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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Researchers found a genetic region that influences the number of coat layers in dogs.

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

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

The Rotterdam Study aims to understand various diseases in older adults.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Researchers found two new genetic variants linked to Alzheimer's disease.

Lack of cystatin M/E causes thin hair and dry skin.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

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