Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Stroke and COL4A2[original query] |
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| Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology 2015 Mar 84 (9): 918-26. Rannikmäe Kristiina, Davies Gail, Thomson Pippa A, Bevan Steve, Devan William J, Falcone Guido J, Traylor Matthew, Anderson Christopher D, Battey Thomas W K, Radmanesh Farid, Deka Ranjan, Woo Jessica G, Martin Lisa J, Jimenez-Conde Jordi, Selim Magdy, Brown Devin L, Silliman Scott L, Kidwell Chelsea S, Montaner Joan, Langefeld Carl D, Slowik Agnieszka, Hansen Björn M, Lindgren Arne G, Meschia James F, Fornage Myriam, Bis Joshua C, Debette Stéphanie, Ikram Mohammad A, Longstreth Will T, Schmidt Reinhold, Zhang Cathy R, Yang Qiong, Sharma Pankaj, Kittner Steven J, Mitchell Braxton D, Holliday Elizabeth G, Levi Christopher R, Attia John, Rothwell Peter M, Poole Deborah L, Boncoraglio Giorgio B, Psaty Bruce M, Malik Rainer, Rost Natalia, Worrall Bradford B, Dichgans Martin, Van Agtmael Tom, Woo Daniel, Markus Hugh S, Seshadri Sudha, Rosand Jonathan, Sudlow Cathie L M, , , , , |
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Neurology 2015 Dec . Traylor Matthew, Zhang Cathy R, Adib-Samii Poneh, Devan William J, Parsons Owen E, Lanfranconi Silvia, Gregory Sarah, Cloonan Lisa, Falcone Guido J, Radmanesh Farid, Fitzpatrick Kaitlin, Kanakis Allison, Barrick Thomas R, Moynihan Barry, Lewis Cathryn M, Boncoraglio Giorgio B, Lemmens Robin, Thijs Vincent, Sudlow Cathie, Wardlaw Joanna, Rothwell Peter M, Meschia James F, Worrall Bradford B, Levi Christopher, Bevan Steve, Furie Karen L, Dichgans Martin, Rosand Jonathan, Markus Hugh S, Rost Natalia, |
| COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology 2017 Sep . Rannikmäe Kristiina, Sivakumaran Vhinoth, Millar Henry, Malik Rainer, Anderson Christopher D, Chong Mike, Dave Tushar, Falcone Guido J, Fernandez-Cadenas Israel, Jimenez-Conde Jordi, Lindgren Arne, Montaner Joan, O'Donnell Martin, Paré Guillaume, Radmanesh Farid, Rost Natalia S, Slowik Agnieszka, Söderholm Martin, Traylor Matthew, Pulit Sara L, Seshadri Sudha, Worrall Brad B, Woo Daniel, Markus Hugh S, Mitchell Braxton D, Dichgans Martin, Rosand Jonathan, Sudlow Cathie L M, |
| Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Brain : a journal of neurology 2019 Oct 142 (10): 3176-3189. Chung Jaeyoon, Marini Sandro, Pera Joanna, Norrving Bo, Jimenez-Conde Jordi, Roquer Jaume, Fernandez-Cadenas Israel, Tirschwell David L, Selim Magdy, Brown Devin L, Silliman Scott L, Worrall Bradford B, Meschia James F, Demel Stacie, Greenberg Steven M, Slowik Agnieszka, Lindgren Arne, Schmidt Reinhold, Traylor Matthew, Sargurupremraj Muralidharan, Tiedt Steffen, Malik Rainer, Debette Stéphanie, Dichgans Martin, Langefeld Carl D, Woo Daniel, Rosand Jonathan, Anderson Christopher |
| Association of COL4A2 Gene Polymorphisms with Lacunar Stroke in Xinjiang Han Populations. Journal of molecular neuroscience : MN 2019 Jun . Liang Chen, Zhang Jiyun, Liu Hai, Ma Jianhua, An Zhiwei, Xia Wen, Zhang Xiaoni |
| Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects. Brain : a journal of neurology 2019 3 142 (4): 1009-1023. Mishra Aniket, Chauhan Ganesh, Violleau Marie-Helene, Vojinovic Dina, Jian Xueqiu, Bis Joshua C, Li Shuo, Saba Yasaman, Grenier-Boley Benjamin, Yang Qiong, Bartz Traci M, Hofer Edith, Soumaré Aïcha, Peng Fen, Duperron Marie-Gabrielle, Foglio Mario, Mosley Thomas H, Schmidt Reinhold, Psaty Bruce M, Launer Lenore J, Boerwinkle Eric, Zhu Yicheng, Mazoyer Bernard, Lathrop Mark, Bellenguez Celine, Van Duijn Cornelia M, Ikram M Arfan, Schmidt Helena, Longstreth W T, Fornage Myriam, Seshadri Sudha, Joutel Anne, Tzourio Christophe, Debette Stephan |
| How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study. Neurology 2019 11 93 (22): e2007-e2020. Tan Rhea Y Y, Traylor Matthew, Megy Karyn, Duarte Daniel, Deevi Sri V V, Shamardina Olga, Mapeta Rutendo P, , Ouwehand Willem H, Gräf Stefan, Downes Kate, Markus Hugh |
| Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke. Stroke 2020 3 51 (4): 1056-1063. Ilinca Andreea, Martinez-Majander Nicolas, Samuelsson Sofie, Piccinelli Paul, Truvé Katarina, Cole John, Kittner Steven, Soller Maria, Kristoffersson Ulf, Tatlisumak Turgut, Puschmann Andreas, Putaala Jukka, Lindgren Ar |
| Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups. Stroke 2020 Feb STROKEAHA119028840. Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau |
| Replication of Top Loci From COL4A1/2 Associated With White Matter Hyperintensity Burden in Patients With Ischemic Stroke. Stroke 2020 11 51 (12): 3751-3755. Li Jiang, Abedi Vida, , Zand Ramin, Griessenauer Christoph |
| Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
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- Page last updated:May 22, 2023
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