V. Garg

发表

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease

Peter White, Sara Fitzgerald-Butt, Kim L. McBride, 2016, Circulation. Cardiovascular genetics.

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Jonathan C. Cohen, D. Srivastava, R. Matsuoka, 2003, Nature.

Mutations in NOTCH1 cause aortic valve disease

D. Srivastava, Alecia N. Muth, V. Garg, 2005, Nature.

Genetic Abnormalities in FOXP1 Are Associated with Congenital Heart Defects

K. McBride, S. Harrison, V. Garg, 2013, Human mutation.

Compacting the heart with Notch

V. Garg, C. Misra, 2013, Nature Medicine.

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

Gustavo Glusman, Paul Scheet, Mark Yandell, 2014, Nature Biotechnology.

Exploring trends and factors related to hookah use among college students: A cross-Sectional survey

V. Garg, Nishu Singla, Ritesh Singla, 2018 .

Another Notch in the Genetic Puzzle of Tetralogy of Fallot.

V. Garg, J. Yasuhara, Adrianna Matos‐Nieves, 2019, Circulation research.

Lifetime prevalence of sexual intercourse and contraception use at last sex among adolescents and young adults with congenital heart disease.

K. McBride, S. Fitzgerald-Butt, C. Gerhardt, 2015, The Journal of adolescent health : official publication of the Society for Adolescent Medicine.

Evidence of Aortopathy in Mice with Haploinsufficiency of Notch1 in Nos3-Null Background

B. Lilly, K. Bosse, V. Garg, 2015, Journal of cardiovascular development and disease.

Molecular genetic mechanisms of congenital heart disease.

V. Garg, T. Z. Choudhury, 2022, Current opinion in genetics & development.

Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery

K. McBride, Gloria A. Zender, S. Fitzgerald-Butt, 2022, PLoS genetics.

Galectin-3 and sST2 as Prognosticators for Heart Failure Requiring Extracorporeal Life Support: Jack n’ Jill

V. Garg, A. Yates, Jianli Bi, 2021, Biomolecules.

Loss of Jagged1 in mature endothelial cells causes vascular dysfunction with alterations in smooth muscle phenotypes.

Patricia E. Mccallinhart, B. Lilly, G. Agarwal, 2022, Vascular pharmacology.

MicroRNA miR 145 Regulates TGFBR 2 Expression and Matrix Synthesis in Vascular Smooth Muscle Cells

B. Lilly, V. Garg, S. Koenig, 2014 .

Percutaneous Patent Ductus Arteriosus (PDA) Closure in Very Preterm Infants: Feasibility and Complications

J. Cheatham, V. Garg, S. Cheatham, 2016, Journal of the American Heart Association.

Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation.

Madhumita Basu, V. Garg, Sheng-Wei Chang, 2014, Human molecular genetics.

and atrioventricular septation

Madhumita Basu, V. Garg, Sheng-Wei Chang, 2014 .

Congenital Heart Disease–Causing Gata4 Mutation Displays Functional Deficits In Vivo

D. Srivastava, W. Pu, N. Sachan, 2012, PLoS genetics.

Growth of the Normal Human Heart

V. Garg, 2012 .

Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.

D. Srivastava, J. Richardson, C. Lo, 2009, Developmental biology.

Inhibition of BKCa channels protects neonatal hearts against myocardial ischemia and reperfusion injury

V. Garg, Harpreet Singh, Devasena Ponnalagu, 2021, bioRxiv.

Early versus delayed umbilical cord clamping in infants with congenital heart disease: a pilot, randomized, controlled trial

T. M. Hoffman, V. Garg, J. Bauer, 2015, Journal of Perinatology.

Assessment of large copy number variants in patients with apparently isolated congenital left‐sided cardiac lesions reveals clinically relevant genomic events

Mahshid S. Azamian, J. Belmont, J. Towbin, 2017, American journal of medical genetics. Part A.

The Role of Lipoprotein(a) in Calcific Aortic Valve Disease: Insights From a Large-Cohort Genetic Study.

V. Garg, 2017, JAMA cardiology.

Patent Ductus Arteriosus: A Contemporary Perspective for the Pediatric and Adult Cardiac Care Provider

Elaine L. Shelton, P. McNamara, M. Mah, 2022, Journal of the American Heart Association.

Single-cell transcriptomic profiling unveils dysregulation of cardiac progenitor cells and cardiomyocytes in a mouse model of maternal hyperglycemia

Xinmin Zhang, Madhumita Basu, Karthik M. Kodigepalli, 2022, Communications Biology.

