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JPH2 Mutant Gene Causes Familial Hypertrophic Cardiomyopathy

JACC. Basic to translational science, 2017-02, Vol.2 (1), p.68-70

Roberts, Robert, MD

2017

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Genetics: Implications for Prevention and Management of Coronary Artery Disease

Journal of the American College of Cardiology, 2016-12, Vol.68 (25), p.2797-2818

2016

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The MOGE(S) Classification for a Phenotype–Genotype Nomenclature of Cardiomyopathy

Journal of the American College of Cardiology, 2013-12, Vol.62 (22), p.2046-2072

2013

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Multiauthored International Publications

Journal of the American College of Cardiology, 2017-05, Vol.69 (18), p.2344-2346

Roberts, Robert, MD

2017

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Introducing JACC: Basic to Translational Science

JACC. Basic to translational science, 2016, Vol.1 (1), p.1-2

2016

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Mendelian Randomization Studies Promise to Shorten the Journey to FDA Approval

JACC. Basic to translational science, 2018-10, Vol.3 (5), p.690-703

Roberts, Robert, MD

2018

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Gene Dosage of the Common Variant 9p21 Predicts Severity of Coronary Artery Disease

Journal of the American College of Cardiology, 2010-08, Vol.56 (6), p.479-486

2010

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A genetic basis for coronary artery disease

Trends in cardiovascular medicine, 2015-04, Vol.25 (3), p.171-178

Roberts, Robert, MD, FRCPC, MACC, FAHA, FRSC, FCAHS, FESC, LLD (Hon.)

2015

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Haptoglobin, the Good and the Bad

Journal of the American College of Cardiology, 2013-02, Vol.61 (7), p.738-740

Roberts, Robert, MD

2013

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Discovery of a Gene Responsible for Sudden Cardiac Death

JACC. Clinical electrophysiology, 2017-03, Vol.3 (3), p.289-290

Roberts, Robert, MD

2017

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Genetics and Genomics of Single-Gene Cardiovascular Diseases

Journal of the American College of Cardiology, 2016-12, Vol.68 (25), p.2831-2849

2016

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Genomics in Cardiovascular Disease

Journal of the American College of Cardiology, 2013-05, Vol.61 (20), p.2029-2037

2013

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PCSK9 Inhibition—A New Thrust in the Prevention of Heart Disease: Genetics Does It Again

Canadian journal of cardiology, 2013-08, Vol.29 (8), p.899-901

Roberts, Robert, MD, FRCPC, MACC

2013

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The Editor’s Roundtable: Current Perspectives on Triglycerides and Atherosclerosis

The American journal of cardiology, 2015

2015

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Kinesin Family Member 6 Variant Trp719Arg Does Not Associate With Angiographically Defined Coronary Artery Disease in the Ottawa Heart Genomics Study

Journal of the American College of Cardiology, 2009-04, Vol.53 (16), p.1471-1472

2009

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Interferon-γ Activates Expression of p15 and p16 Regardless of 9p21.3 Coronary Artery Disease Risk Genotype

Journal of the American College of Cardiology, 2013-01, Vol.61 (2), p.143-147

2013

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Personalized Cardiovascular Medicine: Status in 2012

Canadian journal of cardiology, 2012-11, Vol.28 (6), p.693-699

2012

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Echocardiography: A Requisite Friend of the Cardiac Geneticist

Journal of the American Society of Echocardiography, 2011-07, Vol.24 (7), p.790-791

Roberts, Robert, MD, FRCPC, MACC

2011

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Reply

Journal of the American College of Cardiology, 2014, Vol.63 (23), p.2584-2586

2014

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Genes and Coronary Artery Disease

Journal of the American College of Cardiology, 2012-10, Vol.60 (18), p.1715-1721

2012

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Reply

Journal of the American College of Cardiology, 2011, Vol.57 (13), p.1498-1499

2011

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Genomics in coronary artery disease: Past, present and future

Canadian journal of cardiology, 2010-03, Vol.26, p.56A-59A

2010

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Identification of Myofilament Mutations: Its Role in the Diagnosis and Management of Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2008-06, Vol.83 (6), p.626-627

2008

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The Editor's Roundtable: Health Reform and Its Implications for Cardiovascular Medicine

The American journal of cardiology, 2010-02, Vol.105 (4), p.557-565

2010

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Genomics: Is It Ready for Primetime?

The Medical clinics of North America, 2012, Vol.96 (1), p.113-122

2012

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JPH2 Mutant Gene Causes Familial Hypertrophic Cardiomyopathy

Genetics: Implications for Prevention and Management of Coronary Artery Disease

The MOGE(S) Classification for a Phenotype–Genotype Nomenclature of Cardiomyopathy

Multiauthored International Publications

Introducing JACC: Basic to Translational Science

Mendelian Randomization Studies Promise to Shorten the Journey to FDA Approval

Gene Dosage of the Common Variant 9p21 Predicts Severity of Coronary Artery Disease

A genetic basis for coronary artery disease

Haptoglobin, the Good and the Bad

Discovery of a Gene Responsible for Sudden Cardiac Death

Genetics and Genomics of Single-Gene Cardiovascular Diseases

Genomics in Cardiovascular Disease

PCSK9 Inhibition—A New Thrust in the Prevention of Heart Disease: Genetics Does It Again

The Editor’s Roundtable: Current Perspectives on Triglycerides and Atherosclerosis

Kinesin Family Member 6 Variant Trp719Arg Does Not Associate With Angiographically Defined Coronary Artery Disease in the Ottawa Heart Genomics Study

Interferon-γ Activates Expression of p15 and p16 Regardless of 9p21.3 Coronary Artery Disease Risk Genotype

Personalized Cardiovascular Medicine: Status in 2012

Echocardiography: A Requisite Friend of the Cardiac Geneticist

Reply

Genes and Coronary Artery Disease

Reply

Genomics in coronary artery disease: Past, present and future

Identification of Myofilament Mutations: Its Role in the Diagnosis and Management of Hypertrophic Cardiomyopathy

The Editor's Roundtable: Health Reform and Its Implications for Cardiovascular Medicine

Genomics: Is It Ready for Primetime?

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