R. Hinton

R. Hinton, F. Lim, A. Coleman, 2015, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Somatic growth trajectory in the fetus with hypoplastic left heart syndrome

R. Hinton, J. Cnota, E. Michelfelder, 2013, Pediatric Research.

Aortopathy in the 7q11.23 microduplication syndrome

S. Lalani, R. Hinton, S. Ware, 2015, American journal of medical genetics. Part A.

Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndrome

R. Hinton, S. Ware, V. Pilipenko, 2016, American journal of medical genetics. Part A.

Novel fibrillin 1 mutation in a case of neonatal Marfan syndrome: the increasing importance of early recognition.

R. Hinton, D. Witte, R. Hopkin, 2007, Congenital heart disease.

Genetic contribution to bicuspid aortic valve morphology

R. Hinton, 2011 .

Dilated ascending aorta in a child with ring chromosome 21 syndrome

R. Hinton, A. Rope, H. Saal, 2004, American journal of medical genetics. Part A.

Identification of a common polymorphism in COQ8B acting as a modifier of thoracic aortic aneurysm severity

D. Milewicz, R. Hinton, B. Landis, 2021, HGG advances.

Mouse heart valve structure and function: echocardiographic and morphometric analyses from the fetus through the aged adult.

R. Hinton, K. Yutzey, D. Benson, 2008, American journal of physiology. Heart and circulatory physiology.

Loss of flow responsive Tie1 results in Impaired Aortic valve remodeling.

R. Hinton, H. Baldwin, W. Merryman, 2019, Developmental biology.

Integrin β3 inhibition is a therapeutic strategy for supravalvular aortic stenosis

R. Hinton, Jiesi Luo, G. Tellides, 2016, The Journal of experimental medicine.

Elastin Haploinsufficiency Results in Progressive Aortic Valve Malformation and Latent Valve Disease in a Mouse Model

Varun K. Krishnamurthy, Dean Y. Li, D. Narmoneva, 2010, Circulation research.

The presence of bicuspid aortic valve does not predict ventricular septal defect type

R. Hinton, L. Cripe, W. Border, 2008, American journal of medical genetics. Part A.

Direct effects of oxygenated crystalloid or blood cardioplegia on isolated myocyte contractile function.

R. Hinton, F. Spinale, B. Dorman, 1996, The Journal of thoracic and cardiovascular surgery.

Developmental differences in myocyte contractile response after cardioplegic arrest.

R. Hinton, P. Gillette, J. Stratton, 1996, The Journal of thoracic and cardiovascular surgery.

Molecular Mechanisms of Heart Valve Development and Disease

R. Hinton, K. Yutzey, Christina M. Alfieri, 2016 .

Genetic testing practices in infants with congenital heart disease.

R. Hinton, K. Sund, S. Ware, 2014, Congenital heart disease.

Persistent left superior vena cava: an overlooked feature of CHARGE syndrome?

R. Hinton, S. Ware, P. Goldenberg, 2015 .

Tetrasomy 15q25.2 → qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation

R. Hinton, D. Witte, R. Hopkin, 2012, American journal of medical genetics. Part A.

Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest

R. Hinton, M. Campbell, R. Czosek, 2015, American journal of medical genetics. Part A.

Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.

J. Towbin, R. Hinton, S. Ware, 2012, Journal of cardiac failure.

Hormonal Regulation of Prostaglandin E2 Receptors: Localization and Expression in Rat Cervical Tissue

R. Hinton, R. Ittenbach, P. Grigsby, 2010, Reproductive Sciences.

Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiency.

C. Morris, R. Hinton, D. Benson, 2006, The Journal of heart valve disease.

Significance of reverse orientation of the ductus arteriosus in neonates with pulmonary outflow tract obstruction for early intervention.

R. Hinton, E. Michelfelder, 2006, The American journal of cardiology.

Hypoplastic left heart syndrome is associated with structural and vascular placental abnormalities and leptin dysregulation.

R. Hinton, L. Muglia, J. Cnota, 2015, Placenta.

Approach to Risk Genetic and Environmental Factors Contributing to Cardiovascular Malformation: A Unified

R. Hinton, 2013 .

Hypoplastic left heart syndrome is heritable.

Lisa J. Martin, R. Hinton, L. Cripe, 2007, Journal of the American College of Cardiology.

Immersed smoothed finite element method for fluid–structure interaction simulation of aortic valves

G. Liu, Jianyao Yao, D. Narmoneva, 2012, Computational Mechanics.

First principles.

R. Hinton, Robert B Hinton, 2016, The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha.

Physiological Growth, Remodeling Potential, and Preserved Function of a Novel Bioprosthetic Tricuspid Valve: Tubular Bioprosthesis Made of Small Intestinal Submucosa-Derived Extracellular Matrix.

D. Narmoneva, R. Hinton, M. Taylor, 2015, Journal of the American College of Cardiology.

The family history: reemergence of an established tool.

R. Hinton, Robert B Hinton, 2008, Critical care nursing clinics of North America.

Familial co-occurrence of congenital heart defects follows distinct patterns

Robert H. Anderson, S. Brunak, C. Workman, 2017, European heart journal.

Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

S. Lalani, R. Hinton, C. Maslen, 2015, Journal of cardiovascular development and disease.

Genetic Testing in Pediatric Left Ventricular Noncompaction

R. Hinton, S. Ware, R. Ittenbach, 2017, Circulation. Cardiovascular genetics.

Differential expression of cartilage and bone-related proteins in pediatric and adult diseased aortic valves.

R. Hinton, K. Yutzey, Elaine E. Wirrig, 2011, Journal of molecular and cellular cardiology.

38. Hypoplastic Left Heart Syndrome

R. Hinton, D. Benson, 2012 .

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes

R. Hinton, B. Landis, D. Cooper, 2015, Cardiology in the Young.

Twins With Progressive Thoracic Aortic Aneurysm, Recurrent Dissection and ACTA2 Mutation

R. Hinton, B. Landis, S. Ware, 2014, Pediatrics.

Genetics of Bicuspid Aortic Valve and Calcific Aortic Valve Disease

R. Hinton, 2013 .

Chapter 7 Genetics of Bicuspid Aortic Valve and Calcific Aortic Valve Disease

R. Hinton, 2013 .

Aorta Measurements are Heritable and Influenced by Bicuspid Aortic Valve

Lisa J. Martin, E. Demerath, R. Hinton, 2011, Front. Gene..

Genetics of Cardiovascular Disease in the Young

Lisa J. Martin, R. Hinton, D. Benson, 2012 .

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity

A. Jegga, T. Foroud, R. Hinton, 2017, Journal of Cardiovascular Translational Research.

Preservation of myocyte contractile function after hyperthermic cardioplegic arrest by activation of ATP-sensitive potassium channels.

R. Hinton, F. Spinale, B. Dorman, 1997, Circulation.

Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations

R. Hinton, G. Andelfinger, L. Cripe, 2007, Human Genetics.

A pediatric approach to family history of cardiovascular disease: diagnosis, risk assessment, and management.

R. Hinton, E. Miller, 2014, Pediatric clinics of North America.

Genetic and Environmental Factors Contributing to Cardiovascular Malformation: A Unified Approach to Risk

R. Hinton, 2013, Journal of the American Heart Association.

Horner's syndrome after coronary artery bypass surgery

J. Gold, R. Hinton, M. Heinemann, 1996, Neurology.

Replacement of the Aortic Valve in a Patient with Mucolipidosis III

R. Hinton, S. Ware, L. Cripe, 2009, Cardiology in the Young.

Extracellular Matrix Remodeling and Organization in Developing and Diseased Aortic Valves

R. Hinton, P. Manning, K. Yutzey, 2006, Circulation research.

Maladaptive matrix remodeling and regional biomechanical dysfunction in a mouse model of aortic valve disease.

Varun K. Krishnamurthy, F. Guilak, D. Narmoneva, 2012, Matrix biology : journal of the International Society for Matrix Biology.

Scleraxis Is Required for Cell Lineage Differentiation and Extracellular Matrix Remodeling During Murine Heart Valve Formation In Vivo

R. Hinton, K. Kadler, J. Lincoln, 2008, Circulation research.

Aortic atheroma is related to outcome but not numbers of emboli during coronary bypass.

G. Hartman, J. Gold, F. Yao, 1997, The Annals of thoracic surgery.

KPT-330 Prevents Aortic Valve Calcification via a Novel C/EBPβ Signaling Pathway

R. Hinton, J. Thompson, Karthik M. Kodigepalli, 2021, Circulation research.

Early Aberrant Angiogenesis Due to Elastic Fiber Fragmentation in Aortic Valve Disease

J. Smith, R. Hinton, A. Juraszek, 2013, Journal of cardiovascular development and disease.

Proteomic Alterations Associated with Biomechanical Dysfunction are Early Processes in the Emilin1 Deficient Mouse Model of Aortic Valve Disease

A. Jegga, D. Narmoneva, R. Hinton, 2017, Annals of Biomedical Engineering.

Inhibition of MAPK‐Erk pathway in vivo attenuates aortic valve disease processes in Emilin1‐deficient mouse model

A. Jegga, J. Smith, R. Hinton, 2017, Physiological reports.

Valve Endothelial Cell–Derived Tgf&bgr;1 Signaling Promotes Nuclear Localization of Sox9 in Interstitial Cells Associated With Attenuated Calcification

William C. Ray, R. Hinton, D. Heistad, 2016, Arteriosclerosis, thrombosis, and vascular biology.

COX2 Inhibition Reduces Aortic Valve Calcification In Vivo

R. Hinton, K. Yutzey, Elaine E. Wirrig, 2015, Arteriosclerosis, thrombosis, and vascular biology.

Review of Molecular and Mechanical Interactions in the Aortic Valve and Aorta: Implications for the Shared Pathogenesis of Aortic Valve Disease and Aortopathy

Varun K. Krishnamurthy, L. Hiratzka, J. Smith, 2014, Journal of Cardiovascular Translational Research.

