By Professor Diane Fatkin

Journal articles

Peters S; James PA; Fatkin D; Zentner D, 2022, 'Pregnancy Outcomes in Females With Dilated Cardiomyopathy-Associated Rare Genetic Variants', Circulation: Genomic and Precision Medicine, 15, pp. E003540, http://dx.doi.org/10.1161/CIRCGEN.121.003540

De Bosscher R; Dausin C; Janssens K; Bogaert J; Elliott A; Ghekiere O; Van De Heyning CM; Sanders P; Kalman J; Fatkin D; Herbots L; Willems R; Heidbuchel H; La Gerche A; Claessen G, 2022, 'Rationale and design of the PROspective ATHletic Heart (Pro@Heart) study: Long-term assessment of the determinants of cardiac remodelling and its clinical consequences in endurance athletes', BMJ Open Sport and Exercise Medicine, 8, http://dx.doi.org/10.1136/bmjsem-2022-001309

Peters S; Thompson BA; Perrin M; James P; Zentner D; Kalman JM; Vandenberg JI; Fatkin D, 2022, 'Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated SCN5A Variants: A Systematic Review', Circulation: Genomic and Precision Medicine, 15, pp. E003432, http://dx.doi.org/10.1161/CIRCGEN.121.003432

Paul C; Peters S; Perrin M; Fatkin D; Amerena J, 2022, 'Non-ischaemic dilated cardiomyopathy: recognising the genetic links', Internal Medicine Journal, 53, http://dx.doi.org/10.1111/imj.15921

Al-Kaisey A; Wong G; Young P; Hawson J; Chieng D; Bakshi A; Lacaze P; Giannoulatou E; Kistler P; Fatkin D; Kalman J, 2022, 'Polygenic Risk Scores Identify Atrial Electrophysiological Substrate Abnormalities and Predict Atrial Fibrillation Recurrence Following Catheter Ablation', Heart, Lung and Circulation, 31, pp. S52 - S52, http://dx.doi.org/10.1016/j.hlc.2022.06.027

Lacaze P; Sebra R; Riaz M; Ingles J; Tiller J; Thompson BA; James PA; Fatkin D; Semsarian C; Reid CM; Tonkin AM; Winship I; Schadt E; McNeil JJ, 2021, 'Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent', npj Genomic Medicine, 6, http://dx.doi.org/10.1038/s41525-021-00211-x

Li JV; Ng CA; Cheng D; Zhou Z; Yao M; Guo Y; Yu ZY; Ramaswamy Y; Ju LA; Kuchel PW; Feneley MP; Fatkin D; Cox CD, 2021, 'Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations', Communications Biology, 4, http://dx.doi.org/10.1038/s42003-021-02528-w

Cannata A; Merlo M; Dal Ferro M; Manca P; Paldino A; Barbati G; Graw S; Bromage D; Johnson R; Roy D; Gigli M; Stolfo D; Abbate A; Parkih V; Ashley E; Lakdawala N; Carr-White G; Fatkin D; Mcdonagh T; Taylor M; Mestroni L; Sinagra G, 2021, 'Titin mutations and female sex characterize dilated cardiomyopathy in the elderly', EUROPEAN HEART JOURNAL SUPPLEMENTS, 23, pp. G153 - +, http://dx.doi.org/10.1093/eurheartj/suab142.006

Xu H; Cole JW; Gaynor B; Ryan K; Mitchell BD; Rundek T; Worrall BB; Ellinor PT; Fatkin D; Lubitz SA; Pare G; Leifer D, 2021, 'Abstract 9924: Polygenic Risk Score for PR Interval is Associated with Increased Risk of Ischemic Stroke', Circulation, 144, http://dx.doi.org/10.1161/circ.144.suppl_1.9924

Gigli M; Stolfo D; Graw SL; Merlo M; Gregorio C; Nee Chen S; Dal Ferro M; Paldinomd A; De Angelis G; Brun F; Jirikowic J; Salcedo EE; Turja S; Fatkin D; Johnson R; Van Tintelen JP; Te Riele ASJM; Wilde AAM; Lakdawala NK; Picard K; Miani D; Muser D; Maria Severini G; Calkins H; James CA; Murray B; Tichnell C; Parikh VN; Ashley EA; Reuter C; Song J; Judge DP; McKenna WJ; Taylor MRG; Sinagra G; Mestroni L, 2021, 'Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants', Circulation, 144, pp. 1600 - 1611, http://dx.doi.org/10.1161/CIRCULATIONAHA.121.053521

