Marta Bernués

2.0k total citations
18 papers, 313 citations indexed

About

Marta Bernués is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Marta Bernués has authored 18 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Marta Bernués's work include Cancer Genomics and Diagnostics (5 papers), Chronic Lymphocytic Leukemia Research (4 papers) and Renal and related cancers (4 papers). Marta Bernués is often cited by papers focused on Cancer Genomics and Diagnostics (5 papers), Chronic Lymphocytic Leukemia Research (4 papers) and Renal and related cancers (4 papers). Marta Bernués collaborates with scholars based in Spain and United Kingdom. Marta Bernués's co-authors include Rosa Miró, M.R. Caballı́n, Antoni Gelabert, Carme Casadevall, Josep Egozcue, Esther Prat, Jordi Rosell, Damián Heine‐Suñer, Nancy Govea and Xavier Busquets and has published in prestigious journals such as British Journal of Cancer, Urology and European Journal of Human Genetics.

In The Last Decade

Marta Bernués

17 papers receiving 303 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta Bernués Spain 11 189 100 68 62 61 18 313
Yao‐Shan Fan United States 9 94 0.5× 48 0.5× 19 0.3× 42 0.7× 38 0.6× 19 275
Myriam Goldstein Israel 8 209 1.1× 83 0.8× 70 1.0× 19 0.3× 21 0.3× 10 331
Detlef Trost France 10 224 1.2× 124 1.2× 17 0.3× 16 0.3× 23 0.4× 20 346
Claudia Dellavecchia Italy 9 153 0.8× 220 2.2× 74 1.1× 39 0.6× 18 0.3× 11 408
Lillian Bitner United States 4 128 0.7× 16 0.2× 22 0.3× 46 0.7× 58 1.0× 5 330
Lourdes Badı́a Spain 10 111 0.6× 110 1.1× 45 0.7× 10 0.2× 43 0.7× 28 325
Lan‐Szu Chou United States 5 108 0.6× 76 0.8× 153 2.3× 79 1.3× 16 0.3× 9 352
Marco Garieri Switzerland 10 278 1.5× 156 1.6× 13 0.2× 24 0.4× 17 0.3× 12 435
M.H. Breuning Netherlands 8 219 1.2× 157 1.6× 25 0.4× 51 0.8× 40 0.7× 13 385
Pawan Dhami United Kingdom 9 164 0.9× 41 0.4× 11 0.2× 39 0.6× 14 0.2× 19 344

Countries citing papers authored by Marta Bernués

Since Specialization
Citations

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

Fields of papers citing papers by Marta Bernués

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Bernués

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

All Works

18 of 18 papers shown
1.
Bernués, Marta, Teresa González, Luís A. Corchete, et al.. (2022). t(10;12)(q24;q15): A new cytogenetic marker in hematological malignancies. Cancer Genetics. 264-265. 60–65. 1 indexed citations
2.
Andrade, Bernardo López, Antonio Gutiérrez, María Antonia Durán, et al.. (2015). Acute lymphoblastic leukemia with e1a3 BCR/ABL fusion protein. A report of two cases. Experimental Hematology and Oncology. 5(1). 21–21. 9 indexed citations
3.
Bernués, Marta, María Antonia Durán, Julio Iglesias, et al.. (2014). Genetics of lymphocytes influences the emergence of second cancer in chronic lymphocytic leukemia.. PubMed. 34(5). 2311–4. 1 indexed citations
4.
Rosell, Jordi, et al.. (2011). Structural rearrangements of trisomies are a risk marker of clinical progression in hyperdiploid multiple myeloma.. PubMed. 31(5). 1599–602. 1 indexed citations
5.
Durán, María Antonia, et al.. (2007). dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in Myelodysplastic Syndromes. Leukemia Research. 32(1). 159–161. 10 indexed citations
6.
Rosell, Jordi, Montse Morlá, Daniel Bachiller, et al.. (2007). Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation. European Journal of Human Genetics. 15(6). 658–663. 51 indexed citations
7.
Camps, Jordi, Itziar Salaverría, María J. García, et al.. (2006). Genomic imbalances and patterns of karyotypic variability in mantle-cell lymphoma cell lines. Leukemia Research. 30(8). 923–934. 43 indexed citations
8.
Prat, Esther, Marta Bernués, Javier del Rey, et al.. (2006). Common pattern of unusual chromosome abnormalities in hereditary papillary renal carcinoma. Cancer Genetics and Cytogenetics. 164(2). 142–147. 3 indexed citations
9.
Casas, Sı́lvia, Anna Aventı́n, Teresa Vallespı́, et al.. (2004). Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia. Cancer Genetics and Cytogenetics. 153(1). 16–25. 22 indexed citations
10.
Heine‐Suñer, Damián, Montse Morlá, Xavier Busquets, et al.. (2003). Fragile‐X syndrome and skewed X‐chromosome inactivation within a family: A female member with complete inactivation of the functional X chromosome. American Journal of Medical Genetics Part A. 122A(2). 108–114. 37 indexed citations
11.
Casadevall, Carme, Marta Bernués, M.R. Caballı́n, et al.. (2002). Analysis of kidney tumors by comparative genomic hybridization and conventional cytogenetics. Cancer Genetics and Cytogenetics. 137(1). 49–53. 22 indexed citations
12.
Fuster, Carme, Carme Casadevall, Marta Bernués, et al.. (2001). Comparative genomic hybridization analysis of transitional cell carcinomas of the renal pelvis. Cancer Genetics and Cytogenetics. 127(1). 59–63. 17 indexed citations
13.
Prat, Esther, Marta Bernués, M.R. Caballı́n, et al.. (2001). Detection of chromosomal imbalances in papillary bladder tumors by comparative genomic hybridization. Urology. 57(5). 986–992. 40 indexed citations
14.
Bernués, Marta, Carme Casadevall, M.R. Caballı́n, et al.. (1999). Study of Allelic Losses on 3p, 6q, and 17p in Human Urothelial Cancer. Cancer Genetics and Cytogenetics. 112(1). 42–45. 13 indexed citations
15.
Bernués, Marta, et al.. (1999). Restriction fragment length polymorphism of the L-myc gene is not a prognostic factor in bladder cancer patients. British Journal of Cancer. 79(11-12). 1855–1858. 11 indexed citations
16.
Bernués, Marta, Carme Casadevall, Rosa Miró, et al.. (1998). Analysis of 3p Allelic Losses in Renal Cell Carcinomas. Cancer Genetics and Cytogenetics. 107(2). 121–124. 6 indexed citations
17.
Bernués, Marta, Carme Casadevall, Rosa Miró, et al.. (1995). Cytogenetic characterization of a familial papillary renal cell carcinoma. Cancer Genetics and Cytogenetics. 84(2). 123–127. 18 indexed citations
18.
Bernués, Marta, Carme Casadevall, Rosa Miró, et al.. (1993). A case of transitional cell carcinoma of the bladder with a del(9)(q11q21.2). Cancer Genetics and Cytogenetics. 69(1). 76–77. 8 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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