Schott, Jean Jacques

Top Publications

Top Publications Authored or Co-Authored by "Schott, Jean Jacques"

• 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
• KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

  Nature Genetics, Volume 44, No. 4, Year 2012, Citations 262
• Analysis for Genetic Modifiers of Disease Severity in Patients with Long-QT Syndrome Type 2

  Circulation: Cardiovascular Genetics, Volume 8, No. 3, Year 2015, Citations 57
• SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

  European Heart Journal, Volume 39, No. 31, Year 2018, Citations 51
• Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type i

  International Journal of Cardiology, Volume 207, Year 2016, Citations 49