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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Specific gene variants affect wool traits in Chinese Tan sheep.

The rs1128977 gene variant may affect cholesterol and body measurements.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

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

Mutations in the Whn gene affect hair keratin gene expression differently.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

No significant genetic link to alopecia areata was found in the Jordanian group.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

TCF7L2 gene polymorphism is linked to alopecia areata, but it doesn't affect the success of PRP or conventional treatments.

Older parental age, rural living, and specific genetic mutations increase hypospadias risk in children.

DNA analysis can help tailor alopecia treatment.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

AR polyglycine repeat doesn't cause baldness.

Keratinocyte cytokines and genetic variations influence the development of moles and skin pigmentation.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.