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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Variation in the TCHH gene affects wool curliness in sheep.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

The BASP classification is effective for diagnosing pattern hair loss in Indian men and women.

Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

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

A specific gene change in APCDD1 increases the risk of hair loss.

CARASIL can cause different symptoms even with the same genetic mutation.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Common baldness is likely inherited through multiple genes, not just one.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A genetic hair protein variant is more common in Japanese people and is inherited.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Certain genes influence the direction of hair whorls on the scalp.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

The EDAR gene greatly affects hair thickness in Asian populations.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

LIPH mutations cause woolly hair in some Chinese people.