Véronica Cusin
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 5%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 20
- Connective tissue disorders research 8
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- BRCA gene mutations in cancer 3
-
- Congenital limb and hand anomalies 2
- Co-authors
- Arnold Münnich (6 shared papers)Valérie Cormier‐Daire (4 shared papers)Martine F. Le Merrer (4 shared papers)Valérie Belin (2 shared papers)Delphine Girlich (2 shared papers)Anne Moncla (2 shared papers)Michel J. J. Vekemans (2 shared papers)Annick Toutain (2 shared papers)
In The Last Decade
Véronica Cusin
30 papers receiving 1.3k citations
Véronica Cusin's Hit Papers
Peers
Comparison fields: 5 of 70
- Developmental Biology 79
- Genetics 632
- Genetics 142
- Cellular and Molecular Neuroscience 130
- Endocrinology, Diabetes and Metabolism 98
Countries citing papers authored by Véronica Cusin
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
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.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 294 | |
| 2 | 2010 | 189 | |
| 3 | 2006 | 121 | |
| 4 | 2011 | 108 | |
| 5 | 2003 | 74 | |
| 6 | 2004 | 67 | |
| 7 | 2003 | 54 | |
| 8 | 2001 | 39 | |
| 9 | 2014 | 39 | |
| 10 | 2018 | 39 | |
| 11 | 2018 | 35 | |
| 12 | 2004 | 34 | |
| 13 | 2005 | 34 | |
| 14 | 1999 | 26 | |
| 15 | PFMG2025–integrating genomic medicine into the national healthcare system in France Hit paper breakdown → | 2025 | 26 |
| 16 | 2013 | 23 | |
| 17 | 2021 | 22 | |
| 18 | 2004 | 14 | |
| 19 | 2004 | 14 | |
| 20 | 2005 | 12 |
About Véronica Cusin
Véronica Cusin is a scholar working on Genetics, Developmental Biology, Pathology and Forensic Medicine, Genetics and Pediatrics, Perinatology and Child Health, having authored 31 papers that have together received 1.3k indexed citations. Recurring topics across this work include Connective tissue disorders research (8 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic factors in colorectal cancer (3 papers), BRCA gene mutations in cancer (3 papers), Congenital limb and hand anomalies (2 papers), Hereditary Neurological Disorders (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Developmental Biology (79 citations), Genetics (632 citations), Genetics (142 citations), Cellular and Molecular Neuroscience (130 citations) and Endocrinology, Diabetes and Metabolism (98 citations). Véronica Cusin has collaborated with scholars based in France, Belgium and Lebanon. Frequent co-authors include Arnold Münnich, Valérie Cormier‐Daire, Martine F. Le Merrer, Valérie Belin, Delphine Girlich, Anne Moncla, Michel J. J. Vekemans, Annick Toutain, Géraldine Viot and Laurence Olivier Faivre. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, The American Journal of Human Genetics, Genetics in Medicine and Prenatal Diagnosis.
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.