Research Output per year
Research Output 1991 2019
- 1 - 50 out of 655 results
- Title (ascending)
39
Citations
(Scopus)
2017 AHA/ACC/HRS guideline for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society
Al-Khatib, S. M., Stevenson, W. G., Ackerman, M. J., Bryant, W. J., Callans, D. J., Curtis, A. B., Deal, B. J., Dickfeld, T., Field, M. E., Fonarow, G. C., Gillis, A. M., Granger, C. B., Hammill, S. C., Hlatky, M. A., Joglar, J. A., Kay, G. N., Matlock, D. D., Myerburg, R. J. & Page, R. L., Oct 1 2018, In : Heart Rhythm. 15, 10, p. e73-e189Research output: Contribution to journal › Article
Sudden Cardiac Death
Advisory Committees
Practice Guidelines
Cardiac Arrhythmias
Guidelines
92
Citations
(Scopus)
2017 AHA/ACC/HRS guideline for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Executive summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society
Al-Khatib, S. M., Stevenson, W. G., Ackerman, M. J., Bryant, W. J., Callans, D. J., Curtis, A. B., Deal, B. J., Dickfeld, T., Field, M. E., Fonarow, G. C., Gillis, A. M., Granger, C. B., Hammill, S. C., Hlatky, M. A., Joglar, J. A., Kay, G. N., Matlock, D. D., Myerburg, R. J. & Page, R. L., Oct 1 2018, In : Heart Rhythm. 15, 10, p. e190-e252Research output: Contribution to journal › Article
Sudden Cardiac Death
Advisory Committees
Practice Guidelines
Cardiac Arrhythmias
Guidelines
60
Citations
(Scopus)
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death
Al-Khatib, S. M., Stevenson, W. G., Ackerman, M. J., Bryant, W. J., Callans, D. J., Curtis, A. B., Deal, B. J., Dickfeld, T., Field, M. E., Fonarow, G. C., Gillis, A. M., Granger, C. B., Hammill, S. C., Hlatky, M. A., Joglar, J. A., Kay, G. N., Matlock, D. D., Myerburg, R. J. & Page, R. L., Sep 25 2018, In : Circulation. 138, 13, p. e272-e391Research output: Contribution to journal › Article
Cardiac Electrophysiology
Torsades de Pointes
Ambulatory Monitoring
Cardiac Resynchronization Therapy
Ventricular Premature Complexes
47
Citations
(Scopus)
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society
Al-Khatib, S. M., Stevenson, W. G., Ackerman, M. J., Bryant, W. J., Callans, D. J., Curtis, A. B., Deal, B. J., Dickfeld, T., Field, M. E., Fonarow, G. C., Gillis, A. M., Granger, C. B., Hammill, S. C., Hlatky, M. A., Joglar, J. A., Kay, G. N., Matlock, D. D., Myerburg, R. J. & Page, R. L., Oct 2 2018, In : Journal of the American College of Cardiology. 72, 14, p. 1677-1749 73 p.Research output: Contribution to journal › Article
Cardiac Electrophysiology
Torsades de Pointes
Ambulatory Monitoring
Cardiac Resynchronization Therapy
Ventricular Premature Complexes
86
Citations
(Scopus)
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society
Al-Khatib, S. M., Stevenson, W. G., Ackerman, M. J., Bryant, W. J., Callans, D. J., Curtis, A. B., Deal, B. J., Dickfeld, T., Field, M. E., Fonarow, G. C., Gillis, A. M., Granger, C. B., Hammill, S. C., Hlatky, M. A., Joglar, J. A., Kay, G. N., Matlock, D. D., Myerburg, R. J. & Page, R. L., Oct 2 2018, In : Journal of the American College of Cardiology. 72, 14, p. e91-e220Research output: Contribution to journal › Article
Cardiac Electrophysiology
Torsades de Pointes
Ambulatory Monitoring
Cardiac Resynchronization Therapy
Ventricular Premature Complexes
48
Citations
(Scopus)
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: Executive Summary
