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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
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Abstract
Abstract Bipolar disorder (BD) is a heritable mental illness with complex etiology. We performed a genome-wide association study (GWAS) of 41,917 BD cases and 371,549 controls of European ancestry, which identified 64 associated genomic loci. BD 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 eQTL data implicated 15 genes robustly linked to BD via gene expression, encoding druggable targets such as HTR6, MCHR1, DCLK3 and FURIN. Analyses of BD subtypes indicated high but imperfect genetic correlation between BD type I and II and identified additional associated loci. Together, these results advance our understanding of the biological etiology of BD, identify novel therapeutic leads and prioritize genes for functional follow-up studies.
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“As previous studies and our results suggest, EduYears shows phenotypic correlations and shares genetic components with multiple traits and diseases relevant to medical research, including cognitive function, neurodegeneration and psychiatric disorders43–46”
From Shared genetic architectures of educational attainment in East Asian and European populations (2024) · cites this paper as [46]
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“For psychiatric disorders, summary data from the following GWAS were used: schizophrenia (SCZ; 33,640 cases; 43,456 controls)(19), bipolar disorder (BPD; 41,917 cases; 371,549 controls)(20), depression (as a broader phenotype closely related to major depressive disorder (MDD)) (246,363 cases; 561,190 controls)(21), an…”
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“Although twin studies estimate the heritability of BD to be between 60% and 85%, variations identified through genome-wide association studies (GWAS) account for less than 20% of the disease risk [ 3, 4 ].”
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“…disorders are associated with AMS treatment response, PGSs were calculated using GWAS summary statistics for attention-de fi cit/ hyperactivity disorder (ADHD; [26]), BD [27], major depressive disorder (MDD; [28]), anxiety disorders [29], schizophrenia [30], and generalized epilepsy [31].”
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InfluentialSelf-citationAssociations between mosaic loss and schizophrenia or bipolar disorder of young age
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“…GWASs identified CACNA1C and other voltage-gated calcium-channel subunits as genome-wide significant loci for BD [44,45], while subsequent large-scale meta-analyses extended these findings to SCZ and cross-disorder cohorts, revealing convergent enrichment of calcium-related pathways [42–45].”
InfluentialSelf-citationTransformer-based deep learning enhances discovery in migraine GWAS
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“We also used GWAS summary statistics data of schizophrenia 18 , bipolar disorder 53 , autism spectrum disorder 54 , and major depression disorder 55 obtained from the Psychiatric Genomics Consortium.”
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“[25,26] The study methodology, including participant characteristics and quality control protocols, has been extensively described in prior publications.”
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InfluentialDeficiency of Kif15 impairing synaptic development leads to mood disorder in mice
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“Such an approach is indispensable for achieving a more comprehensive understanding of the factors at play in BD. Thirdly, substantial evidence indicates that genetic factors significantly influence brain function and may underpin conditions like BD [65].”
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“%) are lower than the estimates from family, twin and adoption studies, and that BD-PRS only explains 8% of phenotypic variance in both adults and youth with BD (Birmaher et al., 2022; Jiang et al., 2024; Mullins et al., 2021; Owen and Williams, 2021).”
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“…and 7992 controls) (Forstner et al. 2021), ASD (18,381 cases and 27,969 controls) (Grove et al. 2019), BIP (41,917 cases and 371,549 controls) (Mullins et al. 2021), AN (16,992 cases and 55,525 controls) (Watson et al. 2019), MDD (15,771 cases and 178,777 controls), OCD (2688 cases and 7037…”
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Polygenic risk scores in relation to suicidality among youth with or at risk for bipolar disorder
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“The fi rst cluster comprised the ASD, EPI, and PD, the second included the ADHD and DEP, and the third cluster encompassed the OCD, SCZ, and BIP (Fig.”
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“…studies (GWASs) of depression (246 363 cases and 561 190 controls) (Howard et al., 2019), bipolar disorder (41 917 cases and 371 549 controls) (Mullins et al., 2021), schizophrenia (76 755 cases and 243 649 controls) (Trubetskoy et al., 2022), and anxiety (25 453 cases and 58 113 controls)…”
Self-citationMendelian randomisation analysis to explore the association between cathepsins and bipolar disorder
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“In contrast, individuals with type II BD exhibit a more chronic profile, with a greater duration of depressive episodes over the course of the illness than those with type I. Type II BD presents with recurrent episodes of major depression that persist for a longer duration [4–6].”
BackgroundGenomicSEM Modelling of Diverse Executive Function GWAS Improves Gene Discovery
Perry, L. C., Chevalier, N., & Luciano, M. (2025) · Behavior Genetics · doi:10.1007/s10519-025-10214-4 · Cited by 2
“…attainment (Okbay et al. 2022 ) and 9 different disorders taken from the psychiatric genetics consortium (Arnold et al. 2018; Demontis et al. 2023; Forstner et al. 2021; Grove et al. 2019; Howard et al. 2019; Mullins et al. 2021; Trubets-koy et al. 2022; Watson et al. 2019; Yu et al. 2019).”
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“…with evidence linking (a) BD to single-nucleotide polymorphisms within multiple clock genes, (b) mood variability to polygenic risk scores related to chronotype and low circadian amplitude, and (c) disruptions in sleep/sleep-activity rhythms [46–48] in family members of those diagnosed with BD.”
