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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Seven new genetic risk areas for prostate cancer were found.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Male-to-female skin grafts in mice are rejected due to sex-linked antigens.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

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

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Researchers found 15 new genetic links to skin traits in Japanese women.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Genetic differences affect COVID-19 severity and treatment effectiveness.

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

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

New mutations in the hairless gene may cause hair loss and affect bone development.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

No clear link between specific gene and hair loss in Mexican brothers.

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

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

ESR2 gene linked to female-pattern hair loss.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

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

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.