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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

The document concludes that more research is needed to create suitable diagnostic criteria and understand PCOS in Korean women, and genetics may allow for personalized treatment.

Certain genes may influence hair loss differently in men and women.

DNA markers can help predict male pattern baldness, useful in criminal and missing person cases.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

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

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Nociplastic type pain, common in Chronic Overlapping Pain Conditions, is a complex, heritable trait linked to 24 unique genetic factors and 127 genes, with potential shared mechanisms in cognitive, personality, and metabolic traits.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

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.

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

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A genetic variant linked to hair thinning in Japanese women was found.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Genes linked to wool fineness in sheep have been identified.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

The Orenburg goat breed has unique genetics that require more detailed research and careful breeding.