Items where Division is "Molecular Cardiology"

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Number of items at this level: 122.

A

Austin, Rachel and Quinn, Michael C.J. and Afoakwah, Clifford and Metke-Jimenez, Alejandro and Leroux, Hugo and Atherton, John and Brown, Jaye S. and Wornham, Linda J. and Macciocca, Ivan and de Silva, Michelle G. and Thompson, Tina and Martin, Ellenore M. and Hilton, Desiree and Devery, Sophie and Wu, Kathy H.C. and Jackson, Matilda R. and Correnti, Gemma and Overkov, Angela and Elbracht-Leong, Stefanie and Ingles, Jodie and Scuffham, Paul and Semsarian, Christopher and McGaughran, Julie Investigation of current models of care for genetic heart disease in Australia: A national clinical audit. International Journal of Cardiology (2021), 330 pp. 128-134. ISSN 01675273

Alphonse, Patricia and Virk, Sohaib and Collins, Jhonna and Campbell, Timothy and Thomas, Stuart P. and Semsarian, Christopher and Kumar, Saurabh Prognostic impact of atrial fibrillation in hypertrophic cardiomyopathy: a systematic review. [Review]

Alexander, Peta M.A. and Nugent, Alan W. and Daubeney, Piers E.F. and Lee, Katherine J. and Sleeper, Lynn A. and Schuster, Tibor and Turner, Christian and Davis, Andrew M. and Semsarian, Chris and Colan, Steven D. and Robertson, Terry and Ramsay, James and Justo, Robert and Sholler, Gary F. and King, Ingrid and Weintraub, Robert G. Long-Term Outcomes of Hypertrophic Cardiomyopathy Diagnosed During Childhood. Circulation (2018), 138 (1) pp. 29-36. ISSN 0009-7322

Ai, Tomohiko and Gray, Belinda and Gnanappa, Ganesh Kumar and Bagnall, Richard D. and Femia, Giuseppe and Yeates, Laura and Ingles, Jodie and Burns, Charlotte and Puranik, Rajesh and Grieve, Stuart M. and Semsarian, Christopher and Sy, Raymond W. Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome. PLOS ONE (2018), 13 (4) e0195594. ISSN 1932-6203

B

Butters, Alexandra and Arnott, Clare and Sweeting, Joanna and Winkel, Bo Gregers and Semsarian, Christopher and Ingles, Jodie Sex Disparities in Sudden Cardiac Death. [Review]

Bell, Katy and Doust, Jenny and McGeechan, Kevin and Horvath, Andrea R. and Barratt, Alexandra and Hayen, Andrew and Semsarian, Christopher and Irwig, Les Reply to - Understanding the impact of blood pressure guidelines and variability on hypertension diagnoses. [Editorial Material]

Butters, Alexandra and Semsarian, Caitlin R. and Bagnall, Richard D. and Yeates, Laura and Stafford, Fergus and Burns, Charlotte and Semsarian, Christopher and Ingles, Jodie Clinical Profile and Health Disparities in a Multiethnic Cohort of Patients With Hypertrophic Cardiomyopathy. Circulation: Heart Failure (2021), 14 (3) ISSN 1941-3289

Bennett, Richard and Campbell, Timothy and Eslick, Adam and Pudipeddi, Anand and Hing, Alfred and Yeates, Laura and Hanna, Bernadette and Kumar, Saurabh Ventricular Tachycardia in a Patient With Dilated Cardiomyopathy Caused by a Novel Mutation of Lamin A/C Gene: Insights From Features on Electroanatomic Mapping, Catheter Ablation and Tissue Pathology. Heart, Lung and Circulation (2021), 30 (2) pp. 310-317. ISSN 14439506

Bleakley, Lauren E. and Soh, Ming S. and Bagnall, Richard D. and Sadleir, Lynette G. and Gooley, Samuel and Semsarian, Christopher and Scheffer, Ingrid E. and Berkovic, Samuel F. and Reid, Christopher A. Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy? Frontiers in Neurology (2020), 11 ISSN 1664-2295

Balestrini, Simona and Mikati, Mohamad A. and Álvarez-García-Rovés, Reyes and Carboni, Michael and Hunanyan, Arsen S. and Kherallah, Bassil and McLean, Melissa and Prange, Lyndsey and De Grandis, Elisa and Gagliardi, Alessandra and Pisciotta, Livia and Stagnaro, Michela and Veneselli, Edvige and Campistol, Jaume and Fons, Carmen and Pias-Peleteiro, Leticia and Brashear, Allison and Miller, Charlotte and Samões, Raquel and Brankovic, Vesna and Padiath, Quasar S. and Potic, Ana and Pilch, Jacek and Vezyroglou, Aikaterini and Bye, Ann M.E. and Davis, Andrew M. and Ryan, Monique M. and Semsarian, Christopher and Hollingsworth, Georgina and Scheffer, Ingrid E. and Granata, Tiziana and Nardocci, Nardo and Ragona, Francesca and Arzimanoglou, Alexis and Panagiotakaki, Eleni and Carrilho, Inês and Zucca, Claudio and Novy, Jan and Dzieżyc, Karolina and Parowicz, Marek and Mazurkiewicz-Bełdzińska, Maria and Weckhuysen, Sarah and Pons, Roser and Groppa, Sergiu and Sinden, Daniel S. and Pitt, Geoffrey S. and Tinker, Andrew and Ashworth, Michael and Michalak, Zuzanna and Thom, Maria and Cross, J. Helen and Vavassori, Rosaria and Kaski, Juan P. and Sisodiya, Sanjay M. Cardiac phenotype in ATP1A3-related syndromes. Neurology (2020), 95 (21) e2866-e2879. ISSN 0028-3878

Blue, Gillian M. and Smith, Janine and Sholler, Gary F. and Semsarian, Christopher and Winlaw, David S. Current Practice of Genetic Testing and Counselling in Congenital Heart Disease: An Australian Perspective. [Letter]

Butters, Alexandra and Isbister, Julia C. and Medi, Caroline and Raju, Hariharan and Turner, Christian and Sy, Raymond W. and Semsarian, Christopher and Ingles, Jodie Epidemiology and clinical characteristics of atrial fibrillation in patients with inherited heart diseases. Journal of Cardiovascular Electrophysiology (2020), 31 (2) pp. 465-473. ISSN 1045-3873

Bell, Katy and Doust, Jenny and McGeechan, Kevin and Horvath, Andrea Rita and Barratt, Alexandra and Hayen, Andrew and Semsarian, Christopher and Irwig, Les The potential for overdiagnosis and underdiagnosis because of blood pressure variability: a comparison of the 2017 ACC/AHA, 2018 ESC/ESH and 2019 NICE hypertension guidelines. Journal of Hypertension (2020), 39 (2) pp. 236-242. ISSN 0263-6352

