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Jason Roberts

TitleAssistant Clinical Professor
InstitutionUniversity of California San Francisco
DepartmentDean's Office
AddressUCSF Fresno
Fresno CA 93701
Phone559-499-6500
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Roberts JD. TJP1 Mutations in Arrhythmogenic Cardiomyopathy. Circ Genom Precis Med. 2018 Oct; 11(10):e002337. PMID: 30354307.
      View in: PubMed
    2. Gula LJ, Roberts JD. Early Repolarization in Long QT Syndrome: Modifier of Arrhythmic Risk or Benign Incidental Finding? JACC Clin Electrophysiol. 2018 Sep; 4(9):1245-1247. PMID: 30236401.
      View in: PubMed
    3. Malhi N, So PP, Cheung CC, Laksman ZWM, Healey JS, Chauhan VS, Green MS, Champagne J, Steinberg C, Sanatani S, Angaran P, Duff H, Roberts JD, Arbour L, Leather R, Simpson CS, Tadros R, Talajic M, Gardner M, Siefer C, Krahn AD. Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER). JACC Clin Electrophysiol. 2018 Nov; 4(11):1473-1479. PMID: 30466855.
      View in: PubMed
    4. Lieve KVV, Verhagen J, Wei J, Bos JM, van der Werf C, Rosés I Noguer F, Mancini GMS, Guo W, Wang R, van den Heuvel F, Frohn-Mulder IME, Shimizu W, Nogami A, Horigome H, Roberts JD, Leenhardt A, Crijns HJG, Blank AC, Aiba T, Wiesfeld ACP, Blom NA, Sumitomo N, Till J, Ackerman MJ, Chen SRW, van de Laar IMBH, Wilde AAM. Linking the Heart and the Brain: Neurodevelopmental Disorders In Patients With Catecholaminergic Polymorphic Ventricular Tachycardia. Heart Rhythm. 2018 Aug 28. PMID: 30170228.
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    5. Alhassani S, Deif B, Conacher S, Cunningham KS, Roberts JD. A large familial pathogenic Plakophilin-2 gene (PKP2) deletion manifesting with sudden cardiac death and lone atrial fibrillation: Evidence for alternating atrial and ventricular phenotypes. HeartRhythm Case Rep. 2018 Oct; 4(10):486-489. PMID: 30364518.
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    6. Deif B, Ballantyne B, Almehmadi F, Mikhail M, McIntyre WF, Manlucu J, Yee R, Sapp JL, Roberts JD, Healey JS, Leong-Sit P, Tang AS. Cardiac Resynchronization is Pro-arrhythmic in the Absence of Reverse Ventricular Remodelling: A Systematic Review and Meta-analysis. Cardiovasc Res. 2018 Jul 14. PMID: 30010807.
      View in: PubMed
    7. Roberts JD. Predicting Penetrance of SCN5A Rare Variants: Peering Beyond the Black and White and Into the Shades of Grey. Circ Genom Precis Med. 2018 May; 11(5):e002166. PMID: 29728398.
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    8. Roberts JD. Noncoding Genetic Variation and Gene Expression: Deciphering the Molecular Drivers of Genome-Wide Association Study Signals in Atrial Fibrillation. Circ Genom Precis Med. 2018 Mar; 11(3):e002109. PMID: 29545483.
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    9. Duffett SA, Jolly U, Klein GJ, Roberts JD. Going big in hypertrophic cardiomyopathy: Ablation of ventricular tachycardia in a giant apical aneurysm. J Cardiovasc Electrophysiol. 2018 Jan; 29(1):197-198. PMID: 28940486.
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    10. O'Neal WT, Singleton MJ, Roberts JD, Tereshchenko LG, Sotoodehnia N, Chen LY, Marcus GM, Soliman EZ. Association Between QT-Interval Components and Sudden Cardiac Death: The ARIC Study (Atherosclerosis Risk in Communities). Circ Arrhythm Electrophysiol. 2017 Oct; 10(10). PMID: 29030380.
