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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 gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

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

A specific gene mutation causes severe skin and nail issues and hair loss.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Certain genetic variants may increase the risk of developing PCOS.

CARASIL can cause different symptoms even with the same genetic mutation.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Genetic differences affect COVID-19 severity and treatment effectiveness.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

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

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Variation in the TCHH gene affects wool curliness in sheep.

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

Targeting the TNFRSF1B gene may help treat hair loss.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.