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Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

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

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Researchers found a gene mutation responsible for a rare hair loss condition.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Certain gene changes and hormone levels are linked to female hair loss.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Mice with CBS deficiency are healthier on a low-methionine diet.

The same gene mutation can cause different symptoms in family members.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.