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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Bibliografiset tiedot
Julkaisussa:Int J Bipolar Disord
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer Berlin Heidelberg 2018
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Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6230336/
https://ncbi.nlm.nih.gov/pubmed/30415424
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40345-018-0132-x
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