Single-cell RNA-sequencing analysis of aortic valve interstitial cells demonstrates the regulation of integrin signaling by nitric oxide

Madhumita Basu, S. Manivannan, V. Garg, 2022, Frontiers in Cardiovascular Medicine.

Dynamic Heterogeneity of the Heart Valve Interstitial Cell Population in Mitral Valve Health and Disease

R. Norris, V. Garg, Lindsey J. Anstine, 2015, Journal of cardiovascular development and disease.

Shaping the future heart: transgenerational outcomes of maternal metabolic syndrome.

Madhumita Basu, V. Garg, A. Trask, 2019, American journal of physiology. Heart and circulatory physiology.

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

W. Chung, J. Priest, W. Pu, 2018, Circulation.

Genetics of Valvular Heart Disease

S. LaHaye, V. Garg, J. Lincoln, 2014, Current Cardiology Reports.

Impact of maternal hyperglycemia on cardiac development: Insights from animal models

Madhumita Basu, V. Garg, U. Majumdar, 2021, Genesis.

A Multi-Omics Approach Using a Mouse Model of Cardiac Malformations for Prioritization of Human Congenital Heart Disease Contributing Genes

K. McBride, S. Manivannan, P. White, 2021, Frontiers in Cardiovascular Medicine.

Decoding Genetics of Congenital Heart Disease Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs)

K. McBride, V. Garg, Ming-Tao Zhao, 2021, Frontiers in Cell and Developmental Biology.

Genetics of congenital heart disease: a narrative review of recent advances and clinical implications

V. Garg, J. Yasuhara, 2021, Translational pediatrics.

Endothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract

K. Bosse, V. Garg, F. Radtke, 2016, Journal of the American Heart Association.

Endothelial Notch 1 Is Required for Proper Development of the Semilunar Valves and Cardiac Out fl ow Tract

K. Bosse, V. Garg, F. Radtke, 2016 .

Molecular Basis of Cardiac Development and Congenital Heart Disease

V. Garg, 2012 .

Impact of Mendelian inheritance in cardiovascular disease

K. McBride, V. Garg, 2010, Annals of the New York Academy of Sciences.

Genetics of Congenital Heart Disease

V. Garg, Ashleigh A Richards, 2010, Current cardiology reviews.

Review Insights into the genetic basis of congenital heart disease

Harry Hines Boulevard, V. Garg, 2006 .

Insights into the genetic basis of congenital heart disease

V. Garg, Vidu Garg, 2006, Cellular and Molecular Life Sciences CMLS.

Genetic Underpinnings of Cardiogenesis and Congenital Heart Disease

D. Srivastava, V. Garg, 2005 .

Notch1 Signaling and Aortic Valve Disease: From Human Genetics to Mouse Models

V. Garg, U. Majumdar, Uddalak Majumdar, 2017 .

Genetics of aortic valve disease

V. Garg, J. Yasuhara, R. Ackah, 2023, Current opinion in cardiology.

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects.

D. Srivastava, R. Matsuoka, V. Garg, 1999, Science.

Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development.

D. Srivastava, I. S. Kathiriya, V. Garg, 2001, Developmental biology.

GATA4 sequence variants in patients with congenital heart disease

C. Maslen, E. Goldmuntz, V. Garg, 2007, Journal of Medical Genetics.

congenital heart disease sequence variants in patients with GATA4

C. Maslen, E. Goldmuntz, V. Garg, 2008 .

and E Goldmuntz congenital heart disease sequence variants in patients withGATA 4

C. Maslen, V. Garg, A. Tomita‐Mitchell, 2007 .

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

Mahshid S. Azamian, J. Lupski, S. Leal, 2016, Human molecular genetics.

Fetal and postnatal lung defects reveal a novel and required role for Fgf8 in lung development.

A. Moon, Shibing Yu, K. Albertine, 2010, Developmental biology.

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.

Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

A. Zinn, V. Garg, Sheng-Wei Chang, 2012, Pediatric Cardiology.

Single-Cell RNA Sequencing Reveals Novel Genes Regulated by Hypoxia in the Lung Vasculature

B. Lilly, S. Manivannan, V. Garg, 2022, Journal of Vascular Research.

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

R. Siebert, J. Coselli, K. Devriendt, 2020, bioRxiv.

Molecular genetics of aortic valve disease

V. Garg, Vidu Garg, 2006, Current opinion in cardiology.

Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy

K. McBride, S. Fitzgerald-Butt, Zhe Han, 2019, bioRxiv.

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

A. Zinn, V. Garg, N. Hauser, 2008, Pediatric Research.

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

Lisa J. Martin, Julie A. Phillippi, P. Kirshbom, 2021, HGG advances.

