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Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Male mice with FGF5 mutations grow longer hair than females.

Certain genetic markers may increase or decrease prostate cancer risk.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Genetic marker rs12558842 strongly linked to male hair loss.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A new DSG4 gene mutation causes hair defects in a young girl.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A specific gene mutation causes sparse, brittle hair in a family.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

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

CT60 polymorphism might increase the risk of Alopecia Areata.

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

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

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.