Pathogenic Ischemic Stroke Phenotypes in the NINDS-Stroke Genetics Network-Reference-Cited by-同舟云学术

Pathogenic Ischemic Stroke Phenotypes in the NINDS-Stroke Genetics Network

Published:2014-12 Issue:12 Volume:45 Page:3589-3596
ISSN:0039-2499
Container-title:Stroke
language:en
Short-container-title:Stroke

Author:

Ay Hakan¹,Arsava Ethem Murat¹,Andsberg Gunnar¹,Benner Thomas¹,Brown Robert D.¹,Chapman Sherita N.¹,Cole John W.¹,Delavaran Hossein¹,Dichgans Martin¹,Engström Gunnar¹,Giralt-Steinhauer Eva¹,Grewal Raji P.¹,Gwinn Katrina¹,Jern Christina¹,Jimenez-Conde Jordi¹,Jood Katarina¹,Katsnelson Michael¹,Kissela Brett¹,Kittner Steven J.¹,Kleindorfer Dawn O.¹,Labovitz Daniel L.¹,Lanfranconi Silvia¹,Lee Jin-Moo¹,Lehm Manuel¹,Lemmens Robin¹,Levi Chris¹,Li Linxin¹,Lindgren Arne¹,Markus Hugh S.¹,McArdle Patrick F.¹,Melander Olle¹,Norrving Bo¹,Peddareddygari Leema Reddy¹,Pedersén Annie¹,Pera Joanna¹,Rannikmäe Kristiina¹,Rexrode Kathryn M.¹,Rhodes David¹,Rich Stephen S.¹,Roquer Jaume¹,Rosand Jonathan¹,Rothwell Peter M.¹,Rundek Tatjana¹,Sacco Ralph L.¹,Schmidt Reinhold¹,Schürks Markus¹,Seiler Stephan¹,Sharma Pankaj¹,Slowik Agnieszka¹,Sudlow Cathie¹,Thijs Vincent¹,Woodfield Rebecca¹,Worrall Bradford B.¹,Meschia James F.¹

Affiliation:

1. From the Department of Radiology, AA Martinos Center for Biomedical Imaging (H.A., E.M.A., T.B.), Stroke Service, Department of Neurology (H.A., J.R.), and Center for Human Genetic Research (J.R.), Massachusetts General Hospital, Harvard Medical School, Boston; Department of Neurology and Rehabilitation Medicine, Skåne University Hospital, Lund, Sweden (G.A., H.D., A.L., O.M., B.N.); Department of Neurology, Mayo Clinic Rochester, MN (R.D.B.); Department of Neurology (S.N.C., B.B.W.), Center for...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

Reference16 articles.

1. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke

2. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

3. Common variants at 6p21.1 are associated with large artery atherosclerotic stroke

4. Genetics of Atrial Fibrillation

5. Variants conferring risk of atrial fibrillation on chromosome 4q25

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