All Stories

  1. Expression of Netrin-1 in the developing mouse heart

    Article • Gene Expression Patterns, December 2025, Elsevier

    Vidu Garg

  2. Loss of Methyltransferase and Hypomethylated m6A Sarcomere Transcripts Leading to Early-Onset Dilated Cardiomyopathy

    Article • Circulation, June 2025, Wolters Kluwer Health

    Vidu Garg

  3. Cardiovascular post-acute sequelae of SARS-CoV-2 in children and adolescents: cohort study using electronic health records

    Article • Nature Communications, April 2025, Springer Science + Business Media

    Vidu Garg

  4. Impact of genetic factors on antioxidant rescue of maternal diabetes–associated congenital heart disease

    Article • JCI Insight, December 2024, American Society for Clinical Investigation

    Vidu Garg

  5. Cell-Free RNA Signatures in Maternal Blood with Fetal Congenital Heart Disease

    Article • Circulation Research, October 2024, Wolters Kluwer Health

    Vidu Garg

  6. Case Report: An association of left ventricular outflow tract obstruction with 5p deletions

    Article • Frontiers in Genetics, October 2024, Frontiers

    Vidu Garg

  7. Characterization of an induced pluripotent stem cell line (NCHi013-A) from a 5-year-old male with pulmonary atresia with intact ventricular septum and a biventricular repair

    Article • Stem Cell Research, October 2024, Elsevier

    Vidu Garg

  8. Generation of an induced pluripotent stem cell line (NCHi016-A) from a 5-year-old female with pulmonary atresia with intact ventricular septum and one-and-half ventricle palliation

    Article • Stem Cell Research, October 2024, Elsevier

    Vidu Garg

  9. Generation of iPSC line NCHi015-A from a patient with truncus arteriosus carrying heterozygous variants in KMT2D and NOTCH1

    Article • Stem Cell Research, August 2024, Elsevier

    Vidu Garg

  10. Parental experiences of congenital heart disease transition care highlight the need for family-centered approaches

    Article • Evidence-Based Nursing, July 2024, BMJ

    Vidu Garg

  11. Endocardial HDAC3 is required for myocardial trabeculation

    Article • Nature Communications, May 2024, Springer Science + Business Media

    Vidu Garg

  12. Post-Acute Cardiovascular Outcomes of COVID-19 in Children and Adolescents: An EHR Cohort Study from the RECOVER Project

    Article • May 2024, Cold Spring Harbor Laboratory Press

    Vidu Garg

  13. Associations of Impulsivity and Risky Decision-Making with E-Cigarette-Related Outcomes Among Adolescents with Congenital Heart Disease: Variable- and Person-Oriented Approaches

    Article • Behavioral Medicine, May 2024, Taylor & Francis

    Vidu Garg

  14. Abnormal Progenitor Cell Differentiation and Cardiomyocyte Proliferation in Hypoplastic Right Heart Syndrome

    Article • Circulation, March 2024, Wolters Kluwer Health

    Vidu Garg

  15. Generation and characterization of a human induced pluripotent stem cell line heterozygous for a NOTCH1 mutation (NCHi014-A)

    Article • Stem Cell Research, February 2024, Elsevier

    Vidu Garg

  16. Characterization of an induced pluripotent stem cell line NCHi011-A from a 23-year-old female with Alagille Syndrome harboring a heterozygous JAG1 pathogenic variant

    Article • Stem Cell Research, October 2023, Elsevier

    Vidu Garg

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

    Article • Human Genetics and Genomics Advances, October 2023, Elsevier

    Vidu Garg

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

    Article • Journal of the American Heart Association, September 2023, Wolters Kluwer Health

    Vidu Garg

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

    Article • Pediatric Research, September 2023, Springer Science + Business Media

    Vidu Garg

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

    Article • Stem Cell Research, September 2023, Elsevier

    Vidu Garg

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

    Article • Stem Cell Research, September 2023, Elsevier

    Vidu Garg

  22. Generation of iPSC line NCHi012-A from a patient with Alagille syndrome and heterozygous pathogenic variant in the JAG1 gene

    Article • Stem Cell Research, September 2023, Elsevier

    Vidu Garg

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

    Article • Frontiers in Cardiovascular Medicine, April 2023, Frontiers

    Vidu Garg

  24. Endocardial HDAC3 is required for myocardial trabeculation

    Article • April 2023, Cold Spring Harbor Laboratory Press

    Vidu Garg

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

    Article • Journal of Pediatric Psychology, February 2023, Oxford University Press (OUP)

