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

Jocelyn Laporte

Centre National de la Recherche Scientifique

ORCID: 0000-0001-8256-5862

Also affiliated with Inserm, Institut de génétique et de biologie moléculaire et cellulaire

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 10 papers. Top paper: “Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy”.

Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

Nature Genetics(2024)10.1038/s41588-023-01651-0
N/A
0.901DataRank · unranked
33 citations

Dan Cox, Irina Zaharieva, Valeria Di Leo, J. Sarparanta, Per Harald Jonson +80 more

Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric Cores

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.002
N/A
0.578DataRank · unranked
46 citations

Carl Elias Kutzner, Ying Hu, Xavière Lornage, John Rendu, Tanya Stojkovic +42 more

Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

Nature Communications(2022)10.1038/s41467-022-30015-1
N/A
0.571DataRank · unranked
44 citations

Payam Mohassel, Sandra Donkervoort, Lin Guo, Kevin O’Donovan, Maura Coughlin +53 more

GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome

Annals of Neurology(2020)10.1002/ana.25772
N/A
0.561DataRank · unranked
41 citations

Yaqun Zou, James E. Dunford, Jachinta Rooney, Goutam Chandra, Hui Xiong +29 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

Digenic Inheritance Involving a Muscle Specific Protein Kinase and the Giant Titin Protein Causes a Skeletal Muscle Myopathy

SSRN Electronic Journal(2021)10.2139/ssrn.3801723
N/A
0DataRank · unranked
2 citations

Irina Zaharieva, Valeria Di Leo, Anna Vihola, Neha Wali, Marco Savarese +60 more

Two zebrafish cacna1s loss-of-function variants provide models of mild and severe CACNA1S-related myopathy

Human Molecular Genetics(2023)10.1093/hmg/ddad178
N/A
0DataRank · unranked
3 citations

Linda Groom, Sabrina M. Wang, Emanuela Pannia, Nigel Griffiths, Jenica L.M. Van Gennip +5 more

Dietary pro-oxidant therapy by a vitamin K precursor targets PI 3-kinase VPS34 function

Science(2024)10.1126/science.adk9167
N/A
0DataRank · unranked
56 citations

Shan Kuang, Kaitlin Watrud, Mary R. Doherty, Charlotte Gineste, Grinu Mathew +40 more

Specific heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

medRxiv(2021)10.1101/2021.04.08.21254942
N/A
0DataRank · unranked
2 citations

Payam Mohassel, Sandra Donkervoort, Lin Guo, Kevin J. O’Donovan, Maura Coughlin +53 more

Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy

JCI Insight(2025)10.1172/jci.insight.194868
N/A
0DataRank · unranked
3 citations

F. Rostedt, Charlotte Gineste, Robert A. Seaborne, Hannah F. Dugdale, Vladimir Belhac +12 more