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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

ESR2 gene linked to female-pattern hair loss.

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

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

SB414 may be an effective treatment for atopic dermatitis by reducing swelling and bacterial infection.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

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The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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The study found genetic variations in sheep linked to traits like milk production, growth, and health.

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A gene called HDAC9 might be a new factor in male-pattern baldness.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

A KRT32 gene variant causes loose anagen hair syndrome.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

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Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

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Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

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Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.