Devin Oglesbee

Also affiliated with WinnMed, Mayo Clinic in Arizona, Mayo Clinic in Florida

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 11 papers. Top paper: “A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders”.

A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders

International Journal of Neonatal Screening(2020)10.3390/ijns6020044

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0DataRank · unranked

33 citations

Dimitar K. Gavrilov, Devin Oglesbee, Kimiyo Raymond, Silvia Tortorelli, John J. Hopwood +13 more

Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity

Journal of Clinical Investigation(2021)10.1172/jci136055

N/A

0DataRank · unranked

202 citations

Bryn Reinstadler, Kristin Engelstad, Owen S. Skinner, Erin Stackowitz, Ronald G. Haller +12 more

Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2

Nephrology Dialysis Transplantation(2021)10.1093/ndt/gfab027

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0DataRank · unranked

55 citations

Jason K. Viehman, Ramila A. Mehta, Andrea G. Cogal, Linda Hasadsri, Devin Oglesbee +7 more

Genetic therapy in a mitochondrial disease model suggests a critical role for liver dysfunction in mortality

eLife(2022)10.7554/elife.65488

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0DataRank · unranked

4 citations

Mark Wishman, Roberto Lopez Cervera, MaKayla R. Serres, Jennifer L. Anderson, Shannon R. Holmberg +16 more

An evaluation of untargeted metabolomics methods to characterize inborn errors of metabolism

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.108115

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0DataRank · unranked

13 citations

Coleman Turgeon, Zinandré Stander, Devin Oglesbee, Rachel Wurth

A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseases

Orphanet Journal of Rare Diseases(2024)10.1186/s13023-024-03423-3

N/A

0DataRank · unranked

8 citations

Rory J. Tinker, Rizwan Hamid, Joy D. Cogan, Kimberly Ezell, Devin Oglesbee +4 more

The clinical utility in hospital‐wide use of growth differentiation factor 15 as a biomarker for mitochondrial DNA‐related disorders

Journal of Inherited Metabolic Disease(2024)10.1002/jimd.12821

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0DataRank · unranked

2 citations

Jane Estrella, Devin Oglesbee, Austin Larson, Johan L.K. Van Hove, Andrea Cortés Fernández

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

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0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive condition

Molecular Genetics and Metabolism Reports(2024)10.1016/j.ymgmr.2024.101145

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0DataRank · unranked

0 citations

Yutaka Furuta, Devin Oglesbee, Enikö K. Pivnick, David C. Rinker, Jonathan H. Sheehan +9 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

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0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy

Genetics in Medicine(2025)10.1016/j.gim.2025.101506

N/A

0DataRank · unranked

3 citations

Chu-Ting Chang, A. Declève, Gloria Brunori, W.H. Ludlam, Alden Huang +93 more