Steven B. Bleyl - Concepedia

Author

Steven B. Bleyl

University of Utah

Also Known As

Steven B Bleyl, Steven B. Bleyl, Steven Bleyl

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

University of Utah Intermountain Healthcare ARUP Laboratories (United States)Primary Children's Hospital Kaiser Permanente

About

Steven B. Bleyl is an author at University of Utah specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	923
2	Health Sciences	2	2	344
3	Public Health	2	2	46
4	Engineering	1	1	21
5	Natural Sciences	1	1	34

Steven B. Bleyl

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Xq28-linked noncompaction of the left ventricular myocardium: Prenatal diagnosis and pathologic analysis of affected individuals Steven B. Bleyl, Brian R. Mumford, Mary-Carole Brown-Harrison, American Journal of Medical Genetics Cardiac MuscleHeart FailurePathologyCongenital Heart AnomalyLeft Ventricular Failure	1997	307
Neonatal, Lethal Noncompaction of the Left Ventricular Myocardium Is Allelic with Barth Syndrome Steven B. Bleyl, Brian R. Mumford, Victor Thompson, The American Journal of Human Genetics CardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular DiseaseMedicine	1997	292
Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system Carol S. Bruggers, Steven B. Bleyl, Theodore J. Pysher, Pediatric Blood & Cancer	2010	98
Exome Analysis of a Family With Pleiotropic Congenital Heart Disease Cammon B. Arrington, Steven B. Bleyl, Norisada Matsunami, Circulation Cardiovascular Genetics	2012	80
Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms Steven B. Bleyl, Yukio Saijoh, Noortje A.M. Bax, Human Molecular Genetics	2010	68
Clinical utility of a next generation sequencing panel assay for Marfan and Marfan‐like syndromes featuring aortopathy Whitney Wooderchak‐Donahue, Chad VanSant‐Webb, Tatiana Tvrdik, American Journal of Medical Genetics Part A	2015	65
Cardiac malformations in <i>Pdgfrα</i> mutant embryos are associated with increased expression of WT1 and Nkx2.5 in the second heart field Noortje A.M. Bax, Steven B. Bleyl, R Gallini, Developmental Dynamics	2010	61
Two unique patients with novel microdeletions in 4p16.3 that exclude the WHS critical regions: Implications for critical region designation Sarah T. South, Steven B. Bleyl, John C. Carey American Journal of Medical Genetics Part A	2007	56
Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development Lisa D. Urness, Steven B. Bleyl, Tracy J. Wright, Developmental Biology AngiogenesisCardiovascular DiseaseMedicineFibroblast Growth FactorVascular Biology	2011	52
Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks Mauro Longoni, Kasper Lage, Meaghan Russell, American Journal of Medical Genetics Part A	2012	51

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