BackgroundPopulation clustering of structural brain aging and its association with brain developmentPreprint
Duan, H., Shi, R., Kang, J., Banaschewski, T., Bokde, A. L. W., Büchel, C., Desrivières, S., Flor, H., Grigis, A., Garavan, H., et al. (2024) · eLife · doi:10.7554/elife.94970 · Cited by 6
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“Recent genome-wide association studies (GWASs) have identi fi ed fatty acid desaturase ( FADS1 and FADS2 ) genes, which encode enzymes involved in n-3 and n-6 lipid biosynthesis pathways, as susceptibility genes of BD (top single nucleotide polymorphism [SNP] rs28456) [15, 16].”
BackgroundSelf-citationRethinking the connection between bipolar disorder and epilepsy from genetic perspectives
Huo, J.-H., & Li, M. (2024) · Genomic Psychiatry · doi:10.61373/gp024l.0061 · Cited by 2
Roles of alternative polyadenylation in psychiatric disorder risk
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Self-citationSchizophrenia and risk preference: a bidirectional two-sample mendelian randomization study
Zhao, Y., Guo, W.-L., Zhou, J.-S., & Wang, X.-P. (2024) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-024-01853-5 · Cited by 2
“The summary data of GWAS related to schizophrenia were obtained from a meta-analysis involving GWAS on subjects of European ancestry from The Psychiatric Genomics Consortium (https://www.med.unc.edu/pgc/) [13, 14].”
Tume, C. E., Chick, S. L., Holmans, P., Rees, E., O’Donovan, M. C., Cameron, D., & Bray, N. J. (2024) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2024.100345 · Cited by 2
“371,000 controls) (28), and neuroticism ( .”
Self-citationPutative Risk Biomarkers of Bipolar Disorder in At-risk Youth
Meng, X., Zhang, S., Zhou, S., Ma, Y., Yu, X., & Guan, L. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01219-w · Cited by 3
“Recently, a GWAS study in more than 40,000 patients found 15 genes linked to BD [28].”
Wu, Y., Zhang, C., Zhang, Y., Chen, R., Wang, L., Chang, H., Li, M., Xiao, X., & Li, S. L. (2024) · Psychiatry Research · doi:10.1016/j.psychres.2024.115929 · Cited by 2
Vellucci, L., Simone, G. D., Morley‐Fletcher, S., Buonaguro, E. F., Avagliano, C., Barone, A., Maccari, S., Iasevoli, F., & de Bartolomeis, A. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111032 · Cited by 2
“…autism spectrum disorder, bipolar disorder, and major depressive disorder (Berdenis van Berlekom et al. 2020; Fatemi et al. 2013; Leber et al. 2017; Mullins et al. 2021). disorders involve significantly the impact may the development and Baram this context, it networks using thought to be al.”
Georgiou, A. N., Voskarides, K., Zanos, P., & Chatzittofis, A. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1379922 · Cited by 2
Edwards, A. C., Singh, M., Peterson, R. E., Webb, B. T., & Gentry, A. E. (2024) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32982 · Cited by 2
Vreeker, A., Horsfall, M., Eikelenboom, M., Beerthuizen, A., Bergink, V., Boks, M. P., Hartman, C. A., de Koning, R. M., de Leeuw, M., Maciejewski, D. F., et al. (2024) · BMC Psychiatry · doi:10.1186/s12888-024-05555-z · Cited by 3
“For bipolar disorder, 64 genetic loci have been identified and it is expected that more genetic loci will be identified when sample sizes increase [19].”
BackgroundSelf-citationKanjira, S. C., Adams, M., Jiang, Y.-X., Tian, C., Lewis, C., Kuchenbaecker, K., & McIntosh, A. (2023) · medRxiv · doi:10.1101/2023.12.24.23300412 · Cited by 2
Self-citationGuo, W., Zhao, Y., Liu, J., Zhou, J., & Wang, X. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.12.018 · Cited by 2
Valentim, W. L., Tylee, D. S., & Polimanti, R. A. (2023) · WIREs Mechanisms of Disease · doi:10.1002/wsbm.1635 · Cited by 2
Zhong, Y., Baum, L., Tubbs, J. D., Ye, R., Chen, L. H., Wu, T. T., Hung, S., Tang, C.-P., Ho, T.-I., Moyzis, R. K., et al. (2025) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-025-09626-4 · Cited by 2
“…Genomics Consortium (PGC) summary statistics of five major psychiatric disorders [i.e., ADHD [11], autism spectrum disorder [35], bipolar disorder [36], major depressive disorder [37], and schizophrenia [38] were used as the training datasets to calculate individual-level PGS in our sample.”
Independent inheritance of cognition and bipolar disorder in a family sample
D'Amico, A., Sung, H., Arbona‐Lampaya, A., Freifeld, A., Hosey, K., Garcia, J., Lacbawan, L. N., Besancon, E., Kassem, L., Akula, N., et al. (2024) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.33001 · Cited by 2
“However, it is unknown to what degree cognitive symptoms in BD are a core feature of the illness, as in SCZ, since cognitive impairments could be the result of BD or its treatment.”
InfluentialSelf-citationHu, J., Zhang, Y., Zheng, S., Chen, G.-R., Lin, Y., Kang, D., Lin, Z., & Yao, P. (2023) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2023.05.070 · Cited by 2
Keeping the balance: Trade-offs between human brain evolution, autism, and schizophrenia
Duński, E., & Pękowska, A. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.1009390 · Cited by 5
“There are multiple newly discovered coding and non-coding regions implicated in SCZ, ASD and other ND that await further analysis from the evolutionary and functional standpoints (Demontis et al., 2019; Grove et al., 2019; Howard et al., 2019; Mullins et al., 2021; Wightman et al., 2021; Trubetskoy et al., 2022).”
