Rosa Santacroce

2.9k total citations · 1 hit paper
55 papers, 1.9k citations indexed

About

Rosa Santacroce is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Rosa Santacroce has authored 55 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 18 papers in Hematology and 15 papers in Genetics. Recurrent topics in Rosa Santacroce's work include Hemophilia Treatment and Research (11 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (10 papers) and Blood Coagulation and Thrombosis Mechanisms (8 papers). Rosa Santacroce is often cited by papers focused on Hemophilia Treatment and Research (11 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (10 papers) and Blood Coagulation and Thrombosis Mechanisms (8 papers). Rosa Santacroce collaborates with scholars based in Italy, United States and Germany. Rosa Santacroce's co-authors include Maurizio Margaglione, Giovanna D’Andrea, Elvira Grandone, Massimiliano Chetta, Vincenzo Brancaccio, Rosa D’Ambrosio, P Perna, Maria D’Apolito, Valeria Bafunno and Angelica Leccese and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and International Journal of Molecular Sciences.

In The Last Decade

Rosa Santacroce

54 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin

2004 549 citations Giovanna D’Andrea, Massimiliano Chetta et al. profile →

Peers

Countries citing papers authored by Rosa Santacroce

Since Specialization

Citations

This map shows the geographic impact of Rosa Santacroce'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 Rosa Santacroce with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rosa Santacroce more than expected).

Fields of papers citing papers by Rosa Santacroce

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rosa Santacroce. 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 Rosa Santacroce. The network helps show where Rosa Santacroce may publish in the future.

