M. Tristani-Firouzi

发表

De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes

W. Chung, Yufeng Shen, M. Yandell, 2019, Nature Communications.

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

Yufeng Shen, Alessandro Giardini, Hongyu Zhao, 2017, Nature Genetics.

Exome analysis of a family with Wolff–Parkinson–White syndrome identifies a novel disease locus

Mark Yandell, H Joseph Yost, Brett J. Kennedy, 2015, American journal of medical genetics. Part A.

Mutations in the hminK gene cause long QT syndrome and suppress lKs function

M. Sanguinetti, M. Tristani-Firouzi, M. Keating, 1997, Nature Genetics.

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

S. Subramony, S. Bendahhou, A. George, 2001, Cell.

hERG potassium channels and cardiac arrhythmia

M. Sanguinetti, M. Tristani-Firouzi, 2006, Nature.

Kir 2.1 channelopathies: the Andersen–Tawil syndrome

Martin Tristani-Firouzi, M. Tristani-Firouzi, S. Etheridge, 2010, Pflügers Archiv - European Journal of Physiology.

Zebrafish model for human long QT syndrome

Jan Huisken, Rima Arnaout, Martin Tristani-Firouzi, 2007, Proceedings of the National Academy of Sciences.

Structural Determinants of HERG Channel Block by Clofilium and Ibutilide

Michael C Sanguinetti, Martin Tristani-Firouzi, Derek Leishman, 2004, Molecular Pharmacology.

Genetic and Physiologic Dissection of the Vertebrate Cardiac Conduction System

Herwig Baier, Jan Huisken, Rima Arnaout, 2008, PLoS biology.

Sheet-Like Remodeling of the Transverse Tubular System in Human Heart Failure Impairs Excitation-Contraction Coupling and Functional Recovery by Mechanical Unloading

Dean Y. Li, F. Sachse, M. Tristani-Firouzi, 2017, Circulation.

hERG potassium channels and cardiac

Martin Tristani-Firouzi, M. Tristani-Firouzi, C. Sanguinetti, 2006 .

Molecular Basis for a High-Potency Open-Channel Block of Kv1.5 Channel by the Endocannabinoid Anandamide

F. Sachse, M. Tristani-Firouzi, N. Decher, 2010, Molecular Pharmacology.

Andersen-Tawil and Timothy Syndromes

M. Tristani-Firouzi, S. Etheridge, 2013 .

Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis

R. M. Burr, M. Bamshad, A. Moon, 2011, Proceedings of the National Academy of Sciences.

The absence of insulin signaling in the heart induces changes in potassium channel expression and ventricular repolarization.

M. Tristani-Firouzi, E. Abel, R. Pereira, 2014, American journal of physiology. Heart and circulatory physiology.

Molecular biology of K(+) channels and their role in cardiac arrhythmias.

M. Sanguinetti, M. Tristani-Firouzi, J. Mitcheson, 2001, The American journal of medicine.

De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

B. Gelb, C. Sevim Bayrak, Y. Itan, 2020, Genome Medicine.

A near-infrared fluorescent voltage-sensitive dye allows for moderate-throughput electrophysiological analyses of human induced pluripotent stem cell-derived cardiomyocytes.

I. Benjamin, R. Lux, M. Tristani-Firouzi, 2014, American journal of physiology. Heart and circulatory physiology.

EM-mosaic detects mosaic point mutations that contribute to congenital heart disease

K. B. Manheimer, W. Chung, J. Seidman, 2020, Genome Medicine.

The Application of Root Mean Square Electrocardiography (RMS ECG) for the Detection of Acquired and Congenital Long QT Syndrome

Robert L. Lux, Martin Tristani-Firouzi, R. Lux, 2014, PloS one.

Revisiting the challenges of universal screening for long QT syndrome.

M. Tristani-Firouzi, 2015, Journal of electrocardiology.

Molecular determinants of Kv7.1/KCNE1 channel inhibition by amitriptyline

M. Tristani-Firouzi, J. Sánchez-Chapula, T. Ferrer, 2018, Biochemical pharmacology.

DNA Methylation Reprograms Cardiac Metabolic Gene Expression in End-Stage Human Heart Failure.

