Véronique Geoffroy

2.2k total citations
17 papers, 775 citations indexed

About

Véronique Geoffroy is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Véronique Geoffroy has authored 17 papers receiving a total of 775 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Véronique Geoffroy's work include Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (5 papers) and Hedgehog Signaling Pathway Studies (5 papers). Véronique Geoffroy is often cited by papers focused on Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (5 papers) and Hedgehog Signaling Pathway Studies (5 papers). Véronique Geoffroy collaborates with scholars based in France, Germany and United Kingdom. Véronique Geoffroy's co-authors include Corinne Stoetzel, Hélène Dollfus, Jean Muller, Amélie Piton, Arnaud Kress, Yvan Herenger, Sophie Scheidecker, Uwe Strähle, Christelle Etard and Élise Schaefer and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Bioinformatics.

In The Last Decade

Véronique Geoffroy

17 papers receiving 769 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Véronique Geoffroy France 12 559 510 70 64 58 17 775
Stuart W. Tompson United States 12 482 0.9× 429 0.8× 29 0.4× 48 0.8× 55 0.9× 16 716
Donna M. Muzny United States 15 551 1.0× 456 0.9× 40 0.6× 52 0.8× 19 0.3× 20 854
Nara Sobreira United States 10 325 0.6× 323 0.6× 63 0.9× 25 0.4× 29 0.5× 27 550
Pietro Palumbo Italy 15 314 0.6× 325 0.6× 25 0.4× 49 0.8× 40 0.7× 64 620
Luitgard Graul‐Neumann Germany 19 539 1.0× 457 0.9× 37 0.5× 86 1.3× 44 0.8× 46 884
Angelo Iulianella Canada 17 557 1.0× 281 0.6× 53 0.8× 58 0.9× 15 0.3× 29 754
B Hamel Netherlands 6 402 0.7× 274 0.5× 38 0.5× 40 0.6× 118 2.0× 7 648
Judith Goodship United Kingdom 11 729 1.3× 517 1.0× 28 0.4× 35 0.5× 30 0.5× 13 978
Valérie Layet France 13 506 0.9× 513 1.0× 165 2.4× 32 0.5× 43 0.7× 22 925
Elisa Tassano Italy 15 310 0.6× 272 0.5× 58 0.8× 18 0.3× 42 0.7× 54 596

Countries citing papers authored by Véronique Geoffroy

Since Specialization
Citations

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

Fields of papers citing papers by Véronique Geoffroy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Véronique Geoffroy

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

All Works

17 of 17 papers shown
1.
Estrada‐Cuzcano, Alejandro, Véronique Geoffroy, Julien Tarabeux, et al.. (2023). WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects. International Journal of Molecular Sciences. 24(10). 8729–8729. 5 indexed citations
2.
Geoffroy, Véronique, Thomas Guignard, Arnaud Kress, et al.. (2023). The AnnotSV webserver in 2023: updated visualization and ranking. Nucleic Acids Research. 51(W1). W39–W45. 6 indexed citations
3.
Geoffroy, Véronique, Thomas Guignard, Arnaud Kress, et al.. (2021). AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis. Nucleic Acids Research. 49(W1). W21–W28. 34 indexed citations
4.
Scheidecker, Sophie, Séverine Bär, Corinne Stoetzel, et al.. (2019). Mutations inKARScause a severe neurological and neurosensory disease with optic neuropathy. Human Mutation. 40(10). 1826–1840. 15 indexed citations
5.
Estrada‐Cuzcano, Alejandro, Christelle Etard, Corinne Stoetzel, et al.. (2019). NovelIQCEvariations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish. Human Mutation. 41(1). 240–254. 5 indexed citations
6.
Laugel-Haushalter, Virginie, Séverine Bär, Élise Schaefer, et al.. (2019). A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. Frontiers in Genetics. 10. 504–504. 10 indexed citations
7.
Schaefer, Élise, Corinne Stoetzel, Véronique Geoffroy, et al.. (2019). Identification and Characterization of Known Biallelic Mutations in the IFT27 (BBS19) Gene in a Novel Family With Bardet-Biedl Syndrome. Frontiers in Genetics. 10. 29 indexed citations
8.
Geoffroy, Véronique, Yvan Herenger, Arnaud Kress, et al.. (2018). AnnotSV: an integrated tool for structural variations annotation. Bioinformatics. 34(20). 3572–3574. 207 indexed citations
9.
Stoetzel, Corinne, Véronique Geoffroy, Jean Muller, et al.. (2018). Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning. Frontiers in Physiology. 9. 1329–1329. 9 indexed citations
10.
Bloch‐Zupan, Agnès, Corinne Stoetzel, Julia Meyer, et al.. (2016). Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar. Frontiers in Physiology. 7. 70–70. 11 indexed citations
11.
Stoetzel, Corinne, Séverine Bär, Johan‐Owen De Craene, et al.. (2016). A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi. Nature Communications. 7(1). 13586–13586. 40 indexed citations
12.
Schaefer, Élise, Corinne Stoetzel, Sophie Scheidecker, et al.. (2016). Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet–Biedl syndrome. Journal of Human Genetics. 61(5). 447–450. 57 indexed citations
13.
Scheidecker, Sophie, Christelle Etard, Laurence Haren, et al.. (2015). Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy. The American Journal of Human Genetics. 96(4). 666–674. 50 indexed citations
14.
Geoffroy, Véronique, Cécile Pizot, Claire Redin, et al.. (2015). VaRank: a simple and powerful tool for ranking genetic variants. PeerJ. 3. e796–e796. 47 indexed citations
15.
Scheidecker, Sophie, Christelle Etard, Nathan W. Pierce, et al.. (2013). Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18). Journal of Medical Genetics. 51(2). 132–136. 104 indexed citations
16.
Redin, Claire, Stéphanie Le Gras, Véronique Geoffroy, et al.. (2012). Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes. Journal of Medical Genetics. 49(8). 502–512. 81 indexed citations
17.
Bloch‐Zupan, Agnès, Christelle Etard, Jean Muller, et al.. (2011). Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects. The American Journal of Human Genetics. 89(6). 773–781. 65 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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