Immaculada Ponsa

510 total citations
16 papers, 380 citations indexed

About

Immaculada Ponsa is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Immaculada Ponsa has authored 16 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Surgery. Recurrent topics in Immaculada Ponsa's work include Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (3 papers) and Bladder and Urothelial Cancer Treatments (3 papers). Immaculada Ponsa is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (3 papers) and Bladder and Urothelial Cancer Treatments (3 papers). Immaculada Ponsa collaborates with scholars based in Spain, United States and Netherlands. Immaculada Ponsa's co-authors include Rosa Miró, Xavier Estivill, Lluı́s Armengol, Marga Nadal, Jordi Camps, Miguel Angel Pujana, Mónica Gratacòs, Belén Peral, Rocı́o Martı́n-Santos and Antoni Bulbena and has published in prestigious journals such as Cell, PLoS ONE and Genetics.

In The Last Decade

Immaculada Ponsa

16 papers receiving 362 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Immaculada Ponsa Spain 9 161 156 73 56 50 16 380
Birgitte Bertelsen Denmark 13 195 1.2× 244 1.6× 73 1.0× 67 1.2× 63 1.3× 26 525
Mary O’Driscoll United Kingdom 10 87 0.5× 129 0.8× 37 0.5× 47 0.8× 50 1.0× 20 390
James Colley United Kingdom 8 383 2.4× 241 1.5× 48 0.7× 79 1.4× 61 1.2× 13 539
K N Harikrishnan Australia 12 249 1.5× 552 3.5× 73 1.0× 41 0.7× 24 0.5× 16 722
Katherine Rojas United States 9 263 1.6× 200 1.3× 47 0.6× 24 0.4× 17 0.3× 15 424
Qixi Wu China 14 328 2.0× 290 1.9× 92 1.3× 38 0.7× 39 0.8× 28 568
J CLARK United States 8 127 0.8× 127 0.8× 32 0.4× 124 2.2× 31 0.6× 12 446
M. Kron United States 9 132 0.8× 131 0.8× 42 0.6× 53 0.9× 16 0.3× 20 470
Megan T. Cho United States 20 462 2.9× 508 3.3× 32 0.4× 51 0.9× 27 0.5× 27 838
Christopher Adams United States 11 68 0.4× 373 2.4× 108 1.5× 28 0.5× 36 0.7× 16 518

Countries citing papers authored by Immaculada Ponsa

Since Specialization
Citations

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

Fields of papers citing papers by Immaculada Ponsa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Immaculada Ponsa

This figure shows the co-authorship network connecting the top 25 collaborators of Immaculada Ponsa. A scholar is included among the top collaborators of Immaculada Ponsa 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 Immaculada Ponsa. Immaculada Ponsa 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.
Erola, Pau, María Isabel Álvarez‐Mora, Marcos Díaz‐Gay, et al.. (2018). Quantitative analysis of somatically acquired and constitutive uniparental disomy in gastrointestinal cancers. International Journal of Cancer. 144(3). 513–524. 6 indexed citations
2.
Wangsa, Darawalee, Immaculada Ponsa, Anna Bosch, et al.. (2017). Transcription-dependent radial distribution of TCF7L2 regulated genes in chromosome territories. Chromosoma. 126(5). 655–667. 5 indexed citations
3.
Miró, Rosa, Nora Fernández‐Jiménez, Esther Prat, et al.. (2015). Patterns of somatic uniparental disomy identify novel tumor suppressor genes in colorectal cancer. Carcinogenesis. 36(10). 1103–1110. 16 indexed citations
4.
Gaiser, Timo, Daniela Hirsch, Jonathan Keith Killian, et al.. (2012). Molecular patterns in the evolution of serrated lesion of the colorectum. International Journal of Cancer. 132(8). 1800–1810. 28 indexed citations
5.
Rey, Javier del, Esther Prat, Immaculada Ponsa, et al.. (2010). Centrosome clustering and cyclin D1 gene amplification in double minutes are common events in chromosomal unstable bladder tumors. BMC Cancer. 10(1). 280–280. 18 indexed citations
6.
Morell, Marta, et al.. (2009). Nucleotide, Cytogenetic and Expression Impact of the Human Chromosome 8p23.1 Inversion Polymorphism. PLoS ONE. 4(12). e8269–e8269. 18 indexed citations
7.
Ponsa, Immaculada, Josep Antoni Ramos‐Quiroga, Marta Ribasès, et al.. (2009). Absence of cytogenetic effects in children and adults with attention-deficit/hyperactivity disorder treated with methylphenidate. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 666(1-2). 44–49. 13 indexed citations
8.
Prat, Esther, Javier del Rey, Immaculada Ponsa, et al.. (2009). Comparative Genomic Hybridization Analysis Reveals New Different Subgroups in Early-stage Bladder Tumors. Urology. 75(2). 347–355. 6 indexed citations
9.
Prat, Esther, Javier del Rey, Jordi Camps, et al.. (2008). Genomic Imbalances in Urothelial Cancer: Intratumor Heterogeneity Versus Multifocality. Diagnostic Molecular Pathology. 17(3). 134–140. 8 indexed citations
10.
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
11.
Camps, Jordi, Immaculada Ponsa, Maria Ribas, et al.. (2005). Comprehensive measurement of chromosomal instability in cancer cells: combination of fluorescence in situ hybridization and cytokinesis‐block micronucleus assay. The FASEB Journal. 19(7). 1–19. 41 indexed citations
12.
Tusell, Laura, et al.. (2004). Capping of Radiation-Induced DNA Breaks in Mouse Early Embryos. Journal of Radiation Research. 45(3). 415–422. 6 indexed citations
13.
Ponsa, Immaculada, Joan Francesc Barquinero, Rosa Miró, Josep Egozcue, & Anna Genescà. (2001). Non-disjunction and Chromosome Loss in Gamma-Irradiated Human Lymphocytes: A FluorescenceIn SituHybridization Analysis Using Centromere-Specific Probes. Radiation Research. 155(3). 424–431. 15 indexed citations
14.
Gratacòs, Mónica, Marga Nadal, Rocı́o Martı́n-Santos, et al.. (2001). A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders. Cell. 106(3). 367–379. 156 indexed citations
15.
Ramı́rez, Ángel, Éric Milot, Immaculada Ponsa, et al.. (2001). Sequence and Chromosomal Context Effects on Variegated Expression of Keratin 5/lacZ Constructs in Stratified Epithelia of Transgenic Mice. Genetics. 158(1). 341–350. 39 indexed citations
16.
Ponsa, Immaculada, et al.. (1998). A New Assay to Asses Aneuploidy in Human-Hamster Embryos. Advances in experimental medicine and biology. 444. 185–190. 2 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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