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A genetic marker linked to a type of hair loss was found in most patients studied.

Certain gene variations might be linked to severe acne in women but not in men.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

A gene-based model predicts lung adenocarcinoma outcomes and helps guide treatment decisions.

A specific gene variation in goats is linked to better growth traits.

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

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

A mutation in the Sgkl gene causes defective hair growth in mice.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

A new gene causes hairlessness and skin cysts in rats.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

ESR2 gene linked to female-pattern hair loss.

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, near the hairless gene.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.