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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Hair protein analysis might help identify a person's ethnicity, sex, and age in forensics.

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

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

Genetic factors may influence how well valproic acid works and its side effects in epilepsy treatment.

Monilethrix is linked to a gene cluster on chromosome 12.

GIANT improves brain imaging by using genetics to better map brain regions.

Genetically at-risk healthy people show similar immune issues as those with Pemphigus vulgaris or Alopecia areata.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Gene linked to common hair loss found, may lead to new treatments.

Androgenetic alopecia may cause schizophrenia, but schizophrenia does not cause androgenetic alopecia.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

A new gene mutation linked to a skin condition was found in a Spanish family.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

SNP profiling allows personalized skincare treatments for better results and fewer side effects.

Key genes and factors crucial for hair follicle development and wool traits in Merino sheep were identified.

The hair coat disorder in Schipperkes is similar to Alopecia X and involves increased androstenedione levels and hair cycle arrest.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A female Rottweiler had a rare genetic condition causing mostly hairless skin.

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

Allergies and atopic conditions may increase the risk of developing alopecia areata.

Different body areas in mice produce different hair types due to interactions between skin layers.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

Familial sexual precocity in girls may be more common than previously thought.