Bárbara Marques

913 total citations
19 papers, 272 citations indexed

About

Bárbara Marques is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Bárbara Marques has authored 19 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Hematology. Recurrent topics in Bárbara Marques's work include Genomic variations and chromosomal abnormalities (5 papers), Chronic Myeloid Leukemia Treatments (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Bárbara Marques is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Chronic Myeloid Leukemia Treatments (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Bárbara Marques collaborates with scholars based in Portugal, Mozambique and Belgium. Bárbara Marques's co-authors include Maria Guida Boavida, Paulo Matos, Peter Jordan, Luı́s Vieira, D. David, Jennifer Skaug, Stephen W. Scherer, Sebastian Beck, Fátima Verı́ssimo and Christian Gespach and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and Gene.

In The Last Decade

Bárbara Marques

18 papers receiving 257 citations

Peers

Bárbara Marques
Lauren Véronèse France
Candace J. Poole United States
Tracey Holloway United Kingdom
Rozario Thomas United States
Edward Favours United States
Susana Bizarro Portugal
Kristen L. Karlin United States
Tanya A. Kranenburg United States
Pierre Walrafen France
Nina Weichert‐Leahey United States
Lauren Véronèse France
Bárbara Marques
Citations per year, relative to Bárbara Marques Bárbara Marques (= 1×) peers Lauren Véronèse

Countries citing papers authored by Bárbara Marques

Since Specialization
Citations

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

Fields of papers citing papers by Bárbara Marques

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bárbara Marques

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

All Works

19 of 19 papers shown
1.
Marques, Bárbara, et al.. (2021). SVInterpreter: A Comprehensive Topologically Associated Domain-Based Clinical Outcome Prediction Tool for Balanced and Unbalanced Structural Variants. Frontiers in Genetics. 12. 757170–757170. 6 indexed citations
2.
Ventura, Célia, Paulo Matos, Bárbara Marques, et al.. (2020). Cytotoxicity and genotoxicity of MWCNT-7 and crocidolite: assessment in alveolar epithelial cells versus their coculture with monocyte-derived macrophages. Nanotoxicology. 14(4). 479–503. 27 indexed citations
3.
Marques, Bárbara, et al.. (2017). Very late presentation of a disorder of sex development. Andrologia. 49(10). e12831–e12831. 2 indexed citations
4.
5.
Marques, Bárbara, Cristina Ferreira, Sónia N. Pedro, et al.. (2016). Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report. Molecular Cytogenetics. 9(1). 87–87. 1 indexed citations
6.
David, D., Bárbara Marques, Cristina Ferreira, et al.. (2013). Co-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression. Human Genetics. 132(11). 1287–1299. 16 indexed citations
7.
Marques, Bárbara, et al.. (2013). Farm to School Education Project: Innovative Partnership to Support Student Achievement of Core Knowledge and Competencies and Provide Service-Learning Opportunity through Farm to School. Journal of the Academy of Nutrition and Dietetics. 113(9). A50–A50. 1 indexed citations
8.
Ferreira, Cristina, et al.. (2013). Prenatal diagnosis of mosaic tetrasomy 18p. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 30–31.
9.
10.
David, D., Bárbara Marques, Cristina Ferreira, et al.. (2009). Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5 Mb on chromosome 2q14.1–q14.2. European Journal of Human Genetics. 17(8). 1024–1033. 14 indexed citations
11.
Michels, Evi, Jo Vandesompele, Katleen De Preter, et al.. (2007). ArrayCGH‐based classification of neuroblastoma into genomic subgroups. Genes Chromosomes and Cancer. 46(12). 1098–1108. 55 indexed citations
12.
Vieira, Luı́s, Paulo Matos, Bárbara Marques, et al.. (2006). Three‐way translocation involves MLL, MLLT3, and a novel cell cycle control gene, FLJ10374, in the pathogenesis of acute myeloid leukemia with t(9;11;19)(p22;q23;p13.3). Genes Chromosomes and Cancer. 45(5). 455–469. 8 indexed citations
13.
Vieira, Luı́s, et al.. (2005). Molecular cytogenetic characterization of rearrangements involving 12p in leukemia. Cancer Genetics and Cytogenetics. 157(2). 134–139. 9 indexed citations
14.
Limbert, Catarina, et al.. (2005). [Screening for Y chromosome sequences in patients with Turner syndrome].. PubMed. 15(2). 89–100. 3 indexed citations
15.
David, D., Joana Cardoso, Bárbara Marques, et al.. (2003). Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGFβ2 in the pathogenesis of Peters’ anomaly. Genomics. 81(5). 489–503. 29 indexed citations
16.
Lopes, Maria de Lurdes, et al.. (2002). Pesquisa de sequências do cromossoma Y em indivíduos com síndroma de Turner.. SHILAP Revista de lepidopterología. 1 indexed citations
17.
Vieira, Luı́s, Vanessa G. Oliveira, Bárbara Marques, et al.. (2001). Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2). Cancer Genetics and Cytogenetics. 128(2). 104–107. 24 indexed citations
18.
Matos, Paulo, Jennifer Skaug, Bárbara Marques, et al.. (2000). Small GTPase Rac1: Structure, Localization, and Expression of the Human Gene. Biochemical and Biophysical Research Communications. 277(3). 741–751. 55 indexed citations
19.
Vieira, Luı́s, et al.. (1999). Insertion of the 5′ Part of BCR within the ABL Gene at 9q34 in a Philadelphia-negative Chronic Myeloid Leukemia. Cancer Genetics and Cytogenetics. 114(1). 17–21. 15 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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