🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Jirair K. Bedoyan

University of Pittsburgh

ORCID: 0000-0002-9737-6877

Also affiliated with Children's Hospital of Pittsburgh

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 2%percentile
2.0Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Mitochondrial diseases in North America

Neurology Genetics(2020)10.1212/nxg.0000000000000402
Top 11%
2.0DataRank
Top 11%77 citations

Yuelin Long, Victoria Cooley, Robert Schoenaker, Valentina Emmanuele, Salvatore DiMauro +30 more

Papers

Driven by 10 papers — median percentile 89. Top paper: “Mitochondrial diseases in North America”.

Mitochondrial diseases in North America

Neurology Genetics(2020)10.1212/nxg.0000000000000402
Top 11%
2.0DataRank
Top 11%77 citations

Yuelin Long, Victoria Cooley, Robert Schoenaker, Valentina Emmanuele, Salvatore DiMauro +30 more

Utility of specific amino acid ratios in screening for pyruvate dehydrogenase complex deficiencies and other mitochondrial disorders associated with congenital lactic acidosis and newborn screening prospects

JIMD Reports(2020)10.1002/jmd2.12153
N/A
0DataRank · unranked
15 citations

Rosemary Hage, Ha Kyung Shin, Sharon Linard, Edwin Ferren, Nicole Ducich +11 more

Long-term effects of medical management on growth and weight in individuals with urea cycle disorders

Scientific Reports(2020)10.1038/s41598-020-67496-3
N/A
0DataRank · unranked
19 citations

Sven F. Garbade, Florian Gleich, Andrea Gropman, Pascale de Lonlay, Georg F. Hoffmann +58 more

From genotype to phenotype: Early prediction of disease severity in argininosuccinic aciduria

Human Mutation(2020)10.1002/humu.23983
N/A
0DataRank · unranked
26 citations

Sven F. Garbade, Florian Gleich, Jürgen G. Okun, Sandesh C.S. Nagamani, Andrea Gropman +29 more

Novel presentations associated with a PDHA1 variant – Alternating hemiplegia in Hemizygote proband and Guillain Barre Syndrome in Heterozygote mother

European Journal of Paediatric Neurology(2021)10.1016/j.ejpn.2021.01.006
N/A
0DataRank · unranked
4 citations

George Grahame, Jirair K. Bedoyan, Andrea Gropman, Kuntal Sen

Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC‐E1 structure and function

Journal of Inherited Metabolic Disease(2022)10.1002/jimd.12477
N/A
0DataRank · unranked
8 citations

Jason A. Mears, Jirair K. Bedoyan, Nicole Ducich

Simulations of Pathogenic E1α Variants: Allostery and Impact on Pyruvate Dehydrogenase Complex-E1 Structure and Function

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.17.492373
N/A
0DataRank · unranked
0 citations

Jirair K. Bedoyan, Olexandr Isayev, Hatice Gökcan

Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoin

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107605
N/A
0DataRank · unranked
4 citations

Angela Leshinski, Nicole Ducich, Leigh Anne Flore, April Rasala Lehman, Natasha Shur +10 more

Amino acid ratio combinations as biomarkers for discriminating patients with pyruvate dehydrogenase complex deficiency from other inborn errors of metabolism

Molecular Genetics & Genomic Medicine(2023)10.1002/mgg3.2283
N/A
0DataRank · unranked
4 citations

April N. Lehman, Hatice Gökcan, Lorna Cropcho, Danielle Black, Steven F. Dobrowolski +3 more

Are asymptomatic carriers of OTC deficiency always asymptomatic? A multicentric retrospective study of risk using the UCDC longitudinal study database

Molecular Genetics & Genomic Medicine(2024)10.1002/mgg3.2443
N/A
0DataRank · unranked
12 citations

Rima Izem, Yuelin Long, Jiji Jiang, Laura Konczal, Robert McCarter +3 more