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List of works by Vidu Garg

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

scientific article

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

scientific article

A rare human sequence variant reveals myocardin autoinhibition

scientific article published on 13 October 2008

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

scientific article

Another Notch in the Genetic Puzzle of Tetralogy of Fallot

scientific article published on 01 February 2019

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

scientific article published on 26 November 2013

Chromosomal haplotypes by genetic phasing of human families

scientific article

Compacting the heart with Notch

scientific article published in February 2013

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

scientific article published on May 10, 2012

Corrigendum to "Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease" [J. Mol. Cell. Cardiol. 60 (2013) 27-35]

scientific article published on 31 May 2018

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

article by Ashleigh A Richards et al published October 2008 in Pediatric Research

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

scientific article published on 24 June 2019

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

scientific article

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

scientific article published on 30 July 2015

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

scientific article published on 22 April 2016

Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease.

scientific article published on 11 April 2013

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

scientific article published on 26 September 2016

Erratum: Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development

scholarly article published in European Journal of Human Genetics

Etiology of valvular heart disease-genetic and developmental origins

scientific article published on 07 July 2014

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

scientific article

GATA4 sequence variants in patients with congenital heart disease

scientific article published on December 2007

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

scientific article published on 01 November 2018

Genetic abnormalities in FOXP1 are associated with congenital heart defects

scientific article published on 11 July 2013

Genetic basis of aortic valvular disease.

scientific article published on 2 February 2017

Genetics of congenital heart disease

scientific article published on May 2010

Genetics of valvular heart disease

scientific article

Heredity of bicuspid aortic valve: is family screening indicated?

scientific article published on 01 April 2011

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.

scientific article

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

scientific article

Impact of Mendelian inheritance in cardiovascular disease ⬇️

scientific article published on October 19, 2010

Insights into the genetic basis of congenital heart disease.

scientific article

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

scientific journal article

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

scientific article published on April 2015

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

scientific article published on 01 December 2018

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

scientific article published on 29 May 2015

MicroRNA miR145 regulates TGFBR2 expression and matrix synthesis in vascular smooth muscle cells

scientific article

Mutations in NOTCH1 cause aortic valve disease

scientific article

Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis.

scientific article

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

scientific article published on 26 May 2020

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

scientific article published on 12 February 2016

Pharmacological inhibitor of notch signaling stabilizes the progression of small abdominal aortic aneurysm in a mouse model.

scientific article

Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve

scientific article published on 5 May 2014

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

scientific article published on 01 April 2007

Shaping the future heart: transgenerational outcomes of maternal metabolic syndrome

scientific article published on 15 March 2019

Spectrum of heart disease associated with murine and human GATA4 mutation

scientific journal article

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

scientific article published on 21 February 2012

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

scientific journal article

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

scientific article published on 12 November 2017

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

scientific article

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

scientific article published on 14 July 2016

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