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Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

The Gsdma3 gene is essential for normal hair development in mice.

The Naked gene in mice causes abnormal sebaceous glands and disrupts hair follicle organization.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

A new gene mutation is linked to monilethrix in the studied family.

KRTAP28-1 gene can help breed sheep with finer wool.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

ARHGEF3 is essential for proper hair follicle development in mice.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

The HCR gene contributes to psoriasis risk.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

A gene variation is linked to hair thickness in Asians.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

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

AR gene not major factor in female hair loss; different from male hair loss.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Cantú syndrome may be linked to pituitary adenomas.

Found new possible treatments for hair loss.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

A mutation in the human hairless gene causes alopecia universalis.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

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