Mar Infante

985 total citations
33 papers, 509 citations indexed

About

Mar Infante is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Mar Infante has authored 33 papers receiving a total of 509 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Molecular Biology and 14 papers in Pathology and Forensic Medicine. Recurrent topics in Mar Infante's work include BRCA gene mutations in cancer (18 papers), Cancer Genomics and Diagnostics (14 papers) and Genetic factors in colorectal cancer (14 papers). Mar Infante is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Cancer Genomics and Diagnostics (14 papers) and Genetic factors in colorectal cancer (14 papers). Mar Infante collaborates with scholars based in Spain, United Kingdom and Netherlands. Mar Infante's co-authors include M. Durán, Eladio A. Velasco, Cristina Miner, Eva Esteban‐Cardeñosa, Lucía Pérez‐Cabornero, David J. Sanz, Alberto Acedo, Carolina Velázquez, Miguel de la Hoya and Marta Pineda and has published in prestigious journals such as Clinical Cancer Research, Nature Protocols and International Journal of Molecular Sciences.

In The Last Decade

Mar Infante

33 papers receiving 497 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mar Infante Spain 14 292 245 147 133 89 33 509
Antoine Rousselin France 8 296 1.0× 266 1.1× 88 0.6× 132 1.0× 73 0.8× 11 471
Claude Houdayer France 12 245 0.8× 188 0.8× 50 0.3× 111 0.8× 76 0.9× 15 405
Mario A. Hermsen Netherlands 2 112 0.4× 116 0.5× 145 1.0× 105 0.8× 98 1.1× 2 301
F. B. F. Law Hong Kong 10 228 0.8× 242 1.0× 91 0.6× 127 1.0× 96 1.1× 10 387
Thaddeus Judkins United States 10 247 0.8× 430 1.8× 218 1.5× 192 1.4× 156 1.8× 19 607
Davide Lazzereschi Italy 12 385 1.3× 234 1.0× 66 0.4× 28 0.2× 117 1.3× 14 505
Paraskevi Apostolou Greece 10 211 0.7× 300 1.2× 95 0.6× 130 1.0× 91 1.0× 22 449
Jisha Antony New Zealand 12 276 0.9× 50 0.2× 22 0.1× 31 0.2× 35 0.4× 19 349
Therese Sandberg Sweden 7 189 0.6× 167 0.7× 46 0.3× 70 0.5× 81 0.9× 9 382
Joanna Matyjasik Poland 7 167 0.6× 154 0.6× 85 0.6× 95 0.7× 83 0.9× 11 316

