Emanuela Pannia

Also affiliated with Hospital for Sick Children, Institut thématique Génétique, génomique et bioinformatique, SickKids Foundation

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

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 4 papers. Top paper: “Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum”.

Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum

Genetics in Medicine(2023)10.1016/j.gim.2023.100863

N/A

0DataRank · unranked

6 citations

Ashish R. Deshwar, Harsha Murthy, Daniela D’Agostino, Lucie Dupuis, Balram Gangaram +19 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

microRNA-133a as an indicator of disease progression and treatment response in X-linked myotubular myopathy

Molecular Therapy — Nucleic Acids(2025)10.1016/j.omtn.2025.102507

N/A

0DataRank · unranked

1 citations

Dakota Gustafson, Peter B. MacDonald, Emanuela Pannia, Crizza Ching, Nesrin Sabha +4 more

Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia

Brain(2025)10.1093/brain/awaf273

N/A

0DataRank · unranked

1 citations

Ny Hoang, Jamie C Stark, Sunny Cui, Emanuela Pannia, Chung Ting Tsoi +36 more