Devin Oglesbee

5.8k total citations · 1 hit paper
87 papers, 3.1k citations indexed

About

Devin Oglesbee is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Devin Oglesbee has authored 87 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 34 papers in Clinical Biochemistry and 26 papers in Physiology. Recurrent topics in Devin Oglesbee's work include Metabolism and Genetic Disorders (34 papers), Mitochondrial Function and Pathology (23 papers) and Lysosomal Storage Disorders Research (16 papers). Devin Oglesbee is often cited by papers focused on Metabolism and Genetic Disorders (34 papers), Mitochondrial Function and Pathology (23 papers) and Lysosomal Storage Disorders Research (16 papers). Devin Oglesbee collaborates with scholars based in United States, Canada and Germany. Devin Oglesbee's co-authors include Dietrich Matern, Silvia Tortorelli, Piero Rinaldo, Roderick Capaldi, Robert Aggeler, George T. Hanson, S. James Remington, Roger Y. Tsien, Dimitar Gavrilov and Kimiyo Raymond and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Devin Oglesbee

75 papers receiving 3.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Investigating Mitochondrial Redox Potential with Redox-sensitive Green Fluorescent Protein Indicators

2004 774 citations Devin Oglesbee, Roderick Capaldi et al. Journal of Biological Chemistry profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Devin Oglesbee United States	29	1.9k	905	637	367	342	87	3.1k
Manuel Schiff France	25	1.3k 0.7×	870 1.0×	380 0.6×	200 0.5×	255 0.7×	115	2.3k
P. Vreken Netherlands	34	3.3k 1.8×	1.2k 1.3×	594 0.9×	337 0.9×	307 0.9×	81	4.5k
Cary O. Harding United States	33	1.9k 1.0×	2.0k 2.2×	1.1k 1.7×	291 0.8×	538 1.6×	120	3.4k
Saskia B. Wortmann Netherlands	32	1.9k 1.0×	1.0k 1.1×	302 0.5×	137 0.4×	539 1.6×	122	2.7k
Antònia Ribes Spain	38	2.5k 1.4×	2.1k 2.4×	586 0.9×	377 1.0×	395 1.2×	175	3.9k
Lourdes R. Desviat Spain	36	2.7k 1.5×	2.1k 2.3×	567 0.9×	285 0.8×	415 1.2×	154	3.7k
Margherita Ruoppolo Italy	30	1.5k 0.8×	373 0.4×	344 0.5×	136 0.4×	280 0.8×	116	2.4k
J. Jaeken Belgium	28	2.0k 1.1×	606 0.7×	649 1.0×	191 0.5×	467 1.4×	90	2.8k
Elisabeth Holme Sweden	34	3.0k 1.6×	2.0k 2.2×	404 0.6×	177 0.5×	297 0.9×	80	4.1k
A. H. van Gennip Netherlands	25	1.7k 0.9×	840 0.9×	257 0.4×	303 0.8×	190 0.6×	82	2.8k

Countries citing papers authored by Devin Oglesbee

Since Specialization

Citations

This map shows the geographic impact of Devin Oglesbee'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 Devin Oglesbee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Devin Oglesbee more than expected).

Fields of papers citing papers by Devin Oglesbee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Devin Oglesbee. 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 Devin Oglesbee. The network helps show where Devin Oglesbee may publish in the future.

Co-authorship network of co-authors of Devin Oglesbee

This figure shows the co-authorship network connecting the top 25 collaborators of Devin Oglesbee. A scholar is included among the top collaborators of Devin Oglesbee 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 Devin Oglesbee. Devin Oglesbee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Schultz, Matthew, Amy White, Dawn Peck, et al.. (2025). Clinical utility of untargeted urine oligosaccharide screening. Molecular Genetics and Metabolism. 146(4). 109267–109267.

Turgeon, Coleman, Kari Casas, Ryan Flanagan, et al.. (2024). Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase. Molecular Genetics and Metabolism Reports. 40. 101110–101110. 1 indexed citations

Byeon, Seul Kee, Jin Yong Kim, Roman M. Zenka, et al.. (2024). Development of a Multiplexed Sphingolipids Method for Diagnosis of Inborn Errors of Ceramide Metabolism. Clinical Chemistry. 70(11). 1366–1374. 2 indexed citations

Furuta, Yutaka, Rory J. Tinker, Rizwan Hamid, et al.. (2024). A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseases. Orphanet Journal of Rare Diseases. 19(1). 427–427. 2 indexed citations

Oglesbee, Devin, Linda Hasadsri, Duygu Selcen, et al.. (2024). SMN1 c.5C>G (p.Ala2Gly) missense variant, a challenging molecular SMA diagnosis associated with mild disease, preserves SMN nuclear gems in patient-specific fibroblasts. Frontiers in Genetics. 15. 1406819–1406819. 1 indexed citations

White, Amy, Tiffany Grider, Josef Alawneh, et al.. (2024). P004: Urine polyols for diagnosis of sorbitol dehydrogenase (SORD) deficiency-related peripheral neuropathy*. SHILAP Revista de lepidopterología. 2. 100881–100881.

