Disease: Restless legs syndrome- susceptibility t- 3
- A TRAPPC6B splicing variant associates to restless legs syndrome
- Biological and clinical insights from genetics of insomnia symptoms
- Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome
- Evidence for a genetic association between monoamine oxidase A and restless legs syndrome
- Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome
- Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome
- Genetic factors influencing ferritin levels in 14,126 blood donors: results from the Danish Blood Donor Study
- Genetics of restless legs syndrome
- Lack of Association between Genetic Risk Loci for Restless Legs Syndrome and Multimorbidity
- Large genome-wide association study identifies three novel risk variants for restless legs syndrome
- Mechanisms and therapeutic implications of the placebo effect in neurological and psychiatric conditions
- Polygenic risk score identifies associations between sleep duration and diseases determined from an electronic medical record biobank
- Prevalence and determinants of periodic limb movements in the general population
- Protein tyrosine phosphatase variants in human hereditary disorders and disease susceptibilities
- Restless legs syndrome treatment with dopaminergic drugs
- Revisiting brain iron deficiency in restless legs syndrome using magnetic resonance imaging
- Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome
- The effects of a MAP2K5 microRNA target site SNP on risk for anxiety and depressive disorders
- Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes
- Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome