Josefa Rius

745 total citations
8 papers, 528 citations indexed

About

Josefa Rius is a scholar working on Molecular Biology, Immunology and Hematology. According to data from OpenAlex, Josefa Rius has authored 8 papers receiving a total of 528 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Immunology and 3 papers in Hematology. Recurrent topics in Josefa Rius's work include Inflammasome and immune disorders (6 papers), IL-33, ST2, and ILC Pathways (3 papers) and Autoimmune and Inflammatory Disorders Research (2 papers). Josefa Rius is often cited by papers focused on Inflammasome and immune disorders (6 papers), IL-33, ST2, and ILC Pathways (3 papers) and Autoimmune and Inflammatory Disorders Research (2 papers). Josefa Rius collaborates with scholars based in Spain and United States. Josefa Rius's co-authors include Juan I. Aróstegui, Jordi Yagüe, Susana Plaza, Jordi Vives, Anna Aldea, Eduardo Ramos, Consuelo Modesto, Antonio Naranjo, Julia García-Consuegra and Cristina Arnal and has published in prestigious journals such as Human Mutation, European Journal of Pediatrics and American Journal of Medical Genetics Part A.

In The Last Decade

Josefa Rius

8 papers receiving 514 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Josefa Rius Spain	8	380	245	143	95	93	8	528
Takakazu Yoshioka Japan	6	243 0.6×	205 0.8×	74 0.5×	95 1.0×	56 0.6×	12	401
Elizabeth Drewe United Kingdom	9	611 1.6×	385 1.6×	215 1.5×	34 0.4×	125 1.3×	14	750
Trudy M. Doyle United States	10	226 0.6×	115 0.5×	55 0.4×	265 2.8×	123 1.3×	14	626
Rabia Miray Kışla Ekinci Türkiye	12	163 0.4×	134 0.5×	49 0.3×	17 0.2×	91 1.0×	51	342
J. B. Kuemmerle‐Deschner Germany	7	251 0.7×	140 0.6×	138 1.0×	12 0.1×	83 0.9×	25	350
Beverly Barham United States	6	565 1.5×	345 1.4×	174 1.2×	12 0.1×	71 0.8×	6	646
Sibel Balcı Türkiye	12	141 0.4×	124 0.5×	42 0.3×	16 0.2×	89 1.0×	47	326
Anja Bialkowski Germany	7	201 0.5×	101 0.4×	82 0.6×	17 0.2×	40 0.4×	9	347
Emmanuelle Cochet France	7	607 1.6×	414 1.7×	120 0.8×	24 0.3×	97 1.0×	12	671
Nazife Şule Yaşar Bilge Türkiye	11	168 0.4×	94 0.4×	39 0.3×	11 0.1×	67 0.7×	38	284

Countries citing papers authored by Josefa Rius

Since Specialization

Citations

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

Fields of papers citing papers by Josefa Rius

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josefa Rius

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

All Works

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8 of 8 papers shown

Aróstegui, Juan I., Mariona Pascal, Daniel Clemente, et al.. (2010). A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal‐onset multisystem inflammatory disease: Novel evidence of the role of low‐level mosaicism as the pathophysiologic mechanism underlying mendelian inherited diseases. Arthritis & Rheumatism. 62(4). 1158–1166. 55 indexed citations

Cañete, Juan D., Juan I. Aróstegui, Rubén Queiró, et al.. (2007). An unexpectedly high frequency of MEFV mutations in patients with anti–citrullinated protein antibody–negative palindromic rheumatism. Arthritis & Rheumatism. 56(8). 2784–2788. 51 indexed citations

Aróstegui, Juan I., Cristina Arnal, Rosa Merino, et al.. (2007). NOD2 gene–associated pediatric granulomatous arthritis: Clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin‐1 blockade in a Spanish cohort. Arthritis & Rheumatism. 56(11). 3805–3813. 165 indexed citations

Granell, Miquel, Álvaro Urbano-Ispizúa, Juan I. Aróstegui, et al.. (2006). Effect of NOD2/CARD15 variants in T-cell depleted allogeneic stem cell transplantation.. PubMed. 91(10). 1372–6. 51 indexed citations

Aldea, Anna, Francesc Calafell, Juan I. Aróstegui, et al.. (2004). The west side story:MEFVhaplotype in Spanish FMF patients and controls, and evidence of high LD and a recombination “hot-spot” at theMEFVlocus. Human Mutation. 23(4). 399–399. 35 indexed citations

Aróstegui, Juan I., Anna Aldea, Consuelo Modesto, et al.. (2004). Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene. Arthritis & Rheumatism. 50(12). 4045–4050. 73 indexed citations

Aróstegui, Juan I., Anna Aldea, Josefa Rius, et al.. (2004). Etanercept plus colchicine treatment in a child with tumour necrosis factor receptor-associated periodic syndrome abolishes auto-inflammatory episodes without normalising the subclinical acute phase response. European Journal of Pediatrics. 164(1). 13–16. 33 indexed citations

Aldea, Anna, Josep M. Campistol, Juan I. Aróstegui, et al.. (2003). A severe autosomal‐dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: An unusual familial Mediterranean fever phenotype or another MEFV‐associated periodic inflammatory disorder?. American Journal of Medical Genetics Part A. 124A(1). 67–73. 65 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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