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Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

Low-penetration genes might help personalize colorectal cancer prevention.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Certain gene variations may increase the risk of PCOS in South Indian women.

A specific gene change in APCDD1 increases the risk of hair loss.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Certain gene variations might be linked to severe acne in women but not in men.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

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

No link found between aromatase gene and female hair loss.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

The rs1128977 gene variant may affect cholesterol and body measurements.

CYP11A1 is crucial for skin health and disease by producing important steroids.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

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

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Gene differences affect finasteride side effects in men with hair loss.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Certain genetic variations are linked to hair loss in Mexican men.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Two new gene mutations cause a rare hair disorder.

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

The study found potential new DNA patterns in fertility genes, but further testing is needed.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Lack of cystatin M/E causes thin hair and dry skin.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.