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Molecular Genetic Basis of Hypertrophic Cardiomyopathy

Circulation research, 2021-05, Vol.128 (10), p.1533-1553

Marian, A J

2021

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The Hippo Pathway Is Activated and Is a Causal Mechanism for Adipogenesis in Arrhythmogenic Cardiomyopathy

Circulation research, 2014-01, Vol.114 (3), p.454-468

2014

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Strategic Approaches to Unraveling Genetic Causes of Cardiovascular Diseases

Circulation research, 2011-05, Vol.108 (10), p.1252-1269

2011

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Nuclear Plakoglobin Is Essential for Differentiation of Cardiac Progenitor Cells to Adipocytes in Arrhythmogenic Right Ventricular Cardiomyopathy

Circulation research, 2011-12, Vol.109 (12), p.1342-1353

2011

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The Discovery of the ACE2 Gene

Circulation research, 2013-05, Vol.112 (10), p.1307-1309

Marian, A.J

2013

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Introduction to Cardiovascular Aging Compendium: “Aging as the Quintessential Complex Phenotype”

Circulation research, 2018-09, Vol.123 (7), p.737-739

2018

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MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II

Human molecular genetics, 2007-10, Vol.16 (20), p.2453-2462

2007

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Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 2004-03, Vol.109 (10), p.1284-1291

2004

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Genetic Causality in Complex Traits

Journal of the American College of Cardiology, 2016-02, Vol.67 (4), p.417-419

Marian, A.J., MD

2016

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The Molecular Genetic Basis for Hypertrophic Cardiomyopathy

Journal of molecular and cellular cardiology, 2001-04, Vol.33 (4), p.655-670

2001

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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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A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

Human molecular genetics, 2012-01, Vol.21 (2), p.358-370

2012

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Yeast one-hybrid assays: A historical and technical perspective

Methods (San Diego, Calif.), 2012-08, Vol.57 (4), p.441-447

2012

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Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome

Circulation (New York, N.Y.), 2005-01, Vol.111 (1), p.21-29

2005

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Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy

Circulation (New York, N.Y.), 2001-07, Vol.104 (2), p.128-130

2001

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Prevention of Cardiac Hypertrophy by Atorvastatin in a Transgenic Rabbit Model of Human Hypertrophic Cardiomyopathy

Circulation research, 2005-08, Vol.97 (3), p.285-292

2005

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Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease

Circulation (New York, N.Y.), 2003-07, Vol.108 (4), p.395-398

2003

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Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance

Brain (London, England : 1878), 2007-09, Vol.130 (9), p.2258-2266

2007

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Identification of a Genetic Locus for Familial Atrial Fibrillation

The New England journal of medicine, 1997-03, Vol.336 (13), p.905-911

1997

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Circulation Research and Human Genetic Studies

Circulation research, 2010-07, Vol.107 (1), p.6-8

2010

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Recent advances in the molecular genetics of hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 1995-09, Vol.92 (5), p.1336-1347

1995

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Molecular analysis of primary gastric cancer, corresponding xenografts, and 2 novel gastric carcinoma cell lines reveals novel alterations in gastric carcinogenesis

Human pathology, 2007-06, Vol.38 (6), p.903-913

2007

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Molecular genetic studies of complex phenotypes

Translational research : the journal of laboratory and clinical medicine, 2012-02, Vol.159 (2), p.64-79

Marian, Ali J

2012

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Power Asymmetry and Early Intervention in Divorce

Psychology, public policy, and law, 2023-08, Vol.29 (3), p.383-401

2023

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Molecular Genetic Basis of Hypertrophic Cardiomyopathy

The Hippo Pathway Is Activated and Is a Causal Mechanism for Adipogenesis in Arrhythmogenic Cardiomyopathy

Strategic Approaches to Unraveling Genetic Causes of Cardiovascular Diseases

Nuclear Plakoglobin Is Essential for Differentiation of Cardiac Progenitor Cells to Adipocytes in Arrhythmogenic Right Ventricular Cardiomyopathy

The Discovery of the ACE2 Gene

Introduction to Cardiovascular Aging Compendium: “Aging as the Quintessential Complex Phenotype”

MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II

Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy

Genetic Causality in Complex Traits

The Molecular Genetic Basis for Hypertrophic Cardiomyopathy

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Genomics in Cardiovascular Disease

A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

Yeast one-hybrid assays: A historical and technical perspective

Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome

Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy

Prevention of Cardiac Hypertrophy by Atorvastatin in a Transgenic Rabbit Model of Human Hypertrophic Cardiomyopathy

Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease

Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance

Identification of a Genetic Locus for Familial Atrial Fibrillation

Circulation Research and Human Genetic Studies

Recent advances in the molecular genetics of hypertrophic cardiomyopathy

Molecular analysis of primary gastric cancer, corresponding xenografts, and 2 novel gastric carcinoma cell lines reveals novel alterations in gastric carcinogenesis

Molecular genetic studies of complex phenotypes

Power Asymmetry and Early Intervention in Divorce

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