| Year |
Citation |
Score |
| 2022 |
Barker N, Judge DP. Counseling Family Members and Monitoring for Evidence of Disease in Asymptomatic Carriers of Amyloid Transthyretin Cardiac Amyloidosis. The American Journal of Cardiology. PMID 36216601 DOI: 10.1016/j.amjcard.2022.09.011 |
0.329 |
|
| 2021 |
Ghidoni A, Elliott PM, Syrris P, Calkins H, James CA, Judge DP, Murray B, Barc J, Probst V, Schott JJ, Song JP, Hauer RNW, Hoorntje ET, van Tintelen JP, Schulze-Bahr E, et al. Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features. Circulation. Genomic and Precision Medicine. PMID 33566628 DOI: 10.1161/CIRCGEN.120.003097 |
0.319 |
|
| 2020 |
Brun F, Gigli M, Graw SL, Judge DP, Merlo M, Murray B, Calkins H, Sinagra G, Taylor MR, Mestroni L, James CA. truncations cause arrhythmogenic right ventricular cardiomyopathy. Journal of Medical Genetics. PMID 31924696 DOI: 10.1136/Jmedgenet-2019-106394 |
0.312 |
|
| 2019 |
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM, Hua W, Indik JH, Ingles J, James CA, ... ... Judge DP, et al. 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary. Heart Rhythm. 16: e373-e407. PMID 31676023 DOI: 10.1016/J.Hrthm.2019.09.019 |
0.317 |
|
| 2019 |
Fajardo J, Cummings A, Brown E, Cuomo K, Rhodes P, Woodbury S, Gilotra N, Russell S, Judge D. Clinical pathway to screen for cardiac amyloidosis in heart failure with preserved ejection fraction. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 26: 166-167. PMID 31343333 DOI: 10.1080/13506129.2019.1583178 |
0.363 |
|
| 2019 |
Roberts JD, Murphy NP, Hamilton RM, Lubbers ER, James CA, Kline CF, Gollob MH, Krahn AD, Sturm AC, Musa H, El-Refaey M, Koenig S, Aneq MÅ, Hoorntje ET, Graw SL, ... ... Judge DP, et al. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy. The Journal of Clinical Investigation. 130. PMID 31264976 DOI: 10.1172/Jci125538 |
0.344 |
|
| 2019 |
Brown EE, McMilllan KN, Halushka MK, Ravekes WJ, Knight M, Crosson JE, Judge DP, Murphy AM. Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditis. Cardiology in the Young. 1-5. PMID 31198128 DOI: 10.1017/S1047951119001124 |
0.375 |
|
| 2019 |
Towbin JA, McKenna WJ, Abrams DJ, Ackerman MJ, Calkins H, Darrieux FCC, Daubert JP, de Chillou C, DePasquale EC, Desai MY, Estes NAM, Hua W, Indik JH, Ingles J, James CA, ... ... Judge DP, et al. 2019 HRS Expert Consensus Statement on Evaluation, Risk Stratification, and Management of Arrhythmogenic Cardiomyopathy. Heart Rhythm. PMID 31078652 DOI: 10.1016/J.Hrthm.2019.05.007 |
0.318 |
|
| 2019 |
Cadrin-Tourigny J, Bosman LP, Nozza A, Wang W, Tadros R, Bhonsale A, Bourfiss M, Fortier A, Lie ØH, Saguner AM, Svensson A, Andorin A, Tichnell C, Murray B, Zeppenfeld K, ... ... Judge DP, et al. A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy. European Heart Journal. PMID 30915475 DOI: 10.1093/Eurheartj/Ehz103 |
0.405 |
|
| 2019 |
Parikh VN, Caleshu C, Reuter C, Lazzeroni LC, Ingles J, Garcia J, McCaleb K, Adesiyun T, Sedaghat-Hamedani F, Kumar S, Graw S, Gigli M, Stolfo D, Dal Ferro M, Ing AY, ... ... Judge DP, et al. Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy. Circulation. Heart Failure. 12: e005371. PMID 30871351 DOI: 10.1161/Circheartfailure.118.005371 |
0.316 |
|
| 2018 |
Griffin JM, Judge DP, Zehr KJ, Madrazo J, Rouf R. Four-Chamber Intracardiac Thrombi Complicating Wild-Type TTR Amyloidosis. Case Reports in Cardiology. 2018: 1845962. PMID 30671265 DOI: 10.1155/2018/1845962 |
0.359 |
|
| 2018 |
Bishop E, Brown EE, Fajardo J, Barouch LA, Judge DP, Halushka MK. Seven factors predict a delayed diagnosis of cardiac amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-6. PMID 30169971 DOI: 10.1080/13506129.2018.1498782 |
0.326 |
|
| 2018 |
Murray B, Hoorntje ET, Te Riele ASJM, Tichnell C, van der Heijden JF, Tandri H, van den Berg MP, Jongbloed JDH, Wilde AAM, Hauer RNW, Calkins H, Judge DP, James CA, van Tintelen JP, Dooijes D. Identification of sarcomeric variants in probands with a clinical diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC). Journal of Cardiovascular Electrophysiology. PMID 29709087 DOI: 10.1111/Jce.13621 |
0.441 |
|
| 2018 |
Caulfield TR, Richter JE, Brown EE, Mohammad AN, Judge DP, Atwal PS. Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family. Molecular Genetics & Genomic Medicine. PMID 29700987 DOI: 10.1002/Mgg3.401 |
0.364 |
|
| 2018 |
Orgeron GM, Te Riele A, Tichnell C, Wang W, Murray B, Bhonsale A, Judge DP, Kamel IR, Zimmerman SL, Tandri H, Calkins H, James CA. Performance of the 2015 International Task Force Consensus Statement Risk Stratification Algorithm for Implantable Cardioverter-Defibrillator Placement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. Circulation. Arrhythmia and Electrophysiology. 11: e005593. PMID 29453325 DOI: 10.1161/Circep.117.005593 |
0.321 |
|
| 2017 |
Judge DP, Norris RA. Inheritance Impacts Mitral Valve Insufficiency. Circulation. Cardiovascular Genetics. 10. PMID 28993408 DOI: 10.1161/Circgenetics.117.001920 |
0.342 |
|
| 2017 |
Hoorntje ET, Te Rijdt WP, James CA, Pilichou K, Basso C, Judge DP, Bezzina CR, van Tintelen JP. Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis. Cardiovascular Research. 113: 1521-1531. PMID 28957532 DOI: 10.1093/Cvr/Cvx150 |
0.394 |
|
| 2017 |
Corrado D, Basso C, Judge DP. Arrhythmogenic Cardiomyopathy. Circulation Research. 121: 784-802. PMID 28912183 DOI: 10.1161/CIRCRESAHA.117.309345 |
0.302 |
|
| 2017 |
Gilotra NA, Bhonsale A, James CA, Te Riele ASJ, Murray B, Tichnell C, Sawant A, Ong CS, Judge DP, Russell SD, Calkins H, Tedford RJ. Heart Failure Is Common and Under-Recognized in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia. Circulation. Heart Failure. 10. PMID 28874384 DOI: 10.1161/Circheartfailure.116.003819 |
0.372 |
|
| 2017 |
