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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

A specific gene mutation causes complete hair loss without other health issues.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

A certain gene variation can affect protein production and is linked to male pattern baldness.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

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

Different populations have distinct hair structures related to their ancestry.

Hair root sheaths can be used to accurately analyze genetic markers.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

DNA markers can help predict male pattern baldness, useful in criminal and missing person cases.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

New mutations in the hairless gene may cause hair loss and affect bone development.

A specific gene mutation causes congenital hair loss.

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

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.