Roberta Palla

3.6k total citations
63 papers, 1.9k citations indexed

About

Roberta Palla is a scholar working on Hematology, Immunology and Genetics. According to data from OpenAlex, Roberta Palla has authored 63 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Hematology, 21 papers in Immunology and 18 papers in Genetics. Recurrent topics in Roberta Palla's work include Hemophilia Treatment and Research (21 papers), Complement system in diseases (20 papers) and Platelet Disorders and Treatments (19 papers). Roberta Palla is often cited by papers focused on Hemophilia Treatment and Research (21 papers), Complement system in diseases (20 papers) and Platelet Disorders and Treatments (19 papers). Roberta Palla collaborates with scholars based in Italy, United States and Netherlands. Roberta Palla's co-authors include Flora Peyvandi, Amy D. Shapiro, Marzia Menegatti, Pier Mannuccio Mannucci, Isabella Garagiola, Luca A. Lotta, Carla Valsecchi, Silvia Lavoretano, P.M. Mannucci and Raimondo De Cristofaro and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Roberta Palla

58 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roberta Palla Italy	24	1.1k	808	554	407	248	63	1.9k
K Sawada Japan	25	1.1k 1.0×	552 0.7×	571 1.0×	335 0.8×	227 0.9×	60	2.4k
François Provôt France	24	972 0.8×	2.4k 3.0×	627 1.1×	1.8k 4.5×	163 0.7×	84	3.2k
Lotta Hansson Sweden	27	397 0.3×	806 1.0×	390 0.7×	100 0.2×	224 0.9×	81	2.1k
Ki‐Seong Eom South Korea	25	1.5k 1.3×	583 0.7×	317 0.6×	79 0.2×	96 0.4×	188	2.3k
Katalin Váradi Austria	21	1.5k 1.3×	376 0.5×	556 1.0×	101 0.2×	74 0.3×	55	1.8k
Peter Ganly New Zealand	19	798 0.7×	288 0.4×	823 1.5×	56 0.1×	220 0.9×	58	1.9k
Stephen Harding United Kingdom	16	590 0.5×	191 0.2×	287 0.5×	217 0.5×	70 0.3×	75	1.2k
Efstathios Alexopoulos Greece	23	243 0.2×	552 0.7×	178 0.3×	1.1k 2.6×	279 1.1×	52	1.9k
Bruno Fattizzo Italy	24	1.4k 1.2×	525 0.6×	647 1.2×	109 0.3×	107 0.4×	147	2.3k
Anne‐Laure Sellier‐Leclerc France	15	242 0.2×	562 0.7×	142 0.3×	630 1.5×	169 0.7×	54	1.1k

Countries citing papers authored by Roberta Palla

Since Specialization

Citations

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

Fields of papers citing papers by Roberta Palla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Palla

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Palla. A scholar is included among the top collaborators of Roberta Palla 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 Roberta Palla. Roberta Palla 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

Palla, Roberta, et al.. (2025). The genetic spectrum of rare bleeding disorders. Journal of Thrombosis and Haemostasis. 23(9). 2763–2775.

Palla, Roberta, Marzia Menegatti, Simona Maria Siboni, et al.. (2025). Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database. Research and Practice in Thrombosis and Haemostasis. 9(5). 102960–102960.

Palla, Roberta, et al.. (2025). Effect of DNA methylation on inhibitor development in people with hemophilia A treated with FVIII concentrates. Research and Practice in Thrombosis and Haemostasis. 9(3). 102858–102858.

