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Paper Details

Genetic variation at 16q24.2 is associated with small vessel stroke.
Ann Neurol
54
2017
16q24, CpG, CpG sites, INTERPRETATION 16q24, SVS, ZCCHC14, cerebral small vessel disease, cerebral white matter hyperintensities, cg16596957, chromosome 16q24, genetic variants, intracerebral hemorrhage, ischemic stroke, mRNA, messenger RNA, regulatory elements, rs12445022, single-nucleotide polymorphism, small vessel disease, small vessel stroke, stroke, vascular cognitive impairment, whole blood
Author NameAffiliation
Rainer MalikInstitute for Stroke and Dementia Research, Klinikum der Universitat Munchen, Ludwig-Maximilians University
Mike A NallsNational Institute on Aging
Mike A NallsNational Institute on Aging
Gudmar Thorleifsson
Gudmar Thorleifsson
Carl D LangefeldCenter for Public Health Genomics and Department of Biostatistical Sciences, Wake Forest School of Medicine
Carl D LangefeldCenter for Public Health Genomics and Department of Biostatistical Sciences, Wake Forest School of Medicine
Danish SaleheenPerelman School of Medicine, University of Pennsylvania
Natalia S RostJ. Philip Kistler Stroke Research Center, Massachusetts General Hospital
Tim D SpectorKing's College London
Tim D SpectorKing's College London
Jordana T BellKing's College London
Eilis HannonUniversity of Exeter Medical School, University of Exeter
Jonathan MillUniversity of Exeter Medical School, University of Exeter
Jonathan MillInstitute of Psychiatry, King's College London
Jonathan MillUniversity of Exeter Medical School, University of Exeter
Jonathan MillInstitute of Psychiatry, King's College London
Joshua C BisCardiovascular Health Research Unit, University of Washington
Lenore J LaunerNational Institute on Aging
John W ColeUniversity of Maryland School of Medicine and Baltimore VAMC
Olle MelanderLund University
Donna K ArnettCollege of Public Health, University of Kentucky
Julie A JohnsonDepartment of Pharmacotherapy and Translational Research and Center for Pharmacogenomics, University of Florida
Julie A JohnsonCollege of Medicine, University of Florida
Sara L PulitUniversity Medical Center Utrecht
Quenna WongUniversity of Washington
Stephen S RichCenter for Public Health Genomics, University of Virginia School of Medicine
Paul I W de BakkerJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht
Paul I W de BakkerCenter for Molecular Medicine, University Medical Center Utrecht
Paul I W de BakkerJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht
Paul I W de BakkerCenter for Molecular Medicine, University Medical Center Utrecht
Patrick F McArdleUniversity of Maryland School of Medicine
Daniel WooUniversity of Cincinnati College of Medicine
Huichun XuUniversity of Maryland School of Medicine
Huichun XuUniversity of Maryland School of Medicine
Myriam FornageThe University of Texas Health Science Center at Houston
Kari Stefansson
Kari StefanssonUniversity of Iceland
Kari Stefansson
Kari StefanssonUniversity of Iceland
Unnur Thorsteinsdottir
Unnur ThorsteinsdottirUniversity of Iceland
Unnur Thorsteinsdottir
Unnur ThorsteinsdottirUniversity of Iceland
Solveig GretarsdottirCenter for Public Health Genomics and Department of Biostatistical Sciences, Wake Forest School of Medicine
Jonathan RosandMassachusetts General Hospital
Jonathan RosandUniversity of Cincinnati College of Medicine
Jonathan RosandCenter for Human Genetic Research, Massachusetts General Hospital
Jonathan RosandJ. Philip Kistler Stroke Research Center, Massachusetts General Hospital
Jonathan RosandMassachusetts General Hospital
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