Associated Papers
Relationship between APOE, PER2, PER3 and OX2R Genetic Variants and Neuropsychiatric Symptoms in Patients with Alzheimer's Disease.
Lozano-Tovar S et al.
International Journal of Environmental Research and Public Health, 2023
36901420 (PubMed )
Supplement: ijerph-20-04412-s001.zip › ijerph-2184456-supplementary.pdf
A variant in orexin receptor-2 is associated with self-reported daytime sleepiness in the Japanese population.
Miyagawa T et al.
Journal of Human Genetics, 2022
A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia.
Miyagawa T et al.
Npj Genomic Medicine, 2022
Common activation mechanism of class A GPCRs.
Zhou Q et al.
Elife, 2019
31855179 (PubMed )
Supplement: elife-50279-fig1-data1.xlsx › table1
Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.
Barclay SF et al.
Respiratory Physiology & Neurobiology, 2016
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism
Cluster headache and the hypocretin receptor 2 reconsidered: a genetic association study and meta-analysis.
Weller CM et al.
Cephalalgia : an International Journal of Headache, 2015
Gender-stratified gene and gene-treatment interactions in smoking cessation.
Lee W et al.
The Pharmacogenomics Journal, 2012
21808284 (PubMed )
Supplement: NIHMS305090-supplement-3.pdf
Select a paper to view details