Sofia H. Giacomelli

437 total citations
17 papers, 309 citations indexed

About

Sofia H. Giacomelli is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Sofia H. Giacomelli has authored 17 papers receiving a total of 309 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Hematology, 6 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Sofia H. Giacomelli's work include Platelet Disorders and Treatments (8 papers), Hemophilia Treatment and Research (8 papers) and Blood groups and transfusion (5 papers). Sofia H. Giacomelli is often cited by papers focused on Platelet Disorders and Treatments (8 papers), Hemophilia Treatment and Research (8 papers) and Blood groups and transfusion (5 papers). Sofia H. Giacomelli collaborates with scholars based in Italy, United States and Germany. Sofia H. Giacomelli's co-authors include Giancarlo Castaman, Francesco Rodeghiero, Elena Santagostino, Maria Elisa Mancuso, Serena Sanna, Rosa Santacroce, Stefano Duga, Chiara Biasoli, Giovanna D’Andrea and Francesco Rodeghiero and has published in prestigious journals such as Journal of Thrombosis and Haemostasis, Human Mutation and Thrombosis Research.

In The Last Decade

Sofia H. Giacomelli

17 papers receiving 304 citations

Peers

Sofia H. Giacomelli

HEMAT

IMMUN

GENET

PRM

Galina Tsykunova Norway

Sébastien Lachot France

Christian Reimann Germany

Valeria Calafiore Italy

Maria López‐Pavía Spain

Fernando Roncolato Australia

Sandra Salazar United States

José Antonio Queizán Spain

K R Reynolds United States

Alexander Coltoff United States

Galina Tsykunova Norway

Sofia H. Giacomelli

147 ×0.6

HEMAT

103 ×0.8

21 ×0.5

IMMUN

25 ×0.7

GENET

21 ×0.6

PRM

Citations per year, relative to Sofia H. Giacomelli Sofia H. Giacomelli (= 1×) peers Galina Tsykunova

Countries citing papers authored by Sofia H. Giacomelli

Since Specialization

Citations

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

Fields of papers citing papers by Sofia H. Giacomelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sofia H. Giacomelli. 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 Sofia H. Giacomelli. The network helps show where Sofia H. Giacomelli may publish in the future.

Co-authorship network of co-authors of Sofia H. Giacomelli

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

All Works

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17 of 17 papers shown

Castaman, Giancarlo, Sofia H. Giacomelli, Chiara Biasoli, Laura Contino, & Paolo Radossi. (2019). Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders. European Journal Of Haematology. 103(4). 379–384. 22 indexed citations

Castaman, Giancarlo, Valeria Rimoldi, Sofia H. Giacomelli, & Stefano Duga. (2015). Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations. Thrombosis Research. 136(1). 144–147. 7 indexed citations

Castaman, Giancarlo, Sofia H. Giacomelli, Annarita Tagliaferri, & Francesco Rodeghiero. (2013). A novel heterozygous missense mutation (His127Arg) in a family with inherited cross-reacting material positive factor XI deficiency. Blood Coagulation & Fibrinolysis. 24(6). 670–672. 1 indexed citations

Castaman, Giancarlo, Sofia H. Giacomelli, Sonia Caccia, et al.. (2013). The spectrum of factor XI deficiency in Italy. Haemophilia. 20(1). 106–113. 12 indexed citations

Castaman, Giancarlo, Sofia H. Giacomelli, Tobias Obser, et al.. (2012). Reduced von Willebrand factor secretion is associated with loss of Weibel–Palade body formation. Journal of Thrombosis and Haemostasis. 10(5). 951–958. 14 indexed citations

Pinotti, Mirko, Alessandro Canella, Giuseppe Tagariello, et al.. (2012). Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations. Human Mutation. 33(9). 1373–1376. 16 indexed citations

Castaman, Giancarlo, Sofia H. Giacomelli, Maria Elisa Mancuso, et al.. (2011). Deep intronic variations may cause mild hemophilia A. Journal of Thrombosis and Haemostasis. 9(8). 1541–1548. 54 indexed citations

Castaman, Giancarlo, Manuela Platé, Sofia H. Giacomelli, Francesco Rodeghiero, & Stefano Duga. (2010). Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficiencies. Journal of Thrombosis and Haemostasis. 8(12). 2736–2742. 14 indexed citations

Castaman, Giancarlo, Sofia H. Giacomelli, Maria Elisa Mancuso, et al.. (2010). F8 mRNA studies in haemophilia A patients with different splice site mutations. Haemophilia. 16(5). 786–790. 14 indexed citations

10.

Castaman, Giancarlo, Sofia H. Giacomelli, Tobias Obser, et al.. (2010). Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype. Journal of Thrombosis and Haemostasis. 8(9). 2011–2016. 18 indexed citations

11.

Castaman, Giancarlo, Maria Elisa Mancuso, Sofia H. Giacomelli, et al.. (2009). Molecular and phenotypic determinants of the response to desmopressin in adult patients with mild hemophilia A. Journal of Thrombosis and Haemostasis. 7(11). 1824–1831. 36 indexed citations

12.

Castaman, Giancarlo, Sofia H. Giacomelli, & Francesco Rodeghiero. (2009). Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene. Acta Haematologica. 121(2-3). 106–110. 5 indexed citations

13.

Castaman, Giancarlo, Sofia H. Giacomelli, David Habart, et al.. (2008). Factor XI gene mutations in factor XI deficient patients of the Czech Republic. American Journal of Hematology. 83(12). 916–919. 5 indexed citations

14.

Santacroce, Rosa, Maura Acquila, Donata Belvini, et al.. (2008). Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. Journal of Human Genetics. 53(3). 275–284. 34 indexed citations

15.

Castaman, Giancarlo, et al.. (2007). Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene. Haemophilia. 13(3). 311–316. 13 indexed citations

16.

Castaman, Giancarlo, Sofia H. Giacomelli, Vytautas Ivaškevičius, et al.. (2007). Molecular characterization of five Italian families with inherited severe factor XIII deficiency. Haemophilia. 14(1). 96–102. 7 indexed citations

17.

Rosato, Antonio, Alessia Zoso, Sofia H. Giacomelli, et al.. (2003). The cytotoxic T-lymphocyte response against a poorly immunogenic mammary adenocarcinoma is focused on a single immunodominant class I epitope derived from the gp70 Env product of an endogenous retrovirus.. PubMed. 63(9). 2158–63. 37 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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