Verónica Seidel

411 total citations
9 papers, 191 citations indexed

About

Verónica Seidel is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Verónica Seidel has authored 9 papers receiving a total of 191 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Verónica Seidel's work include Congenital limb and hand anomalies (3 papers), Genetic Syndromes and Imprinting (2 papers) and Orthopedic Surgery and Rehabilitation (2 papers). Verónica Seidel is often cited by papers focused on Congenital limb and hand anomalies (3 papers), Genetic Syndromes and Imprinting (2 papers) and Orthopedic Surgery and Rehabilitation (2 papers). Verónica Seidel collaborates with scholars based in Spain, Gambia and United Kingdom. Verónica Seidel's co-authors include Stephen Owens, Miguel Constância, Gusztáv Bélteki, Ken K. Ong, Wendy N. Cooper, Andrew M. Prentice, Batbayar Khulan, Cathy E. Elks, Nabeel A. Affara and David B. Dunger and has published in prestigious journals such as PEDIATRICS, The FASEB Journal and The Pediatric Infectious Disease Journal.

In The Last Decade

Verónica Seidel

9 papers receiving 188 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Verónica Seidel Spain	5	87	77	51	36	28	9	191
Wilhelmina H. Stokvis‐Brantsma Netherlands	6	215 2.5×	64 0.8×	236 4.6×	3 0.1×	20 0.7×	6	351
M Osztovics United States	8	56 0.6×	99 1.3×	92 1.8×	10 0.3×	14 0.5×	34	207
E. Kervancıoglu Türkiye	11	59 0.7×	63 0.8×	47 0.9×		24 0.9×	18	414
A. Dalleac France	8	108 1.2×	92 1.2×	55 1.1×		13 0.5×	10	440
Mariateresa Sessa Italy	9	58 0.7×	237 3.1×	163 3.2×	2 0.1×	15 0.5×	13	313
Monika Schiesser Germany	9	51 0.6×	47 0.6×	61 1.2×	12 0.3×	15 0.5×	14	260
Fabiana Faja Italy	9	83 1.0×	35 0.5×	50 1.0×		21 0.8×	19	300
Danni Zhou China	11	61 0.7×	63 0.8×	20 0.4×		31 1.1×	35	342
Achamma Chandy India	9	102 1.2×	84 1.1×	46 0.9×		29 1.0×	19	397
L. Memo Italy	7	131 1.5×	77 1.0×	150 2.9×	4 0.1×	7 0.3×	11	241

Countries citing papers authored by Verónica Seidel

Since Specialization

Citations

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

Fields of papers citing papers by Verónica Seidel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verónica Seidel

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

All Works

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9 of 9 papers shown

Carcavilla, Atilano, José L. Santomé, Verónica Seidel, et al.. (2023). Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment. Journal of Clinical Medicine. 12(15). 5003–5003. 3 indexed citations

Díaz, Francisca, Manuel Parrón, Silvia Modamio‐Høybjør, et al.. (2023). Evolution of clinical and radiological presentations of spondyloepimetaphyseal dysplasia, RPL13‐related: Description of 11 further cases. Clinical Genetics. 104(1). 100–106. 2 indexed citations

Seidel, Verónica, et al.. (2021). Novel biallelic variant in BBS9 causative of Bardet–Biedl syndrome: expanding the spectrum of disease-causing genetic alterations. BMC Medical Genomics. 14(1). 91–91. 4 indexed citations

Pérez‐Grijalba, Virginia, María López, Judith Armstrong, et al.. (2019). New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients. Molecular Genetics & Genomic Medicine. 7(11). e972–e972. 13 indexed citations

López, María, et al.. (2018). Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum. BMC Medical Genetics. 19(1). 36–36. 27 indexed citations

López, María, et al.. (2016). First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant. BMC Medical Genetics. 17(1). 97–97. 17 indexed citations

Cooper, Wendy N., Batbayar Khulan, Stephen Owens, et al.. (2012). DNA methylation profiling at imprinted loci after periconceptional micronutrient supplementation in humans: results of a pilot randomized controlled trial. The FASEB Journal. 26(5). 1782–1790. 98 indexed citations

Mǔr, Antonio, et al.. (2005). ACANTHOSIS NIGRICANS AS AN ADVERSE EFFECT OF HIGHLY ACTIVE ANTIRETROVIRAL THERAPY IN AN ADOLESCENT GIRL WITH HUMAN IMMUNODEFICIENCY VIRUS INFECTION. The Pediatric Infectious Disease Journal. 24(8). 742–743. 4 indexed citations

López-Vílchez, María Ángeles, Verónica Seidel, Magı́ Farré, et al.. (2005). Areca-Nut Abuse and Neonatal Withdrawal Syndrome. PEDIATRICS. 117(1). e129–e131. 23 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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