BackgroundA higher genetic risk for depression is a greater risk factor for cardiovascular disease in women
Jiang, J.-Y., Singh, K., Davis, L. K., Wray, N., & Shah, S. H. (2022) · medRxiv · doi:10.1101/2022.10.08.22280805 · Cited by 2
Self-citationNew drug targets in psychiatry: Neurobiological considerations in the genomics era
Harrison, P. J., Mould, A. W., & Tunbridge, E. M. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104763 · Cited by 1
“Thus, there is significant overlap in GWAS-identified candidate risk genes between psychiatric illnesses, particularly between schizophrenia and bipolar disorder (Mullins et al., 2021; Consortium et al., 2020).”
BackgroundSchizophrenia and Bipolar Polygenic Risk Scores in Relation to Intracranial Volume
de Zwarte, S. D., Brouwer, R., Kahn, R., & van Haren, N. V. (2022) · Genes · doi:10.3390/genes13040695 · Cited by 2
“There is no evidence of a significant genetic correlation between either disorder and ICV based on the findings from genome wide association studies (GWAS) of schizophrenia and bipolar disorder [14,15]; however, genetic overlap between schizophrenia and ICV has been suggested through conditional false discovery rate a…”
BackgroundSelf-citationHsa-miR-19b-3p and Hsa-miR-23b-3P are the candidate biomarkers for bipolar disorder
Davarinejad, O., Foruzandeh, Z., Mohammadi, P., Golmohammadi, F., Ghavi, D., Alivand, M. R., Chogan, M., Zhaleh, H., & Rahmati, Y. (2022) · Informatics in Medicine Unlocked · doi:10.1016/j.imu.2022.100959 · Cited by 2
Taylor-Desir, M. J., Balls‐Berry, J. E., McElroy, S. L., Bond, D. J., Vallender, E. J., Ladner, M. E., Coombes, B. J., Jackson, L., Arceo, D., Caples, F. V., et al. (2022) · Journal of Racial and Ethnic Health Disparities · doi:10.1007/s40615-022-01228-3 · Cited by 2
“The recent Psychiatric Genomics Consortium (PGC) genome-wide association study (GWAS) included more than 40,000 BD cases and discovered 64 genome-wide significant associations, but all participants were European; patients of East Asian and African ancestries were only included in follow-up analyses [13].”
BackgroundSelf-citationSugawara, H., Bundo, M., Kasahara, T., Nakachi, Y., Ueda, J., Kubota-Sakashita, M., Iwamoto, K., & Kato, T. (2022) · Molecular Brain · doi:10.1186/s13041-021-00894-4 · Cited by 2
“A recent genome-wide association study revealed that BD is a polygenic disorder caused by multiple genetic risks with small effect sizes [1].”
BackgroundEmotional cognition subgroups in unaffected first-degree relatives of patients with mood disorders
Kjærstad, H. L., Varo, C., Meluken, I., Vieta, E., Vinberg, M., Kessing, L. V., & Miskowiak, K. W. (2021) · Psychological Medicine · doi:10.1017/s0033291721004165 · Cited by 4
Self-citationDissecting Biological Pathways of Psychopathology using Cognitive GenomicsPreprint
Lam, M., Chen, C., Hill, W. D., Xia, C., Tian, R., Levey, D. F., Gelernter, J. E., Stein, M. B., Biogen Biobank team, Hatoum, A. S., et al. (2021) · medRxiv · doi:10.1101/2021.07.20.21260487 · Cited by 2
Self-citationThe moving target of psychiatric diagnosis
Alda, M. (2021) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.210098 · Cited by 5
Self-citationWestern, D., Yang, C., Timsina, J., Liu, M., Wang, C., Campbell, M. C., Kotzbauer, P., Perlmutter, J. S., Schindler, S. E., Morris, J. C., et al. (2026) · Science Translational Medicine · doi:10.1126/scitranslmed.adz2016 · Cited by 1
Xia, P.-H., Wesseldijk, L., Lu, Y., Sikström, S., de Manzano, Ö., Vach, V., Ullén, F., & Mosing, M. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03925-5 · Cited by 1
Okewole, A., Bourque, V.-R., Koko, M., Huguet, G., Børglum, A. D., Grove, J., Jacquemont, S., Baron‐Cohen, S., & Warrier, V. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03880-1 · Cited by 1
Self-citationZeng, L., Khan, A., Fitzgerald, K. C., Lama, T., Chen, J., Li, R., Harroud, A., Compston, A., Sawcer, S. J., Kermode, A. G., et al. (2026) · Nature Genetics · doi:10.1038/s41588-026-02731-7 · Cited by 5
“…variants, we evaluated our updated list of 236 MS susceptibility SNPs (Supplementary Table 4) across other GWAS, including MS severity 2 , 12 autoimmune diseases 37–44 , 4 neurodegenerative diseases 45–48 , 4 psychiatric disorders/traits 49–52 and 3 metabolic traits 53,54 (Supplementary Table 8).”
