In the current work, we analysed 4,685 sporadic FTD cases and 15,308 controls looking for common genetic determinants for sFTD. We identified associations at the MAPT, APOE and MOBP loci with FTD, suggesting potential common genetic denominators across multiple neurological conditions (i.e. FTD, PSP, ALS, AD, PD and CBD). The summary statistics provided here include - marker, position, p-value, OR and std-err - for the above dataset.
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