Steven B. Bleyl
University of Utah(US)
Publications by Year
Research Areas
Congenital heart defects research, Congenital Heart Disease Studies, Genomics and Rare Diseases, Cardiomyopathy and Myosin Studies, Genomic variations and chromosomal abnormalities
Most-Cited Works
- Larsen's Human Embryology(2014)
- → Xq28-linked noncompaction of the left ventricular myocardium: Prenatal diagnosis and pathologic analysis of affected individuals(1997)307 cited
- → Neonatal, Lethal Noncompaction of the Left Ventricular Myocardium Is Allelic with Barth Syndrome(1997)292 cited
- → Global implementation of genomic medicine: We are not alone(2015)242 cited
- → Development of the Heart(2009)101 cited
- → Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system(2010)98 cited
- → Exome Analysis of a Family With Pleiotropic Congenital Heart Disease(2012)80 cited
- → Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms(2010)68 cited
- → Clinical utility of a next generation sequencing panel assay for Marfan and Marfan‐like syndromes featuring aortopathy(2015)67 cited
- → Cardiac malformations in Pdgfrα mutant embryos are associated with increased expression of WT1 and Nkx2.5 in the second heart field(2010)61 cited