O. Wever-Pinzon, Chae-Myeong Ha, M. Tristani-Firouzi, 2019, American journal of physiology. Heart and circulatory physiology.

Early post-zygotic mutations contribute to congenital heart disease

K. B. Manheimer, W. Chung, J. Seidman, 2019, bioRxiv.

Deriving Cardiomyocytes from Human Amniocytes

H. Yost, Ryan Sunderland, B. Demarest, 2018, bioRxiv.

Structural Determinants and Biophysical Properties of hERG1 Channel Gating

F. Sachse, M. Sanguinetti, M. Tristani-Firouzi, 2013 .

Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors

K. B. Manheimer, W. Chung, J. Seidman, 2017, bioRxiv.

Voltage sensitivity of M2 muscarinic receptors underlies the delayed rectifier‐like activation of ACh‐gated K+ current by choline in feline atrial myocytes

F. Sachse, M. Tristani-Firouzi, J. Sánchez-Chapula, 2013, The Journal of physiology.

The Pulmonary Circulation in Health and Disease

S. Archer, E. K. Weir, M. Tristani-Firouzi, 2002 .

Oxygen-induced constriction of rabbit ductus arteriosus occurs via inhibition of a 4-aminopyridine-, voltage-sensitive potassium channel.

S. Archer, E. K. Weir, M. Tristani-Firouzi, 1996, The Journal of clinical investigation.

Addressing ethical and laboratory challenges for initiation of a rapid whole genome sequencing program

M. Yandell, J. Botkin, D. Dimmock, 2021, Journal of Clinical and Translational Science.

Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

W. Chung, J. Seidman, A. Sharp, 2020, PLoS genetics.

An Fgf 8 mouse mutant phenocopies human 22 q 11 deletion syndrome

M. Capecchi, J. Brewer, A. Moon, 2002 .

Neither cardiac mitochondrial DNA variation or copy number contribute to congenital heart disease risk

J. Seidman, Yufeng Shen, D. Bernstein, 2022, The American Journal of Human Genetics.

R E V I E W A R T I C L E The primary periodic paralyses: diagnosis, pathogenesis and treatment

R. Griggs, M. Tristani-Firouzi, L. Ptáček, 2005 .

Estimation of offspring genetic risk scores using parental genotypes.

A. Quinlan, T. Workalemahu, M. Tristani-Firouzi, 2022, medRxiv.

Congenital long QT 3 in the pediatric population.

S. Seslar, B. Cuneo, M. Tristani-Firouzi, 2012, The American journal of cardiology.

A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations.

J. Mason, M. Tristani-Firouzi, S. Etheridge, 2003, Journal of the American College of Cardiology.

Somatic mosaicism contributes to phenotypic variation in Timothy syndrome

A. Wilde, A. Rope, M. Tristani-Firouzi, 2011, American journal of medical genetics. Part A.

A multicenter, prospective, cross-sectional, genotype-phenotype and longitudinal natural history study of Andersen-Tawil syndrome

R. Griggs, M. Tristani-Firouzi, V. Sansone, 2022, medRxiv.

Chapter 6 Delayed Rectifier Potassium Channels in Normal and Abnormal Cardiac Repolarization

M. Sanguinetti, M. Tristani-Firouzi, 1999 .

Polymorphic ventricular tachycardia associated with mutations in KCNJ2.

M. Tristani-Firouzi, 2004, Heart rhythm.

Resuscitated sudden cardiac death in Andersen-Tawil syndrome.

K. Airey, M. Tristani-Firouzi, S. Etheridge, 2009, Heart rhythm.

Atrium‐specific ion channels in the zebrafish—A role of IKACh in atrial repolarization

M. Tristani-Firouzi, P. Lundegaard, A. Lopez-Izquierdo, 2018, Acta physiologica.

Voltage-induced structural modifications on M2 muscarinic receptor and their functional implications when interacting with iperoxo.

M. Tristani-Firouzi, José J. De Jesús-Pérez, T. Ferrer, 2020, Biochemical pharmacology.

Congenital long QT syndrome in children identified by family screening.

