Disease: Restless legs syndrome- susceptibility t- 6
- A genetic risk factor for periodic limb movements in sleep
- Biological and clinical insights from genetics of insomnia symptoms
- Extrapyramidal syndromes associated with selective serotonin reuptake inhibitors: a case-control study using spontaneous reports
- Family study of restless legs syndrome in Quebec, Canada: clinical characterization of 671 familial cases
- Further studies on periodic limb movement disorder and restless legs syndrome in children with attention-deficit hyperactivity disorder
- Genetic factors influencing ferritin levels in 14,126 blood donors: results from the Danish Blood Donor Study
- Genetic markers of Restless Legs Syndrome in Parkinson disease
- Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
- Genome-wide estimates of heritability and genetic correlations in essential tremor
- Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q
- Large genome-wide association study identifies three novel risk variants for restless legs syndrome
- Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate
- MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels
- Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome
- Phenocopies in families with essential tremor and restless legs syndrome challenge Mendelian laws. Epigenetics might provide answers
- Prevalence and determinants of periodic limb movements in the general population
- Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
- Restless legs syndrome and pregnancy
- Restless Legs Syndrome and Sleep-Related Movement Disorders
- Restless legs syndrome treatment with dopaminergic drugs
- Restless legs syndrome, rapid eye movement sleep behavior disorder, and hypersomnia in patients with two parkin mutations
- Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity
- Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate
- RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity
- The 14q restless legs syndrome locus in the French Canadian population
- Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes