Table 1.
Ischemic stroke cases genotyped as part of the SiGN study and previously genotyped control groups, according to study site*.
Site | Location | Genotype platform | Cases (n) | Controls (n) |
---|---|---|---|---|
CASES GENOTYPED THROUGH SiGN (US SITES) | ||||
GASROS | Boston, USA | Illumina HumanOmni 5M Exome | 470 | |
GCNKSS | Greater Cincinnati region, USA | Illumina HumanOmni 5M Exome | 499 | |
ISGS | Multi-center, USA | Illumina HumanOmni 5M Exome | 187 | |
MCISS | New Jersey, USA | Illumina HumanOmni 5M Exome | 630 | |
MIAMISR | Miami, USA | Illumina HumanOmni 5M Exome | 299 | |
NHS | National sample, USA | Illumina HumanOmni 5M Exome | 316 | |
NOMAS(S) | Manhattan, USA | Illumina HumanOmni 5M Exome | 363 | |
REGARDS | National sample, USA | Illumina HumanOmni 5M Exome | 311 | |
SPS3 | Multi-center; USA; Latin America, Spain | Illumina HumanOmni 5M Exome | 962 | |
SWISS | Multi-center, USA | Illumina HumanOmni 5M Exome | 271 | |
WHI | National sample, USA | Illumina HumanOmni 5M Exome | 458 | |
WUSTL | St. Louis, USA | Illumina HumanOmni 5M Exome | 455 | |
CASES GENOTYPED THROUGH SiGN (INTERNATIONAL SITES) | ||||
BASICMAR | Barcelona, Spain | Illumina HumanOmni 5M Exome | 930 | |
BRAINS | London, England | Illumina HumanOmni 5M Exome | 114 | |
GRAZ | Graz, Austria | Illumina HumanOmni 5M Exome | 639 | |
KRAKOW | Krakow, Poland | Illumina HumanOmni 5M Exome | 952 | 776 |
LEUVEN | Leuven, Belgium | Illumina HumanOmni 5M Exome | 482 | 468 |
LUND | Lund, Sweden | Illumina HumanOmni 5M Exome | 651 | |
SAHLSIS | Gothenburg, Sweden | Illumina HumanOmni 5M Exome | 800 | |
PREVIOUSLY GENOTYPED CONTROL GROUPS | ||||
HABC | Multi-center, USA | Illumina 1M-Duo | 2802 | |
HRS | Multi-center, USA | Illumina HumanOmni 2.5M | 12507 | |
OAI | Multi-center, USA | Illumina HumanOmni 2.5M | 4011 | |
ADHD | Barcelona, Spain | Illumina HumanOmni 1M | 435 | |
GRAZ | Graz, Austria | Illumina 610 | 829 | |
INMA | Barcelona, Spain | Illumina HumanOmni 1M | 1061 | |
KORA | Southern Germany | Illumina Human 550 | 820 | |
WTCCC | United Kingdom | Illumina 660 | 5186 |
SiGN cases genotyped at the Center for Inherited Diseases (CIDR) on the Illumina HumanOmni 5M Exome array.