Gualtierotti, Roberta, Erica Scalambrino, Marigrazia Clerici, et al.. (2024). Predictive parameters for spontaneous joint bleeding during emicizumab prophylaxis. Blood Advances. 8(11). 2901–2907. 6 indexed citations

Peyvandi, Flora, Paolo Bucciarelli, Carla Valsecchi, et al.. (2020). IgG subclasses as biomarkers for persistence of factor VIII inhibitors in previously untreated patients with severe haemophilia A. British Journal of Haematology. 192(3). 621–625. 2 indexed citations

Messori, Andrea, Flora Peyvandi, Sabrina Trippoli, et al.. (2018). High-titre inhibitors in previously untreated patients with severe haemophilia A receiving recombinant or plasma-derived factor VIII: a budget-impact analysis.. Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano). 16(2). 215–220. 3 indexed citations

Rosendaal, Frits R., Roberta Palla, Isabella Garagiola, Pier Mannuccio Mannucci, & Flora Peyvandi. (2017). Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis. Blood. 130(15). 1757–1759. 28 indexed citations

Palla, Roberta, Simona Maria Siboni, Marzia Menegatti, Khaled M. Musallam, & Flora Peyvandi. (2016). Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders. Thrombosis Research. 148. 128–134. 22 indexed citations

Mancini, Ilaria, Carla Valsecchi, Luca A. Lotta, et al.. (2014). FRETS-VWF73 rather than CBA assay reflects ADAMTS13 proteolytic activity in acquired thrombotic thrombocytopenic purpura patients. Thrombosis and Haemostasis. 112(8). 297–303. 19 indexed citations

10.

Vučelić, D., Danijela Miković, Nebojša Antonijević, et al.. (2013). Diagnostic relevance of ADAMTS13 activity: Evaluation of 28 patients with thrombotic thrombocytopenic purpura - hemolytic uremic syndrome clinical diagnosis. Srpski arhiv za celokupno lekarstvo. 141(7-8). 466–474. 1 indexed citations

11.

Peyvandi, Flora, Roberta Palla, Luca A. Lotta, et al.. (2010). ADAMTS‐13 assays in thrombotic thrombocytopenic purpura. Journal of Thrombosis and Haemostasis. 8(4). 631–640. 77 indexed citations

12.

Lotta, Luca A., et al.. (2009). ADAMTS13mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura. Human Mutation. 31(1). 11–19. 120 indexed citations

13.

Lancellotti, Stefano, Vincenzo De Filippis, Nicola Pozzi, et al.. (2009). Formation of methionine sulfoxide by peroxynitrite at position 1606 of von Willebrand factor inhibits its cleavage by ADAMTS-13: A new prothrombotic mechanism in diseases associated with oxidative stress. Free Radical Biology and Medicine. 48(3). 446–456. 53 indexed citations

14.

Palla, Roberta, Silvia Lavoretano, R Lombardi, et al.. (2008). The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura. Haematologica. 94(2). 289–293. 16 indexed citations

15.

Tripodi, Armando, Flora Peyvandi, Veena Chantarangkul, et al.. (2008). Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS‐13). Journal of Thrombosis and Haemostasis. 6(9). 1534–1541. 38 indexed citations

16.

Cristofaro, Raimondo De, Flora Peyvandi, Roberta Palla, et al.. (2005). Role of Chloride Ions in Modulation of the Interaction between von Willebrand Factor and ADAMTS-13. Journal of Biological Chemistry. 280(24). 23295–23302. 38 indexed citations

17.

Cristofaro, Raimondo De, Andrea Carotti, Sepideh Akhavan, et al.. (2005). The natural mutation by deletion of Lys9 in the thrombin A‐chain affects the pK_a value of catalytic residues, the overall enzyme's stability and conformational transitions linked to Na⁺ binding. FEBS Journal. 273(1). 159–169. 27 indexed citations

18.

Peyvandi, Flora, Raimondo De Cristofaro, Isabella Garagiola, et al.. (2004). The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency. British Journal of Haematology. 127(5). 576–584. 5 indexed citations

19.

Garagiola, Isabella, Roberta Palla, & Flora Peyvandi. (2003). Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiency—misdiagnosis by direct sequence analysis using a PCR product. Prenatal Diagnosis. 23(9). 731–734. 6 indexed citations

20.

Emdin, Michele, Marcello Piacenti, Vincenzo Panichi, et al.. (1989). Ultrafiltration: A Rational Treatment for Heart Failure. Cardiology. 76(5). 384–390. 10 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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