Al-Khatib, S. M., Stevenson, W. G., Ackerman, M. J., Bryant, W. J., Callans, D. J., Curtis, A. B., Deal, B. J., Dickfeld, T., Field, M. E., Fonarow, G. C., Gillis, A. M., Granger, C. B., Hammill, S. C., Hlatky, M. A., Joglar, J. A., Kay, G. N., Matlock, D. D., Myerburg, R. J. & Page, R. L., Sep 25 2018, In : Circulation. 138, 13, p. e210-e271Research output: Contribution to journal › Article
Cardiac Electrophysiology
Torsades de Pointes
Ambulatory Monitoring
Cardiac Resynchronization Therapy
Ventricular Premature Complexes
9
Citations
(Scopus)
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy
Towbin, J. A., McKenna, W. J., Abrams, D. J., Ackerman, M. J., Calkins, H., Darrieux, F. C. C., Daubert, J. P., de Chillou, C., DePasquale, E. C., Desai, M. Y., Estes, N. A. M., Hua, W., Indik, J. H., Ingles, J., James, C. A., John, R. M., Judge, D. P., Keegan, R., Krahn, A. D., Link, M. S. & 10 others, , Nov 2019, In : Heart rhythm. 16, 11, p. e301-e372Research output: Contribution to journal › Article
Open Access
Risk Management
Cardiomyopathies
Arrhythmogenic Right Ventricular Dysplasia
Cardiac Arrhythmias
Heart Valve Diseases
2
Citations
(Scopus)
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary
Towbin, J. A., McKenna, W. J., Abrams, D. J., Ackerman, M. J., Calkins, H., Darrieux, F. C. C., Daubert, J. P., de Chillou, C., DePasquale, E. C., Desai, M. Y., Estes, N. A. M., Hua, W., Indik, J. H., Ingles, J., James, C. A., John, R. M., Judge, D. P., Keegan, R., Krahn, A. D., Link, M. S. & 10 others, , Nov 2019, In : Heart rhythm. 16, 11, p. e373-e407Research output: Contribution to journal › Article
Open Access
Risk Management
Cardiomyopathies
Arrhythmogenic Right Ventricular Dysplasia
Cardiac Arrhythmias
Heart Valve Diseases
99
Citations
(Scopus)
Abnormal electrocardiographic findings in athletes: Recognising changes suggestive of cardiomyopathy
Drezner, J. A., Ashley, E., Baggish, A. L., Börjesson, M., Corrado, D., Owens, D. S., Patel, A., Pelliccia, A., Vetter, V. L., Ackerman, M. J., Anderson, J., Asplund, C. A., Cannon, B. C., DiFiori, J., Fischbach, P., Froelicher, V., Harmon, K. G., Heidbuchel, H., Marek, J., Paul, S. & 6 others, , Feb 2013, In : British Journal of Sports Medicine. 47, 3, p. 137-152 16 p.Research output: Contribution to journal › Article
Cardiomyopathies
Athletes
Electrocardiography
Sudden Cardiac Death
Sports Medicine
85
Citations
(Scopus)
Abnormal electrocardiographic findings in athletes: Recognising changes suggestive of primary electrical disease
Drezner, J. A., Ackerman, M. J., Cannon, B. C., Corrado, D., Heidbuchel, H., Prutkin, J. M., Salerno, J. C., Anderson, J., Ashley, E., Asplund, C. A., Baggish, A. L., Börjesson, M., DiFiori, J. P., Fischbach, P., Froelicher, V., Harmon, K. G., Marek, J., Owens, D. S., Paul, S., Pelliccia, A. & 5 others, , Feb 2013, In : British Journal of Sports Medicine. 47, 3, p. 153-167 15 p.Research output: Contribution to journal › Article
Athletes
Electrocardiography
Sudden Cardiac Death
Channelopathies
Sports Medicine
21
Citations
(Scopus)
A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesis
Hennessey, J. A., Boczek, N. J., Jiang, Y. H., Miller, J. D., Patrick, W., Pfeiffer, R., Sutphin, B. S., Tester, D. J., Barajas-Martinez, H., Ackerman, M. J., Antzelevitch, C., Kanter, R. & Pitt, G. S., 2014, In : PLoS One. 9, 9, e106982.Research output: Contribution to journal › Article
Cardiac Arrhythmias
inactivation
Genes
arrhythmia
Long QT Syndrome
11
Citations
(Scopus)
A case for inclusion of genetic counselors in cardiac care
