Luca Stefanucci

5.7k total citations
5 papers, 97 citations indexed

About

Luca Stefanucci is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Luca Stefanucci has authored 5 papers receiving a total of 97 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Hematology and 2 papers in Genetics. Recurrent topics in Luca Stefanucci's work include Cancer-related gene regulation (2 papers), Hemoglobinopathies and Related Disorders (1 paper) and RNA modifications and cancer (1 paper). Luca Stefanucci is often cited by papers focused on Cancer-related gene regulation (2 papers), Hemoglobinopathies and Related Disorders (1 paper) and RNA modifications and cancer (1 paper). Luca Stefanucci collaborates with scholars based in United Kingdom, France and Netherlands. Luca Stefanucci's co-authors include Xiaoyu Chen, Vincent Mouly, Josephine M. Janssen, Ignazio Maggio, Jin Liu, Manuel A.F.V. Gonçalves, Mattia Frontini, José Padilla, Françis Couturaud and Karola Rehnström and has published in prestigious journals such as Nucleic Acids Research, PLoS Genetics and Thrombosis and Haemostasis.

In The Last Decade

Luca Stefanucci

5 papers receiving 97 citations

Peers

Luca Stefanucci

MB

GENET

HEMAT

PHYSI

Yajie Zhao United Kingdom

Itziar Cossío Spain

Lin-ya Tang United States

Beth A. Miller United States

Eric Bartell United States

Juan Pablo Trujillo‐Quintero Spain

Flávia Piazzon Brazil

Ajoy Aloysius India

Catrina M. Loucks Canada

Ursula M. Schick United States

Yajie Zhao United Kingdom

Luca Stefanucci

80 ×1.0

MB

53 ×1.6

GENET

8 ×0.7

GENET

9 ×1.1

HEMAT

11 ×1.4

PHYSI

Citations per year, relative to Luca Stefanucci Luca Stefanucci (= 1×) peers Yajie Zhao

Countries citing papers authored by Luca Stefanucci

Since Specialization

Citations

This map shows the geographic impact of Luca Stefanucci's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Luca Stefanucci with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luca Stefanucci more than expected).

Fields of papers citing papers by Luca Stefanucci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luca Stefanucci. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Luca Stefanucci. The network helps show where Luca Stefanucci may publish in the future.

Co-authorship network of co-authors of Luca Stefanucci

This figure shows the co-authorship network connecting the top 25 collaborators of Luca Stefanucci. A scholar is included among the top collaborators of Luca Stefanucci based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Luca Stefanucci. Luca Stefanucci is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Stefanucci, Luca & Mattia Frontini. (2022). Non‐coding genetic variation in regulatory elements determines thrombosis and hemostasis phenotypes. Journal of Thrombosis and Haemostasis. 20(8). 1759–1765. 2 indexed citations

2.

Morena‐Barrio, Belén de la, Jonathan Stephens, María Eugenia de la Morena‐Barrio, et al.. (2022). Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency. Thrombosis and Haemostasis. 122(8). 1369–1378. 14 indexed citations

3.

Morange, Pierre‐Emmanuel, Franck Peiretti, Lénaïck Gourhant, et al.. (2021). A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant. PLoS Genetics. 17(1). e1009284–e1009284. 9 indexed citations

4.

Meli, Athinoula, Amy Frary, Karola Rehnström, et al.. (2021). Familial pseudohyperkalemia induces significantly higher levels of extracellular potassium in early storage of red cell concentrates without affecting other standard measures of quality: A case control and allele frequency study. Transfusion. 61(8). 2439–2449. 8 indexed citations

5.

Maggio, Ignazio, Luca Stefanucci, Josephine M. Janssen, et al.. (2016). Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations. Nucleic Acids Research. 44(3). 1449–1470. 64 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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