Original language | English |
---|---|
Pages (from-to) | 678-85 |
Number of pages | 8 |
Journal | Neurology |
Volume | 83 |
Issue number | 8 |
DOIs | |
Publication status | Published - 19 Aug 2014 |
Keywords
- Brain Ischemia
- Cerebral Hemorrhage
- Chromosomes, Human, Pair 12
- Genetic Predisposition to Disease
- Genome-Wide Association Study
- Genotype
- Humans
- Polymorphism, Single Nucleotide
- Risk
- Stroke
Access to Document
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
In: Neurology, Vol. 83, No. 8, 19.08.2014, p. 678-85.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
AU - Kilarski, Laura L
AU - Achterberg, Sefanja
AU - Devan, William J
AU - Traylor, Matthew
AU - Malik, Rainer
AU - Lindgren, Arne
AU - Pare, Guillame
AU - Sharma, Pankaj
AU - Slowik, Agniesczka
AU - Thijs, Vincent
AU - Walters, Matthew
AU - Worrall, Bradford B
AU - Sale, Michele M
AU - Algra, Ale
AU - Kappelle, L Jaap
AU - Wijmenga, Cisca
AU - Norrving, Bo
AU - Sandling, Johanna K
AU - Rönnblom, Lars
AU - Goris, An
AU - Franke, Andre
AU - Sudlow, Cathie
AU - Rothwell, Peter M
AU - Levi, Christopher
AU - Holliday, Elizabeth G
AU - Fornage, Myriam
AU - Psaty, Bruce
AU - Gretarsdottir, Solveig
AU - Thorsteinsdottir, Unnar
AU - Seshadri, Sudha
AU - Mitchell, Braxton D
AU - Kittner, Steven
AU - Clarke, Robert
AU - Hopewell, Jemma C
AU - Bis, Joshua C
AU - Boncoraglio, Giorgio B
AU - Meschia, James
AU - Ikram, M Arfan
AU - Hansen, Bjorn M
AU - Montaner, Joan
AU - Thorleifsson, Gudmar
AU - Stefanson, Kari
AU - Rosand, Jonathan
AU - de Bakker, Paul I W
AU - Farrall, Martin
AU - Dichgans, Martin
AU - Markus, Hugh S
AU - Bevan, Steve
AU - GARNET Collaborative Research Group, Wellcome Trust Case Control Consortium 2, Australian Stroke Genetic Collaborative, the METASTROKE Consortium, and the International Stroke Genetics Consortium
N1 - © 2014 American Academy of Neurology.
PY - 2014/8/19
Y1 - 2014/8/19
KW - Brain Ischemia
KW - Cerebral Hemorrhage
KW - Chromosomes, Human, Pair 12
KW - Genetic Predisposition to Disease
KW - Genome-Wide Association Study
KW - Genotype
KW - Humans
KW - Polymorphism, Single Nucleotide
KW - Risk
KW - Stroke
U2 - 10.1212/WNL.0000000000000707
DO - 10.1212/WNL.0000000000000707
M3 - Article
C2 - 25031287
SN - 0028-3878
VL - 83
SP - 678
EP - 685
JO - Neurology
JF - Neurology
IS - 8
ER -