Erin T. Strovel

1.1k total citations
16 papers, 528 citations indexed

About

Erin T. Strovel is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Erin T. Strovel has authored 16 papers receiving a total of 528 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cell Biology, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Erin T. Strovel's work include Genomics and Rare Diseases (3 papers), Click Chemistry and Applications (2 papers) and Vitamin D Research Studies (2 papers). Erin T. Strovel is often cited by papers focused on Genomics and Rare Diseases (3 papers), Click Chemistry and Applications (2 papers) and Vitamin D Research Studies (2 papers). Erin T. Strovel collaborates with scholars based in United States, Cameroon and India. Erin T. Strovel's co-authors include William A. Gahl, Marjan Huizing, Daniel J. Sussman, Dianqing Wu, Raymond E. Boissy, Yang Zhao, Rangaprasad Sarangarajan, Yair Anikster, Lisa M. Hartnell and Diana L. Fitzpatrick and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Molecular Biology of the Cell.

In The Last Decade

Erin T. Strovel

15 papers receiving 515 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Erin T. Strovel United States 11 272 261 73 72 68 16 528
Arturo Incao United States 12 126 0.5× 176 0.7× 86 1.2× 28 0.4× 36 0.5× 15 355
S.H. Kidson South Africa 14 164 0.6× 164 0.6× 16 0.2× 48 0.7× 78 1.1× 23 387
Yoel Smicun United States 11 251 0.9× 389 1.5× 15 0.2× 63 0.9× 100 1.5× 14 547
Chin-To Fong United States 9 108 0.4× 198 0.8× 46 0.6× 85 1.2× 53 0.8× 9 450
Chetan K. Rane United States 8 90 0.3× 305 1.2× 22 0.3× 38 0.5× 21 0.3× 12 512
N. Meier Germany 10 156 0.6× 256 1.0× 30 0.4× 43 0.6× 5 0.1× 11 487
Huiping Shi China 15 113 0.4× 321 1.2× 216 3.0× 101 1.4× 59 0.9× 54 754
Gabriela Calounova Sweden 15 49 0.2× 185 0.7× 61 0.8× 219 3.0× 10 0.1× 24 420
Yossi Gottfried Israel 10 76 0.3× 459 1.8× 69 0.9× 65 0.9× 7 0.1× 11 604

Countries citing papers authored by Erin T. Strovel

Since Specialization
Citations

This map shows the geographic impact of Erin T. Strovel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Erin T. Strovel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erin T. Strovel more than expected).

Fields of papers citing papers by Erin T. Strovel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erin T. Strovel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Erin T. Strovel. The network helps show where Erin T. Strovel may publish in the future.

Co-authorship network of co-authors of Erin T. Strovel

This figure shows the co-authorship network connecting the top 25 collaborators of Erin T. Strovel. A scholar is included among the top collaborators of Erin T. Strovel based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Erin T. Strovel. Erin T. Strovel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Bollino, Dominique, Anusha Ganapati Bhat, Xinrong Ma, et al.. (2024). Long-acting Erwinia chrysanthemi, Pegcrisantaspase, induces alternate amino acid biosynthetic pathways in a preclinical model of pancreatic ductal adenocarcinoma. SHILAP Revista de lepidopterología. 12(1). 19–19.
2.
Massingham, Lauren, Jonathan A. Bernstein, David P. Gardner, et al.. (2022). 2022 Association of Professors of Human and Medical Genetics (APHMG) consensus–based update of the core competencies for undergraduate medical education in genetics and genomics. Genetics in Medicine. 24(10). 2167–2179. 7 indexed citations
3.
Strovel, Erin T., Kristina Cusmano‐Ozog, Tim Wood, & Chunli Yu. (2022). Measurement of lysosomal enzyme activities: A technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 24(4). 769–783. 11 indexed citations
4.
Bollino, Dominique, Xinrong Ma, Brandon Carter‐Cooper, et al.. (2022). Erwinia asparaginase (crisantaspase) increases plasma levels of serine and glycine. Frontiers in Oncology. 12. 1035537–1035537. 3 indexed citations
5.
Emadi, Ashkan, Bandish Kapadia, Dominique Bollino, et al.. (2020). Venetoclax and pegcrisantaspase for complex karyotype acute myeloid leukemia. Leukemia. 35(7). 1907–1924. 23 indexed citations
6.
Bisordi, Katharine, et al.. (2019). Newborn Screening Long Term Follow-Up in the Medical Home. International Journal of Neonatal Screening. 5(3). 25–25. 2 indexed citations
7.
Strovel, Erin T., Tina M. Cowan, Anna I. Scott, & Barry Wolf. (2017). Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics. Genetics in Medicine. 19(10). 1–10. 40 indexed citations
8.
Greene, Carol L., Erin T. Strovel, Elaine Spector, et al.. (2016). The M405V allele of the glutaryl-CoA dehydrogenase gene is an important marker for glutaric aciduria type I (GA-I) low excretors. Molecular Genetics and Metabolism. 119(1-2). 50–56. 11 indexed citations
9.
Hoffman, Jodi D., Valerie Greger, Erin T. Strovel, et al.. (2013). Next‐generation DNA sequencing of HEXA: a step in the right direction for carrier screening. Molecular Genetics & Genomic Medicine. 1(4). 260–268. 19 indexed citations
10.
Pindolia, Kirit, Megan Jordan, Caiying Guo, et al.. (2010). Development and characterization of a mouse with profound biotinidase deficiency: A biotin-responsive neurocutaneous disorder. Molecular Genetics and Metabolism. 102(2). 161–169. 20 indexed citations
11.
Cowan, Tina M. & Erin T. Strovel. (2008). Management and Quality Assurance in the Biochemical Genetics Laboratory. Current Protocols in Human Genetics. 59(1). Unit 17.7–Unit 17.7. 3 indexed citations
12.
Kleta, Robert, David J. Aughton, Michael J. Rivkin, et al.. (2003). Biochemical and molecular analyses of infantile free sialic acid storage disease in North American children. American Journal of Medical Genetics Part A. 120A(1). 28–33. 28 indexed citations
13.
Huizing, Marjan, Charles D. Scher, Erin T. Strovel, et al.. (2002). Nonsense Mutations in ADTB3A Cause Complete Deficiency of the β3A Subunit of Adaptor Complex-3 and Severe Hermansky-Pudlak Syndrome Type 2. Pediatric Research. 51(2). 150–158. 119 indexed citations
14.
Huizing, Marjan, Rangaprasad Sarangarajan, Erin T. Strovel, et al.. (2001). AP-3 Mediates Tyrosinase but Not TRP-1 Trafficking in Human Melanocytes. Molecular Biology of the Cell. 12(7). 2075–2085. 132 indexed citations
15.
Strovel, Erin T., Dianqing Wu, & Daniel J. Sussman. (2000). Protein Phosphatase 2Cα Dephosphorylates Axin and Activates LEF-1-dependent Transcription. Journal of Biological Chemistry. 275(4). 2399–2403. 90 indexed citations
16.
Strovel, Erin T. & Daniel J. Sussman. (1999). Transient Overexpression of Murine Dishevelled Genes Results in Apoptotic Cell Death. Experimental Cell Research. 253(2). 637–648. 20 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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