Christopher S. Fraser

Biochemistry, Genetics and Molecular BiologyMaterials Science

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: “Structure of a human 48 S translational initiation complex”.

Structure of a human 48 S translational initiation complex

Science(2020)10.1126/science.aba4904

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0DataRank · unranked

286 citations

Masaaki Sokabe, S.H.W. Kraatz, Yuliya Gordiyenko, Mark Skehel, Christopher S. Fraser +2 more

eIF5B and eIF1A remodel human translation initiation complexes to mediate ribosomal subunit joining

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.09.471821

N/A

0DataRank · unranked

4 citations

Rosslyn Grosely, Masaaki Sokabe, Carlos Alvarado, Jinfan Wang, Elizabeth Montabana +7 more

eIF5B and eIF1A reorient initiator tRNA to allow ribosomal subunit joining

Nature(2022)10.1038/s41586-022-04858-z

N/A

0DataRank · unranked

81 citations

Rosslyn Grosely, Masaaki Sokabe, Carlos Alvarado, Jinfan Wang, Elizabeth Montabana +7 more

Human eukaryotic initiation factor 4E (eIF4E) and the nucleotide-bound state of eIF4A regulate eIF4F binding to RNA

Journal of Biological Chemistry(2022)10.1016/j.jbc.2022.102368

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0DataRank · unranked

19 citations

Masaaki Sokabe, Nancy Villa, William C. Merrick, Christopher S. Fraser, Mario Servulo Izidoro

The structure of a human translation initiation complex reveals two independent roles for the helicase eIF4A

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.07.519490

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0DataRank · unranked

11 citations

Masaaki Sokabe, Irene Díaz‐López, Yuliya Gordiyenko, Christopher S. Fraser, V. Ramakrishnan +1 more

Monitoring RNA restructuring in a human cell-free extract reveals eIF4A-dependent and eIF4A-independent unwinding activity

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.14.520460

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0DataRank · unranked

1 citations

Christopher S. Fraser, Mattie H. O’Sullivan

Monitoring RNA restructuring in a human cell-free extract reveals eIF4A-dependent and eIF4A-independent unwinding activity

Journal of Biological Chemistry(2023)10.1016/j.jbc.2023.104936

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0DataRank · unranked

11 citations

Christopher S. Fraser, Mattie H. O’Sullivan

The structure of a human translation initiation complex reveals two independent roles for the helicase eIF4A

Nature Structural & Molecular Biology(2024)10.1038/s41594-023-01196-0

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0DataRank · unranked

93 citations

Masaaki Sokabe, Irene Díaz‐López, Yuliya Gordiyenko, Christopher S. Fraser, V. Ramakrishnan +1 more

Human eukaryotic initiation factor 4G directly binds the 40S ribosomal subunit to promote efficient translation

Journal of Biological Chemistry(2024)10.1016/j.jbc.2024.107242

N/A

0DataRank · unranked

11 citations

Christopher S. Fraser, Nancy Villa

Human tumor suppressor protein Pdcd4 binds at the mRNA entry channel in the 40S small ribosomal subunit

Nature Communications(2024)10.1038/s41467-024-50672-8

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0DataRank · unranked

14 citations

Masaaki Sokabe, Irene Díaz‐López, Yuliya Gordiyenko, Philipp K. Zuber, Yifei Du +4 more

FMRP drives mRNP targets into translationally silenced complexes

Molecular Cell(2025)10.1016/j.molcel.2025.06.012

N/A

0DataRank · unranked

1 citations

Hana Cho, Elizabeth Abshire, Christoph Pröschel, Shuhei Mitsutomi, Hanae Sato +5 more