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The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

STK11 gene polymorphism does not predict metformin response in PCOS.

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

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

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Male pattern baldness is linked to specific genetic variations in the androgen receptor gene.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Certain gene variations may increase the risk of PCOS in South Indian women.

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

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.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A new gene mutation is linked to monilethrix in the studied family.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Different forms of finasteride dissolve and remain stable differently, affecting capsule quality.

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

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

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

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.