Burns, Charlotte and Yeates, Laura and Semsarian, Christopher and Ingles, Jodie Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial. BMJ Open (2019), 9 (1) e026627. ISSN 2044-6055

Bates, Kezia and Sweeting, Joanna and Yeates, Laura and McDonald, Kristie and Semsarian, Christopher and Ingles, Jodie Psychological adaptation to molecular autopsy findings following sudden cardiac death in the young. Genetics in Medicine (2019), 21 (6) pp. 1452-1456. ISSN 1098-3600

Blanch, Bianca and Lago, Luise P and Sy, Raymond and Harris, Phillip J and Semsarian, Christopher and Ingles, Jodie Implantable cardioverter–defibrillator therapy in Australia, 2002–2015. Medical Journal of Australia (2018), 209 (3) pp. 123-129. ISSN 0025-729X

Bonner, Carissa and Spinks, Catherine and Semsarian, Christopher and Barratt, Alex and Ingles, Jodie and McCaffery, Kirsten Psychosocial Impact of a Positive Gene Result for Asymptomatic Relatives at Risk of Hypertrophic Cardiomyopathy. Journal of Genetic Counseling (2018), 27 (5) pp. 1040-1048. ISSN 1059-7700

Bagnall, Richard D. and Ingles, Jodie and Dinger, Marcel E. and Cowley, Mark J. and Ross, Samantha Barratt and Minoche, André E. and Lal, Sean and Turner, Christian and Colley, Alison and Rajagopalan, Sulekha and Berman, Yemima and Ronan, Anne and Fatkin, Diane and Semsarian, Christopher Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology (2018), 72 (4) pp. 419-429. ISSN 07351097

C

Clemens, Daniel J. and Gray, Belinda and Bagnall, Richard D. and Tester, David J. and Giudicessi, John R. and Maleszewski, Joseph J. and Crotti, Lia and Schwartz, Peter J. and Matthews, Emma and Semsarian, Christopher and Behr, Elijah R. and Ackerman, Michael J. Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims. [Letter]

Clemens, Daniel J. and Gray, Belinda and Bagnall, Richard D. and Tester, David J. and Dotzler, Steven M. and Giudicessi, John R. and Matthews, Emma and Semsarian, Christopher and Behr, Elijah R. and Ackerman, Michael J. Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population. Circulation: Genomic and Precision Medicine (2020), 13 (2) ISSN 2574-8300

Clemens, Daniel J. and Gray, Belinda and Bagnall, Richard D. and Tester, David J. and Dotzler, Steven M. and Giudicessi, John R. and Matthews, Emma and Semsarian, Christopher and Behr, Elijah R. and Ackerman, Michael J. Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population. Circulation: Genomic and Precision Medicine (2020), 13 (2) ISSN 2574-8300

D

Dries, Annika M. and Kirillova, Anna and Reuter, Chloe M. and Garcia, John and Zouk, Hana and Hawley, Megan and Murray, Brittney and Tichnell, Crystal and Pilichou, Kalliopi and Protonotarios, Alexandros and Medeiros-Domingo, Argelia and Kelly, Melissa A. and Baras, Aris and Ingles, Jodie and Semsarian, Christopher and Bauce, Barbara and Celeghin, Rudy and Basso, Cristina and Jongbloed, Jan D. H. and Nussbaum, Robert L. and Funke, Birgit and Cerrone, Marina and Mestroni, Luisa and Taylor, Matthew R. G. and Sinagra, Gianfranco and Merlo, Marco and Saguner, Ardan M. and Elliott, Perry M. and Syrris, Petros and van Tintelen, J. Peter and James, Cynthia A. and Haggerty, Christopher M. and Parikh, Victoria N. The genetic architecture of Plakophilin 2 cardiomyopathy. Genetics in Medicine (2021), 23 (10) pp. 1961-1968. ISSN 1098-3600

Daniels, Matthew J. and Fusi, Luca and Semsarian, Christopher and Naidu, Srihari S. Myosin Modulation in Hypertrophic Cardiomyopathy and Systolic Heart Failure: Getting Inside the Engine. [Editorial Material]

Dennis, Mark and Elder, Alexander and Semsarian, Christopher and Orchard, John and Brouwer, Isabel and Puranik, Rajesh A 10-year review of sudden death during sporting activities. Heart Rhythm (2018), 15 (10) pp. 1477-1483. ISSN 15475271

E

Eberly, Lauren A. and Day, Sharlene M. and Ashley, Euan A. and Jacoby, Daniel L. and Jefferies, John Lynn and Colan, Steven D. and Rossano, Joseph W. and Semsarian, Christopher and Pereira, Alexandre C. and Olivotto, Iacopo and Ingles, Jodie and Seidman, Christine E. and Channaoui, Nadine and Cirino, Allison L. and Han, Larry and Ho, Carolyn Y. and Lakdawala, Neal K. Association of Race With Disease Expression and Clinical Outcomes Among Patients With Hypertrophic Cardiomyopathy. JAMA Cardiology (2020), 5 (1) p. 83. ISSN 2380-6583

F

Femia, Giuseppe and Zhu, Danyi and Choudhary, Preeti and Ross, Samantha B. and Muthurangu, Vivek and Richmond, David and Celermajer, David S. and Semsarian, Christopher and Puranik, Rajesh Long term clinical outcomes associated with CMR quantified isolated left ventricular non-compaction in adults. International Journal of Cardiology (2021), 328 pp. 235-240. ISSN 01675273

Femia, Giuseppe and Langlois, Neil and Raleigh, Jim and Gray, Belinda and Othman, Farrah and Perumal, Sunthara Rajan and Semsarian, Christopher and Puranik, Rajesh Comparison of conventional autopsy with post-mortem magnetic resonance, computed tomography in determining the cause of unexplained death. Forensic Science, Medicine and Pathology (2021), 17 (1) pp. 10-18. ISSN 1547-769X

Femia, Giuseppe and Langlois, Neil and Raleigh, Jim and Perumal, Sunthara Rajan and Semsarian, Christopher and Puranik, Rajesh Post-mortem cardiac magnetic resonance parameters in normal and diseased conditions. Cardiovascular Diagnosis and Therapy (2021), 11 (2) pp. 373-382. ISSN 22233652

Femia, Giuseppe and Semsarian, Christopher and Ross, Samantha B. and Celermajer, David and Puranik, Rajesh Left Ventricular Non-Compaction: Review of the Current Diagnostic Challenges and Consequences in Athletes. [Review]

