Is associated with lacunar ischemic stroke ...
Document type :
Article dans une revue scientifique: Article original
PMID :
Permalink :
Title :
Is associated with lacunar ischemic stroke and deep ich: meta-analyses among 21,500 cases and 40,600 controls
Author(s) :
Rannikmae, Kristiina [Auteur]
Sivakumaran, Vhinoth [Auteur]
Millar, Henry [Auteur]
Malik, Rainer [Auteur]
Anderson, Christopher D. [Auteur]
Chong, Mike [Auteur]
Dave, Tushar [Auteur]
Falcone, Guido J. [Auteur]
Fernandez-Cadenas, Israel [Auteur]
Jimenez-Conde, Jordi [Auteur]
Lindgren, Arne G. [Auteur]
Montaner, Joan [Auteur]
O''donnell, Martin J. [Auteur]
Pare, Guillaume [Auteur]
Radmanesh, Farid [Auteur]
Rost, Natalia S. [Auteur]
Slowik, Agnieszka [Auteur]
Soderholm, Martin [Auteur]
Traylor, Matthew [Auteur]
Pulit, Sara L. [Auteur]
Seshadri, Sudha [Auteur]
Worrall, Bradford B. [Auteur]
Woo, Daniel [Auteur]
Markus, Hugh S. [Auteur]
Mitchell, Braxton D. [Auteur]
Dichgans, Martin [Auteur]
Rosand, Jonathan [Auteur]
Sudlow, Cathie L. M. [Auteur]
Sivakumaran, Vhinoth [Auteur]
Millar, Henry [Auteur]
Malik, Rainer [Auteur]
Anderson, Christopher D. [Auteur]
Chong, Mike [Auteur]
Dave, Tushar [Auteur]
Falcone, Guido J. [Auteur]
Fernandez-Cadenas, Israel [Auteur]
Jimenez-Conde, Jordi [Auteur]
Lindgren, Arne G. [Auteur]
Montaner, Joan [Auteur]
O''donnell, Martin J. [Auteur]
Pare, Guillaume [Auteur]
Radmanesh, Farid [Auteur]
Rost, Natalia S. [Auteur]
Slowik, Agnieszka [Auteur]
Soderholm, Martin [Auteur]
Traylor, Matthew [Auteur]
Pulit, Sara L. [Auteur]
Seshadri, Sudha [Auteur]
Worrall, Bradford B. [Auteur]
Woo, Daniel [Auteur]
Markus, Hugh S. [Auteur]
Mitchell, Braxton D. [Auteur]
Dichgans, Martin [Auteur]
Rosand, Jonathan [Auteur]
Sudlow, Cathie L. M. [Auteur]
Journal title :
Neurology
Abbreviated title :
Neurology
Volume number :
89
Pages :
1829-1839
Publication date :
2017-10-24
ISSN :
1526-632X
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
OBJECTIVE: To determine whether common variants in familial cerebral small vessel disease (SVD) genes confer risk of sporadic cerebral SVD.
METHODS: We meta-analyzed genotype data from individuals of European ancestry to ...
Show more >OBJECTIVE: To determine whether common variants in familial cerebral small vessel disease (SVD) genes confer risk of sporadic cerebral SVD. METHODS: We meta-analyzed genotype data from individuals of European ancestry to determine associations of common single nucleotide polymorphisms (SNPs) in 6 familial cerebral SVD genes (COL4A1COL4A2NOTCH3HTRA1TREX1CECR1 RESULTS: A locus in COL4A2p-4p-8p-5HTRA1p-4p-4COL4A2HTRA1 CONCLUSIONS: These results provide evidence of shared genetic determinants and suggest common pathophysiologic mechanisms of distinct ischemic and hemorrhagic cerebral SVD stroke phenotypes, offering new insights into the causal mechanisms of cerebral SVD.Show less >
Show more >OBJECTIVE: To determine whether common variants in familial cerebral small vessel disease (SVD) genes confer risk of sporadic cerebral SVD. METHODS: We meta-analyzed genotype data from individuals of European ancestry to determine associations of common single nucleotide polymorphisms (SNPs) in 6 familial cerebral SVD genes (COL4A1COL4A2NOTCH3HTRA1TREX1CECR1 RESULTS: A locus in COL4A2p-4p-8p-5HTRA1p-4p-4COL4A2HTRA1 CONCLUSIONS: These results provide evidence of shared genetic determinants and suggest common pathophysiologic mechanisms of distinct ischemic and hemorrhagic cerebral SVD stroke phenotypes, offering new insights into the causal mechanisms of cerebral SVD.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CHU Lille
CNRS
Inserm
Université de Lille
CNRS
Inserm
Université de Lille
Collections :
Research team(s) :
Troubles cognitifs dégénératifs et vasculaires
Submission date :
2019-11-27T14:31:22Z