Véronica Cusin

1.5k citations
13 papers · 725 · h-index 12

Impact in

  • Genetics top 10%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Neurogenetic and Muscular Disorders Research
    • Genomic variations and chromosomal abnormalities

Papers in

    • RNA modifications and cancer 4
    • RNA Research and Splicing 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Neurogenetic and Muscular Disorders Research 2
    • Genomic variations and chromosomal abnormalities 2

Véronica Cusin

13 papers receiving 709 citations

Peers

Véronica Cusin
Comparison fields: 5 of 53
  • Genetics 288
  • Genetics 86
  • Developmental Biology 16
  • Urology 35
  • Molecular Biology 399
Replace Jan Murken with:
Jan Murken Germany
J. Kunze Germany
K. O. J. Simola Finland
Lanying Song United States
Ghislaine Plessis France
V. Ventruto Italy
Rudolf A. Pfeiffer Germany
Andreas Dufke Germany
Rowdy Meijer Netherlands
Carol A. Crowe United States
Véronica Cusin relative to Jan Murken Germany Jan Murken's profile →
Citations per field
00.5×
Jan Murken · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Véronica Cusin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Véronica Cusin Line = papers co-authored together Véronica Cusin links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 1998258
2 2010172
3 200462
4 200343
5 200036
6 200429
7 201827
8 200526
9 199821
10 199920
11 200414
12 200412
13
[Clinical spectrum of prenatal tetralogy of Fallot].
20005

About Véronica Cusin

Véronica Cusin is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Physiology, having authored 13 papers that have together received 725 indexed citations. Recurring topics across this work include RNA modifications and cancer (4 papers), Congenital Anomalies and Fetal Surgery (3 papers), RNA Research and Splicing (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Asthma and respiratory diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Genetics (288 citations), Genetics (86 citations), Developmental Biology (16 citations), Urology (35 citations) and Molecular Biology (399 citations). Véronica Cusin has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Arnold Münnich, Valérie Cormier‐Daire, Géraldine Viot, Michel Vekemans, Annick Toutain, Delphine Girlich, Anne Moncla, Martine Le Merrer, Laurence Faivre and Christel Thauvin‐Robinet. Their work appears in journals such as Gastric Cancer, American Journal of Respiratory and Critical Care Medicine, Prenatal Diagnosis, European Journal of Human Genetics and Acta Paediatrica.

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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