Hannah Bogardus
ScholarGPS® ID: 84458743059076
Affiliation History
Field
Medicine
Discipline
Pediatrics
Metrics Summary
Publication Count
5
Predicted Citations
153
Predicted h-index
5
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus (journal article) Haematologica, volume 99, issue 9, pages e168-e170 (2014). |
Cytochrome P450 2C8 ω3-Long-Chain Polyunsaturated Fatty Acid Metabolites Increase Mouse Retinal Pathologic Neovascularization—Brief Report (journal article) Arteriosclerosis, Thrombosis, and Vascular Biology, volume 34, issue 3, pages 581-586 (2014). |
Journal of Biological Chemistry, volume 288, issue 12, pages 8433-8444 (2013). |
A de novo band 3 mutation in hereditary spherocytosis (journal article) Pediatric Blood & Cancer, volume 58, issue 6, pages 1004-1004 (2012). |
Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy (journal article) Blood, volume 118, issue 21, pages 1030-1030 (2011). |