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11 p, 1.9 MB |
Genetic basis of lacunar stroke : a pooled analysis of individual patient data and genome-wide association studies
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Traylor, Matthew (Clinical Pharmacology and The Barts Heart Centre and NIHR Barts Biomedical Research Centre, Barts Health NHS Trust, William Harvey Research Institute, Queen Mary University of London, London, UK) ;
Persyn, Elodie (King's College London) ;
Tomppo, Liisa (Helsinki University Hospital (Finlàndia)) ;
Klasson, Sofia (Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden) ;
Abedi, Vida (Department of Molecular and Functional Genomics, Weis Center for Research, Geisinger Health System, Danville, PA, USA) ;
Bakker, Mark K. (Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, Netherlands) ;
Torres, Nuria (Institut d'Investigació Biomèdica Sant Pau) ;
Li, Linxin (University of Oxford. Nuffield Department of Clinical Neuroscience) ;
Bell, Steven (Unversity of Cambridge) ;
Rutten-Jacobs, Loes (Product Development Personalized Health Care, F Hoffmann-La Roche, Basel, Switzerland) ;
Tozer, Daniel J. (Clinical Neurosciences, University of Cambridge, Cambridge, UK) ;
Griessenauer, Christoph J. (Institute of Neurointervention, Paracelsus Medical University, Salzburg, Austria) ;
Zhang, Yanfei (Genomic Medicine Institute, Geisinger Health System, Danville, PA, USA) ;
Pedersen, Annie (Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden) ;
Sharma, Pankaj (Institute of Cardiovascular Research, Royal Holloway University of London, London, UK) ;
Jimenez-Conde, Jordi (Institut Hospital del Mar d'Investigacions Mèdiques) ;
Rundek, Tatjana (University of Miami. Miller School of Medicine) ;
Grewal, Raji P. (Neuroscience Institute, Saint Francis Medical Center, School of Health and Medical Sciences, Seton Hall University, South Orange, NJ, USA) ;
Lindgren, Arne (Lund University (Lund, Suècia)) ;
Meschia, James F. (Mayo Clinic (Jacksonville, Estats Units d'Amèrica)) ;
Salomaa, Veikko (Finnish Institute for Health and Welfare (Helsinki, Finlàndia)) ;
Havulinna, Aki S (Institute for Molecular Medicine Finland (FIMM HiLIFE), Helsinki, Finland) ;
Kourkoulis, Christina (Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA) ;
Crawford, Katherine (Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA) ;
Marini, Sandro (Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA) ;
Mitchell, Braxton D. (Geriatrics Research and Education Clinical Center, Baltimore Veterans Administration Medical Center, Baltimore, MD, USA) ;
Kittner, Steven J. (Geriatrics Research and Education Clinical Center, Baltimore Veterans Administration Medical Center, Baltimore, MD, USA) ;
Rosand, Jonathan (Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA) ;
Dichgans, Martin (Munich Cluster for Systems Neurology (SyNergy), Munich, Germany) ;
Jern, Christina (Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden) ;
Strbian, Daniel (Helsinki University Hospital (Finlàndia)) ;
Fernandez-Cadenas, Israel (Hospital Universitari Vall d'Hebron. Institut de Recerca) ;
Zand, Ramin (Neuroscience Institute, Geisinger Health System, Danville, PA, USA) ;
Ruigrok, Ynte (Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, Netherlands) ;
Rost, Natalia (Massachusetts General Hospital (Boston)) ;
Lemmens, Robin (University Hospitals Leuven (Bèlgica)) ;
Rothwell, Peter M. (University of Oxford. Nuffield Department of Clinical Neuroscience) ;
Anderson, Christopher D. (Program in Medical & Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA) ;
Wardlaw, Joanna (Centre for Clinical Brain Sciences, UK Dementia Research Institute and Row Fogo Centre for Research into the Ageing Brain, University of Edinburgh, Edinburgh, UK) ;
Lewis, Cathryn M. (King's College London. Social, Genetic, and Developmental Psychiatry Centre) ;
Markus, Hugh S. (Clinical Neurosciences, University of Cambridge, Cambridge, UK) ;
Universitat Autònoma de Barcelona
The genetic basis of lacunar stroke is poorly understood, with a single locus on 16q24 identified to date. We sought to identify novel associations and provide mechanistic insights into the disease. [...]