McGrath-Cadell L; Hesselson S; Tarr I; Iismaa SE; Bax M; Junday K; Dunwoodie SE; Fatkin D; Kovacic J; Muller DWM; Giannoulatou E; Graham RM, 2021, 'Spontaneous Coronary Artery Dissection (SCAD) and a family history of aortic artery dissection, a case series', European Heart Journal, 42, http://dx.doi.org/10.1093/eurheartj/ehab724.2787

Patel PN; Ito K; Willcox JAL; Haghighi A; Jang MY; Gorham JM; Depalma SR; Lam L; McDonough B; Johnson R; Lakdawala NK; Roberts A; Barton PJR; Cook SA; Fatkin D; Seidman CE; Seidman JG, 2021, 'Contribution of Noncanonical Splice Variants to TTN Truncating Variant Cardiomyopathy', Circulation: Genomic and Precision Medicine, 14, pp. E003389, http://dx.doi.org/10.1161/CIRCGEN.121.003389

Giudicessi JR; Ackerman MJ; Fatkin D; Kovacic JC, 2021, 'Precision Medicine Approaches to Cardiac Arrhythmias: JACC Focus Seminar 4/5 (vol 77, pg 2573, 2021)', JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 78, http://dx.doi.org/10.1016/j.jacc.2021.05.032

Fatkin D; Calkins H; Elliott P; James CA; Peters S; Kovacic JC, 2021, 'Contemporary and Future Approaches to Precision Medicine in Inherited Cardiomyopathies: JACC Focus Seminar 3/5', Journal of the American College of Cardiology, 77, pp. 2551 - 2572, http://dx.doi.org/10.1016/j.jacc.2020.12.072

Giudicessi JR; Ackerman MJ; Fatkin D; Kovacic JC, 2021, 'Precision Medicine Approaches to Cardiac Arrhythmias: JACC Focus Seminar 4/5', Journal of the American College of Cardiology, 77, pp. 2573 - 2591, http://dx.doi.org/10.1016/j.jacc.2021.03.325

Pineda S; Nikolova-Krstevski V; Leimena C; Atkinson AJ; Altekoester AK; Cox CD; Jacoby A; Huttner IG; Ju YK; Soka M; Ohanian M; Trivedi G; Kalvakuri S; Birker K; Johnson R; Molenaar P; Kuchar D; Allen DG; Van Helden DF; Harvey RP; Hill AP; Bodmer R; Vogler G; Dobrzynski H; Ocorr K; Fatkin D, 2021, 'Conserved Role of the Large Conductance Calcium-Activated Potassium Channel, KCa1.1, in Sinus Node Function and Arrhythmia Risk', Circulation: Genomic and Precision Medicine, 14, pp. E003144, http://dx.doi.org/10.1161/CIRCGEN.120.003144

Yu ZY; Gong H; Wu J; Dai Y; Kesteven SH; Fatkin D; Martinac B; Graham RM; Feneley MP, 2021, 'Cardiac Gq Receptors and Calcineurin Activation Are Not Required for the Hypertrophic Response to Mechanical Left Ventricular Pressure Overload', Frontiers in Cell and Developmental Biology, 9, http://dx.doi.org/10.3389/fcell.2021.639509

Taliun D; Harris DN; Kessler MD; Carlson J; Szpiech ZA; Torres R; Taliun SAG; Corvelo A; Gogarten SM; Kang HM; Pitsillides AN; LeFaive J; Lee SB; Tian X; Browning BL; Das S; Emde AK; Clarke WE; Loesch DP; Shetty AC; Blackwell TW; Smith AV; Wong Q; Liu X; Conomos MP; Bobo DM; Aguet F; Albert C; Alonso A; Ardlie KG; Arking DE; Aslibekyan S; Auer PL; Barnard J; Barr RG; Barwick L; Becker LC; Beer RL; Benjamin EJ; Bielak LF; Blangero J; Boehnke M; Bowden DW; Brody JA; Burchard EG; Cade BE; Casella JF; Chalazan B; Chasman DI; Chen YDI; Cho MH; Choi SH; Chung MK; Clish CB; Correa A; Curran JE; Custer B; Darbar D; Daya M; de Andrade M; DeMeo DL; Dutcher SK; Ellinor PT; Emery LS; Eng C; Fatkin D; Fingerlin T; Forer L; Fornage M; Franceschini N; Fuchsberger C; Fullerton SM; Germer S; Gladwin MT; Gottlieb DJ; Guo X; Hall ME; He J; Heard-Costa NL; Heckbert SR; Irvin MR; Johnsen JM; Johnson AD; Kaplan R; Kardia SLR; Kelly T; Kelly S; Kenny EE; Kiel DP; Klemmer R; Konkle BA; Kooperberg C; Köttgen A; Lange LA; Lasky-Su J; Levy D; Lin X; Lin KH; Liu C; Loos RJF, 2021, 'Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program', Nature, 590, pp. 290 - 299, http://dx.doi.org/10.1038/s41586-021-03205-y

