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A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

No link found between aromatase gene and female hair loss.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Hairless gene not strongly linked to baldness.

Finasteride side effects in young men may be linked to specific gene variations.

Haplogroup X found in Altaian population supports Amerindian origin.

A specific gene mutation causes Olmsted syndrome.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A gene mutation causes woolly hair in a Syrian patient.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

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

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

Hair loss gene linked to prostate issues.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Longer CAG repeats in gene linked to more severe hair loss in females.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

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

A gene called BMAL1 plays a role in controlling hair growth.

MC4R gene variants not linked to female hair loss.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Certain gene variations are linked to better memory in healthy Chinese women.