Ryan E. Loy

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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: “Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene”.

Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene

UNC Libraries(2020)10.17615/hrbk-2487

N/A

0DataRank · unranked

4 citations

Michael Rose, Farshid Ghassemi, Susan Treves, Stefan Buk, Caroline A. Sewry +15 more

Muscle weakness in Ryr1 I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca 2+ ion permeation and release from the sarcoplasmic reticulum

UNC Libraries(2020)10.17615/c8af-7374

N/A

0DataRank · unranked

2 citations

Robert T. Dirksen, David H. MacLennan, Gerhard Meissner, Murat Orynbayev, W. Melzer +5 more