Feingold B, Mahle WT, Auerbach S, Clemens P, Domenighetti AA, Jefferies JL, Judge DP, Lal AK, Markham LW, Parks WJ, Tsuda T, Wang PJ, Yoo SJ. Management of Cardiac Involvement Associated With Neuromuscular Diseases: A Scientific Statement From the American Heart Association. Circulation. PMID 28838934 DOI: 10.1161/Cir.0000000000000526 |
0.375 |
|
| 2017 |
Cirino AL, Harris S, Lakdawala NK, Michels M, Olivotto I, Day SM, Abrams DJ, Charron P, Caleshu C, Semsarian C, Ingles J, Rakowski H, Judge DP, Ho CY. Role of Genetic Testing in Inherited Cardiovascular Disease: A Review. Jama Cardiology. PMID 28793145 DOI: 10.1001/Jamacardio.2017.2352 |
0.312 |
|
| 2017 |
Lee YZJ, Judge DP. The Role of Genetics in Peripartum Cardiomyopathy. Journal of Cardiovascular Translational Research. PMID 28776299 DOI: 10.1007/S12265-017-9764-Y |
0.343 |
|
| 2017 |
Rouf R, MacFarlane EG, Takimoto E, Chaudhary R, Nagpal V, Rainer PP, Bindman JG, Gerber EE, Bedja D, Schiefer C, Miller KL, Zhu G, Myers L, Amat-Alarcon N, Lee DI, ... ... Judge DP, et al. Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice. Jci Insight. 2. PMID 28768908 DOI: 10.1172/Jci.Insight.91588 |
0.333 |
|
| 2017 |
Houston BA, Judge DP, Brown E, Halushka M, Barouch LA. Giant Ring Mitochondria in a Patient with Heart Failure and Cerebral White Matter Disease Due to MT-TL1 Mitochondrial Gene Mutation. Journal of Cardiac Failure. PMID 28624653 DOI: 10.1016/J.Cardfail.2017.06.001 |
0.322 |
|
| 2017 |
Orgeron GM, James CA, Te Riele A, Tichnell C, Murray B, Bhonsale A, Kamel IR, Zimmerman SL, Judge DP, Crosson J, Tandri H, Calkins H. Implantable Cardioverter-Defibrillator Therapy in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Predictors of Appropriate Therapy, Outcomes, and Complications. Journal of the American Heart Association. 6. PMID 28588093 DOI: 10.1161/Jaha.117.006242 |
0.375 |
|
| 2017 |
Gupta R, Tichnell C, Murray B, Rizzo S, Te Riele A, Tandri H, Judge DP, Thiene G, Basso C, Calkins H, James CA. Comparison of Features of Fatal Versus Nonfatal Cardiac Arrest in Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. The American Journal of Cardiology. PMID 28506445 DOI: 10.1016/J.Amjcard.2017.03.251 |
0.368 |
|
| 2017 |
Bhonsale A, Te Riele AS, Sawant AC, Groeneweg JA, James CA, Murray B, Tichnell C, Mast TP, van der Pols MJ, Cramer MJ, Dooijes D, van der Heijden JF, Tandri H, van Tintelen JP, Judge DP, et al. Cardiac Phenotype and Long Term Prognosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia Patients with Late Presentation. Heart Rhythm. PMID 28215569 DOI: 10.1016/J.Hrthm.2017.02.013 |
0.415 |
|
| 2017 |
Mast TP, James CA, Calkins H, Teske AJ, Tichnell C, Murray B, Loh P, Russell SD, Velthuis BK, Judge DP, Dooijes D, Tedford RJ, van der Heijden JF, Tandri H, Hauer RN, et al. Evaluation of Structural Progression in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. Jama Cardiology. PMID 28097316 DOI: 10.1001/Jamacardio.2016.5034 |
0.396 |
|
| 2017 |
Cho GS, Lee DI, Tampakakis E, Murphy S, Andersen P, Uosaki H, Chelko S, Chakir K, Hong I, Seo K, Chen HV, Chen X, Basso C, Houser SR, Tomaselli GF, ... ... Judge DP, et al. Neonatal Transplantation Confers Maturation of PSC-Derived Cardiomyocytes Conducive to Modeling Cardiomyopathy. Cell Reports. 18: 571-582. PMID 28076798 DOI: 10.1016/J.Celrep.2016.12.040 |
0.302 |
|
| 2017 |
Te Riele AS, Agullo-Pascual E, James CA, Leo-Macias A, Cerrone M, Zhang M, Lin X, Lin B, Sobreira NL, Amat-Alarcon N, Marsman RF, Murray B, Tichnell C, van der Heijden JF, Dooijes D, ... ... Judge DP, et al. Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis. Cardiovascular Research. 113: 102-111. PMID 28069705 DOI: 10.1093/Cvr/Cvw234 |
0.398 |
|
| 2017 |
Chelko S, Keceli G, Andersen P, Amat-Codina N, Agrimi J, Bedja D, Halushka M, James C, Calkins H, Judge D, Paolocci N. Altered Thioredoxin-AIF Crosstalk Underlies Exercise-induced Cardiac Cell Death in Arrhythmogenic Cardiomyopathy Free Radical Biology and Medicine. 112: 110-111. DOI: 10.1016/J.Freeradbiomed.2017.10.165 |
0.334 |
|
| 2016 |
Houston BA, Schneider AL, Vaishnav J, Cromwell DM, Miller PE, Faridi KF, Shah A, Sciortino C, Whitman G, Tedford RJ, Stevens GR, Judge DP, Russell SD, Rouf R. Angiotensin II antagonism is associated with reduced risk for gastrointestinal bleeding caused by arteriovenous malformations in patients with left ventricular assist devices. The Journal of Heart and Lung Transplantation : the Official Publication of the International Society For Heart Transplantation. PMID 28169115 DOI: 10.1016/J.Healun.2016.12.016 |
0.309 |
|
| 2016 |
Ton VK, Bhonsale A, Gilotra NA, Halushka MK, Steenbergen C, Almansa J, Brown E, Tedford RJ, Wittstein I, Sharma K, Russell SD, Judge DP. Baseline Characteristics Predict the Presence of Amyloid on Endomyocardial Biopsy. Journal of Cardiac Failure. PMID 28011000 DOI: 10.1016/J.Cardfail.2016.12.006 |
0.377 |
|
| 2016 |
Judge DP, Lee YZ, Sharma K. Untangling Wild-Type Transthyretin Amyloidosis. Journal of the American College of Cardiology. 68: 1021-3. PMID 27585506 DOI: 10.1016/J.Jacc.2016.06.032 |
0.353 |
|
| 2016 |
Maurer MS, Hanna M, Grogan M, Dispenzieri A, Witteles R, Drachman B, Judge DP, Lenihan DJ, Gottlieb SS, Shah SJ, Steidley DE, Ventura H, Murali S, Silver MA, Jacoby D, et al. Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey). Journal of the American College of Cardiology. 68: 161-72. PMID 27386769 DOI: 10.1016/J.Jacc.2016.03.596 |
0.342 |
|
| 2016 |
Chelko SP, Asimaki A, Andersen P, Bedja D, Amat-Alarcon N, DeMazumder D, Jasti R, MacRae CA, Leber R, Kleber AG, Saffitz JE, Judge DP. Central role for GSK3β in the pathogenesis of arrhythmogenic cardiomyopathy. Jci Insight. 1. PMID 27170944 DOI: 10.1172/Jci.Insight.85923 |
0.345 |
|
| 2016 |
