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Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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

New genes linked to male pattern baldness were found on chromosome 20p11.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A KRT32 gene variant causes loose anagen hair syndrome.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

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

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

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

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

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

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A gene variation is linked to hair thickness in Asians.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

These gene variations are not linked to alopecia areata in Egyptians.

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

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.