2021 -  10.1016/S1474-4422(21)00031-4
The Lancet neurology, Vol. 20 (may 2021) , p. 351-361
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13 p, 1.4 MB |
Genome-wide association meta-analysis of functional outcome after ischemic stroke
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Söderholm, Martin (Skåne University Hospital (Suècia)) ;
Pedersen, Annie (Department of Clinical Neuroscience. Institute of Neuroscience and Physiology. Sahlgrenska Academy. University of Gothenburg) ;
Lorentzen, Erik (Sahlgrenska University Hospital (Suècia)) ;
Stanne, Tara M. (Institute of Biomedicine) ;
Bevan, Steve (Bioinformatics Core Facility. University of Gothenburg) ;
Olsson, Maja (Institute of Biomedicine) ;
Cole, John W. ;
Fernandez-Cadenas, Israel (Hospital de la Santa Creu i Sant Pau (Barcelona, Catalunya)) ;
Hankey, Graeme J. (Medical School. The University of Western Australia, Perth; Department of Neurology) ;
Jimenez-Conde, Jordi (Institut Hospital del Mar d'Investigacions Mèdiques) ;
Jood, Katarina (Department of Clinical Genetics and Genomics) ;
Lee, Jin-Moo (Department of Neurology. Washington University School of Medicine, St. Louis, MO) ;
Lemmens, Robin (University Hospitals Leuven (Bèlgica)) ;
Levi, Christopher R (School of Medicine and Public Health) ;
Mitchell, Braxton D. (Priority Research Centre for Stroke and Traumatic Brain Injury. University of Newcastle) ;
Norrving, Bo (Skåne University Hospital (Suècia)) ;
Rannikmäe, Kristiina (University of Maryland. Department of Medicine) ;
Rost, Natalia S. (Geriatric Research. Education. and Clinical Center. Veterans Affairs Medical Center) ;
Rosand, Jonathan (Massachusetts General Hospital (Boston)) ;
Rothwell, Peter M. (Broad Institute of MIT and Harvard) ;
Scott, Rodney (University of Virginia. Departments of Neurology and Health Evaluation Sciences) ;
Strbian, Daniel (Massachusetts General Hospital (Boston)) ;
Sturm, Jonathan W. (VIB. Center for Brain and Disease Research) ;
Sudlow, Cathie (University of Maryland. Department of Medicine) ;
Traylor, Matthew (University of Oxford. Nuffield Department of Clinical Neurosciences.) ;
Thijs, Vincent (University of Cambridge. Department of ClinicalNeurosciences) ;
Tatlisumak, Turgut (Stroke Division. Florey Institute for Neuroscience and Mental Health. University of Melbourne) ;
Woo, Daniel (Austin Health. Department of Neurology) ;
Worrall, Bradford B. (University of Cincinnati. Department of Neurology and Rehabilitation) ;
Maguire, Jane M. (HunterMedical Research Centre. PRC Stroke and Brain Injury) ;
Lindgren, Arne (Skåne University Hospital (Suècia)) ;
Jern, Christina (University of Lincoln. School of Life Sciences) ;
Universitat Autònoma de Barcelona
ObjectiveTo discover common genetic variants associated with poststroke outcomes using a genome-wide association (GWA) study. MethodsThe study comprised 6,165 patients with ischemic stroke from 12 studies in Europe, the United States, and Australia included in the GISCOME (Genetics of Ischaemic Stroke Functional Outcome) network. [...]
2019 - 10.1212/WNL.0000000000007138
Neurology, Vol. 92 Núm. 12 (19 2019) , p. E1271-E1283
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