Santiago CF; Huttner IG; Fatkin D, 2021, 'Mechanisms of TTNtv-related dilated cardiomyopathy: Insights from zebrafish models', Journal of Cardiovascular Development and Disease, 8, pp. 1 - 18, http://dx.doi.org/10.3390/jcdd8020010

Guo Y; Merten AL; Schöler U; Yu ZY; Cvetkovska J; Fatkin D; Feneley MP; Martinac B; Friedrich O, 2021, 'In vitro cell stretching technology (IsoStretcher) as an approach to unravel Piezo1-mediated cardiac mechanotransduction', Progress in Biophysics and Molecular Biology, 159, pp. 22 - 33, http://dx.doi.org/10.1016/j.pbiomolbio.2020.07.003

Peters S; Johnson R; Zentner D; James P; Kalman JM; Fatkin D, 2021, 'Long-Term Efficacy and Safety of Sodium Channel Antagonists in Patients With p.R222Q SCN5A-Related Arrhythmic Dilated Cardiomyopathy', JACC: Clinical Electrophysiology, 7, pp. 126 - 128, http://dx.doi.org/10.1016/j.jacep.2020.09.023

Iismaa SE; Hesselson S; McGrath-Cadell L; Muller DW; Fatkin D; Giannoulatou E; Kovacic J; Graham RM, 2021, 'Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women', Heart Lung and Circulation, 30, pp. 27 - 35, http://dx.doi.org/10.1016/j.hlc.2020.05.110

Peters S; Thompson B; Perrin M; James P; Zentner D; Kalman J; Fatkin D, 2021, 'Arrhythmias are a Requisite Feature of SCN5A Mediated Dilated Cardiomyopathy: A Systematic Review of Variants', Heart, Lung and Circulation, 30, pp. S95 - S95, http://dx.doi.org/10.1016/j.hlc.2021.06.015

Bax M; Junday K; Hesselson S; Iismaa S; Tarr I; McGrath-Cadell L; Dunwoodie S; Fatkin D; Kovacic J; Muller D; Giannoulatou E; Graham R, 2021, 'Modelling Spontaneous Coronary Artery Dissection With iPSC-Derived Vascular Cells', Heart, Lung and Circulation, 30, pp. S131 - S131, http://dx.doi.org/10.1016/j.hlc.2021.06.089

McGrath-Cadell L; Iismaa SE; Hesselson S; Muller DW; Fatkin D; Giannoulatou E; Kovacic JC; Graham RM, 2021, 'Recent Updates on Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia', International Journal of Integrative Cardiology, 3, http://dx.doi.org/10.47275/2690-862x-121

McGrath-Cadell L; Hesselson S; Tarr I; Iismaa S; Bax M; Junday K; Dunwoodie S; Fatkin D; Kovacic J; Muller D; Giannoulatou E; Graham B, 2021, 'Spontaneous Coronary Artery Dissection (SCAD) and a Family History of Aortic Artery Dissection—A Case Series', Heart, Lung and Circulation, 30, pp. S252 - S252, http://dx.doi.org/10.1016/j.hlc.2021.06.350

Santiago C; Huttner I; Chand R; Humphreys D; Young P; Ward A; Fatkin D, 2021, 'TTNtv Carriers do not Have Increased Susceptibility to Chemotherapy-Induced Cardiomyopathy', Heart, Lung and Circulation, 30, pp. S97 - S97, http://dx.doi.org/10.1016/j.hlc.2021.06.018

