Raquel Flores

1.6k total citations
23 papers, 994 citations indexed

About

Raquel Flores is a scholar working on Molecular Biology, Developmental Neuroscience and Genetics. According to data from OpenAlex, Raquel Flores has authored 23 papers receiving a total of 994 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Developmental Neuroscience and 4 papers in Genetics. Recurrent topics in Raquel Flores's work include Williams Syndrome Research (12 papers), Congenital heart defects research (8 papers) and Nuclear Receptors and Signaling (3 papers). Raquel Flores is often cited by papers focused on Williams Syndrome Research (12 papers), Congenital heart defects research (8 papers) and Nuclear Receptors and Signaling (3 papers). Raquel Flores collaborates with scholars based in Spain, Australia and Austria. Raquel Flores's co-authors include Mónica Bayés, Luis A. Pérez‐Jurado, L.A. Pérez Jurado, Ivon Cuscó, Clara Serra‐Juhé, Anna Antonell, Miguel Del Campo, Núria Torán, Jesús Argente and Gabriel Ángel Martos‐Moreno and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Immunology and Development.

In The Last Decade

Raquel Flores

20 papers receiving 975 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raquel Flores Spain 14 410 350 274 118 113 23 994
Yoshimasa Sakamoto Japan 17 594 1.4× 140 0.4× 110 0.4× 291 2.5× 199 1.8× 75 1.1k
Patricia I. Bader United States 18 619 1.5× 45 0.1× 584 2.1× 77 0.7× 94 0.8× 32 1.1k
Anna Krawisz United States 10 270 0.7× 36 0.1× 234 0.9× 90 0.8× 211 1.9× 25 856
Karen Nygard Canada 17 348 0.8× 25 0.1× 168 0.6× 66 0.6× 51 0.5× 37 908
Nathalie Van der Aa Belgium 19 412 1.0× 37 0.1× 388 1.4× 84 0.7× 49 0.4× 26 809
Pedro Moreira Portugal 17 341 0.8× 33 0.1× 168 0.6× 53 0.4× 204 1.8× 37 1.0k
Jing Gao China 18 372 0.9× 34 0.1× 48 0.2× 83 0.7× 53 0.5× 85 1.0k
Wang Ch Taiwan 9 420 1.0× 31 0.1× 308 1.1× 52 0.4× 66 0.6× 41 767
S Nakazawa Japan 22 415 1.0× 29 0.1× 90 0.3× 166 1.4× 38 0.3× 51 1.2k
Shin Okazaki Japan 12 243 0.6× 50 0.1× 160 0.6× 112 0.9× 49 0.4× 79 620

Countries citing papers authored by Raquel Flores

Since Specialization
Citations

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

Fields of papers citing papers by Raquel Flores

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raquel Flores

This figure shows the co-authorship network connecting the top 25 collaborators of Raquel Flores. A scholar is included among the top collaborators of Raquel Flores 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 Raquel Flores. Raquel Flores 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.
Balayo, Tina, Sharna Lunn, Ulla-Maj Fiúza, et al.. (2025). N2B27 media formulations influence gastruloid development. Development. 152(22).
2.
Kuebler, Bernd, Begoña Arán, Raquel Flores, et al.. (2020). Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion). Stem Cell Research. 49. 102087–102087. 2 indexed citations
3.
4.
Codina‐Solà, Marta, et al.. (2019). Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome. Journal of Medical Genetics. 56(12). 801–808. 11 indexed citations
5.
Serra‐Juhé, Clara, Gabriel Ángel Martos‐Moreno, Raquel Flores, et al.. (2019). Heterozygous rare genetic variants in non-syndromic early-onset obesity. International Journal of Obesity. 44(4). 830–841. 39 indexed citations
6.
7.
Serra‐Juhé, Clara, Gabriel Ángel Martos‐Moreno, Raquel Flores, et al.. (2017). Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants. PLoS Genetics. 13(5). e1006657–e1006657. 26 indexed citations
8.
Muñoz, José Luís Bernal, et al.. (2016). C-Reactive Protein and Procalcitonin as Early Markers of Septic Complications after Laparoscopic Sleeve Gastrectomy in Morbidly Obese Patients Within an Enhanced Recovery After Surgery Program. Journal of the American College of Surgeons. 222(5). 831–837. 28 indexed citations
9.
Serra‐Juhé, Clara, et al.. (2015). DNA methylation abnormalities in congenital heart disease. Epigenetics. 10(2). 167–177. 94 indexed citations
10.
Flores, Raquel, et al.. (2014). Lateral preference in Williams–Beuren syndrome is associated with cognition and language. European Child & Adolescent Psychiatry. 24(9). 1025–1033. 7 indexed citations
11.
Argente, Jesús, Raquel Flores, Bhupendra Verma, et al.. (2014). Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency. EMBO Molecular Medicine. 6(3). 299–306. 74 indexed citations
12.
Martos‐Moreno, Gabriel Ángel, et al.. (2013). Quimerismo hemático en gemelos dicigóticos concebidos por fertilización in vitro. Anales de Pediatría. 79(4). 248–252. 1 indexed citations
13.
Flores, Raquel, et al.. (2012). Ganado ovino. Variantes génicas de alta prolificidad. 12–13.
14.
Rodríguez‐Santiago, Benjamín, Beatriz Sobrino, Clara Serra‐Juhé, et al.. (2009). Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia. Molecular Psychiatry. 15(10). 1023–1033. 73 indexed citations
15.
Antonell, Anna, Miguel Del Campo, Liane Kaufmann, et al.. (2009). Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams–Beuren syndrome neurocognitive profile. Journal of Medical Genetics. 47(5). 312–320. 91 indexed citations
16.
Cuscó, Ivon, Roser Corominas, Mónica Bayés, et al.. (2008). Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion. Genome Research. 18(5). 683–694. 56 indexed citations
17.
Castelo‐Branco, Miguel, Raquel Sebastião, Aldina Reis, et al.. (2007). Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders. Journal of Clinical Investigation. 117(12). 3720–9. 36 indexed citations
18.
Campo, Miguel Del, Anna Antonell, Francisco J. Muñoz, et al.. (2006). Hemizygosity at the NCF1 Gene in Patients with Williams-Beuren Syndrome Decreases Their Risk of Hypertension. The American Journal of Human Genetics. 78(4). 533–542. 75 indexed citations
19.
Antonell, Anna, et al.. (2006). Síndrome de Williams: aspectos clínicos y bases moleculares. Revista de Neurología. 42(S01). S069–S069. 8 indexed citations
20.
Bayés, Mónica, et al.. (2003). Mutational Mechanisms of Williams-Beuren Syndrome Deletions. The American Journal of Human Genetics. 73(1). 131–151. 241 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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