Carlos Daniel De Brasi

852 total citations
42 papers, 561 citations indexed

About

Carlos Daniel De Brasi is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Carlos Daniel De Brasi has authored 42 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Hematology, 31 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Carlos Daniel De Brasi's work include Cancer-related gene regulation (23 papers), Hemophilia Treatment and Research (22 papers) and Chronic Myeloid Leukemia Treatments (9 papers). Carlos Daniel De Brasi is often cited by papers focused on Cancer-related gene regulation (23 papers), Hemophilia Treatment and Research (22 papers) and Chronic Myeloid Leukemia Treatments (9 papers). Carlos Daniel De Brasi collaborates with scholars based in Argentina, United Kingdom and Brazil. Carlos Daniel De Brasi's co-authors include Irene Larripa, Liliana Carmen Rossetti, Claudia Pamela Radic, D. J. Bowen, Anne Goodeve, R. Bianco, Peter W. Collins, Irene Szijan, Florencia Giliberto and Michele Bianchini and has published in prestigious journals such as Blood, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Carlos Daniel De Brasi

42 papers receiving 538 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carlos Daniel De Brasi Argentina 14 402 392 70 60 25 42 561
Jürgen Groet United Kingdom 12 213 0.5× 243 0.6× 98 1.4× 63 1.1× 46 1.8× 15 502
Kristen S. Jahn United States 5 440 1.1× 72 0.2× 52 0.7× 78 1.3× 37 1.5× 5 530
Claudio Macias-Treviño United States 6 428 1.1× 69 0.2× 87 1.2× 168 2.8× 51 2.0× 10 559
L. Alexander Liggett United States 7 193 0.5× 79 0.2× 92 1.3× 26 0.4× 26 1.0× 7 446
Brian Gibbs United States 5 123 0.3× 98 0.3× 98 1.4× 36 0.6× 33 1.3× 8 254
Shu Yau United Kingdom 8 130 0.3× 49 0.1× 90 1.3× 42 0.7× 38 1.5× 10 258
Kimihiko Banno Japan 9 182 0.5× 45 0.1× 44 0.6× 25 0.4× 12 0.5× 12 272
Paul V. Dellorusso United States 7 159 0.4× 214 0.5× 22 0.3× 64 1.1× 6 0.2× 7 422
Dorothée Cailley France 8 166 0.4× 84 0.2× 215 3.1× 46 0.8× 73 2.9× 10 388
Cong Peng China 5 160 0.4× 90 0.2× 38 0.5× 167 2.8× 74 3.0× 12 290

Countries citing papers authored by Carlos Daniel De Brasi

Since Specialization
Citations

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

Fields of papers citing papers by Carlos Daniel De Brasi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carlos Daniel De Brasi. 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 Carlos Daniel De Brasi. The network helps show where Carlos Daniel De Brasi may publish in the future.

Co-authorship network of co-authors of Carlos Daniel De Brasi

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos Daniel De Brasi. A scholar is included among the top collaborators of Carlos Daniel De Brasi 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 Carlos Daniel De Brasi. Carlos Daniel De Brasi 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.
2.
Rossetti, Liliana Carmen, et al.. (2023). Assessment of interleukin-10 promoter variant (−1082A/G) and cytokine production in patients with hemolytic uremic syndrome. Frontiers in Pediatrics. 11. 1210158–1210158. 2 indexed citations
3.
4.
Mazzanti, Chiara Maria, Liliana Carmen Rossetti, Claudia Pamela Radic, et al.. (2020). Analysis of complex structural variants in the DMD gene in one family. Neuromuscular Disorders. 31(3). 253–263. 4 indexed citations
5.
Radic, Claudia Pamela, Daniela Neme, Irene Larripa, et al.. (2019). Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia. European Journal of Human Genetics. 27(4). 603–611. 1 indexed citations
6.
Radic, Claudia Pamela, et al.. (2015). F8 intron 22 inversions and SNP rs73563631 in unrelated families with severe haemophilia A: clinical features and gene testing implications. Thrombosis and Haemostasis. 115(3). 678–681. 4 indexed citations
7.
Citterio, Cintia E., Liliana Carmen Rossetti, Martine Doco‐Fenzy, et al.. (2013). Novel mutational mechanism in the thyroglobulin gene: Imperfect DNA inversion as a cause for hereditary hypothyroidism. Molecular and Cellular Endocrinology. 381(1-2). 220–229. 14 indexed citations
8.
Giliberto, Florencia, et al.. (2013). Symptomatic female carriers of Duchenne muscular dystrophy (DMD): Genetic and clinical characterization. Journal of the Neurological Sciences. 336(1-2). 36–41. 39 indexed citations
9.
Rossetti, Liliana Carmen, Claudia Pamela Radic, Daniela Neme, et al.. (2013). Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risks. Haemophilia. 19(4). 511–518. 10 indexed citations
10.
Rossetti, Liliana Carmen, R. Bianco, Irene Larripa, et al.. (2012). Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B. Thrombosis and Haemostasis. 109(1). 24–33. 31 indexed citations
11.
Brasi, Carlos Daniel De, et al.. (2010). BAX/BCL-XL gene expression ratio inversely correlates with disease progression in chronic myeloid leukemia. Blood Cells Molecules and Diseases. 45(3). 192–196. 12 indexed citations
12.
Rossetti, Liliana Carmen, Claudia Pamela Radic, M. Candela, et al.. (2007). Sixteen novel hemophilia A causative mutations in the first Argentinian series of severe molecular defects. Haematologica. 92(6). 842–845. 21 indexed citations
13.
Bianchini, Michele, et al.. (2007). Determination of BCR-ABL Overexpression by Correlating qRT-PCR and IP-FISH in Imatinib Treated CML Patients.. Blood. 110(11). 1958–1958. 1 indexed citations
14.
Rossetti, Liliana Carmen, et al.. (2004). Analysis of factor VIII gene intron 1 inversion in Argentinian families with severe haemophilia A and a review of the literature. Blood Coagulation & Fibrinolysis. 15(7). 569–572. 19 indexed citations
15.
Rossetti, Liliana Carmen, Anne Goodeve, Irene Larripa, & Carlos Daniel De Brasi. (2004). Homeologous recombination between AluSx-sequences as a cause of hemophilia. Human Mutation. 24(5). 440–440. 30 indexed citations
16.
Brasi, Carlos Daniel De, et al.. (2004). Feasibility of a cost-effective approach to evaluate short tandem repeat markers suitable for chimerism follow-up. Molecular Diagnosis. 8(2). 87–91. 6 indexed citations
17.
Brasi, Carlos Daniel De, et al.. (2003). Rapid detection of exon 1 NRAS gene mutations using universal heteroduplex generator technology. Human Mutation. 21(2). 132–137. 4 indexed citations
18.
Brasi, Carlos Daniel De, D. J. Bowen, Peter W. Collins, & Irene Larripa. (2002). The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human males. Journal of Human Genetics. 47(5). 239–242. 2 indexed citations
19.
Bowen, D. J., Carlos Daniel De Brasi, Irene Larripa, & Peter W. Collins. (2000). A new polymorphism in the human factor VIII gene: implications for linkage analysis in haemophilia A and for the evolution of int22h sequences. British Journal of Haematology. 111(2). 544–548. 7 indexed citations
20.
Brasi, Carlos Daniel De, Irma Slavutsky, & Irene Larripa. (1996). [Molecular genetics of hemophilia A].. PubMed. 56(5 Pt 1). 509–17. 3 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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