Benson DW - Search Results

1

Analysis of Ellis van Creveld syndrome gene products: implications for cardiovascular development and disease.

Sund KL, Roelker S, Ramachandran V, Durbin L, Benson DW. Sund KL, et al. Among authors: benson dw. Hum Mol Genet. 2009 May 15;18(10):1813-24. doi: 10.1093/hmg/ddp098. Epub 2009 Feb 27. Hum Mol Genet. 2009. PMID: 19251731 Free PMC article.

2

Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations.

Martin LJ, Ramachandran V, Cripe LH, Hinton RB, Andelfinger G, Tabangin M, Shooner K, Keddache M, Benson DW. Martin LJ, et al. Among authors: benson dw. Hum Genet. 2007 Apr;121(2):275-84. doi: 10.1007/s00439-006-0316-9. Epub 2007 Jan 4. Hum Genet. 2007. PMID: 17203300

3

Looking down the atrioventricular canal.

Benson DW, Sund KL. Benson DW, et al. Cardiovasc Res. 2010 Nov 1;88(2):205-6. doi: 10.1093/cvr/cvq302. Epub 2010 Sep 20. Cardiovasc Res. 2010. PMID: 20855523 Free PMC article. No abstract available.

4

Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.

Ye M, Coldren C, Liang X, Mattina T, Goldmuntz E, Benson DW, Ivy D, Perryman MB, Garrett-Sinha LA, Grossfeld P. Ye M, et al. Among authors: benson dw. Hum Mol Genet. 2010 Feb 15;19(4):648-56. doi: 10.1093/hmg/ddp532. Epub 2009 Nov 26. Hum Mol Genet. 2010. PMID: 19942620 Free PMC article.

5

KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes.

Andelfinger G, Tapper AR, Welch RC, Vanoye CG, George AL Jr, Benson DW. Andelfinger G, et al. Among authors: benson dw. Am J Hum Genet. 2002 Sep;71(3):663-8. doi: 10.1086/342360. Epub 2002 Jul 29. Am J Hum Genet. 2002. PMID: 12148092 Free PMC article.

6

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

Rajagopal SK, Ma Q, Obler D, Shen J, Manichaikul A, Tomita-Mitchell A, Boardman K, Briggs C, Garg V, Srivastava D, Goldmuntz E, Broman KW, Benson DW, Smoot LB, Pu WT. Rajagopal SK, et al. Among authors: benson dw. J Mol Cell Cardiol. 2007 Dec;43(6):677-85. doi: 10.1016/j.yjmcc.2007.06.004. Epub 2007 Jun 21. J Mol Cell Cardiol. 2007. PMID: 17643447 Free PMC article.

7

The complex genetics of hypoplastic left heart syndrome.

Liu X, Yagi H, Saeed S, Bais AS, Gabriel GC, Chen Z, Peterson KA, Li Y, Schwartz MC, Reynolds WT, Saydmohammed M, Gibbs B, Wu Y, Devine W, Chatterjee B, Klena NT, Kostka D, de Mesy Bentley KL, Ganapathiraju MK, Dexheimer P, Leatherbury L, Khalifa O, Bhagat A, Zahid M, Pu W, Watkins S, Grossfeld P, Murray SA, Porter GA Jr, Tsang M, Martin LJ, Benson DW, Aronow BJ, Lo CW. Liu X, et al. Among authors: benson dw. Nat Genet. 2017 Jul;49(7):1152-1159. doi: 10.1038/ng.3870. Epub 2017 May 22. Nat Genet. 2017. PMID: 28530678 Free PMC article.

8

Genetic origins of pediatric heart disease.

Benson DW. Benson DW. Pediatr Cardiol. 2010 Apr;31(3):422-9. doi: 10.1007/s00246-009-9607-y. Epub 2009 Dec 23. Pediatr Cardiol. 2010. PMID: 20033147 Review.

9

The presence of bicuspid aortic valve does not predict ventricular septal defect type.

Hor KN, Border WL, Cripe LH, Benson DW, Hinton RB. Hor KN, et al. Among authors: benson dw. Am J Med Genet A. 2008 Dec 15;146A(24):3202-5. doi: 10.1002/ajmg.a.32609. Am J Med Genet A. 2008. PMID: 19012349 Free PMC article.

10

Elastin haploinsufficiency results in progressive aortic valve malformation and latent valve disease in a mouse model.

Hinton RB, Adelman-Brown J, Witt S, Krishnamurthy VK, Osinska H, Sakthivel B, James JF, Li DY, Narmoneva DA, Mecham RP, Benson DW. Hinton RB, et al. Among authors: benson dw. Circ Res. 2010 Aug 20;107(4):549-57. doi: 10.1161/CIRCRESAHA.110.221358. Epub 2010 Jun 24. Circ Res. 2010. PMID: 20576933 Free PMC article.

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