Femia, Giuseppe and Semsarian, Christopher and Langlois, Neil and McGuire, Mark and Raleigh, James and Taylor, Andrew and Puranik, Rajesh Post-Mortem Imaging Adjudicated Sudden Death: Causes and Controversies. Heart, Lung and Circulation (2019), 28 (1) pp. 15-21. ISSN 14439506

G

Ghidoni, Alice and Elliott, Perry M. and Syrris, Petros and Calkins, Hugh and James, Cynthia A. and Judge, Daniel P. and Murray, Brittney and Barc, Julien and Probst, Vincent and Schott, Jean Jacques and Song, Jiang-Ping and Hauer, Richard N.W. and Hoorntje, Edgar T. and van Tintelen, J. Peter and Schulze-Bahr, Eric and Hamilton, Robert M. and Mittal, Kirti and Semsarian, Christopher and Behr, Elijah R. and Ackerman, Michael J. and Basso, Cristina and Parati, Gianfranco and Gentilini, Davide and Kotta, Maria-Christina and Mayosi, Bongani M. and Schwartz, Peter J. and Crotti, Lia Cadherin 2-Related Arrhythmogenic Cardiomyopathy. Circulation: Genomic and Precision Medicine (2021), 14 (2) ISSN 2574-8300

Gray, Belinda and Semsarian, Christopher Genetic Testing for Inherited Cardiovascular Disease: Implications of the AHA Scientific Statement for Cardiologists. [Editorial Material]

Gray, Belinda and Semsarian, Christopher and Fatkin, Diane and Ingles, Jodie and Atherton, John J. and Davis, Andrew M. and Sanders, Prashanthan and Pachter, Nicholas and Skinner, Jonathan R. and Stiles, Martin K. Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement. Heart, Lung and Circulation (2020), 29 (7) e85-e87. ISSN 14439506

Gray, Belinda and Semsarian, Christopher Utility of genetic testing in athletes. [Review]

Grover, Suchi and Lloyd, Rachael and Perry, Rebecca and Lou, Pey Wen and Haan, Eric and Yeates, Laura and Woodman, Richard and Atherton, John J and Semsarian, Chris and Selvanayagam, Joseph B Assessment of myocardial oxygenation, strain, and diastology in MYBPC3-related hypertrophic cardiomyopathy: a cardiovascular magnetic resonance and echocardiography study. European Heart Journal - Cardiovascular Imaging (2019), 20 (8) pp. 932-938. ISSN 2047-2404

Gray, Belinda and Ackerman, Michael J. and Semsarian, Christopher and Behr, Elijah R. Evaluation After Sudden Death in the Young. Circulation: Arrhythmia and Electrophysiology (2019), 12 (8) ISSN 1941-3149

Gray, Belinda and Semsarian, Christopher Editorial commentary: Will the real long QT genes please stand up. Trends in Cardiovascular Medicine (2018), 28 (7) pp. 465-466. ISSN 10501738

Gray, Belinda and Hasdemir, Can and Ingles, Jodie and Aiba, Takeshi and Makita, Naomasa and Probst, Vincent and Wilde, Arthur A.M. and Newbury-Ecob, Ruth and Sheppard, Mary N. and Semsarian, Christopher and Sy, Raymond W. and Behr, Elijah R. Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants. Heart Rhythm (2018), 15 (7) pp. 1051-1057. ISSN 15475271

H

Holliday, Mira and Singer, Emma S. and Ross, Samantha B. and Lim, Seakcheng and Lal, Sean and Ingles, Jodie and Semsarian, Christopher and Bagnall, Richard D. Transcriptome Sequencing of Patients With Hypertrophic Cardiomyopathy Reveals Novel Splice-Altering Variants in MYBPC3. Circulation: Genomic and Precision Medicine (2021), 14 (2) ISSN 2574-8300

Hamilton-Craig, Christian and McGavigan, Andrew and Semsarian, Chris and Martin, Andrew and Atherton, John and Stanton, Tony and La Gerche, Andre and Taylor, Andrew J. and Haqqani, Haris The Cardiac Society of Australia and New Zealand Position Statement on the Diagnosis and Management of Arrhythmogenic Right Ventricular Cardiomyopathy (2019 Update). Heart, Lung and Circulation (2020), 29 (1) pp. 40-48. ISSN 14439506

Helms, Adam S. and Thompson, Andrea D. and Glazier, Amelia A. and Hafeez, Neha and Kabani, Samat and Rodriguez, Juliani and Yob, Jaime M. and Woolcock, Helen and Mazzarotto, Francesco and Lakdawala, Neal K. and Wittekind, Samuel G. and Pereira, Alexandre C. and Jacoby, Daniel L. and Colan, Steven D. and Ashley, Euan A. and Saberi, Sara and Ware, James S. and Ingles, Jodie and Semsarian, Christopher and Michels, Michelle and Olivotto, Iacopo and Ho, Carolyn Y. and Day, Sharlene M. Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy. Circulation: Genomic and Precision Medicine (2020), 13 (5) pp. 396-405. ISSN 2574-8300

Holliday, Mira and Ross, Samantha Barratt and Lim, Seakcheng and Mangala, Melissa and Hill, Adam and Szappanos, Henrietta Cserne and Hool, Livia and Semsarian, Christopher Development of induced pluripotent stem cells from a patient with hypertrophic cardiomyopathy who carries the pathogenic myosin heavy chain 7 mutation p.Arg403Gln. Stem Cell Research (2018), 33 pp. 269-273. ISSN 18735061

Holliday, Mira and Ross, Samantha Barratt and Lim, Seakcheng and Semsarian, Christopher Generation of an induced pluripotent stem cell line from a hypertrophic cardiomyopathy patient with a pathogenic myosin binding protein C (MYBPC3) p.Arg502Trp mutation. Stem Cell Research (2018), 33 pp. 56-59. ISSN 18735061

I

Isbister, Julia C. and Sy, Raymond W. and Semsarian, Christopher Cardiac arrhythmias in epilepsy: Troublemaker, accomplice, or innocent bystander? [Editorial Material]

Isbister, Julia C. and Nowak, Natalie and Butters, Alexandra and Yeates, Laura and Gray, Belinda and Sy, Raymond W. and Ingles, Jodie and Bagnall, Richard D. and Semsarian, Christopher “Concealed cardiomyopathy” as a cause of previously unexplained sudden cardiac arrest. International Journal of Cardiology (2021), 324 pp. 96-101. ISSN 01675273

Isbister, Julia C. and Krahn, Andrew D. and Semsarian, Christopher and Sy, Raymond W. Brugada Syndrome: Clinical Care Amidst Pathophysiological Uncertainty. [Review]

Ingles, Jodie and Semsarian, Christopher Making the case for cascade screening among families with inherited heart disease. Heart Rhythm (2020), 17 (1) pp. 113-114. ISSN 15475271

