Shiyu Luo

Central South University of Forestry and Technology

Also affiliated with Central South University, Chinese Academy of Sciences, Institute of Subtropical Agriculture, Zhanjiang Experimental Station

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 12 papers. Top paper: “Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse model”.

Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse model

JCI Insight(2022)10.1172/jci.insight.157336

N/A

0.460DataRank · unranked

12 citations

Jasmine Lin, Jeffrey J. Widrick, Shiyu Luo, Gu Li, Tracy Zhang +5 more

Striated Preferentially Expressed Protein Kinase (SPEG)-Deficient Skeletal Muscles Display Fewer Satellite Cells with Reduced Proliferation and Delayed Differentiation

American Journal Of Pathology(2020)10.1016/j.ajpath.2020.08.012

N/A

0DataRank · unranked

6 citations

Jasmine Lin, Samantha M. Rosen, Tian Zhang, Shideh Kazerounian, Shiyu Luo +2 more

Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature

Journal of genetics and genomics/Journal of Genetics and Genomics(2021)10.1016/j.jgg.2021.02.008

N/A

0DataRank · unranked

41 citations

Sen Zhao, Chenxi Yu, Di Wu, Zihui Yan, Lijun Fan +25 more

A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings

PLoS Genetics(2021)10.1371/journal.pgen.1009639

N/A

0DataRank · unranked

7 citations

Michal Dibus, Alicia Casey, Christina Yee, Sara O. Vargas, Shiyu Luo +15 more

Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.18.562924

N/A

0DataRank · unranked

1 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more

Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complex

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.24.538136

N/A

0DataRank · unranked

0 citations

Jasmine Lin, Shiyu Luo, Klaus Schmitz‐Abe, Rohan Agrawal, Melissa Meng +6 more

The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation

Clinica Chimica Acta(2024)10.1016/j.cca.2024.119765

N/A

0DataRank · unranked

3 citations

S.D. Rollins, Klaus Schmitz‐Abe, Amy Tam, Qifei Li, Jiahai Shi +4 more

HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells

Disease Models & Mechanisms(2024)10.1242/dmm.050557

N/A

0DataRank · unranked

3 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more

Integrated multi‐omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex

Journal of Cachexia Sarcopenia and Muscle(2024)10.1002/jcsm.13470

N/A

0DataRank · unranked

4 citations

Jasmine Lin, Shiyu Luo, Klaus Schmitz‐Abe, Rohan Agrawal, Melissa Meng +6 more

The Solute Carrier Family 26 Member 9 Is a Modifier of the Rapidly Progressing Cystic Fibrosis Associated with F508del CFTR Mutations

medRxiv(2024)10.1101/2024.01.04.23300546

N/A

0DataRank · unranked

0 citations

S.D. Rollins, Klaus Schmitz‐Abe, Amy Tam, Qifei Li, Jiahai Shi +4 more

SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

Human Molecular Genetics(2020)10.1093/hmg/ddaa276

N/A

0DataRank · unranked

13 citations

Qifei Li, Jasmine Lin, Quinn Murphy, Isabelle Marty, Tracy Zhang +3 more

Unique signatures of highly constrained genes across publicly available genomic databases

Genetics in Medicine(2025)10.1016/j.gim.2025.101413

N/A

0DataRank · unranked

0 citations

Qifei Li, S. Greene, Michela Borrelli, Shiyu Luo, Madesh C. Ramesh +2 more