Véronica Cusin

1.5k total citations
13 papers, 721 citations indexed

About

Véronica Cusin is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Véronica Cusin has authored 13 papers receiving a total of 721 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in Véronica Cusin's work include RNA modifications and cancer (4 papers), Congenital Anomalies and Fetal Surgery (3 papers) and RNA Research and Splicing (3 papers). Véronica Cusin is often cited by papers focused on RNA modifications and cancer (4 papers), Congenital Anomalies and Fetal Surgery (3 papers) and RNA Research and Splicing (3 papers). Véronica Cusin collaborates with scholars based in France, Italy and United States. Véronica Cusin's co-authors include Arnold Münnich, Annick Toutain, Valérie Cormier‐Daire, Delphine Girlich, Michel Vekemans, Géraldine Viot, Anne Moncla, Martine Le Merrer, Laurence Faivre and William Camu and has published in prestigious journals such as Nature Genetics, American Journal of Respiratory and Critical Care Medicine and The American Journal of Human Genetics.

In The Last Decade

Véronica Cusin

13 papers receiving 703 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Véronica Cusin France	12	443	309	97	91	86	13	721
Pierre Miniou France	13	611 1.4×	185 0.6×	91 0.9×	87 1.0×	162 1.9×	15	752
V. Ventruto Italy	17	479 1.1×	288 0.9×	77 0.8×	37 0.4×	81 0.9×	48	792
P N Ray Canada	13	643 1.5×	225 0.7×	83 0.9×	116 1.3×	136 1.6×	17	783
Carol A. Crowe United States	17	582 1.3×	318 1.0×	119 1.2×	53 0.6×	70 0.8×	28	904
Caroline J. Formstone United Kingdom	18	665 1.5×	158 0.5×	84 0.9×	175 1.9×	77 0.9×	26	1.1k
Silvestre Oltra Spain	20	626 1.4×	478 1.5×	39 0.4×	41 0.5×	84 1.0×	69	1.1k
Ann‐Charlotte Thuresson Sweden	20	655 1.5×	485 1.6×	81 0.8×	41 0.5×	53 0.6×	34	1.1k
Alex Magee United Kingdom	12	507 1.1×	537 1.7×	120 1.2×	71 0.8×	149 1.7×	20	913
Yvonne J. Vos Netherlands	19	520 1.2×	240 0.8×	103 1.1×	112 1.2×	36 0.4×	42	1.0k
Kit Doudney United Kingdom	13	500 1.1×	298 1.0×	73 0.8×	123 1.4×	58 0.7×	25	762

Countries citing papers authored by Véronica Cusin

Since Specialization

Citations

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

Fields of papers citing papers by Véronica Cusin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Véronica Cusin

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

All Works

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13 of 13 papers shown

Benusiglio, Patrick R., Chrystelle Colas, Erell Guillerm, et al.. (2018). Clinical implications of CTNNA1 germline mutations in asymptomatic carriers. Gastric Cancer. 22(4). 899–903. 26 indexed citations

Latour, Philippe, Christel Thauvin‐Robinet, P Soichot, et al.. (2010). A Major Determinant for Binding and Aminoacylation of tRNAAla in Cytoplasmic Alanyl-tRNA Synthetase Is Mutated in Dominant Axonal Charcot-Marie-Tooth Disease. The American Journal of Human Genetics. 86(1). 77–82. 171 indexed citations

Callier, Patrick, Laurence Faivre, Véronica Cusin, et al.. (2005). Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome. American Journal of Medical Genetics Part A. 137A(2). 204–207. 26 indexed citations

Clermont, Olivier, Philippe Burlet, Paule Bénit, et al.. (2004). Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations. Human Mutation. 24(5). 417–427. 61 indexed citations

Faivre, Laurence, Thierry Rousseau, Nicole Laurent, et al.. (2004). Prenatal overgrowth and mosaic trisomy 15q25‐qter including the IGF1 receptor gene. Prenatal Diagnosis. 24(5). 393–395. 14 indexed citations

Viollet, Louis, Mohammed Zarhrate, Isabelle Maystadt, et al.. (2004). Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families. European Journal of Human Genetics. 12(6). 483–488. 12 indexed citations

Biancalana, Valérie, Chérif Beldjord, A. Taillandier, et al.. (2004). Five years of molecular diagnosis of Fragile X syndrome (1997–2001): A collaborative study reporting 95% of the activity in France. American Journal of Medical Genetics Part A. 129A(3). 218–224. 29 indexed citations

Thauvin‐Robinet, Christel, Laurence Faivre, Véronica Cusin, et al.. (2003). Cloacal exstrophy in an infant with 9q34.1‐qter deletion resulting from a de novo unbalanced translocation between chromosome 9q and Yq. American Journal of Medical Genetics Part A. 126A(3). 303–307. 43 indexed citations

Malerba, Giovanni, Elisabetta Trabetti, Roberta Galavotti, et al.. (2000). Linkage Analysis of Chromosome 12 Markers in Italian Families with Atopic Asthmatic Children. American Journal of Respiratory and Critical Care Medicine. 162(4). 1587–1590. 36 indexed citations

10.

Azancot, A., et al.. (2000). [Clinical spectrum of prenatal tetralogy of Fallot].. PubMed. 93(5). 587–93. 5 indexed citations

11.

Cormier‐Daire, Valérie, Véronica Cusin, Géraldine Viot, et al.. (1999). SHOX gene mutations and deletions in dyschondrosteosis or Leri‐Weill syndrome. Acta Paediatrica. 88(s433). 55–59. 20 indexed citations

12.

Cusin, Véronica, Géraldine Viot, Delphine Girlich, et al.. (1998). SHOX mutations in dyschondrosteosis (Leri-Weill syndrome). Nature Genetics. 19(1). 67–69. 257 indexed citations

13.

Trabetti, Elisabetta, Véronica Cusin, Giovanni Malerba, et al.. (1998). Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population.. Journal of Medical Genetics. 35(8). 680–681. 21 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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