Houston BA, Kalathiya RJ, Hsu S, Loungani R, Davis ME, Coffin ST, Haglund N, Maltais S, Keebler ME, Leary PJ, Judge DP, Stevens GR, Rickard J, Sciortino CM, Whitman GJ, et al. Right ventricular afterload sensitivity dramatically increases after left ventricular assist device implantation: A multi-center hemodynamic analysis. The Journal of Heart and Lung Transplantation : the Official Publication of the International Society For Heart Transplantation. PMID 27041496 DOI: 10.1016/J.Healun.2016.01.1225 |
0.336 |
|
| 2016 |
Bales ND, Johnson NM, Judge DP, Murphy AM. Comprehensive Versus Targeted Genetic Testing in Children with Hypertrophic Cardiomyopathy. Pediatric Cardiology. PMID 26936621 DOI: 10.1007/S00246-016-1358-Y |
0.362 |
|
| 2016 |
Coelho T, Merlini G, Bulawa CE, Fleming JA, Judge DP, Kelly JW, Maurer MS, Planté-Bordeneuve V, Labaudinière R, Mundayat R, Riley S, Lombardo I, Huertas P. Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis. Neurology and Therapy. PMID 26894299 DOI: 10.1007/S40120-016-0040-X |
0.302 |
|
| 2016 |
Asimaki A, Protonotarios A, James CA, Chelko SP, Tichnell C, Murray B, Tsatsopoulou A, Anastasakis A, Te Riele A, Kléber AG, Judge DP, Calkins H, Saffitz JE. Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells. Circulation. Arrhythmia and Electrophysiology. 9: e003688. PMID 26850880 DOI: 10.1161/Circep.115.003688 |
0.393 |
|
| 2016 |
Te Riele AS, James CA, Murray B, Tichnell C, Amat-Alarcon N, Burks K, Tandri H, Calkins H, Polydefkis M, Judge DP. Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. Journal of Cardiovascular Translational Research. PMID 26733327 DOI: 10.1007/S12265-015-9670-0 |
0.415 |
|
| 2016 |
Vargas JD, Manichaikul A, Liu C, Rich S, Post W, Judge D, Bluemke D. COMMON GENETIC VARIANTS AND LEFT VENTRICULAR STRUCTURE IN THE MULTI-ETHNIC STUDY OF ATHEROSCLEROSIS Journal of the American College of Cardiology. 67: 1835. DOI: 10.1016/S0735-1097(16)31836-8 |
0.351 |
|
| 2015 |
Te Riele ASJM, James CA, Sawant AC, Bhonsale A, Groeneweg JA, Mast TP, Murray B, Tichnell C, Dooijes D, van Tintelen JP, Judge DP, van der Heijden JF, Crosson J, Hauer RNW, Calkins H, et al. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset Disease. Jacc. Clinical Electrophysiology. 1: 551-560. PMID 29759408 DOI: 10.1016/J.Jacep.2015.08.004 |
0.348 |
|
| 2015 |
Judge DP, Neamatalla H, Norris RA, Levine RA, Butcher JT, Vignier N, Kang KH, Nguyen Q, Bruneval P, Perier MC, Messas E, Jeunemaitre X, de Vlaming A, Markwald R, Carrier L, et al. Targeted Mybpc3 Knock-Out Mice with Cardiac Hypertrophy Exhibit Structural Mitral Valve Abnormalities. Journal of Cardiovascular Development and Disease. 2: 48-65. PMID 26819945 DOI: 10.3390/Jcdd2020048 |
0.337 |
|
| 2015 |
Levine RA, Hagége AA, Judge DP, Padala M, Dal-Bianco JP, Aikawa E, Beaudoin J, Bischoff J, Bouatia-Naji N, Bruneval P, Butcher JT, Carpentier A, Chaput M, Chester AH, Clusel C, et al. Mitral valve disease-morphology and mechanisms. Nature Reviews. Cardiology. PMID 26483167 DOI: 10.1038/Nrcardio.2015.161 |
0.394 |
|
| 2015 |
Katritsis G, Shah AS, James CA, Murray B, Tichnell C, Judge DP, Calkins H, Tedford RJ. Surgical Correction of Tricuspid Regurgitation in Patients with ARVD/C. Heartrhythm Case Reports. 1: 326-330. PMID 26405649 DOI: 10.1016/J.Hrcr.2015.05.001 |
0.398 |
|
| 2015 |
Sawant AC, Te Riele AS, Tichnell C, Murray B, Bhonsale A, Tandri H, Judge DP, Calkins H, James CA. Safety of American Heart Association-recommended minimum exercise for desmosomal mutation carriers. Heart Rhythm : the Official Journal of the Heart Rhythm Society. PMID 26321091 DOI: 10.1016/J.Hrthm.2015.08.035 |
0.311 |
|
| 2015 |
Te Riele AS, James CA, Groeneweg JA, Sawant AC, Kammers K, Murray B, Tichnell C, van der Heijden JF, Judge DP, Dooijes D, van Tintelen JP, Hauer RN, Calkins H, Tandri H. Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy. European Heart Journal. PMID 26314686 DOI: 10.1093/Eurheartj/Ehv387 |
0.361 |
|
| 2015 |
McNally EM, Kaltman JR, Benson DW, Canter CE, Cripe LH, Duan D, Finder JD, Hoffman EP, Judge DP, Kertesz N, Kinnett K, Kirsch R, Metzger JM, Pearson GD, Rafael-Fortney JA, et al. Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy. Circulation. 131: 1590-8. PMID 25940966 DOI: 10.1161/Circulationaha.114.015151 |
0.424 |
|
| 2015 |
Khan M, Wasim A, Mirrakhimov AE, McMahon BA, Judge DP, Chu LC, Banavali A, Zeidan AM. Case report of a patient with left ventricular assistance device undergoing chemotherapy for a new diagnosis of lung cancer. Case Reports in Oncological Medicine. 2015: 163727. PMID 25874142 DOI: 10.1155/2015/163727 |
0.361 |
|
| 2015 |
Maurer MS, Grogan DR, Judge DP, Mundayat R, Packman J, Lombardo I, Quyyumi AA, Aarts J, Falk RH. Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomes. Circulation. Heart Failure. 8: 519-26. PMID 25872787 DOI: 10.1161/Circheartfailure.113.000890 |
0.376 |
|
| 2015 |
Groeneweg JA, Bhonsale A, James CA, Te Riele AS, Dooijes D, Tichnell C, Murray B, Wiesfeld AC, Sawant AC, Kassamali B, Atsma DE, Volders PG, de Groot NM, de Boer K, Zimmerman SL, ... ... Judge DP, et al. Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members. Circulation. Cardiovascular Genetics. 8: 437-46. PMID 25820315 DOI: 10.1161/Circgenetics.114.001003 |
0.352 |
|
| 2015 |
Damy T, Judge DP, Kristen AV, Berthet K, Li H, Aarts J. Cardiac findings and events observed in an open-label clinical trial of tafamidis in patients with non-Val30Met and non-Val122Ile hereditary transthyretin amyloidosis. Journal of Cardiovascular Translational Research. 8: 117-27. PMID 25743445 DOI: 10.1007/S12265-015-9613-9 |
0.393 |
|
| 2015 |
