Rafael Valdés‐Mas

16.0k total citations · 2 hit papers
23 papers, 1.8k citations indexed

About

Rafael Valdés‐Mas is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Rafael Valdés‐Mas has authored 23 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Rafael Valdés‐Mas's work include Chronic Lymphocytic Leukemia Research (4 papers), Genetic factors in colorectal cancer (4 papers) and DNA Repair Mechanisms (3 papers). Rafael Valdés‐Mas is often cited by papers focused on Chronic Lymphocytic Leukemia Research (4 papers), Genetic factors in colorectal cancer (4 papers) and DNA Repair Mechanisms (3 papers). Rafael Valdés‐Mas collaborates with scholars based in Spain, Germany and Israel. Rafael Valdés‐Mas's co-authors include Carlos López-Otı́n, Xosé S. Puente, Eran Elinav, Neus Villamor, Elı́as Campo, Sı́lvia Beà, Mally Dori-Bachash, Clea Bárcena, Nuria Garatachea and Carlota Rubio-Pérez and has published in prestigious journals such as Nature, Science and Nature Medicine.

In The Last Decade

Rafael Valdés‐Mas

23 papers receiving 1.8k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice

2019 452 citations Clea Bárcena, Rafael Valdés‐Mas et al. Nature Medicine profile →
Non-coding recurrent mutations in chronic lymphocytic leukaemia

2016 377 citations Xosé S. Puente, Sı́lvia Beà et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rafael Valdés‐Mas Spain	15	1.1k	350	273	241	233	23	1.8k
Wei‐Shiung Lian Taiwan	26	951 0.9×	91 0.3×	195 0.7×	206 0.9×	106 0.5×	94	2.0k
Markus Seifert Austria	30	877 0.8×	414 1.2×	1.1k 3.9×	276 1.1×	149 0.6×	81	3.2k
Antonella Vetuschi Italy	26	835 0.8×	115 0.3×	113 0.4×	125 0.5×	468 2.0×	69	2.2k
Huaqing Wang China	24	862 0.8×	214 0.6×	220 0.8×	106 0.4×	66 0.3×	49	1.7k
Rong Zeng China	26	945 0.9×	110 0.3×	185 0.7×	92 0.4×	103 0.4×	113	2.0k
Yun Huang China	22	718 0.7×	180 0.5×	92 0.3×	69 0.3×	99 0.4×	78	1.5k
Aaron Burberry United States	14	1.1k 1.0×	67 0.2×	367 1.3×	191 0.8×	111 0.5×	16	1.9k
Mingcan Yu United States	21	1.1k 1.0×	143 0.4×	45 0.2×	262 1.1×	222 1.0×	34	2.1k
Hongqi Zhang China	29	868 0.8×	289 0.8×	38 0.1×	263 1.1×	250 1.1×	153	2.5k

Countries citing papers authored by Rafael Valdés‐Mas

Since Specialization

Citations

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

Fields of papers citing papers by Rafael Valdés‐Mas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rafael Valdés‐Mas. 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 Rafael Valdés‐Mas. The network helps show where Rafael Valdés‐Mas may publish in the future.

Co-authorship network of co-authors of Rafael Valdés‐Mas

This figure shows the co-authorship network connecting the top 25 collaborators of Rafael Valdés‐Mas. A scholar is included among the top collaborators of Rafael Valdés‐Mas 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 Rafael Valdés‐Mas. Rafael Valdés‐Mas 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

Cahn, Avivit, Valery Istomin, Sarah Israel, et al.. (2024). Diagnosis and Risk Factors of Prediabetes and Diabetes in People Living With Human Immunodeficiency Virus: Evaluation of Clinical and Microbiome Parameters. The Journal of Infectious Diseases. 230(2). 411–420. 2 indexed citations

Dougherty, Michael W., Rafael Valdés‐Mas, Kevin M. Wernke, et al.. (2023). The microbial genotoxin colibactin exacerbates mismatch repair mutations in colorectal tumors. Neoplasia. 43. 100918–100918. 19 indexed citations

Kviatcovsky, Denise, Rafael Valdés‐Mas, Sara Federici, & Eran Elinav. (2023). Phage therapy in noncommunicable diseases. Science. 382(6668). 266–267. 15 indexed citations