Self-citationGlaser, B., Bazezew, M., Bragantini, D., Hegemann, L., Orm, S., Morgan, M., Bishop, S. L., Valand, S. B., Hannigan, L., & Havdahl, A. (2026) · Autism · doi:10.1177/13623613261474929 · Cited by 1
“…Demontis et al., 2023), anorexia nervosa (Termorshuizen et al., 2025), anxiety (Purves et al., 2020), autism (Grove et al., 2019), bipolar disorder (Mullins et al., 2021), childhood maltreatment (Warrier et al., 2021), educational attainment (Lee et al., 2018), insomnia (Watanabe et al., 2019),…”
Identifying independent causal cell types for human diseases and risk variants
Kim, A., Zhang, Z., Legros, C., Wang, H., Lu, Z., de Smith, A. J., Moore, J. E., Durvasula, A., Mancuso, N., & Gazal, S. (2026) · Cell Genomics · doi:10.1016/j.xgen.2026.101325 · Cited by 14
Martone, A., Folego-Temoteo, I., Fries, G. R., Docherty, A. R., Ashley‐Koch, A. E., Apter, A., Baca-García, E., Balázs, J., Barzilay, S., Bobes, J., et al. (2026) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2026.112821 · Cited by 2
Self-citationFrom Synapses to Circuits, the Role of KIBRA and the WWC Family in Adaptive Brain Function
Volk, L. J. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70514 · Cited by 1
Seo, Y. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27136084 · Cited by 1
“A GWAS can identify risk loci enriched in neuronal and synaptic genes, including ion-channel-associated pathways [119–122].”
Genomic relationship between polyendocrine metabolic ovarian syndrome and bipolar disorder
Jaholkowski, P. P., Tesfaye, M., Fominykh, V., Parekh, P., Wiström, E. D., Parker, N., Koch, E. M., Bauer, A. E., Trzaskoma, P., Rokicki, J., et al. (2026) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2026.112903 · Cited by 2
Self-citationSchizophrenia and bipolar disorder: a comparative analysis of genetic and brain network connectivity
Ren, H., Liu, Y.-J., Huang, Y.-Q., Tang, Y.-G., Xiao, L.-L., Wu, Y.-L., Liu, S.-Y., Yin, Y., Ma, Q., Dai, M.-H., et al. (2026) · Psychological Medicine · doi:10.1017/s0033291726104413 · Cited by 1
“For BD and SCZ, we used the GWAS results of BD conducted by Mullins et al. (Mullins et al., 2021) including 41,917 cases and 371,549 controls, and those of SCZ conducted by Trubetskoy et al. (Trubetskoy et al., 2022) including 76,755 cases and 243,649 controls.”
Immune dysfunction in psychiatric disorders: emerging genomic insights
McGrath, I. M., & Lynall, M.-E. (2026) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2026.102467
Shah, K., Totty, M. S., Bach, S. V., Valentine, M. R., Chandra, A., AlGrain, H. A., Divecha, H. R., Miller, R. A., Siewe, F. R. M., Kwon, S. H., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117500 · Cited by 5
Wang, M., Galvin, V. C., Joyce, M. K. P., Datta, D., Yang, S., Disney, A. A., & Arnsten, A. F. T. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.06.008 · Cited by 2
Rødevand, L. N., Rahman, Z., Jahołkowski, P., Parker, N., Valdimarsdóttir, U. A., Smeland, O. B., Tesfaye, M., Parekh, P., Frei, O., Djurovic, S., et al. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106304 · Cited by 1
“13,14 Thus, we aimed to elucidate the potential role of smoking in the genetic relationship between SCZ, BIP and BMI.”
InfluentialSelf-citationAryal, S., Geng, C., Yin, M. A., Kwon, M. J., Farsi, Z., Goble, N., Asan, A. S., Brenner, K. S., Shepard, N., Geller, A., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117436 · Cited by 7
Niu, M.-Q., Chen, C., & Maes, M. (2026) · The European Physical Journal Special Topics · doi:10.1140/epjs/s11734-026-02369-w · Cited by 1
Tesfaye, M., Stavrum, A.-K., Höffler, K. D., O’Connell, K. S., David, F. S., Garrett, M. E., Hesam-Shariati, S., Overs, B. J., Pisanu, C., Spano, L., et al. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106284
“2,43 BD subtypes may have underlying biological differences; hence, discoveries reported in studies of BD may not necessarily apply to BDII.”
Self-citationSex-specific impact of vitamin D and B9 concentrations on neuroticism: a polygenic score-based study
Алфимова, М. В., Голимбет, В. Е., Semina, E. V., & Chaika, Y. A. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2026.1788663 · Cited by 1
Wang, X., Luo, L., Chang, S., & Yang, L. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03606-3 · Cited by 1
LaMarca, E. A., Saito, A., Plaza-Jennings, A. L., Espeso‐Gil, S., Hellmich, A., Fernando, M. B., Javidfar, B., Liao, W., Estill, M. S., Townsley, K. G., et al. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-04009-2 · Cited by 5
“In contrast, variants linked to schizophrenia risk [74 – 76], bipolar disorder [77], seizure disorder [78], or autoimmune disease [79] showed no signi fi cant enrichment for R-loop primed genes (Fig.”
Astrocyte fatty acid metabolism as a driver of risk for major depressive disorder
Fitzgerald, E., O’Toole, N., Pokhvisneva, I., Nestler, E. J., Turecki, G., Nagy, C., & Meaney, M. J. (2026) · Nature Communications · doi:10.1038/s41467-026-71542-5 · Cited by 1
“Genes present in >5 networks were also enriched in GWAS of common variants for bipolar disorder 29 ( p =2.2e-7; MAGMA) and schizophrenia 30 ( p =1.5e-5; MAGMA; Fig.”
