Carmen Orellana

2.1k total citations
65 papers, 828 citations indexed

About

Carmen Orellana is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Carmen Orellana has authored 65 papers receiving a total of 828 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 32 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Carmen Orellana's work include Genomic variations and chromosomal abnormalities (25 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Prenatal Screening and Diagnostics (11 papers). Carmen Orellana is often cited by papers focused on Genomic variations and chromosomal abnormalities (25 papers), Genetics and Neurodevelopmental Disorders (13 papers) and Prenatal Screening and Diagnostics (11 papers). Carmen Orellana collaborates with scholars based in Spain, Uruguay and Netherlands. Carmen Orellana's co-authors include Francisco Martı́nez, Silvestre Oltra, Mónica Rosello, Sandra Monfort, Sonia Mayo, Victoria Castel, Alfonso Caro‐Llopis, Elena Grau, Adela Cañete and Jaime M. Monti and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and British Journal of Pharmacology.

In The Last Decade

Carmen Orellana

60 papers receiving 814 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carmen Orellana Spain 19 440 400 115 106 103 65 828
Silvestre Oltra Spain 20 626 1.4× 478 1.2× 109 0.9× 177 1.7× 185 1.8× 69 1.1k
James Lespinasse France 15 702 1.6× 619 1.5× 77 0.7× 108 1.0× 132 1.3× 35 1.4k
Ahmet Okay Çağlayan Türkiye 18 482 1.1× 390 1.0× 141 1.2× 58 0.5× 58 0.6× 79 1.1k
Birgit Zirn Germany 19 689 1.6× 419 1.0× 167 1.5× 129 1.2× 61 0.6× 33 1.1k
Alice Goldenberg France 20 678 1.5× 565 1.4× 91 0.8× 40 0.4× 50 0.5× 49 1.1k
Geert Vandeweyer Belgium 19 496 1.1× 414 1.0× 48 0.4× 50 0.5× 72 0.7× 48 980
Monika Cohen Germany 11 551 1.3× 488 1.2× 98 0.9× 38 0.4× 32 0.3× 13 859
Karen Buysse Belgium 15 456 1.0× 633 1.6× 169 1.5× 28 0.3× 66 0.6× 19 959
Thomas Schwarzbraun Austria 14 517 1.2× 252 0.6× 38 0.3× 36 0.3× 125 1.2× 26 852
Christel Thauvin‐Robinet France 21 762 1.7× 532 1.3× 116 1.0× 78 0.7× 70 0.7× 80 1.4k

Countries citing papers authored by Carmen Orellana

Since Specialization
Citations

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

Fields of papers citing papers by Carmen Orellana

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmen Orellana

This figure shows the co-authorship network connecting the top 25 collaborators of Carmen Orellana. A scholar is included among the top collaborators of Carmen Orellana 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 Carmen Orellana. Carmen Orellana 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.
Avetisyan, Gayane, Marion G. Valerio, Carmen Orellana, et al.. (2025). Atypical B-Cell Acute Lymphoblastic Leukemia with iAMP21 in the Context of Constitutional Ring Chromosome 21: A Case Report and Review of the Genetic Insights. International Journal of Molecular Sciences. 26(1). 357–357. 1 indexed citations
5.
6.
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.
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
9.
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
10.
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
11.
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
12.
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
13.
Yáñez, Yania, Elena Grau, Silvestre Oltra, et al.. (2011). Minimal disease detection in peripheral blood and bone marrow from patients with non-metastatic neuroblastoma. Journal of Cancer Research and Clinical Oncology. 137(8). 1263–1272. 20 indexed citations
14.
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
15.
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
16.
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
17.
Orellana, Carmen, Sandra Monfort, Marion Rosello, et al.. (2009). Duplication of the Williams–Beuren critical region: case report and further delineation of the phenotypic spectrum. BMJ Case Reports. 2009. bcr0620091996–bcr0620091996. 1 indexed citations
18.
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
19.
Orellana, Carmen, Francisco Martı́nez, Victoria Castel, et al.. (1998). A Novel TP53 Germ-Line Mutation Identified in a Girl with a Primitive Neuroectodermal Tumor and Her Father. Cancer Genetics and Cytogenetics. 105(2). 103–108. 8 indexed citations
20.
Orellana, Carmen, et al.. (1987). Inhibition of adrenomedullary catecholamine release by propranolol isomers and clonidine involving mechanisms unrelated to adrenoceptors. British Journal of Pharmacology. 92(4). 795–801. 18 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Silvestre Oltra Breakdown of academic impact, for papers by James Lespinasse Breakdown of academic impact, for papers by Ahmet Okay Çağlayan Breakdown of academic impact, for papers by Birgit Zirn Breakdown of academic impact, for papers by Alice Goldenberg Breakdown of academic impact, for papers by Geert Vandeweyer Breakdown of academic impact, for papers by Monika Cohen Breakdown of academic impact, for papers by Karen Buysse Breakdown of academic impact, for papers by Thomas Schwarzbraun Breakdown of academic impact, for papers by Christel Thauvin‐Robinet
Rankless by CCL
2026