Bhonsale A, Groeneweg JA, James CA, Dooijes D, Tichnell C, Jongbloed JD, Murray B, te Riele AS, van den Berg MP, Bikker H, Atsma DE, de Groot NM, Houweling AC, van der Heijden JF, Russell SD, ... ... Judge DP, et al. Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers. European Heart Journal. 36: 847-55. PMID 25616645 DOI: 10.1093/Eurheartj/Ehu509 |
0.405 |
|
| 2015 |
Philips B, te Riele AS, Sawant A, Kareddy V, James CA, Murray B, Tichnell C, Kassamali B, Nazarian S, Judge DP, Calkins H, Tandri H. Outcomes and ventricular tachycardia recurrence characteristics after epicardial ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 716-25. PMID 25530221 DOI: 10.1016/J.Hrthm.2014.12.018 |
0.391 |
|
| 2015 |
Rastegar N, Zimmerman SL, Te Riele AS, James C, Burt JR, Bhonsale A, Murray B, Tichnell C, Judge D, Calkins H, Tandri H, Bluemke DA, Kamel IR. Spectrum of Biventricular Involvement on CMR Among Carriers of ARVD/C-Associated Mutations. Jacc. Cardiovascular Imaging. 8: 863-4. PMID 25457767 DOI: 10.1016/J.Jcmg.2014.09.009 |
0.432 |
|
| 2015 |
Castaño A, Drachman BM, Judge D, Maurer MS. Natural history and therapy of TTR-cardiac amyloidosis: emerging disease-modifying therapies from organ transplantation to stabilizer and silencer drugs. Heart Failure Reviews. 20: 163-78. PMID 25408161 DOI: 10.1007/S10741-014-9462-7 |
0.385 |
|
| 2015 |
Milting H, Klauke B, Christensen AH, Müsebeck J, Walhorn V, Grannemann S, Münnich T, Šari? T, Rasmussen TB, Jensen HK, Mogensen J, Baecker C, Romaker E, Laser KT, zu Knyphausen E, ... ... Judge DP, et al. The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus. European Heart Journal. 36: 872-81. PMID 24598986 DOI: 10.1093/Eurheartj/Ehu077 |
0.371 |
|
| 2015 |
Ton V, Bhonsale A, Halushka MK, Steenbergen C, Kasper E, Tedford RJ, Wittstein I, Sharma K, Russell S, Judge DP. Baseline Characteristics Predict the Presence of Amyloid on Endomyocardial Biopsy Among Patients With Heart Failure With Preserved Ejection Fraction Journal of Cardiac Failure. 21: S17. DOI: 10.1016/J.Cardfail.2015.06.085 |
0.335 |
|
| 2014 |
Ton VK, Mukherjee M, Judge DP. Transthyretin cardiac amyloidosis: pathogenesis, treatments, and emerging role in heart failure with preserved ejection fraction. Clinical Medicine Insights. Cardiology. 8: 39-44. PMID 25628512 DOI: 10.4137/CMC.S15719 |
0.3 |
|
| 2014 |
Sawant AC, Bhonsale A, te Riele AS, Tichnell C, Murray B, Russell SD, Tandri H, Tedford RJ, Judge DP, Calkins H, James CA. Exercise has a disproportionate role in the pathogenesis of arrhythmogenic right ventricular dysplasia/cardiomyopathy in patients without desmosomal mutations. Journal of the American Heart Association. 3: e001471. PMID 25516436 DOI: 10.1161/Jaha.114.001471 |
0.373 |
|
| 2014 |
Molina O G, Judge D, Campbell W, Chahal H, Mugmon M. Transthyretin cardiac amyloidosis: an under-diagnosed cause of heart failure. Journal of Community Hospital Internal Medicine Perspectives. 4: 25500. PMID 25432650 DOI: 10.3402/Jchimp.V4.25500 |
0.452 |
|
| 2014 |
Leung DG, Herzka DA, Thompson WR, He B, Bibat G, Tennekoon G, Russell SD, Schuleri KH, Lardo AC, Kass DA, Thompson RE, Judge DP, Wagner KR. Sildenafil does not improve cardiomyopathy in Duchenne/Becker muscular dystrophy. Annals of Neurology. 76: 541-9. PMID 25042693 DOI: 10.1002/Ana.24214 |
0.34 |
|
| 2014 |
te Riele AS, James CA, Rastegar N, Bhonsale A, Murray B, Tichnell C, Judge DP, Bluemke DA, Zimmerman SL, Kamel IR, Calkins H, Tandri H. Yield of serial evaluation in at-risk family members of patients with ARVD/C. Journal of the American College of Cardiology. 64: 293-301. PMID 25034067 DOI: 10.1016/J.Jacc.2014.04.044 |
0.325 |
|
| 2014 |
Asimaki A, Kapoor S, Plovie E, Karin Arndt A, Adams E, Liu Z, James CA, Judge DP, Calkins H, Churko J, Wu JC, MacRae CA, Kléber AG, Saffitz JE. Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy. Science Translational Medicine. 6: 240ra74. PMID 24920660 DOI: 10.1126/Scitranslmed.3008008 |
0.413 |
|
| 2014 |
Perera JL, Johnson NM, Judge DP, Crosson JE. Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia. Pediatric Cardiology. 35: 1206-12. PMID 24880466 DOI: 10.1007/S00246-014-0917-3 |
0.45 |
|
| 2014 |
Shenje LT, Andersen P, Halushka MK, Lui C, Fernandez L, Collin GB, Amat-Alarcon N, Meschino W, Cutz E, Chang K, Yonescu R, Batista DA, Chen Y, Chelko S, Crosson JE, ... ... Judge DP, et al. Mutations in Alström protein impair terminal differentiation of cardiomyocytes. Nature Communications. 5: 3416. PMID 24595103 DOI: 10.1038/Ncomms4416 |
0.334 |
|
| 2014 |
Philips B, Madhavan S, James CA, te Riele AS, Murray B, Tichnell C, Bhonsale A, Nazarian S, Judge DP, Calkins H, Tandri H, Cheng A. Arrhythmogenic right ventricular dysplasia/cardiomyopathy and cardiac sarcoidosis: distinguishing features when the diagnosis is unclear. Circulation. Arrhythmia and Electrophysiology. 7: 230-6. PMID 24585727 DOI: 10.1161/Circep.113.000932 |
0.406 |
|
| 2014 |
Cerrone M, Lin X, Zhang M, Agullo-Pascual E, Pfenniger A, Chkourko Gusky H, Novelli V, Kim C, Tirasawadichai T, Judge DP, Rothenberg E, Chen HS, Napolitano C, Priori SG, Delmar M. Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype. Circulation. 129: 1092-103. PMID 24352520 DOI: 10.1161/Circulationaha.113.003077 |
0.395 |
|
| 2014 |
Liu D, Wang CJ, Judge DP, Halushka MK, Ni J, Habashi JP, Moslehi J, Bedja D, Gabrielson KL, Xu H, Qian F, Huso D, Dietz HC, Germino GG, Watnick T. A Pkd1-Fbn1 genetic interaction implicates TGF-β signaling in the pathogenesis of vascular complications in autosomal dominant polycystic kidney disease. Journal of the American Society of Nephrology : Jasn. 25: 81-91. PMID 24071006 DOI: 10.1681/Asn.2012050486 |
0.342 |
|
| 2014 |
Agullo-Pascual E, Lin X, Bu L, Bin L, Zhang M, Cerrone M, Fowler S, Murray B, te Riele A, James C, Tichnell C, Calkins H, Rothenberg E, Judge D, Delmar M. SUPER-RESOLUTION IMAGING IN HIPSC-CMS TO STUDY ARRHYTHMOGENIC CARDIOMYOPATHY IN A PATIENT WITH AN SCN5A MUTATION Heart Rhythm. 11: 2135. DOI: 10.1016/J.Hrthm.2014.09.030 |
