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Both HLA-B and MICA are independently linked to alopecia areata.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Researchers found two new genetic variants linked to Alzheimer's disease.

A new mutation in mice causes crooked whiskers and messy hair.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

Ritlecitinib significantly improves scalp hair regrowth in alopecia areata patients over time.

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The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

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Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Anti-DFS70 antibodies can help identify nonsystemic autoimmune conditions in SLE patients.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Ritlecitinib may be more effective for severe alopecia areata than conventional treatments.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

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Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.