Ntalla I; Weng LC; Cartwright JH; Hall AW; Sveinbjornsson G; Tucker NR; Choi SH; Chaffin MD; Roselli C; Barnes MR; Mifsud B; Warren HR; Hayward C; Marten J; Cranley JJ; Concas MP; Gasparini P; Boutin T; Kolcic I; Polasek O; Rudan I; Araujo NM; Lima-Costa MF; Ribeiro ALP; Souza RP; Tarazona-Santos E; Giedraitis V; Ingelsson E; Mahajan A; Morris AP; Del Greco M F; Foco L; Gögele M; Hicks AA; Cook JP; Lind L; Lindgren CM; Sundström J; Nelson CP; Riaz MB; Samani NJ; Sinagra G; Ulivi S; Kähönen M; Mishra PP; Mononen N; Nikus K; Caulfield MJ; Dominiczak A; Padmanabhan S; Montasser ME; O’Connell JR; Ryan K; Shuldiner AR; Aeschbacher S; Conen D; Risch L; Thériault S; Hutri-Kähönen N; Lehtimäki T; Lyytikäinen LP; Raitakari OT; Barnes CLK; Campbell H; Joshi PK; Wilson JF; Isaacs A; Kors JA; van Duijn CM; Huang PL; Gudnason V; Harris TB; Launer LJ; Smith AV; Bottinger EP; Loos RJF; Nadkarni GN; Preuss MH; Correa A; Mei H; Wilson J; Meitinger T; Müller-Nurasyid M; Peters A; Waldenberger M; Mangino M; Spector TD; Rienstra M; van de Vegte YJ; van der Harst P; Verweij N; Kääb S; Schramm K; Sinner MF; Strauch K; Cutler MJ; Fatkin D; London B; Olesen M; Roden DM, 2020, 'Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction', Nature Communications, 11, http://dx.doi.org/10.1038/s41467-020-15706-x

Carss KJ; Baranowska AA; Armisen J; Webb TR; Hamby SE; Premawardhana D; Al-Hussaini A; Wood A; Wang Q; Deevi SVV; Vitsios D; Lewis SH; Kotecha D; Bouatia-Naji N; Hesselson S; Iismaa SE; Tarr I; McGrath-Cadell L; Muller DW; Dunwoodie SL; Fatkin D; Graham RM; Giannoulatou E; Samani NJ; Petrovski S; Haefliger C; Adlam D, 2020, 'Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing', Circulation: Genomic and Precision Medicine, 13, pp. E003030, http://dx.doi.org/10.1161/CIRCGEN.120.003030

Wong GR; Nalliah CJ; Lee G; Voskoboinik A; Prabhu S; Parameswaran R; Sugumar H; Anderson RD; Ling LH; McLellan A; Johnson R; Sanders P; Kistler PM; Fatkin D; Kalman JM, 2020, 'Genetic Susceptibility to Atrial Fibrillation Is Associated With Atrial Electrical Remodeling and Adverse Post-Ablation Outcome', JACC: Clinical Electrophysiology, 6, pp. 1509 - 1521, http://dx.doi.org/10.1016/j.jacep.2020.05.031

Akhtar MM; Lorenzini M; Cicerchia M; Ochoa JP; Hey TM; Sabater Molina M; Restrepo-Cordoba MA; Dal Ferro M; Stolfo D; Johnson R; Larrañaga-Moreira JM; Robles-Mezcua A; Rodriguez-Palomares JF; Casas G; Peña-Peña ML; Lopes LR; Gallego-Delgado M; Franaszczyk M; Laucey G; Rangel-Sousa D; Basurte M; Palomino-Doza J; Villacorta E; Bilinska Z; Limeres Freire J; Garcia Pinilla JM; Barriales-Villa R; Fatkin D; Sinagra G; Garcia-Pavia P; Gimeno JR; Mogensen J; Monserrat L; Elliott PM, 2020, 'Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene', Circulation: Heart Failure, 13, pp. E006832, http://dx.doi.org/10.1161/CIRCHEARTFAILURE.119.006832

Gray B; Semsarian C; Fatkin D; Ingles J; Atherton JJ; Davis AM; Sanders P; Pachter N; Skinner JR; Stiles MK, 2020, 'Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement', Heart Lung and Circulation, 29, pp. e85 - e87, http://dx.doi.org/10.1016/j.hlc.2020.04.006

