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Autor:
Knol, Maria J., Lu, Dongwei, Traylor, Matthew, Adams, Hieab H.H., Romero, José Rafael J., Smith, Albert V., Fornage, Myriam, Hofer, Edith, Liu, Junfeng, Hostettler, Isabel C., Luciano, Michelle, Trompet, Stella, Giese, Anne-Katrin, Hilal, Saima, van den Akker, Erik B., Vojinovic, Dina, Li, Shuo, Sigurdsson, Sigurdur, van der Lee, Sven J., Jack, Clifford R., Wilson, Duncan, Yilmaz, Pinar, Satizabal, Claudia L., Liewald, David C.M., van der Grond, Jeroen, Chen, Christopher, Saba, Yasaman, van der Lugt, Aad, Bastin, Mark E., Windham, B. Gwen, Cheng, Ching Yu, Pirpamer, Lukas, Kantarci, Kejal, Himali, Jayandra J., Yang, Qiong, Morris, Zoe, Beiser, Alexa S., Tozer, Daniel J., Vernooij, Meike W., Amin, Najaf, Beekman, Marian, Koh, Jia Yu, Stott, David J., Houlden, Henry, Schmidt, Reinhold, Gottesman, Rebecca F., MacKinnon, Andrew D., DeCarli, Charles, Gudnason, Vilmundur, Deary, Ian J., van Duijn, Cornelia M., Slagboom, P. Eline, Wong, Tien Yin, Rost, Natalia S., Jukema, J. Wouter, Mosley, Thomas H., Werring, David J., Schmidt, Helena, Wardlaw, Joanna M., Ikram, M. Arfan, Seshadri, Sudha, Launer, Lenore J., Markus, Hugh S.
Publikováno v:
Neurology
article-version (Version of Record) 3
article-version (Version of Record) 3
Objective To identify common genetic variants associated with the presence of brain microbleeds (BMBs). Methods We performed genome-wide association studies in 11 population-based cohort studies and 3 case–control or case-only stroke cohorts. Genot