Neus Romo

824 total citations
16 papers, 657 citations indexed

About

Neus Romo is a scholar working on Immunology, Epidemiology and Molecular Biology. According to data from OpenAlex, Neus Romo has authored 16 papers receiving a total of 657 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Immunology, 6 papers in Epidemiology and 5 papers in Molecular Biology. Recurrent topics in Neus Romo's work include Immune Cell Function and Interaction (10 papers), T-cell and B-cell Immunology (8 papers) and Cytomegalovirus and herpesvirus research (6 papers). Neus Romo is often cited by papers focused on Immune Cell Function and Interaction (10 papers), T-cell and B-cell Immunology (8 papers) and Cytomegalovirus and herpesvirus research (6 papers). Neus Romo collaborates with scholars based in Spain, United States and China. Neus Romo's co-authors include Miguel López‐Botet, Ana Angulo, Giuliana Magri, Aura Muntasell, Andrea Sáez‐Borderías, Maria Pia Cosma, Umberto Di Vicino, Mónica Gumá, Daniela Sanges and Alessandro Moretta and has published in prestigious journals such as Journal of Clinical Investigation, Blood and The Journal of Immunology.

In The Last Decade

Neus Romo

16 papers receiving 648 citations

Peers

Neus Romo

IMMUN

EPIDE

ONCOL

CMN

Hugh H. Reid Australia

J. Ludovic Croxford United States

Nina Chu United States

William C. Hatch United States

Pierre Grenot France

Susan Westmoreland United States

Simone C. Wuest United States

Afonso R. M. Almeida Portugal

Victoria Tüngler Germany

Jenny Gu United States

Hugh H. Reid Australia

Neus Romo

444 ×1.0

IMMUN

99 ×0.4

EPIDE

84 ×0.5

73 ×1.1

ONCOL

13 ×0.3

CMN

Citations per year, relative to Neus Romo Neus Romo (= 1×) peers Hugh H. Reid

Countries citing papers authored by Neus Romo

Since Specialization

Citations

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

Fields of papers citing papers by Neus Romo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neus Romo

This figure shows the co-authorship network connecting the top 25 collaborators of Neus Romo. A scholar is included among the top collaborators of Neus Romo 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 Neus Romo. Neus Romo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Arumugam, K., Lukas Vlahos, Davide Carnevali, et al.. (2020). The Master Regulator Protein BAZ2B Can Reprogram Human Hematopoietic Lineage-Committed Progenitors into a Multipotent State. Cell Reports. 33(10). 108474–108474. 19 indexed citations

Nakagawa, Shoma, et al.. (2019). Controlled ploidy reduction of pluripotent 4n cells generates 2n cells during mouse embryo development. Science Advances. 5(10). eaax4199–eaax4199. 10 indexed citations

Sanges, Daniela, et al.. (2016). Reprogramming Müller glia via in vivo cell fusion regenerates murine photoreceptors. Journal of Clinical Investigation. 126(8). 3104–3116. 62 indexed citations

Sanges, Daniela, Neus Romo, Umberto Di Vicino, et al.. (2013). Wnt/β-Catenin Signaling Triggers Neuron Reprogramming and Regeneration in the Mouse Retina. Cell Reports. 4(2). 271–286. 75 indexed citations

Muntasell, Aura, Andrea Vera, Neus Romo, et al.. (2013). NKG2C zygosity influences CD94/NKG2C receptor function and the NK‐cell compartment redistribution in response to human cytomegalovirus. European Journal of Immunology. 43(12). 3268–3278. 74 indexed citations

Martínez‐Pomar, Natalia, et al.. (2012). Functional impact of A91V mutation of the PRF1 perforin gene. Human Immunology. 74(1). 14–17. 13 indexed citations

Hengel, Hartmut, Alessandro Moretta, Miguel López‐Botet, et al.. (2011). immune evasion strategies cytomegalovirus-infected myeloid dendritic cells overcoming viral NKp46 and DNAM-1 NK-cell receptors drive the response to human. 2 indexed citations

Romo, Neus, Giuliana Magri, Aura Muntasell, et al.. (2011). Natural killer cell-mediated response to human cytomegalovirus-infected macrophages is modulated by their functional polarization. Journal of Leukocyte Biology. 90(4). 717–726. 60 indexed citations

Romo, Neus, Montserrat Fitó, Mónica Gumá, et al.. (2011). Association of Atherosclerosis With Expression of the LILRB1 Receptor By Human NK and T-Cells Supports the Infectious Burden Hypothesis. Arteriosclerosis Thrombosis and Vascular Biology. 31(10). 2314–2321. 31 indexed citations

10.

Monsiváis‐Urenda, Adriana, Daniel E. Noyola, Christian A. García‐Sepúlveda, et al.. (2010). Influence of human cytomegalovirus infection on the NK cell receptor repertoire in children. European Journal of Immunology. 40(5). 1418–1427. 72 indexed citations

11.

Rodríguez, José, Andrea Sáez‐Borderías, Elvira Munteis, et al.. (2010). Natural killer receptors distribution in multiple sclerosis: Relation to clinical course and interferon-beta therapy. Clinical Immunology. 137(1). 41–50. 22 indexed citations

12.

Sáez‐Borderías, Andrea, Neus Romo, Francisco Ruiz‐Cabello, et al.. (2010). Natural killer cell receptor expression reflects the role of human cytomegalovirus in the pathogenesis of a subset of CD4+ T-cell large granular lymphocytosis. Human Immunology. 72(3). 226–228. 4 indexed citations

13.

Magri, Giuliana, Aura Muntasell, Neus Romo, et al.. (2010). NKp46 and DNAM-1 NK-cell receptors drive the response to human cytomegalovirus-infected myeloid dendritic cells overcoming viral immune evasion strategies. Blood. 117(3). 848–856. 103 indexed citations

14.

Sáez‐Borderías, Andrea, Neus Romo, Giuliana Magri, et al.. (2009). IL-12-Dependent Inducible Expression of the CD94/NKG2A Inhibitory Receptor Regulates CD94/NKG2C+ NK Cell Function. The Journal of Immunology. 182(2). 829–836. 61 indexed citations

15.

Sánchez, Antonio, José Rodríguez, Elisa Cisneros, et al.. (2009). Multiple sclerosis associates with LILRA3 deletion in Spanish patients. Genes and Immunity. 10(6). 579–585. 37 indexed citations

16.

Castellvı́-Bel, Sergi, Antoni Castells, Cameron N. Johnstone, et al.. (2003). Evaluation of PARVG located on 22q13 as a candidate tumor suppressor gene for colorectal and breast cancer. Cancer Genetics and Cytogenetics. 144(1). 80–82. 12 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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