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Arne Lindgren

Showing results (101-110 of 115) with videos related to

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Neurology|July 18, 2014
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12Laura L Kilarski, Sefanja Achterberg, William J Devan, et al.
Neurology|March 4, 2016
Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaborationRainer Malik, Matthew Traylor, Sara L Pulit, et al.
Frontiers in Neuroscience|July 29, 2021
MRI Radiomic Signature of White Matter Hyperintensities Is Associated With Clinical PhenotypesMartin Bretzner, Anna K Bonkhoff, Markus D Schirmer, et al.
Stroke|November 8, 2014
Pathogenic ischemic stroke phenotypes in the NINDS-stroke genetics networkHakan Ay, Ethem Murat Arsava, Gunnar Andsberg, et al.
JAMA Neurology|February 7, 2019
Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity: A Meta-analysisSandro Marini, Katherine Crawford, Andrea Morotti, et al.
Stroke|January 7, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2Yu-Ching Cheng, Tara M Stanne, Anne-Katrin Giese, et al.
Annals of Neurology|October 8, 2016
Genetic variants in CETP increase risk of intracerebral hemorrhageChristopher D Anderson, Guido J Falcone, Chia-Ling Phuah, et al.
Circulation Research|December 25, 2018
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional OutcomeMarina Mola-Caminal, Caty Carrera, Carolina Soriano-Tárraga, et al.
Annals of Neurology|December 21, 2016
Genetic variation at 16q24.2 is associated with small vessel strokeMatthew Traylor, Rainer Malik, Mike A Nalls, et al.
American Journal of Human Genetics|March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhageDaniel Woo, Guido J Falcone, William J Devan, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Neurology|July 18, 2014
Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12Laura L Kilarski, Sefanja Achterberg, William J Devan, et al.
Neurology|March 4, 2016
Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaborationRainer Malik, Matthew Traylor, Sara L Pulit, et al.
Frontiers in Neuroscience|July 29, 2021
MRI Radiomic Signature of White Matter Hyperintensities Is Associated With Clinical PhenotypesMartin Bretzner, Anna K Bonkhoff, Markus D Schirmer, et al.
Stroke|November 8, 2014
Pathogenic ischemic stroke phenotypes in the NINDS-stroke genetics networkHakan Ay, Ethem Murat Arsava, Gunnar Andsberg, et al.
JAMA Neurology|February 7, 2019
Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity: A Meta-analysisSandro Marini, Katherine Crawford, Andrea Morotti, et al.
Stroke|January 7, 2016
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2Yu-Ching Cheng, Tara M Stanne, Anne-Katrin Giese, et al.
Annals of Neurology|October 8, 2016
Genetic variants in CETP increase risk of intracerebral hemorrhageChristopher D Anderson, Guido J Falcone, Chia-Ling Phuah, et al.
Circulation Research|December 25, 2018
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional OutcomeMarina Mola-Caminal, Caty Carrera, Carolina Soriano-Tárraga, et al.
Annals of Neurology|December 21, 2016
Genetic variation at 16q24.2 is associated with small vessel strokeMatthew Traylor, Rainer Malik, Mike A Nalls, et al.
American Journal of Human Genetics|March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhageDaniel Woo, Guido J Falcone, William J Devan, et al.
Pageof 12