diagnosis cannot be achieved easily because of the enormous...
14.
Dan H, Song X, Li J, Xing Y, Li T
Ophthalmic Genet
. 2016 Jul;
38(3):206-210.
PMID: 27428514
Background: Schubert-Bornschein congenital stationary night blindness (CSNB) is a rare retinal disorder that may lead to severe visual impairment in patients. The aim of this study was to detect mutations...
15.
Zhou L, Li T, Song X, Li Y, Li H, Dan H
Mol Vis
. 2015 Mar;
21:213-23.
PMID: 25802485
Purpose: Mutations in the NYX gene are known to cause complete congenital stationary night blindness (CSNB1), which is always accompanied by high myopia. In this study, we aimed to investigate...