Ingles, Jodie and Semsarian, Christopher Time to Rethink the Genetic Architecture of Long QT Syndrome. [Editorial Material]

Isbister, Julia and Semsarian, Christopher Cardiovascular genomics and sudden cardiac death in the young. Australian Journal of General Practice (2019), 48 (3) pp. 90-95. ISSN 2208794X

Ingles, Jodie and Goldstein, Jennifer and Thaxton, Courtney and Caleshu, Colleen and Corty, Edward W. and Crowley, Stephanie B. and Dougherty, Kristen and Harrison, Steven M. and McGlaughon, Jennifer and Milko, Laura V. and Morales, Ana and Seifert, Bryce A. and Strande, Natasha and Thomson, Kate and Peter van Tintelen, J. and Wallace, Kathleen and Walsh, Roddy and Wells, Quinn and Whiffin, Nicola and Witkowski, Leora and Semsarian, Christopher and Ware, James S. and Hershberger, Ray E. and Funke, Birgit Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes. Circulation: Genomic and Precision Medicine (2019), 12 (2) ISSN 2574-8300

Ingles, Jodie and Semsarian, Christopher Response by Ingles and Semsarian to Letter Regarding Article, “Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events”. Circulation: Genomic and Precision Medicine (2019), 12 (3) ISSN 2574-8300

Isbister, Julia and Semsarian, Christopher Sudden cardiac death: an update. Internal Medicine Journal (2019), 49 (7) pp. 826-833. ISSN 1444-0903

Ingles, Jodie and Semsarian, Christopher An Unexpected FLNC Phenotype. Mayo Clinic Proceedings (2019), 94 (5) pp. 751-753. ISSN 00256196

Ingles, Jodie and Bagnall, Richard D and Yeates, Laura and McGrady, Michele and Berman, Yemima and Whalley, David and Duflou, Johan and Semsarian, Christopher Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events. Circulation: Genomic and Precision Medicine (2018), 11 (11) ISSN 2574-8300

Ingles, Jodie and Semsarian, Christopher Family Matters. Circulation: Genomic and Precision Medicine (2018), 11 (4) ISSN 2574-8300

Ingles, Jodie and Bagnall, Richard D. and Semsarian, Christopher Genetic Testing for Cardiomyopathies in Clinical Practice. Heart Failure Clinics (2018), 14 (2) pp. 129-137. ISSN 15517136

J

Jordan, Elizabeth and Peterson, Laiken and Ai, Tomohiko and Asatryan, Babken and Bronicki, Lucas and Brown, Emily and Celeghin, Rudy and Edwards, Matthew and Fan, Judy and Ingles, Jodie and James, Cynthia A. and Jarinova, Olga and Johnson, Renee and Judge, Daniel P. and Lahrouchi, Najim and Lekanne Deprez, Ronald H. and Lumbers, R. Thomas and Mazzarotto, Francesco and Medeiros Domingo, Argelia and Miller, Rebecca L. and Morales, Ana and Murray, Brittney and Peters, Stacey and Pilichou, Kalliopi and Protonotarios, Alexandros and Semsarian, Christopher and Shah, Palak and Syrris, Petros and Thaxton, Courtney and van Tintelen, J. Peter and Walsh, Roddy and Wang, Jessica and Ware, James and Hershberger, Ray E. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Circulation (2021), 144 (1) pp. 7-19. ISSN 0009-7322

K

Kelly, Melissa A and Caleshu, Colleen and Morales, Ana and Buchan, Jillian and Wolf, Zena and Harrison, Steven M and Cook, Stuart and Dillon, Mitchell W and Garcia, John and Haverfield, Eden and Jongbloed, Jan D H and Macaya, Daniela and Manrai, Arjun and Orland, Kate and Richard, Gabriele and Spoonamore, Katherine and Thomas, Matthew and Thomson, Kate and Vincent, Lisa M and Walsh, Roddy and Watkins, Hugh and Whiffin, Nicola and Ingles, Jodie and van Tintelen, J Peter and Semsarian, Christopher and Ware, James S and Hershberger, Ray and Funke, Birgit Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel. Genetics in Medicine (2018), 20 (3) pp. 351-359. ISSN 1098-3600

L

Lim, Wei-Wen and Neo, Melissa and Thanigaimani, Shivshankar and Kuklik, Pawel and Ganesan, Anand N. and Lau, Dennis H. and Tsoutsman, Tatiana and Kalman, Jonathan M. and Semsarian, Christopher and Saint, David A. and Sanders, Prashanthan Electrophysiological and Structural Remodeling of the Atria in a Mouse Model of Troponin-I Mutation Linked Hypertrophic Cardiomyopathy: Implications for Atrial Fibrillation. International Journal of Molecular Sciences (2021), 22 (13) p. 6941. ISSN 1422-0067

Lacaze, Paul and Sebra, Robert and Riaz, Moeen and Ingles, Jodie and Tiller, Jane and Thompson, Bryony A. and James, Paul A. and Fatkin, Diane and Semsarian, Christopher and Reid, Christopher M. and Tonkin, Andrew M. and Winship, Ingrid and Schadt, Eric and McNeil, John J. Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent. NPJ Genomic Medicine (2021), 6 (1) ISSN 2056-7944

Lakdawala, Neal K. and Olivotto, Iacopo and Day, Sharlene M. and Han, Larry and Ashley, Euan A. and Michels, Michelle and Ingles, Jodie and Semsarian, Christopher and Jacoby, Daniel and Jefferies, John L. and Colan, Steven D. and Pereira, Alexandre C. and Rossano, Joseph W. and Wittekind, Sam and Ware, James S. and Saberi, Sara and Helms, Adam S. and Cirino, Allison L. and Leinwand, Leslie A. and Seidman, Christine E. and Ho, Carolyn Y. Associations Between Female Sex, Sarcomere Variants and Clinical Outcomes in Hypertrophic Cardiomyopathy. Circulation: Genomic and Precision Medicine (2020), ISSN 2574-8300

Lieve, Krystien V.V. and Dusi, Veronica and van der Werf, Christian and Bos, J. Martijn and Lane, Conor M. and Stokke, Mathis Korseberg and Roston, Thomas M. and Djupsjöbacka, Aurora and Wada, Yuko and Denjoy, Isabelle and Bundgaard, Henning and Noguer, Ferran Roses I. and Semsarian, Christopher and Robyns, Tomas and Hofman, Nynke and Tanck, Michael W. and van den Berg, Maarten P. and Kammeraad, Janneke A.E. and Krahn, Andrew D. and Clur, Sally-Ann B. and Sacher, Frederic and Till, Jan and Skinner, Jonathan R. and Tfelt-Hansen, Jacob and Probst, Vincent and Leenhardt, Antoine and Horie, Minoru and Swan, Heikki and Roberts, Jason D. and Sanatani, Shubhayan and Haugaa, Kristina H. and Schwartz, Peter J. and Ackerman, Michael J. and Wilde, Arthur A.M. Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation: Arrhythmia and Electrophysiology (2020), 13 (3) ISSN 1941-3149

