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studies Children: Item: Title: Introduction Item: Title: Methods Children: Item: Title: Study design and phenotype definitions Item: Title: Genotyping and imputation Item: Title: Statistical analysis Item: Title: Role of the funding source Item: Title: Results Item: Title: Discussion Item: Title: Acknowledgments Item: Title: References Info: Title: Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies Author: Matthew Traylor PhD Subject: The Lancet Neurology, 20 (2021) 351-361. doi:10.1016/S1474-4422(21)00031-4 Keywords: Creator: Elsevier Producer: Acrobat Distiller 6.0 for Windows CreationDate: Sat Apr 10 11:54:24 CEST 2021 ModDate: Tue Apr 20 15:14:22 CEST 2021 ID: 0x9a7509befed52f49a10fbb3f84566fcf, 0x85ae9970b0860441bc100332b37e4525 Filters: FilterPipeline: FlateDecode FilterPipeline: DCTDecode Images: Image: NisoImageMetadata: FormatName: image/jpg CompressionScheme: JPEG ImageWidth: 1364 ImageHeight: 683 ColorSpace: CMYK 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BaseEncoding: WinAnsiEncoding Differences: true ToUnicode: true Font: BaseFont: BBUNWL+Shaker2Lancet-Regular FontSubset: true FirstChar: 32 LastChar: 150 FontDescriptor: FontName: BBUNWL+Shaker2Lancet-Regular Flags: Nonsymbolic FontBBox: -158, -241, 1019, 980 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: BBUNWL+Shaker2Lancet-Italic FontSubset: true FirstChar: 24 LastChar: 122 FontDescriptor: FontName: BBUNWL+Shaker2Lancet-Italic Flags: Nonsymbolic, Italic FontBBox: -177, -241, 960, 980 FontFile3: true EncodingDictionary: BaseEncoding: WinAnsiEncoding Differences: true ToUnicode: true Font: BaseFont: BBUNWL+Shaker2Lancet-Italic FontSubset: true FirstChar: 1 LastChar: 143 FontDescriptor: FontName: BBUNWL+Shaker2Lancet-Italic Flags: Nonsymbolic, Italic FontBBox: -177, -241, 960, 980 FontFile3: true EncodingDictionary: BaseEncoding: WinAnsiEncoding Differences: true XMP: application/pdf doi:10.1016/S1474-4422(21)00031-4 Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies Matthew Traylor PhD Elodie Persyn PhD Liisa Tomppo MD Sofia Klasson MSc Vida Abedi PhD Mark K Bakker MSc Nuria Torres PhD Linxin Li DPhil Steven Bell PhD Loes Rutten-Jacobs PhD Daniel J Tozer PhD Christoph J Griessenauer MD Yanfei Zhang PhD Annie Pedersen MD Prof Pankaj Sharma MD Prof Jordi Jimenez-Conde MD Prof Tatjana Rundek MD Prof Raji P Grewal MD Prof Arne Lindgren MD Prof James F Meschia MD Prof Veikko Salomaa MD Aki Havulinna DSc Christina Kourkoulis BS Katherine Crawford BS Sandro Marini MD Prof Braxton D Mitchell PhD Prof Steven J Kittner MD Prof Jonathan Rosand MD Prof Martin Dichgans MD Prof Christina Jern MD Daniel Strbian MD Israel Fernandez-Cadenas PhD Ramin Zand MD Ynte Ruigrok MD Prof Natalia Rost MD Robin Lemmens MD Prof Peter M Rothwell FMedSci Christopher D Anderson MD Prof Joanna Wardlaw FRCR Prof Cathryn M Lewis PhD Prof Hugh S Markus FMedSci Helsinki Stroke, Study Dutch Parelsnoer Institute-Cerebrovascular Accident (CVA) Study Group National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network UK DNA Lacunar Stroke Study Investigators International Stroke Genetics Consortium The Lancet Neurology, 20 (2021) 351-361. doi:10.1016/S1474-4422(21)00031-4 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license journal The Lancet Neurology Copyright © 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. 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