G. Hamard

492 total citations
6 papers, 357 citations indexed

About

G. Hamard is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, G. Hamard has authored 6 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Nephrology. Recurrent topics in G. Hamard's work include Muscle Physiology and Disorders (2 papers), Sexual Differentiation and Disorders (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). G. Hamard is often cited by papers focused on Muscle Physiology and Disorders (2 papers), Sexual Differentiation and Disorders (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). G. Hamard collaborates with scholars based in France, Germany and United States. G. Hamard's co-authors include A Kahn, Michiko Niwa‐Kawakita, Sabine Colnot, Thomas Decaens, Christine Perret, Marco Giovannini, Cécile Godard, Jamel Chelly, J.‐C. Kaplan and Hélène Gilgenkrantz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Hepatology.

In The Last Decade

G. Hamard

6 papers receiving 354 citations

Peers

G. Hamard
Floriane Pez France
Masumi Yoshie Japan
Jana Samarin Germany
A. Nigel Brooks United Kingdom
Henry C. Yang United States
Hae Yoen Jung South Korea
Hui Rao China
Enkhjargal Batmunkh Hungary
Debbie K.W. Hsu United States
Eric Shi United States
Floriane Pez France
G. Hamard
Citations per year, relative to G. Hamard G. Hamard (= 1×) peers Floriane Pez

Countries citing papers authored by G. Hamard

Since Specialization
Citations

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

Fields of papers citing papers by G. Hamard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Hamard

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

All Works

6 of 6 papers shown
1.
Philippe, Aurélie, Stefanie Weber, Christophe Houbron, et al.. (2008). A missense mutation in podocin leads to early and severe renal disease in mice. Kidney International. 73(9). 1038–1047. 30 indexed citations
2.
Colnot, Sabine, Thomas Decaens, Michiko Niwa‐Kawakita, et al.. (2004). Liver-targeted disruption ofApcin mice activates β-catenin signaling and leads to hepatocellular carcinomas. Proceedings of the National Academy of Sciences. 101(49). 17216–17221. 238 indexed citations
3.
Colnot, Sabine, Thomas Decaens, Michiko Niwa‐Kawakita, et al.. (2003). 504 Hepatic invalidation of the tumor suppressor gene. Hepatology. 38. 402–402. 1 indexed citations
4.
Chelly, Jamel, Hélène Gilgenkrantz, Jean‐Philippe Hugnot, et al.. (1991). Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.. Journal of Clinical Investigation. 88(4). 1161–1166. 46 indexed citations
5.
Chelly, Jamel, Hélène Gilgenkrantz, Jean‐Philippe Hugnot, et al.. (1991). Application to the Analysis of Truncated Transcripts of the Dystrophin Gene in Nonmuscle Cultured Cells from Duchenne and Becker Patients. 7 indexed citations
6.
Chelly, Jamel, F. Marlhens, B. Le Marec, et al.. (1986). De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy. Human Genetics. 74(2). 193–196. 35 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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