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Certain gene variations may increase the risk of hair loss in Egyptians.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain gene combinations may affect prostate cancer risk, and GSTP1 methylation is linked to tumor aggressiveness.

A KRT32 gene variant causes loose anagen hair syndrome.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Scientists discovered two versions of a new human hair keratin gene.

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

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Vitamin D receptor gene variations are not linked to alopecia areata.

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

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

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