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Martin Dichgans

Showing results (471-480 of 526) with videos related to

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Nature Genetics|September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic strokeElizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, et al.
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study ProtocolGuido J Falcone, Stacey Q Wolfe, Marialuisa Zedde, et al.
Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|February 1, 2017
STROKOG (stroke and cognition consortium): An international consortium to examine the epidemiology, diagnosis, and treatment of neurocognitive disorders in relation to cerebrovascular diseasePerminder S Sachdev, Jessica W Lo, John D Crawford, et al.
Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Nature Genetics|November 25, 2014
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissectionStéphanie Debette, Yoichiro Kamatani, Tiina M Metso, et al.
Molecular Psychiatry|March 23, 2019
The BDNF<sub>Val66Met</sub> SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer's diseaseNicolai Franzmeier, Jinyi Ren, Alexander Damm, 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.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Pageof 53

Showing results (471-480 of 526) with videos related to

Sort By:
Pageof 53
Nature Genetics|September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic strokeElizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, et al.
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study ProtocolGuido J Falcone, Stacey Q Wolfe, Marialuisa Zedde, et al.
Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|February 1, 2017
STROKOG (stroke and cognition consortium): An international consortium to examine the epidemiology, diagnosis, and treatment of neurocognitive disorders in relation to cerebrovascular diseasePerminder S Sachdev, Jessica W Lo, John D Crawford, et al.
Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Nature Genetics|November 25, 2014
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissectionStéphanie Debette, Yoichiro Kamatani, Tiina M Metso, et al.
Molecular Psychiatry|March 23, 2019
The BDNF<sub>Val66Met</sub> SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer's diseaseNicolai Franzmeier, Jinyi Ren, Alexander Damm, 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.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Pageof 53