Self-citation
Metadata
- Authors
- Mullins, N., Forstner, A. J., O’Connell, K. S., Coombes, B., Coleman, J. R. I., Qiao, Z., Als, T. D., Bigdeli, T. B., Børte, S., Bryois, J., Charney, A. W., Drange, O. K., Gandal, M. J., Hagenaars, S. P., Ikeda, M., Kamitaki, N., Kim, M., Krebs, K., Panagiotaropoulou, G., Schilder, B. M., Sloofman, L. G., Steinberg, S., Trubetskoy, V., Winsvold, B. S., Won, H.-H., Abramova, L., Adorjan, K., Agerbo, E., Al Eissa, M., Albani, D., Alliey-Rodriguez, N., Anjorin, A., Antilla, V., Antoniou, A., Awasthi, S., Baek, J. H., Bækvad-Hansen, M., Bass, N., Bauer, M., Beins, E. C., Bergen, S. E., Birner, A., Bøcker Pedersen, C., Bøen, E., Boks, M. P., Bosch, R., Brum, M., Brumpton, B. M., Brunkhorst-Kanaan, N., Budde, M., Bybjerg-Grauholm, J., Byerley, W., Cairns, M., Casas, M., Cervantes, P., Clarke, T.-K., Cruceanu, C., Cuellar-Barboza, A., Cunningham, J., Curtis, D., Czerski, P. M., Dale, A. M., Dalkner, N., David, F. S., Degenhardt, F., Djurovic, S., Dobbyn, A. L., Douzenis, A., Elvsåshagen, T., Escott-Price, V., Ferrier, I. N., Fiorentino, A., Foroud, T. M., Forty, L., Frank, J., Frei, O., Freimer, N. B., Frisén, L., Gade, K., Garnham, J., Gelernter, J., Giørtz Pedersen, M., Gizer, I. R., Gordon, S. D., Gordon-Smith, K., Greenwood, T. A., Grove, J., Guzman-Parra, J., Ha, K., Haraldsson, M., Hautzinger, M., Heilbronner, U., Hellgren, D., Herms, S., Hoffmann, P., Holmans, P. A., Huckins, L., Jamain, S., Johnson, J. S., Kalman, J. L., Kamatani, Y., Kennedy, J. L., Kittel-Schneider, S., Knowles, J. A., Kogevinas, M., Koromina, M., Kranz, T. M., Kranzler, H. R., Kubo, M., Kupka, R., Kushner, S. A., Lavebratt, C., Lawrence, J., Leber, M., Lee, H.-J., Lee, P. H., Levy, S. E., Lewis, C., Liao, C., Lucae, S., Lundberg, M., MacIntyre, D. J., Magnusson, S. H., Maier, W., Maihofer, A., Malaspina, D., Maratou, E., Martinsson, L., Mattheisen, M., McCarroll, S. A., McGregor, N. W., McGuffin, P., McKay, J. D., Medeiros, H., Medland, S. E., Millischer, V., Montgomery, G. W., Moran, J. L., Morris, D. W., Mühleisen, T. W., O’Brien, N., O’Donovan, C., Olde Loohuis, L. M., Oruc, L., Papiol, S., Pardiñas, A. F., Perry, A., Pfennig, A., Porichi, E., Potash, J. B., Quested, D., Raj, T., Rapaport, M. H., DePaulo, J. R., Regeer, E. J., Rice, J. P., Rivas, F., Rivera, M., Roth, J., Roussos, P., Ruderfer, D. M., Sánchez-Mora, C., Schulte, E. C., Senner, F., Sharp, S., Shilling, P. D., Sigurdsson, E., Sirignano, L., Slaney, C., Smeland, O. B., Smith, D. J., Sobell, J. L., Søholm Hansen, C., Soler Artigas, M., Spijker, A. T., Stein, D. J., Strauss, J. S., Świątkowska, B., Terao, C., Thorgeirsson, T. E., Toma, C., Tooney, P., Tsermpini, E.-E., Vawter, M. P., Vedder, H., Walters, J. T. R., Witt, S. H., Xi, S., Xu, W., Yang, J. M. K., Young, A. H., Young, H., Zandi, P. P., Zhou, H., Zillich, L., Psychiatry, H. A.-I., Adolfsson, R., Agartz, I., Alda, M., Alfredsson, L., Babadjanova, G., Backlund, L., Baune, B. T., Bellivier, F., Bengesser, S., Berrettini, W. H., Blackwood, D. H. R., Boehnke, M., Børglum, A. D., Breen, G., Carr, V. J., Catts, S., Corvin, A., Craddock, N., Dannlowski, U., Dikeos, D., Esko, T., Etain, B., Ferentinos, P., Frye, M., Fullerton, J. M., Gawlik, M., Gershon, E. S., Goes, F. S., Green, M. J., Grigoroiu-Serbanescu, M., Hauser, J., Henskens, F., Hillert, J., Hong, K. S., Hougaard, D. M., Hultman, C. M., Hveem, K., Iwata, N., Jablensky, A. V., Jones, I., Jones, L. A., Kahn, R. S., Kelsoe, J. R., Kirov, G., Landén, M., Leboyer, M., Lewis, C. M., Li, Q. S., Lissowska, J., Lochner, C., Loughland, C., Martin, N. G., Mathews, C. A., Mayoral, F., McElroy, S. L., McIntosh, A. M., McMahon, F. J., Melle, I., Michie, P., Milani, L., Mitchell, P. B., Morken, G., Mors, O., Mortensen, P. B., Mowry, B., Müller-Myhsok, B., Myers, R. M., Neale, B. M., Nievergelt, C. M., Nordentoft, M., Nöthen, M. M., O’Donovan, M. C., Oedegaard, K. J., Olsson, T., Owen, M. J., Paciga, S. A., Pantelis, C., Pato, C., Pato, M. T., Patrinos, G. P., Perlis, R. H., Posthuma, D., Ramos-Quiroga, J. A., Reif, A., Reininghaus, E. Z., Ribasés, M., Rietschel, M., Ripke, S., Rouleau, G. A., Saito, T., Schall, U., Schalling, M., Schofield, P. R., Schulze, T. G., Scott, L. J., Scott, R. J., Serretti, A., Shannon Weickert, C., Smoller, J. W., Stefansson, H., Stefansson, K., Stordal, E., Streit, F., Sullivan, P. F., Turecki, G., Vaaler, A. E., Vieta, E., Vincent, J. B., Waldman, I. D., Weickert, T. W., Werge, T., Wray, N. R., Zwart, J.-A., Biernacka, J. M., Nurnberger, J. I., Cichon, S., Edenberg, H. J., Stahl, E. A., McQuillin, A., Di Florio, A., Ophoff, R. A., & Andreassen, O. A.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- University of Bonn (DE)