0.311 |
|
| 2013 |
Camm CF, James CA, Tichnell C, Murray B, Bhonsale A, te Riele AS, Judge DP, Tandri H, Calkins H. Prevalence of atrial arrhythmias in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1661-8. PMID 23994726 DOI: 10.1016/J.Hrthm.2013.08.032 |
0.407 |
|
| 2013 |
Te Riele AS, James CA, Philips B, Rastegar N, Bhonsale A, Groeneweg JA, Murray B, Tichnell C, Judge DP, Van Der Heijden JF, Cramer MJ, Velthuis BK, Bluemke DA, Zimmerman SL, Kamel IR, et al. Mutation-positive arrhythmogenic right ventricular dysplasia/cardiomyopathy: the triangle of dysplasia displaced. Journal of Cardiovascular Electrophysiology. 24: 1311-20. PMID 23889974 DOI: 10.1111/Jce.12222 |
0.429 |
|
| 2013 |
James CA, Bhonsale A, Tichnell C, Murray B, Russell SD, Tandri H, Tedford RJ, Judge DP, Calkins H. Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers. Journal of the American College of Cardiology. 62: 1290-7. PMID 23871885 DOI: 10.1016/J.Jacc.2013.06.033 |
0.386 |
|
| 2013 |
te Riele AS, James CA, Bhonsale A, Groeneweg JA, Camm CF, Murray B, Tichnell C, van der Heijden JF, Dooijes D, Judge DP, Hauer RN, Tandri H, Calkins H. Malignant arrhythmogenic right ventricular dysplasia/cardiomyopathy with a normal 12-lead electrocardiogram: a rare but underrecognized clinical entity. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1484-91. PMID 23816439 DOI: 10.1016/J.Hrthm.2013.06.022 |
0.412 |
|
| 2013 |
te Riele AS, Bhonsale A, James CA, Rastegar N, Murray B, Burt JR, Tichnell C, Madhavan S, Judge DP, Bluemke DA, Zimmerman SL, Kamel IR, Calkins H, Tandri H. Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers. Journal of the American College of Cardiology. 62: 1761-9. PMID 23810894 DOI: 10.1016/J.Jacc.2012.11.087 |
0.396 |
|
| 2013 |
Perrin MJ, Angaran P, Laksman Z, Zhang H, Porepa LF, Rutberg J, James C, Krahn AD, Judge DP, Calkins H, Gollob MH. Exercise testing in asymptomatic gene carriers exposes a latent electrical substrate of arrhythmogenic right ventricular cardiomyopathy. Journal of the American College of Cardiology. 62: 1772-9. PMID 23810883 DOI: 10.1016/J.Jacc.2013.04.084 |
0.356 |
|
| 2013 |
Bhonsale A, James CA, Tichnell C, Murray B, Madhavan S, Philips B, Russell SD, Abraham T, Tandri H, Judge DP, Calkins H. Risk stratification in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers. Circulation. Arrhythmia and Electrophysiology. 6: 569-78. PMID 23671136 DOI: 10.1161/Circep.113.000233 |
0.425 |
|
| 2013 |
Kane MS, Lindsay ME, Judge DP, Barrowman J, Ap Rhys C, Simonson L, Dietz HC, Michaelis S. LMNA-associated cardiocutaneous progeria: an inherited autosomal dominant premature aging syndrome with late onset. American Journal of Medical Genetics. Part A. 161: 1599-611. PMID 23666920 DOI: 10.1002/Ajmg.A.35971 |
0.356 |
|
| 2013 |
Kim C, Wong J, Wen J, Wang S, Wang C, Spiering S, Kan NG, Forcales S, Puri PL, Leone TC, Marine JE, Calkins H, Kelly DP, Judge DP, Chen HS. Studying arrhythmogenic right ventricular dysplasia with patient-specific iPSCs. Nature. 494: 105-10. PMID 23354045 DOI: 10.1038/Nature11799 |
0.372 |
|
| 2013 |
Murray B, Wagle R, Amat-Alarcon N, Wilkens A, Stephens P, Zackai EH, Goldmuntz E, Calkins H, Deardorff MA, Judge DP. A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome. American Journal of Medical Genetics. Part A. 161: 371-6. PMID 23307527 DOI: 10.1002/ajmg.a.35733 |
0.326 |
|
| 2013 |
Maleszewski JJ, Murray DL, Dispenzieri A, Grogan M, Pereira NL, Jenkins SM, Judge DP, Caturegli P, Vrana JA, Theis JD, Dogan A, Halushka MK. Relationship between monoclonal gammopathy and cardiac amyloid type. Cardiovascular Pathology : the Official Journal of the Society For Cardiovascular Pathology. 22: 189-94. PMID 23102805 DOI: 10.1016/J.Carpath.2012.09.001 |
0.311 |
|
| 2013 |
Liang HY, Tops L, Tandri H, James C, Tichnell C, Bax J, Judge D, Calkins H, Abraham T. Presence of plakophilin-2 mutation in arrhythmogenic right ventricular dysplasia cardiomyopathy is associated with worse left ventricular mechanics European Heart Journal. 34: P2911-P2911. DOI: 10.1093/Eurheartj/Eht309.P2911 |
0.424 |
|
| 2013 |
Damy T, Judge D, Dogan A, Slama M, Berthet K, Planté-Bordeneuve V. 075: Cardiac safety and tolerability, and effects on cardiac function of tafamidis in patients with non-V30M TTR-FAP Archives of Cardiovascular Diseases Supplements. 5: 25. DOI: 10.1016/S1878-6480(13)71005-X |
0.424 |
|
| 2013 |
Cerrone M, Lin X, Zhang M, Agullo-Pascual E, Pfenniger A, Gusky HC, Novelli V, Kim C, Tirasawadischai T, Judge DP, Rothenberg E, Chen HV, Napolitano C, Priori SG, Delmar M. Missense Mutations in Plakophilin-2 Can Cause Brugada Syndrome Phenotype By Decreasing Sodium Current and Nav1.5 Membrane Localization Heart Rhythm. 10: 1743. DOI: 10.1016/J.Hrthm.2013.09.019 |
0.367 |
|
| 2012 |
Tan BY, Judge DP. A clinical approach to a family history of sudden death. Circulation. Cardiovascular Genetics. 5: 697-705. PMID 23250900 DOI: 10.1161/Circgenetics.110.959437 |
0.323 |
|
| 2012 |
Gould RA, Sinha R, Aziz H, Rouf R, Dietz HC, Judge DP, Butcher J. Multi-scale biomechanical remodeling in aging and genetic mutant murine mitral valve leaflets: insights into Marfan syndrome. Plos One. 7: e44639. PMID 22984535 DOI: 10.1371/Journal.Pone.0044639 |
0.344 |
|
| 2012 |
Ruberg FL, Maurer MS, Judge DP, Zeldenrust S, Skinner M, Kim AY, Falk RH, Cheung KN, Patel AR, Pano A, Packman J, Grogan DR. Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS). American Heart Journal. 164: 222-228.e1. PMID 22877808 DOI: 10.1016/J.Ahj.2012.04.015 |
0.383 |
|
| 2012 |
