Eric Helmenstine

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 5 papers. Top paper: “The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing”.

The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing

Blood Advances(2020)10.1182/bloodadvances.2019001127

N/A

0DataRank · unranked

60 citations

Eric Helmenstine, Lisa Pieterse, Bing Li, Christopher D. Gocke, Joshua Donaldson +8 more

Cell-specific regulation of gene expression using splicing-dependent frameshifting

Nature Communications(2022)10.1038/s41467-022-33523-2

N/A

0DataRank · unranked

39 citations

Alexei M. Bygrave, Clayton P. Santiago, Rogger P. Carmen‐Orozco, Vickie Trinh, Minzhong Yu +31 more

Cell-specific regulation of gene expression using splicing-dependent frameshifting

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.02.481623

N/A

0DataRank · unranked

2 citations

Alexei M. Bygrave, Clayton P. Santiago, Rogger P. Carmen‐Orozco, Vickie Trinh, Minzhong Yu +29 more

The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts

Research Square(2023)10.21203/rs.3.rs-2802265/v1

N/A

0DataRank · unranked

2 citations

Jonathan P. Ling, Jian Zhang, Eric Helmenstine, Wencke Walter, Riley E. Bergman +15 more

The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts

Blood Advances(2024)10.1182/bloodadvances.2023011260

N/A

0DataRank · unranked

8 citations

Jonathan P. Ling, Jian Zhang, Eric Helmenstine, Wencke Walter, Panagiotis Tsakiroglou +19 more