Vicenç Català

523 total citations
14 papers, 271 citations indexed

About

Vicenç Català is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Vicenç Català has authored 14 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 5 papers in Plant Science. Recurrent topics in Vicenç Català's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Chromosomal and Genetic Variations (5 papers). Vicenç Català is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Chromosomal and Genetic Variations (5 papers). Vicenç Català collaborates with scholars based in Spain, United States and France. Vicenç Català's co-authors include Francesca Vidal, Josep Santaló, J. Egozcue, Joan Blanco, Pedro N. Barri, Gloria Calderón, Carla Giménez, Anna Veiga, A. Estop and L. Bassas and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Cytogenetic and Genome Research.

In The Last Decade

Vicenç Català

14 papers receiving 224 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vicenç Català Spain 10 191 92 89 71 70 14 271
M. Codina‐Pascual Spain 11 256 1.3× 164 1.8× 95 1.1× 178 2.5× 175 2.5× 15 411
K. Burns Canada 6 203 1.1× 113 1.2× 105 1.2× 129 1.8× 97 1.4× 8 324
R. Martin Canada 5 213 1.1× 150 1.6× 137 1.5× 116 1.6× 78 1.1× 7 329
Áine Rattigan United Kingdom 10 394 2.1× 30 0.3× 167 1.9× 91 1.3× 274 3.9× 10 483
Ewa Wiland Poland 11 191 1.0× 128 1.4× 106 1.2× 129 1.8× 109 1.6× 31 332
T. Hassold United States 6 132 0.7× 208 2.3× 47 0.5× 32 0.5× 67 1.0× 8 315
Kathy Hildebrand Canada 9 244 1.3× 189 2.1× 157 1.8× 187 2.6× 112 1.6× 10 442
Rubén Martín‐Arenas Spain 6 89 0.5× 57 0.6× 50 0.6× 27 0.4× 66 0.9× 12 162
Wouter G. van Inzen Netherlands 9 87 0.5× 113 1.2× 130 1.5× 26 0.4× 93 1.3× 10 293
Aïda Pujol Spain 10 145 0.8× 203 2.2× 125 1.4× 47 0.7× 76 1.1× 15 340

Countries citing papers authored by Vicenç Català

Since Specialization
Citations

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

Fields of papers citing papers by Vicenç Català

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vicenç Català

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

All Works

14 of 14 papers shown
1.
Baena, Neus, et al.. (2015). A 11.7-Mb Paracentric Inversion in Chromosome 1q Detected in Prenatal Diagnosis Associated with Familial Intellectual Disability. Cytogenetic and Genome Research. 146(2). 109–114. 14 indexed citations
2.
Cirigliano, Vincenzo, et al.. (2013). Supernumerary Ring Chromosome: An Etiology for Pallister-Killian Syndrome?. Fetal Diagnosis and Therapy. 34(3). 172–175. 18 indexed citations
3.
Plaja, Alberto, Elisabet Lloveras, Cristina Martínez-Bouzas, et al.. (2013). Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: A possible recurrent chromosome aberration. American Journal of Medical Genetics Part A. 161(9). 2363–2368. 20 indexed citations
4.
Català, Vicenç, et al.. (2013). Mosaicos cromosómicos en vellosidad corial. 24(3). 99–107. 1 indexed citations
5.
Mayo, Sonia, Sandra Monfort, Mónica Rosello, et al.. (2011). De novo Interstitial Triplication of <i>MECP2</i> in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation. Cytogenetic and Genome Research. 135(2). 93–101. 19 indexed citations
6.
Blanco, Joan, et al.. (2011). Hidden mosaicism in patients with Klinefelter's syndrome: implications for genetic reproductive counselling. Human Reproduction. 26(12). 3486–3493. 32 indexed citations
7.
Morales, Carmen, Irene Mademont‐Soler, Núria Clusellas, et al.. (2010). Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues. European Journal of Medical Genetics. 53(4). 197–200. 17 indexed citations
8.
Vicente, Asunción, et al.. (2009). Phylloid Hypomelanosis and Mosaic Partial Trisomy 13. Archives of Dermatology. 145(5). 576–8. 22 indexed citations
9.
Plaja, Alberto, et al.. (2004). Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24. Fertility and Sterility. 82(6). 1666–1671. 4 indexed citations
10.
11.
Vidal, Francesca, Vicenç Català, Josep Santaló, et al.. (1993). Preimplantation diagnosis: Sephadex filtration and human serum albumin gradients do not select spermatozoa by sex chromosome: a fluorescent in-situ hybridization study. Human Reproduction. 8(10). 1740–1743. 68 indexed citations
12.
Estop, A., Vicenç Català, & Josep Santaló. (1990). Chromosome constitution of highly motile mouse sperm. Molecular Reproduction and Development. 27(2). 168–172. 8 indexed citations
13.
Català, Vicenç, A. Estop, Josep Santaló, & J. Egozcue. (1988). Sexual immaturity and maternal age: incidence of aneuploidy and polyploidy in first-cleavage mouse embryos. Cytogenetic and Genome Research. 48(4). 233–237. 13 indexed citations
14.
Santaló, Josep, et al.. (1987). Chromosomes of mouse embryos in vivo and in vitro: effect of manipulation, maternal age and gamete ageing*. Human Reproduction. 2(8). 717–719. 5 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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