Nitric oxide prevents aortic valve calcification by S-nitrosylation of USP9X to activate NOTCH signaling

E. Aikawa, S. Cole, Madhumita Basu, 2020, Science Advances.

Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis

V. Garg, L. Villeneuve, M. Mamarbachi, 2018, Journal of cellular physiology.

Use of Machine Learning to Classify High Risk Variants of Uncertain Significance in Lamin A/C Cardiac Disease.

K. McBride, J. Leonard, P. White, 2021, Heart rhythm.

Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association

M. Perez, C. Fox, D. Roden, 2016, Circulation. Cardiovascular genetics.

Chromosomal haplotypes by genetic phasing of human families.

Jared C. Roach, Gustavo Glusman, David J. Galas, 2011, American journal of human genetics.

Epigenetic mechanisms underlying maternal diabetes-associated risk of congenital heart disease.

Madhumita Basu, K. Jiao, Zhe Han, 2017, JCI insight.

Measuring genetic knowledge: a brief survey instrument for adolescents and adults

A. Bodine, K. McBride, S. Fitzgerald-Butt, 2016, Clinical genetics.

Notch1 haploinsufficiency causes ascending aortic aneurysms in mice.

B. Lilly, S. LaHaye, V. Garg, 2017, JCI insight.

MicroRNA miR145 Regulates TGFBR2 Expression and Matrix Synthesis in Vascular Smooth Muscle Cells

B. Lilly, V. Garg, S. Koenig, 2015, Circulation research.

A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L

D. Srivastava, Kathryn N. Ivey, V. Garg, 2001, Mechanisms of Development.

Human Stem Cell Models of SARS-CoV-2 Infection in the Cardiovascular System

M. Peeples, V. Garg, Ming-Tao Zhao, 2021, Stem Cell Reviews and Reports.

In Vivo and In Vitro Genetic Models of Congenital Heart Disease.

V. Garg, J. Yasuhara, U. Majumdar, 2019, Cold Spring Harbor perspectives in biology.

Impaired Human Cardiac Cell Development due to NOTCH1 Deficiency

Joe Z. Zhang, V. Garg, I. Deschênes, 2022, Circulation research.

Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms

Madhumita Basu, V. Garg, 2018, Birth defects research.

Etiology of valvular heart disease-genetic and developmental origins.

V. Garg, J. Lincoln, 2014, Circulation journal : official journal of the Japanese Circulation Society.

Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease.

B. Lilly, S. LaHaye, K. Bosse, 2013, Journal of molecular and cellular cardiology.

Cardiomyocyte Proliferation and Maturation: Two Sides of the Same Coin for Heart Regeneration

V. Garg, Ming-Tao Zhao, Shi-qiao Ye, 2020, Frontiers in Cell and Developmental Biology.

A Randomized Clinical Trial Demonstrating Feasibility and Preliminary Efficacy of a Videoconference-Delivered Physical Activity Lifestyle Intervention Among Adolescents With a Congenital Heart Defect.

J. Rausch, J. Jackson, V. Garg, 2021, Annals of behavioral medicine : a publication of the Society of Behavioral Medicine.

Probing single ventricle heart defects with patient‐derived induced pluripotent stem cells and emerging technologies

V. Garg, Ming-Tao Zhao, Karen Texter, 2022, Birth defects research.

Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors

E. Zmuda, K. McBride, S. Fitzgerald-Butt, 2019, Pediatric Cardiology.

Single-cell Transcriptomic Profiling Unveils Cardiac Cell-type Specific Response to Maternal Hyperglycemia Underlying the Risk of Congenital Heart Defects

Madhumita Basu, Xinmin Zhang, Karthik M. Kodigepalli, 2021, bioRxiv.

Maternal hyperglycemia impedes second heart field-derived cardiomyocyte differentiation to elevate the risk of congenital heart defects

Madhumita Basu, Xinmin Zhang, Karthik M. Kodigepalli, 2021 .

The Association of Global and Disease-Related Stress With Susceptibility to and Use of E-Cigarettes and Marijuana Among Adolescents With Congenital Heart Disease.

