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A gene variant increases the risk of a type of hair loss by affecting hair protein production.

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

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

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

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A new gene variant causes curly coats in some dog breeds.

These gene variations are not linked to alopecia areata in Egyptians.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A specific gene mutation causes a severe skin disorder in a family.

Researchers found two new genetic variants linked to Alzheimer's disease.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

JAK1 gene variation may increase alopecia areata risk.

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

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

AR polyglycine repeat doesn't cause baldness.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

A KRT32 gene variant causes loose anagen hair syndrome.

Gene differences affect finasteride side effects in men with hair loss.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.