Corrado Mammì

774 total citations
28 papers, 389 citations indexed

About

Corrado Mammì is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Corrado Mammì has authored 28 papers receiving a total of 389 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Hematology and 8 papers in Genetics. Recurrent topics in Corrado Mammì's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Acute Myeloid Leukemia Research (3 papers). Corrado Mammì is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Acute Myeloid Leukemia Research (3 papers). Corrado Mammì collaborates with scholars based in Italy, Greece and United States. Corrado Mammì's co-authors include Carmelo Laganà, Manuela Priolo, Gianluca Sottilotta, Angela Sparago, Vincenzo Oriana, Flavia Cerrato, Andrea Riccio, Vincenzo Lombardo, Franco Meschi and Ornella Massa and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Molecular Phylogenetics and Evolution.

In The Last Decade

Corrado Mammì

26 papers receiving 379 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Corrado Mammì Italy 8 201 135 110 93 80 28 389
Shinichiro Miyagawa Japan 12 146 0.7× 39 0.3× 83 0.8× 86 0.9× 81 1.0× 20 376
Maria Carolina Salerno Italy 12 109 0.5× 44 0.3× 96 0.9× 139 1.5× 15 0.2× 24 350
Mariangela Cisternino Italy 14 228 1.1× 71 0.5× 274 2.5× 251 2.7× 20 0.3× 23 594
Celia D. Delozier United States 9 154 0.8× 25 0.2× 90 0.8× 9 0.1× 65 0.8× 14 312
Subbiah Sridhar India 11 52 0.3× 80 0.6× 45 0.4× 115 1.2× 18 0.2× 35 302
Nadine Lucidarme France 10 88 0.4× 73 0.5× 78 0.7× 144 1.5× 69 0.9× 14 372
Amer Budayr United States 10 62 0.3× 89 0.7× 183 1.7× 75 0.8× 13 0.2× 12 621
B.B. Jacobsen Denmark 6 147 0.7× 92 0.7× 51 0.5× 105 1.1× 9 0.1× 9 385
Stephen Hyer United Kingdom 12 97 0.5× 237 1.8× 72 0.7× 454 4.9× 10 0.1× 18 614
G. Mortimer Ireland 12 65 0.3× 42 0.3× 101 0.9× 39 0.4× 8 0.1× 35 382

Countries citing papers authored by Corrado Mammì

Since Specialization
Citations

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

Fields of papers citing papers by Corrado Mammì

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corrado Mammì

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

All Works

20 of 20 papers shown
1.
Floris, Matteo, Myriam Alcalay, Annalaura Montella, et al.. (2024). Pharmacogenetics in Italy: current landscape and future prospects. Human Genomics. 18(1). 78–78. 2 indexed citations
2.
Alesi, Viola, Silvia Genovese, Silvia Di Tommaso, et al.. (2024). Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency. Human Genomics. 18(1). 29–29. 1 indexed citations
3.
4.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Natural history of MRAS‐related Noonan syndrome: Evidence of mild adult‐onset left ventricular hypertrophy and neuropsychiatric features. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(2). 160–166.
5.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants. European Journal of Human Genetics. 31(7). 805–814. 4 indexed citations
6.
Augimeri, Giuseppina, Diego Sisci, Maria Stefania Sinicropi, et al.. (2023). Association between HMGCR, CRP, and CETP gene polymorphisms and metabolic/inflammatory serum profile in healthy adolescents. Journal of Translational Medicine. 21(1). 718–718. 2 indexed citations
7.
Priolo, Manuela, Andrea Ciolfi, Luca Pannone, et al.. (2022). SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction. Clinical Genetics. 102(1). 12–21. 2 indexed citations
8.
Zelasco, Samanta, Cinzia Giordano, Catia Morelli, et al.. (2022). LPL, FNDC5 and PPARγ gene polymorphisms related to body composition parameters and lipid metabolic profile in adolescents from Southern Italy. Journal of Translational Medicine. 20(1). 107–107. 5 indexed citations
9.
Olíva, Esther Natalie, Roberto Latagliata, Elena Sabattini, et al.. (2021). Accuracy of bone marrow histochemical TP53 expression compared to the detection of TP53 somatic mutations in patients with myelodysplastic syndromes harbouring a del5q cytogenetic abnormality.. PubMed. 11(4). 417–426. 2 indexed citations
10.
11.
Passanisi, Stefano, et al.. (2014). Treatment of Transient Neonatal Diabetes Mellitus: Insulin Pump or Insulin Glargine? Our Experience. Diabetes Technology & Therapeutics. 16(12). 880–884. 11 indexed citations
12.
Martino, Bruno, Corrado Mammì, Francesca Ronco, et al.. (2014). On the Absence of Calreticulin (CALR) Mutations in Chronic Myeloprolierative Neoplasms (MPNs) with Splanchnic Venous Thrombosis (SVT): Experience from a Single Institution. Blood. 124(21). 3198–3198. 3 indexed citations
13.
Morabito, Fortunato, Stefan Hohaus, Corrado Mammì, et al.. (2011). Role of glutathione-s-transferase (gst) polymorphisms in patients with advanced hodgkin lymphoma: results from the hd2000 GISL trial. Leukemia & lymphoma. 53(3). 406–410. 3 indexed citations
14.
Iafusco, Dario, Ornella Massa, B Pasquino, et al.. (2011). Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births. Acta Diabetologica. 49(5). 405–408. 115 indexed citations
15.
Famà, Angelo, Angela Rago, Chiara Marzano, et al.. (2010). [Budd-Chiari syndrome and splanchnic vein thrombosis: masked myeloproliferative neoplasms and JAK2V617F].. PubMed. 161(2). 169–71. 1 indexed citations
16.
Sottilotta, Gianluca, et al.. (2009). High Incidence of Factor V Leiden and Prothrombin G20210A in Healthy Southern Italians. Clinical and Applied Thrombosis/Hemostasis. 15(3). 356–359. 17 indexed citations
17.
Lucia, Eugenio, Bruno Martino, Corrado Mammì, et al.. (2008). The incidence of JAK2 V617F mutation in bcr/abl-negative chronic myeloproliferative disorders: assessment by two different detection methods. Leukemia & lymphoma. 49(10). 1907–1915. 6 indexed citations
18.
Priolo, Manuela, Angela Sparago, Corrado Mammì, et al.. (2008). MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment. European Journal of Human Genetics. 16(5). 565–571. 57 indexed citations
19.
Sottilotta, Gianluca, et al.. (2005). Genetic prothrombotic risk factors in women with unexplained pregnancy loss. Thrombosis Research. 117(6). 681–684. 38 indexed citations
20.
Luca, Francesca, Nicholas P. Anagnou, G. Ciavarella, et al.. (2003). Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects. Molecular Phylogenetics and Evolution. 28(3). 387–395. 51 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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