Maja Di Rocco

Also affiliated with Istituti di Ricovero e Cura a Carattere Scientifico

Medicine

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: “Patients with ACVR1R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva”.

Patients with ACVR1R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva

Orphanet Journal of Rare Diseases(2020)10.1186/s13023-020-01465-x

N/A

0.746DataRank · unranked

15 citations

Carmen De Cunto, Geneviève Baujat, Kelly L. Wentworth, Donna R. Grogan, Matthew A. Brown +9 more

Dysregulation of FLVCR1a-dependent mitochondrial calcium handling in neural progenitors causes congenital hydrocephalus

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101647

N/A

0DataRank · unranked

7 citations

Dibyanti Mukherjee, Massimo Bonora, Christoph P. Bagowski, Jeannette Nardelli, Livia Metani +34 more