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Jason Roberts

Title(s)Assistant Clinical Professor, Dean's Office
SchoolSchool of Medicine
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. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. An International Multi-Center Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2- Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation. 2020 Jul 22. Ng K, Titus EW, Lieve KV, Roston TM, Mazzanti A, Deiter FH, Denjoy I, Ingles J, Till J, Robyns T, Connors SP, Steinberg C, Abrams DJ, Pang B, Scheinman MM, Bos JM, Duffett SA, van der Werf C, Maltret A, Green MS, Rutberg J, Balaji S, Cadrin-Tourigny J, Orland KM, Knight LM, Brateng C, Wu J, Tang AS, Skanes AC, Manlucu J, Healey JS, January CT, Krahn AD, Collins KK, Maginot KR, Fischbach P, Etheridge SP, Eckhardt LL, Hamilton RM, Ackerman MJ, Rosés I Noguer F, Semsarian C, Jura N, Leenhardt A, Gollob MH, Priori SG, Sanatani S, Wilde AAM, Deo RC, Roberts JD. PMID: 32693635.
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    2. Arrhythmogenic Cardiomyopathy: Molecular Insights for Improved Therapeutic Design. J Cardiovasc Dev Dis. 2020 May 26; 7(2). Stevens TL, Wallace MJ, Refaey ME, Roberts JD, Koenig SN, Mohler PJ. PMID: 32466575.
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    3. Exercise and arrhythmic risk in TMEM43 p.S358L arrhythmogenic right ventricular cardiomyopathy. Heart Rhythm. 2020 Feb 29. Paulin FL, Hodgkinson KA, MacLaughlan S, Stuckless SN, Templeton C, Shah S, Bremner H, Roberts JD, Young TL, Parfrey PS, Connors SP. PMID: 32120009.
      View in: PubMed   Mentions: 1     Fields:    
    4. The evolution of gene-guided management of inherited arrhythmia syndromes: Peering beyond monogenic paradigms towards comprehensive genomic risk scores. J Cardiovasc Electrophysiol. 2020 Feb 27. Rowe MK, Roberts JD. PMID: 32107815.
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    5. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia. Circ Arrhythm Electrophysiol. 2020 Mar; 13(3):e007471. Lieve KVV, Dusi V, van der Werf C, Bos JM, Lane CM, Stokke MK, Roston TM, Djupsjöbacka A, Wada Y, Denjoy I, Bundgaard H, Noguer FRI, Semsarian C, Robyns T, Hofman N, Tanck MW, van den Berg MP, Kammeraad JAE, Krahn AD, Clur SB, Sacher F, Till J, Skinner JR, Tfelt-Hansen J, Probst V, Leenhardt A, Horie M, Swan H, Roberts JD, Sanatani S, Haugaa KH, Schwartz PJ, Ackerman MJ, Wilde AAM. PMID: 32063070.
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    6. Initially unexplained cardiac arrest in children and adolescents: A national experience from the Canadian Pediatric Heart Rhythm Network. Heart Rhythm. 2020 Jun; 17(6):975-981. Cunningham T, Roston TM, Franciosi S, Liu MC, Atallah J, Escudero CA, Udupa S, Roberts JD, Dhillon S, Dallaire F, Fournier A, Fatah M, Hamilton R, Sanatani S. PMID: 32036023.
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    7. An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition. Circulation. 2020 Feb 11; 141(6):429-439. Roberts JD, Asaki SY, Mazzanti A, Bos JM, Tuleta I, Muir AR, Crotti L, Krahn AD, Kutyifa V, Shoemaker MB, Johnsrude CL, Aiba T, Marcondes L, Baban A, Udupa S, Dechert B, Fischbach P, Knight LM, Vittinghoff E, Kukavica D, Stallmeyer B, Giudicessi JR, Spazzolini C, Shimamoto K, Tadros R, Cadrin-Tourigny J, Duff HJ, Simpson CS, Roston TM, Wijeyeratne YD, El Hajjaji I, Yousif MD, Gula LJ, Leong-Sit P, Chavali N, Landstrom AP, Marcus GM, Dittmann S, Wilde AAM, Behr ER, Tfelt-Hansen J, Scheinman MM, Perez MV, Kaski JP, Gow RM, Drago F, Aziz PF, Abrams DJ, Gollob MH, Skinner JR, Shimizu W, Kaufman ES, Roden DM, Zareba W, Schwartz PJ, Schulze-Bahr E, Etheridge SP, Priori SG, Ackerman MJ. PMID: 31941373.
