Associated Papers
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes.
Fan Q et al.
Nature Communications, 2023
Association of HERPUD1 genetic variant rs2217332 with age-related macular degeneration and polypoidal choroidal vasculopathy in an Indian cohort.
Alagappan LP et al.
Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie, 2023
Clonal germinal center B cells function as a niche for T-cell lymphoma.
Fujisawa M et al.
Blood, 2022
35921527 (PubMed )
Supplement: BLOOD_BLD-2022-015451-mmc1.xlsx › supplemental_Table_6
Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.
Sha Y et al.
Bmc Medical Genetics, 2019
31370824 (PubMed )
Supplement: 12881_2019_864_MOESM2_ESM.xlsx › Sheet1
Evaluation of the association of C5 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
Liu K et al.
Eye and Vision (london, England), 2019
Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East Asians.
Fan Q et al.
Journal of Human Genetics, 2017
A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy.
Huang L et al.
Nature Genetics, 2016
Genetic Association of Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy.
Chen LJ
Asia-pacific Journal of Ophthalmology (philadelphia, Pa.), 0
Latest Development on Genetics of Common Retinal Diseases.
Chen LJ et al.
Asia-pacific Journal of Ophthalmology (philadelphia, Pa.), 0
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