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    11. Roberts JD, Krahn AD, Ackerman MJ, Rohatgi RK, Moss AJ, Nazer B, Tadros R, Gerull B, Sanatani S, Wijeyeratne YD, Baruteau AE, Muir AR, Pang B, Cadrin-Tourigny J, Talajic M, Rivard L, Tester DJ, Liu T, Whitman IR, Wojciak J, Conacher S, Gula LJ, Leong-Sit P, Manlucu J, Green MS, Hamilton R, Healey JS, Lopes CM, Behr ER, Wilde AA, Gollob MH, Scheinman MM. Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? Circ Arrhythm Electrophysiol. 2017 Aug; 10(8). PMID: 28794082.
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    12. Mellor G, Laksman ZWM, Tadros R, Roberts JD, Gerull B, Simpson CS, Klein GJ, Champagne J, Talajic M, Gardner M, Steinberg C, Arbour L, Birnie DH, Angaran P, Leather R, Sanatani S, Chauhan VS, Seifer C, Healey JS, Krahn AD. Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry). Circ Cardiovasc Genet. 2017 Jun; 10(3). PMID: 28600387.
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    13. Roberts JD, Soliman EZ, Alonso A, Vittinghoff E, Chen LY, Loehr L, Marcus GM. Electrocardiographic intervals associated with incident atrial fibrillation: Dissecting the QT interval. Heart Rhythm. 2017 05; 14(5):654-660. PMID: 28189824.
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    14. Swayne LA, Murphy NP, Asuri S, Chen L, Xu X, McIntosh S, Wang C, Lancione PJ, Roberts JD, Kerr C, Sanatani S, Sherwin E, Kline CF, Zhang M, Mohler PJ, Arbour LT. Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome. Circ Cardiovasc Genet. 2017 Jan; 10(1). PMID: 28196901.
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    15. Roberts JD, Gollob MH, Young C, Connors SP, Gray C, Wilton SB, Green MS, Zhu DW, Hodgkinson KA, Poon A, Li Q, Orr N, Tang AS, Klein GJ, Wojciak J, Campagna J, Olgin JE, Badhwar N, Vedantham V, Marcus GM, Kwok PY, Deo RC, Scheinman MM. Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia. JACC Clin Electrophysiol. 2017 Mar; 3(3):276-288. PMID: 29759522.
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    16. Roberts JD, Marcus GM. Ablatogenomics: can genotype guide catheter ablation for cardiac arrhythmias? Pharmacogenomics. 2016 Oct 28. PMID: 27790939.
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    17. Steinberg C, Padfield GJ, Champagne J, Sanatani S, Angaran P, Andrade JG, Roberts JD, Healey JS, Chauhan VS, Birnie DH, Janzen M, Gerull B, Klein GJ, Leather R, Simpson CS, Seifer C, Talajic M, Gardner M, Krahn AD. Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry. Circ Arrhythm Electrophysiol. 2016 Sep; 9(9). PMID: 27635072.
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    18. Roberts JD, Yang J, Gladstone RA, Longoria J, Whitman IR, Dewland TA, Miller C, Robles A, Poon A, Seiler B, Laframboise WA, Olgin JE, Kwok PY, Marcus GM. Atrial Fibrillation Associated Genetic Variants and Left Atrial Histology: Evaluation for Molecular Sub-Phenotypes. J Cardiovasc Electrophysiol. 2016 Aug 30. PMID: 27574037.
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    19. Roberts JD, Hu D, Heckbert SR, Alonso A, Dewland TA, Vittinghoff E, Liu Y, Psaty BM, Olgin JE, Magnani JW, Huntsman S, Burchard EG, Arking DE, Bibbins-Domingo K, Harris TB, Perez MV, Ziv E, Marcus GM. Genetic Investigation Into the Differential Risk of Atrial Fibrillation Among Black and White Individuals. JAMA Cardiol. 2016 Jul 01; 1(4):442-50. PMID: 27438321.