J. Rausch, A. Ferketich, J. Jackson, 2023, Journal of pediatric psychology.

Inhibition of Notch1 Signaling Reduces Abdominal Aortic Aneurysm in Mice by Attenuating Macrophage-Mediated Inflammation

H. Kuivaniemi, V. Garg, N. Huang, 2012, Arteriosclerosis, thrombosis, and vascular biology.

Spectrum of heart disease associated with murine and human GATA4 mutation.

Karl W Broman, Deepak Srivastava, Ani Manichaikul, 2007, Journal of molecular and cellular cardiology.

Beyond genetics: focusing on maternal environment for congenital heart disease prevention

Madhumita Basu, V. Garg, 2013, Evidence-Based Medicine.

Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated GATA4 mutation

S. LaHaye, V. Garg, S. Koenig, 2019, Disease Models & Mechanisms.

Congenital aortic valve stenosis: from pathophysiology to molecular genetics and the need for novel therapeutics

Amee M. Bigelow, V. Garg, J. Yasuhara, 2023, Frontiers in Cardiovascular Medicine.

Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve

K. McBride, S. Fitzgerald-Butt, M. Mah, 2017, Pediatric Cardiology.

Inhibitory Role of Notch1 in Calcific Aortic Valve Disease

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

Genetic basis of aortic valvular disease

V. Garg, J. Lincoln, S. Koenig, 2017, Current opinion in cardiology.

Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve

K. McBride, S. Fitzgerald-Butt, P. White, 2014, BMC Medical Genomics.

Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve

K. McBride, S. Fitzgerald-Butt, P. White, 2014, BMC Medical Genomics.

Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve

K. McBride, S. Fitzgerald-Butt, S. LaHaye, 2014, Pediatric Research.

miR‐145 transgenic mice develop cardiopulmonary complications leading to postnatal death

B. Lilly, Karthik M. Kodigepalli, S. Manivannan, 2021, Physiological reports.

Pharmacological Inhibitor of Notch Signaling Stabilizes the Progression of Small Abdominal Aortic Aneurysm in a Mouse Model

H. Kuivaniemi, V. Garg, S. Koenig, 2014, Journal of the American Heart Association.

Identification of GATA6 Sequence Variants in Patients With Congenital Heart Defects

D. Srivastava, V. Garg, S. Koenig, 2010, Pediatric Research.

Identification of GATA6 sequence variants in patients with congenital heart defects.

D. Srivastava, V. Garg, S. Koenig, 2010, Pediatric research.

A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death.

J. Joglar, V. Garg, H. Yin, 2009, Heart rhythm.

phenotypic modulation and the response to injury? Can microRNAs control vascular smooth muscle

W. Sessa, B. Lilly, V. Garg, 2015 .

Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease

N. Abate, M. Chandalia, I. S. Kathiriya, 2007, American journal of medical genetics. Part A.

Subtype‐specific cardiomyocytes for precision medicine: Where are we now?

V. Garg, Ming-Tao Zhao, Ningyi Shao, 2020, Stem cells.

Endocardial HDAC3 is required for myocardial trabeculation

M. Looso, V. Garg, C. Cai, 2023, bioRxiv.

Notch Signaling in Aortic Valve Development and Disease

V. Garg, 2016 .

Heredity of bicuspid aortic valve: is family screening indicated?

K. McBride, V. Garg, 2011, Heart.

Generation of an induced pluripotent stem cell line (NCHi010-A) from a 6-year-old female with down syndrome and without congenital heart disease.

K. Manickam, V. Garg, Ming-Tao Zhao, 2023, Stem cell research.

Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects.

V. Garg, Ming-Tao Zhao, Karen Texter, 2023, Stem cell research.

Natian and Ryabhatta—graphical user interfaces to create, analyze and visualize single-cell transcriptomic datasets

S. Manivannan, V. Garg, 2021, bioRxiv.

Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitis.

Amee M. Bigelow, V. Garg, M. Galantowicz, 2023, Pediatric research.

A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.

Mahshid S. Azamian, S. Lalani, B. Landis, 2023, Journal of the American Heart Association.

Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated GATA4 mutation

S. LaHaye, V. Garg, S. Koenig, 2019, Disease Models & Mechanisms.

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome

M. Werler, M. Bamshad, T. Ojala, 2023, HGG advances.

Cardiovascular Development and Disease Evidence of Aortopathy in Mice with Haploinsufficiency of Notch1 in Nos3-null Background

B. Lilly, K. Bosse, V. Garg, 2022 .