Paloma Ropero

708 total citations
85 papers, 443 citations indexed

About

Paloma Ropero is a scholar working on Genetics, Hematology and Physiology. According to data from OpenAlex, Paloma Ropero has authored 85 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Genetics, 50 papers in Hematology and 15 papers in Physiology. Recurrent topics in Paloma Ropero's work include Hemoglobinopathies and Related Disorders (64 papers), Iron Metabolism and Disorders (46 papers) and Erythrocyte Function and Pathophysiology (15 papers). Paloma Ropero is often cited by papers focused on Hemoglobinopathies and Related Disorders (64 papers), Iron Metabolism and Disorders (46 papers) and Erythrocyte Function and Pathophysiology (15 papers). Paloma Ropero collaborates with scholars based in Spain, Italy and Chile. Paloma Ropero's co-authors include Ana Villegas, Fernando A. González, Eduardo Anguita, Jorge Martínez Nieto, D Espinós, Silvia de la Iglesia, Marta Polo, José M. Ladero, José A. G. Agúndez and Celina Benavente and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Hepatology and European Journal of Cancer.

In The Last Decade

Paloma Ropero

76 papers receiving 437 citations

Peers

Paloma Ropero

GENET

HEMAT

PHYSI

PPCH

Thanusak Tatu Thailand

Iswari Setianingsih Indonesia

Xiao-Fen Zhan China

Duantida Songdej Thailand

Disma Renda Italy

Corrado Masciullo Italy

Egemen Tütüncüoğlu United States

Pratibha Sawant India

Paola Cerani Italy

Rayra Pereira Santiago Brazil

Thanusak Tatu Thailand

Paloma Ropero

469 ×1.5

GENET

429 ×1.6

HEMAT

119 ×1.5

70 ×0.9

PHYSI

191 ×3.1

PPCH

Citations per year, relative to Paloma Ropero Paloma Ropero (= 1×) peers Thanusak Tatu

Countries citing papers authored by Paloma Ropero

Since Specialization

Citations

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

Fields of papers citing papers by Paloma Ropero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paloma Ropero

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

All Works

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20 of 20 papers shown

Ropero, Paloma, et al.. (2025). Phenotype of sickle cell disease. Correlation of haplotypes and polymorphisms in cluster β, BCL11A, and HBS1L−MYB. Pilot study. Frontiers in Medicine. 12. 1347026–1347026.

Nieto, Jorge Martínez, et al.. (2025). An HBB Intron 1 Variant (c.92 + 9C > T) Suggestive of β-Thalassemia Trait. Hemoglobin. 49(5). 358–360.

Ropero, Paloma, et al.. (2022). Does size matter? Two new deletions in the HBB gene cause β0-thalassemia. Annals of Hematology. 101(7). 1465–1471.

Ropero, Paloma, et al.. (2021). Hb Maruchi [α165 (E14) Ala>Pro; HBA1: c.196G>C]: A new thalassemia hemoglobinopathy related to the alpha1 globin gene. Clinical Biochemistry. 92. 77–81. 1 indexed citations

González, Yolanda, et al.. (2020). Why is the novel Hb Miguel Servet visualised by CE-HPLC newborn and not by the CE-HPLC β-thalassaemia programme?. Journal of Clinical Pathology. 74(3). 198–201. 2 indexed citations

Ropero, Paloma, Fernando A. González, Jorge Martínez Nieto, et al.. (2019). C>A substitution in NT 46 of the 3’ UTR region (the α complex protected region) of the alpha-1 globin gene: a non-deletional mutation or polymorphism?. Journal of Clinical Pathology. 73(1). 14–16. 1 indexed citations

Nieto, Jorge Martínez, et al.. (2019). Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014. Annals of Hematology. 98(7). 1537–1545. 6 indexed citations

Torrejón, María José, et al.. (2017). Hb Moncloa: A new variant of haemoglobin that interferes in the quantification of Hb A1c. Clinical Biochemistry. 50(9). 521–524. 6 indexed citations

Villegas, Ana, Fernando A. González, Jorge Martínez Nieto, et al.. (2016). Haemoglobinopathies that occur with decreased HbA ₂ levels: a gene mutation set involving the δ gene at a Spanish centre. Journal of Clinical Pathology. 70(1). 75–80. 4 indexed citations

10.

Alonso‐Domínguez, Juan Manuel, Jesús Villarrubia, M Sopena, et al.. (2015). Reticulocyte parameters of delta beta thalassaemia trait, beta thalassaemia trait and iron deficiency anaemia. Journal of Clinical Pathology. 69(2). 149–154. 9 indexed citations

11.

Nieto, Jorge Martínez, et al.. (2014). Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype. Journal of Human Genetics. 59(10). 585–587. 2 indexed citations

12.

Ropero, Paloma, et al.. (2009). Diagnóstico prenatal de hemoglobinopatías y talasemias. Medicina Clínica. 132(2). 53–56. 3 indexed citations

13.

Villegas, Ana, et al.. (2008). Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group. Annals of Hematology. 88(3). 235–238. 17 indexed citations

14.

Ropero, Paloma, et al.. (2008). Origin of the Frameshift Codons 41/42 (–TCTT) Mutation in the First Cases Described in the Spanish Population. Hemoglobin. 32(5). 513–519.

15.

Ropero, Paloma, et al.. (2007). Hemoglobina Fannin-Lubbock II [β111(G13)Val → Leu y β119(GH2)Gly → Asp]: descripción de 4 nuevos casos. Medicina Clínica. 129(10). 379–381. 4 indexed citations

16.

Ropero, Paloma, et al.. (2006). Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in a cohort of 1,000 neonates in Madrid (Spain). Annals of Hematology. 85(5). 323–6. 9 indexed citations

17.

Villegas, Ana, Paloma Ropero, Fernando A. González, et al.. (2003). Hb Santander [β34(B16)Val→Asp (GTC→GAC)]: A New Unstable Variant Found as a De Novo Mutation in a Spanish Patient. Hemoglobin. 27(1). 31–35. 5 indexed citations

18.

Juncà, Jordi, et al.. (2002). Characterization of a new hemoglobin variant: Hb Badalona (β31[B13]Leu→Val). Annals of Hematology. 81(4). 179–181. 2 indexed citations

19.

Villegas, Ana, et al.. (1998). High incidence of the CD8/9 (+G) beta 0-thalassemia mutation in Spain.. PubMed. 83(12). 1066–8. 5 indexed citations

20.

Ropero, Paloma, et al.. (1996). Hb J-Baltimore [β16(A13)GLY→ASP] Associated with β⁺Thalassemia in a Spanish Family. Hemoglobin. 20(1). 79–84. 3 indexed citations

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