All Stories

  1. 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

  2. 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

  3. 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

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

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

    Vidu Garg

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

    Article • Circulation Research, February 2019, Wolters Kluwer Health

    Vidu Garg

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

    Article • Birth Defects Research, December 2018, Wiley

    Vidu Garg

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

    Article • Circulation, November 2018, Wolters Kluwer Health

    Vidu Garg

  8. 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

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

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

    Vidu Garg

  10. Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis

    Article • Journal of Cellular Physiology, September 2017, Wiley

    Vidu Garg

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

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

    Vidu Garg

  12. 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

  13. Genetic basis of aortic valvular disease

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

    Vidu Garg

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

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

    Vidu Garg

  15. 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

  16. 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

  17. 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

  18. 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

  19. 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

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

    Article • Clinical Genetics, June 2015, Wiley

    Vidu Garg

  21. 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

  22. 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

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

    Article • Circulation Research, October 2014, Wolters Kluwer Health

    Vidu Garg

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

    Article • Nature Biotechnology, May 2014, Nature

    Vidu Garg

  25. 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

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

    Article • Pediatric Research, May 2014, Nature

    Vidu Garg

  27. Genetics of Valvular Heart Disease

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

    Vidu Garg

  28. 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

  29. Etiology of Valvular Heart Disease

    Article • Circulation Journal, January 2014, Japanese Circulation Society

    Vidu Garg

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

    Article • Evidence-Based Medicine, November 2013, BMJ

    Vidu Garg

  31. Genetic Abnormalities inFOXP1Are Associated with Congenital Heart Defects

    Article • Human Mutation, July 2013, Wiley

    Vidu Garg

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

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

    Vidu Garg

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

    Article • Circulation Research, February 2013, Wolters Kluwer Health

    Vidu Garg

  34. Compacting the heart with Notch

    Article • Nature Medicine, February 2013, Nature

    Vidu Garg

  35. 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

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

    Article • PLoS Genetics, May 2012, PLOS

    Vidu Garg

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

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

    Vidu Garg

  38. 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

  39. Inhibitory Role of Notch1 in Calcific Aortic Valve Disease

    Article • PLoS ONE, November 2011, PLOS

    Vidu Garg

  40. Chromosomal Haplotypes by Genetic Phasing of Human Families

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

    Vidu Garg

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

    Article • Heart, April 2011, BMJ

    Vidu Garg

  42. 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

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

    Article • Developmental Biology, November 2010, Elsevier

    Vidu Garg

  44. Impact of Mendelian inheritance in cardiovascular disease

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

    Vidu Garg

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

    Article • Pediatric Research, October 2010, Nature

    Vidu Garg

  46. Genetics of Congenital Heart Disease

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

    Vidu Garg

  47. 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

  48. 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

  49. EXPRESSION PATTERNS OF BASONUCLIN 2 IN PENILE TISSUE

    Article • The Journal of Urology, April 2009, Elsevier

    Vidu Garg

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

    Article • Developmental Biology, February 2009, Elsevier

    Vidu Garg

  51. A Rare Human Sequence Variant Reveals Myocardin Autoinhibition

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

    Vidu Garg

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

    Article • Pediatric Research, October 2008, Nature

    Vidu Garg

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

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

    Vidu Garg

  54. GATA4 sequence variants in patients with congenital heart disease

    Article • Journal of Medical Genetics, September 2007, BMJ

    Vidu Garg

  55. 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

  56. Molecular genetics of aortic valve disease

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

    Vidu Garg

  57. Insights into the genetic basis of congenital heart disease

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

    Vidu Garg

  58. Mutations in NOTCH1 cause aortic valve disease

    Article • Nature, July 2005, Nature

    Vidu Garg

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

    Article • Nature, July 2003, Nature

    Vidu Garg

  60. 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

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

    Article • Developmental Biology, July 2001, Elsevier

    Vidu Garg

  62. 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