Disease: Restless legs syndrome- susceptibility t- 5
- A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1
- Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population
- 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
- Genetic markers of Restless Legs Syndrome in Parkinson disease
- Genetics of restless legs syndrome
- Genome-wide estimates of heritability and genetic correlations in essential tremor
- Haplotype Association of the <em>MAP2K5</em> Gene with Antipsychotics-Induced Symptoms of Restless Legs Syndrome among Patients with Schizophrenia
- Haplotype Association of the MAP2K5 Gene with Antipsychotics-Induced Symptoms of Restless Legs Syndrome among Patients with Schizophrenia
- Identification of Restless Legs Syndrome Genes by Mutational Load Analysis
- 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
- Protein tyrosine phosphatase variants in human hereditary disorders and disease susceptibilities
- Tef polymorphism is associated with sleep disturbances in patients with Parkinson's disease
- The effects of a MAP2K5 microRNA target site SNP on risk for anxiety and depressive disorders
- TOX3 regulates neural progenitor identity
- 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