Davide Komla‐Ebri

2.4k total citations
6 papers, 191 citations indexed

About

Davide Komla‐Ebri is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Davide Komla‐Ebri has authored 6 papers receiving a total of 191 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 Oncology. Recurrent topics in Davide Komla‐Ebri's work include Connective tissue disorders research (6 papers), Fibroblast Growth Factor Research (4 papers) and Bone health and treatments (2 papers). Davide Komla‐Ebri is often cited by papers focused on Connective tissue disorders research (6 papers), Fibroblast Growth Factor Research (4 papers) and Bone health and treatments (2 papers). Davide Komla‐Ebri collaborates with scholars based in France, Switzerland and United Kingdom. Davide Komla‐Ebri's co-authors include Nabil Kaci, Laurence Legeai‐Mallet, Federico Di Rocco, Martin Biosse Duplan, Catherine Benoist-Lasselin, Arnold Münnich, Yann Heuzé, Michaela Kneissel, Ina Krämer and Emilie Mugniery and has published in prestigious journals such as Journal of Clinical Investigation, Human Molecular Genetics and JCI Insight.

In The Last Decade

Davide Komla‐Ebri

5 papers receiving 191 citations

Peers

Davide Komla‐Ebri

MB

GENET

ONCOL

PRM

RHEUM

Maha Faden Saudi Arabia

Virginie Grybek France

Anne Dieux France

Wiebke Ahrens Germany

Pauline Marzin France

Mafalda Mucciolo Italy

Emma Miles United Kingdom

Paolo Bordogna Italy

Eveline W Blom Netherlands

Hanneke Basart Netherlands

Maha Faden Saudi Arabia

Davide Komla‐Ebri

93 ×0.7

MB

100 ×0.7

GENET

31 ×1.3

ONCOL

17 ×0.8

PRM

22 ×1.0

RHEUM

Citations per year, relative to Davide Komla‐Ebri Davide Komla‐Ebri (= 1×) peers Maha Faden

Countries citing papers authored by Davide Komla‐Ebri

Since Specialization

Citations

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

Fields of papers citing papers by Davide Komla‐Ebri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Davide Komla‐Ebri. 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 Davide Komla‐Ebri. The network helps show where Davide Komla‐Ebri may publish in the future.

Co-authorship network of co-authors of Davide Komla‐Ebri

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

All Works

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6 of 6 papers shown

1.

Komla‐Ebri, Davide, Yann Heuzé, Nabil Kaci, et al.. (2023). Hypochondroplasia gain-of-function mutation in FGFR3 causes defective bone mineralization in mice. JCI Insight. 8(12). 6 indexed citations

2.

Dambroise, Emilie, et al.. (2019). Animal models of craniosynostosis. Neurochirurgie. 65(5). 202–209. 12 indexed citations

3.

Duplan, Martin Biosse, Davide Komla‐Ebri, Yann Heuzé, et al.. (2016). Meckel’s and condylar cartilages anomalies in achondroplasia result in defective development and growth of the mandible. Human Molecular Genetics. 25(14). ddw153–ddw153. 32 indexed citations

4.

Komla‐Ebri, Davide, Emilie Dambroise, Ina Krämer, et al.. (2016). Tyrosine kinase inhibitor NVP-BGJ398 functionally improves FGFR3-related dwarfism in mouse model. Journal of Clinical Investigation. 126(5). 1871–1884. 78 indexed citations

5.

Rocco, Federico Di, Martin Biosse Duplan, Yann Heuzé, et al.. (2014). FGFR3 mutation causes abnormal membranous ossification in achondroplasia. Human Molecular Genetics. 23(11). 2914–2925. 63 indexed citations

6.

Duplan, Martin Biosse, Yann Heuzé, Davide Komla‐Ebri, et al.. (2014). Disturbed cartilages of the mandible in achondroplasia are associated with defective mandible shape and position. Bone Abstracts.

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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