Literature DB >> 8480595

Causes of congenital heart diseases: old and new modes, mechanisms, and models.

J J Nora1.   

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Year:  1993        PMID： 8480595     DOI： 10.1016/0002-8703(93)91014-6

Source DB:  PubMed          Journal:  Am Heart J        ISSN： 0002-8703            Impact factor:   4.749


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  11 in total

1.  The keeshond defect in cardiac conotruncal development is oligogenic.

Authors:  Petra Werner; Michael G Raducha; Ulana Prociuk; Elaine A Ostrander; Richard S Spielman; Ewen F Kirkness; Donald F Patterson; Paula S Henthorn
Journal:  Hum Genet       Date:  2005-02-12       Impact factor: 4.132

2.  Molecular cloning, chromosomal mapping, and characterization of the human cardiac-specific homeobox gene hCsx.

Authors:  D Turbay; S B Wechsler; K M Blanchard; S Izumo
Journal:  Mol Med       Date:  1996-01       Impact factor: 6.354

3.  Genetic factors in the development of cardiovascular anomalies.

Authors:  R Abdulla
Journal:  Pediatr Cardiol       Date:  1997 Jul-Aug       Impact factor: 1.655

4.  History of Our Understanding of the Causes of Congenital Heart Disease.

Authors:  Bruce D Gelb
Journal:  Circ Cardiovasc Genet       Date:  2015-06

5.  Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.

Authors:  Kim L McBride; Ricardo Pignatelli; Mark Lewin; Trang Ho; Susan Fernbach; Andres Menesses; Wilbur Lam; Suzanne M Leal; Norman Kaplan; Paul Schliekelman; Jeffrey A Towbin; John W Belmont
Journal:  Am J Med Genet A       Date:  2005-04-15       Impact factor: 2.802

Review 6.  Approach to congenital heart disease in the neonate.

Authors:  Usha S Krishnan
Journal:  Indian J Pediatr       Date:  2002-06       Impact factor: 1.967

7.  Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions.

Authors:  Mark B Lewin; Kim L McBride; Ricardo Pignatelli; Susan Fernbach; Ana Combes; Andres Menesses; Wilbur Lam; Louis I Bezold; Norman Kaplan; Jeffrey A Towbin; John W Belmont
Journal:  Pediatrics       Date:  2004-09       Impact factor: 7.124

Review 8.  Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies.

Authors:  Di Yu; Lei Yang; Shutong Shen; Changfeng Fan; Weiyan Zhang; Xuming Mo
Journal:  Pediatr Cardiol       Date:  2014-06-10       Impact factor: 1.655

9.  Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations.

Authors:  Javier T Granados-Riveron; Mark Pope; Frances A Bu'lock; Christopher Thornborough; Jacqueline Eason; Kerry Setchfield; Ami Ketley; Edwin P Kirk; Diane Fatkin; Michael P Feneley; Richard P Harvey; J David Brook
Journal:  Congenit Heart Dis       Date:  2011-10-20       Impact factor: 2.007

10.  The Hole and the Whole: Lessons from Manipulation of Nipbl Deficiency.

Authors:  Bruce D Gelb
Journal:  PLoS Biol       Date:  2016-09-08       Impact factor: 8.029
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