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Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics

BACKGROUND: Disentangling the etiology of common, complex diseases is a major challenge in genetic research. For bipolar disorder (BD), several genome-wide association studies (GWAS) have been performed. Similar to other complex disorders, major breakthroughs in explaining the high heritability of B...

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Detalles Bibliográficos
Autores principales: Breuer, René, Mattheisen, Manuel, Frank, Josef, Krumm, Bertram, Treutlein, Jens, Kassem, Layla, Strohmaier, Jana, Herms, Stefan, Mühleisen, Thomas W., Degenhardt, Franziska, Cichon, Sven, Nöthen, Markus M., Karypis, George, Kelsoe, John, Greenwood, Tiffany, Nievergelt, Caroline, Shilling, Paul, Shekhtman, Tatyana, Edenberg, Howard, Craig, David, Szelinger, Szabolcs, Nurnberger, John, Gershon, Elliot, Alliey-Rodriguez, Ney, Zandi, Peter, Goes, Fernando, Schork, Nicholas, Smith, Erin, Koller, Daniel, Zhang, Peng, Badner, Judith, Berrettini, Wade, Bloss, Cinnamon, Byerley, William, Coryell, William, Foroud, Tatiana, Guo, Yirin, Hipolito, Maria, Keating, Brendan, Lawson, William, Liu, Chunyu, Mahon, Pamela, McInnis, Melvin, Murray, Sarah, Nwulia, Evaristus, Potash, James, Rice, John, Scheftner, William, Zöllner, Sebastian, McMahon, Francis J., Rietschel, Marcella, Schulze, Thomas G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230336/
https://www.ncbi.nlm.nih.gov/pubmed/30415424
http://dx.doi.org/10.1186/s40345-018-0132-x