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Correction to: Journal of Neurology https://doi.org/10.1007/s00415-022-11109-8
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Table 2 Association results in the replication sample. For each SNP, the association data in the replication cohort and results from the meta-analyses between discovery and replication cohorts (including and not including the NonIT-EUR cohort) are reported. Results for the genome-wide Italian approach are reported in the upper panel (A), while results for the approaches including the NonIT-EUR are reported in panel B (discovery sample derived from ITAGWAS alone) and C (SNPs identified through the meta-analysis between ITAGWAS and ITAiChip). A1: reference allele (the same as defined in table 1); OR: odds ratio; L95: lower-bound of 95%-confidence interval; U95: upper bound of 95%-confidence interval; P: P-value of association; I2: heterogeneity index. The SNPs with an association beyond the multiple testing correction (Bonferroni threshold of P-value: 1.7 × 10–3, 3.6 × 10–3, 6.25 × 10–3 respectively for A, B and C) are highlighted in bold. No significant association was found in the replication cohort for SNPs selected through the Italian genome-wide approach.
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Sorosina, M., Barizzone, N., Clarelli, F. et al. Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility. J Neurol 269, 4523–4524 (2022). https://doi.org/10.1007/s00415-022-11216-6
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DOI: https://doi.org/10.1007/s00415-022-11216-6