Genetic diagnosis in pediatric cardiomyopathy: clinical application and research perspectives

Por Ware, Stephanie M.
Publicado em 2011

Use of FOXJ1CreER(2T) mice for inducible deletion of embryonic node gene expression

Por Wang, Shuyun, Ware, Stephanie M.
Publicado em 2009

The Role of the Geneticist and Genetic Counselor in an ACHD Clinic

Por Parrott, Ashley, Ware, Stephanie M.
Publicado em 2012

Importance of genetic evaluation and testing in pediatric cardiomyopathy

Por Tariq, Muhammad, Ware, Stephanie M
Publicado no World J Cardiol (2014)

Genetic and Developmental Basis of Cardiovascular Malformations

Por Azhar, Mohamad, Ware, Stephanie M.
Publicado no Clin Perinatol (2016)

New Genetic Insights into Congenital Heart Disease

Por Ware, Stephanie M., Jefferies, John Lynn
Publicado em 2012

Toward Personalized Medicine: Does Genetic Diagnosis of Pediatric Cardiomyopathy Influence Patient Management?

Por Lee, Teresa M., Ware, Stephanie M.
Publicado no Prog Pediatr Cardiol (2015)

The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges

Por Landis, Benjamin J., Ware, Stephanie M.
Publicado no Front Cardiovasc Med (2016)

Heart Failure in Pediatric Patients with Congenital Heart Disease

Por Hinton, Robert B., Ware, Stephanie M.
Publicado no Circ Res (2017)

Genetic and functional analyses of ZIC3 variants in congenital heart disease

Por Cowan, Jason, Tariq, Muhammad, Ware, Stephanie M.
Publicado em 2014

A Mouse Model of Conduction System Patterning Abnormalities in Heterotaxy Syndrome

Por Czosek, Richard J., Haaning, Allison, Ware, Stephanie M.
Publicado em 2010

Spectrum of Clinical Diseases Caused By Disorders of Primary Cilia

Por Ware, Stephanie M., Aygun, Meral Gunay-, Hildebrandt, Friedhelm
Publicado em 2011

Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice

Por Quinn, Malgorzata E., Haaning, Allison, Ware, Stephanie M.
Publicado em 2012

Heterotaxy-spectrum heart defects in Zic3 hypomorphic mice

Por Haaning, Allison M., Quinn, Malgorzata E., Ware, Stephanie M.
Publicado em 2013

Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease

Por Bedard, James E. J., Haaning, Allison M., Ware, Stephanie M.
Publicado em 2011

An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis

Por Cast, Ashley E., Gao, Chunlei, Amack, Jeffrey D., Ware, Stephanie M.
Publicado em 2012

Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative Genomics

Por Rindler, Tara N., Hinton, Robert B., Salomonis, Nathan, Ware, Stephanie M.
Publicado no Sci Rep (2017)

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

Por Tariq, Muhammad, Belmont, John W, Lalani, Seema, Smolarek, Teresa, Ware, Stephanie M
Publicado em 2011

Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling

Por Freeze, Samantha L., Landis, Benjamin J., Ware, Stephanie M., Helm, Benjamin M.
Publicado no J Genet Couns (2016)

Zic3 is required in the migrating primitive streak for node morphogenesis and left–right patterning

Por Sutherland, Mardi J., Wang, Shuyun, Quinn, Malgorzata E., Haaning, Allison, Ware, Stephanie M.
Publicado em 2013