M

Marston, Nicholas A and Han, Larry and Olivotto, Iacopo and Day, Sharlene M and Ashley, Euan A and Michels, Michelle and Pereira, Alexandre C and Ingles, Jodie and Semsarian, Christopher and Jacoby, Daniel and Colan, Steven D and Rossano, Joseph W and Wittekind, Samuel G and Ware, James S and Saberi, Sara and Helms, Adam S and Ho, Carolyn Y Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathy. European Heart Journal (2021), 42 (20) pp. 1988-1996. ISSN 0195-668X

Mattivi, Connor L. and Bos, J. Martijn and Bagnall, Richard D. and Nowak, Natalie and Giudicessi, John R. and Ommen, Steve R. and Semsarian, Christopher and Ackerman, Michael J. Clinical Utility of a Phenotype-Enhanced MYH7 -Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic Testing. Circulation: Genomic and Precision Medicine (2020), 13 (5) pp. 453-459. ISSN 2574-8300

Marstrand, Peter and Han, Larry and Day, Sharlene M. and Olivotto, Iacopo and Ashley, Euan A. and Michels, Michelle and Pereira, Alexandre C. and Wittekind, Samuel G. and Helms, Adam and Saberi, Sara and Jacoby, Daniel and Ware, James S. and Colan, Steven D. and Semsarian, Christopher and Ingles, Jodie and Lakdawala, Neal K. and Ho, Carolyn Y. Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction. Circulation (2020), 141 (17) pp. 1371-1383. ISSN 0009-7322

McDonald, Kristie and Sharpe, Louise and Yeates, Laura and Semsarian, Christopher and Ingles, Jodie Needs analysis of parents following sudden cardiac death in the young. Open Heart (2020), 7 (2) e001120. ISSN 2053-3624

Moonen, Avalon and Lal, Sean and Ingles, Jodie and Yeates, Laura and Semsarian, Chris and Puranik, Raj Prevalence of Anderson-Fabry disease in a cohort with unexplained late gadolinium enhancement on cardiac MRI. International Journal of Cardiology (2020), 304 pp. 122-124. ISSN 01675273

Miron, Anastasia and Lafreniere-Roula, Myriam and Steve Fan, Chun-Po and Armstrong, Katey R. and Dragulescu, Andreea and Papaz, Tanya and Manlhiot, Cedric and Kaufman, Beth and Butts, Ryan J. and Gardin, Letizia and Stephenson, Elizabeth A. and Howard, Taylor S. and Aziz, Pete F. and Balaji, Seshadri and Ladouceur, Virginie Beauséjour and Benson, Lee N. and Colan, Steven D. and Godown, Justin and Henderson, Heather T. and Ingles, Jodie and Jeewa, Aamir and Jefferies, John L. and Lal, Ashwin K. and Mathew, Jacob and Jean-St-Michel, Emilie and Michels, Michelle and Nakano, Stephanie J. and Olivotto, Iacopo and Parent, John J. and Pereira, Alexandre C. and Semsarian, Christopher and Whitehill, Robert D. and Wittekind, Samuel G. and Russell, Mark W. and Conway, Jennifer and Richmond, Marc E. and Villa, Chet and Weintraub, Robert G. and Rossano, Joseph W. and Kantor, Paul F. and Ho, Carolyn Y. and Mital, Seema A Validated Model for Sudden Cardiac Death Risk Prediction in Pediatric Hypertrophic Cardiomyopathy. Circulation (2020), 142 (3) pp. 217-229. ISSN 0009-7322

Maurizi, Niccolò and Michels, Michelle and Rowin, Ethan J. and Semsarian, Christopher and Girolami, Francesca and Tomberli, Benedetta and Cecchi, Franco and Maron, Martin S. and Olivotto, Iacopo and Maron, Barry J. Clinical Course and Significance of Hypertrophic Cardiomyopathy Without Left Ventricular Hypertrophy. Circulation (2019), 139 (6) pp. 830-833. ISSN 0009-7322

Minoche, Andre E. and Horvat, Claire and Johnson, Renee and Gayevskiy, Velimir and Morton, Sarah U. and Drew, Alexander P. and Woo, Kerhan and Statham, Aaron L. and Lundie, Ben and Bagnall, Richard D. and Ingles, Jodie and Semsarian, Christopher and Seidman, J. G. and Seidman, Christine E. and Dinger, Marcel E. and Cowley, Mark J. and Fatkin, Diane Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy. Genetics in Medicine (2019), 21 (3) pp. 650-662. ISSN 1098-3600

Minoche, Andre E. and Horvat, Claire and Johnson, Renee and Gayevskiy, Velimir and Morton, Sarah U. and Drew, Alexander P. and Woo, Kerhan and Statham, Aaron L. and Lundie, Ben and Bagnall, Richard D. and Ingles, Jodie and Semsarian, Christopher and Seidman, J. G. and Seidman, Christine E. and Dinger, Marcel E. and Cowley, Mark J. and Fatkin, Diane Response to Brodehl et al. Genetics in Medicine (2019), 21 (5) pp. 1248-1249. ISSN 1098-3600

Moore, Benjamin and Semsarian, Christopher and Chan, Kim H. and Sy, Raymond W. Sudden Cardiac Death and Ventricular Arrhythmias in Hypertrophic Cardiomyopathy. Heart, Lung and Circulation (2019), 28 (1) pp. 146-154. ISSN 14439506

Maron, Barry J. and Casey, Susan A. and Olivotto, Iacopo and Sherrid, Mark V. and Semsarian, Christopher and Autore, Camillo and Ahmed, Aisha and Boriani, Giuseppe and Francia, Pietro and Winters, Stephen L. and Giudici, Michael and Koulova, Anna and Garberich, Ross and Rowin, Ethan J. and Sears, Samuel F. and Maron, Martin S. and Spirito, Paolo Clinical Course and Quality of Life in High-Risk Patients With Hypertrophic Cardiomyopathy and Implantable Cardioverter-Defibrillators. Circulation: Arrhythmia and Electrophysiology (2018), 11 (4) ISSN 1941-3149

