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Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

No significant genetic link to alopecia areata was found in the Jordanian group.

Mutations in the HOXC13 gene cause hair and nail development issues.

The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Researchers found 24 genes that change significantly and affect cashmere growth in goats; this could help increase cashmere production.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Researchers created a new mouse model for studying scleroderma.

Hair follicles can be used to study gene mutations in Stargardt disease.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

Gene variations may increase oxidative stress in male pattern baldness.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.