Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease.

Journal of medical genetics - 1 Jul 2011

Schormair Barbara, Plag Jens, Kaffe Maria, Gross Nadine, Czamara Darina, Samtleben Walter, Lichtner Peter, Ströhle Andreas, Stefanidis Ioannis, Vainas Andreas, Dardiotis Efthimios, Sakkas George K, Gieger Christian, Müller-Myhsok Bertram, Meitinger Thomas, Heemann Uwe, Hadjigeorgiou Georgios M, Oexle Konrad, Winkelmann Juliane

Abstract excerpt

BACKGROUND: Restless legs syndrome (RLS) is a sleep related movement disorder that occurs both in an idiopathic form and in symptomatic varieties. RLS is a frequent and distressing comorbidity in end stage renal disease (ESRD). For idiopathic RLS (iRLS), genetic risk factors have been identified, but their role in RLS in ESRD has not been investigated yet. Therefore, a case-control association study of these...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Germany
Share to Greece

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeodomain Proteins

Share to Kidney Failure, Chronic

Share to Myeloid Ecotropic Viral Integration Site 1 Protein

Share to Neoplasm Proteins

Share to Nerve Tissue Proteins

Share to Restless Legs Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 21572129
DOI: 10.1136/jmg.2010.087858
PMCID: PMC3122881

Genes

BTBD9
MEIS1
SKOR1
PTPRD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease.PMID 21572129Read ↗

Association of candidate genetic variants with restless legs syndrome in end stage renal disease: a multicenter case-control study in Taiwan.Semantic proximity Read ↗

Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population.Semantic proximity Read ↗

Association of BTBD9 and MAP2K5/SKOR1 With Restless Legs Syndrome in Chinese Population.Semantic proximity Read ↗

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.Semantic proximity Read ↗

A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1.Semantic proximity Read ↗

Genetic markers of Restless Legs Syndrome in Parkinson disease.Semantic proximity Read ↗

Replication of restless legs syndrome loci in three European populations.Semantic proximity Read ↗

Restless legs syndrome: an update on genetics and future perspectives.Semantic proximity Read ↗

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.Semantic proximity Read ↗

Periodic leg movements during sleep are associated with polymorphisms in BTBD9, TOX3/BC034767, MEIS1, MAP2K5/SKOR1, and PTPRD.Semantic proximity Read ↗

Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.Semantic proximity Read ↗

Restless legs syndrome in Czech patients with multiple sclerosis: an epidemiological and genetic study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.