- Oslo University Hospital (NO)
- Mayo Clinic (US)
- King's College London (GB)
- The University of Queensland (AU)
- Aarhus University (DK)
- SUNY Downstate Health Sciences University (US)
- Karolinska Institutet (SE)
- Norwegian University of Science and Technology (NO)
- University of California, Los Angeles (US)
- Fujita Health University (JP)
- Broad Institute (US)
- University of Tartu (EE)
- Stiftung Charité (DE)
- deCODE Genetics (Iceland) (IS)
- Samsung (South Korea) (KR)
- Mental Health Research Center of Russian Academy of Medical Sciences (RU)
- Institut für Psychiatrische Phänomik und Genomik (DE)
- Mario Negri Institute for Pharmacological Research (IT)
- Berkshire Healthcare NHS Foundation Trust (GB)
- National and Kapodistrian University of Athens (GR)
- Samsung Medical Center (KR)
- University College London (GB)
- University Hospital Carl Gustav Carus (DE)
- Medical University of Graz (AT)
- Diakonhjemmet Hospital (NO)
- University Medical Center Utrecht (NL)
- Universitat Autònoma de Barcelona (ES)
- University Hospital Frankfurt (DE)
- University of California, San Francisco (US)
- University of Newcastle Australia (AU)
- McGill University Health Centre (CA)
- University of Edinburgh (GB)
- Queen Mary University of London (GB)
- Poznan University of Medical Sciences (PL)
- University of California San Diego (US)
- Newcastle University (GB)
- Indiana University Indianapolis (US)
- Cardiff University (GB)
- Heidelberg University (DE)
- Universitätsmedizin Göttingen (DE)
- Dalhousie University (CA)
- Yale University (US)
- University of Missouri (US)
- QIMR Berghofer Medical Research Institute (AU)
- Seoul National University (KR)
- National University Hospital of Iceland (IS)
- University of Tübingen (DE)
- Inserm (FR)
- RIKEN Center for Integrative Medical Sciences (JP)
- Centre for Addiction and Mental Health (CA)
- Barcelona Institute for Global Health (ES)
- University of Patras (GR)
- Philadelphia VA Medical Center (US)
- GGZ inGeest (NL)
- Erasmus MC (NL)
- Karolinska University Hospital (SE)
- North East London NHS Foundation Trust (GB)
- University Hospital Cologne (DE)
- Korea University (KR)
- Harvard University (US)
- HudsonAlpha Institute for Biotechnology (US)
- Montreal Neurological Institute and Hospital (CA)
- Max Planck Institute of Psychiatry (DE)
- Stellenbosch University (ZA)
- Centre international de recherche sur le cancer (FR)
- Ollscoil na Gaillimhe – University of Galway (IE)
- Forschungszentrum Jülich (DE)
- University of Worcester (GB)
- Johns Hopkins University (US)
- Oxford Health NHS Foundation Trust (GB)
- Emory University (US)
- Washington University in St. Louis (US)
- Instituto de Investigación Biomédica de Málaga (ES)
- Universidad de Granada (ES)
- Universitätsklinikum Würzburg (DE)
- Vanderbilt University Medical Center (US)
- University of Southern California (US)
- PsyQ (NL)
- South African Medical Research Council (ZA)
- Nofer Institute of Occupational Medicine (PL)
- University of California, Irvine (US)
- University of Toronto (CA)
- National Health Service (GB)
- Umeå University (SE)
- University of Pennsylvania (US)
- University of Michigan (US)
- Trinity College Dublin (IE)
- UNSW Sydney (AU)
- University of Chicago (US)
- Statens Serum Institut (DK)
- The University of Western Australia (AU)
- The Maria Sklodowska-Curie National Research Institute of Oncology (PL)
- University of Florida (US)
- Lindner Center of HOPE (US)
- National Institute of Mental Health (US)
- University of Oslo (NO)
- Massachusetts General Hospital (US)
- University of Copenhagen (DK)
- Haukeland University Hospital (NO)
- Pfizer (United States) (US)
- The University of Melbourne (AU)
- Neuroscience Research Australia (AU)
- University of North Carolina at Chapel Hill (US)
- St Olav's University Hospital (NO)
- Centro de Investigación Biomédica en Red de Salud Mental (ES)
- SUNY Upstate Medical University (US)
- Corresponding author
- Mullins, Niamh
- Andreassen, Ole A.