Bart NK; Thomas L; Korczyk D; Atherton JJ; Stewart GJ; Fatkin D, 2020, 'Amyloid Cardiomyopathy', Heart Lung and Circulation, 29, pp. 575 - 583, http://dx.doi.org/10.1016/j.hlc.2019.11.019

Peters S; Johnson R; Birch S; Zentner D; Hershberger RE; Fatkin D, 2020, 'Familial Dilated Cardiomyopathy', Heart Lung and Circulation, 29, pp. 566 - 574, http://dx.doi.org/10.1016/j.hlc.2019.11.018

Gladding PA; Legget M; Fatkin D; Larsen P; Doughty R, 2020, 'Polygenic Risk Scores in Coronary Artery Disease and Atrial Fibrillation', Heart Lung and Circulation, 29, pp. 634 - 640, http://dx.doi.org/10.1016/j.hlc.2019.12.004

Kessler MD; Loesch DP; Perry JA; Heard-Costa NL; Taliun D; Cade BE; Wang H; Daya M; Ziniti J; Datta S; Celedón JC; Soto-Quiros ME; Avila L; Weiss ST; Barnes K; Redline SS; Vasan RS; Johnson AD; Mathias RA; Hernandez R; Wilson JG; Nickerson DA; Abecasis G; Browning SR; Zöllner S; O'Connell JR; Mitchell BD; National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium ; TOPMed Population Genetics Working Group ; O'Connor TD, 2020, 'De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.', Proc Natl Acad Sci U S A, 117, pp. 2560 - 2569, http://dx.doi.org/10.1073/pnas.1902766117

Fatkin D; Johnson R, 2020, 'Variants of Uncertain Significance and “Missing Pathogenicity”', Journal of the American Heart Association, 9, http://dx.doi.org/10.1161/JAHA.119.015588

Santiago C; Chand R; Humphreys D; Young P; Ward A; Huttner I; Fatkin D, 2020, '002 Titin Truncation Provides a Sensitised Template for Cardio-Depressant Effects of Alcohol', Heart, Lung and Circulation, 29, pp. S37 - S38, http://dx.doi.org/10.1016/j.hlc.2020.09.009

Situ Y; Baric J; Han W; Law M; Fatkin D; Graham R, 2020, '055 Prevalence and Patient Awareness of Cardiovascular Risk Factors in a Community-Based Australian Cohort', Heart, Lung and Circulation, 29, pp. S62 - S62, http://dx.doi.org/10.1016/j.hlc.2020.09.062

Fatkin D; Huttner IG; Kovacic JC; Seidman JG; Seidman CE, 2019, 'Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review', Journal of the American College of Cardiology, 74, pp. 2921 - 2938, http://dx.doi.org/10.1016/j.jacc.2019.10.011

McGrath-Cadell L; Hesselson S; Iismaa SE; Mishra K; Wong CMY; Fatkin D; Dunwoodie SL; Harvey R; Holloway CJ; Muller DWM; Giannoulatou E; Graham RM, 2019, 'P5540Familial clustering of spontaneous coronary artery dissection', European Heart Journal, 40, http://dx.doi.org/10.1093/eurheartj/ehz746.0486

Minoche AE; Horvat C; Johnson R; Gayevskiy V; Morton SU; Drew AP; Woo K; Statham AL; Lundie B; Bagnall RD; Ingles J; Semsarian C; Seidman JG; Seidman CE; Dinger ME; Cowley MJ; Fatkin D, 2019, 'Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy', Genetics in Medicine, 21, pp. 650 - 662, http://dx.doi.org/10.1038/s41436-018-0084-7

