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

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

Polygenic risk scores can predict the risk and outcomes of benign prostatic hyperplasia.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

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

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Six new hair loss factors in men not linked to female hair loss.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

PCOS is likely inherited in families, increasing risk for first-degree relatives.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

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

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

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

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

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

A KRT32 gene variant causes loose anagen hair syndrome.

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

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

HLA-DRB5 and other genes may be linked to alopecia universalis.