Mor, Uria, Yotam Cohen, Rafael Valdés‐Mas, et al.. (2022). Dimensionality reduction of longitudinal ’omics data using modern tensor factorizations. PLoS Computational Biology. 18(7). e1010212–e1010212. 20 indexed citations

Federici, Sara, Denise Kviatcovsky, Rafael Valdés‐Mas, & Eran Elinav. (2022). Microbiome-phage interactions in inflammatory bowel disease. Clinical Microbiology and Infection. 29(6). 682–688. 39 indexed citations

Montassier, Emmanuel, Rafael Valdés‐Mas, Éric Batard, et al.. (2021). Probiotics impact the antibiotic resistance gene reservoir along the human GI tract in a person-specific and antibiotic-dependent manner. Nature Microbiology. 6(8). 1043–1054. 145 indexed citations

Tazón‐Vega, Bárbara, Pau Abrisqueta, Juan C. Nieto, et al.. (2021). Immunological and genetic kinetics from diagnosis to clinical progression in chronic lymphocytic leukemia. Biomarker Research. 9(1). 37–37. 5 indexed citations

Grosheva, Inna, Danping Zheng, Maayan Levy, et al.. (2020). High-Throughput Screen Identifies Host and Microbiota Regulators of Intestinal Barrier Function. Gastroenterology. 159(5). 1807–1823. 142 indexed citations

Bueno, Clara, Fernando J. Calero‐Nieto, Xiaonan Wang, et al.. (2019). Enhanced hemato-endothelial specification during human embryonic differentiation through developmental cooperation between AF4-MLL and MLL-AF4 fusions. Haematologica. 104(6). 1189–1201. 14 indexed citations

10.

Bárcena, Clea, Rafael Valdés‐Mas, Pablo Mayoral, et al.. (2019). Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice. Nature Medicine. 25(8). 1234–1242. 452 indexed citations breakdown →

11.

Mur, Pilar, Ann‐Sofie Jemth, Nuno Amaral, et al.. (2018). Germline variation in the oxidative DNA repair genesNUDT1andOGG1is not associated with hereditary colorectal cancer or polyposis. Human Mutation. 39(9). 1214–1225. 5 indexed citations

12.

Mur, Pilar, Susanna Aussó, Gemma Aiza, et al.. (2016). Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis. Scientific Reports. 6(1). 20697–20697. 6 indexed citations

13.

Puente, Xosé S., Sı́lvia Beà, Rafael Valdés‐Mas, et al.. (2016). Non-coding recurrent mutations in chronic lymphocytic leukaemia. Nature. 534(7607). S11–S12. 377 indexed citations breakdown →

14.

Bellido, Fernando, Marta Pineda, Gemma Aiza, et al.. (2015). POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance. Genetics in Medicine. 18(4). 325–332. 175 indexed citations

15.

Toma, Claudio, Bàrbara Torrico, Amaia Hervás, et al.. (2015). Common and rare variants of microRNA genes in autism spectrum disorders. The World Journal of Biological Psychiatry. 16(6). 376–386. 30 indexed citations

16.

Castellsagué, Joan, Bernat Gel, Juana Fernández‐Rodríguez, et al.. (2015). Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine. EMBO Molecular Medicine. 7(5). 608–627. 34 indexed citations

17.

Valdés‐Mas, Rafael, Jesús Gutiérrez‐Abril, Xosé S. Puente, & Carlos López-Otı́n. (2015). Chronic lymphocytic leukemia: looking into the dark side of the genome. Cell Death and Differentiation. 23(1). 7–9. 2 indexed citations

18.

Valdés‐Mas, Rafael, Ana Gutiérrez‐Fernández, Juan Gómez, et al.. (2014). Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy. Nature Communications. 5(1). 5326–5326. 126 indexed citations

19.

Toma, Claudio, Bàrbara Torrico, Amaia Hervás, et al.. (2013). Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations. Molecular Psychiatry. 19(7). 784–790. 88 indexed citations

20.

Valdés‐Mas, Rafael, Sı́lvia Beà, Diana Puente, Carlos López-Otı́n, & Xosé S. Puente. (2012). Estimation of Copy Number Alterations from Exome Sequencing Data. PLoS ONE. 7(12). e51422–e51422. 13 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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