Association of common genetic variants with brain microbleeds: A genome-wide association study

To identify common genetic variants associated with the presence of brain microbleeds (BMBs). We performed genome-wide association studies in 11 population-based cohort studies and 3 case-control or case-only stroke cohorts. Genotypes were imputed to the Haplotype Reference Consortium or 1000 Genome...

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Vydáno v:	Neurology Ročník 95; číslo 24; s. e3331
Hlavní autoři:	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, Jr, 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
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	United States 15.12.2020
Témata:	Aged Aged, 80 and over Alleles Apolipoprotein E2 - genetics Apolipoprotein E4 - genetics Apolipoproteins E - genetics Case-Control Studies Cerebral Hemorrhage - diagnostic imaging Cerebral Hemorrhage - epidemiology Cerebral Hemorrhage - genetics Cerebral Hemorrhage - pathology Cerebral Small Vessel Diseases - epidemiology Cerebral Small Vessel Diseases - genetics Cohort Studies Female Genetic Predisposition to Disease Genome-Wide Association Study Humans Magnetic Resonance Imaging Male Middle Aged Polymorphism, Single Nucleotide Risk White Matter - diagnostic imaging White Matter - pathology
ISSN:	1526-632X, 1526-632X
On-line přístup:	Zjistit podrobnosti o přístupu
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