Advances in the treatment of aortic valve disease: is it time for companion diagnostics?

R. Hinton, Robert B Hinton, 2014, Current opinion in pediatrics.

TGF-β mediates early angiogenesis and latent fibrosis in an Emilin1-deficient mouse model of aortic valve disease

R. Hinton, G. Bressan, A. Opoka, 2014, Disease Models & Mechanisms.

Insufficient versican cleavage and Smad2 phosphorylation results in bicuspid aortic and pulmonary valves.

R. Hinton, M. Weinstein, H. Osińska, 2013, Journal of molecular and cellular cardiology.

Bicuspid Aortic Valve and Thoracic Aortic Aneurysm: Three Patient Populations, Two Disease Phenotypes, and One Shared Genotype

R. Hinton, 2012, Cardiology research and practice.

Preservation of myocyte contractile function after hypothermic, hyperkalemic cardioplegic arrest with 2, 3-butanedione monoxime.

R. Hinton, F. Spinale, B. Dorman, 1996, The Journal of thoracic and cardiovascular surgery.

Angiogenic microenvironment augments impaired endothelial responses under diabetic conditions.

Jennifer R. Hurley, D. Narmoneva, R. Hinton, 2014, American journal of physiology. Cell physiology.

MALDI Imaging Mass Spectrometry as a Lipidomic Approach to Heart Valve Research.

J. Mayer, D. Bichell, R. Caprioli, 2016, The Journal of heart valve disease.

Potassium channel opener-augmented cardioplegia: protection of myocyte contractility with chronic left ventricular dysfunction.

R. Hinton, F. Spinale, B. Dorman, 1997, Circulation.

Twist1 promotes heart valve cell proliferation and extracellular matrix gene expression during development in vivo and is expressed in human diseased aortic valves.

R. Hinton, Santanu Chakraborty, K. Yutzey, 2010, Developmental biology.

Prenatal Head Growth and White Matter Injury in Hypoplastic Left Heart Syndrome

R. Hinton, G. Andelfinger, D. Benson, 2008, Pediatric Research.

Inhibitory Role of Notch1 in Calcific Aortic Valve Disease

H. Garner, R. Hinton, V. Garg, 2011, PloS one.

Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve.

Lisa J. Martin, R. Hinton, L. Cripe, 2009, Journal of the American College of Cardiology.

Risk factors for aortic valve disease in bicuspid aortic valve: A family‐based study

Lisa J. Martin, R. Hinton, D. Benson, 2011, American journal of medical genetics. Part A.

Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosa.

J. Towbin, R. Hinton, S. Ware, 2012, Circulation. Heart failure.

Abnormalities of placental development and function are associated with the different fetal growth patterns of hypoplastic left heart syndrome and transposition of the great arteries.

R. Hinton, J. Cnota, H. Jones, 2020, Placenta.

Abnormalities of placental development and function are associated with the different fetal growth patterns of hypoplastic left heart syndrome and transposition of the great arteries

R. Hinton, J. Cnota, H. Jones, 2018, bioRxiv.

Clinical Stratification of Pediatric Patients with Idiopathic Thoracic Aortic Aneurysm.

Lisa J. Martin, R. Hinton, B. Landis, 2015, The Journal of pediatrics.

A fetus with hypertrophic cardiomyopathy, restrictive, and single-ventricle physiology, and a beta-myosin heavy chain mutation.

R. Hinton, S. Ware, B. Marino, 2010, The Journal of pediatrics.

Asymmetric Cell–Matrix and Biomechanical Abnormalities in Elastin Insufficiency Induced Aortopathy

Varun K. Krishnamurthy, J. Wansapura, D. Narmoneva, 2014, Annals of Biomedical Engineering.

Microcephaly is associated with early adverse neurologic outcomes in hypoplastic left heart syndrome

R. Hinton, P. Manning, J. Cnota, 2013, Pediatric Research.

Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing

R. Hinton, B. Landis, S. Ware, 2016, American Journal of Medical Genetics. Part A.

Heart Failure in Pediatric Patients With Congenital Heart Disease.

R. Hinton, S. Ware, 2017, Circulation research.

Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve.

R. Hinton, L. Cripe, M. Tabangin, 2009, Journal of the American College of Cardiology.

Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing

R. Hinton, B. Landis, S. Ware, 2016, American journal of medical genetics. Part A.

Regional structure-function relationships in mouse aortic valve tissue.

Varun K. Krishnamurthy, F. Guilak, D. Narmoneva, 2011, Journal of biomechanics.

Cardiovascular Development and Disease Cross Talk between Notch Signaling and Biomechanics in Human Aortic Valve Disease Pathogenesis

J. Smith, D. Narmoneva, R. Hinton, 2022 .

Periostin Is Required for Maturation and Extracellular Matrix Stabilization of Noncardiomyocyte Lineages of the Heart

R. Markwald, R. Hinton, J. Molkentin, 2008, Circulation research.

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes

R. Hinton, B. Landis, D. Cooper, 2015, Cardiology in the Young.