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Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
Traylor M, Persyn E, Tomppo L, Klasson S, Abedi V, Bakker MK, Torres N, Li L, Bell S, Rutten-Jacobs L, Tozer DJ, Griessenauer CJ, Zhang Y, Pedersen A, Sharma P, Jimenez-Conde J, Rundek T, Grewal RP, Lindgren A, Meschia JF, Salomaa V, Havulinna A, Kourkoulis C, Crawford K, Marini S, Mitchell BD, Kittner SJ, Rosand J, Dichgans M, Jern C, Strbian D, Fernandez-Cadenas I, Zand R, Ruigrok Y, Rost N, Lemmens R, Rothwell PM, Anderson CD, Wardlaw J, Lewis CM, Markus HS; 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. Traylor M, et al. Among authors: rutten jacobs l. Lancet Neurol. 2021 May;20(5):351-361. doi: 10.1016/S1474-4422(21)00031-4. Epub 2021 Mar 25. Lancet Neurol. 2021. PMID: 33773637 Free PMC article.
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.
Debette S, Kamatani Y, Metso TM, Kloss M, Chauhan G, Engelter ST, Pezzini A, Thijs V, Markus HS, Dichgans M, Wolf C, Dittrich R, Touzé E, Southerland AM, Samson Y, Abboud S, Béjot Y, Caso V, Bersano A, Gschwendtner A, Sessa M, Cole J, Lamy C, Medeiros E, Beretta S, Bonati LH, Grau AJ, Michel P, Majersik JJ, Sharma P, Kalashnikova L, Nazarova M, Dobrynina L, Bartels E, Guillon B, van den Herik EG, Fernandez-Cadenas I, Jood K, Nalls MA, De Leeuw FE, Jern C, Cheng YC, Werner I, Metso AJ, Lichy C, Lyrer PA, Brandt T, Boncoraglio GB, Wichmann HE, Gieger C, Johnson AD, Böttcher T, Castellano M, Arveiler D, Ikram MA, Breteler MM, Padovani A, Meschia JF, Kuhlenbäumer G, Rolfs A, Worrall BB; International Stroke Genetics Consortium; Ringelstein EB, Zelenika D, Tatlisumak T, Lathrop M, Leys D, Amouyel P, Dallongeville J; CADISP Group. Debette S, et al. Nat Genet. 2015 Jan;47(1):78-83. doi: 10.1038/ng.3154. Epub 2014 Nov 24. Nat Genet. 2015. PMID: 25420145 Free PMC article.
Common NOTCH3 Variants and Cerebral Small-Vessel Disease.
Rutten-Jacobs LC, Traylor M, Adib-Samii P, Thijs V, Sudlow C, Rothwell PM, Boncoraglio G, Dichgans M, Bevan S, Meschia J, Levi C, Rost NS, Rosand J, Hassan A, Markus HS. Rutten-Jacobs LC, et al. Stroke. 2015 Jun;46(6):1482-7. doi: 10.1161/STROKEAHA.114.008540. Epub 2015 May 7. Stroke. 2015. PMID: 25953367 Free PMC article. Clinical Trial.
Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex.
Traylor M, Rutten-Jacobs LC, Holliday EG, Malik R, Sudlow C, Rothwell PM, Maguire JM, Koblar SA, Bevan S, Boncoraglio G, Dichgans M, Levi C, Lewis CM, Markus HS. Traylor M, et al. Stroke. 2015 Nov;46(11):3042-7. doi: 10.1161/STROKEAHA.115.009816. Epub 2015 Oct 6. Stroke. 2015. PMID: 26443828 Free PMC article.
Structural network efficiency predicts conversion to dementia.
Tuladhar AM, van Uden IW, Rutten-Jacobs LC, Lawrence A, van der Holst H, van Norden A, de Laat K, van Dijk E, Claassen JA, Kessels RP, Markus HS, Norris DG, de Leeuw FE. Tuladhar AM, et al. Neurology. 2016 Mar 22;86(12):1112-9. doi: 10.1212/WNL.0000000000002502. Epub 2016 Feb 17. Neurology. 2016. PMID: 26888983 Free PMC article.
Accelerated development of cerebral small vessel disease in young stroke patients.
Arntz RM, van den Broek SM, van Uden IW, Ghafoorian M, Platel B, Rutten-Jacobs LC, Maaijwee NA, Schaapsmeerders P, Schoonderwaldt HC, van Dijk EJ, de Leeuw FE. Arntz RM, et al. Neurology. 2016 Sep 20;87(12):1212-9. doi: 10.1212/WNL.0000000000003123. Epub 2016 Aug 12. Neurology. 2016. PMID: 27521431 Free PMC article.
69 results