Circ Cardiovasc Genet -- Table of Contents (2 [5])

Volume 2, Issue 5; October, 2009

Editorial
Original Articles
Methods in Genetics and Clinical Interpretation

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	Editorial
	Desmosome Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy: Important Insight but Only Part of the Picture Jeffrey E. Saffitz Circ Cardiovasc Genet. 2009;2:415-417, doi:10.1161/CIRCGENETICS.109.909366 Extract \| Full Text \| PDF
	Original Articles
	Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study Zahurul A. Bhuiyan, Jan D.H. Jongbloed, Jasper van der Smagt, Paola M. Lombardi, Ans C.P. Wiesfeld, Marcel Nelen, Meyke Schouten, Roselie Jongbloed, Moniek G.P.J. Cox, Marleen van Wolferen, Luz M. Rodriguez, Isabelle C. van Gelder, Hennie Bikker, Albert J.H. Suurmeijer, Maarten P. van den Berg, Marcel M.A.M. Mannens, Richard N.W. Hauer, Arthur A.M. Wilde, and J. Peter van Tintelen Circ Cardiovasc Genet. 2009;2:418-427; published online before print August 1 2009, doi:10.1161/CIRCGENETICS.108.839829 Abstract \| Full Text \| PDF \| Supplemental Data \| Clinical Perspective
	Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy A. Dénise den Haan, Boon Yew Tan, Michelle N. Zikusoka, Laura Ibañez Lladó, Rahul Jain, Amy Daly, Crystal Tichnell, Cynthia James, Nuria Amat-Alarcon, Theodore Abraham, Stuart D. Russell, David A. Bluemke, Hugh Calkins, Darshan Dalal, and Daniel P. Judge Circ Cardiovasc Genet. 2009;2:428-435; published online before print June 3 2009, doi:10.1161/CIRCGENETICS.109.858217 Abstract \| Full Text \| PDF \| Data Supplement \| Clinical Perspective
	Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic Cardiomyopathy Juan Pablo Kaski, Petros Syrris, Maria Teresa Tome Esteban, Sharon Jenkins, Antonios Pantazis, John E. Deanfield, William J. McKenna, and Perry M. Elliott Circ Cardiovasc Genet. 2009;2:436-441; published online before print July 16 2009, doi:10.1161/CIRCGENETICS.108.821314 Abstract \| Full Text \| PDF \| Clinical Perspective
	Sarcomere Mutations in Cardiomyopathy With Left Ventricular Hypertrabeculation Lisa M. Dellefave, Peter Pytel, Stephanie Mewborn, Bassem Mora, Deborah L. Guris, Savitri Fedson, Darrel Waggoner, Ivan Moskowitz, and Elizabeth M. McNally Circ Cardiovasc Genet. 2009;2:442-449; published online before print July 24 2009, doi:10.1161/CIRCGENETICS.109.861955 Abstract \| Full Text \| PDF \| Clinical Perspective
	High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese Population Hsiang-Yu Lin, Kah-Wai Chong, Ju-Hui Hsu, Hsiao-Chi Yu, Chun-Che Shih, Cheng-Hung Huang, Shing-Jong Lin, Chen-Huan Chen, Chuan-Chi Chiang, Huey-Jane Ho, Pi-Chang Lee, Chuan-Hong Kao, Kang-Hsiang Cheng, Chuen Hsueh, and Dau-Ming Niu Circ Cardiovasc Genet. 2009;2:450-456; published online before print July 24 2009, doi:10.1161/CIRCGENETICS.109.862920 Abstract \| Full Text \| PDF \| Clinical Perspective
	Distinct Early Signaling Events Resulting From the Expression of the PRKAG2 R302Q Mutant of AMPK Contribute to Increased Myocardial Glycogen Karalyn D. Folmes, Anita Y.M. Chan, Debby P.Y. Koonen, Thomas C. Pulinilkunnil, István Baczkó, Beth E. Hunter, Stephanie Thorn, Michael F. Allard, Robert Roberts, Michael H. Gollob, Peter E. Light, and Jason R.B. Dyck Circ Cardiovasc Genet. 2009;2:457-466; published online before print July 15 2009, doi:10.1161/CIRCGENETICS.108.834564 Abstract \| Full Text \| PDF \| Clinical Perspective
	Genetic Variation at the Proprotein Convertase Subtilisin/Kexin Type 5 Gene Modulates High-Density Lipoprotein Cholesterol Levels Iulia Iatan, Zari Dastani, Ron Do, Daphna Weissglas-Volkov, Isabelle Ruel, Jenny C. Lee, Adriana Huertas-Vazquez, Marja-Riitta Taskinen, Annik Prat, Nabil G. Seidah, Päivi Pajukanta, James C. Engert, and Jacques Genest Circ Cardiovasc Genet. 2009;2:467-475; published online before print August 22 2009, doi:10.1161/CIRCGENETICS.109.877811 Abstract \| Full Text \| PDF \| Clinical Perspective
	EPHB4 Gene Polymorphisms and Risk of Intracranial Hemorrhage in Patients With Brain Arteriovenous Malformations Shantel Weinsheimer, Helen Kim, Ludmila Pawlikowska, Yongmei Chen, Michael T. Lawton, Stephen Sidney, Pui-Yan Kwok, Charles E. McCulloch, and William L. Young Circ Cardiovasc Genet. 2009;2:476-482; published online before print August 22 2009, doi:10.1161/CIRCGENETICS.109.883595 Abstract \| Full Text \| PDF \| Data Supplement \| Clinical Perspective
	A Common Copy Number Variation on Chromosome 6 Association With the Gene Expression Level of Endothelin 1 in Transformed B Lymphocytes From Three Racial Groups Yan V. Sun, Patricia A. Peyser, and Sharon L.R. Kardia Circ Cardiovasc Genet. 2009;2:483-488; published online before print August 2 2009, doi:10.1161/CIRCGENETICS.109.848754 Abstract \| Full Text \| PDF \| Data Supplement \| Clinical Perspective
	Refining Molecular Pathways Leading to Calcific Aortic Valve Stenosis by Studying Gene Expression Profile of Normal and Calcified Stenotic Human Aortic Valves Yohan Bossé, Ahmed Miqdad, Dominique Fournier, Andrée Pépin, Philippe Pibarot, and Patrick Mathieu Circ Cardiovasc Genet. 2009;2:489-498; published online before print July 8 2009, doi:10.1161/CIRCGENETICS.108.820795 Abstract \| Full Text \| PDF \| Data Supplement \| Clinical Perspective
	Variation in the 4q25 Chromosomal Locus Predicts Atrial Fibrillation After Coronary Artery Bypass Graft Surgery Simon C. Body, Charles D. Collard, Stanton K. Shernan, Amanda A. Fox, Kuang-Yu Liu, Marylyn D. Ritchie, Tjörvi E. Perry, Jochen D. Muehlschlegel, Sary Aranki, Brian S. Donahue, Mias Pretorius, Juan-Carlos Estrada, Patrick T. Ellinor, Christopher Newton-Cheh, Christine E. Seidman, J.G. Seidman, Daniel S. Herman;, Peter Lichtner, Thomas Meitinger, Arne Pfeufer, Stefan Kääb, Nancy J. Brown, Dan M. Roden, and Dawood Darbar Circ Cardiovasc Genet. 2009;2:499-506; published online before print August 2 2009, doi:10.1161/CIRCGENETICS.109.849075 Abstract \| Full Text \| PDF \| Supplemental Data \| Clinical Perspective
	Alcohol Intake, Myocardial Infarction, Biochemical Risk Factors, and Alcohol Dehydrogenase Genotypes Janne S. Tolstrup, Morten Grønbæk, and Børge G. Nordestgaard Circ Cardiovasc Genet. 2009;2:507-514; published online before print August 22 2009, doi:10.1161/CIRCGENETICS.109.873604 Abstract \| Full Text \| PDF \| Clinical Perspective
	Common Variation in the Platelet Receptor P2RY12 Gene Is Associated With Residual On-Clopidogrel Platelet Reactivity in Patients Undergoing Elective Percutaneous Coronary Interventions Goran Rudez, Heleen J. Bouman, Jochem W. van Werkum, Frank W.G. Leebeek, Adrian Kruit, Hendrik J.T. Ruven, Jurriën M. ten Berg, Moniek P.M. de Maat, and Christian M. Hackeng Circ Cardiovasc Genet. 2009;2:515-521; published online before print July 24 2009, doi:10.1161/CIRCGENETICS.109.861799 Abstract \| Full Text \| PDF \| Data Supplement \| Clinical Perspective
	Functional Variant Disrupts Insulin Induction of USF1: Mechanism for USF1-Associated Dyslipidemias Jussi Naukkarinen, Emma Nilsson, Heikki A. Koistinen, Sanni Söderlund, Valeriya Lyssenko, Allan Vaag, Pernille Poulsen, Leif Groop, Marja-Riitta Taskinen, and Leena Peltonen Circ Cardiovasc Genet. 2009;2:522-529; published online before print June 12 2009, doi:10.1161/CIRCGENETICS.108.840421 Abstract \| Full Text \| PDF \| Data Supplement \| Clinical Perspective
	Methods in Genetics and Clinical Interpretation
	Single-Nucleotide Polymorphism Bioinformatics: A Comprehensive Review of Resources Andrew D. Johnson Circ Cardiovasc Genet. 2009;2:530-536, doi:10.1161/CIRCGENETICS.109.872010 Extract \| Full Text \| PDF \| Data Supplement