van der Zwaag PA, van Rijsingen IA, Asimaki A, Jongbloed JD, van Veldhuisen DJ, Wiesfeld AC, Cox MG, van Lochem LT, de Boer RA, Hofstra RM, Christiaans I, van Spaendonck-Zwarts KY, Lekanne dit Deprez RH, Judge DP, Calkins H, et al. Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy. European Journal of Heart Failure. 14: 1199-207. PMID 22820313 DOI: 10.1093/Eurjhf/Hfs119 |
0.428 |
|
| 2012 |
Judge DP. The complex genetics of atrial fibrillation. Journal of the American College of Cardiology. 60: 1182-4. PMID 22818066 DOI: 10.1016/J.Jacc.2012.04.031 |
0.34 |
|
| 2012 |
Philips B, Madhavan S, James C, Tichnell C, Murray B, Dalal D, Bhonsale A, Nazarian S, Judge DP, Russell SD, Abraham T, Calkins H, Tandri H. Outcomes of catheter ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. Arrhythmia and Electrophysiology. 5: 499-505. PMID 22492430 DOI: 10.1161/Circep.111.968677 |
0.362 |
|
| 2012 |
Lakdawala NK, Funke BH, Baxter S, Cirino AL, Roberts AE, Judge DP, Johnson N, Mendelsohn NJ, Morel C, Care M, Chung WK, Jones C, Psychogios A, Duffy E, Rehm HL, et al. Genetic testing for dilated cardiomyopathy in clinical practice. Journal of Cardiac Failure. 18: 296-303. PMID 22464770 DOI: 10.1016/J.Cardfail.2012.01.013 |
0.33 |
|
| 2012 |
Noureldin RA, Liu S, Nacif MS, Judge DP, Halushka MK, Abraham TP, Ho C, Bluemke DA. The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance. Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society For Cardiovascular Magnetic Resonance. 14: 17. PMID 22348519 DOI: 10.1186/1532-429X-14-17 |
0.418 |
|
| 2012 |
Hong TT, Cogswell R, James CA, Kang G, Pullinger CR, Malloy MJ, Kane JP, Wojciak J, Calkins H, Scheinman MM, Tseng ZH, Ganz P, De Marco T, Judge DP, Shaw RM. Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 9: 961-7. PMID 22300662 DOI: 10.1016/J.Hrthm.2012.01.024 |
0.414 |
|
| 2012 |
Tedford RJ, James C, Judge DP, Tichnell C, Murray B, Bhonsale A, Philips B, Abraham T, Dalal D, Halushka MK, Tandri H, Calkins H, Russell SD. Cardiac transplantation in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Journal of the American College of Cardiology. 59: 289-90. PMID 22240135 DOI: 10.1016/J.Jacc.2011.09.051 |
0.417 |
|
| 2012 |
Groeneweg J, Bhonsale A, James C, van der Heijden J, Murray B, Wilde A, Tichnell C, Jongbloed J, Tandri H, van Tintelen J, Judge D, Hauer R, Calkins H, Dooijes D. Prediction of Pathogenicity of Missense Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Heart Rhythm. 9: 1917. DOI: 10.1016/J.Hrthm.2012.09.113 |
0.379 |
|
| 2011 |
Bhonsale A, James CA, Tichnell C, Murray B, Gagarin D, Philips B, Dalal D, Tedford R, Russell SD, Abraham T, Tandri H, Judge DP, Calkins H. Incidence and predictors of implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary prevention. Journal of the American College of Cardiology. 58: 1485-96. PMID 21939834 DOI: 10.1016/J.Jacc.2011.06.043 |
0.307 |
|
| 2011 |
Hagège AA, Bruneval P, Levine RA, Desnos M, Neamatalla H, Judge DP. The mitral valve in hypertrophic cardiomyopathy: old versus new concepts. Journal of Cardiovascular Translational Research. 4: 757-66. PMID 21909825 DOI: 10.1007/S12265-011-9319-6 |
0.407 |
|
| 2011 |
Judge DP, Markwald RR, Hagège AA, Levine RA. Translational research on the mitral valve: from developmental mechanisms to new therapies. Journal of Cardiovascular Translational Research. 4: 699-701. PMID 21901526 DOI: 10.1007/S12265-011-9320-0 |
0.406 |
|
| 2011 |
Judge DP, Rouf R, Habashi J, Dietz HC. Mitral valve disease in Marfan syndrome and related disorders. Journal of Cardiovascular Translational Research. 4: 741-7. PMID 21866385 DOI: 10.1007/S12265-011-9314-Y |
0.361 |
|
| 2011 |
Judge DP, Kass DA, Thompson WR, Wagner KR. Pathophysiology and therapy of cardiac dysfunction in Duchenne muscular dystrophy. American Journal of Cardiovascular Drugs : Drugs, Devices, and Other Interventions. 11: 287-94. PMID 21812510 DOI: 10.2165/11594070-000000000-00000 |
0.395 |
|
| 2011 |
Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, Camm AJ, Ellinor PT, Gollob M, Hamilton R, Hershberger RE, Judge DP, Le Marec H, McKenna WJ, Schulze-Bahr E, et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 13: 1077-109. PMID 21810866 DOI: 10.1093/Europace/Eur245 |
0.332 |
|
| 2011 |
Judge DP. Cardiovascular genetics provides new insights for early onset arrhythmogenic right ventricular dysplasia/cardiomyopathy. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 1696-7. PMID 21798228 DOI: 10.1016/J.Hrthm.2011.07.024 |
0.362 |
|
| 2011 |
Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, Camm AJ, Ellinor PT, Gollob M, Hamilton R, Hershberger RE, Judge DP, Le Marec H, McKenna WJ, Schulze-Bahr E, et al. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 1308-39. PMID 21787999 DOI: 10.1016/J.Hrthm.2011.05.020 |
0.35 |
|
| 2011 |
Judge DP. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: a family affair. Circulation. 123: 2661-3. PMID 21670239 DOI: 10.1161/Circulationaha.111.031724 |
0.399 |
|
| 2011 |
Kapplinger JD, Landstrom AP, Salisbury BA, Callis TE, Pollevick GD, Tester DJ, Cox MG, Bhuiyan Z, Bikker H, Wiesfeld AC, Hauer RN, van Tintelen JP, Jongbloed JD, Calkins H, Judge DP, et al. Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise. Journal of the American College of Cardiology. 57: 2317-27. PMID 21636032 DOI: 10.1016/J.Jacc.2010.12.036 |
0.344 |
|
| 2011 |
Jain R, Tandri H, Daly A, Tichnell C, James C, Abraham T, Judge DP, Calkins H, Dalal D. Reader- and instrument-dependent variability in the electrocardiographic assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Journal of Cardiovascular Electrophysiology. 22: 561-8. PMID 21114702 DOI: 10.1111/J.1540-8167.2010.01961.X |
0.362 |
|
| 2011 |
Bhonsale A, James C, Tichnell C, Murray B, Philips B, Russell S, Abraham T, Tandri H, Judge D, Calkins H. Arrhythmic Risk Stratification in Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated Desmosomal Mutations Heart Rhythm. 8: 1827-1828. DOI: 10.1016/J.Hrthm.2011.09.052 |
