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Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

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

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Gene variation affects prostate issues and hair loss.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Hair loss gene linked to prostate issues.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Certain gene variations are found in people with polycystic ovary syndrome.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A gene variation is linked to hair thickness in Asians.

Certain gene variations are significantly linked to hair loss, especially in white people.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Genetic differences may influence male pattern hair loss in Russians.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.