Alessandra Splendore

639 total citations
16 papers, 392 citations indexed

About

Alessandra Splendore is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Alessandra Splendore has authored 16 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Hematology. Recurrent topics in Alessandra Splendore's work include Craniofacial Disorders and Treatments (6 papers), Acute Myeloid Leukemia Research (4 papers) and RNA modifications and cancer (3 papers). Alessandra Splendore is often cited by papers focused on Craniofacial Disorders and Treatments (6 papers), Acute Myeloid Leukemia Research (4 papers) and RNA modifications and cancer (3 papers). Alessandra Splendore collaborates with scholars based in Brazil, United States and Argentina. Alessandra Splendore's co-authors include Maria Rita Passos‐Bueno, Cibele Masotti, Athena M. Cherry, Melanie A. Manning, Swaroop Aradhya, Maria S. Pombo‐de‐Oliveira, Elias O. Silva, Denise P. Cavalcanti, A. Richieri‐Costa and Luís Garcia Alonso and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and BMC Cancer.

In The Last Decade

Alessandra Splendore

16 papers receiving 383 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alessandra Splendore Brazil 11 227 172 58 48 47 16 392
Aziza Sbiti Morocco 9 133 0.6× 211 1.2× 69 1.2× 15 0.3× 45 1.0× 19 387
Vasilios Zachariadis Sweden 11 90 0.4× 157 0.9× 38 0.7× 100 2.1× 16 0.3× 20 392
Gabriel A. Quinlan Australia 6 76 0.3× 437 2.5× 28 0.5× 25 0.5× 17 0.4× 8 489
Fátima Godinho Portugal 7 52 0.2× 190 1.1× 29 0.5× 54 1.1× 51 1.1× 12 389
M Stefanova Germany 12 208 0.9× 196 1.1× 77 1.3× 12 0.3× 6 0.1× 29 474
Nobuko Yamanaka Canada 12 26 0.1× 143 0.8× 116 2.0× 58 1.2× 26 0.6× 15 347
Rika Kawagoe Japan 7 45 0.2× 282 1.6× 59 1.0× 37 0.8× 13 0.3× 9 367
Ayala Aviram Israel 8 161 0.7× 168 1.0× 75 1.3× 12 0.3× 7 0.1× 9 328
Karen J. Harrison Canada 10 252 1.1× 248 1.4× 23 0.4× 23 0.5× 7 0.1× 17 461
Vera Uliana Italy 13 189 0.8× 163 0.9× 19 0.3× 17 0.4× 8 0.2× 30 377

Countries citing papers authored by Alessandra Splendore

Since Specialization
Citations

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

Fields of papers citing papers by Alessandra Splendore

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessandra Splendore

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

All Works

16 of 16 papers shown
1.
Mansur, Marcela Braga, Rocı́o Hassan, Alessandra Splendore, et al.. (2012). Impact of complex NOTCH1 mutations on survival in paediatric T-cell leukaemia. BMC Cancer. 12(1). 9–9. 29 indexed citations
2.
Mansur, Marcela Braga, et al.. (2009). T-cell lymphoblastic leukemia in early childhood presents NOTCH1 mutations and MLL rearrangements. Leukemia Research. 34(4). 483–486. 13 indexed citations
3.
Li, Hong Hua, Madhuri Roy, Corinne M. Spencer, et al.. (2009). Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice. EMBO Molecular Medicine. 1(1). 50–65. 74 indexed citations
4.
Masotti, Cibele, Tudor C. Poerner, Alessandra Splendore, et al.. (2007). Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity. European Journal of Human Genetics. 16(2). 145–152. 25 indexed citations
5.
Aradhya, Swaroop, Melanie A. Manning, Alessandra Splendore, & Athena M. Cherry. (2007). Whole‐genome array‐CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features. American Journal of Medical Genetics Part A. 143A(13). 1431–1441. 42 indexed citations
6.
Magalhães, Isis Quezado, et al.. (2006). GATA1 mutations in acute leukemia in children with Down syndrome. Cancer Genetics and Cytogenetics. 166(2). 112–116. 14 indexed citations
7.
Masotti, Cibele, Lucia Armelin‐Correa, Alessandra Splendore, et al.. (2005). A functional SNP in the promoter region of TCOF1 is associated with reduced gene expression and YY1 DNA–protein interaction. Gene. 359. 44–52. 23 indexed citations
8.
Splendore, Alessandra, et al.. (2005). TCOF1 mutation database: Novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature. Human Mutation. 25(5). 429–434. 31 indexed citations
9.
Splendore, Alessandra, Isis Quezado Magalhães, & Maria S. Pombo‐de‐Oliveira. (2005). GATA1mutations in myeloproliferative disorders: nomenclature standardization and review of the literature. Human Mutation. 26(4). 390–392. 1 indexed citations
10.
Splendore, Alessandra, et al.. (2005). Transient Neonatal Myeloproliferative Disorder Without Down Syndrome and Detection of GATA1 Mutation. Journal of Pediatric Hematology/Oncology. 27(1). 50–52. 12 indexed citations
11.
Emerenciano, Mariana, et al.. (2005). Influência da metileno-tetrahidrofolato redutase na patogênese das leucemias agudas infantis. SHILAP Revista de lepidopterología. 51(4). 289–295. 2 indexed citations
12.
Splendore, Alessandra, Ethylin Wang Jabs, Têmis Maria Félix, & Maria Rita Passos‐Bueno. (2003). Parental origin of mutations in sporadic cases of Treacher Collins syndrome. European Journal of Human Genetics. 11(9). 718–722. 32 indexed citations
13.
Passos‐Bueno, Maria Rita & Alessandra Splendore. (2001). Síndrome de Treacher Collins: aspectos clínicos, genéticos e moleculares. Revista de Medicina. 80(1). 52–56. 5 indexed citations
14.
Splendore, Alessandra, et al.. (2001). Centro de Estudos do Genoma Humano:. Revista Neurociências. 20(2). 194–199. 1 indexed citations
15.
Splendore, Alessandra, Elias O. Silva, Luís Garcia Alonso, et al.. (2000). High mutation detection rate inTCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes. Human Mutation. 16(4). 315–322. 85 indexed citations
16.
Splendore, Alessandra, Elias O. Silva, Luís Garcia Alonso, et al.. (2000). High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes. Human Mutation. 16(4). 315–315. 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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