Agnès Bloch‐Zupan

2.9k total citations
75 papers, 1.5k citations indexed

About

Agnès Bloch‐Zupan is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, Agnès Bloch‐Zupan has authored 75 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 30 papers in Rheumatology and 18 papers in Genetics. Recurrent topics in Agnès Bloch‐Zupan's work include dental development and anomalies (33 papers), Bone and Dental Protein Studies (26 papers) and Oral and Maxillofacial Pathology (17 papers). Agnès Bloch‐Zupan is often cited by papers focused on dental development and anomalies (33 papers), Bone and Dental Protein Studies (26 papers) and Oral and Maxillofacial Pathology (17 papers). Agnès Bloch‐Zupan collaborates with scholars based in France, United Kingdom and Germany. Agnès Bloch‐Zupan's co-authors include Paul Ashley, J V Ruch, Hélène Dollfus, Étienne Mornet, Manuel P. Mark, Marie‐Cécile Manière, Virginie Laugel-Haushalter, François Clauss, Yves Alembik and Alan J. Mighell and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Agnès Bloch‐Zupan

72 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Agnès Bloch‐Zupan France 22 852 578 324 242 221 75 1.5k
Dominique Hotton France 21 865 1.0× 719 1.2× 157 0.5× 314 1.3× 64 0.3× 43 1.2k
Sadakazu Ejiri Japan 26 866 1.0× 316 0.5× 182 0.6× 278 1.1× 88 0.4× 63 1.7k
Claire Bardet France 18 267 0.3× 288 0.5× 147 0.5× 150 0.6× 100 0.5× 35 936
Brigitte Baroukh France 22 348 0.4× 226 0.4× 104 0.3× 314 1.3× 72 0.3× 44 1.4k
Maria Ransjö Sweden 21 615 0.7× 122 0.2× 133 0.4× 188 0.8× 57 0.3× 64 1.2k
Yutaka Maruoka Japan 17 510 0.6× 148 0.3× 126 0.4× 320 1.3× 53 0.2× 56 1.1k
Figen Seymen Türkiye 27 1.3k 1.5× 1.1k 1.9× 318 1.0× 508 2.1× 15 0.1× 104 2.1k
Akihiro Hosoya Japan 24 827 1.0× 258 0.4× 109 0.3× 225 0.9× 21 0.1× 71 1.4k
Yoshinobu Shibasaki Japan 21 828 1.0× 197 0.3× 206 0.6× 396 1.6× 63 0.3× 52 1.7k
Shibin Yu China 21 352 0.4× 612 1.1× 79 0.2× 225 0.9× 35 0.2× 55 1.2k

Countries citing papers authored by Agnès Bloch‐Zupan

Since Specialization
Citations

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

Fields of papers citing papers by Agnès Bloch‐Zupan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Agnès Bloch‐Zupan. 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 Agnès Bloch‐Zupan. The network helps show where Agnès Bloch‐Zupan may publish in the future.

