Ana Rath

9.9k total citations · 2 hit papers
51 papers, 2.9k citations indexed

About

Ana Rath is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Ana Rath has authored 51 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 15 papers in Molecular Biology and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Ana Rath's work include Genomics and Rare Diseases (29 papers), Biomedical Text Mining and Ontologies (10 papers) and Cystic Fibrosis Research Advances (7 papers). Ana Rath is often cited by papers focused on Genomics and Rare Diseases (29 papers), Biomedical Text Mining and Ontologies (10 papers) and Cystic Fibrosis Research Advances (7 papers). Ana Rath collaborates with scholars based in France, Germany and Italy. Ana Rath's co-authors include Annie Olry, J. P. Chevrel, Valérie Serrière-Lanneau, Yann Le Cam, Charlotte Rodwell, Daniel N. Murphy, Deborah M. Lambert, Stéphanie Nguengang Wakap, Ségolène Aymé and Bruno Urbero and has published in prestigious journals such as PLoS ONE, Nature Reviews Drug Discovery and Agriculture Ecosystems & Environment.

In The Last Decade

Ana Rath

50 papers receiving 2.8k citations

Hit Papers

Estimating cumulative point prevalence of rare diseases: ... 2019 2026 2021 2023 2019 2019 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ana Rath France 24 1.2k 816 542 333 296 51 2.9k
Manuel Posada de la Paz Spain 37 854 0.7× 687 0.8× 375 0.7× 424 1.3× 282 1.0× 219 4.1k
Domenica Taruscio Italy 36 1.1k 0.9× 1.1k 1.3× 315 0.6× 420 1.3× 351 1.2× 194 3.8k
Peter A. Kanetsky United States 37 646 0.5× 1.2k 1.5× 596 1.1× 303 0.9× 112 0.4× 115 5.2k
John I. Allen United States 35 772 0.6× 400 0.5× 842 1.6× 609 1.8× 240 0.8× 136 4.9k
William E. Winter United States 32 1.5k 1.3× 613 0.8× 1.9k 3.6× 281 0.8× 126 0.4× 137 5.1k
Bingshu E. Chen Canada 33 436 0.4× 707 0.9× 703 1.3× 551 1.7× 134 0.5× 147 4.0k
Zornitza Stark Australia 31 2.1k 1.8× 1.4k 1.7× 174 0.3× 247 0.7× 238 0.8× 151 3.6k
Eleanor Sanderson United Kingdom 26 2.4k 2.0× 1.1k 1.4× 617 1.1× 280 0.8× 291 1.0× 66 5.3k
Ayako Matsuda Japan 24 497 0.4× 447 0.5× 679 1.3× 377 1.1× 58 0.2× 94 2.5k
Elizabeth Garrett United States 28 324 0.3× 884 1.1× 563 1.0× 334 1.0× 444 1.5× 82 3.4k

Countries citing papers authored by Ana Rath

Since Specialization
Citations

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

Fields of papers citing papers by Ana Rath

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ana Rath

This figure shows the co-authorship network connecting the top 25 collaborators of Ana Rath. A scholar is included among the top collaborators of Ana Rath 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 Ana Rath. Ana Rath 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.
Weber, Stefanie, et al.. (2024). Coding undiagnosed rare disease patients in health information systems: recommendations from the RD-CODE project. Orphanet Journal of Rare Diseases. 19(1). 28–28. 3 indexed citations
2.
Pozza, Laura Visonà Dalla, Paola Facchin, Clara Cavero‐Carbonell, et al.. (2023). ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability. Orphanet Journal of Rare Diseases. 18(1). 267–267. 8 indexed citations
3.
Lagorce, David, Leslie Matalonga, Ida Paramonov, et al.. (2023). Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report. European Journal of Human Genetics. 32(2). 182–189. 5 indexed citations
4.
Fiore, Mathieu, Marie‐Christine Alessi, Céline Falaise, et al.. (2023). Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders. Orphanet Journal of Rare Diseases. 18(1). 171–171. 7 indexed citations
5.
Olry, Annie, Marc Hanauer, Valérie Serrière-Lanneau, et al.. (2018). Harmonising phenomics information for a better interoperability in the rare disease field. European Journal of Medical Genetics. 61(11). 706–714. 16 indexed citations
6.
Djurisic, Snezana, Ana Rath, Silvio Garattini, et al.. (2017). Barriers to the conduct of randomised clinical trials within all disease areas. Trials. 18(1). 360–360. 103 indexed citations
7.
Neugebauer, Edmund, Ana Rath, Michaela Eikermann, et al.. (2017). Specific barriers to the conduct of randomised clinical trials on medical devices. Trials. 18(1). 427–427. 67 indexed citations
9.
Julkowska, Daria, Christopher P. Austin, Christine M. Cutillo, et al.. (2017). The importance of international collaboration for rare diseases research: a European perspective. Gene Therapy. 24(9). 562–571. 60 indexed citations
10.
Laville, Martine, Bérénice Segrestin, Maud Alligier, et al.. (2017). Evidence-based practice within nutrition: what are the barriers for improving the evidence and how can they be dealt with?. Trials. 18(1). 425–425. 24 indexed citations
11.
Walker, C. E., Geoff Davis, Laura Miller, et al.. (2016). The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort. Genetics in Medicine. 19(5). 546–552. 77 indexed citations
12.
Aymé, Ségolène, et al.. (2015). Rare diseases in ICD11: making rare diseases visible in health information systems through appropriate coding. Orphanet Journal of Rare Diseases. 10(1). 35–35. 92 indexed citations
13.
Rath, Ana, et al.. (2013). Orphanet et son réseau : où trouver une information validée sur les maladies rares. Revue Neurologique. 169. S3–S8. 30 indexed citations
14.
Köhler, Sebastian, Sandra C. Doelken, Ana Rath, Ségolène Aymé, & Peter N. Robinson. (2012). Ontological phenotype standards for neurogenetics. Human Mutation. 33(9). 1333–1339. 16 indexed citations
15.
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
16.
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
17.
Korenkov, Michael, A. Paul, Stefan Sauerland, et al.. (2001). Classification and surgical treatment of incisional hernia. Langenbeck s Archives of Surgery. 386(1). 65–73. 198 indexed citations
18.
Rath, Ana, et al.. (2000). Experimental study on the in vivo behaviour of a new collagen glue in lung surgery. European Journal of Cardio-Thoracic Surgery. 17(1). 8–13. 17 indexed citations
19.
Forster, D.H., Gérard Krause, Petra Gastmeier, et al.. (2000). Can quality circles improve hospital-acquired infection control?. Journal of Hospital Infection. 45(4). 302–310. 27 indexed citations
20.
Gastmeier, Petra, D. Sohr, Ana Rath, et al.. (2000). Repeated prevalence investigations on nosocomial infections for continuous surveillance. Journal of Hospital Infection. 45(1). 47–53. 40 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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