Exome sequencing in a family with restless legs syndrome

Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

(2011) Juliane Winkelmann et al.   PLoS Genetics

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

The cadherin Fat2 is required for planar cell polarity in the Drosophila ovary

(2009) I. Viktorinova et al.   DEVELOPMENT

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions (“mimics”)

(2009) Wayne A. Hening et al.   SLEEP MEDICINE

Cadherins as Targets for Genetic Diseases

(2009) A. El-Amraoui et al.   Cold Spring Harbor Perspectives in Biology

Childhood-onset restless legs syndrome: Clinical and genetic features of 22 families

(2008) Hiltrud Muhle et al.   MOVEMENT DISORDERS

Autosomal-dominant locus for restless legs syndrome in French-Canadians on chromosome 16p12.1

(2008) Anastasia Levchenko et al.   MOVEMENT DISORDERS

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

(2008) Barbara Schormair et al.   NATURE GENETICS

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

(2008) Leanne M Dibbens et al.   NATURE GENETICS

Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13

(2008) David Kemlink et al.   NEUROGENETICS