Aurore Germain

654 total citations
5 papers, 372 citations indexed

About

Aurore Germain is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Aurore Germain has authored 5 papers receiving a total of 372 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Ophthalmology and 2 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Aurore Germain's work include Retinal Development and Disorders (4 papers), Retinal Diseases and Treatments (3 papers) and Retinal Imaging and Analysis (1 paper). Aurore Germain is often cited by papers focused on Retinal Development and Disorders (4 papers), Retinal Diseases and Treatments (3 papers) and Retinal Imaging and Analysis (1 paper). Aurore Germain collaborates with scholars based in France, Spain and United Kingdom. Aurore Germain's co-authors include Christina Zeitz, Isabelle Audo, Aline Antonio, Saddek Mohand‐Saïd, José‐Alain Sahel, Shomi S. Bhattacharya, Marie‐Elise Lancelot, Mélanie Letexier, Thierry Léveillard and Kinga M. Bujakowska and has published in prestigious journals such as Cellular Signalling, Human Mutation and Orphanet Journal of Rare Diseases.

In The Last Decade

Aurore Germain

5 papers receiving 367 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aurore Germain France	5	317	193	68	56	42	5	372
Trushna Desai United States	7	251 0.8×	229 1.2×	70 1.0×	71 1.3×	78 1.9×	8	418
Mor Hanany Israel	8	381 1.2×	185 1.0×	123 1.8×	55 1.0×	36 0.9×	12	448
Heather T. Daggett United States	9	264 0.8×	78 0.4×	27 0.4×	51 0.9×	80 1.9×	10	351
Tomokazu Takeuchi Japan	11	265 0.8×	144 0.7×	35 0.5×	42 0.8×	37 0.9×	28	319
Roberto Bonelli Australia	10	155 0.5×	151 0.8×	21 0.3×	84 1.5×	25 0.6×	25	307
Denise J. Morgan United States	7	274 0.9×	189 1.0×	25 0.4×	109 1.9×	15 0.4×	11	421
Orla Galvin United Kingdom	7	147 0.5×	101 0.5×	31 0.5×	34 0.6×	25 0.6×	10	224
Jean-Louis Dufier France	7	173 0.5×	85 0.4×	61 0.9×	37 0.7×	18 0.4×	8	288
Xavier Gérard France	10	347 1.1×	69 0.4×	126 1.9×	34 0.6×	49 1.2×	17	404
Ximena Corso‐Díaz United States	9	200 0.6×	83 0.4×	34 0.5×	36 0.6×	12 0.3×	13	274

Countries citing papers authored by Aurore Germain

Since Specialization

Citations

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

Fields of papers citing papers by Aurore Germain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurore Germain

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

All Works

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5 of 5 papers shown

1.

Audo, Isabelle, Kinga M. Bujakowska, Thierry Léveillard, et al.. (2012). Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet Journal of Rare Diseases. 7(1). 8–8. 125 indexed citations

2.

Bujakowska, Kinga M., Isabelle Audo, Saddek Mohand‐Saïd, et al.. (2011). CRB1 mutations in inherited retinal dystrophies. Human Mutation. 33(2). 306–315. 149 indexed citations

3.

Audo, Isabelle, Saddek Mohand‐Saïd, Claire‐Marie Dhaenens, et al.. (2011). RP1 and autosomal dominant rod-cone dystrophy: Novel mutations, a review of published variants, and genotype-phenotype correlation. Human Mutation. 33(1). 73–80. 31 indexed citations

4.

Audo, Isabelle, Marie‐Elise Lancelot, Saddek Mohand‐Saïd, et al.. (2011). Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort. Human Mutation. 32(4). E2091–103. 23 indexed citations

5.

Szabo‐Fresnais, Nicolas, Florence Lefebvre, Aurore Germain, Rodolphe Fischmeister, & Martine Pomérance. (2010). A new regulation of IL-6 production in adult cardiomyocytes by β-adrenergic and IL-1β receptors and induction of cellular hypertrophy by IL-6 trans-signalling. Cellular Signalling. 22(7). 1143–1152. 44 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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