M. Tristani-Firouzi, S. Etheridge, E. Saarel, 2008, The American journal of cardiology.

Interactions between S4-S5 Linker and S6 Transmembrane Domain Modulate Gating of HERG K+ Channels*

M. Sanguinetti, M. Tristani-Firouzi, Jun Chen, 2002, The Journal of Biological Chemistry.

A NOVEL APPROACH TO DIFFERENTIATING CARDIAC FIBROBLASTS FROM INDUCED PLURIPOTENT STEM CELLS

M. Tristani-Firouzi, Alexander Sperber, 2022 .

Nebulized nitric oxide/nucleophile adduct reduces chronic pulmonary hypertension.

S. Archer, M. Tristani-Firouzi, T. Hutsell, 1996, Cardiovascular research.

Mitochondrial calcium uniporter stabilization preserves energetic homeostasis during Complex I impairment

S. Franklin, M. Tristani-Firouzi, S. Sommakia, 2022, Nature Communications.

The mitochondrial calcium uniporter compensates for Complex I dysfunction

S. Franklin, M. Tristani-Firouzi, S. Sommakia, 2021 .

Flecainide Suppresses Bidirectional Ventricular Tachycardia and Reverses Tachycardia‐Induced Cardiomyopathy in Andersen‐Tawil Syndrome

M. Tristani-Firouzi, L. Ptáček, O. Pellizzón, 2007, Journal of cardiovascular electrophysiology.

Diversity of response in vascular smooth muscle cells to changes in oxygen tension.

D. Cornfield, D. Peterson, S. Archer, 1997, Kidney international.

Pharmacological Conversion of a Cardiac Inward Rectifier into an Outward Rectifier Potassium Channel

M. Tristani-Firouzi, J. Sánchez-Chapula, Eloy G. Moreno-Galindo, 2016, Molecular Pharmacology.

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Kathleen M. Chen, K. B. Manheimer, G. Marth, 2020, Nature Genetics.

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.

M. Capecchi, J. Brewer, A. Moon, 2002, Development.

Contribution of rare transmitted and de novo variants among 2 , 871 1 congenital heart disease probands

Deepak, Stephan J Sanders, W. Chung, 2017 .

De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease

Michael F Swartz, K. B. Manheimer, W. Chung, 2020, Circulation. Genomic and precision medicine.

Functional and Pharmacological Analysis of Cardiomyocytes Differentiated from Human Peripheral Blood Mononuclear-Derived Pluripotent Stem Cells

A. Moreno, I. Benjamin, R. Lux, 2014, Stem cell reports.

Inhibition of Notch signaling rescues cardiovascular development in Kabuki Syndrome

H. Yost, B. Demarest, M. Tristani-Firouzi, 2018, bioRxiv.

A Functional Assay for Sick Sinus Syndrome Genetic Variants

M. Tristani-Firouzi, N. Bowles, C. Jou, 2017, Cellular Physiology and Biochemistry.

Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association

B. Gelb, P. Kannankeril, A. Sturm, 2021, Circulation. Genomic and precision medicine.

GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm

W. Chung, J. Seidman, D. Srivastava, 2020, eLife.

A Poisson binomial-based statistical testing framework for comorbidity discovery across electronic health record datasets

M. Yandell, A. Henrie, S. Wesołowski, 2021, Nature Computational Science.

A Poisson binomial based statistical testing framework for comprehensive comorbidity discovery across massive Electronic Health Record datasets

M. Yandell, A. Henrie, S. Wesołowski, 2021, medRxiv.

Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics

P. Bayrak-Toydemir, N. Longo, Josue A Flores-Daboub, 2022, Pediatric Research.

Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome*

Martin Tristani-Firouzi, Saïd Bendahhou, Ying-Hui Fu, 2003, Journal of Biological Chemistry.

Efficient Precision Genome Editing in iPSCs via Genetic Co-targeting with Selection

I. Benjamin, J. Verbsky, D. Dimmock, 2017, Stem cell reports.

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Hubert Kwiecinski, Rabi Tawil, Martin Tristani-Firouzi, 2002, The Journal of clinical investigation.

