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A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

ESR2 gene variations may be linked to female pattern hair loss.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

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

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

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Certain gene variations are linked to better memory in healthy Chinese women.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

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

Male pattern baldness is linked to specific genetic variations in the androgen receptor gene.

Two gene areas linked to male pattern baldness found, more research needed.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Haplogroup X found in Altaian population supports Amerindian origin.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Robertsonian translocation can cause recurrent miscarriages.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

Somatic BHD mutations are rare in Japanese renal tumors.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Researchers found a gene mutation responsible for a rare hair loss condition.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.