N

Ng, Kevin and Titus, Erron W. and Lieve, Krystien V. and Roston, Thomas M. and Mazzanti, Andrea and Deiter, Frederick H. and Denjoy, Isabelle and Ingles, Jodie and Till, Jan and Robyns, Tomas and Connors, Sean P. and Steinberg, Christian and Abrams, Dominic J. and Pang, Benjamin and Scheinman, Melvin M. and Bos, J. Martijn and Duffett, Stephen A. and van der Werf, Christian and Maltret, Alice and Green, Martin S. and Rutberg, Julie and Balaji, Seshadri and Cadrin-Tourigny, Julia and Orland, Kate M. and Knight, Linda M. and Brateng, Caitlin and Wu, Jeremy and Tang, Anthony S. and Skanes, Allan C. and Manlucu, Jaimie and Healey, Jeff S. and January, Craig T. and Krahn, Andrew D. and Collins, Kathryn K. and Maginot, Kathleen R. and Fischbach, Peter and Etheridge, Susan P. and Eckhardt, Lee L. and Hamilton, Robert M. and Ackerman, Michael J. and Noguer, Ferran Rosés I. and Semsarian, Christopher and Jura, Natalia and Leenhardt, Antoine and Gollob, Michael H. and Priori, Silvia G. and Sanatani, Shubhayan and Wilde, Arthur A.M. and Deo, Rahul C. and Roberts, Jason D. An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2 -Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation (2020), 142 (10) pp. 932-947. ISSN 0009-7322

Nalliah, Chrishan J and Mahajan, Rajiv and Elliott, Adrian D and Haqqani, Haris and Lau, Dennis H and Vohra, Jitendra K and Morton, Joseph B and Semsarian, Christopher and Marwick, Thomas and Kalman, Jonathan M and Sanders, Prashanthan Mitral valve prolapse and sudden cardiac death: a systematic review and meta-analysis. Heart (2018), 105 (2) pp. 144-151. ISSN 1355-6037

O

Orchard, Jessica J. and Orchard, John W. and Raju, Hariharan and La Gerche, Andre and Puranik, Rajesh and Semsarian, Chris Comparison between a 6‑lead smartphone ECG and 12‑lead ECG in athletes. Journal of Electrocardiology (2021), 66 pp. 95-97. ISSN 00220736

Orchard, Jessica J. and Orchard, John W. and La Gerche, Andre and Kountouris, Alex and Raju, Hariharan and Young, Mark and Puranik, Rajesh and Semsarian, Chris Audit of a cardiac screening policy for elite Australian cricketers. Journal of Science and Medicine in Sport (2020), 23 (6) pp. 541-547. ISSN 14402440

Orchard, Jessica J and Orchard, John W and La Gerche, Andre and Semsarian, Christopher Cardiac screening of athletes: consensus needed for clinicians on indications for follow-up echocardiography testing. [Editorial Material]

Orchard, Jessica J. and Neubeck, Lis and Orchard, John W. and Puranik, Rajesh and Raju, Hariharan and Freedman, Ben and La Gerche, Andre and Semsarian, Christopher ECG-based cardiac screening programs: Legal, ethical, and logistical considerations. Heart Rhythm (2019), 16 (10) pp. 1584-1591. ISSN 15475271

Oomen, Ad W.G.J. and Semsarian, Christopher and Puranik, Rajesh and Sy, Raymond W. Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy: Progress and Pitfalls. Heart, Lung and Circulation (2018), 27 (11) pp. 1310-1317. ISSN 14439506

Orchard, Jessica J and Orchard, John W and La Gerche, Andre and Raju, Hariharan and Semsarian, Christopher Misclassification of cricket in the American College of Cardiology (ACC) Task Force classification of sports. [Editorial Material]

P

Paratz, Elizabeth D. and Smith, Karen and Ball, Jocasta and van Heusden, Alexander and Zentner, Dominica and Parsons, Sarah and Morgan, Natalie and Thompson, Tina and James, Paul and Pflaumer, Andreas and Semsarian, Christopher and Stub, Dion and Liew, Danny and La Gerche, Andre The economic impact of sudden cardiac arrest. Resuscitation (2021), 163 pp. 49-56. ISSN 03009572

Paratz, Elizabeth D. and Rowsell, Luke and van Heusden, Alexander and Zentner, Dominica and Parsons, Sarah and Morgan, Natalie and Thompson, Tina and James, Paul and Pflaumer, Andreas and Semsarian, Christopher and Ingles, Jodie and Case, Rosalind and Ball, Jocasta and Smith, Karen and Stub, Dion and La Gerche, Andre The End Unexplained Cardiac Death (EndUCD) Registry for Young Australian Sudden Cardiac Arrest. Heart, Lung and Circulation (2021), 30 (5) pp. 714-720. ISSN 14439506

Paratz, Elizabeth D. and Costello, Ben and Rowsell, Luke and Morgan, Natalie and Smith, Karen and Thompson, Tina and Semsarian, Chris and Pflaumer, Andreas and James, Paul and Stub, Dion and La Gerche, André and Zentner, Dominica and Parsons, Sarah Can post-mortem coronary artery calcium scores aid diagnosis in young sudden death? Forensic Science, Medicine and Pathology (2020), ISSN 1547-769X

Paratz, Elizabeth Davida and Rowsell, Luke and Zentner, Dominica and Parsons, Sarah and Morgan, Natalie and Thompson, Tina and James, Paul and Pflaumer, Andreas and Semsarian, Christopher and Smith, Karen and Stub, Dion and La Gerche, Andre Cardiac arrest and sudden cardiac death registries: a systematic review of global coverage. [Review]

Paratz, Elizabeth and Semsarian, Christopher and La Gerche, Andre Mind the gap: Knowledge deficits in evaluating young sudden cardiac death. [Review]

Papoutsidakis, Nikolaos and Heitner, Stephen and Ingles, Jodie and Semsarian, Christopher and Mannello, Meghan and Salberg, Lisa and Waldman, Cynthia and Vaccaro, Benjamin and Maurizi, Niccolo and Olivotto, Iacopo and Jacoby, Daniel Participation in thrill-seeking activities by patients with hypertrophic cardiomyopathy: Individual preferences, adverse events and physician attitude. American Heart Journal (2019), 214 pp. 28-35. ISSN 00028703

R

Repetti, Giuliana G. and Kim, Yuri and Pereira, Alexandre C. and Ingles, Jodie and Russell, Mark W. and Lakdawala, Neal K. and Ho, Carolyn Y. and Day, Sharlene and Semsarian, Christopher and McDonough, Barbara and DePalma, Steven R. and Quiat, Daniel and Green, Eric M. and Seidman, Christine E. and Seidman, J. G. Discordant clinical features of identical hypertrophic cardiomyopathy twins. Proceedings of the National Academy of Sciences (2021), 118 (10) e2021717118. ISSN 0027-8424

