🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Qifei Li

Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine

ORCID: 0000-0002-0069-8512
Biochemistry, Genetics and Molecular BiologyMedicineEngineering

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 15 papers. Top paper: “Carbon monoxide-induced autophagy enhances human mesenchymal stromal cell function via paracrine actions in murine polymicrobial sepsis”.

Carbon monoxide-induced autophagy enhances human mesenchymal stromal cell function via paracrine actions in murine polymicrobial sepsis

Molecular Therapy(2024)10.1016/j.ymthe.2024.05.018
N/A
0.594DataRank · unranked
15 citations

Sailaja Ghanta, Qifei Li, Anthony M. Lamattina, Ekaterina Murzin, James A. Lederer +5 more

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

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

High number of candidate gene variants are identified as disease‐causing in a period of 4 years

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63509
N/A
0DataRank · unranked
5 citations

Qifei Li, Jill A. Madden, Casie A. Genetti, Catherine A. Brownstein, Klaus Schmitz‐Abe +3 more

Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytes

Basic Research in Cardiology(2023)10.1007/s00395-023-01029-7
N/A
0DataRank · unranked
1 citations

He Huang, Yanshuang Wu, Chang Shu, Narae Hwang, Qifei Li +9 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

“It’s hard to wait”: Provider perspectives on current genomic care in safety-net NICUs

Genetics in Medicine(2024)10.1016/j.gim.2024.101177
N/A
0DataRank · unranked
5 citations

Monica H. Wojcik, Sonia Hills, Jessica Douglas, Pankaj B. Agrawal, Tyler Allcroft +26 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

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