Voltage‐dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits

M. Sanguinetti, M. Tristani-Firouzi, 1998, The Journal of physiology.

Effective variant filtering and expected candidate variant yield in studies of rare human disease

Brent S. Pedersen, A. Quinlan, J. Schiffman, 2021, npj Genomic Medicine.

The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele

Brett J. Kennedy, C. Ball, J. Carlquist, 2021, Nature Communications.

Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics

P. Bayrak-Toydemir, N. Longo, Josue A Flores-Daboub, 2022, Pediatric Research.

De novo variants in exomes of congenital heart disease patients identify risk genes and pathways

B. Gelb, Y. Itan, M. Tristani-Firouzi, 2020, Genome Medicine.

An explainable artificial intelligence approach for predicting cardiovascular outcomes using electronic health records

K. Eilbeck, M. Yandell, A. Henrie, 2021, medRxiv.

Regional Specificity of Human ether-a'-go-go-related Gene Channel Activation and Inactivation Gating*

Michael C Sanguinetti, Martin Tristani-Firouzi, M. Sanguinetti, 2005, Journal of Biological Chemistry.

Gating currents associated with intramembrane charge displacement in HERG potassium channels

Michael C Sanguinetti, Martin Tristani-Firouzi, Anthony Varghese, 2003, Proceedings of the National Academy of Sciences of the United States of America.

PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

E. Behr, S. Bendahhou, Ying-Hui Fu, 2003, Neurology.

Sudden cardiac death in Andersen-Tawil syndrome.

E. Schulze-Bahr, M. Tristani-Firouzi, S. Etheridge, 2007, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

S. Cannon, R. Griggs, M. Tristani-Firouzi, 2006, Brain : a journal of neurology.

The Molecular Basis of the Long QT Syndrome

M. Sanguinetti, M. Tristani-Firouzi, 2001 .

An explainable AI approach for discovering social determinants of health and risk interactions for stroke in patients with atrial fibrillation

W. Watkins, E. Hernandez, M. Tristani-Firouzi, 2023, medRxiv.

Rapid progression of long-segment coarctation in a patient with Williams' syndrome

M. Tristani-Firouzi, Cammon B. Arrington, M. Puchalski, 2005, Cardiology in the Young.

Andersen‐Tawil syndrome: Prospective cohort analysis and expansion of the phenotype

M. Tristani-Firouzi, S. Etheridge, L. Ptáček, 2006, American journal of medical genetics. Part A.

Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations: Characteristic T-U–Wave Patterns Predict the KCNJ2 Genotype

P. Schwartz, M. Ackerman, G. Vincent, 2005, Circulation.

Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease

W. Chung, J. Seidman, Yufeng Shen, 2020, JAMA cardiology.

Adrenergic receptor genotypes influence postoperative outcomes in infants in the Single‐Ventricle Reconstruction Trial

M. Lafreniere-Roula, S. B. Wechsler, J. Newburger, 2017, The Journal of thoracic and cardiovascular surgery.

Chloroquine Blocks a Mutant Kir2.1 Channel Responsible for Short QT Syndrome and Normalizes Repolarization Properties in silico

Frank B. Sachse, Martin Tristani-Firouzi, F. Sachse, 2009, Cellular Physiology and Biochemistry.

The S4–S5 linker couples voltage sensing and activation of pacemaker channels

Jun Chen, John S. Mitcheson, Martin Tristani-Firouzi, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Family Screening After Sudden Death in a Population-Based Study of Children.

D. Roden, M. Yandell, P. Kannankeril, 2022, Pediatrics.

Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia

Gabor T. Marth, Thomas J. Nicholas, G. Marth, 2022, Molecular genetics & genomic medicine.

The pharmacokinetics of methadone and its metabolites in neonates, infants, and children

Steven Edward Kern, M. Tristani-Firouzi, R. Ward, 2014, Paediatric anaesthesia.

Chronic infusion of nitric oxide in experimental pulmonary hypertension: pulmonary pressure-flow analysis.

S. Archer, M. Tristani-Firouzi, V. Hampl, 1996, The European respiratory journal.

The molecular basis of chloroquine block of the inward rectifier Kir2.1 channel

Frank B. Sachse, Martin Tristani-Firouzi, F. Sachse, 2008, Proceedings of the National Academy of Sciences.

