Reassessment of candidate gene studies for idiopathic restless legs syndrome in a large genome-wide association study dataset of European ancestry

Association of BST1 polymorphism with idiopathic restless legs syndrome in Chinese population

(2021) Yumeng Huang et al.   Sleep and Breathing

Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome

(2021) Félix Javier Jiménez-Jiménez et al.   Frontiers in Pharmacology

Genome-wide enhancer maps link risk variants to disease genes

(2021) Joseph Nasser et al.   NATURE

Discovery and implications of polygenicity of common diseases

(2021) Peter M. Visscher et al.   SCIENCE

Powerful gene-based testing by integrating long-range chromatin interactions and knockoff genotypes

(2021) Shiyang Ma et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Association Between CLOCK Gene Variants and Restless Legs Syndrome in Koreans

(2021) Jae Eun Seo et al.   Psychiatry Investigation

Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification

(2020) Camille M. Moore et al.   HUMAN HEREDITY

Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome

(2020) Félix Javier Jiménez-Jiménez et al.   JOURNAL OF NEUROLOGY

Large genome-wide association study identifies three novel risk variants for restless legs syndrome

(2020) Maria Didriksen et al.   Communications Biology

No Support for Historical Candidate Gene or Candidate Gene-by-Interaction Hypotheses for Major Depression Across Multiple Large Samples

(2019) Richard Border et al.   AMERICAN JOURNAL OF PSYCHIATRY

ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies

(2019) Yaowu Liu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Benefits and limitations of genome-wide association studies

(2019) Vivian Tam et al.   NATURE REVIEWS GENETICS

How genome-wide association studies (GWAS) made traditional candidate gene studies obsolete

(2019) Laramie E. Duncan et al.   NEUROPSYCHOPHARMACOLOGY

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

(2019) Sara Bandres‐Ciga et al.   MOVEMENT DISORDERS

Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome

(2018) Félix Javier Jiménez-Jiménez et al.   PHARMACOGENOMICS JOURNAL

Genetics of restless legs syndrome: An update

(2018) Félix J. Jiménez-Jiménez et al.   SLEEP MEDICINE REVIEWS

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

(2017) Barbara Schormair et al.   LANCET NEUROLOGY

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome

(2017) Félix Javier Jiménez-Jiménez et al.   SLEEP

GeneHancer: genome-wide integration of enhancers and target genes in GeneCards

(2017) Simon Fishilevich et al.   Database-The Journal of Biological Databases and Curation

Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome

(2017) Félix Javier Jiménez-Jiménez et al.   SLEEP

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

(2016) Félix Javier Jiménez-Jiménez et al.   JOURNAL OF NEURAL TRANSMISSION

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome

(2015) Elena García-Martín et al.   MEDICINE

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population

(2015) Félix Javier Jiménez-Jiménez et al.   MEDICINE

MAGMA: Generalized Gene-Set Analysis of GWAS Data

(2015) Christiaan A. de Leeuw et al.   PLoS Computational Biology

Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome

(2014) Félix Javier Jiménez-Jiménez et al.   JOURNAL OF NEURAL TRANSMISSION

Restless legs syndrome/Willis–Ekbom disease diagnostic criteria: updated International Restless Legs Syndrome Study Group (IRLSSG) consensus criteria – history, rationale, description, and significance

(2014) Richard P. Allen et al.   SLEEP MEDICINE

Dopamine receptor D3 (DRD3) gene rs6280 variant and risk for restless legs syndrome

(2013) Félix Javier Jiménez-Jiménez et al.   SLEEP MEDICINE

The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome

(2013) Félix Javier Jiménez-Jiménez et al.   SLEEP MEDICINE

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome

(2012) Angela Roco et al.   JOURNAL OF NEURAL TRANSMISSION

Exome sequencing in a family with restless legs syndrome

(2012) Anne Weissbach et al.   MOVEMENT DISORDERS

Replication in Genome-Wide Association Studies

(2010) Peter Kraft et al.   STATISTICAL SCIENCE

Quantifying and correcting for the winner's curse in genetic association studies

(2009) Rui Xiao et al.   GENETIC EPIDEMIOLOGY

Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome

(2007) Juliane Winkelmann et al.   MOVEMENT DISORDERS