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Genomics of Bipolar Disorder: What the Clinician Needs to Know

McQuillin, A; Ophoff, RA; (2025) Genomics of Bipolar Disorder: What the Clinician Needs to Know. Psychiatric Clinics of North America , 48 (2) pp. 331-341. 10.1016/j.psc.2025.01.009.

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Abstract

Bipolar disorder (BD) affects approximately 2% of the global population, characterized by alternating episodes of mania or hypomania, and depression. It comprises two main types: bipolar I disorder, marked by severe manic episodes, and bipolar II disorder, defined by milder hypomanic episodes. Individuals often experience rapid cycling and significant comorbidities, leading to decreased productivity and increased mortality rates. Early diagnosis and intervention are crucial for better outcomes. Both genetic and environmental factors contribute to BD's etiology, with genetic research promising improved diagnosis, novel therapeutic targets, and societal understanding that may help destigmatize the disorder.

Type: Article
Title: Genomics of Bipolar Disorder: What the Clinician Needs to Know
Location: United States
DOI: 10.1016/j.psc.2025.01.009
Publisher version: https://doi.org/10.1016/j.psc.2025.01.009
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Bipolar Disorder, Bipolar Disorder Subtypes, Pharmacogenetic, Genetic, Genomic, Twin
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Division of Psychiatry
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Division of Psychiatry > Mental Health Neuroscience
URI: https://discovery.ucl.ac.uk/id/eprint/10213964
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