3-OST-7 Regulates BMP-Dependent Cardiac Contraction

F. Sachse, H. Yost, M. Tristani-Firouzi, 2013, PLoS biology.

Modeling effects of voltage dependent properties of the cardiac muscarinic receptor on human sinus node function

Gunnar Seemann, Frank B Sachse, Robin Moss, 2018, PLoS Comput. Biol..

Conformational changes in the M2 muscarinic receptor induced by membrane voltage and agonist binding

M. Tristani-Firouzi, J. Sánchez-Chapula, R. Navarro-Polanco, 2011, The Journal of physiology.

Functional Effects of Mutations in KvLQT1 that Cause Long QT Syndrome

M. Sanguinetti, M. Tristani-Firouzi, M. Keating, 1999, Journal of cardiovascular electrophysiology.

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects

Nicolas F. Fernandez, W. Chung, D. Srivastava, 2020, JACC. Basic to translational science.

An In Vivo Cardiac Assay to Determine the Functional Consequences of Putative Long QT Syndrome Mutations

Xiaoming Sheng, Martin Tristani-Firouzi, M. Tristani-Firouzi, 2013, Circulation research.

Genetic, demographic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart disease

B. McCrindle, E. Hernandez, T. Miller, 2022, medRxiv.

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

Deanne M. Taylor, H. Hakonarson, B. Morrow, 2021, Genes.

The Long and Short of It: Insights Into the Short QT Syndrome.

M. Tristani-Firouzi, 2014, Journal of the American College of Cardiology.

Electrocardiograms in Healthy North American Children in the Digital Age

F. Trachtenberg, C. Berul, M. Tristani-Firouzi, 2018, Circulation. Arrhythmia and electrophysiology.

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Gabor T. Marth, Kathleen M. Chen, K. B. Manheimer, 2020, Nature Genetics.

Blebbistatin Effectively Uncouples the Excitation-Contraction Process in Zebrafish Embryonic Heart

Kenneth W. Spitzer, Martin Tristani-Firouzi, M. Tristani-Firouzi, 2010, Cellular Physiology and Biochemistry.

Development of a Portable Tool to Identify Patients With Atrial Fibrillation Using Clinical Notes From the Electronic Medical Record

Hawkins C. Gay, M. Yandell, D. Lloyd‐Jones, 2020, Circulation. Cardiovascular quality and outcomes.

Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity

W. Chung, J. Seidman, Yufeng Shen, 2022, Circulation. Genomic and precision medicine.

Care recommendations for the investigation and management of children with skeletal muscle channelopathies

Jacqueline A Palace, M. Tristani-Firouzi, S. Vicart, 2023, Pediatric Neurology.

Tamoxifen Inhibition of Kv7.2/Kv7.3 Channels

M. Tristani-Firouzi, M. Shapiro, J. Sánchez-Chapula, 2013, PloS one.

The S4-S5 Linker Directly Couples Voltage Sensor Movement to the Activation Gate in the Human Ether-á-go-go-related Gene (hERG) K+ Channel*

M. Tristani-Firouzi, T. Ferrer, D. Piper, 2006, Journal of Biological Chemistry.

CRISPR/Cas9‐Directed Gene Editing for the Generation of Loss‐of‐Function Mutants in High‐Throughput Zebrafish F0 Screens

H. Yost, B. Bisgrove, M. Tristani-Firouzi, 2017, Current protocols in molecular biology.

Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes

K. Pollard, Matthew Aguirre, J. Priest, 2023, Circulation. Genomic and precision medicine.

Relaxation gating of the acetylcholine‐activated inward rectifier K+ current is mediated by intrinsic voltage sensitivity of the muscarinic receptor

Frank B Sachse, Eloy G Moreno-Galindo, Ricardo A Navarro-Polanco, 2011, The Journal of physiology.

Andersen-Tawil syndrome: an ever-expanding phenotype?

M. Tristani-Firouzi, 2006, Heart rhythm.

Modeling of IK1 mutations in human left ventricular myocytes and tissue.

