Genetic Liability to Insomnia and Cardiovascular Disease Risk

被引:46
作者
Larsson, Susanna C. [1 ,2 ]
Markus, Hugh S. [3 ]
机构
[1] Karolinska Inst, Unit Cardiovasc & Nutr Epidemiol, Inst Environm Med, S-17177 Stockholm, Sweden
[2] Uppsala Univ, Dept Surg Sci, Uppsala, Sweden
[3] Univ Cambridge, Stroke Res Grp, Dept Clin Neurosci, Cambridge, England
基金
瑞典研究理事会;
关键词
cardiovascular diseases; Mendelian randomization analysis; sleep; sleep initiation and maintenance disorders; stroke;
D O I
10.1161/CIRCULATIONAHA.119.041830
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:796 / 798
页数:3
相关论文
共 5 条
  • [1] Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
    Aragam, Krishna G.
    Chaffin, Mark
    Levinson, Rebecca T.
    McDermott, Gregory
    Choi, Seung Hoan
    Shoemaker, M. Benjamin
    Haas, Mary E.
    Weng, Lu-Chen
    Lindsay, Mark E.
    Smith, J. Gustav j
    Newton-Cheh, Christopher
    Roden, Dan M.
    London, Barry
    Wells, Quinn S.
    Ellinor, Patrick T.
    Kathiresan, Sekar
    Lubitz, Steven A.
    Bloom, Heather L.
    Dudley, Samuel C.
    Ellinor, Patrick T.
    Shalaby, Alaa A.
    Weiss, Raul
    Gutmann, Rebecca
    Saba, Samir
    [J]. CIRCULATION, 2019, 139 (04) : 489 - 501
  • [2] Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
    Jansen, Philip R.
    Watanabe, Kyoko
    Stringer, Sven
    Skene, Nathan
    Bryois, Julien
    Hammerschlag, Anke R.
    de Leeuw, Christiaan A.
    Benjamins, Jeroen S.
    Munoz-Manchado, Ana B.
    Nagel, Mats
    Savage, Jeanne E.
    Tiemeier, Henning
    White, Tonya
    Tung, Joyce Y.
    Hinds, David A.
    Vacic, Vladimir
    Wang, Xin
    Sullivan, Patrick F.
    van der Sluis, Sophie
    Polderman, Tinca J. C.
    Smit, August B.
    Hjerling-Leffler, Jens
    Van Someren, Eus J. W.
    Posthuma, Danielle
    Agee, Michelle
    Alipanahi, Babak
    Auton, Adam
    Bell, Robert K.
    Bryc, Katarzyna
    Elson, Sarah L.
    Fontanillas, Pierre
    Furlotte, Nicholas A.
    Huber, Karen E.
    Kleinman, Aaron
    Litterman, Nadia K.
    McCreight, Jennifer C.
    McIntyre, Matthew H.
    Mountain, Joanna L.
    Noblin, Elizabeth S.
    Northover, Carrie A. M.
    Pitts, Steven J.
    Sathirapongsasuti, J. Fah
    Sazonova, Olga, V
    Shelton, Janie F.
    Shringarpure, Suyash
    Tian, Chao
    Wilson, Catherine H.
    [J]. NATURE GENETICS, 2019, 51 (03) : 394 - +
  • [3] Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
    Malik, Rainer
    Chauhan, Ganesh
    Traylor, Matthew
    Sargurupremraj, Muralidharan
    Okada, Yukinori
    Mishra, Aniket
    Rutten-Jacobs, Loes
    Giese, Anne-Katrin
    van der Laan, Sander W.
    Gretarsdottir, Solveig
    Anderson, Christopher D.
    Chong, Michael
    Adams, Hieab H. H.
    Ago, Tetsuro
    Almgren, Peter
    Amouyel, Philippe
    Ay, Hakan
    Bartz, Traci M.
    Benavente, Oscar R.
    Bevan, Steve
    Boncoraglio, Giorgio B.
    Brown, Robert D., Jr.
    Butterworth, Adam S.
    Carrera, Caty
    Carty, Cara L.
    Chasman, Daniel I.