Arscott, P., Caleshu, C., Kotzer, K., Kreykes, S., Kruisselbrink, T., Orland, K., Rigelsky, C., Smith, E., Spoonamore, K., Haidle, J. L., Marvin, M., Ackerman, M. J., Hadi, A., Mani, A., Ommen, S. & Cherny, S., 2016, In : Cardiology in Review. 24, 2, p. 49-55 7 p.Research output: Contribution to journal › Article
Genetic Testing
Cardiology
Heart Diseases
Delivery of Health Care
Costs and Cost Analysis
140
Citations
(Scopus)
A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation
Ye, B., Valdivia, C. R., Ackerman, M. J. & Makielski, J. C., Apr 2003, In : Physiological Genomics. 12, p. 187-193 7 p.Research output: Contribution to journal › Article
Cardiac Arrhythmias
Clone Cells
Mutation
Gene Library
Ion Channels
16
Citations
(Scopus)
Acquired long QT syndrome secondary to cesium chloride supplement
Vyas, H., Johnson, K., Houlihan, R., Bauer, B. A. & Ackerman, M. J., Dec 2006, In : Journal of Alternative and Complementary Medicine. 12, 10, p. 1011-1014 4 p.Research output: Contribution to journal › Article
Long QT Syndrome
Syncope
Physicians
cesium chloride
4
Citations
(Scopus)
Acquired QT prolongation associated with esophagitis and acute weight loss: How to evaluate a prolonged QT interval
Koch, J. J., Porter, C. J. & Ackerman, M. J., Oct 2005, In : Pediatric Cardiology. 26, 5, p. 646-650 5 p.Research output: Contribution to journal › Article
Esophagitis
Weight Loss
Electrocardiography
Long QT Syndrome
Herpes Simplex
54
Citations
(Scopus)
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: Recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel
ClinGen Cardiovascular Clinical Domain Working Group, Mar 1 2018, In : Genetics in Medicine. 20, 3, p. 351-359 9 p.Research output: Contribution to journal › Article
Adenosine Monophosphate
Cardiomyopathies
Social Adjustment
Genes
Molecular Pathology
48
Citations
(Scopus)
A functional and structural study of tropon in C mutations related to hypertrophic cardiomyopathy
Pinto, J. R., Parvatiyar, M. S., Jones, M. A., Liang, J., Ackerman, M. J. & Potter, J. D., Jul 10 2009, In : Journal of Biological Chemistry. 284, 28, p. 19090-19100 11 p.Research output: Contribution to journal › Article
Troponin C
Hypertrophic Cardiomyopathy
Troponin
Mutation
Myosins
31
Citations
(Scopus)
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation
Bartos, D. C., Anderson, J. B., Bastiaenen, R., Johnson, J. N., Gollob, M. H., Tester, D. J., Burgess, D. E., Homfray, T., Behr, E. R., Ackerman, M. J., Guicheney, P. & Delisle, B. P., May 2013, In : Journal of Cardiovascular Electrophysiology. 24, 5, p. 562-569 8 p.Research output: Contribution to journal › Article
Penetrance
Atrial Fibrillation
Mutation
Action Potentials
Sudden Cardiac Death
14
Citations
(Scopus)
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation
Bartos, D. C., Giudicessi, J. R., Tester, D. J., Ackerman, M. J., Ohno, S., Horie, M., Gollob, M. H., Burgess, D. E. & Delisle, B. P., Mar 2014, In : Heart Rhythm. 11, 3, p. 459-468 10 p.Research output: Contribution to journal › Article
Cyclic AMP-Dependent Protein Kinases
Phosphorylation
Action Potentials
Phenotype
Mutation
36
Citations
(Scopus)
Allelic dropout in long QT syndrome genetic testing: A possible mechanism underlying false-negative results
Tester, D. J., Cronk, L. B., Carr, J. L., Schulz, V., Salisbury, B. A., Judson, R. S. & Ackerman, M. J., Jul 2006, In : Heart Rhythm. 3, 7, p. 815-821 7 p.Research output: Contribution to journal › Article
Long QT Syndrome
Genetic Testing
Exons
Single Nucleotide Polymorphism
Genotype
92
Citations
(Scopus)
alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.