0.403 |
|
| 2011 |
Maleszewski J, Murray D, Dispenzieri A, Judge D, Caturegli P, Vrana J, Theis J, Dogan A, Halushka M. 531 Monoclonal Gammopathy of Undetermined Significance (MGUS) Does Not Predict Cardiac Amyloid Type The Journal of Heart and Lung Transplantation. 30: S179. DOI: 10.1016/J.Healun.2011.01.542 |
0.329 |
|
| 2010 |
Judge DP, Rouf R. Use of genetics in the clinical evaluation and management of heart failure. Current Treatment Options in Cardiovascular Medicine. 12: 566-77. PMID 21063933 DOI: 10.1007/S11936-010-0092-7 |
0.416 |
|
| 2010 |
Tan BY, Jain R, den Haan AD, Chen Y, Dalal D, Tandri H, Amat-Alarcon N, Daly A, Tichnell C, James C, Calkins H, Judge DP. Shared desmosome gene findings in early and late onset arrhythmogenic right ventricular dysplasia/cardiomyopathy. Journal of Cardiovascular Translational Research. 3: 663-73. PMID 20857253 DOI: 10.1007/S12265-010-9224-4 |
0.404 |
|
| 2010 |
Jain R, Dalal D, Daly A, Tichnell C, James C, Evenson A, Abraham T, Tan BY, Tandri H, Russell SD, Judge D, Calkins H. Response to letters regarding article, "electrocardiographic features of arrhythmogenic right ventricular dysplasia" Circulation. 121: e406. DOI: 10.1161/Circulationaha.109.929158 |
0.346 |
|
| 2009 |
den Haan AD, Tan BY, Zikusoka MN, Lladó LI, Jain R, Daly A, Tichnell C, James C, Amat-Alarcon N, Abraham T, Russell SD, Bluemke DA, Calkins H, Dalal D, Judge DP. Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. Cardiovascular Genetics. 2: 428-35. PMID 20031617 DOI: 10.1161/Circgenetics.109.858217 |
0.432 |
|
| 2009 |
Judge DP. Use of genetics in the clinical evaluation of cardiomyopathy. Jama. 302: 2471-6. PMID 19996403 DOI: 10.1001/Jama.2009.1787 |
0.406 |
|
| 2009 |
Judge DP. Phenotypic diversity arising from a single mutation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 6: 1584-5. PMID 19786372 DOI: 10.1016/J.Hrthm.2009.08.008 |
0.318 |
|
| 2009 |
Jain R, Dalal D, Daly A, Tichnell C, James C, Evenson A, Jain R, Abraham T, Tan BY, Tandri H, Russell SD, Judge D, Calkins H. Electrocardiographic features of arrhythmogenic right ventricular dysplasia. Circulation. 120: 477-87. PMID 19635971 DOI: 10.1161/Circulationaha.108.838821 |
0.346 |
|
| 2009 |
Kittleson MM, Skojec DV, Wittstein IS, Champion HC, Judge DP, Barouch LA, Halushka M, Hare JM, Kasper EK, Russell SD. The change in B-type natriuretic peptide levels over time predicts significant rejection in cardiac transplant recipients. The Journal of Heart and Lung Transplantation : the Official Publication of the International Society For Heart Transplantation. 28: 704-9. PMID 19560699 DOI: 10.1016/J.Healun.2009.04.019 |
0.305 |
|
| 2009 |
Ruberg FL, Judge DP, Maurer MS. Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected]. Journal of Cardiac Failure. 15: 464. PMID 19477408 DOI: 10.1016/J.Cardfail.2009.04.003 |
0.353 |
|
| 2009 |
Tandri H, Asimaki A, Abraham T, Dalal D, Tops L, Jain R, Saffitz JE, Judge DP, Russell SD, Halushka M, Bluemke DA, Kass DA, Calkins H. Prolonged RV endocardial activation duration: a novel marker of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 6: 769-75. PMID 19419906 DOI: 10.1016/J.Hrthm.2009.02.031 |
0.392 |
|
| 2009 |
Dalal D, Tandri H, Judge DP, Amat N, Macedo R, Jain R, Tichnell C, Daly A, James C, Russell SD, Abraham T, Bluemke DA, Calkins H. Morphologic variants of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy a genetics-magnetic resonance imaging correlation study. Journal of the American College of Cardiology. 53: 1289-99. PMID 19358943 DOI: 10.1016/J.Jacc.2008.12.045 |
0.396 |
|
| 2008 |
Judge DP, Johnson NM. Genetic evaluation of familial cardiomyopathy. Journal of Cardiovascular Translational Research. 1: 144-54. PMID 20559909 DOI: 10.1007/S12265-008-9025-1 |
0.343 |
|
| 2008 |
Awad MM, Calkins H, Judge DP. Mechanisms of disease: Molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy Nature Clinical Practice Cardiovascular Medicine. 5: 258-267. PMID 18382419 DOI: 10.1038/Ncpcardio1182 |
0.455 |
|
| 2008 |
Frazier A, Judge DP, Schulman SP, Johnson N, Holmes KW, Murphy AM. Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations. Pediatric Cardiology. 29: 846-50. PMID 18175163 DOI: 10.1007/S00246-007-9177-9 |
0.4 |
|
| 2008 |
Judge DP, Dietz HC. Therapy of Marfan syndrome Annual Review of Medicine. 59: 43-59. PMID 17845137 DOI: 10.1146/Annurev.Med.59.103106.103801 |
0.31 |
|
| 2008 |
Judge DP. E713K in desmoglein-2 and arrhythmogenic right ventricular dysplasia/cardiomyopathy Nature Reviews Cardiology. 5. DOI: 10.1038/Ncpcardio1351 |
0.387 |
|
| 2007 |
Dalal D, Jain R, Tandri H, Dong J, Eid SM, Prakasa K, Tichnell C, James C, Abraham T, Russell SD, Sinha S, Judge DP, Bluemke DA, Marine JE, Calkins H. Long-Term Efficacy of Catheter Ablation of Ventricular Tachycardia in Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Journal of the American College of Cardiology. 50: 432-440. PMID 17662396 DOI: 10.1016/J.Jacc.2007.03.049 |
0.372 |
|
| 2007 |
Prakasa KR, Wang J, Tandri H, Dalal D, Bomma C, Chojnowski R, James C, Tichnell C, Russell S, Judge D, Corretti M, Bluemke D, Calkins H, Abraham TP. Utility of Tissue Doppler and Strain Echocardiography in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy American Journal of Cardiology. 100: 507-512. PMID 17659937 DOI: 10.1016/J.Amjcard.2007.03.053 |
0.309 |
|
| 2007 |
Fenton H, Judge DP, Yuh DD, Halushka MK. Intracardiac Giant Cells After Left Ventricular Assist Device Placement Journal of Heart and Lung Transplantation. 26: 417-420. PMID 17403488 DOI: 10.1016/J.Healun.2007.01.013 |
0.373 |
|
| 2006 |
