Singleton Deletions Throughout the Genome Increase Risk of Bipolar Disorder

An overall burden of rare structural genomic variants has not been reported in Bipolar Disorder (BD), although there have been reports of cases with microduplication and microdeletion. Here, we present a genome wide copy number variant (CNV) survey of 1001 cases and 1034 controls using the Affymetri...

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Autors principals: Zhang, Dandan, Cheng, Lijun, Qian, Yudong, Alliey-Rodriguez, Ney, Kelsoe, John R., Greenwood, Tiffany, Nievergelt, Caroline, Barrett, Thomas B., McKinney, Rebecca, Schork, Nicholas, Smith, Erin N., Bloss, Cinnamon, Nurnberger, John, Edenberg, Howard J., Foroud, Tatiana, Sheftner, William, Lawson, William B., Nwulia, Evaritus A., Hipolito, Maria, Coryell, William, Rice, John, Byerley, William, McMahon, Francis, Schulze, Thomas G., Berrettini, Wade, Potash, James B., Belmonte, Pamela L., Zandi, Peter P., McInnis, Melvin, Zöllner, Sebastian, Craig, David, Szelinger, Szabolics, Koller, Daniel, Christian, Susan L., Liu, Chunyu, Gershon, Elliot S.
Format: Artigo
Idioma:Inglês
Publicat: 2008
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2735188/
https://ncbi.nlm.nih.gov/pubmed/19114987
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2008.144
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