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    20. Krahn AD, Healey JS, Gerull B, Angaran P, Chakrabarti S, Sanatani S, Arbour L, Laksman ZW, Carroll SL, Seifer C, Green M, Roberts JD, Talajic M, Hamilton R, Gardner M. The Canadian Arrhythmogenic Right Ventricular Cardiomyopathy Registry: Rationale, Design, and Preliminary Recruitment. Can J Cardiol. 2016 12; 32(12):1396-1401. PMID: 27474350.
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    21. Gula LJ, Skanes AC, Klein GJ, Jenkyn KB, Redfearn DP, Manlucu J, Roberts JD, Yee R, Tang AS, Leong-Sit P. Atrial flutter and atrial fibrillation ablation - sequential or combined? A cost-benefit and risk analysis of primary prevention pulmonary vein ablation. Heart Rhythm. 2016 07; 13(7):1441-8. PMID: 26944890.
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    22. Roberts JD, Gerstenfeld EP. Concomitant Isolation of the Pulmonary Veins and Posterior Wall Using a Box Lesion Set in a Patient with Persistent Atrial Fibrillation and Variant Pulmonary Venous Anatomy. Card Electrophysiol Clin. 2016 Mar; 8(1):145-9. PMID: 26920183.
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    23. Roberts JD, Klein GJ. Rare Disease and Low Event Rates: Challenges for Refining Risk Stratification in Brugada Syndrome. Can J Cardiol. 2016 11; 32(11):1294.e1-1294.e3. PMID: 27084074.
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    24. Roberts JD, Dewland TA, Glidden DV, Hoffmann TJ, Arking DE, Chen LY, Psaty BM, Olgin JE, Alonso A, Heckbert SR, Marcus GM. Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation. Am Heart J. 2016 May; 175:9-17. PMID: 27179719; PMCID: PMC4873713 [Available on 05/01/17].
    25. Roberts JD, Marcus GM. Pseudo Pseudo A-A-V Response: What is the Mechanism? Pacing Clin Electrophysiol. 2015 Oct; 38(10):1223-4. PMID: 26010744.
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    26. Roberts JD, Marcus GM. The burgeoning field of ablatogenomics. Circ Arrhythm Electrophysiol. 2015 Apr; 8(2):258-60. PMID: 25900988.
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    27. Johnson CJ, Roberts JD, James JH, Hoffmayer KS, Badhwar N, Ku IA, Zhao S, Naeger DM, Rao RK, O'Connell JW, De Marco T, Botvinick EH, Scheinman MM. Comparison of radionuclide angiographic synchrony analysis to echocardiography and magnetic resonance imaging for the diagnosis of arrhythmogenic right ventricular cardiomyopathy. Heart Rhythm. 2015 Jun; 12(6):1268-75. PMID: 25744613.
      View in: PubMed
    28. Roberts JD, Longoria J, Poon A, Gollob MH, Dewland TA, Kwok PY, Olgin JE, Deo RC, Marcus GM. Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation. Circ Cardiovasc Genet. 2015 Feb; 8(1):50-7. PMID: 25406240; PMCID: PMC4334693.
    29. Roberts JD, Dewland TA, Longoria J, Fitzpatrick AL, Ziv E, Hu D, Lin J, Glidden DV, Psaty BM, Burchard EG, Blackburn EH, Olgin JE, Heckbert SR, Marcus GM. Telomere length and the risk of atrial fibrillation: insights into the role of biological versus chronological aging. Circ Arrhythm Electrophysiol. 2014 Dec; 7(6):1026-32. PMID: 25381796; PMCID: PMC4294941.
    30. Roberts JD, Gollob MH. A contemporary review on the genetic basis of atrial fibrillation. Methodist Debakey Cardiovasc J. 2014 Jan-Mar; 10(1):18-24. PMID: 24932358; PMCID: PMC4051329.
    31. Roberts JD, Hsu JC, Aouizerat BE, Pullinger CR, Malloy MJ, Kane JP, Olgin JE, Marcus GM. Impact of a 4q25 genetic variant in atrial flutter and on the risk of atrial fibrillation after cavotricuspid isthmus ablation. J Cardiovasc Electrophysiol. 2014 Mar; 25(3):271-277. PMID: 24237655; PMCID: PMC3947706.