Ross, Samantha Barratt and Singer, Emma S. and Driscoll, Elizabeth and Nowak, Natalie and Yeates, Laura and Puranik, Rajesh and Sy, Raymond W. and Rajagopalan, Sulekha and Barratt, Alexandra and Ingles, Jodie and Bagnall, Richard D. and Semsarian, Christopher Genetic architecture of left ventricular noncompaction in adults. Human Genome Variation (2020), 7 (1) ISSN 2054-345X

Ross, Samantha and Holliday, Mira and Lim, Seakcheng and Semsarian, Christopher Characterization of the first induced pluripotent stem cell line generated from a patient with autosomal dominant catecholaminergic polymorphic ventricular tachycardia due to a heterozygous mutation in cardiac calsequestrin-2. Stem Cell Research (2019), 37 p. 101450. ISSN 18735061

Ross, Samantha B and McGeechan, Kevin and Barratt, Alexandra and Semsarian, Christopher Overdiagnosis of left ventricular non-compaction in adults: the data tells the story. European Heart Journal (2019), 40 (38) p. 3206. ISSN 0195-668X

Ross, Samantha Barratt and Semsarian, Christopher Clinical and Genetic Complexities of Left Ventricular Noncompaction. JAMA Cardiology (2018), 3 (11) p. 1033. ISSN 2380-6583

Ross, Samantha Barratt and Fraser, Stuart T. and Semsarian, Christopher Induced pluripotent stem cell technology and inherited arrhythmia syndromes. Heart Rhythm (2018), 15 (1) pp. 137-144. ISSN 15475271

Richardson, Ebony and Spinks, Catherine and Davis, Andrew and Turner, Christian and Atherton, John and McGaughran, Julie and Semsarian, Christopher and Ingles, Jodie Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood. Journal of Genetic Counseling (2018), 27 (3) pp. 549-557. ISSN 1059-7700

S

Stiles, Martin K. and Wilde, Arthur A. M. and Abrams, Dominic J. and Ackerman, Michael J. and Albert, Christine M. and Behr, Elijah R. and Chugh, Sumeet S. and Cornel, Martina C. and Gardner, Karen and Ingles, Jodie and James, Cynthia A. and Juang, Jyh‐Ming Jimmy and Kääb, Stefan and Kaufman, Elizabeth S. and Krahn, Andrew D. and Lubitz, Steven A. and MacLeod, Heather and Morillo, Carlos A. and Nademanee, Koonlawee and Probst, Vincent and Saarel, Elizabeth V. and Sacilotto, Luciana and Semsarian, Christopher and Sheppard, Mary N. and Shimizu, Wataru and Skinner, Jonathan R. and Tfelt‐Hansen, Jacob and Wang, Dao Wu 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families. Journal of Arrhythmia (2021), ISSN 1880-4276

Stiles, Martin K. and Wilde, Arthur A.M. and Abrams, Dominic J. and Ackerman, Michael J. and Albert, Christine M. and Behr, Elijah R. and Chugh, Sumeet S. and Cornel, Martina C. and Gardner, Karen and Ingles, Jodie and James, Cynthia A. and Jimmy Juang, Jyh-Ming and Kääb, Stefan and Kaufman, Elizabeth S. and Krahn, Andrew D. and Lubitz, Steven A. and MacLeod, Heather and Morillo, Carlos A. and Nademanee, Koonlawee and Probst, Vincent and Saarel, Elizabeth V. and Sacilotto, Luciana and Semsarian, Christopher and Sheppard, Mary N. and Shimizu, Wataru and Skinner, Jonathan R. and Tfelt-Hansen, Jacob and Wang, Dao Wu 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families. Heart Rhythm (2021), 18 (1) e1-e50. ISSN 15475271

Soh, Ming S. and Bagnall, Richard D. and Bennett, Mark F. and Bleakley, Lauren E. and Mohamed Syazwan, Erlina S. and Marie Phillips, A. and Chiam, Mathew D. F. and McKenzie, Chaseley E. and Hildebrand, Michael and Crompton, Douglas and Bahlo, Melanie and Semsarian, Christopher and Scheffer, Ingrid E. and Berkovic, Samuel F. and Reid, Christopher A. Loss‐of‐function variants in K v 11.1 cardiac channels as a biomarker for SUDEP. Annals of Clinical and Translational Neurology (2021), ISSN 2328-9503

Semsarian, Christopher and Ingles, Jodie and Ross, Samantha Barratt and Dunwoodie, Sally L. and Bagnall, Richard D. and Kovacic, Jason C. Precision Medicine in Cardiovascular Disease: Genetics and Impact on Phenotypes. Journal of the American College of Cardiology (2021), 77 (20) pp. 2517-2530. ISSN 07351097

Semsarian, Christopher and Davis, Lindsay The Wait is Over: The 2020 American Heart Association/American College of Cardiology (AHA/ACC) Hypertrophic Cardiomyopathy Guidelines Have Arrived. [Editorial Material]

Singer, Emma S. and Ross, Samantha B. and Skinner, Jon R. and Weintraub, Robert G. and Ingles, Jodie and Semsarian, Christopher and Bagnall, Richard D. Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death. Genetics in Medicine (2020), ISSN 1098-3600

Skinner, Jonathan R. and Atherton, John J. and Semsarian, Christopher Genetic Cardiovascular Conditions – It's All About Family. [Editorial Material]

Semsarian, Christopher and Semsarian, Caitlin R. Variable Penetrance in Hypertrophic Cardiomyopathy: In Search of the Holy Grail. [Editorial Material]

Semsarian, Christopher and Orchard, Jessica and Gray, Belinda and Orchard, John When do athletes benefit from cardiac genetic testing? [Editorial Material]

Semsarian, Christopher Genome sequencing for sale on the NHS. BMJ (2019), l789. ISSN 0959-8138

Singer, Emma S. and Ingles, Jodie and Semsarian, Christopher and Bagnall, Richard D. Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic Cardiomyopathy. Circulation: Genomic and Precision Medicine (2019), 12 (1) ISSN 2574-8300

Semsarian, Christopher and Ingles, Jodie and Bagnall, Richard D. Revisiting Genome Sequencing Data in Light of Novel Disease Gene Associations. Journal of the American College of Cardiology (2019), 73 (11) pp. 1365-1366. ISSN 07351097

Semsarian, Christopher and Ho, Carolyn Y Screening children at risk for hypertrophic cardiomyopathy: balancing benefits and harms. European Heart Journal (2019), ISSN 0195-668X

Semsarian, Christopher and Ho, Carolyn Y Screening children at risk for hypertrophic cardiomyopathy: balancing benefits and harms. European Heart Journal (2019), ISSN 0195-668X

Semsarian, Christopher and Barratt, Alexandra and McGeechan, Kevin and Puranik, Rajesh and Blanch, Bianca and Jones, Katherine and Ross, Samantha B A systematic review and meta-analysis of the prevalence of left ventricular non-compaction in adults. [Review]

