https://doi.org/10.1111/jcmm.16385
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Shangyi Fu
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64
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15
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18
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Shangyi Fu is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Retinal Development and Disorders & Skin Protection and Aging & Cutaneous Melanoma Detection and Management. The author has an h-index of 15, co-authored 55 publications.
ORCID: 0000-0003-0499-3495Papers by this author
worksProstate adenocarcinoma and COVID‐19: The possible impacts of <i>TMPRSS2</i> expressions in susceptibility to SARS‐CoV‐2
2021 · Journal of Cellular and Molecular Medicine · 29 citations
A novel, homozygous nonsense variant of the <i>CDHR1</i> gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis
2018 · Journal of Cellular and Molecular Medicine · 21 citations
https://doi.org/10.1111/jcmm.13841
A novel splicing mutation in the <i>PRPH2</i> gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree
2019 · Journal of Cellular and Molecular Medicine · 21 citations
https://doi.org/10.1111/jcmm.14278
Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant
2018 · British Journal of Ophthalmology · 15 citations
https://doi.org/10.1136/bjophthalmol-2018-312347
Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
2022 · Molecules · 9 citations
https://doi.org/10.3390/molecules27217413
Novel, pathogenic insertion variant of <scp>GSDME</scp> associates with autosomal dominant hearing loss in a large Chinese pedigree
2023 · Journal of Cellular and Molecular Medicine · 7 citations
https://doi.org/10.1111/jcmm.18004
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