Anna Ruiz

1.7k total citations
34 papers, 872 citations indexed

About

Anna Ruiz is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Anna Ruiz has authored 34 papers receiving a total of 872 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Oncology and 9 papers in Genetics. Recurrent topics in Anna Ruiz's work include Cutaneous Melanoma Detection and Management (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Anna Ruiz is often cited by papers focused on Cutaneous Melanoma Detection and Management (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Anna Ruiz collaborates with scholars based in Spain, United Kingdom and United States. Anna Ruiz's co-authors include Susana Puig, T Castel, Xavier Estivill, Michael Lynch, Josep Malvehy, Jaume Reventós, Miguel Abal, Eva Colás, Eugeni Saigí and Anna Ferrer and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Anna Ruiz

32 papers receiving 863 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Ruiz Spain 17 499 331 323 129 110 34 872
Daniel Voskas Canada 9 795 1.6× 297 0.9× 268 0.8× 163 1.3× 69 0.6× 17 1.0k
Catherine Clarke United Kingdom 14 430 0.9× 190 0.6× 313 1.0× 96 0.7× 49 0.4× 18 830
Mary K. Washington United States 6 595 1.2× 179 0.5× 480 1.5× 214 1.7× 59 0.5× 10 996
Ryosuke Osada Japan 13 481 1.0× 192 0.6× 235 0.7× 46 0.4× 97 0.9× 20 807
Gaëlle Bouvencourt Belgium 6 697 1.4× 305 0.9× 811 2.5× 116 0.9× 287 2.6× 7 1.3k
Mandy Wahlbuhl Germany 8 710 1.4× 209 0.6× 267 0.8× 117 0.9× 45 0.4× 15 940
Ursina Zürrer‐Härdi Switzerland 9 605 1.2× 240 0.7× 538 1.7× 100 0.8× 102 0.9× 13 966
Johanne Dubail France 15 347 0.7× 220 0.7× 161 0.5× 173 1.3× 40 0.4× 23 758
C. W. Perrett United Kingdom 17 491 1.0× 193 0.6× 185 0.6× 80 0.6× 54 0.5× 31 1.2k
Walid K. Chatila United States 14 386 0.8× 300 0.9× 323 1.0× 77 0.6× 186 1.7× 50 878

Countries citing papers authored by Anna Ruiz

Since Specialization
Citations

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

Fields of papers citing papers by Anna Ruiz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Ruiz

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Ruiz. A scholar is included among the top collaborators of Anna Ruiz 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 Anna Ruiz. Anna Ruiz 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.
Trujillo‐Quintero, Juan Pablo, Anna Brunet‐Vega, Nino Spataro, et al.. (2025). A Novel RHEB Germline Variant Associated With Intellectual Disability and Epilepsy: Expanding the Spectrum of mTORopathies. Clinical Genetics. 108(2). 218–223.
2.
Spataro, Nino, Elisabeth Gabau, Juan Pablo Trujillo‐Quintero, et al.. (2024). Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome. Frontiers in Genetics. 15. 1291063–1291063. 1 indexed citations
3.
Spataro, Nino, Juan Pablo Trujillo‐Quintero, Elisabeth Gabau, et al.. (2023). High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders. Genes. 14(3). 708–708. 3 indexed citations
4.
Marcé‐Grau, Anna, et al.. (2021). Muscarinic acetylcholine receptor M1 mutations causing neurodevelopmental disorder and epilepsy. Human Mutation. 42(10). 1215–1220. 4 indexed citations
5.
Hümmer, Stefan, Elisabeth Gabau, Míriam Guitart, et al.. (2021). The Novel KIF1A Missense Variant (R169T) Strongly Reduces Microtubule Stimulated ATPase Activity and Is Associated With NESCAV Syndrome. Frontiers in Neuroscience. 15. 618098–618098. 12 indexed citations
6.
Gabau, Elisabeth, Carme Brun i Gasca, Steven Laurie, et al.. (2021). New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PLoS ONE. 16(10). e0258766–e0258766. 14 indexed citations
7.
Esteba‐Castillo, Susanna, Neus Baena, Anna Ruiz, et al.. (2018). High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders. Behavior Genetics. 48(4). 323–336. 16 indexed citations
8.
Baena, Neus, Elisabeth Gabau, Adrijan Sarajlija, et al.. (2017). Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature. BMC Medical Genetics. 18(1). 137–137. 5 indexed citations
9.
Pedrola, Núria, Laura Devis, Irene Campoy, et al.. (2015). Nidogen 1 and Nuclear Protein 1: novel targets of ETV5 transcription factor involved in endometrial cancer invasion. Clinical & Experimental Metastasis. 32(5). 467–478. 48 indexed citations
10.
Ruiz, Anna, Gemma Llort, Neus Baena, et al.. (2014). Genetic Testing in Hereditary Breast and Ovarian Cancer Using Massive Parallel Sequencing. BioMed Research International. 2014. 1–8. 13 indexed citations
11.
Pericay, Carles, Anna Ferrer, E. Dotor, et al.. (2013). microRNA expression profile in stage III colorectal cancer: Circulating miR-18a and miR-29a as promising biomarkers. Oncology Reports. 30(1). 320–326. 142 indexed citations
12.
Majem, Blanca, Josep Castellví, Sílvia Cabrera, et al.. (2012). Analysis of Gene Expression Regulated by the ETV5 Transcription Factor in OV90 Ovarian Cancer Cells Identifies FOXM1 Overexpression in Ovarian Cancer. Molecular Cancer Research. 10(7). 914–924. 24 indexed citations
13.
Cabrera, Sílvia, Marta Llauradó, Josep Castellví, et al.. (2011). Generation and characterization of orthotopic murine models for endometrial cancer. Clinical & Experimental Metastasis. 29(3). 217–227. 24 indexed citations
14.
Llauradó, Marta, Miguel Abal, Josep Castellví, et al.. (2011). ETV5 transcription factor is overexpressed in ovarian cancer and regulates cell adhesion in ovarian cancer cells. International Journal of Cancer. 130(7). 1532–1543. 41 indexed citations
15.
Yakobson, Emanuel, Shlomit Eisenberg, David Halle, et al.. (2003). A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families. European Journal of Human Genetics. 11(4). 288–296. 19 indexed citations
16.
Ruiz, Anna, Miguel Ángel Pujana, & Xavier Estivill. (2000). Isolation and characterisation of a novel human gene (C9orf11) on chromosome 9p21, a region frequently deleted in human cancer. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1517(1). 128–134. 5 indexed citations
17.
Ruiz, Anna, Susana Puig, Josep Malvehy, et al.. (1999). CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia. Journal of Medical Genetics. 36(6). 490–493. 41 indexed citations
18.
Ruiz, Anna, Susana Puig, Michael Lynch, T Castel, & Xavier Estivill. (1998). Retention of theCDKN2A locus and low frequency of point mutations in primary and metastasic cutaneous malignant melanoma. International Journal of Cancer. 76(3). 312–316. 38 indexed citations
19.
20.
Puig, Susana, Anna Ruiz, & Conxi Lázaro. (1994). Several loci at chromosome 9p are involved in early and late stages of growth of cutaneous malignant melanoma. The American Journal of Human Genetics. 55. 1 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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