Wu, G., Ai, T., Kim, J. J., Mohapatra, B., Xi, Y., Li, Z., Abbasi, S., Purevjav, E., Samani, K., Ackerman, M. J., Qi, M., Moss, A. J., Shimizu, W., Towbin, J. A., Cheng, J. & Vatta, M., Aug 2008, In : Circulation. Arrhythmia and electrophysiology. 1, 3, p. 193-201 9 p.Research output: Contribution to journal › Article
Long QT Syndrome
Sodium Channels
Mutation
HEK293 Cells
Cardiac Myocytes
122
Citations
(Scopus)
A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors
Tester, D. J., Dura, M., Carturan, E., Reiken, S., Wronska, A., Marks, A. R. & Ackerman, M. J., Jun 2007, In : Heart Rhythm. 4, 6, p. 733-739 7 p.Research output: Contribution to journal › Article
Ryanodine Receptor Calcium Release Channel
Sudden Infant Death
Mutation
Diastole
HEK293 Cells
64
Citations
(Scopus)
A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathy
Vasile, V. C., Ommen, S. R., Edwards, W. D. & Ackerman, M. J., Jul 7 2006, In : Biochemical and Biophysical Research Communications. 345, 3, p. 998-1003 6 p.Research output: Contribution to journal › Article
Vinculin
Hypertrophic Cardiomyopathy
Missense Mutation
Mutation
Proteins
2
Citations
(Scopus)
A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene
Ding, Y., Long, P. A., Bos, J. M., Shih, Y. H., Ma, X., Sundsbak, R. S., Chen, J., Jiang, Y., Zhao, L., Hu, X., Wang, J., Shi, Y., Ackerman, M. J., Lin, X., Ekker, S. C., Redfield, M. M., Olson, T. M. & Xu, X. H., Apr 20 2017, In : JCI insight. 2, 8Research output: Contribution to journal › Article
Open Access
47
Citations
(Scopus)
A mutation in telethonin alters Nav1.5 function
Mazzone, A., Strege, P. R., Tester, D. J., Bernard, C. E., Faulkner, G., De Giorgio, R., Makielski, J. C., Stanghellini, V., Gibbons, S. J., Ackerman, M. J. & Farrugia, G., Jun 13 2008, In : Journal of Biological Chemistry. 283, 24, p. 16537-16544 8 p.Research output: Contribution to journal › Article
Intestinal Pseudo-Obstruction
Mutation
Sodium Channels
Ion Channels
Romano-Ward Syndrome
A mutation in telethonin alters Nav1.5 function (Journal of Biological Chemistry (2008) 283 (16537-16544))
Mazzone, A., Strege, P. R., Tester, D. J., Bernard, C. E., Faulkner, G., De Giorgio, R., Makielski, J. C., Stanghellini, V., Gibbons, S. J., Ackerman, M. J. & Farrugia, G., Aug 8 2008, In : Journal of Biological Chemistry. 283, 32, p. 22336 1 p.Research output: Contribution to journal › Article
Mutation
27
Citations
(Scopus)
A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation
Parvatiyar, M. S., Landstrom, A. P., Figueiredo-Freitas, C., Potter, J. D., Ackerman, M. J. & Pinto, J. R., Sep 14 2012, In : Journal of Biological Chemistry. 287, 38, p. 31845-31855 11 p.Research output: Contribution to journal › Article
Troponin C
Hypertrophic Cardiomyopathy
Ventricular Fibrillation
Mutation
Sudden Cardiac Death
12
Citations
(Scopus)
An algorithm for QT interval monitoring in neonatal intensive care units
Helfenbein, E. D., Ackerman, M. J., Rautaharju, P. M., Zhou, S. H., Gregg, R. E., Lindauer, J. M., Miller, D., Wang, J. J., Kresge, S. S., Babaeizadeh, S., Feild, D. Q. & Michaud, F. P., Nov 2007, In : Journal of Electrocardiology. 40, 6 SUPPL. 1Research output: Contribution to journal › Article
Neonatal Intensive Care Units
