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Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci Open
Vitiligo is an autoimmune disease with a strong genetic component, characterized by areas of depigmented skin resulting from loss of epidermal melanocytes. Genetic factors are known to play key roles in vitiligo through discoveries in asso…
Epigenome-wide association data implicates DNA methylation-mediated genetic risk in psoriasis Open
Background Psoriasis is a chronic inflammatory skin disease characterized by epidermal hyperproliferation and altered keratinocyte differentiation and inflammation and is caused by the interplay of genetic and environmental factors. Previo…
Oculocutaneous Albinism with Squamous Cell Carcinoma, Bowen's Disease and Actinic Keratosis: A Case Report Open
Introduction Oculocutaneous albinism (OCA) is an autosomal recessive disorder characterized by defects in melanin synthesis that affect the skin, eyes, ears, and hair to varying degrees. Because of the melanin deficiency, albino patients a…
View article: Genotype combination contributes to psoriasis: An exhaustive algorithm perspective
Genotype combination contributes to psoriasis: An exhaustive algorithm perspective Open
Researchers have learned that nearly all conditions and diseases have a genetic component. With the benefit of technological advances, many single-nucleotide polymorphisms (SNPs) have been found to be associated with the risk of complex di…
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Issue Information Open
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Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci Open
Vitiligo is an autoimmune disease with a strong genetic component, characterized by areas of depigmented skin resulting from loss of epidermal melanocytes. Genetic factors are known to play key roles in vitiligo through discoveries in asso…