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A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

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

A gene variation is linked to hair thickness in Asians.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Targeting IL-15 may help treat Alopecia Areata.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Certain gene variations may increase the risk and severity of alopecia areata.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

CT60 polymorphism might increase the risk of Alopecia Areata.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

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

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Haplogroup X found in Altaian population supports Amerindian origin.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

RXRα is crucial for proper immune response and links diet to immune function.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

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

New genetic mutations causing hair loss were found in a Chinese family.

Certain genetic variations are linked to hair loss in Mexican men.