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Two specific genetic markers increase the risk of hair loss in Asian populations.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

The visfatin GT genotype may increase the risk of Alopecia Areata.

Gene variation affects prostate issues and hair loss.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

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

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

New mutations in the hairless gene may cause hair loss and affect bone development.

Two gene variants cause white spots in cattle.

A mutation in the KRT25 gene causes woolly hair and hair loss.

New genetic variants linked to albinism were found in Pakistani families.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

A specific gene mutation causes severe skin and nail issues and hair loss.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.