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Certain gene variations may increase the risk of hair loss in Egyptians.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

C-scores can help predict gain-of-function and loss-of-function mutations.

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

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

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

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A specific gene mutation causes a severe skin disorder in a family.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The visfatin GT genotype may increase the risk of Alopecia Areata.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Trichotillomania may have a genetic link to psychiatric disorders.

A specific gene variant may increase the risk of developing Alopecia Areata.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new mouse mutation causes skin and hair defects due to a gene change.

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

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

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