    Chen, Wei-Min
    Cole, John W.
    Correa, Adolfo
    Cotlarciuc, Ioana
    Cruchaga, Carlos
    Danesh, John
    de Bakker, Paul I. W.
    DeStefano, Anita L.
    den Hoed, Marcel
    Duan, Qing
    Engelter, Stefan T.
    Falcone, Guido J.
    Gottesman, Rebecca F.
    Grewal, Raji P.
    Gudnason, Vilmundur
    Gustafsson, Stefan
    Haessler, Jeffrey
    Harris, Tamara B.
    Hassan, Ahamad
    Havulinna, Aki S.
    Heckbert, Susan R.
    Holliday, Elizabeth G.
    Howard, George
    Hsu, Fang-Chi
    [J]. NATURE GENETICS, 2018, 50 (04) : 524 - +
  • [4] A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
    Nikpay, Majid
    Goel, Anuj
    Won, Hong-Hee
    Hall, Leanne M.
    Willenborg, Christina
    Kanoni, Stavroula
    Saleheen, Danish
    Kyriakou, Theodosios
    Nelson, Christopher P.
    Hopewell, Jemma C.
    Webb, Thomas R.
    Zeng, Lingyao
    Dehghan, Abbas
    Alver, Maris
    Armasu, Sebastian M.
    Auro, Kirsi
    Bjonnes, Andrew
    Chasman, Daniel I.
    Chen, Shufeng
    Ford, Ian
    Franceschini, Nora
    Gieger, Christian
    Grace, Christopher
    Gustafsson, Stefan
    Huang, Jie
    Hwang, Shih-Jen
    Kim, Yun Kyoung
    Kleber, Marcus E.
    Lau, King Wai
    Lu, Xiangfeng
    Lu, Yingchang
    Lyytikainen, Leo-Pekka
    Mihailov, Evelin
    Morrison, Alanna C.
    Pervjakova, Natalia
    Qu, Liming
    Rose, Lynda M.
    Salfati, Elias
    Saxena, Richa
    Scholz, Markus
    Smith, Albert V.
    Tikkanen, Emmi
    Uitterlinden, Andre
    Yang, Xueli
    Zhang, Weihua
    Zhao, Wei
    de Andrade, Mariza
    de Vries, Paul S.
    van Zuydam, Natalie R.
    Anand, Sonia S.
    [J]. NATURE GENETICS, 2015, 47 (10) : 1121 - +
  • [5] Multi-ethnic genome-wide association study for atrial fibrillation
    Roselli, Carolina
    Chaffin, Mark D.
    Weng, Lu-Chen
    Aeschbacher, Stefanie
    Ahlberg, Gustav
    Albert, Christine M.
    Almgren, Peter
    Alonso, Alvaro
    Anderson, Christopher D.
    Aragam, Krishna G.
    Arking, Dan E.
    Barnard, John
    Bartz, Traci M.
    Benjamin, Emelia J.
    Bihlmeyer, Nathan A.
    Bis, Joshua C.
    Bloom, Heather L.
    Boerwinkle, Eric
    Bottinger, Erwin B.
    Brody, Jennifer A.
    Calkins, Hugh
    Campbell, Archie
    Cappola, Thomas P.
    Carlquist, John
    Chasman, Daniel I.
    Chen, Lin Y.
    Chen, Yii-Der Ida
    Choi, Eue-Keun
    Choi, Seung Hoan
    Christophersen, Ingrid E.
    Chung, Mina K.
    Cole, John W.
    Conen, David
    Cook, James
    Crijns, Harry J.
    Cutler, Michael J.
    Damrauer, Scott M.
    Daniels, Brian R.
    Darbar, Dawood
    Delgado, Graciela
    Denny, Joshua C.
    Dichgans, Martin
    Doerr, Marcus
    Dudink, Elton A.
    Dudley, Samuel C.
    Esa, Nada
    Esko, Tonu
    Eskola, Markku
    Fatkin, Diane
    Felix, Stephan B.
    [J]. NATURE GENETICS, 2018, 50 (09) : 1225 - +