Matthew J. Rardin

MedicineBiochemistry, Genetics and Molecular BiologyChemistry

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 2 papers. Top paper: “SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease”.

SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease

Nature Communications(2020)10.1038/s41467-020-19743-4

N/A

0DataRank · unranked

81 citations

Sanna Matilainen, Jesse G. Meyer, Pieti W. Pallijeff, J. Wall Richard, Christopher J. Carroll +21 more

A novel splice variant of Elp3/Kat9 regulates mitochondrial tRNA modification and function

Scientific Reports(2022)10.1038/s41598-022-18114-x

N/A

0DataRank · unranked

4 citations

Hyunsun Jo, Indra Heckenbach, Ritesh Tiwari, Herbert G. Kasler, Chad A. Lerner +7 more