    Vidu Garg

  26. Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutation

    Article • Stem Cell Research, February 2023, Elsevier

    Vidu Garg

  27. Genetics of aortic valve disease

    Article • Current Opinion in Cardiology, January 2023, Wolters Kluwer Health

    Vidu Garg

  28. Impaired Human Cardiac Cell Development due to NOTCH1 Deficiency

    Article • Circulation Research, January 2023, Wolters Kluwer Health

    Vidu Garg

  29. A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

    Article • Genetics in Medicine Open, January 2023, Elsevier

    Vidu Garg

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

    Article • Frontiers in Cardiovascular Medicine, October 2022, Frontiers

    Vidu Garg

  31. Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS)

    Article • Stem Cell Research, October 2022, Elsevier

    Vidu Garg

  32. Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS)

    Article • Stem Cell Research, October 2022, Elsevier

    Vidu Garg

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

    Article • Journal of the American Heart Association, September 2022, Wolters Kluwer Health

    Vidu Garg

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

    Article • Communications Biology, August 2022, Springer Science + Business Media

    Vidu Garg

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

    Article • Vascular Pharmacology, August 2022, Elsevier

    Vidu Garg

  36. Molecular genetic mechanisms of congenital heart disease

    Article • Current Opinion in Genetics & Development, August 2022, Elsevier

    Vidu Garg

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

    Article • PLoS Genetics, June 2022, PLOS

    Vidu Garg

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

    Article • Cell Death Discovery, April 2022, Springer Science + Business Media

    Vidu Garg

  39. Use of machine learning to classify high-risk variants of uncertain significance in lamin A/C cardiac disease

    Article • Heart Rhythm, April 2022, Elsevier

    Vidu Garg

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

    Article • Birth Defects Research, February 2022, Wiley

    Vidu Garg

  41. Calcific aortic valve disease: novel insights into nitric oxide signalling

    Article • European Heart Journal, February 2022, Oxford University Press (OUP)

    Vidu Garg

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

    Article • Journal of Vascular Research, January 2022, Karger Publishers

    Vidu Garg

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

    Article • Annals of Behavioral Medicine, December 2021, Oxford University Press (OUP)

    Vidu Garg

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

    Article • November 2021, Cold Spring Harbor Laboratory Press

    Vidu Garg

  45. Gender Differences in Physical Activity Engagement Among Adolescents With Congenital Heart Disease

    Article • Journal of Pediatric Psychology, November 2021, Oxford University Press (OUP)

    Vidu Garg

  46. Correction to: Human Stem Cell Models of SARS‑CoV‑2 Infection in the Cardiovascular System

    Article • Stem Cell Reviews and Reports, October 2021, Springer Science + Business Media

    Vidu Garg

  47. Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

    Article • PLoS Genetics, September 2021, PLOS

    Dr. Yasset Perez-Riverol, Vidu Garg

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

    Article • genesis, September 2021, Wiley

    Vidu Garg

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

    Article • Translational Pediatrics, September 2021, AME Publishing Company

    Vidu Garg

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

    Article • Physiological Reports, September 2021, Wiley

    Vidu Garg

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

    Article • Frontiers in Cardiovascular Medicine, August 2021, Frontiers

    Vidu Garg

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

    Article • Stem Cell Reviews and Reports, August 2021, Springer Science + Business Media

    Vidu Garg

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

    Article • PLoS Genetics, July 2021, PLOS

    Dr. Yasset Perez-Riverol, Vidu Garg

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

    Article • Human Genetics and Genomics Advances, July 2021, Elsevier

    Vidu Garg

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

    Article • June 2021, Cold Spring Harbor Laboratory Press

    Vidu Garg

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

    Article • May 2021, Cold Spring Harbor Laboratory Press

    Vidu Garg

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

    Article • Science Advances, February 2021, American Association for the Advancement of Science

    Vidu Garg

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

    Article • Biomolecules, January 2021, MDPI AG

    Vidu Garg

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

    Article • Frontiers in Cell and Developmental Biology, January 2021, Frontiers

    Vidu Garg

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

    Article • Frontiers in Cell and Developmental Biology, October 2020, Frontiers

    Vidu Garg

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

    Article • August 2020, Cold Spring Harbor Laboratory Press

    Vidu Garg

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

    Article • June 2020, Cold Spring Harbor Laboratory Press

    Dr. Yasset Perez-Riverol, Vidu Garg

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

    Article • PLoS Genetics, May 2020, PLOS

    Sihem Darouich, Vidu Garg

  64. Subtype-specific cardiomyocytes for precision medicine: Where are we now?

    Article • Stem Cells, April 2020, Oxford University Press (OUP)

