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Author Details
Full Name
Hayan Jouni
Affiliation
Mayo Clinic
ORCID
Career Start Year
2010
Papers
51
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35084701
[18]F-FDG/[13]N-ammonia cardiac PET findings in ATTR cardiac amyloidosis.
J Nucl Cardiol
2023
34176680
Mitral Valve Cleft-like Indentations in Hypertrophic Obstructive Cardiomyopathy: Insights From Intraoperative Three-Dimensional Transesophageal Echocardiography.
J Cardiothorac Vasc Anesth
2022
35561958
Averaged Transaortic Mean Gradient during Atrial Fibrillation Does Not Accurately Reflect Aortic Stenosis Severity.
J Am Soc Echocardiogr
2022
35245669
Unfavorable Tricuspid Annulus Dynamics: A Novel Concept to Explain Development of Tricuspid Regurgitation in Atrial Fibrillation.
J Am Soc Echocardiogr
2022
34820769
Predictors of inducible ischemia with radionuclide stress testing: Choosing the right patients when the patients are changing.
J Nucl Cardiol
2022
34320381
Rituximab for the Treatment of Refractory Cardiac Sarcoidosis: A Single-Center Experience.
J Card Fail
2022
31111450
Suppressing physiologic 18-fluorodeoxyglucose uptake in patients undergoing positron emission tomography for cardiac sarcoidosis: The effect of a structured patient preparation protocol.
J Nucl Cardiol
2021
33724363
Atrial fibrillation is associated with large beat-to-beat variability in mitral and tricuspid annulus dimensions.
Eur Heart J Cardiovasc Imaging
2021
30771161
Diagnostic performance of F[18] FDG PET in cardiac sarcoidosis: Are we getting closer to the truth?
J Nucl Cardiol
2020
32061605
Large, Unpredictable Beat-To-Beat Variability of Mitral Annulus Size in Atrial Fibrillation: Implications for Percutaneous Interventions.
JACC Cardiovasc Interv
2020
32370835
Artificial Intelligence in Cardiology: Present and Future.
Mayo Clin Proc
2020
30792945
Electronic health record access by patients as an indicator of information seeking and sharing for cardiovascular health promotion in social networks: Secondary analysis of a randomized clinical trial.
Prev Med Rep
2019
29435464
Solving a Mystery . . . 8 Years Later.
J Investig Med High Impact Case Rep
2018
28062272
Disclosing Genetic Risk for Coronary Heart Disease: Attitudes Toward Personal Information in Health Records.
Am J Prev Med
2017
28386791
Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI-GENES) Randomized Clinical Trial.
J Genet Couns
2017
29208597
Unraveling Inflammation and Oxidative Stress in Cardiac Sarcoidosis.
Circ Cardiovasc Imaging
2017
28779015
Effect of Disclosing Genetic Risk for Coronary Heart Disease on Information Seeking and Sharing: The MI-GENES Study (Myocardial Infarction Genes).
Circ Cardiovasc Genet
2017
28687538
Temporal Trends of Single-Photon Emission Computed Tomography Myocardial Perfusion Imaging in Patients With Coronary Artery Disease: A 22-Year Experience From a Tertiary Academic Medical Center.
Circ Cardiovasc Imaging
2017
27993947
Shared decision-making following disclosure of coronary heart disease genetic risk: results from a randomized clinical trial.
J Investig Med
2017
27859518
Ixazomib cardiotoxicity: A possible class effect of proteasome inhibitors.
Am J Hematol
2017
25708169
Disclosing genetic risk for coronary heart disease: effects on perceived personal control and genetic counseling satisfaction.
Clin Genet
2016
27264231
Temporal trends of single-photon emission computed tomography myocardial perfusion imaging in patients without prior coronary artery disease: A 22-year experience at a tertiary academic medical center.
Am Heart J
2016
26915630
Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial).
Circulation
2016
26169577
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.
Pharmacogenomics J
2016
25625086
Ventricular septal defect and bivalvular endocarditis.
Avicenna J Med
2015
26271327
Design of a randomized controlled trial of disclosing genomic risk of coronary heart disease: the Myocardial Infarction Genes (MI-GENES) study.
BMC Med Genomics
2015
26030142
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.
PLoS One
2015
24026423
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Hum Genet
2014
25009551
The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study.
Front Genet
2014
25005442
Family history as a risk factor for carotid artery stenosis.
Stroke
2014
24760576
Images in vascular medicine. Twenty-eight years later: A case of superior vena cava aneurysm secondary to cystic hygroma.
Vasc Med
2014
24525054
Cleft posterior mitral leaflet resembling a tri-leaflet mitral valve: a novel phenotypic association with hypertrophic cardiomyopathy.
Eur Heart J
2014
24632283
Fabry disease with resting outflow obstruction masquerading as hypertrophic cardiomyopathy.
J Am Coll Cardiol
2014
23899785
'Popcorn thrombus': a case of massive intracardiac thromboembolism.
Heart
2014
23315613
The diagnosis of apical hypertrophic cardiomyopathy with myocardial perfusion imaging.
Heart
2013
26425586
Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study: A Case Series.
J Investig Med High Impact Case Rep
2013
26425574
Hypercalcemia, Renal Failure, and Skull Lytic Lesions: Follicular Lymphoma Masquerading as Multiple Myeloma.
J Investig Med High Impact Case Rep
2013
25125939
Clinical Correlates of Autosomal Chromosomal Abnormalities in an Electronic Medical Record-Linked Genome-Wide Association Study: A Case Series.
J Investig Med
2013
24136363
Downstream clinical implications of abnormal myocardial perfusion single-photon emission computed tomography based on appropriate use criteria.
J Nucl Cardiol
2013
23696099
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study.
G3 (Bethesda)
2013
23658142
A skin rash and what lies beneath: paraneoplastic pemphigus, an atypical presentation of follicular cell lymphoma.
Am J Hematol
2013
23595034
Diagnosis of achalasia on transthoracic echocardiography with the use of oral contrast.
Circ J
2013
23449431
Eclipse of the right ventricular outflow tract: natural history of a sinus of valsalva aneurysm.
J Am Coll Cardiol
2013
23263154
Images in vascular medicine. The mystery of a crimson leg: a case of Klippel-Trenaunay-Weber syndrome.
Vasc Med
2013
22096207
Serum N-terminal pro-B-type natriuretic peptide levels are associated with functional capacity in patients with peripheral arterial disease.
Angiology
2012
23188868
Danger above: a classic case of an unruptured right sinus of Valsalva aneurysm.
BMJ Case Rep
2012
23047997
A classic case of amyloid cardiomyopathy.
BMJ Case Rep
2012
22560525
Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits.
Mayo Clin Proc
2012
20947817
Increased serum N-terminal pro-B-type natriuretic peptide levels in patients with medial arterial calcification and poorly compressible leg arteries.
Arterioscler Thromb Vasc Biol
2011
20981332
Superparamagnetic bifunctional bisphosphonates nanoparticles: a potential MRI contrast agent for osteoporosis therapy and diagnostic.
J Osteoporos
2010
1 - 50 of 51
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Queen's University
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Dan M Roden
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Teri A Manolio
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Rex L Chisholm
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
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Abel N Kho
Northwestern University Feinberg School of Medicine
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Dana C Crawford
Cleveland Institute for Computational Biology, Case Western Reserve University
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