| Urgent guidance for navigating and circumventing the QTc-prolonging and torsadogenic potential of possible pharmacotherapies for coronavirus disease 19 (COVID-19) JR Giudicessi, PA Noseworthy, PA Friedman, MJ Ackerman Mayo Clinic Proceedings 95 (6), 1213-1221, 2020 | 487 | 2020 |
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ... Nature genetics 46 (8), 826-836, 2014 | 324 | 2014 |
| Transient outward current (Ito) gain-of-function mutations in the KCND3-encoded Kv4. 3 potassium channel and Brugada syndrome JR Giudicessi, D Ye, DJ Tester, L Crotti, A Mugione, VV Nesterenko, ... Heart rhythm 8 (7), 1024-1032, 2011 | 274 | 2011 |
| Spectrum and prevalence of mutations involving BrS1-through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing … L Crotti, CA Marcou, DJ Tester, S Castelletti, JR Giudicessi, M Torchio, ... Journal of the American College of Cardiology 60 (15), 1410-1418, 2012 | 235 | 2012 |
| Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes JR Giudicessi, MJ Ackerman Translational Research 161 (1), 1-14, 2013 | 231 | 2013 |
| European heart rhythm association (EHRA)/heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus … AAM Wilde, C Semsarian, MF Márquez, AS Shamloo, MJ Ackerman, ... Europace 24 (8), 1307-1367, 2022 | 211 | 2022 |
| Genotype-and phenotype-guided management of congenital long QT syndrome JR Giudicessi, MJ Ackerman Current problems in cardiology 38 (10), 417-455, 2013 | 192 | 2013 |
| Variants in the 3′ untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an … AS Amin, JR Giudicessi, AJ Tijsen, AM Spanjaart, YJ Reckman, ... European heart journal 33 (6), 714-723, 2012 | 173 | 2012 |
| The genetic architecture of long QT syndrome: a critical reappraisal JR Giudicessi, AAM Wilde, MJ Ackerman Trends in cardiovascular medicine 28 (7), 453-464, 2018 | 140 | 2018 |
| Potassium-channel mutations and cardiac arrhythmias—diagnosis and therapy JR Giudicessi, MJ Ackerman Nature Reviews Cardiology 9 (6), 319-332, 2012 | 138 | 2012 |
| Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long … NJ Boczek, JM Best, DJ Tester, JR Giudicessi, S Middha, JM Evans, ... Circulation: Cardiovascular Genetics 6 (3), 279-289, 2013 | 126 | 2013 |
| Enhanced Classification of Brugada Syndrome–Associated and Long-QT Syndrome–Associated Genetic Variants in the SCN5A-Encoded Nav1.5 Cardiac Sodium … JD Kapplinger, JR Giudicessi, D Ye, DJ Tester, TE Callis, CR Valdivia, ... Circulation: Cardiovascular Genetics 8 (4), 582-595, 2015 | 102 | 2015 |
| Artificial intelligence–enabled assessment of the heart rate corrected QT interval using a mobile electrocardiogram device JR Giudicessi, M Schram, JM Bos, CD Galloway, JB Shreibati, ... Circulation 143 (13), 1274-1286, 2021 | 101 | 2021 |
| Genetic susceptibility for COVID-19–associated sudden cardiac death in African Americans JR Giudicessi, DM Roden, AAM Wilde, MJ Ackerman Heart rhythm 17 (9), 1487-1492, 2020 | 101 | 2020 |
| Classification and reporting of potentially proarrhythmic common genetic variation in long QT syndrome genetic testing JR Giudicessi, DM Roden, AAM Wilde, MJ Ackerman Circulation 137 (6), 619-630, 2018 | 87 | 2018 |
| Novel mutations in the KCND3‐encoded Kv4.3 K+ channel associated with autopsy‐negative sudden unexplained death JR Giudicessi, D Ye, CJ Kritzberger, VV Nesterenko, DJ Tester, ... Human mutation 33 (6), 989-997, 2012 | 79 | 2012 |
| Cardiovascular safety of prokinetic agents: a focus on drug‐induced arrhythmias JR Giudicessi, MJ Ackerman, M Camilleri Neurogastroenterology & Motility 30 (6), e13302, 2018 | 67 | 2018 |
| Precision cardiovascular medicine: state of genetic testing JR Giudicessi, IJ Kullo, MJ Ackerman Mayo Clinic Proceedings 92 (4), 642-662, 2017 | 66 | 2017 |
| Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome JR Giudicessi, JD Kapplinger, DJ Tester, M Alders, BA Salisbury, ... Circulation: Cardiovascular Genetics 5 (5), 519-528, 2012 | 65 | 2012 |
| Characterization of SEMA3A-Encoded Semaphorin as a Naturally Occurring Kv4.3 Protein Inhibitor and its Contribution to Brugada Syndrome NJ Boczek, D Ye, EK Johnson, W Wang, L Crotti, DJ Tester, F Dagradi, ... Circulation research 115 (4), 460-469, 2014 | 63 | 2014 |
