Inflammatory and infectious upper respiratory diseases (ICD-10: J30-J39), such as diseases
of the sinonasal tract, pharynx and larynx, are growing health problems yet their genomic …

Vitiligo is characterized by death or functional defects of epidermal melanocytes through still
controversial pathogenic process. Previously, we showed that mitochondria-driven pre …

Background: The association between circulating vitamin D levels and risk of vitiligo was
inconsistent among observational studies, and whether these observed associations were …

Autoimmune Addison's disease (AAD) is a rare but life-threatening endocrine disorder
caused by an autoimmune destruction of the adrenal cortex. A previous genome-wide …

Oculocutaneous albinism (OCA), which is roughly divided into non‐syndromic and
syndromic OCA, is a group of autosomal recessive disorders caused by mutations in genes …

Background: Vitiligo is an acquired depigmenting skin disorder with multifactorial
pathogenesis including genetic, autoimmune, and neuronal factors. Both humoral-and cell …

The association of molecular variants with phenotypic variation is a main issue in biology,
often tackled with genome‐wide association studies (GWAS). GWAS are challenging, with …

Purpose Vitiligo is an acquired depigmented skin disorder. Though genetic background,
autoimmune dysregulation, and oxidative stress were reported involved in the development …

As the circadian clock regulates fundamental biological processes, disrupted clocks are
often observed in patients and diseased tissues. Determining the circadian time of the …

Background Vitiligo is a long-term skin disease characterized by the loss of pigment in the
skin. The current therapeutic approaches are limited. Although the anti-vitiligo mechanisms …