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Certain gene variations might increase the risk of a hair loss condition in Koreans.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Memantine may slightly improve memory in people with Down syndrome, but more research is needed.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

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

Researchers found two new genetic variants linked to Alzheimer's disease.

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

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

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

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

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.

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

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Mutations in the SNRPE gene cause hereditary hair loss.

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

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

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

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.