Spotlight

TOC Spotlight File

Volume 2, Issue 5; October, 2009

Editorial

Desmosome Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy: Important Insight but Only Part of the Picture

Original Articles

Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study

Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic Cardiomyopathy

Sarcomere Mutations in Cardiomyopathy With Left Ventricular Hypertrabeculation

High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese Population

Distinct Early Signaling Events Resulting From the Expression of the PRKAG2 R302Q Mutant of AMPK Contribute to Increased Myocardial Glycogen

Genetic Variation at the Proprotein Convertase Subtilisin/Kexin Type 5 Gene Modulates High-Density Lipoprotein Cholesterol Levels

EPHB4 Gene Polymorphisms and Risk of Intracranial Hemorrhage in Patients With Brain Arteriovenous Malformations

A Common Copy Number Variation on Chromosome 6 Association With the Gene Expression Level of Endothelin 1 in Transformed B Lymphocytes From Three Racial Groups

Refining Molecular Pathways Leading to Calcific Aortic Valve Stenosis by Studying Gene Expression Profile of Normal and Calcified Stenotic Human Aortic Valves

Variation in the 4q25 Chromosomal Locus Predicts Atrial Fibrillation After Coronary Artery Bypass Graft Surgery

Alcohol Intake, Myocardial Infarction, Biochemical Risk Factors, and Alcohol Dehydrogenase Genotypes

Common Variation in the Platelet Receptor P2RY12 Gene Is Associated With Residual On-Clopidogrel Platelet Reactivity in Patients Undergoing Elective Percutaneous Coronary Interventions

Functional Variant Disrupts Insulin Induction of USF1: Mechanism for USF1-Associated Dyslipidemias

Methods in Genetics and Clinical Interpretation

Single-Nucleotide Polymorphism Bioinformatics: A Comprehensive Review of Resources

Spotlight