- ORCID
- Mullins, Niamh
- Forstner, Andreas J.
- O’Connell, Kevin S.
- Coombes, Brandon
- Coleman, Jonathan R. I.
- Qiao, Zhen
- Als, Thomas D.
- Bigdeli, Tim B.
- Børte, Sigrid
- Bryois, Julien
- Charney, Alexander W.
- Drange, Ole Kristian
- Gandal, Michael J.
- Hagenaars, Saskia P.
- Ikeda, Masashi
- Kamitaki, Nolan
- Kim, Minsoo
- Krebs, Kristi
- Panagiotaropoulou, Georgia
- Schilder, Brian M.
- Sloofman, Laura G.
- Steinberg, Stacy
- Trubetskoy, Vassily
- Winsvold, Bendik S.
- Won, Hong-Hee
- Adorjan, Kristina
- Agerbo, Esben
- Albani, Diego
- Antoniou, Anastasia
- Awasthi, Swapnil
- Baek, Ji Hyun
- Bass, Nicholas
- Bauer, Michael
- Beins, Eva C.
- Bergen, Sarah E.
- Birner, Armin
- Bøen, Erlend
- Boks, Marco P.
- Bosch, Rosa
- Brumpton, Ben M.
- Budde, Monika
- Byerley, William
- Cairns, Murray
- Cervantes, Pablo
- Clarke, Toni-Kim
- Cruceanu, Cristiana
- Cunningham, Julie
- Curtis, David
- Czerski, Piotr M.
- Dale, Anders M.
- Dalkner, Nina
- David, Friederike S.
- Degenhardt, Franziska
- Djurovic, Srdjan
- Dobbyn, Amanda L.
- Elvsåshagen, Torbjørn
- Ferrier, I. Nicol
- Fiorentino, Alessia
- Foroud, Tatiana M.
- Forty, Liz
- Frank, Josef
- Frei, Oleksandr
- Freimer, Nelson B.
- Frisén, Louise
- Gade, Katrin
- Garnham, Julie
- Gelernter, Joel
- Gizer, Ian R.
- Gordon, Scott D.
- Greenwood, Tiffany A.
- Grove, Jakob
- Ha, Kyooseob
- Haraldsson, Magnus
- Hautzinger, Martin
- Heilbronner, Urs
- Herms, Stefan
- Hoffmann, Per
- Holmans, Peter A.
- Huckins, Laura
- Jamain, Stéphane
- Johnson, Jessica S.
- Kalman, Janos L.
- Kennedy, James L.
- Knowles, James A.
- Kogevinas, Manolis
- Koromina, Maria
- Kranz, Thorsten M.
- Kranzler, Henry R.
- Kubo, Michiaki
- Kupka, Ralph
- Kushner, Steven A.
- Lavebratt, Catharina
- Lawrence, Jacob
- Leber, Markus
- Lee, Heon-Jeong
- Lee, Phil H.
- Levy, Shawn E.
- Liao, Calwing
- Lucae, Susanne
- MacIntyre, Donald J.
- Maihofer, Adam
- Malaspina, Dolores
- Maratou, Eirini
- Martinsson, Lina
- Mattheisen, Manuel
- McCarroll, Steven A.
- McGregor, Nathaniel W.
- McKay, James D.
- Medeiros, Helena
- Medland, Sarah E.
- Millischer, Vincent
- Montgomery, Grant W.
- Moran, Jennifer L.
- Morris, Derek W.
- Mühleisen, Thomas W.
- O’Brien, Niamh
- O’Donovan, Claire
- Papiol, Sergi
- Pardiñas, Antonio F.
- Perry, Amy
- Pfennig, Andrea
- Potash, James B.
- Quested, Digby
- Raj, Towfique
- Rapaport, Mark H.
- DePaulo, J. Raymond
- Regeer, Eline J.
- Rice, John P.
- Rivera, Margarita
- Roth, Julian
- Roussos, Panos
- Ruderfer, Douglas M.
- Schulte, Eva C.
- Senner, Fanny
- Sharp, Sally
- Shilling, Paul D.
- Sirignano, Lea
- Slaney, Claire
- Smeland, Olav B.
- Sobell, Janet L.
- Stein, Dan J.
- Świątkowska, Beata
- Terao, Chikashi
- Thorgeirsson, Thorgeir E.
- Tooney, Paul
- Tsermpini, Evangelia-Eirini
- Vawter, Marquis P.
- Vedder, Helmut
- Walters, James T. R.
- Witt, Stephanie H.
- Xu, Wei
- Yang, Jessica Mei Kay
- Young, Allan H.
- Young, Hannah
- Zandi, Peter P.
- Zhou, Hang
- Zillich, Lea
- Adolfsson, Rolf
- Agartz, Ingrid
- Alda, Martin
- Alfredsson, Lars
- Backlund, Lena
- Baune, Bernhard T.