Adlam D; Olson TM; Combaret N; Kovacic JC; Iismaa SE; Al-Hussaini A; O'Byrne MM; Bouajila S; Georges A; Mishra K; Braund PS; d'Escamard V; Huang S; Margaritis M; Nelson CP; de Andrade M; Kadian-Dodov D; Welch CA; Mazurkiewicz S; Jeunemaitre X; Motreff P; Belle L; Dupouy P; Barnay P; Meneveau N; Gilard M; Rioufol G; Range G; Brunel P; Delarche N; Filippi E; Le Bivic L; Harbaoui B; Benamer H; Cayla G; Varenne O; Manzo-Silberman SP; Silvain J; Spaulding C; Caussin C; Gerbaud E; Valy Y; Koning R; Lhermusier T; Champin S; Salengro E; Fluttaz A; Zabalawi A; Cottin Y; Teiger E; Saint-Etienne C; Ducrocq G; Marliere S; Boiffard E; Aubry P; Georges JL; Bresson D; De Poli F; Karrillon G; Roule V; Bali L; Valla M; Gerbay A; Houpe D; Dubreuil O; Monnier A; Mayaud N; Manchuelle A; Commeau P; Bedossa M; Wong CMY; Giannoulatou E; Sweeting M; Muller D; Wood A; McGrath-Cadell L; Fatkin D; Dunwoodie SL; Harvey R; Holloway C; Empana JP; Jouven X; Nikpay M; Goel A; Won HH; Hall LM; Willenborg C; Kanoni S; Saleheen D; Kyriakou T; Hopewell JC; Webb TR; Zeng L; Dehghan A; Alver M; Armasu SM; Auro K; Bjonnes A; Chasman DI; Chen S, 2019, 'Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection', Journal of the American College of Cardiology, 73, pp. 58 - 66, http://dx.doi.org/10.1016/j.jacc.2018.09.085

Horvat C; Johnson R; Lam L; Munro J; Mazzarotto F; Roberts AM; Herman DS; Parfenov M; Haghighi A; McDonough B; DePalma SR; Keogh AM; Macdonald PS; Hayward CS; Roberts A; Barton PJR; Felkin LE; Giannoulatou E; Cook SA; Seidman JG; Seidman CE; Fatkin D, 2019, 'A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy', Genetics in Medicine, 21, pp. 133 - 143, http://dx.doi.org/10.1038/s41436-018-0036-2

Peters S; Kumar S; Elliott P; Kalman JM; Fatkin D, 2019, 'Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management', Heart Lung and Circulation, 28, pp. 31 - 38, http://dx.doi.org/10.1016/j.hlc.2018.09.010

Fatkin D; Huttner IG; Johnson R, 2019, 'Genetics of atrial cardiomyopathy', Current Opinion in Cardiology, 34, pp. 275 - 281, http://dx.doi.org/10.1097/HCO.0000000000000610

McGrath-Cadell L; Hesselson S; Iismaa S; Mishra K; Wong C; Fatkin D; Dunwoodie S; Harvey R; Holloway C; Muller D; Giannoulatou E; Graham R, 2019, 'Familial Clustering of Spontaneous Coronary Artery Dissection', Heart, Lung and Circulation, 28, pp. S330 - S330, http://dx.doi.org/10.1016/j.hlc.2019.06.454

Wong G; Nalliah C; Voskoboinik A; Lee G; Prabhu S; Sugumar H; Parameswaran R; Anderson R; McLellan A; Ling L; Morton J; Johnson R; Kistler P; Fatkin D; Kalman J, 2019, 'Genetic Susceptibility to Atrial Fibrillation at the chr 4q25 Locus is Associated with Left Atrial Electrical Remodelling', Heart, Lung and Circulation, 28, pp. S132 - S132, http://dx.doi.org/10.1016/j.hlc.2019.06.003

Johnson R; Peters S; Ingles J; Correnti G; Ingrey A; Mountain H; Zentner D; Thompson T; Oates E; Ronan A; Pachter N; Haan E; Van Spaendonck-Zwarts K; Semsarian C; McGaughran J; Atherton J; James P; Fatkin D, 2019, 'Penetrance of Dilated Cardiomyopathy in Families with Truncating TTN Variants: a National Perspective', Heart, Lung and Circulation, 28, pp. S140 - S140, http://dx.doi.org/10.1016/j.hlc.2019.06.019

Burns C; Hoorntje E; Corden B; Parikh V; Thompson T; Marsili L; Gray B; Reuter C; Bagnall R; Correnti G; Duflou J; Fatkin D; Fietz M; Haan E; Lam L; Goldblatt J; McCarthy H; Pachter N; Vohra J; Whiffin N; Zentner D; Wheeler M; Ashley E; Semsarian C; Ware J; van Tintelen P; Ingles J, 2019, 'Truncating Variants in the Desmoplakin Gene Cause a Distinct Arrhythmogenic Cardiomyopathy', Heart, Lung and Circulation, 28, pp. S134 - S134, http://dx.doi.org/10.1016/j.hlc.2019.06.007

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