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

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

Mutations in the SNRPE gene cause hereditary hair loss.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A gene mutation in mice causes permanent hair loss and skin issues.

The hair keratin variant is mostly found in Caucasians.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Björnstad syndrome causes twisted hair from birth.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Curved human hair has different structures on each side, which might cause its shape and is similar to wool.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

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

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Using special RNA to target a mutant gene fixed hair problems in mice.

A mutation in mice causes hair loss and immune problems.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Hair fiber shape and curvature are not significantly linked when ancestry is considered.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

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

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Mutations in the HOXC13 gene cause hair and nail development issues.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

A mutation in the Sgkl gene causes defective hair growth in mice.

Certain IL-18 gene variations may increase the risk of alopecia areata.

PRP helps hair growth in common hair loss disorder.