Elena Bussaglia

2.2k total citations
35 papers, 1.6k citations indexed

About

Elena Bussaglia is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Elena Bussaglia has authored 35 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Genetics and 11 papers in Hematology. Recurrent topics in Elena Bussaglia's work include Acute Myeloid Leukemia Research (11 papers), Genetic factors in colorectal cancer (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Elena Bussaglia is often cited by papers focused on Acute Myeloid Leukemia Research (11 papers), Genetic factors in colorectal cancer (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Elena Bussaglia collaborates with scholars based in Spain, France and Italy. Elena Bussaglia's co-authors include Xavier Matías‐Guiu, Jaime Prat, Lluís Catasús, Cristina Pons, Alberto Gallardo, Helena Lagarda, Julie Irving, Pilar Fernández Machín, Montserrat Baiget and Jaime Prat and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Elena Bussaglia

34 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Bussaglia Spain 18 900 422 403 309 257 35 1.6k
Bernd Kazmierczak Germany 24 617 0.7× 138 0.3× 232 0.6× 39 0.1× 179 0.7× 58 1.5k
Sylke Wanschura Germany 21 585 0.7× 187 0.4× 304 0.8× 30 0.1× 160 0.6× 35 1.4k
John B. McIntyre Canada 19 538 0.6× 276 0.7× 248 0.6× 337 1.1× 208 0.8× 37 1.4k
Helena Kiefel Germany 17 605 0.7× 83 0.2× 112 0.3× 59 0.2× 341 1.3× 23 1.2k
Katrin E. Rhodes United States 13 575 0.6× 41 0.1× 69 0.2× 117 0.4× 560 2.2× 21 1.3k
Carol Berger United States 22 831 0.9× 38 0.1× 63 0.2× 141 0.5× 296 1.2× 43 1.6k
Kimberley Howarth United Kingdom 15 631 0.7× 56 0.1× 82 0.2× 30 0.1× 347 1.4× 20 1.4k
Robert T. Jones United States 8 513 0.6× 42 0.1× 77 0.2× 168 0.5× 380 1.5× 20 1.2k
Christina Evers Germany 16 293 0.3× 95 0.2× 114 0.3× 30 0.1× 110 0.4× 33 743

Countries citing papers authored by Elena Bussaglia

Since Specialization
Citations

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

Fields of papers citing papers by Elena Bussaglia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Bussaglia

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Bussaglia. A scholar is included among the top collaborators of Elena Bussaglia 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 Elena Bussaglia. Elena Bussaglia 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.
Hernández‐Álvarez, María Isabel, Matilde Parreño, Elena Bussaglia, et al.. (2025). D816V KIT mutation induces mitochondrial morphologic and functional changes through BNIP3 downregulation in human myeloid cell lines ROSA and TF-1. Experimental Hematology. 145. 104748–104748.
2.
Torrent, Montserrat, et al.. (2020). Many signs, one mutation: Early onset of de novo GATA2 deficiency syndrome. A case report. SHILAP Revista de lepidopterología. 8(12). 3192–3196. 2 indexed citations
3.
Bussaglia, Elena, Marta Pratcorona, Laura San‐Segundo, et al.. (2020). Application of a digital PCR method for WT1 to myeloid neoplasms in CR and deep ELN WT1 molecular response (< 10 copies). Annals of Hematology. 99(4). 765–772. 5 indexed citations
4.
Garrido, Ana, Elena Bussaglia, Marta Pratcorona, et al.. (2019). Bone marrow WT1 levels in patients with myeloid neoplasms treated with 5‐azacytidine: Identification of responding patients. European Journal Of Haematology. 103(3). 208–214. 6 indexed citations
5.
Bosch, Anna, et al.. (2019). Ultrastructural, cytogenetic, and molecular findings in mast cell leukemia: Case report. SHILAP Revista de lepidopterología. 7(7). 1395–1398. 2 indexed citations
6.
Nomdedéu, Josep, Montserrat Hoyos, Jordi Esteve, et al.. (2012). Adverse impact of IDH1 and IDH2 mutations in primary AML: Experience of the Spanish CETLAM group. Leukemia Research. 36(8). 990–997. 32 indexed citations
7.
Lasa, Adriana, Camino Estivill, Elena Bussaglia, et al.. (2009). WT1 monitoring in core binding factor AML: Comparison with specific chimeric products. Leukemia Research. 33(12). 1643–1649. 17 indexed citations
8.
Ferrán, Marta, Elena Bussaglia, Xavier Matías‐Guiu, & Ramón M. Pujol. (2009). Bilateral and symmetrical palmoplantar punctate keratoses in childhood: a possible clinical clue for an early diagnosis ofPTENhamartoma-tumour syndrome. Clinical and Experimental Dermatology. 34(5). e28–e30. 4 indexed citations
9.
Velasco, Ana, Elena Bussaglia, Judit Pallarés, et al.. (2006). PIK3CA gene mutations in endometrial carcinoma. Correlation with PTEN and K-RAS alterations☆. Human Pathology. 37(11). 1465–1472. 117 indexed citations
10.
Irving, Julie, Lluís Catasús, Alberto Gallardo, et al.. (2005). Synchronous endometrioid carcinomas of the uterine corpus and ovary: alterations in the β-catenin (CTNNB1) pathway are associated with independent primary tumors and favorable prognosis. Human Pathology. 36(6). 605–619. 86 indexed citations
11.
12.
Catasús, Lluís, Xavier Matías‐Guiu, Elena Bussaglia, et al.. (2003). Molecular pathology of atypical polypoid adenomyoma of the uterus. Human Pathology. 34(8). 784–788. 26 indexed citations
13.
Bussaglia, Elena, Ramón M. Pujol, Manuel Martín González, et al.. (2002). PTEN Mutations in Eight Spanish Families and One Brazilian Family with Cowden Syndrome. Journal of Investigative Dermatology. 118(4). 639–644. 16 indexed citations
14.
Matías‐Guiu, Xavier, Helena Lagarda, Lluís Catasús, et al.. (2002). Clonality Analysis in Synchronous or Metachronous Tumors of the Female Genital Tract. International Journal of Gynecological Pathology. 21(3). 205–211. 33 indexed citations
15.
Cuscó, Ivon, M. J. Barceló, Elisabeth del Río, et al.. (2001). Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases. Human Genetics. 108(3). 222–229. 36 indexed citations
16.
Matías‐Guiu, Xavier, Lluís Catasús, Elena Bussaglia, et al.. (2001). Molecular pathology of endometrial hyperplasia and carcinoma. Human Pathology. 32(6). 569–577. 245 indexed citations
17.
Bussaglia, Elena, et al.. (2000). PTEN mutations in endometrial carcinomas: A molecular and clinicopathologic analysis of 38 cases. Human Pathology. 31(3). 312–317. 139 indexed citations
18.
Bussaglia, Elena, et al.. (2000). Loss of Heterozygosity on Chromosome 17q in Epithelial Ovarian Tumors: Association with Carcinomas with Serous Differentiation. International Journal of Gynecological Pathology. 19(2). 152–157. 22 indexed citations
19.
Bayés, Mónica, Amalia Martı́nez-Mir, Elena Bussaglia, et al.. (1998). A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.. Journal of Medical Genetics. 35(2). 141–145. 26 indexed citations
20.
Bussaglia, Elena, Olivier Clermont, Eduardo F. Tizzano, et al.. (1995). A frame–shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients. Nature Genetics. 11(3). 335–337. 184 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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