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    8. Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest. Eur Heart J. 2019 09 14; 40(35):2953-2961. van der Werf C, Lieve KV, Bos JM, Lane CM, Denjoy I, Roses-Noguer F, Aiba T, Wada Y, Ingles J, Leren IS, Rudic B, Schwartz PJ, Maltret A, Sacher F, Skinner JR, Krahn AD, Roston TM, Tfelt-Hansen J, Swan H, Robyns T, Ohno S, Roberts JD, van den Berg MP, Kammeraad JA, Probst V, Kannankeril PJ, Blom NA, Behr ER, Borggrefe M, Haugaa KH, Semsarian C, Horie M, Shimizu W, Till JA, Leenhardt A, Ackerman MJ, Wilde AA. PMID: 31145795.
      View in: PubMed   Mentions: 1     Fields:    
    9. Diagnostic evaluation and arrhythmia mechanisms in survivors of unexplained cardiac arrest. Pacing Clin Electrophysiol. 2019 10; 42(10):1320-1330. Deif B, Roberts JD. PMID: 31411341.
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    10. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy. J Clin Invest. 2019 07 02; 129(8):3171-3184. 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, Davies RW, Rafiq MA, Koopmann TT, Aafaqi S, Fatah M, Chiasson DA, Taylor MR, Simmons SL, Han M, van Opbergen CJ, Wold LE, Sinagra G, Mittal K, Tichnell C, Murray B, Codima A, Nazer B, Nguyen DT, Marcus FI, Sobriera N, Lodder EM, van den Berg MP, Spears DA, Robinson JF, Ursell PC, Green AK, Skanes AC, Tang AS, Gardner MJ, Hegele RA, van Veen TA, Wilde AA, Healey JS, Janssen PM, Mestroni L, van Tintelen JP, Calkins H, Judge DP, Hund TJ, Scheinman MM, Mohler PJ. PMID: 31264976.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    11. Comparison of Ajmaline and Procainamide Provocation Tests in the Diagnosis of Brugada Syndrome. JACC Clin Electrophysiol. 2019 04; 5(4):504-512. Cheung CC, Mellor G, Deyell MW, Ensam B, Batchvarov V, Papadakis M, Roberts JD, Leather R, Sanatani S, Healey JS, Chauhan VS, Birnie DH, Champagne J, Angaran P, Klein GJ, Yee R, Simpson CS, Talajic M, Gardner M, Yeung-Lai-Wah JA, Chakrabarti S, Laksman ZW, Sharma S, Behr ER, Krahn AD. PMID: 31000106.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    12. QT-Interval Assessment in Left Bundle Branch Block: Deciphering Normal Within Abnormal. Can J Cardiol. 2019 07; 35(7):802-804. Roberts JD, Gula LJ. PMID: 31292074.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    13. Alcohol consumption and leukocyte telomere length. Sci Rep. 2019 02 05; 9(1):1404. Dixit S, Whooley MA, Vittinghoff E, Roberts JD, Heckbert SR, Fitzpatrick AL, Lin J, Leung C, Mukamal KJ, Marcus GM. PMID: 30723310.
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    14. Thyroid Function and the Risk of Atrial Fibrillation: Exploring Potentially Causal Relationships Through Mendelian Randomization. JAMA Cardiol. 2019 02 01; 4(2):97-99. Roberts JD. PMID: 30673080.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    15. Pregnancy in Catecholaminergic Polymorphic Ventricular Tachycardia. JACC Clin Electrophysiol. 2019 03; 5(3):387-394. Cheung CC, Lieve KV, Roston TM, van der Ree MH, Deyell MW, Andrade JG, Laksman ZW, Nannenberg EA, Tadros R, Pang B, Rutberg J, Green MS, Conacher S, Seifer CM, Roberts JD, Steinberg C, Sanatani S, Wilde AA, Krahn AD. PMID: 30898243.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    16. Challenge and Impact of Quinidine Access in Sudden Death Syndromes: A National Experience. JACC Clin Electrophysiol. 2019 03; 5(3):376-382. Malhi N, Cheung CC, Deif B, Roberts JD, Gula LJ, Green MS, Pang B, Sultan O, Konieczny KM, Angaran P, Dorian P, Lashevsky I, Healey JS, Alak A, Tadros R, Andorin A, Steinberg C, Ayala-Paredes F, Simpson CS, Atallah J, Krahn AD. PMID: 30898241.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    17. TJP1 Mutations in Arrhythmogenic Cardiomyopathy. Circ Genom Precis Med. 2018 10; 11(10):e002337. Roberts JD. PMID: 30354307.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    18. Early Repolarization in Long QT Syndrome: Modifier of Arrhythmic Risk or Benign Incidental Finding? JACC Clin Electrophysiol. 2018 09; 4(9):1245-1247. Gula LJ, Roberts JD. PMID: 30236401.
