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

ESR2 gene linked to female-pattern hair loss.

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

The MTR gene affects wool quality and production in Chinese Merino sheep.

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

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

SQSTM1 is linked to increased risk of alopecia areata.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

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

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

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

ESR2 gene variations may be linked to female pattern hair loss.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A specific gene variation in goats is linked to better growth traits.

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

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Certain genetic markers may increase or decrease prostate cancer risk.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A unique gene mutation was found in a family with monilethrix.