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| Home > Publications database > Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. > print |
| 001 | 892948 | ||
| 005 | 20250813203211.0 | ||
| 024 | 7 | _ | |a 10.1038/s41588-021-00857-4 |2 doi |
| 024 | 7 | _ | |a pmid:34002096 |2 pmid |
| 024 | 7 | _ | |a 1061-4036 |2 ISSN |
| 024 | 7 | _ | |a 1546-1718 |2 ISSN |
| 024 | 7 | _ | |a 2128/29943 |2 Handle |
| 024 | 7 | _ | |a altmetric:106004916 |2 altmetric |
| 024 | 7 | _ | |a WOS:000651382200001 |2 WOS |
| 037 | _ | _ | |a FZJ-2021-02447 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 570 |
| 100 | 1 | _ | |a Mullins, Niamh |0 P:(DE-HGF)0 |b 0 |e Corresponding author |
| 245 | _ | _ | |a Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. |
| 260 | _ | _ | |a London |c 2021 |b Macmillan Publishers Limited, part of Springer Nature |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1754992218_25206 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 520 | _ | _ | |a Bipolar disorder is a heritable mental illness with complex etiology. We performed a genome-wide association study of 41,917 bipolar disorder cases and 371,549 controls of European ancestry, which identified 64 associated genomic loci. Bipolar disorder risk alleles were enriched in genes in synaptic signaling pathways and brain-expressed genes, particularly those with high specificity of expression in neurons of the prefrontal cortex and hippocampus. Significant signal enrichment was found in genes encoding targets of antipsychotics, calcium channel blockers, antiepileptics and anesthetics. Integrating expression quantitative trait locus data implicated 15 genes robustly linked to bipolar disorder via gene expression, encoding druggable targets such as HTR6, MCHR1, DCLK3 and FURIN. Analyses of bipolar disorder subtypes indicated high but imperfect genetic correlation between bipolar disorder type I and II and identified additional associated loci. Together, these results advance our understanding of the biological etiology of bipolar disorder, identify novel therapeutic leads and prioritize genes for functional follow-up studies. |
| 536 | _ | _ | |a 525 - Decoding Brain Organization and Dysfunction (POF4-525) |0 G:(DE-HGF)POF4-525 |c POF4-525 |f POF IV |x 0 |
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| 773 | _ | _ | |a 10.1038/s41588-021-00857-4 |0 PERI:(DE-600)1494946-5 |n 6 |p 817-829 |t Nature genetics |v 53 |y 2021 |x 1546-1718 |
| 856 | 4 | _ | |u https://juser.fz-juelich.de/record/892948/files/Mullins_etal_2021_Genome-wide%20association%20study%20of%20over%2040%2C000%20bipolar%20disorder%20cases.docx |y Published on 2021-05-17. Available in OpenAccess from 2021-11-17. |
| 856 | 4 | _ | |u https://juser.fz-juelich.de/record/892948/files/Mullins_etal_Nat.%20Genet._2021.pdf |y Restricted |
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