Literature DB >> 15937089

Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study.

D Lambrechts, K Devriendt, D A Driscoll, E Goldmuntz, M Gewillig, R Vlietinck, D Collen, P Carmeliet.   

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Year:  2005        PMID： 15937089      PMCID： PMC1736071          DOI： 10.1136/jmg.2004.026443

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  19 in total

Review 1.  Probing human cardiovascular congenital disease using transgenic mouse models.

Authors:  Paige Snider; Simon J Conway
Journal:  Prog Mol Biol Transl Sci       Date:  2011       Impact factor: 3.622

2.  NRP1 haploinsufficiency predisposes to the development of Tetralogy of Fallot.

Authors:  Ivan Duran; Jessica Tenney; Carmen M Warren; Anna Sarukhanov; Fabiana Csukasi; Mark Skalansky; Maria L Iruela-Arispe; Deborah Krakow
Journal:  Am J Med Genet A       Date:  2018-01-24       Impact factor: 2.802

Review 3.  Genetic testing in congenital heart disease: A clinical approach.

Authors:  Marie A Chaix; Gregor Andelfinger; Paul Khairy
Journal:  World J Cardiol       Date:  2016-02-26

4.  Mesenchymal stem cell-based HSP70 promoter-driven VEGFA induction by resveratrol promotes angiogenesis in a mouse model.

Authors:  Young-Bin Chen; Ying-Wei Lan; Tsai-Hsien Hung; Lih-Geeng Chen; Kong-Bung Choo; Winston T K Cheng; Hsuan-Shu Lee; Kowit-Yu Chong
Journal:  Cell Stress Chaperones       Date:  2015-04-10       Impact factor: 3.667

Review 5.  Craniofacial Phenotypes and Genetics of DiGeorge Syndrome.

Authors:  Noriko Funato
Journal:  J Dev Biol       Date:  2022-05-13

6.  Patient genotypes impact survival after surgery for isolated congenital heart disease.

Authors:  Daniel Seung Kim; Jerry H Kim; Amber A Burt; David R Crosslin; Nancy Burnham; Donna M McDonald-McGinn; Elaine H Zackai; Susan C Nicolson; Thomas L Spray; Ian B Stanaway; Deborah A Nickerson; Mark W Russell; Hakon Hakonarson; J William Gaynor; Gail P Jarvik
Journal:  Ann Thorac Surg       Date:  2014-05-06       Impact factor: 4.330

7.  Genetics of congenital heart disease.

Authors:  Ashleigh A Richards; Vidu Garg
Journal:  Curr Cardiol Rev       Date:  2010-05

8.  Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome.

Authors:  Elizabeth Goldmuntz; Deborah A Driscoll; Beverly S Emanuel; Donna McDonald-McGinn; Minghua Mei; Elaine Zackai; Laura E Mitchell
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-02

9.  Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.

Authors:  Helen R Griffin; Darroch H Hall; Ana Topf; James Eden; A Graham Stuart; Jonathan Parsons; Ian Peart; John E Deanfield; John O'Sullivan; Sonya V Babu-Narayan; Michael A Gatzoulis; Frances A Bu'lock; Shoumo Bhattacharya; Jamie Bentham; Martin Farrall; Javier Granados Riveron; J David Brook; John Burn; Heather J Cordell; Judith A Goodship; Bernard Keavney
Journal:  PLoS One       Date:  2009-03-24       Impact factor: 3.240

10.  Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.

Authors:  Miriam S Reuter; Rajiv R Chaturvedi; Rebekah K Jobling; Giovanna Pellecchia; Omar Hamdan; Wilson W L Sung; Thomas Nalpathamkalam; Pratyusha Attaluri; Candice K Silversides; Rachel M Wald; Christian R Marshall; Simon G Williams; Bernard D Keavney; Bhooma Thiruvahindrapuram; Stephen W Scherer; Anne S Bassett
Journal:  Circ Genom Precis Med       Date:  2021-07-30
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