Countries citing papers authored by Mar Infante

Since Specialization
Citations

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

Fields of papers citing papers by Mar Infante

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mar Infante

This figure shows the co-authorship network connecting the top 25 collaborators of Mar Infante. A scholar is included among the top collaborators of Mar Infante 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 Mar Infante. Mar Infante 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.
Bueno‐Martínez, Elena, Pedro Pérez‐Segura, Mar Infante, et al.. (2023). Systematic Minigene-Based Splicing Analysis and Tentative Clinical Classification of 52 CHEK2 Splice-Site Variants. Clinical Chemistry. 70(1). 319–338. 5 indexed citations
2.
Ferreira, Rita, et al.. (2023). Multigene germline testing usefulness instead of BRCA1/2 single screening in triple negative breast cancer cases. Pathology - Research and Practice. 247. 154514–154514. 1 indexed citations
3.
Durán, M., et al.. (2023). Multiomics insights on the onset, progression, and metastatic evolution of breast cancer. Frontiers in Oncology. 13. 1292046–1292046. 3 indexed citations
4.
5.
Infante, Mar, et al.. (2022). Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?. International Journal of Molecular Sciences. 23(19). 11499–11499. 8 indexed citations
6.
Bueno‐Martínez, Elena, Sara Carvalho, Jamie Allen, et al.. (2021). RAD51D Aberrant Splicing in Breast Cancer: Identification of Splicing Regulatory Elements and Minigene-Based Evaluation of 53 DNA Variants. Cancers. 13(11). 2845–2845. 12 indexed citations
7.
Velázquez, Carolina, et al.. (2020). A comprehensive custom panel evaluation for routine hereditary cancer testing: improving the yield of germline mutation detection. Journal of Translational Medicine. 18(1). 232–232. 16 indexed citations
8.
Velázquez, Carolina, et al.. (2018). A PALB2 truncating mutation: Implication in cancer prevention and therapy of Hereditary Breast and Ovarian Cancer. The Breast. 43. 91–96. 7 indexed citations
9.
Infante, Mar, M. Durán, Alberto Acedo, et al.. (2013). The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins. Carcinogenesis. 34(11). 2505–2511. 14 indexed citations
10.
Pérez‐Cabornero, Lucía, et al.. (2013). Genotype–phenotype correlation in MMR mutation-positive families with Lynch syndrome. International Journal of Colorectal Disease. 28(9). 1195–1201. 17 indexed citations
11.
Acedo, Alberto, David J. Sanz, M. Durán, et al.. (2012). Comprehensive splicing functional analysis of DNA variants of the BRCA2 gene by hybrid minigenes. Breast Cancer Research. 14(3). R87–R87. 43 indexed citations
12.
Pérez‐Cabornero, Lucía, et al.. (2011). Frequency of Rearrangements in Lynch Syndrome Cases Associated with MSH2 : Characterization of a New Deletion Involving both EPCAM and the 5′ Part of MSH2. Cancer Prevention Research. 4(10). 1556–1562. 24 indexed citations
13.
Pérez‐Cabornero, Lucía, Mar Infante, Eladio A. Velasco, et al.. (2011). Characterization of New Founder Alu-Mediated Rearrangements in MSH2 Gene Associated with a Lynch Syndrome Phenotype. Cancer Prevention Research. 4(10). 1546–1555. 15 indexed citations
14.
Sanz, David J., Alberto Acedo, Mar Infante, et al.. (2010). A High Proportion of DNA Variants of BRCA1 and BRCA2 Is Associated with Aberrant Splicing in Breast/Ovarian Cancer Patients. Clinical Cancer Research. 16(6). 1957–1967. 84 indexed citations
15.
Infante, Mar, M. Durán, Adriana Lasa, et al.. (2009). Two founder BRCA2 mutations predispose to breast cancer in young women. Breast Cancer Research and Treatment. 122(2). 567–571. 8 indexed citations
16.
Velasco, Eladio A., Mar Infante, M. Durán, et al.. (2007). Heteroduplex analysis by capillary array electrophoresis for rapid mutation detection in large multiexon genes. Nature Protocols. 2(1). 237–246. 37 indexed citations
17.
Infante, Mar, M. Durán, Eva Esteban‐Cardeñosa, Cristina Miner, & Eladio A. Velasco. (2006). High proportion of novel mutations of BRCA1 and BRCA2 in breast/ovarian cancer patients from Castilla-León (central Spain). Journal of Human Genetics. 51(7). 611–617. 30 indexed citations
18.
Velasco, Eladio A., Mar Infante, M. Durán, et al.. (2005). Rapid mutation detection in complex genes by heteroduplex analysis with capillary array electrophoresis. Electrophoresis. 26(13). 2539–2552. 19 indexed citations
19.
Durán, M., Eva Esteban‐Cardeñosa, Eladio A. Velasco, Mar Infante, & Cristina Miner. (2003). Mutational analysis ofBRCA2in Spanish breast cancer patients from Castilla-Leon: Identification of four novel truncating mutations. Human Mutation. 21(4). 448–448. 19 indexed citations
20.
Cusumano, Ana María, et al.. (1997). Latin American registry of dialysis and renal transplantation: 1993 annual dialysis data report. Nephrology Dialysis Transplantation. 12(12). 2521–2527. 34 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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