María Roqué

660 total citations
37 papers, 483 citations indexed

About

María Roqué is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, María Roqué has authored 37 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Oncology. Recurrent topics in María Roqué's work include Epigenetics and DNA Methylation (14 papers), Cancer-related gene regulation (5 papers) and Genomics and Chromatin Dynamics (5 papers). María Roqué is often cited by papers focused on Epigenetics and DNA Methylation (14 papers), Cancer-related gene regulation (5 papers) and Genomics and Chromatin Dynamics (5 papers). María Roqué collaborates with scholars based in Argentina, United States and Australia. María Roqué's co-authors include Diego M. Marzese, Laura M. Vargas‐Roig, Marı́a Teresita Branham, Javier I. J. Orozco, Francisco E. Gago, Emanuel Campoy, Eduardo Pusiol, Dave S.�B. Hoon, S Iorcansky and Boris Elsner and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

María Roqué

35 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
María Roqué Argentina	12	333	107	103	73	66	37	483
Dagmar Arnold United States	8	403 1.2×	141 1.3×	91 0.9×	102 1.4×	46 0.7×	11	630
Shi‐He Liu United States	14	219 0.7×	116 1.1×	77 0.7×	27 0.4×	48 0.7×	26	394
Cláudia Miranda Italy	11	223 0.7×	143 1.3×	52 0.5×	92 1.3×	35 0.5×	15	411
Daniel Hormaechea‐Agulla Spain	10	222 0.7×	68 0.6×	71 0.7×	76 1.0×	27 0.4×	12	579
Melania E. Mercado-Pimentel United States	10	362 1.1×	115 1.1×	122 1.2×	21 0.3×	39 0.6×	12	493
Kristen D. Hadfield United Kingdom	8	232 0.7×	117 1.1×	105 1.0×	25 0.3×	137 2.1×	11	514
Samornmas Kanngurn Thailand	11	239 0.7×	134 1.3×	101 1.0×	23 0.3×	33 0.5×	25	442
Seham Skah France	8	232 0.7×	97 0.9×	76 0.7×	201 2.8×	127 1.9×	11	498
Rong‐Liang Shi China	15	138 0.4×	142 1.3×	72 0.7×	181 2.5×	30 0.5×	28	431
J.P. Leek United Kingdom	13	205 0.6×	70 0.7×	42 0.4×	33 0.5×	69 1.0×	31	402

Countries citing papers authored by María Roqué

Since Specialization

Citations

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

Fields of papers citing papers by María Roqué

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María Roqué

This figure shows the co-authorship network connecting the top 25 collaborators of María Roqué. A scholar is included among the top collaborators of María Roqué 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 María Roqué. María Roqué 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

Real, Sebastián, et al.. (2022). CDC42 as an epigenetic regulator of ID4 in triple-negative breast tumors. Breast Cancer. 29(3). 562–573. 4 indexed citations

Marzese, Diego M., et al.. (2019). Mitochondrial stress triggers a pro-survival response through epigenetic modifications of nuclear DNA. Cellular and Molecular Life Sciences. 76(7). 1397–1417. 10 indexed citations

Campoy, Emanuel, Marı́a Teresita Branham, Luis S. Mayorga, & María Roqué. (2019). Intratumor heterogeneity index of breast carcinomas based on DNA methylation profiles. BMC Cancer. 19(1). 328–328. 5 indexed citations

Campoy, Emanuel, et al.. (2018). Epigenetic regulation of ID4 in breast cancer: tumor suppressor or oncogene?. Clinical Epigenetics. 10(1). 111–111. 21 indexed citations

Roqué, María, et al.. (2018). A frame-shift deletion in the PURA gene associates with a new clinical finding: Hypoglycorrhachia. Is GLUT1 a new PURA target?. Molecular Genetics and Metabolism. 123(3). 331–336. 20 indexed citations

Campoy, Emanuel, Marı́a Teresita Branham, Angela Mathison, et al.. (2016). Asymmetric Cancer Hallmarks in Breast Tumors on Different Sides of the Body. PLoS ONE. 11(7). e0157416–e0157416. 7 indexed citations

Branham, Marı́a Teresita, Emanuel Campoy, Richard L. Branham, et al.. (2015). Epigenetic regulation of ID4 in the determination of the BRCAness phenotype in breast cancer. Breast Cancer Research and Treatment. 155(1). 13–23. 12 indexed citations

Marzese, Diego M., Richard A. Scolyer, María Roqué, et al.. (2014). DNA methylation and gene deletion analysis of brain metastases in melanoma patients identifies mutually exclusive molecular alterations. Neuro-Oncology. 16(11). 1499–1509. 52 indexed citations

Branham, Marı́a Teresita, et al.. (2012). Methylation profile of triple-negative breast carcinomas. Oncogenesis. 1(7). e17–e17. 49 indexed citations

10.

Marzese, Diego M., Dave S.�B. Hoon, Kelly K. Chong, et al.. (2012). DNA Methylation Index and Methylation Profile of Invasive Ductal Breast Tumors. Journal of Molecular Diagnostics. 14(6). 613–622. 28 indexed citations

11.

Vargas, Ana Lía, et al.. (2011). Detección de alteraciones numéricas en el gen dys y su asociación con rasgos clínicos. Medicina-buenos Aires. 71(2). 151–157. 1 indexed citations

12.

Marzese, Diego M., Francisco E. Gago, Laura M. Vargas‐Roig, & María Roqué. (2010). Simultaneous analysis of the methylation profile of 26 cancer related regions in invasive breast carcinomas by MS-MLPA and drMS-MLPA. Molecular and Cellular Probes. 24(5). 271–280. 19 indexed citations

13.

Bátiz, Luis Federico, Ruth Roales‐Buján, Luis‐Manuel Rodríguez‐Pérez, et al.. (2009). A simple PCR-based genotyping method for M105I mutation of alpha-SNAP enhances the study of early pathological changes in hyh phenotype. Molecular and Cellular Probes. 23(6). 281–290. 18 indexed citations

14.

Giliberto, Florencia, et al.. (2008). Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion. Muscle & Nerve. 39(2). 239–243. 51 indexed citations

15.

Marzese, Diego M., et al.. (2008). MLPA mutation detection in Argentine HNPCC and FAP families. Familial Cancer. 8(1). 67–73. 5 indexed citations

16.

Real, Sebastián, et al.. (2007). Polymorphism of the FABP2 gene: a population frequency analysis and an association study with cardiovascular risk markers in Argentina. BMC Medical Genetics. 8(1). 39–39. 10 indexed citations

17.

Real, Sebastián, et al.. (2006). Development of a Premature Stop Codon-detection method based on a bacterial two-hybrid system. BMC Biotechnology. 6(1). 38–38. 4 indexed citations

18.

Roqué, María, et al.. (2002). A PCR-mutagenesis strategy for rapid detection of mutations in codon 634 of the retproto-oncogene related to MEN 2A.. BMC Medical Genetics. 3(1). 4–4. 4 indexed citations

19.

Sansó, Gabriela, Horacio M. Domené, Eduardo Pusiol, et al.. (2002). Very early detection of RET proto‐oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children. Cancer. 94(2). 323–330. 89 indexed citations

20.

Roqué, María, et al.. (2001). Population screening if F508del (ΔF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina. Human Mutation. 18(2). 167–167. 6 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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