    Vidu Garg

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

    Article • Cold Spring Harbor Perspectives in Biology, December 2019, Cold Spring Harbor Laboratory Press

    Vidu Garg

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

    Article • October 2019, Cold Spring Harbor Laboratory Press

    Vidu Garg

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

    Article • Pediatric Cardiology, September 2019, Springer Science + Business Media

    Vidu Garg

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

    Article • Disease Models & Mechanisms, May 2019, The Company of Biologists

    Vidu Garg

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

    Article • AJP Heart and Circulatory Physiology, May 2019, American Physiological Society

    Vidu Garg

  70. Another Notch in the Genetic Puzzle of Tetralogy of Fallot

    Article • Circulation Research, February 2019, Wolters Kluwer Health

    Vidu Garg

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

    Article • Birth Defects Research, December 2018, Wiley

    Vidu Garg

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

    Article • Circulation, November 2018, Wolters Kluwer Health

    Vidu Garg

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

    Article • Journal of Molecular and Cellular Cardiology, August 2018, Elsevier

    Vidu Garg

  74. The Role of Lipoprotein(a) in Calcific Aortic Valve Disease

    Article • JAMA Cardiology, January 2018, American Medical Association (AMA)

    Vidu Garg

  75. Notch1 haploinsufficiency causes ascending aortic aneurysms in mice

    Article • JCI Insight, November 2017, American Society for Clinical Investigation

    Vidu Garg

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

    Article • JCI Insight, October 2017, American Society for Clinical Investigation

    Vidu Garg

  77. Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis

    Article • Journal of Cellular Physiology, September 2017, Wiley

    Vidu Garg

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

    Article • Pediatric Cardiology, September 2017, Springer Science + Business Media

    Vidu Garg

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

    Article • American Journal of Medical Genetics Part A, June 2017, Wiley

    Vidu Garg

  80. Genetic basis of aortic valvular disease

    Article • Current Opinion in Cardiology, May 2017, Wolters Kluwer Health

    Vidu Garg

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

    Article • Circulation Cardiovascular Genetics, October 2016, Wolters Kluwer Health

    Vidu Garg

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

    Article • Circulation Cardiovascular Genetics, August 2016, Wolters Kluwer Health

    Vidu Garg

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

    Article • Journal of the American Heart Association, April 2016, Wolters Kluwer Health

    Vidu Garg

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

    Article • Human Molecular Genetics, March 2016, Oxford University Press (OUP)

    Vidu Garg

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

    Article • Journal of the American Heart Association, February 2016, Wolters Kluwer Health

    Vidu Garg

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

    Article • Journal of Cardiovascular Development and Disease, August 2015, MDPI AG

    Vidu Garg

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

    Article • Journal of Perinatology, July 2015, Springer Science + Business Media

    Vidu Garg

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

    Article • Clinical Genetics, June 2015, Wiley

    Vidu Garg

  89. Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

    Article • Journal of Cardiovascular Development and Disease, April 2015, MDPI AG

    Vidu Garg

  90. Lifetime Prevalence of Sexual Intercourse and Contraception Use at Last Sex Among Adolescents and Young Adults With Congenital Heart Disease

    Article • Journal of Adolescent Health, April 2015, Elsevier

    Vidu Garg

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

    Article • Journal of Cardiovascular Development and Disease, March 2015, MDPI AG

    Vidu Garg

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

    Article • Journal of the American Heart Association, October 2014, Wolters Kluwer Health

    Vidu Garg

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

    Article • Circulation Research, October 2014, Wolters Kluwer Health

    Vidu Garg

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

    Article • Nature Biotechnology, May 2014, Nature

    Vidu Garg

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

    Article • Human Molecular Genetics, May 2014, Oxford University Press (OUP)

    Vidu Garg

  96. Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve

    Article • Pediatric Research, May 2014, Nature

    Vidu Garg

  97. Genetics of Valvular Heart Disease

    Article • Current Cardiology Reports, April 2014, Springer Science + Business Media