- Bellivier, Frank
- Bengesser, Susanne
- Berrettini, Wade H.
- Blackwood, Douglas H. R.
- Boehnke, Michael
- Børglum, Anders D.
- Breen, Gerome
- Carr, Vaughan J.
- Catts, Stanley
- Corvin, Aiden
- Dannlowski, Udo
- Dikeos, Dimitris
- Esko, Tõnu
- Ferentinos, Panagiotis
- Frye, Mark
- Fullerton, Janice M.
- Gawlik, Micha
- Gershon, Elliot S.
- Goes, Fernando S.
- Green, Melissa J.
- Hauser, Joanna
- Hillert, Jan
- Hong, Kyung Sue
- Hougaard, David M.
- Hultman, Christina M.
- Hveem, Kristian
- Iwata, Nakao
- Jablensky, Assen V.
- Jones, Ian
- Jones, Lisa A.
- Kahn, René S.
- Kelsoe, John R.
- Kirov, George
- Landén, Mikael
- Leboyer, Marion
- Lewis, Cathryn M.
- Li, Qingqin S.
- Lissowska, Jolanta
- Loughland, Carmel
- Martin, Nicholas G.
- Mathews, Carol A.
- McElroy, Susan L.
- McIntosh, Andrew M.
- McMahon, Francis J.
- Melle, Ingrid
- Michie, Patricia
- Milani, Lili
- Mitchell, Philip B.
- Morken, Gunnar
- Mors, Ole
- Mortensen, Preben Bo
- Mowry, Bryan
- Myers, Richard M.
- Neale, Benjamin M.
- Nievergelt, Caroline M.
- Nordentoft, Merete
- Nöthen, Markus M.
- O’Donovan, Michael C.
- Oedegaard, Ketil J.
- Olsson, Tomas
- Owen, Michael J.
- Paciga, Sara A.
- Pato, Carlos
- Pato, Michele T.
- Patrinos, George P.
- Perlis, Roy H.
- Reif, Andreas
- Reininghaus, Eva Z.
- Ribasés, Marta
- Rietschel, Marcella
- Ripke, Stephan
- Rouleau, Guy A.
- Saito, Takeo
- Schall, Ulrich
- Schalling, Martin
- Schofield, Peter R.
- Schulze, Thomas G.
- Scott, Laura J.
- Scott, Rodney J.
- Serretti, Alessandro
- Smoller, Jordan W.
- Stordal, Eystein
- Streit, Fabian
- Sullivan, Patrick F.
- Turecki, Gustavo
- Vieta, Eduard
- Vincent, John B.
- Waldman, Irwin D.
- Weickert, Thomas W.
- Werge, Thomas
- Wray, Naomi R.
- Zwart, John-Anker
- Biernacka, Joanna M.
- Cichon, Sven
- Edenberg, Howard J.
- Stahl, Eli A.
- McQuillin, Andrew
- Ophoff, Roel A.
- Andreassen, Ole A.
- Venue
- Nature Genetics
- Published
- 2021-05-17
- Volume
- 53
- Issue
- 6
- Pages
- 817-829
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- PMC
- PMC8192451
- OpenAlex
- W3162259891
- Cited by
- 1,517
- References
- 129
- Citations by year
- 2026: 232 · 2025: 369 · 2024: 387 · 2023: 255 · 2022: 204 · 2021: 68
- FWCI
- 41.13
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Nature Genetics (publishedVersion, other-oa)
- medRxiv (acceptedVersion, cc-by)
- PubMed (publishedVersion)
- Kölner Universitäts PublikationsServer (Universität zu Köln) (publishedVersion)
- Pure Amsterdam UMC (publishedVersion, cc-by)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion, other-oa)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion, other-oa)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion, other-oa)
- VU Research Portal (publishedVersion, other-oa)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion, cc-by-sa)
- ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Institutional Repository of the University of Granada (University of Granada) (acceptedVersion, cc-by-nc-nd)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (acceptedVersion)
- IUScholarWorks (Indiana University) (submittedVersion, other-oa)
- ScholarWorks @ UTRGV (The University of Texas Rio Grande Valley) (submittedVersion, other-oa)
- Worcester Research and Publications (University of Worcester) (submittedVersion, other-oa)
- UWA Profiles and Research Repository (UWA) (submittedVersion, other-oa)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion, other-oa)
- HAL (submittedVersion, other-oa)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- UCL Discovery (University College London) (submittedVersion)
- Open access LMU (Ludwid Maxmilian's Universitat Munchen) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Minerva Access (University of Melbourne) (submittedVersion)
- Hirsla (Landspítali University Hospital) (submittedVersion)
- Hirsla (Landspítali University Hospital) (submittedVersion, other-oa)
- NOVA (University of Newcastle Australia) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Funders
- U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (U01 MH109528, U01 MH094421, U01 MH085520)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Keywords
- bipolar disorder, genome-wide association study, genetic susceptibility loci, prefrontal cortex, hippocampus, expression quantitative trait loci, melanin-concentrating hormone receptor 1, furin, bipolar disorder subtypes, genetic correlation, drug repurposing, European ancestry
- MeSH terms
- Bipolar Disorder, Chromosomes, Human, Humans, Major Histocompatibility Complex, Phenotype, Risk Factors, Genome, Human, Case-Control Studies, Genetic Predisposition to Disease, Multifactorial Inheritance, Quantitative Trait Loci, Genome-Wide Association Study
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