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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

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

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Genetic discoveries are leading to new treatments for alopecia areata.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

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

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

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

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A new mutation in the HR gene causes hair loss in a specific family.

No significant link was found between the studied genes and female hair loss in the Polish population.

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

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

A mutation in the human hairless gene causes alopecia universalis.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.