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The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Genetics may play a significant role in gender dysphoria.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Long non-coding RNAs affect feather growth in chickens in ways that don't follow traditional genetic rules.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Guard hair length is positively correlated with guard hair diameter and down fiber length, but negatively correlated with variation in guard hair diameter and down fiber diameter.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Alopecia areata in these mice is inherited, more common in young females, and can be treated with triamcinolone acetonide.

The naked mutation in mice causes hair loss and helps identify keratin genes.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Overexpressing ovine β-catenin in mice skin increases hair follicle density and growth.

Black hairs have more pigment-related genes, while gray hairs have more keratin-related genes.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

Certain metabolites can either protect against or increase the risk of hair loss.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

Certain gene variations are found in people with polycystic ovary syndrome.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Wool traits in sheep are controlled by many genes and environmental factors.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Genetic testing is crucial for diagnosing rare hair loss disorders.