Genome-wide association analysis identifies genetic variations in subjects with myalgic encephalomyelitis/chronic fatigue syndrome
Authors: Schlauch, K A; Khaiboullina, S F; De Meirleir, K L; Rawat, S; Petereit, J; Rizvanov, A A; Blatt, N; Mijatovic, T; Kulick, D; Palotás, A; Lombardi, V C
Translational Psychiatry,
9 Feb 2016
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Discussion on S4ME
Cohorts in this study
Phenotype:
ME/CFS,
ME/CFS - Canadian Consensus Criteria (CCC) 2003,
ME/CFS - Fukuda (1994 CDC),
Post-exertional malaise (PEM)
AGPAT3,
ARHGEF3,
ARMC9,
ATAD1,
CCDC157,
CCDC7,
CELF4,
CLEC4M,
EPHA6,
FBLN5,
GRIK3,
KRT18P33,
MAP7,
NBAT1,
PITX1-AS1,
PTDSS1,
RECK,
SLCO3A1,
TOX3,
TRA,
TRD,
UBAC2
Search for these genes
Notes
- Genes from "Table 1. Twenty-three most significant SNPs based on the GWAS and genotypic association test P-value."
- Five additional genes highlighted in the Results and Discussion