Eva Barroso

675 total citations
23 papers, 437 citations indexed

About

Eva Barroso is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Eva Barroso has authored 23 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 3 papers in Immunology. Recurrent topics in Eva Barroso's work include Craniofacial Disorders and Treatments (4 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Eva Barroso is often cited by papers focused on Craniofacial Disorders and Treatments (4 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Eva Barroso collaborates with scholars based in Spain, United States and Australia. Eva Barroso's co-authors include Karen E. Heath, Sara Benito‐Sanz, Ángel Campos‐Barros, Gloría Ribas, Lara P. Fernández, Roger L. Milne, Javier Benı́tez, Pablo Lapunzina, José Ignacio Arias and Beatriz Paumard‐Hernández and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, International Journal of Cancer and Carcinogenesis.

In The Last Decade

Eva Barroso

22 papers receiving 430 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eva Barroso Spain	11	289	245	66	37	28	23	437
Marjan M. Nezarati Canada	10	198 0.7×	232 0.9×	25 0.4×	26 0.7×	43 1.5×	17	447
Sandra Corbani Lebanon	10	163 0.6×	225 0.9×	26 0.4×	12 0.3×	51 1.8×	23	387
Ewelina Bukowska‐Olech Poland	11	147 0.5×	157 0.6×	15 0.2×	22 0.6×	21 0.8×	41	273
Mehrnaz Narooie-Nejad Iran	8	88 0.3×	82 0.3×	88 1.3×	21 0.6×	54 1.9×	21	313
Yan-Fang Guo China	11	174 0.6×	245 1.0×	21 0.3×	58 1.6×	26 0.9×	15	431
Ho‐Ming Luk China	13	267 0.9×	249 1.0×	25 0.4×	18 0.5×	27 1.0×	67	471
Sergio A. Cuevas‐Covarrubias Mexico	11	167 0.6×	280 1.1×	16 0.2×	25 0.7×	17 0.6×	41	418
Jennifer L. Asimit United Kingdom	11	397 1.4×	206 0.8×	17 0.3×	16 0.4×	17 0.6×	22	501
Emilie Ait‐Yahya France	7	151 0.5×	171 0.7×	23 0.3×	21 0.6×	39 1.4×	18	366
Amy Knight Johnson United States	12	164 0.6×	196 0.8×	15 0.2×	20 0.5×	19 0.7×	16	396

Countries citing papers authored by Eva Barroso

Since Specialization

Citations

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

Fields of papers citing papers by Eva Barroso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Barroso

This figure shows the co-authorship network connecting the top 25 collaborators of Eva Barroso. A scholar is included among the top collaborators of Eva Barroso 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 Eva Barroso. Eva Barroso 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

Barroso, Eva, et al.. (2020). A novel mutation in the ZNF462 gene c.3306dup; p.(Gln1103Thrfs*10) is associated to Weiss-Kruszka syndrome. A case report. Acta Clinica Belgica. 77(1). 118–121. 8 indexed citations

Darras, Natasha, Shannon Rego, Pierre‐Marie Martin, et al.. (2019). Developmental and epileptic encephalopathy in two siblings with a novel, homozygous missense variant in SCN1B. American Journal of Medical Genetics Part A. 179(11). 2190–2195. 13 indexed citations

Barroso, Eva, et al.. (2018). Orbital and peri-orbital amyloidosis: a report of four cases. Orbit. 38(2). 148–153. 8 indexed citations

Barroso, Eva, et al.. (2018). Transcaruncular rectus tendon fixation to the orbit and frontalis flap for complete third nerve palsy. Orbit. 38(1). 13–18. 1 indexed citations

Barroso, Eva, et al.. (2018). Primary Intraocular Malignant Rhabdoid Tumor Without Extrascleral Compromise. Journal of Pediatric Ophthalmology & Strabismus. 55(6). e7–e9. 1 indexed citations

Gordo, Gema, Jair Tenorio, Pedro Arias, et al.. (2017). mTOR mutations in Smith‐Kingsmore syndrome: Four additional patients and a review. Clinical Genetics. 93(4). 762–775. 29 indexed citations

Valdeolivas, Sara, Fabiana Piscitelli, Roberta Verde, et al.. (2016). Analysis of endocannabinoid signaling elements and related proteins in lymphocytes of patients with Dravet syndrome. Pharmacology Research & Perspectives. 4(2). e00220–e00220. 15 indexed citations

Paumard‐Hernández, Beatriz, Eva Barroso, Sara Benito‐Sanz, et al.. (2014). Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants. European Journal of Human Genetics. 23(7). 907–914. 41 indexed citations

Benito‐Sanz, Sara, José Luís Royo, Eva Barroso, et al.. (2012). Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer. Journal of Medical Genetics. 49(7). 442–450. 55 indexed citations

10.

Barroso, Eva, et al.. (2012). Achondroplasia with 47, xxy karyotype: a case report of the neonatal diagnosis of an extremely unusual association. BMC Pediatrics. 12(1). 88–88. 3 indexed citations

11.

Aza‐Carmona, Miriam, Eva Barroso, Damián Heine‐Suñer, et al.. (2011). Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia. European Journal of Human Genetics. 19(12). 1218–1225. 8 indexed citations

12.

Barroso, Eva, et al.. (2011). Mild isolated craniosynostosis due to a novel FGFR3 mutation, p.Ala334Thr. American Journal of Medical Genetics Part A. 155(12). 3050–3053. 11 indexed citations

13.

Barroso, Eva, Sara Benito‐Sanz, Patricia Yuste‐Checa, et al.. (2010). Identification of the first de novo PAR1 deletion downstream of SHOX in an individual diagnosed with Léri–Weill dyschondrosteosis (LWD). European Journal of Medical Genetics. 53(4). 204–207. 6 indexed citations

14.

Barroso, Eva, Lara P. Fernández, Roger L. Milne, et al.. (2008). Genetic analysis of the vitamin D receptor gene in two epithelial cancers: melanoma and breast cancer case-control studies. BMC Cancer. 8(1). 385–385. 54 indexed citations

15.

Fernández, Lara P., Roger L. Milne, Eva Barroso, et al.. (2006). Estrogen and progesterone receptor gene polymorphisms and sporadic breast cancer risk: A Spanish case‐control study. International Journal of Cancer. 119(2). 467–471. 27 indexed citations

16.

Barroso, Eva. (2006). FANCD2 associated with sporadic breast cancer risk. Carcinogenesis. 27(9). 1930–1937. 33 indexed citations

17.

Barroso, Eva, et al.. (2005). Corrección de la ptosis palpebral mediante conjuntivo-müllerectomía. 29–34. 1 indexed citations

18.

Ribas, Gloría, Anna González‐Neira, Antonio Salas, et al.. (2005). Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes. Human Genetics. 118(6). 669–679. 58 indexed citations

19.

Barroso, Eva, et al.. (2004). Hemangioma intraóseo primario del techo orbitario. 12(2). 4. 1 indexed citations

20.

Barroso, Eva, et al.. (1999). Resultados en el tratamiento del pterigión con mitomicina C a dosis bajas. Archivos de la Sociedad Española de Oftalmologia. 74(2). 67–70.

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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