    Vidu Garg

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

    Article • BMC Medical Genomics, January 2014, Springer Science + Business Media

    Vidu Garg

  99. Etiology of Valvular Heart Disease

    Article • Circulation Journal, January 2014, Japanese Circulation Society

    Vidu Garg

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

    Article • Evidence-Based Medicine, November 2013, BMJ

    Vidu Garg

  101. Genetic Abnormalities inFOXP1Are Associated with Congenital Heart Defects

    Article • Human Mutation, July 2013, Wiley

    Vidu Garg

  102. Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease

    Article • Journal of Molecular and Cellular Cardiology, July 2013, Elsevier

    Vidu Garg

  103. The Congenital Heart Disease Genetic Network Study: Rationale, Design, and Early Results

    Article • Circulation Research, February 2013, Wolters Kluwer Health

    Vidu Garg

  104. Compacting the heart with Notch

    Article • Nature Medicine, February 2013, Nature

    Vidu Garg

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

    Article • Arteriosclerosis Thrombosis and Vascular Biology, October 2012, Wolters Kluwer Health

    Vidu Garg

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

    Article • PLoS Genetics, May 2012, PLOS

    Vidu Garg

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

    Article • Pediatric Cardiology, February 2012, Springer Science + Business Media

    Vidu Garg

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

    Article • European Journal of Human Genetics, February 2012, Nature

    Vidu Garg

  109. Inhibitory Role of Notch1 in Calcific Aortic Valve Disease

    Article • PLOS One, November 2011, PLOS

    Vidu Garg

  110. Chromosomal Haplotypes by Genetic Phasing of Human Families

    Article • The American Journal of Human Genetics, September 2011, Elsevier

    Vidu Garg

  111. Heredity of bicuspid aortic valve: is family screening indicated?

    Article • Heart, April 2011, BMJ

    Vidu Garg

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

    Article • European Journal of Human Genetics, February 2011, Nature

    Vidu Garg

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

    Article • Developmental Biology, November 2010, Elsevier

    Vidu Garg

  114. Impact of Mendelian inheritance in cardiovascular disease

    Article • Annals of the New York Academy of Sciences, October 2010, Wiley

    Vidu Garg

  115. Identification of GATA6 Sequence Variants in Patients With Congenital Heart Defects

    Article • Pediatric Research, October 2010, Nature

    Vidu Garg

  116. Genetics of Congenital Heart Disease

    Article • Current Cardiology Reviews, May 2010, Bentham Science Publishers

    Vidu Garg

  117. ABSENCE OF ABDOMINAL ANEURYSM IN ADULTS WITH COARCTATION AND/OR BICUSPID AORTIC VALVE - IS THIS REALLY AN “AORTOPATHY”?

    Article • Journal of the American College of Cardiology, March 2010, Elsevier

    Vidu Garg

  118. 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

    Article • Heart Rhythm, May 2009, Elsevier

    Vidu Garg

  119. EXPRESSION PATTERNS OF BASONUCLIN 2 IN PENILE TISSUE

    Article • The Journal of Urology, April 2009, Elsevier

    Vidu Garg

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

    Article • Developmental Biology, February 2009, Elsevier

    Vidu Garg

  121. A Rare Human Sequence Variant Reveals Myocardin Autoinhibition

    Article • Journal of Biological Chemistry, October 2008, American Society for Biochemistry & Molecular Biology (ASBMB)

    Vidu Garg

  122. Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

    Article • Pediatric Research, October 2008, Nature

    Vidu Garg

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

    Article • Journal of Molecular and Cellular Cardiology, December 2007, Elsevier

    Vidu Garg

  124. GATA4 sequence variants in patients with congenital heart disease

    Article • Journal of Medical Genetics, September 2007, BMJ

    Vidu Garg

  125. Screening and biochemical analysis ofGATA4sequence variations identified in patients with congenital heart disease

    Article • American Journal of Medical Genetics Part A, April 2007, Wiley

    Vidu Garg

  126. Molecular genetics of aortic valve disease

    Article • Current Opinion in Cardiology, May 2006, Wolters Kluwer Health

    Vidu Garg

  127. Insights into the genetic basis of congenital heart disease

    Article • Cellular and Molecular Life Sciences, March 2006, Springer Science + Business Media

    Vidu Garg

  128. Mutations in NOTCH1 cause aortic valve disease

    Article • Nature, July 2005, Nature

    Vidu Garg

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

    Article • Nature, July 2003, Nature

    Vidu Garg

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

    Article • Mechanisms of Development, October 2001, Elsevier

    Vidu Garg

  131. Tbx1, a DiGeorge Syndrome Candidate Gene, Is Regulated by Sonic Hedgehog during Pharyngeal Arch Development

    Article • Developmental Biology, July 2001, Elsevier

    Vidu Garg

  132. A Molecular Pathway Revealing a Genetic Basis for Human Cardiac and Craniofacial Defects

    Article • Science, February 1999, American Association for the Advancement of Science

    Vidu Garg