Awad MM, Dalal D, Tichnell C, James C, Tucker A, Abraham T, Spevak PJ, Calkins H, Judge DP. Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2 Human Mutation. 27: 1157. PMID 17041889 DOI: 10.1002/Humu.9461 |
0.392 |
|
| 2006 |
Dalal D, James C, Devanagondi R, Tichnell C, Tucker A, Prakasa K, Spevak PJ, Bluemke DA, Abraham T, Russell SD, Calkins H, Judge DP. Penetrance of Mutations in Plakophilin-2 Among Families With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Journal of the American College of Cardiology. 48: 1416-1424. PMID 17010805 DOI: 10.1016/J.Jacc.2006.06.045 |
0.409 |
|
| 2006 |
Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, Tucker A, Russell SD, Bluemke DA, Dietz HC, Calkins H, Judge DP. DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy American Journal of Human Genetics. 79: 136-142. PMID 16773573 DOI: 10.1086/504393 |
0.425 |
|
| 2006 |
Bilchick KC, Judge DP, Calkins H, Marine JE. Use of a Coronary Sinus Lead and Biventricular ICD to Correct a Sensing Abnormality in a Patient with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Journal of Cardiovascular Electrophysiology. 17: 317-320. PMID 16643408 DOI: 10.1111/J.1540-8167.2005.00298.X |
0.383 |
|
| 2006 |
Robinson PN, Arteaga-Solis E, Baldock C, Collod-Béroud G, Booms P, De Paepe A, Dietz HC, Guo G, Handford PA, Judge DP, Kielty CM, Loeys B, Milewicz DM, Ney A, Ramirez F, et al. The molecular genetics of Marfan syndrome and related disorders. Journal of Medical Genetics. 43: 769-87. PMID 16571647 DOI: 10.1136/Jmg.2005.039669 |
0.326 |
|
| 2006 |
Eldadah ZA, Rosen B, Hay I, Edvardsen T, Jayam V, Dickfeld T, Meininger GR, Judge DP, Hare J, Lima JB, Calkins H, Berger RD. The benefit of upgrading chronically right ventricle–paced heart failure patients to resynchronization therapy demonstrated by strain rate imaging Heart Rhythm. 3: 435-442. PMID 16567291 DOI: 10.1016/J.Hrthm.2005.12.003 |
0.358 |
|
| 2006 |
Dalal D, Molin LH, Piccini J, Tichnell C, James C, Bomma C, Prakasa K, Towbin JA, Marcus FI, Spevak PJ, Bluemke DA, Abraham T, Russell SD, Calkins H, Judge DP. Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2. Circulation. 113: 1641-9. PMID 16549640 DOI: 10.1161/Circulationaha.105.568642 |
0.435 |
|
| 2006 |
Habashi J, Judge D, Holm T, Cohn R, Loeys B, Cooper T, Myers L, Klein E, Liu G, Calvi C, Podowski M, Neptune E, Halushka M, Bedja D, Gabrielson K, et al. Losartan in Marfan Syndrome—Beyond Blood Pressure Lowering Journal of the American Society of Nephrology. 17: 1759-1764. DOI: 10.1681/Asn.2006050508 |
0.31 |
|
| 2005 |
Dalal D, Nasir K, Bomma C, Prakasa K, Tandri H, Piccini J, Roguin A, Tichnell C, James C, Russell SD, Judge DP, Abraham T, Spevak PJ, Bluemke DA, Calkins H. Arrhythmogenic right ventricular dysplasia: a United States experience. Circulation. 112: 3823-32. PMID 16344387 DOI: 10.1161/Circulationaha.105.542266 |
0.386 |
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| 2005 |
Judge DP, Dietz HC. Marfan's syndrome. Lancet (London, England). 366: 1965-76. PMID 16325700 DOI: 10.1016/S0140-6736(05)67789-6 |
0.333 |
|
| 2005 |
Khakoo AY, Halushka MK, Rame JE, Rodriguez ER, Kasper EK, Judge DP. Reversible cardiomyopathy caused by administration of interferon alpha. Nature Clinical Practice. Cardiovascular Medicine. 2: 53-7. PMID 16265343 DOI: 10.1038/Ncpcardio0069 |
0.352 |
|
| 2005 |
Loeys BL, Chen J, Neptune ER, Judge DP, Podowski M, Holm T, Meyers J, Leitch CC, Katsanis N, Sharifi N, Xu FL, Myers LA, Spevak PJ, Cameron DE, De Backer J, et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nature Genetics. 37: 275-81. PMID 15731757 DOI: 10.1038/Ng1511 |
0.363 |
|
| 2004 |
Hay I, Melenovsky V, Fetics BJ, Judge DP, Kramer A, Spinelli J, Reister C, Kass DA, Berger RD. Short-Term Effects of Right-Left Heart Sequential Cardiac Resynchronization in Patients With Heart Failure, Chronic Atrial Fibrillation, and Atrioventricular Nodal Block Circulation. 110: 3404-3410. PMID 15557370 DOI: 10.1161/01.Cir.0000148177.82319.C7 |
0.396 |
|
| 2004 |
Judge DP, Biery NJ, Keene DR, Geubtner J, Myers L, Huso DL, Sakai LY, Dietz HC. Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome. The Journal of Clinical Investigation. 114: 172-81. PMID 15254584 DOI: 10.1172/Jci20641 |
0.343 |
|
| 2004 |
Ng CM, Cheng A, Myers LA, Martinez-Murillo F, Jie C, Bedja D, Gabrielson KL, Hausladen JMW, Mecham RP, Judge DP, Dietz HC. TGF-β–dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome Journal of Clinical Investigation. 114: 1586-1592. DOI: 10.1172/Jci200422715 |
0.34 |
|
| 2004 |
Hay I, Melenovsky V, Fetics BJ, Hare J, Judge D, Kramer A, Reister C, Pastore J, Conville R, Kass DA, Berger R. 879-6 Left ventricular pre-excitation is superior to right ventricular pre-excitation in sequential biventricular pacing for heart failure Journal of the American College of Cardiology. 43. DOI: 10.1016/S0735-1097(04)90649-3 |
0.374 |
|
| 2004 |
Hay I, Melenovsky V, Fetics BJ, Hare J, Judge D, Kramer A, Reister C, Pastore J, Conville R, Kass DA, Berger R. 879-2 Does heart rate regularization with biventricular pacing itself enhance net cardiac function in heart failure patients with chronic atrial fibrillation? Journal of the American College of Cardiology. 43. DOI: 10.1016/S0735-1097(04)90645-6 |
0.375 |
|
| 2003 |
Hutchinson S, Furger A, Halliday D, Judge DP, Jefferson A, Dietz HC, Firth H, Handford PA. Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype? Human Molecular Genetics. 12: 2269-76. PMID 12915484 DOI: 10.1093/Hmg/Ddg241 |
0.342 |
|
| 2001 |
Judge DP, Biery NJ, Dietz HC. Characterization of microsatellite markers flanking FBN1: utility in the diagnostic evaluation for Marfan syndrome. American Journal of Medical Genetics. 99: 39-47. PMID 11170092 DOI: 10.1002/1096-8628(20010215)99:1<39::Aid-Ajmg1114>3.0.Co;2-3 |
0.323 |
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