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    19. Cardiac resynchronization is pro-arrhythmic in the absence of reverse ventricular remodelling: a systematic review and meta-analysis. Cardiovasc Res. 2018 09 01; 114(11):1435-1444. 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. PMID: 30010807.
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    20. Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER). JACC Clin Electrophysiol. 2018 11; 4(11):1473-1479. 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. PMID: 30466855.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    21. Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm. 2019 02; 16(2):220-228. Lieve KVV, Verhagen JMA, 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. PMID: 30170228.
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    22. 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. Alhassani S, Deif B, Conacher S, Cunningham KS, Roberts JD. PMID: 30364518.
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    23. Personalizing therapy for atrial fibrillation: the role of stem cell and in silico disease models. Cardiovasc Res. 2018 06 01; 114(7):931-943. Barichello S, Roberts JD, Backx P, Boyle PM, Laksman Z. PMID: 29648634.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimalsCells
    24. Predicting Penetrance of SCN5A Rare Variants: Peering Beyond the Black and White and Into the Shades of Grey. Circ Genom Precis Med. 2018 05; 11(5):e002166. Roberts JD. PMID: 29728398.
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    25. Noncoding Genetic Variation and Gene Expression: Deciphering the Molecular Drivers of Genome-Wide Association Study Signals in Atrial Fibrillation. Circ Genom Precis Med. 2018 03; 11(3):e002109. Roberts JD. PMID: 29545483.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    26. Going big in hypertrophic cardiomyopathy: Ablation of ventricular tachycardia in a giant apical aneurysm. J Cardiovasc Electrophysiol. 2018 01; 29(1):197-198. Duffett SA, Jolly U, Klein GJ, Roberts JD. PMID: 28940486.
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    27. Association Between QT-Interval Components and Sudden Cardiac Death: The ARIC Study (Atherosclerosis Risk in Communities). Circ Arrhythm Electrophysiol. 2017 Oct; 10(10). O'Neal WT, Singleton MJ, Roberts JD, Tereshchenko LG, Sotoodehnia N, Chen LY, Marcus GM, Soliman EZ. PMID: 29030380.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    28. 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). 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. PMID: 28794082.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    29. 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). 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. PMID: 28600387.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    30. Brugada Syndrome: Evolving Insights and Emerging Treatment Strategies. J Innov Card Rhythm Manag. 2017 Feb; 8(2):2613-2622. Duffett SA, Roberts JD. PMID: 32477767.
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    31. Electrocardiographic intervals associated with incident atrial fibrillation: Dissecting the QT interval. Heart Rhythm. 2017 05; 14(5):654-660. Roberts JD, Soliman EZ, Alonso A, Vittinghoff E, Chen LY, Loehr L, Marcus GM. PMID: 28189824.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    32. 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). 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. PMID: 28196901.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    33. Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia. JACC Clin Electrophysiol. 2017 03; 3(3):276-288. 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. PMID: 29759522.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    34. Ablatogenomics: can genotype guide catheter ablation for cardiac arrhythmias? Pharmacogenomics. 2016 Nov; 17(17):1931-1940. Roberts JD, Marcus GM. PMID: 27790939.
      View in: PubMed   Mentions: 1     Fields:    
    35. Atrial Fibrillation Associated Genetic Variants and Left Atrial Histology: Evaluation for Molecular Sub-Phenotypes. J Cardiovasc Electrophysiol. 2016 Nov; 27(11):1264-1270. 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. PMID: 27574037.
