P50-HL74731/HL/NHLBI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2004	2
2005	1
2006	2
2007	4
2008	2
2009	1
2010	3
2011	2
2012	1
2013	4
2014	2
2015	1
2019	1
2020	2
2024	0

1

Site specific gene delivery in the cardiovascular system.

Fishbein I, Stachelek SJ, Connolly JM, Wilensky RL, Alferiev I, Levy RJ. Fishbein I, et al. J Control Release. 2005 Dec 5;109(1-3):37-48. doi: 10.1016/j.jconrel.2005.09.031. Epub 2005 Nov 17. J Control Release. 2005. PMID: 16298010 Review.

2

The genetic contribution to congenital heart disease.

Goldmuntz E. Goldmuntz E. Pediatr Clin North Am. 2004 Dec;51(6):1721-37, x. doi: 10.1016/j.pcl.2004.08.006. Pediatr Clin North Am. 2004. PMID: 15561182 Review.

3

Morbidity in children and adolescents after surgical correction of truncus arteriosus communis.

O'Byrne ML, Mercer-Rosa L, Zhao H, Zhang X, Yang W, Cassedy A, Fogel MA, Rychik J, Tanel RE, Marino BS, Paridon S, Goldmuntz E. O'Byrne ML, et al. Am Heart J. 2013 Sep;166(3):512-8. doi: 10.1016/j.ahj.2013.05.023. Epub 2013 Jul 16. Am Heart J. 2013. PMID: 24016501 Free PMC article.

4

X-chromosome association studies of congenital heart defects.

Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE; Pediatric Cardiac Genomics Consortium. Agopian AJ, et al. Am J Med Genet A. 2020 Jan;182(1):250-254. doi: 10.1002/ajmg.a.61411. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729158 Free PMC article. No abstract available.

5

Quantifying pulmonary regurgitation and right ventricular function in surgically repaired tetralogy of Fallot: a comparative analysis of echocardiography and magnetic resonance imaging.

Mercer-Rosa L, Yang W, Kutty S, Rychik J, Fogel M, Goldmuntz E. Mercer-Rosa L, et al. Circ Cardiovasc Imaging. 2012 Sep 1;5(5):637-43. doi: 10.1161/CIRCIMAGING.112.972588. Epub 2012 Aug 6. Circ Cardiovasc Imaging. 2012. PMID: 22869820 Free PMC article.

6

NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects.

Lupo PJ, Mitchell LE, Goldmuntz E. Lupo PJ, et al. Birth Defects Res A Clin Mol Teratol. 2011 Jan;91(1):61-5. doi: 10.1002/bdra.20745. Epub 2010 Dec 1. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21254360 Free PMC article.

7

22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.

Mercer-Rosa L, Paridon SM, Fogel MA, Rychik J, Tanel RE, Zhao H, Zhang X, Yang W, Shults J, Goldmuntz E. Mercer-Rosa L, et al. Circ Cardiovasc Genet. 2015 Feb;8(1):74-81. doi: 10.1161/CIRCGENETICS.114.000819. Epub 2015 Jan 5. Circ Cardiovasc Genet. 2015. PMID: 25561045 Free PMC article.

8

GATA4 sequence variants in patients with congenital heart disease.

Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E. Tomita-Mitchell A, et al. J Med Genet. 2007 Dec;44(12):779-83. doi: 10.1136/jmg.2007.052183. J Med Genet. 2007. PMID: 18055909 Free PMC article.

9

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.

Roessler E, Pei W, Ouspenskaia MV, Karkera JD, Veléz JI, Banerjee-Basu S, Gibney G, Lupo PJ, Mitchell LE, Towbin JA, Bowers P, Belmont JW, Goldmuntz E, Baxevanis AD, Feldman B, Muenke M. Roessler E, et al. Mol Genet Metab. 2009 Sep-Oct;98(1-2):225-34. doi: 10.1016/j.ymgme.2009.05.005. Epub 2009 May 27. Mol Genet Metab. 2009. PMID: 19553149 Free PMC article.

10

In vivo biomechanical assessment of triglycidylamine crosslinked pericardium.

Sacks MS, Hamamoto H, Connolly JM, Gorman RC, Gorman JH 3rd, Levy RJ. Sacks MS, et al. Biomaterials. 2007 Dec;28(35):5390-8. doi: 10.1016/j.biomaterials.2007.08.021. Epub 2007 Sep 5. Biomaterials. 2007. PMID: 17822757 Free PMC article.

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