Co-authorship network of co-authors of Rosa Santacroce

This figure shows the co-authorship network connecting the top 25 collaborators of Rosa Santacroce. A scholar is included among the top collaborators of Rosa Santacroce 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 Rosa Santacroce. Rosa Santacroce is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing Study 2025 ·International Journal of Molecular Sciences ·Maria D’Apolito, Francesco Santoro, (unknown), (unknown), Rosa Santacroce, (unknown), (unknown), Giovanna D’Andrea, Natale Daniele Brunetti, Maurizio Margaglione	2
2	A Report on a Targeted Screening Population for Alpha-1-Antitrypsin Deficiency (AATD) in Central-Southern Italy 2024 ·Archivos de Bronconeumología ·Giulia Scioscia, Rosa Santacroce, Pasquale Tondo, (unknown), Piera Soccio, (unknown), (unknown), Angelica Leccese, (unknown), (unknown), (unknown), Maria Pia Foschino Barbaro, Maurizio Margaglione, Donato Lacedonia	1
3	Uncovering a Genetic Diagnosis in a Pediatric Patient by Whole Exome Sequencing: A Modeling Investigation in Wiedemann–Steiner Syndrome 2024 ·Genes ·Ighli di Bari, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Grazia Pia Palladino, Maria Pia Patrizio, (unknown), Rosa Santacroce, Maria D’Apolito, Giovanna D’Andrea, (unknown), Ciro Leonardo Pierri, Maurizio Margaglione	0
4	Contact System Activation and Bradykinin Generation in Patients With Idiopathic Angioedema 2024 ·Journal of Investigational Allergology and Clinical Immunology ·Chiara Suffritti, (unknown), (unknown), Samantha Griffini, Elena Grovetti, Rosa Santacroce, Maurizio Margaglione, Massimo Cugno	1
5	The Role of Genetics in the Management of Heart Failure Patients 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Michele Correale, Natale Daniele Brunetti, Rosa Santacroce, Massimo Iacoviello, Maurizio Margaglione	6
6	A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis 2023 ·Genes ·Maria D’Apolito, Francesco Santoro, Rosa Santacroce, Giorgia Cordisco, (unknown), (unknown), Pier Luigi Pellegrino, Natale Daniele Brunetti, Maurizio Margaglione	6
7	A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema 2020 ·Allergy ·(unknown), Maria D’Apolito, Maria Bova, Francesco Bellanti, Stefania Loffredo, Giovanna D’Andrea, Mariano Intrieri, Angelica Petraroli, Angela Bruna Maffione, Giuseppe Spadaro, Rosa Santacroce, Maurizio Margaglione	83
8	Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria 2019 ·BMC Pregnancy and Childbirth ·Elvira Grandone, Pasquale Martinelli, Michela Villani, Gennaro Vecchione, Lucia Fischetti, Angelica Leccese, Rosa Santacroce, Gaetano Corso, Maurizio Margaglione	4
9	Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes 2019 ·Journal of Interventional Cardiac Electrophysiology ·(unknown), (unknown), Rosa Santacroce, Grazia Casavecchia, Michele Correale, Francesca Guastafierro, Angelica Leccese, Giorgia Cordisco, Riccardo Ieva, (unknown), Matteo Di Biase, Maurizio Margaglione, Natale Daniele Brunetti	4
10	Use of Catridecacog in a Patient with Severe Factor XIII Deficiency Undergoing Surgery 2019 ·SHILAP Revista de lepidopterología ·Gianluca Sottilotta, (unknown), Vincenzo Oriana, (unknown), Rosa Santacroce, (unknown)	2
11	Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema 2017 ·Journal of Allergy and Clinical Immunology ·Valeria Bafunno, Davide Firinu, Maria D’Apolito, Giorgia Cordisco, Stefania Loffredo, Angelica Leccese, Maria Bova, Maria Pina Barca, Rosa Santacroce, Marco Cicardi, Stefano Del Giacco, Maurizio Margaglione	196
12	Characterization of patients with angioedema without wheals: The importance of F12 gene screening 2015 ·Clinical Immunology ·Davide Firinu, Valeria Bafunno, Gennaro Vecchione, Maria Pina Barca, Paolo Emilio Manconi, Rosa Santacroce, Maurizio Margaglione, Stefano R. Del Giacco	24
13	The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype 2015 ·Systems Biology in Reproductive Medicine ·Rosa Santacroce, (unknown), Angelica Leccese, (unknown), Mattia Gentile, Maurizio Margaglione	3
14	Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 2015 ·Thrombosis and Haemostasis ·Donatella Colaizzo, Lucio Amitrano, Maria Anna Guardascione, (unknown), Giovanni Luca Tiscia, Giovanna D’Andrea, Rosa Santacroce, Elvira Grandone, Maurizio Margaglione	10
15	Deep intronic variations may cause mild hemophilia A 2011 ·Journal of Thrombosis and Haemostasis ·Giancarlo Castaman, Sofia H. Giacomelli, Maria Elisa Mancuso, Giovanna D’Andrea, Rosa Santacroce, Serena Sanna, Elena Santagostino, P.M. Mannucci, Anne Goodeve, Francesco Rodeghiero	54
16	Detection of New Deletions in a Group of Italian Patients with Hemophilia A by Multiplex Ligation–Dependent Probe Amplification 2009 ·Genetic Testing and Molecular Biomarkers ·Rosa Santacroce, (unknown), Valeria Bafunno, Francesco Sessa, Massimiliano Chetta, (unknown), Nenad Bukvić, Giovanna D’Andrea, (unknown), Maurizio Margaglione	4
17	Coexistence of β-Thalassemia and Hereditary Hemochromatosis in Homozygosity: A Possible Synergic Effect? 2009 ·Hemoglobin ·Nenad Bukvić, (unknown), Francesco Sessa, (unknown), Maria Grazia Roberti, Rosa Santacroce, Maurizio Margaglione	3
18	Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia 2006 ·Haemophilia ·Rosa Santacroce, Gennaro Vecchione, (unknown), Francesco Sessa, (unknown), Donatella Colaizzo, Elvira Grandone, Maurizio Margaglione	27
19	Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss 2002 ·Human Mutation ·Alessandro Ferraris, Eric Rappaport, Rosa Santacroce, Eleanor S. Pollak, Ian D. Krantz, (unknown), (unknown), Maurizio Margaglione, Gabriella Restagno, Bruno Dallapiccola, Saul Surrey, Paolo Fortina	15
20	Simple two-color array-based approach for mutation detection 2000 ·European Journal of Human Genetics ·Paolo Fortina, Kathleen Delgrosso, (unknown), Rosa Santacroce, Stéphane Moutereau, (unknown), David A. Graves, Steven E. McKenzie, Saul Surrey	23

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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