C. Mediano

431 total citations
12 papers, 244 citations indexed

About

C. Mediano is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, C. Mediano has authored 12 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 8 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in C. Mediano's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (3 papers). C. Mediano is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (3 papers). C. Mediano collaborates with scholars based in Spain, Netherlands and Palestinian Territory. C. Mediano's co-authors include Alberto Plaja, Teresa Vendrell, Clara Serra‐Juhé, María Ángeles Mori, Pablo Lapunzina, D.F.C.M. Smeets, Olaya Villa, Luis A. Pérez‐Jurado, Elena Mansilla and Lidia García‐Pérez and has published in prestigious journals such as Breast Cancer Research and Treatment, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

C. Mediano

12 papers receiving 233 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Mediano Spain 8 163 159 76 32 26 12 244
Jiadi Wen United States 9 124 0.8× 125 0.8× 84 1.1× 18 0.6× 16 0.6× 22 264
Carolyn Trunca United States 9 199 1.2× 152 1.0× 98 1.3× 96 3.0× 31 1.2× 14 301
Cathy Sullivan United States 5 174 1.1× 170 1.1× 72 0.9× 38 1.2× 13 0.5× 7 276
Florence Amblard France 10 147 0.9× 75 0.5× 122 1.6× 23 0.7× 26 1.0× 21 276
M. Crocker United Kingdom 9 183 1.1× 68 0.4× 88 1.2× 52 1.6× 15 0.6× 16 245
Michael Freidine United States 9 169 1.0× 292 1.8× 80 1.1× 44 1.4× 57 2.2× 10 396
Anna Ruggeri Italy 10 197 1.2× 255 1.6× 122 1.6× 31 1.0× 24 0.9× 13 402
Eveline Wesby–van Swaay Netherlands 9 177 1.1× 91 0.6× 97 1.3× 25 0.8× 42 1.6× 14 287
Moncef Benkhalifa France 7 98 0.6× 110 0.7× 128 1.7× 21 0.7× 28 1.1× 8 314
Robert‐Jan Galjaard Netherlands 8 180 1.1× 94 0.6× 179 2.4× 20 0.6× 71 2.7× 10 326

Countries citing papers authored by C. Mediano

Since Specialization
Citations

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

Fields of papers citing papers by C. Mediano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Mediano

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

All Works

12 of 12 papers shown
1.
Mediano, C., et al.. (2011). Increased MLL gene rearrangements in amniocytes from fetuses of mothers who smoke. Leukemia Research. 35(8). 1066–1069. 6 indexed citations
2.
Armengol, Lluı́s, Julián Nevado, Clara Serra‐Juhé, et al.. (2011). Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis. Human Genetics. 131(3). 513–523. 69 indexed citations
3.
Bádenas, Célia, Laia Rodríguez‐Revenga, Carmen Morales, et al.. (2010). Assessment of QF-PCR as the First Approach in Prenatal Diagnosis. Journal of Molecular Diagnostics. 12(6). 828–834. 44 indexed citations
4.
Dı́ez, Orland, Sara Gutiérrez‐Enríquez, C. Mediano, et al.. (2009). A novel de novo BRCA2 mutation of paternal origin identified in a Spanish woman with early onset bilateral breast cancer. Breast Cancer Research and Treatment. 121(1). 221–225. 9 indexed citations
5.
Cirigliano, Vincenzo, M. Paz Cañadas, Alberto Plaja, et al.. (2003). Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR. Prenatal Diagnosis. 23(8). 629–633. 19 indexed citations
6.
Farrán-Codina, Inmaculada, et al.. (2002). Early amniocentesis with the filtration technique: neonatal outcome in 123 singleton pregnancies. Prenatal Diagnosis. 22(10). 859–863. 2 indexed citations
7.
Plaja, Alberto, et al.. (2001). Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease. American Journal of Medical Genetics. 98(3). 216–223. 37 indexed citations
8.
Vendrell, Teresa, et al.. (2001). Apparent coexistence of a neocentromere with an alphoid classic centromere. 1(44). 52–52. 1 indexed citations
9.
Plaja, Alberto, et al.. (2001). Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis. American Journal of Medical Genetics. 104(1). 37–41. 22 indexed citations
10.
Plaja, Alberto, C. Mediano, Inmaculada Farrán-Codina, et al.. (1998). Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.. PubMed. 41(1). 52–5. 5 indexed citations
11.
Plaja, Alberto, et al.. (1994). Terminal deletion of Xp in a dysmorphic anencephalic fetus. Prenatal Diagnosis. 14(5). 410–412. 18 indexed citations
12.
Plaja, Alberto, et al.. (1994). Terminal deletion of 6p: report of a new case.. PubMed. 37(4). 196–9. 12 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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