Literature DB >> 26546205

Combining clinical databases with genetic studies to help advance the causation model of congenital heart disease.

Christoph P Hornik1, R Thomas Collins2, Robert D B Jaquiss1, Jeffrey P Jacobs3, Marshall L Jacobs4, Sara K Pasquali5, Amelia S Wallace1, Kevin D Hill1.   

Abstract

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Year:  2015        PMID： 26546205      PMCID： PMC5483952          DOI： 10.1016/j.jtcvs.2015.08.006

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN： 0022-5223            Impact factor:   5.209


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  3 in total

Review 1.  Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literature.

Authors:  Yuri A Zarate; Tiffany Lepard; Elizabeth Sellars; Julie A Kaylor; Maria P Alfaro; Charles Sailey; G Bradley Schaefer; R Thomas Collins
Journal:  Am J Med Genet A       Date:  2014-05-20       Impact factor: 2.802

2.  The Congenital Heart Disease Genetic Network Study: rationale, design, and early results.

Authors:  Bruce Gelb; Martina Brueckner; Wendy Chung; Elizabeth Goldmuntz; Jonathan Kaltman; Juan Pablo Kaski; Richard Kim; Jennie Kline; Laura Mercer-Rosa; George Porter; Amy Roberts; Ellen Rosenberg; Howard Seiden; Christine Seidman; Lynn Sleeper; Sharon Tennstedt; Jonathan Kaltman; Charlene Schramm; Kristin Burns; Gail Pearson; Ellen Rosenberg
Journal:  Circ Res       Date:  2013-02-15       Impact factor: 17.367

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

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

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