Co-authorship network of co-authors of Agnès Bloch‐Zupan

This figure shows the co-authorship network connecting the top 25 collaborators of Agnès Bloch‐Zupan. A scholar is included among the top collaborators of Agnès Bloch‐Zupan 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 Agnès Bloch‐Zupan. Agnès Bloch‐Zupan 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.
Chevalier, Claire, et al.. (2025). Ripply3 overdosage induces mid-face shortening through Tbx1 downregulation in Down syndrome models. PLoS Genetics. 21(9). e1011873–e1011873. 1 indexed citations
2.
Bloch‐Zupan, Agnès, et al.. (2024). Prevalence of tooth agenesis and supernumerary teeth related to different Thai cleft lip and cleft palate populations. BMC Oral Health. 24(1). 960–960. 1 indexed citations
3.
Bugueno, Isaac Maximiliano, et al.. (2024). Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations. Genes & Diseases. 11(5). 101303–101303. 2 indexed citations
4.
Smith, Claire E. L., Virginie Laugel-Haushalter, Ummey Hany, et al.. (2024). Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of Medical Genetics. 61(7). 689–698. 2 indexed citations
5.
Canceill, Thibault, et al.. (2023). Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic review. International Orthodontics. 21(4). 100789–100789. 3 indexed citations
6.
Manière, Marie‐Cécile, et al.. (2023). Primary failure of eruption: From molecular diagnosis to therapeutic management. Journal of Oral Biology and Craniofacial Research. 13(2). 169–176. 7 indexed citations
7.
Bouchet, Jérôme, Ali Nassif, Sandrine Lorimier, et al.. (2021). COVID-19 and Dentistry in 72 Questions: An Overview of the Literature. Journal of Clinical Medicine. 10(4). 779–779. 15 indexed citations
8.
Kunz, Felix, Hülya Kayserili, Alina T. Midro, et al.. (2020). Characteristic dental pattern with hypodontia and short roots in Fraser syndrome. American Journal of Medical Genetics Part A. 182(7). 1681–1689. 7 indexed citations
9.
Molitor, Anne, Zhichao Miao, Agnès Bloch‐Zupan, et al.. (2019). Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitis. Journal of Human Genetics. 64(7). 689–694. 11 indexed citations
10.
Witkos, Tomasz M., Sheila Unger, John A. Follit, et al.. (2019). Hypomorphic mutations of TRIP11 cause odontochondrodysplasia. JCI Insight. 4(3). 61 indexed citations
11.
Underbjerg, Line, Hans Gjørup, Agnès Bloch‐Zupan, et al.. (2018). Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review. Frontiers in Physiology. 9. 701–701. 11 indexed citations
12.
Dure‐Molla, Muriel de La, et al.. (2014). Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. Orphanet Journal of Rare Diseases. 9(1). 84–84. 62 indexed citations
13.
Laugel-Haushalter, Virginie, Corinne Stoetzel, Jean Muller, et al.. (2014). A Novel Mutation in the <b><i>ROGDI</i></b> Gene in a Patient with Kohlschütter-Tönz Syndrome. Molecular Syndromology. 5(6). 293–298. 15 indexed citations
14.
Bloch‐Zupan, Agnès, Yves Alembik, B Doray, et al.. (2012). Oro-Dental Features In Hypophosphatasia : A Valuable Phenotype For Disease Diagnosis And Evaluation Of Future Treatment Outcomes. Revistes Científiques de la University of Barcelona (University of Barcelona). 51(1). 13. 1 indexed citations
15.
Bloch‐Zupan, Agnès, et al.. (2008). Snail expression in early osteogenesis, in vivo and in vitro. UCL Discovery (University College London). 1 indexed citations
16.
Bloch‐Zupan, Agnès. (2007). Genetische Störungen der Zahnentwicklung und Dentition. Medizinische Genetik. 19(4). 399–406.
17.
Bloch‐Zupan, Agnès, et al.. (2001). R-twist gene expression during rat palatogenesis. The International Journal of Developmental Biology. 45(2). 397–404. 19 indexed citations
18.
Bloch‐Zupan, Agnès. (2001). Is the Fluoride Concentration Limit of 1,500 ppm in Cosmetics (EU Guideline) Still Up-to-Date?. Caries Research. 35(Suppl. 1). 22–25. 19 indexed citations
19.
Goldberg, Michel, et al.. (1993). [Lysosomal storage diseases, genetic or drug-induced? effect of glycosaminoglycan and sphingolipid disorders on dental tissues].. SPIRE - Sciences Po Institutional REpository. 1 indexed citations
20.
Mark, Manuel P., Agnès Bloch‐Zupan, & J V Ruch. (1992). Effects of retinoids on tooth morphogenesis and cytodifferentiations, in vitro. The International Journal of Developmental Biology. 36(4). 517–526. 33 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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