F. Sachse, G. Seemann, M. Tristani-Firouzi, 2007, American journal of physiology. Heart and circulatory physiology.

Molecular Coupling in the Human ether-a-go-go-related gene-1 (hERG1) K+ Channel Inactivation Pathway

M. Tristani-Firouzi, E. Perozo, David Medovoy, 2011, The Journal of Biological Chemistry.

Maternal mosaicism in long QT syndrome due to a pathogenic variant in KCNH2

M. Vatta, M. Tristani-Firouzi, S. Etheridge, 2020, HeartRhythm case reports.

Cooperative Interactions Between R531 and Acidic Residues in the Voltage Sensing Module of hERG1 Channels

F. Sachse, M. Sanguinetti, M. Tristani-Firouzi, 2008, Cellular Physiology and Biochemistry.

Kv1.5 open channel block by the antiarrhythmic drug disopyramide: molecular determinants of block.

M. Tristani-Firouzi, N. Decher, J. Sánchez-Chapula, 2008, Journal of pharmacological sciences.

Mortality and Sudden death risk in middle-aged persons with epilepsy -- a UK Biobank study

E. So, V. Somers, M. Tristani-Firouzi, 2023, medRxiv.

Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease

Parth N. Patel, J. Seidman, Yufeng Shen, 2023, Circulation. Genomic and precision medicine.

EM-mosaic detects mosaic point mutations that contribute to congenital heart disease

K. B. Manheimer, W. Chung, J. Seidman, 2020, Genome Medicine.

Expanding the phenotype of CACNA1C mutation disorders

T. Bunch, M. Tristani-Firouzi, L. Meyers, 2021, Molecular genetics & genomic medicine.

Ventilation-induced pulmonary vasodilation at birth is modulated by potassium channel activity.

D. Cornfield, S. Archer, M. Tristani-Firouzi, 1996, The American journal of physiology.

Evidence for Early Vessel Involvement in the Dysfunctional Myocardium of Takayasu's Arteritis

M. Tristani-Firouzi, R. Shaddy, J. Breinholt, 2001, Pediatric Cardiology.

Calcium Channel Dysfunction in Inherited Cardiac Arrhythmia Syndromes

M. Tristani-Firouzi, S. Etheridge, 2011 .

Modification of hERG1 channel gating by Cd2+

F. Sachse, M. Sanguinetti, M. Tristani-Firouzi, 2010, The Journal of general physiology.

Familial Associations of Prevalence and Cause-Specific Mortality for Thoracic Aortic Disease and Bicuspid Aortic Valve in a Large-Population Database

A. Presson, J. Tonna, M. Tristani-Firouzi, 2023, Circulation.

American Heart Association's Children's Strategically Focused Research Network Experience

L. Hou, D. Labarthe, A. Fagerlin, 2023, Journal of the American Heart Association.

Andersen‐Tawil syndrome: Prospective cohort analysis and expansion of the phenotype

J. Kramer, Ying-Hui Fu, M. Tristani-Firouzi, 2006, American journal of medical genetics. Part A.

An In Vivo Cardiac Assay to Determine the Functional Consequences of Putative Long QT Syndrome Mutations

M. Tristani-Firouzi, C. Jou, X. Sheng, 2013, Circulation research.

Structural determinants and biophysical properties of HERG and KCNQ1 channel gating.

M. Sanguinetti, M. Tristani-Firouzi, 2003, Journal of molecular and cellular cardiology.

Pediatric and Familial Genetic Arrhythmia Syndromes: Evaluation of Bidirectional Ventricular Tachycardia—Differential Diagnosis

M. Tristani-Firouzi, S. Etheridge, Mary C. Niu, 2023, Cardiac Electrophysiology Clinics.

Gating of Cardiac Delayed Rectifier K + Channels

M. Sanguinetti, M. Tristani-Firouzi, 2004 .

The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

M. Yandell, M. Tristani-Firouzi, S. Etheridge, 2024, Genome medicine.

Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac Surgery

M. Tristani-Firouzi, M. Yandell, E. J. Hernandez, 2024, medRxiv.

Cardiovascular Disease Burden, Mortality and Sudden Death Risk in Epilepsy -- a UK Biobank study.

V. Somers, M. Tristani-Firouzi, I. Limongelli, 2023, The Canadian journal of cardiology.