Mónica Rosello

1.7k total citations
41 papers, 535 citations indexed

About

Mónica Rosello is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mónica Rosello has authored 41 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 22 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mónica Rosello's work include Genomic variations and chromosomal abnormalities (23 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Prenatal Screening and Diagnostics (9 papers). Mónica Rosello is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Prenatal Screening and Diagnostics (9 papers). Mónica Rosello collaborates with scholars based in Spain, United States and India. Mónica Rosello's co-authors include Francisco Martı́nez, Carmen Orellana, Sandra Monfort, Silvestre Oltra, Sonia Mayo, Alfonso Caro‐Llopis, Míriam Guitart, Peter Marynen, Joris Vermeesch and Guy Froyen and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and BioMed Research International.

In The Last Decade

Mónica Rosello

36 papers receiving 525 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mónica Rosello Spain 14 360 295 95 47 36 41 535
Maria Descartes United States 16 431 1.2× 399 1.4× 94 1.0× 60 1.3× 62 1.7× 34 720
Hiba Risheg United States 10 403 1.1× 374 1.3× 164 1.7× 53 1.1× 28 0.8× 13 640
Tracy Brandt United States 10 399 1.1× 286 1.0× 82 0.9× 35 0.7× 35 1.0× 14 581
Simona Cavani Italy 16 393 1.1× 313 1.1× 160 1.7× 82 1.7× 23 0.6× 31 692
Luigina Spaccini Italy 13 159 0.4× 208 0.7× 104 1.1× 22 0.5× 19 0.5× 47 455
Sara Loddo Italy 13 402 1.1× 277 0.9× 123 1.3× 59 1.3× 16 0.4× 39 639
Roel Hordijk Netherlands 15 520 1.4× 409 1.4× 184 1.9× 100 2.1× 21 0.6× 22 739
Bénédicte Demeer France 12 264 0.7× 169 0.6× 63 0.7× 22 0.5× 25 0.7× 22 373
Ho‐Ming Luk China 13 267 0.7× 249 0.8× 100 1.1× 19 0.4× 29 0.8× 67 471
Michèle Mathieu France 9 310 0.9× 341 1.2× 64 0.7× 32 0.7× 17 0.5× 18 622

Countries citing papers authored by Mónica Rosello

Since Specialization
Citations

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

Fields of papers citing papers by Mónica Rosello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mónica Rosello

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

All Works

20 of 20 papers shown
1.
Menao, Sebastián, Laia Pedrola, Carmen Orellana, et al.. (2025). Clinical Utility of Opportunistic Genome-Wide cfDNA Prenatal Screening in Intermediate-Risk Pregnancies. Genes. 16(11). 1344–1344.
2.
Caro‐Llopis, Alfonso, Mónica Rosello, Silvestre Oltra, et al.. (2025). Genetic landscape of hereditary transthyretin amyloidosis in Spain: a multicentric retrospective study. Amyloid. 32(4). 324–334.
3.
Orellana, Carmen, Mónica Rosello, Amparo Sanchís, et al.. (2025). Utility of Optical Genome Mapping for Accurate Detection and Fine-Mapping of Structural Variants in Elusive Rare Diseases. International Journal of Molecular Sciences. 26(3). 1244–1244.
4.
5.
Monfort, Sandra, Carmen Orellana, Silvestre Oltra, et al.. (2021). Prevalence of pathogenic copy number variants among children conceived by donor oocyte. Scientific Reports. 11(1). 6752–6752. 2 indexed citations
6.
Rosello, Mónica, Alfonso Caro‐Llopis, Carmen Orellana, et al.. (2020). Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing. Pediatric Research. 90(2). 284–288. 26 indexed citations
7.
Reina, Purificación Marín, et al.. (2019). Mixed Phenotype of Langer–Giedion's and Cornelia de Lange's Syndromes in an 8q23.3-q24.1 Microdeletion without TRPS1 Deletion. Journal of Pediatric Genetics. 9(1). 53–57. 1 indexed citations
8.
Fieremans, Nathalie, Hilde Van Esch, Maureen Holvoet, et al.. (2016). Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern. Human Mutation. 37(8). 804–811. 65 indexed citations
9.
Preikšaitienė, Eglė, Alfonso Caro‐Llopis, Silvestre Oltra, et al.. (2015). A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next‐generation sequencing causes CK syndrome. American Journal of Medical Genetics Part A. 167(6). 1342–1348. 7 indexed citations
10.
Mayo, Sonia, Sandra Monfort, Mónica Rosello, et al.. (2015). In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients. BioMed Research International. 2015. 1–8. 3 indexed citations
11.
Martı́nez, Francisco, Purificación Marín Reina, Antonio Pérez Aytés, et al.. (2015). Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes. Pediatric Research. 78(5). 533–539. 28 indexed citations
12.
López-Carrasco, Amparo, Sandra Monfort, Mónica Rosello, et al.. (2013). Localización cromosómica de duplicaciones submicroscópicas en pacientes con trastornos del neurodesarrollo para identificar casos con alto riesgo de recurrencia familiar. Medicina Clínica. 142(12). 531–537. 3 indexed citations
13.
Rosello, Mónica, et al.. (2012). Determinación del perfil de enfermería en las unidades de cuidados intensivos cardiológicos según sus competencias. Dialnet (Universidad de la Rioja). 51–58. 2 indexed citations
14.
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
15.
Monfort, Sandra, Silvestre Oltra, Mónica Rosello, et al.. (2011). Partial Duplication of 18q Including a Distal Critical Region for Edwards Syndrome in a Patient with Normal Phenotype and Oligoasthenospermia: Case Report. Cytogenetic and Genome Research. 133(1). 78–83. 7 indexed citations
16.
Rosello, Mónica, et al.. (2009). Submicroscopic Duplication of the Wolf-Hirschhorn Critical Region with a 4p Terminal Deletion. Cytogenetic and Genome Research. 125(2). 103–108. 11 indexed citations
17.
Rosello, Mónica, et al.. (2009). Rare chromosomal complement of trisomy 21 in a boy conceived by IVF and cryopreservation. Reproductive BioMedicine Online. 19(3). 415–417. 2 indexed citations
18.
Rosello, Mónica, Sandra Monfort, Carmen Orellana, et al.. (2007). Deleción subtelomérica 9qter: definición del síndrome y origen parental en 2 pacientes. Medicina Clínica. 128(11). 419–421. 4 indexed citations
19.
Martı́nez, Francisco, Ana M. León, Sandra Monfort, et al.. (2006). Robust, Easy, and Dose-Sensitive Methylation Test for the Diagnosis of Prader–Willi and Angelman Syndromes. Genetic Testing. 10(3). 174–177. 8 indexed citations
20.
Orellana, Carmen, Lourdes Badı́a, Francisco Martı́nez, et al.. (2006). Recombinant X chromosome in a prenatal diagnosis. Cytogenetic and Genome Research. 112(3-4). 337–340. 3 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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