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. Author manuscript; available in PMC: 2014 Aug 4.
Published in final edited form as: Neurobiol Aging. 2012 Mar 23;33(8):1849.e5–1849.18. doi: 10.1016/j.neurobiolaging.2012.02.014

Table 1.

Summary of sample information

Dataset Sample size AD status (AD/controls) Gender (male/female) Genotyping chip Mean AAD (AD/controls) Origin
Mayo 434 220/214 246/188 Illumina 300 73.5/71.7 USA
NIMH 46 46/0 12/34 Illumina 610 78.1/- USA
WashU 332 294/38 140/192 Illumina 610 84.1/86.1 USA
Belfast 235 213/22 99/136 Illumina 610 82.2/83.1 UK
Bristol 59 43/16 21/38 Illumina 610 82.5/81.6 UK
London 238 194/44 83/155 Illumina 610 86.1/83.0 UK
Manchester 1 1/0 0/1 Illumina 610 79.0/- UK
Nottingham 39 35/4 18/21 Illumina 610 83.6/79.5 UK
Oxford 1 1/0 0/1 Illumina 610 79.5/- UK
Pooled 1385 1047/338 619/766 81.5/76.1

Genome-wide association studies (GWAS) data were obtained from a total of 9 centers, 3 from the USA (NIMH, WashU, and Mayo) and 6 from the UK (Nottingham, Bristol, Manchester, Belfast, Oxford, and London). Sample size, number of cases and controls, and gender for each cohort are as indicated together with details of the mean age at death in years for cases and controls and the genotyping chip used in each study. “-” means the information is not applicable.

Key: AAD, age at death; AD, Alzheimer’s disease; NIMH, National Institute of Mental Health; WashU, Washington University.