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Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

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

Variation in the TCHH gene affects wool curliness in sheep.

Three genes linked to the development of trichilemmal cysts were found.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

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

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Two new gene mutations cause a rare hair disorder.

CT60 polymorphism might increase the risk of Alopecia Areata.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

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

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Genetic variants in specific genes cause a type of hair loss.

A specific gene change in APCDD1 increases the risk of hair loss.

Certain gene variations are linked to the thickness of cashmere goat hair.