Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

BACKGROUND. Genetic risk for bipolar disorder (BD) is conferred through many common alleles, while a role for rare copy number variants (CNVs) is less clear. BD subtypes schizoaffective disorder bipolar type (SAB), bipolar I disorder (BD I) and bipolar II disorder (BD II) differ according to the pro...

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Julkaisussa:Biol Psychiatry
Päätekijät: Charney, Alexander W., Stahl, Eli A., Green, Elaine K., Chen, Chia-Yen, Moran, Jennifer L., Chambert, Kimberly, Belliveau, Richard A., Forty, Liz, Gordon-Smith, Katherine, Lee, Phil H., Bromet, Evelyn J, Buckley, Peter F, Escamilla, Michael A, Fanous, Ayman H., Fochtmann, Laura J, Lehrer, Douglas S., Malaspina, Dolores, Marder, Stephen R., Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Rakofsky, Jeffrey J., Rapaport, Mark H., Medeiros, Helena, Sobell, Janet L., Backlund, Lena, Bergen, Sarah E., Juréus, Anders, Schalling, Martin, Lichtenstein, Paul, Knowles, James A., Burdick, Katherine E., Jones, Ian, Jones, Lisa A, Hultman, Christina M., Perlis, Roy, Purcell, Shaun M., McCarroll, Steven A., Pato, Carlos N., Pato, Michele T., Florio, Ariana Di, Craddock, Nick, Landén, Mikael, Smoller, Jordan W., Ruderfer, Douglas M., Sklar, Pamela
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2018
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6586545/
https://ncbi.nlm.nih.gov/pubmed/30686506
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2018.12.009
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