Skip to Main Content

Paper Details

ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.
Nat Commun
5
2023
ADRA2A, IRX1, RP, Raynaud's phenomenon, allele, catecholamine, causal genes, genomic regions, glucose, hypersensitivity to catecholamine-induced vasospasms, mirtazapine, pain, risk genes, rs12653958, rs7090046, tissues, ulcers, vasospastic disorder
Author NameAffiliation
Spiros DenaxasInstitute of Health Informatics, University College London
Spiros Denaxas
Spiros DenaxasBritish Heart Foundation Data Science Centre
Spiros DenaxasNational Institute of Health Research University College London Hospitals Biomedical Research Centre
Eric R GamazonDivision of Genetic Medicine and Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Eric R GamazonDivision of Genetic Medicine and Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Mark J CaulfieldWilliam Harvey Research Institute, Queen Mary University of London
Mark J CaulfieldWilliam Harvey Research Institute, Queen Mary University of London
Claudia LangenbergBerlin Institute of Health at Charite-Universitatsmedizin Berlin
Claudia LangenbergUniversity of Cambridge
Claudia LangenbergPrecision Healthcare University Research Institute, Queen Mary University of London
  • 1 - 11

Datasets

Release 1.2