Large-scale genome-wide association analysis of bipolar disorder identifies a 
new susceptibility locus near ODZ4

Sklar, P.; Ripke, S.; Scott, L. J.; Andreassen, O. A.; Cichon, S.; Craddock, N.; Edenberg, H. J.; Nurnberger, J. I.; Rietschel, M.; Blackwood, D.; Corvin, A.; Flickinger, M.; Guan, W.; Mattingsdal, M.; McQuillin, A.; Kwan, P.; Wienker, T. F.; Daly, M.; Dudbridge, F.; Holmans, P. A.; Lin, D.; Burmeister, M.; Greenwood, T. A.; Hamshere, M. L.; Muglia, P.; Smith, E. N.; Zandi, P. P.; Nievergelt, C. M.; McKinney, R.; Shilling, P. D.; Schork, N. J.; Bloss, C. S.; Foroud, T.; Koller, D. L.; Gershon, E. S.; Liu, C.; Badner, J. A.; Scheftner, W. A.; Lawson, W. B.; Nwulia, E. A.; Hipolito, M.; Coryell, W.; Rice, J.; Byerley, W.; McMahon, F. J.; Schulze, T. G.; Berrettini, W.; Lohoff, F. W.; Potash, J. B.; Mahon, P. B.; McInnis, M. G.; Zollner, S.; Zhang, P.; Craig, D. W.; Szelinger, S.; Barrett, T. B.; Breuer, R.; Meier, S.; Strohmaier, J.; Witt, S. H.; Tozzi, F.; Farmer, A.; McGuffin, P.; Strauss, J.; Xu, W.; Kennedy, J. L.; Vincent, J. B.; Matthews, K.; Day, R.; Ferreira, M. A.; O'Dushlaine, C.; Perlis, R.; Raychaudhuri, S.; Ruderfer, D.; Hyoun, P. L.; Smoller, J. W.; Li, J.; Absher, D.; Thompson, R. C.; Meng, F. G.; Schatzberg, A. F.; Bunney, W. E.; Barchas, J. D.; Jones, E. G.; Watson, S. J.; Myers, R. M.; Akil, H.; Boehnke, M.; Chambert, K.; Moran, J.; Scolnick, E.; Djurovic, S.; Melle, I.; Morken, G.; Gill, M.; Morris, D.; Quinn, E.; Muhleisen, T. W.; Degenhardt, F. A.; Mattheisen, M.

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

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Wienker, T. F.
Clinical Genetics (Thomas F. Wienker), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Li, J.
Systems Biology (Christoph Wierling), Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Citation

Sklar, P., Ripke, S., Scott, L. J., Andreassen, O. A., Cichon, S., Craddock, N., et al. (2011). Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet, 43(10), 977-83. Retrieved from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=21926972 http://www.nature.com/ng/journal/v43/n10/pdf/ng.943.pdf.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-7971-A

Abstract

We conducted a combined genome-wide association study (GWAS) of 7,481 individuals with bipolar disorder (cases) and 9,250 controls as part of the Psychiatric GWAS Consortium. Our replication study tested 34 SNPs in 4,496 independent cases with bipolar disorder and 42,422 independent controls and found that 18 of 34 SNPs had P < 0.05, with 31 of 34 SNPs having signals with the same direction of effect (P = 3.8 x 10(-7)). An analysis of all 11,974 bipolar disorder cases and 51,792 controls confirmed genome-wide significant evidence of association for CACNA1C and identified a new intronic variant in ODZ4. We identified a pathway comprised of subunits of calcium channels enriched in bipolar disorder association intervals. Finally, a combined GWAS analysis of schizophrenia and bipolar disorder yielded strong association evidence for SNPs in CACNA1C and in the region of NEK4-ITIH1-ITIH3-ITIH4. Our replication results imply that increasing sample sizes in bipolar disorder will confirm many additional loci.