These are essentially genetic variants that primarily contribute to bipolar disorder risk, as opposed to just being mere markers of it.

Novel Human Genetics Evidence Confirms Estimates of Genetic Prevalence, Underdiagnosis, and Potentially Greater Symptom Burden of Gain-of-Function CASR Variants Associated with ADH1 ...

- By examining over 100 unique variants associated with the CASR gene causative of ADH1, the average frequency of gain-of-function CASR variants was ~3.7 per 100,000, closely aligned to previously ...

A Pokemon fan artist creates new regional variants for Nosepass and Probopass, creatures introduced in Gen 3 and 4, respectively.

Men who carry two copies of a common genetic variant are twice as likely to develop dementia than women with the same mutations, according to a new study from Australian researchers. This ...

A novel genetic variant may be a driving force behind the development of metabolic dysfunction–associated steatotic liver disease (MASLD) in some cases, according to researchers at the Mayo ...

Resources are available to help physicians when they encounter variants of unknown significance during genetic testing, Troy R. Torgerson, MD, PhD, said during Updates in Primary Immunodeficiency ...

The data highlight relevant differences in variants associated with LAC patients, including founder and recurrent variants, while showcasing potential features that might be relevant in oncology ...

Certain common genetic changes might make some people with focal epilepsy less responsive to seizure medications, finds a new global study.

Every person carries a unique combination of genetic variants from birth, and these inherited differences quietly shape how our cells function throughout life.