Electrocardiography
Heart Rate
Pediatrics
Neonatal Intensive Care
5
Citations
(Scopus)
An Association of Hippocampal Malformations and Sudden Death? We Need More Data
Ackerman, M. J., Andrew, T. A., Baker, A. M., Devinsky, O., Downs, J. C. U., Keens, T., Kuntz, J., Lin, P., Lear-Kaul, K. C., Reichard, R. & Robinson, D. A., Mar 26 2016, (Accepted/In press) In : Forensic Science, Medicine, and Pathology. p. 1-3 3 p.Research output: Contribution to journal › Article
Sudden Cardiac Death
Sudden Death
Hippocampus
10
Citations
(Scopus)
An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis
Chatterjee, D., Fatah, M., Akdis, D., Spears, D. A., Koopmann, T. T., Mittal, K., Rafiq, M. A., Cattanach, B. M., Zhao, Q., Healey, J. S., Ackerman, M. J., Bos, J. M., Sun, Y., Maynes, J. T., Brunckhorst, C., Medeiros-Domingo, A., Duru, F., Saguner, A. M. & Hamilton, R. M., Nov 21 2018, In : European Heart Journal. 39, 44, p. 3932-3944 13 p.Research output: Contribution to journal › Article
Desmoglein 2
Arrhythmogenic Right Ventricular Dysplasia
Autoantibodies
Antibodies
Mutation
96
Citations
(Scopus)
Anesthesia for patients with congenital long QT syndrome
Kies, S. J., Pabelick, C. M., Hurley, H. A., White, R. D. & Ackerman, M. J., Jan 2005, In : Anesthesiology. 102, 1, p. 204-210 7 p.Research output: Contribution to journal › Article
Long QT Syndrome
Torsades de Pointes
Anesthesia
Sudden Cardiac Death
Anesthetics
13
Citations
(Scopus)
Anesthesia for videoscopic left cardiac sympathetic denervation in children with congenital long QT syndrome and catecholaminergic polymorphic ventricular tachycardia - A case series
Kenyon, C. A., Flick, R., Moir, C., Ackerman, M. J. & Pabelick, C. M., May 2010, In : Paediatric Anaesthesia. 20, 5, p. 465-470 6 p.Research output: Contribution to journal › Article
Long QT Syndrome
Sympathectomy
Anesthesia
Anesthetics
Premedication
36
Citations
(Scopus)
Anesthetic management of patients with Brugada syndrome: A case series and literature review
Kloesel, B., Ackerman, M. J., Sprung, J., Narr, B. J. & Weingarten, T. N., Sep 2011, In : Canadian Journal of Anesthesia. 58, 9, p. 824-836 13 p.Research output: Contribution to journal › Article
Brugada Syndrome
Anesthetics
Anesthesia
Propofol
Hyperkalemia
388
Citations
(Scopus)
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
Kapplinger, J. D., Tester, D. J., Alders, M., Benito, B., Berthet, M., Brugada, J., Brugada, P., Fressart, V., Guerchicoff, A., Harris-Kerr, C., Kamakura, S., Kyndt, F., Koopmann, T. T., Miyamoto, Y., Pfeiffer, R., Pollevick, G. D., Probst, V., Zumhagen, S., Vatta, M., Towbin, J. A. & 9 others, , Jan 2010, In : Heart Rhythm. 7, 1, p. 33-46 14 p.Research output: Contribution to journal › Article
Brugada Syndrome
Sodium Channels
Genetic Testing
Mutation
Healthy Volunteers
30
Citations
(Scopus)
A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia
Tan, B. H., Iturralde-Torres, P., Medeiros-Domingo, A., Nava, S., Tester, D. J., Valdivia, C. R., Tusié-Luna, T., Ackerman, M. J. & Makielski, J. C., Dec 1 2007, In : Cardiovascular Research. 76, 3, p. 409-417 9 p.Research output: Contribution to journal › Article
Sick Sinus Syndrome
Ventricular Tachycardia
Mutation
Phenotype