White, Amy, Dawn Peck, Dimitar Gavrilov, et al.. (2024). Sensitivity of transferrin isoform analysis for PMM2-CDG. Molecular Genetics and Metabolism. 143(1-2). 108564–108564. 1 indexed citations

White, Amy, Devin Oglesbee, Dietrich Matern, et al.. (2023). A new test method for biochemical analysis of plasmalogens in dried blood spots and erythrocytes from patients with peroxisomal disorders. Journal of Inherited Metabolic Disease. 46(6). 1159–1169. 1 indexed citations

Sharma, Rohit, Kristin Engelstad, Owen S. Skinner, et al.. (2021). Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity. Journal of Clinical Investigation. 131(2). 133 indexed citations

10.

Preston, Graeme, Tim L. Emmerzaal, Silvia Radenkovic, et al.. (2021). Cerebellar and multi-system metabolic reprogramming associated with trauma exposure and post-traumatic stress disorder (PTSD)-like behavior in mice. Neurobiology of Stress. 14. 100300–100300. 9 indexed citations

11.

Mousa, Omar Y., Brian D. Juran, Bryan M. McCauley, et al.. (2020). Bile Acid Profiles in Primary Sclerosing Cholangitis and Their Ability to Predict Hepatic Decompensation. Hepatology. 74(1). 281–295. 68 indexed citations

12.

Peck, Dawn, Jean M. Lacey, Amy White, et al.. (2020). Incorporation of Second-Tier Biomarker Testing Improves the Specificity of Newborn Screening for Mucopolysaccharidosis Type I. International Journal of Neonatal Screening. 6(1). 10–10. 28 indexed citations

13.

Palomaki, Glenn E., Caleb Bupp, Anthony R. Gregg, et al.. (2019). Laboratory screening and diagnosis of open neural tube defects, 2019 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 22(3). 462–474. 18 indexed citations

14.

Pierce, Brandon L., Tong Lin, Maria Argos, et al.. (2019). A missense variant in FTCD is associated with arsenic metabolism and toxicity phenotypes in Bangladesh. PLoS Genetics. 15(3). e1007984–e1007984. 16 indexed citations

15.

Perales‐Clemente, Ester, Jared M. Evans, Frank J. Secreto, et al.. (2016). Natural underlying mt DNA heteroplasmy as a potential source of intra‐person hi PSC variability. The EMBO Journal. 35(18). 1979–1990. 59 indexed citations

16.

Baudhuin, Linnea M., Susan A. Lagerstedt, Eric W. Klee, et al.. (2015). Confirming Variants in Next-Generation Sequencing Panel Testing by Sanger Sequencing. Journal of Molecular Diagnostics. 17(4). 456–461. 85 indexed citations

17.

Matern, Dietrich, Devin Oglesbee, & Silvia Tortorelli. (2013). Newborn screening for lysosomal storage disorders and other neuronopathic conditions. PubMed. 17(3). 247–253. 33 indexed citations

18.

Magera, Mark J, Wendy J. Introne, Silvia Tortorelli, et al.. (2010). Homogentisic acid interference in routine urine creatinine determination. Molecular Genetics and Metabolism. 100(1). 103–104. 12 indexed citations

19.

Oglesbee, Devin, Jean M. Lacey, Mark J Magera, et al.. (2008). Second-Tier Test for Quantification of Alloisoleucine and Branched-Chain Amino Acids in Dried Blood Spots to Improve Newborn Screening for Maple Syrup Urine Disease (MSUD). Clinical Chemistry. 54(3). 542–549. 89 indexed citations

20.

Murray, James, Bing Zhang, Steven W. Taylor, et al.. (2003). The Subunit Composition of the Human NADH Dehydrogenase Obtained by Rapid One-step Immunopurification. Journal of Biological Chemistry. 278(16). 13619–13622. 91 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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