Bruno Urbero

495 total citations
8 papers, 292 citations indexed

About

Bruno Urbero is a scholar working on Genetics, Molecular Biology and Artificial Intelligence. According to data from OpenAlex, Bruno Urbero has authored 8 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Artificial Intelligence. Recurrent topics in Bruno Urbero's work include Genomics and Rare Diseases (6 papers), Biomedical Text Mining and Ontologies (2 papers) and Semantic Web and Ontologies (2 papers). Bruno Urbero is often cited by papers focused on Genomics and Rare Diseases (6 papers), Biomedical Text Mining and Ontologies (2 papers) and Semantic Web and Ontologies (2 papers). Bruno Urbero collaborates with scholars based in France and United Kingdom. Bruno Urbero's co-authors include Ségolène Aymé, Annie Olry, Ana Rath, Ferdinand Dhombres, Michel Kress, Xavier Le Goff, Mick F. Tuite, Jean‐Pierre Tassan, Ian Stansfield and Lily Eurwilaichitr and has published in prestigious journals such as Biochimie, Human Mutation and Clinical Rheumatology.

In The Last Decade

Bruno Urbero

8 papers receiving 289 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bruno Urbero France	5	185	158	31	20	15	8	292
Christine Mundlos Germany	6	256 1.4×	236 1.5×	75 2.4×	31 1.6×	22 1.5×	14	396
William Broomall United States	8	217 1.2×	50 0.3×	20 0.6×	9 0.5×	9 0.6×	13	327
David Berman United States	6	175 0.9×	145 0.9×	17 0.5×	65 3.3×	7 0.5×	9	326
Moira Lee United States	1	205 1.1×	111 0.7×	20 0.6×	74 3.7×	23 1.5×	2	321
Marta Bleda Spain	9	189 1.0×	79 0.5×	12 0.4×	41 2.0×	11 0.7×	14	280
Marta Gîrdea Canada	7	177 1.0×	250 1.6×	45 1.5×	70 3.5×	11 0.7×	12	346
Benjamin Livesey United Kingdom	8	293 1.6×	185 1.2×	6 0.2×	55 2.8×	5 0.3×	13	438
Lora Ziyabari United States	3	220 1.2×	122 0.8×	21 0.7×	75 3.8×	24 1.6×	4	350
Anne Sturcke United States	2	209 1.1×	115 0.7×	20 0.6×	74 3.7×	23 1.5×	3	327
Karen He United States	6	83 0.4×	69 0.4×	29 0.9×	46 2.3×	13 0.9×	12	230

Countries citing papers authored by Bruno Urbero

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Urbero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Urbero

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

1.

Rath, Ana, et al.. (2012). Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users. Human Mutation. 33(5). 803–808. 223 indexed citations

2.

Dhombres, Ferdinand, Pierre-Yves Vandenbussche, Ana Rath, et al.. (2011). OntoOrpha: An Ontology to Support Edition and Audit of Knowledge of Rare Diseases in ORPHANET.. 3 indexed citations

3.

Aymé, Ségolène, et al.. (2007). Maladies rares: quelles sources d'information pour les professionnels de santé et les malades?. Réanimation. 16(4). 276–280. 3 indexed citations

4.

Urbero, Bruno, et al.. (2006). Utilisation d’un annuaire des services spécialisés et orientation dans le système de soins: l’exemple d’Orphanet dans les maladies rares. Revue d Épidémiologie et de Santé Publique. 54(1). 41–53. 6 indexed citations

5.

Aymé, Ségolène, et al.. (1998). [Information on rare diseases: the Orphanet project].. PubMed. 19 Suppl 3. 376S–377S. 17 indexed citations

6.

Aymé, Ségolène, et al.. (1998). Information sur les maladies rares : le projet Orphanet. La Revue de Médecine Interne. 19. 376–377. 19 indexed citations

7.

Urbero, Bruno, Lily Eurwilaichitr, Ian Stansfield, et al.. (1997). Expression of the release factor eRF1 (Sup45p) gene of higher eukaryotes in yeast and mammalian tissues. Biochimie. 79(1). 27–36. 18 indexed citations

8.

Pla, Marika, et al.. (1996). The Absence of Human β2-microglobulin Increasesthe Occurrence of Ankylosing Enthesopathy in HLA-B27 Transgenic Mice. Clinical Rheumatology. 15(S1). 28–31. 3 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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