Erin T. Strovel - Concepedia

Concepedia

Author

Erin T. Strovel

University of Maryland, Baltimore

Also Known As

Erin Strovel, Erin T Strovel, Erin T. Strovel

26

Publications

1.1K

Citations

14

H-Index

43

Concepts

All Affiliations

University of Maryland, Baltimore Stanford University Wayne State University Harvard University Eunice Kennedy Shriver National Institute of Child Health and Human Development

ET

About

Erin T. Strovel is an author at University of Maryland, Baltimore specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	730
2	Natural Sciences	2	2	34
3	Biochemistry	2	2	34
4	Cell Biology	2	2	43
5	Cellular Physiology	1	1	21

Erin T. Strovel

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14

Publications

1.1K

Citations

14

H-Index

	Year	Citations
Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project David McHugh, Cynthia A. Cameron, José E. Abdenur, Genetics in Medicine Metabolic SyndromeNewborn ScreeningMetabolic DisorderMass SpectrometryPediatrics	2011	349
AP-3 Mediates Tyrosinase but Not TRP-1 Trafficking in Human Melanocytes Marjan Huizing, Rangaprasad Sarangarajan, Erin T. Strovel, Molecular Biology of the Cell	2001	153
Nonsense Mutations in ADTB3A Cause Complete Deficiency of the β3A Subunit of Adaptor Complex-3 and Severe Hermansky-Pudlak Syndrome Type 2 Marjan Huizing, Charles D. Scher, Erin T. Strovel, Pediatric Research β3A SubunitGenetic DisorderGeneticsMolecular GeneticsNonsense Mutations	2002	151
Protein Phosphatase 2Cα Dephosphorylates Axin and Activates LEF-1-dependent Transcription Erin T. Strovel, Dianqing Wu, Daniel J. Sussman Journal of Biological Chemistry	2000	117
Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics Erin T. Strovel, Tina M. Cowan, Anna I. Scott, Genetics in Medicine Molecular Diagnostic TechniquesGenetic DisorderMedicineGeneticsBioanalysis	2017	60
Asparaginase Erwinia chrysanthemi effectively depletes plasma glutamine in adult patients with relapsed/refractory acute myeloid leukemia Ashkan Emadi, Jennie Y. Law, Erin T. Strovel, Cancer Chemotherapy and Pharmacology Plasma GlutamineMedicineAdult PatientsHematologyAsparaginase Erwinia Chrysanthemi	2017	53
Biochemical and molecular analyses of infantile free sialic acid storage disease in North American children Robert Kleta, David J. Aughton, Michael J. Rivkin, American Journal of Medical Genetics Part A GeneticsPathologySubstrate Reduction TherapyMolecular GeneticsDisease Gene Identification	2003	40
Venetoclax and pegcrisantaspase for complex karyotype acute myeloid leukemia Ashkan Emadi, Bandish Kapadia, Dominique Bollino, Leukemia Hematological MalignancyHematologyPathologyMyeloid Neoplasia	2020	35
Next‐generation <scp>DNA</scp> sequencing of <i><scp>HEXA</scp></i>: a step in the right direction for carrier screening Jodi D. Hoffman, Valerie Greger, Erin T. Strovel, Molecular Genetics & Genomic Medicine	2013	29
Development and characterization of a mouse with profound biotinidase deficiency: A biotin-responsive neurocutaneous disorder Kirit Pindolia, Megan Jordan, Caiying Guo, Molecular Genetics and Metabolism Skin DevelopmentCutaneous BiologyWound HealingProfound Biotinidase DeficiencyDermatology	2010	22

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