Sweeting, Joanna and Ingles, Jodie and Ball, Kylie and Semsarian, Christopher A Control Theory-Based Pilot Intervention to Increase Physical Activity in Patients With Hypertrophic Cardiomyopathy. The American Journal of Cardiology (2018), 122 (5) pp. 866-871. ISSN 00029149

Sweeting, Joanna and Ingles, Jodie and Ball, Kylie and Semsarian, Christopher Daily Step Count as a Simple Marker of Disease Severity in Hypertrophic Cardiomyopathy. Heart, Lung and Circulation (2018), 27 (6) pp. 752-755. ISSN 14439506

Sweeting, Joanna and Semsarian, Christopher Sudden Cardiac Death in Athletes. Heart, Lung and Circulation (2018), 27 (9) pp. 1072-1077. ISSN 14439506

Semsarian, Christopher Update on the Diagnosis and Management of Hypertrophic Cardiomyopathy. Heart, Lung and Circulation (2018), 27 (3) pp. 276-279. ISSN 14439506

T

Thompson, Andrea D. and Helms, Adam S. and Kannan, Anamika and Yob, Jaime and Lakdawala, Neal K. and Wittekind, Samuel G. and Pereira, Alexandre C. and Jacoby, Daniel L. and Colan, Steven D. and Ashley, Euan A. and Saberi, Sara and Ware, James S. and Ingles, Jodie and Semsarian, Christopher and Michels, Michelle and Mazzarotto, Francesco and Olivotto, Iacopo and Ho, Carolyn Y. and Day, Sharlene M. Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation. Genetics in Medicine (2021), ISSN 1098-3600

Towbin, Jeffrey A. and McKenna, William J. and Abrams, Dominic J. and Ackerman, Michael J. and Calkins, Hugh and Darrieux, Francisco C.C. and Daubert, James P. and de Chillou, Christian and DePasquale, Eugene C. and Desai, Milind Y. and Estes, N.A. Mark and Hua, Wei and Indik, Julia H. and Ingles, Jodie and James, Cynthia A. and John, Roy M. and Judge, Daniel P. and Keegan, Roberto and Krahn, Andrew D. and Link, Mark S. and Marcus, Frank I. and McLeod, Christopher J. and Mestroni, Luisa and Priori, Silvia G. and Saffitz, Jeffrey E. and Sanatani, Shubhayan and Shimizu, Wataru and van Tintelen, J. Peter and Wilde, Arthur A.M. and Zareba, Wojciech 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary. Heart Rhythm (2019), 16 (11) e373-e407. ISSN 15475271

Tester, David J. and Wong, Leonie C.H. and Chanana, Pritha and Gray, Belinda and Jaye, Amie and Evans, Jared M. and Evans, Margaret and Fleming, Peter and Jeffrey, Iona and Cohen, Marta and Tfelt-Hansen, Jacob and Simpson, Michael A. and Behr, Elijah R. and Ackerman, Michael J. Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome. The Journal of Pediatrics (2018), 203 423-428.e11. ISSN 00223476

V

van der Werf, Christian and Lieve, Krystien V and Bos, J Martijn and Lane, Conor M and Denjoy, Isabelle and Roses-Noguer, Ferran and Aiba, Takeshi and Wada, Yuko and Ingles, Jodie and Leren, Ida S and Rudic, Boris and Schwartz, Peter J and Maltret, Alice and Sacher, Frederic and Skinner, Jonathan R and Krahn, Andrew D and Roston, Thomas M and Tfelt-Hansen, Jacob and Swan, Heikki and Robyns, Tomas and Ohno, Seiko and Roberts, Jason D and van den Berg, Maarten P and Kammeraad, Janneke A and Probst, Vincent and Kannankeril, Prince J and Blom, Nico A and Behr, Elijah R and Borggrefe, Martin and Haugaa, Kristina H and Semsarian, Christopher and Horie, Minoru and Shimizu, Wataru and Till, Janice A and Leenhardt, Antoine and Ackerman, Michael J and Wilde, Arthur A Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest. European Heart Journal (2019), 40 (35) pp. 2953-2961. ISSN 0195-668X

W

Wong, Eugene K. and Bartels, Kirsten and Hathaway, Julie and Burns, Charlotte and Yeates, Laura and Semsarian, Christopher and Krahn, Andrew D. and Virani, Alice and Ingles, Jodie Perceptions of genetic variant reclassification in patients with inherited cardiac disease. European Journal of Human Genetics (2019), 27 (7) pp. 1134-1142. ISSN 1018-4813

Wong, Nathan and Cheung, Helena and Solly, Emma and Vanags, Laura and Ritchie, William and Nicholls, Stephen and Ng, Martin and Bursill, Christina and Tan, Joanne Exploring the Roles of CREBRF and TRIM2 in the Regulation of Angiogenesis by High-Density Lipoproteins. International Journal of Molecular Sciences (2018), 19 (7) p. 1903. ISSN 1422-0067

Y

Yeates, Laura and McDonald, Kristie and Burns, Charlotte and Semsarian, Christopher and Carter, Stacy and Ingles, Jodie Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study. European Journal of Human Genetics (2021), ISSN 1018-4813

Yeates, Laura and Ingles, Jodie and Gray, Belinda and Singarayar, Suresh and Sy, Raymond W. and Semsarian, Christopher and Bagnall, Richard D. A balanced translocation disrupting SCN5A in a family with Brugada syndrome and sudden cardiac death. Heart Rhythm (2019), 16 (2) pp. 231-238. ISSN 15475271

Z

Zhang, Xiaolei and Walsh, Roddy and Whiffin, Nicola and Buchan, Rachel and Midwinter, William and Wilk, Alicja and Govind, Risha and Li, Nicholas and Ahmad, Mian and Mazzarotto, Francesco and Roberts, Angharad and Theotokis, Pantazis I. and Mazaika, Erica and Allouba, Mona and de Marvao, Antonio and Pua, Chee Jian and Day, Sharlene M. and Ashley, Euan and Colan, Steven D. and Michels, Michelle and Pereira, Alexandre C. and Jacoby, Daniel and Ho, Carolyn Y. and Olivotto, Iacopo and Gunnarsson, Gunnar T. and Jefferies, John L. and Semsarian, Chris and Ingles, Jodie and O’Regan, Declan P. and Aguib, Yasmine and Yacoub, Magdi H. and Cook, Stuart A. and Barton, Paul J. R. and Bottolo, Leonardo and Ware, James S. Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions. Genetics in Medicine (2020), ISSN 1098-3600

This list was generated on Sun Oct 24 03:45:53 2021 UTC.