Penetrance
53
Citations
(Scopus)
A novel disease gene for Brugada syndrome: Sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5
Ishikawa, T., Sato, A., Marcou, C. A., Tester, D. J., Ackerman, M. J., Crotti, L., Schwartz, P. J., On, Y. K., Park, J. E., Nakamura, K., Hiraoka, M., Nakazawa, K., Sakurada, H., Arimura, T., Makita, N. & Kimura, A., Dec 2012, In : Circulation: Arrhythmia and Electrophysiology. 5, 6, p. 1098-1107 10 p.Research output: Contribution to journal › Article
Brugada Syndrome
Membrane Proteins
Mutation
Genes
Sarcoplasmic Reticulum
41
Citations
(Scopus)
A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family
Ackerman, M. J., Schroeder, J. J., Berry, R., Schaid, D. J., Porter, C. B. J., Michels, V. V. & Thibodeau, S. N., Aug 1998, In : Pediatric Research. 44, 2, p. 148-153 6 p.Research output: Contribution to journal › Article
Near Drowning
Long QT Syndrome
Mutation
Electrocardiography
Genotype
73
Citations
(Scopus)
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents
Hu, D., Barajas-Martínez, H., Medeiros-Domingo, A., Crotti, L., Veltmann, C., Schimpf, R., Urrutia, J., Alday, A., Casis, O., Pfeiffer, R., Burashnikov, E., Caceres, G., Tester, D. J., Wolpert, C., Borggrefe, M., Schwartz, P., Ackerman, M. J. & Antzelevitch, C., May 2012, In : Heart Rhythm. 9, 5, p. 760-769 10 p.Research output: Contribution to journal › Article
Brugada Syndrome
Sudden Infant Death
Sodium Channels
Immunoprecipitation
Exons
74
Citations
(Scopus)
A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine
Valdivia, C. R., Ackerman, M. J., Tester, D. J., Wada, T., McCormack, J., Ye, B. & Makielski, J. C., 2002, In : Cardiovascular Research. 55, 2, p. 279-289 11 p.Research output: Contribution to journal › Article
Mexiletine
Cardiac Arrhythmias
Sodium Channels
Mutation
Sodium
28
Citations
(Scopus)
A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood
Van Driest, S. L., Will, M. L., Atkins, D. L. & Ackerman, M. J., Nov 15 2002, In : American Journal of Cardiology. 90, 10, p. 1123-1127 5 p.Research output: Contribution to journal › Article
Hypertrophic Cardiomyopathy
Sudden Cardiac Death
Mutation
Tropomyosin
Missense Mutation
1
Citation
(Scopus)
A Novel Truncating Variant in FLNC-Encoded Filamin C May Serve as a Proarrhythmic Genetic Substrate for Arrhythmogenic Bileaflet Mitral Valve Prolapse Syndrome
Bains, S., Tester, D. J., Asirvatham, S. J., Noseworthy, P., Ackerman, M. J. & Giudicessi, J. R., Jan 1 2019, In : Mayo Clinic proceedings.Research output: Contribution to journal › Article
Filamins
Mitral Valve Prolapse
Mothers
Exome
Ambulatory Monitoring
2
Citations
(Scopus)
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel
Ye, D., Tester, D. J., Zhou, W., Papagiannis, J. & Ackerman, M. J., Feb 1 2019, In : Heart Rhythm. 16, 2, p. 270-278 9 p.Research output: Contribution to journal › Article
Monovalent Cations
L-Type Calcium Channels
Missense Mutation
Nifedipine
Bradycardia
41
Citations
(Scopus)
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome
Limpitikul, W. B., Dick, I. E., Tester, D. J., Boczek, N. J., Limphong, P., Yang, W., Choi, M. H., Babich, J., Disilvestre, D., Kanter, R. J., Tomaselli, G. F., Ackerman, M. J. & Yue, D. T., Jan 6 2017, In : Circulation Research. 120, 1, p. 39-48 10 p.Research output: Contribution to journal › Article
