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

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Rare genetic variants contribute to male pattern hair loss, but there's no link to severe COVID-19.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

ILC1-like cells can cause alopecia areata by themselves.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

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

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Certain gene variations increase the risk of alopecia areata in Koreans.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Genetically at-risk healthy people show similar immune issues as those with Pemphigus vulgaris or Alopecia areata.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A new therapy for a skin blistering condition has not been developed yet.

The LMNA mutation affects skin structure even in asymptomatic carriers.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Genetic marker rs12558842 strongly linked to male hair loss.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

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

Mutant keratins cause inflammation in Epidermolysis Bullosa Simplex, suggesting targeting them could help treat the disorder.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Keratin mutations cause skin diseases and could lead to new treatments.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.