Redon, Richard

Top Publications

Top Publications Authored or Co-Authored by "Redon, Richard"

• Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

  Nature Genetics, Volume 45, No. 9, Year 2013, Citations 480
• Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study

  Cardiovascular Research, Volume 106, No. 3, Year 2015, Citations 118
• Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

  The Lancet Rheumatology, Volume 2, No. 2, Year 2020, Citations 85
• Mutations in FAM111b cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis

  American Journal of Human Genetics, Volume 93, No. 6, Year 2013, Citations 81
• Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy

  American Journal of Human Genetics, Volume 99, No. 3, Year 2016, Citations 75