Long QT Syndrome
Precision Medicine
Calmodulin
Induced Pluripotent Stem Cells
Clustered Regularly Interspaced Short Palindromic Repeats
1
Citation
(Scopus)
Architectural T-Wave Analysis and Identification of On-Therapy Breakthrough Arrhythmic Risk in Type 1 and Type 2 Long-QT Syndrome
Sugrue, A., Rohatgi, R. K., Noseworthy, P., Kremen, V., Bos, J. M., Qiang, B., Sapir, Y., Attia, Z. I., Scott, C. G., Brady, P., Asirvatham, S. J., Friedman, P. A. & Ackerman, M. J., Nov 1 2017, In : Circulation. Arrhythmia and electrophysiology. 10, 11Research output: Contribution to journal › Article
Romano-Ward Syndrome
Long QT Syndrome
Electrocardiography
Therapeutics
Gravitation
3
Citations
(Scopus)
Are longitudinal, natural history studies the next step in genotype-phenotype translational genomics in hypertrophic cardiomyopathy?
Ackerman, M. J., Van Driest, S. L. & Bos, M., Nov 1 2005, In : Journal of the American College of Cardiology. 46, 9, p. 1744-1746 3 p.Research output: Contribution to journal › Article
Hypertrophic Cardiomyopathy
Protein Biosynthesis
Genomics
Natural History
Longitudinal Studies
24
Citations
(Scopus)
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: Risk stratification of perinatal long-QT syndrome
Cuneo, B. F., Etheridge, S. P., Horigome, H., Sallee, D., Moon-Grady, A., Weng, H. Y., Ackerman, M. J. & Woodrow Benson, D., Oct 2013, In : Circulation: Arrhythmia and Electrophysiology. 6, 5, p. 946-951 6 p.Research output: Contribution to journal › Article
Long QT Syndrome
Cardiac Arrhythmias
Torsades de Pointes
Genotype
Phenotype
9
Citations
(Scopus)
Arrhythmia risk in long QT syndrome: Beyond the disease-causative mutation
Giudicessi, J. R. & Ackerman, M. J., Aug 2013, In : Circulation: Cardiovascular Genetics. 6, 4, p. 313-316 4 p.Research output: Contribution to journal › Article
KCNQ1 Potassium Channel
Long QT Syndrome
Ion Channels
Single Nucleotide Polymorphism
Cardiac Arrhythmias
Arrhythmias and arrhythmia management in hypertrophic cardiomyopathy
Bos, J. M., Ommen, S. R. & Ackerman, M. J., Jul 1 2013, Electrical Diseases of the Heart. Springer-Verlag London Ltd, Vol. 2. p. 7-24 18 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
Hypertrophic Cardiomyopathy
Cardiomyopathies
Cardiac Arrhythmias
Sudden Cardiac Death
Genetic Testing
Arrhythmias and arrhythmia management in hypertrophic cardiomyopathy
Martijn Bos, J., Ommen, S. R. & Ackerman, M. J., Jan 1 2013, Electrical Diseases of the Heart: Volume 2: Diagnosis and Treatment, Second Edition. Springer-Verlag London Ltd, p. 7-24 18 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
Hypertrophic Cardiomyopathy
Cardiomyopathies
Cardiac Arrhythmias
Sudden Cardiac Death
Genetic Testing
11
Citations
(Scopus)
Arrhythmogenic biophysical phenotype for SCN5A mutation S1787N depends upon splice variant background and intracellular acidosis
Hu, R. M., Tan, B. H., Tester, D. J., Song, C., He, Y., Dovat, S., Peterson, B. Z., Ackerman, M. J. & Makielski, J. C., Apr 29 2015, In : PLoS One. 10, 4, e0124921.Research output: Contribution to journal › Article
acidosis
Acidosis
Protein Isoforms
Phenotype
mutation