Publications by authors named "Elizabeth A Varga"

13Publications

Thrombocytopenia Pitfalls: Misdiagnosing Type 2B von Willebrand Disease as Ethylenediaminetetraacetic Acid-Dependent Pseudothrombocytopenia.

J Pediatr 2016 Aug 20;175:238-238.e1. Epub 2016 May 20.

Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio.

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August 2016

Homocysteine and MTHFR Mutations.

Circulation 2015 Jul;132(1):e6-9

From Hemophilia and Thrombosis Center and Clot Connect Program (www.clotconnect.org), University of North Carolina School of Medicine, Chapel Hill (S.M.); Division of Hematology/Oncology/Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, OH (E.A.V.); and The Ohio State University College of Medicine, Columbus (E.A.V.).

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July 2015

You want to do what? My mother's choice to have direct-to-consumer genetic testing.

J Genet Couns 2012 Jun 11;21(3):382-5. Epub 2012 Apr 11.

Division of Hematology/Oncology/BMT, Nationwide Children's Hospital, The Ohio State University, Columbus, OH, USA.

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June 2012

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.

Autism Res 2010 Jun;3(3):137-41

Center for Molecular and Human Genetics, Research Institute at Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

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June 2010

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

Genet Med 2009 Feb;11(2):111-7

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

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February 2009

Social and ethical controversies in thrombophilia testing and update on genetic risk factors for venous thromboembolism.

Semin Thromb Hemost 2008 Sep 28;34(6):549-61. Epub 2008 Nov 28.

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

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September 2008

Genetics in the context of thrombophilia.

J Thromb Thrombolysis 2008 Feb 19;25(1):2-5. Epub 2007 Oct 19.

Division of Molecular and Human Genetics, Columbus Children's Research Institute, Wexner 4, Columbus, OH 43205, USA.

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February 2008

Genetic counseling for inherited thrombophilias.

J Thromb Thrombolysis 2008 Feb 19;25(1):6-9. Epub 2007 Oct 19.

Division of Molecular and Human Genetics, Columbus Children's Research Institute, Wexner 4, Columbus, OH 43205, USA.

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February 2008

Cardiology patient pages. Homocysteine and MTHFR mutations: relation to thrombosis and coronary artery disease.

Circulation 2005 May;111(19):e289-93

Department of Internal Medicine, of Human Genetics, The Ohio State University, Columbus, Ohio, USA.

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May 2005

Cardiology patient pages. Prothrombin 20210 mutation (factor II mutation).

Circulation 2004 Jul;110(3):e15-8

Division of Maternal-Fetal Medicine, University of Kansas Medical Center, Kansas, USA.

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July 2004