Emanuela Carlotti

1.6k total citations
20 papers, 579 citations indexed

About

Emanuela Carlotti is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Emanuela Carlotti has authored 20 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pathology and Forensic Medicine, 8 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Emanuela Carlotti's work include Lymphoma Diagnosis and Treatment (11 papers), Chronic Lymphocytic Leukemia Research (8 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Emanuela Carlotti is often cited by papers focused on Lymphoma Diagnosis and Treatment (11 papers), Chronic Lymphocytic Leukemia Research (8 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Emanuela Carlotti collaborates with scholars based in United Kingdom, Italy and United States. Emanuela Carlotti's co-authors include Stefano Bombardieri, Costantino Pitzalis, Elisa Corsiero, Federico Pratesi, William H. Robinson, Paola Migliorini, Jude Fitzgibbon, T. Andrew Lister, John G. Gribben and Sameena Iqbal and has published in prestigious journals such as Blood, The Journal of Immunology and PLoS ONE.

In The Last Decade

Emanuela Carlotti

20 papers receiving 576 citations

Peers

Emanuela Carlotti
Karin E. Summers United Kingdom
Marybeth Nelson United States
Heather Horne United States
Zhen Fan United States
C Lavignac France
PM Kluin Netherlands
Karin E. Summers United Kingdom
Emanuela Carlotti
Citations per year, relative to Emanuela Carlotti Emanuela Carlotti (= 1×) peers Karin E. Summers

Countries citing papers authored by Emanuela Carlotti

Since Specialization
Citations

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

Fields of papers citing papers by Emanuela Carlotti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuela Carlotti

This figure shows the co-authorship network connecting the top 25 collaborators of Emanuela Carlotti. A scholar is included among the top collaborators of Emanuela Carlotti 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 Emanuela Carlotti. Emanuela Carlotti 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.
Debernardi, Silvana, Łukasz Liszka, Chara Ntala, et al.. (2023). Molecular characteristics of early‐onset pancreatic ductal adenocarcinoma. Molecular Oncology. 18(3). 677–690. 3 indexed citations
2.
Carlotti, Emanuela, Marc Williams, Biancastella Cereser, et al.. (2023). Hepatocytes undergo punctuated expansion dynamics from a periportal stem cell niche in normal human liver. Journal of Hepatology. 79(2). 417–432. 5 indexed citations
3.
Michaeli, Miri, et al.. (2022). Mutational patterns along different evolution paths of follicular lymphoma. Frontiers in Oncology. 12. 1029995–1029995. 1 indexed citations
4.
Carlotti, Emanuela, William Murray‐Brown, Kevin Blighe, et al.. (2022). High-throughput sequencing of IgH gene in minor salivary glands from Sjögren's syndrome patients reveals dynamic B cell recirculation between ectopic lymphoid structures. Clinical and Experimental Rheumatology. 40(12). 2363–2372. 3 indexed citations
6.
Carlotti, Emanuela, Shamzah Araf, Jessica Okosun, et al.. (2020). IGHV sequencing reveals acquired N-glycosylation sites as a clonal and stable event during follicular lymphoma evolution. Blood. 135(11). 834–844. 20 indexed citations
7.
Carlotti, Emanuela, Shamzah Araf, Jessica Okosun, et al.. (2018). Immunoglobulin Variable Region Gene Sequences Reveal N-Glycosylation Motifs As an Early and Stable Event in Follicular Lymphoma Pathology. Blood. 132(Supplement 1). 4101–4101. 1 indexed citations
8.
Carlotti, Emanuela, David Wrench, Guglielmo Rosignoli, et al.. (2015). High Throughput Sequencing Analysis of the Immunoglobulin Heavy Chain Gene from Flow-Sorted B Cell Sub-Populations Define the Dynamics of Follicular Lymphoma Clonal Evolution. PLoS ONE. 10(9). e0134833–e0134833. 26 indexed citations
9.
Corsiero, Elisa, Stefano Bombardieri, Emanuela Carlotti, et al.. (2015). Single cell cloning and recombinant monoclonal antibodies generation from RA synovial B cells reveal frequent targeting of citrullinated histones of NETs. Annals of the Rheumatic Diseases. 75(10). 1866–1875. 151 indexed citations
10.
Corsiero, Elisa, Emanuela Carlotti, Hedda Wardemann, et al.. (2014). A1.31 Monoclonal antibodies from CD19+ synovial B cells of RA patients with tertiary lymphoid structures display a strong immunoreactivity towards citrullinated histones from neutrophils NETs. Annals of the Rheumatic Diseases. 73. A13–A13. 1 indexed citations
11.
Wrench, David, Christine F. Skibola, Lucía Conde, et al.. (2011). SNP rs6457327 in the HLA region on chromosome 6p is predictive of the transformation of follicular lymphoma. Blood. 117(11). 3147–3150. 15 indexed citations
12.
Wrench, David, Ajanthah Sangaralingam, Ciarán Ó’Riain, et al.. (2010). TNFRSF14 and EZH2 Mutations, Chr2p Gain and Copy Number Changes Targeting Genes Whose Proteins Interact with the Microenvironment In Transformed Follicular Lymphoma. Blood. 116(21). 799–799. 1 indexed citations
14.
O’Shea, Derville, Ciarán Ó’Riain, Claire Taylor, et al.. (2008). The presence of TP53 mutation at diagnosis of follicular lymphoma identifies a high-risk group of patients with shortened time to disease progression and poorer overall survival. Blood. 112(8). 3126–3129. 87 indexed citations
15.
Pulsoni, Alessandro, Irene Della Starza, Emanuela M. Ghia, et al.. (2007). Stage I/II follicular lymphoma: spread of bcl‐2/IgH+ cells in blood and bone marrow from primary site of disease and possibility of clearance after involved field radiotherapy. British Journal of Haematology. 137(3). 216–220. 18 indexed citations
16.
Fitzgibbon, Jude, Sameena Iqbal, Andrew Davies, et al.. (2007). Genome-wide detection of recurring sites of uniparental disomy in follicular and transformed follicular lymphoma. Leukemia. 21(7). 1514–1520. 55 indexed citations
17.
Carlotti, Emanuela, Giuseppe A. Palumbo, Elena Oldani, et al.. (2007). Fc RIIIA and Fc RIIA polymorphisms do not predict clinical outcome of follicular non-Hodgkin's lymphoma patients treated with sequential CHOP and rituximab. Haematologica. 92(8). 1127–1130. 76 indexed citations
18.
Carlotti, Emanuela, David Wrench, Sameena Iqbal, et al.. (2007). Determining the Mechanism of Transformation of Follicular Lymphoma into Diffuse Large B Cell Lymphoma.. Blood. 110(11). 181–181. 1 indexed citations
19.
Carlotti, Emanuela, Giuseppe A. Palumbo, Elena Oldani, et al.. (2005). Bone Marrow BCL2/IgH+ Cells at Diagnosis and Not FCGRIIIA Polymorphism Predict Response in Follicular Non-Hodgkin’s Lymphoma Patients Treated with Sequential CHOP and Rituximab.. Blood. 106(11). 985–985. 1 indexed citations
20.
Carlotti, Emanuela, Ricardo Amaru, Sarah Slater, et al.. (2002). Molecular characterization of a new recombination of the SIL/TAL‐1 locus in a child with T‐cell acute lymphoblastic leukaemia. British Journal of Haematology. 118(4). 1011–1018. 13 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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