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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:Biol Psychiatry
المؤلفون الرئيسيون: 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
التنسيق: Artigo
اللغة:Inglês
منشور في: 2018
الموضوعات:
Article
الوصول للمادة أونلاين: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
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!

مواد مشابهة