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Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A KRT32 gene variant causes loose anagen hair syndrome.

New mutations in the DSG4 gene cause a rare hair condition.

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Vitamin D receptor gene variations are not linked to alopecia areata.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A new gene mutation causes long hair in some Maine Coon cats.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

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

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

CAG repeat polymorphism and prostate zone volume are not reliable markers of long-term androgen sensitivity.

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 genetic variations in the AR and ERβ genes can affect androgen levels in women.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A genetic marker linked to a type of hair loss was found in most patients studied.