    32. Roberts JD, Gollob MH. Early repolarization: a rare primary arrhythmic syndrome and common modifier of arrhythmic risk. J Cardiovasc Electrophysiol. 2013 Jul; 24(7):837-43. PMID: 23631702.
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    33. Ellinor PT, Lunetta KL, Albert CM, Glazer NL, Ritchie MD, Smith AV, Arking DE, Müller-Nurasyid M, Krijthe BP, Lubitz SA, Bis JC, Chung MK, Dörr M, Ozaki K, Roberts JD, Smith JG, Pfeufer A, Sinner MF, Lohman K, Ding J, Smith NL, Smith JD, Rienstra M, Rice KM, Van Wagoner DR, Magnani JW, Wakili R, Clauss S, Rotter JI, Steinbeck G, Launer LJ, Davies RW, Borkovich M, Harris TB, Lin H, Völker U, Völzke H, Milan DJ, Hofman A, Boerwinkle E, Chen LY, Soliman EZ, Voight BF, Li G, Chakravarti A, Kubo M, Tedrow UB, Rose LM, Ridker PM, Conen D, Tsunoda T, Furukawa T, Sotoodehnia N, Xu S, Kamatani N, Levy D, Nakamura Y, Parvez B, Mahida S, Furie KL, Rosand J, Muhammad R, Psaty BM, Meitinger T, Perz S, Wichmann HE, Witteman JC, Kao WH, Kathiresan S, Roden DM, Uitterlinden AG, Rivadeneira F, McKnight B, Sjögren M, Newman AB, Liu Y, Gollob MH, Melander O, Tanaka T, Stricker BH, Felix SB, Alonso A, Darbar D, Barnard J, Chasman DI, Heckbert SR, Benjamin EJ, Gudnason V, Kääb S. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet. 2012 Apr 29; 44(6):670-5. PMID: 22544366; PMCID: PMC3366038.
    34. Roberts JD, Wells GA, Le May MR, Labinaz M, Glover C, Froeschl M, Dick A, Marquis JF, O'Brien E, Goncalves S, Druce I, Stewart A, Gollob MH, So DY. Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial. Lancet. 2012 May 05; 379(9827):1705-11. PMID: 22464343.
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    35. Roberts JD, Gollob MH. Distinguishing pathogenic mutations from innocuous rare variants in gene discovery for Brugada syndrome. Can J Cardiol. 2012 Mar-Apr; 28(2):160-1. PMID: 22336521.
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    36. Roberts JD, So DY, Lambert AS, Ruel M. Successful surgical repair of ventricular double rupture. Can J Cardiol. 2011 Nov-Dec; 27(6):868.e5-7. PMID: 22118020.
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    37. Gollob MH, Redpath CJ, Roberts JD. The short QT syndrome: proposed diagnostic criteria. J Am Coll Cardiol. 2011 Feb 15; 57(7):802-12. PMID: 21310316.
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    38. Roberts JD, Gollob MH. The genetic and clinical features of cardiac channelopathies. Future Cardiol. 2010 Jul; 6(4):491-506. PMID: 20608822.
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    39. Roberts JD, Davies RW, Lubitz SA, Thibodeau IL, Nery PB, Birnie DH, Benjamin EJ, Lemery R, Ellinor PT, Gollob MH. Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation. Europace. 2010 Aug; 12(8):1078-83. PMID: 20543198; PMCID: PMC2910603.
    40. Roberts JD, Gollob MH. Impact of genetic discoveries on the classification of lone atrial fibrillation. J Am Coll Cardiol. 2010 Feb 23; 55(8):705-12. PMID: 20170805.
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    41. Roberts JD, Veinot JP, Rutberg J, Gollob MH. Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy. Cardiovasc Pathol. 2010 Sep-Oct; 19(5):316-20. PMID: 19632136.
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