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    36. 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 09; 9(9). 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. PMID: 27635072.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    37. Genetic Investigation Into the Differential Risk of Atrial Fibrillation Among Black and White Individuals. JAMA Cardiol. 2016 07 01; 1(4):442-50. 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. PMID: 27438321.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    38. The Canadian Arrhythmogenic Right Ventricular Cardiomyopathy Registry: Rationale, Design, and Preliminary Recruitment. Can J Cardiol. 2016 12; 32(12):1396-1401. 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. PMID: 27474350.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    39. 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. Gula LJ, Skanes AC, Klein GJ, Jenkyn KB, Redfearn DP, Manlucu J, Roberts JD, Yee R, Tang AS, Leong-Sit P. PMID: 26944890.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansPHPublic Health
    40. 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. Roberts JD, Gerstenfeld EP. PMID: 26920183.
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    41. 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. Roberts JD, Klein GJ. PMID: 27084074.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    42. Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation. Am Heart J. 2016 05; 175:9-17. Roberts JD, Dewland TA, Glidden DV, Hoffmann TJ, Arking DE, Chen LY, Psaty BM, Olgin JE, Alonso A, Heckbert SR, Marcus GM. PMID: 27179719.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    43. Pseudo Pseudo A-A-V Response: What is the Mechanism? Pacing Clin Electrophysiol. 2015 Oct; 38(10):1223-4. Roberts JD, Marcus GM. PMID: 26010744.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    44. The burgeoning field of ablatogenomics. Circ Arrhythm Electrophysiol. 2015 Apr; 8(2):258-60. Roberts JD, Marcus GM. PMID: 25900988.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    45. 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. 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. PMID: 25744613.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    46. Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation. Circ Cardiovasc Genet. 2015 Feb; 8(1):50-7. Roberts JD, Longoria J, Poon A, Gollob MH, Dewland TA, Kwok PY, Olgin JE, Deo RC, Marcus GM. PMID: 25406240.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCellsCTClinical Trials
    47. 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. 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. PMID: 25381796.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    48. A contemporary review on the genetic basis of atrial fibrillation. Methodist Debakey Cardiovasc J. 2014 Jan-Mar; 10(1):18-24. Roberts JD, Gollob MH. PMID: 24932358.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimals
    49. 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. Roberts JD, Hsu JC, Aouizerat BE, Pullinger CR, Malloy MJ, Kane JP, Olgin JE, Marcus GM. PMID: 24237655.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    50. Early repolarization: a rare primary arrhythmic syndrome and common modifier of arrhythmic risk. J Cardiovasc Electrophysiol. 2013 Jul; 24(7):837-43. Roberts JD, Gollob MH. PMID: 23631702.
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    51. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet. 2012 Apr 29; 44(6):670-5. 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. PMID: 22544366.
      View in: PubMed   Mentions: 213     Fields:    Translation:Humans
    52. 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. 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. PMID: 22464343.
      View in: PubMed   Mentions: 80     Fields:    Translation:Humans
    53. Distinguishing pathogenic mutations from innocuous rare variants in gene discovery for Brugada syndrome. Can J Cardiol. 2012 Mar-Apr; 28(2):160-1. Roberts JD, Gollob MH. PMID: 22336521.
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    54. Successful surgical repair of ventricular double rupture. Can J Cardiol. 2011 Nov-Dec; 27(6):868.e5-7. Roberts JD, So DY, Lambert AS, Ruel M. PMID: 22118020.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    55. The short QT syndrome: proposed diagnostic criteria. J Am Coll Cardiol. 2011 Feb 15; 57(7):802-12. Gollob MH, Redpath CJ, Roberts JD. PMID: 21310316.
      View in: PubMed   Mentions: 45     Fields:    Translation:Humans
    56. The genetic and clinical features of cardiac channelopathies. Future Cardiol. 2010 Jul; 6(4):491-506. Roberts JD, Gollob MH. PMID: 20608822.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    57. Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation. Europace. 2010 Aug; 12(8):1078-83. Roberts JD, Davies RW, Lubitz SA, Thibodeau IL, Nery PB, Birnie DH, Benjamin EJ, Lemery R, Ellinor PT, Gollob MH. PMID: 20543198.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    58. Impact of genetic discoveries on the classification of lone atrial fibrillation. J Am Coll Cardiol. 2010 Feb 23; 55(8):705-12. Roberts JD, Gollob MH. PMID: 20170805.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
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