Véronica Cusin

1.5k citations

13 papers · 721 indexed · h-index 12

Impact in

Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Neurogenetic and Muscular Disorders Research
Developmental Biology top 10%

Papers in ⓘ

Molecular Biology 7
- RNA modifications and cancer 4
- RNA Research and Splicing 3
Genetics 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Neurogenetic and Muscular Disorders Research 2
- Genomic variations and chromosomal abnormalities 2
- Animal Genetics and Reproduction 1

Co-authors: Arnold Münnich (4 shared papers)Géraldine Viot (2 shared papers)Michel Vekemans (2 shared papers)Delphine Girlich (2 shared papers)Valérie Cormier‐Daire (2 shared papers)Annick Toutain (2 shared papers)Martine Le Merrer (1 shared paper)Anne Moncla (1 shared paper)
Journals: Human Mutation (1 paper)Acta Paediatrica (1 paper)The American Journal of Human Genetics (1 paper)European Journal of Human Genetics (1 paper)Nature Genetics (1 paper)
Partner nations: France Italy United States

In The Last Decade

Véronica Cusin

13 papers receiving 703 citations

Peers

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

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13 of 13 papers shown

#	Work
1	SHOX mutations in dyschondrosteosis (Leri-Weill syndrome) Nature Genetics ·Valérie Belin, Véronica Cusin, Géraldine Viot, Delphine Girlich, Annick Toutain, Anne Moncla, Michel Vekemans, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire	1998	257
2	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 ·Philippe Latour, Christel Thauvin‐Robinet, Chantal Baudelet-Méry, P Soichot, Véronica Cusin, Laurence Faivre, Marie-Claire Locatelli, Martine Mayençon, Annie Sarcey, Emmanuel Broussolle, William Camu, Albert David, Robert Rousson	2010	171
3	Molecular analysis of SMA patients without homozygous SMN1 deletions using a new strategy for identification of SMN1 subtle mutations Human Mutation ·Olivier Clermont, Philippe Burlet, Paule Bénit, Dominique Chanterau, Pascale Saugier-Véber, Arnold Münnich, Véronica Cusin	2004	61
4	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 ·Christel Thauvin‐Robinet, Laurence Faivre, Véronica Cusin, Philippe Khau Van Kien, Patrick Callier, Keith L. Parker, Marc Fellous, Joséphine Borgnon, E Gounot, Frédéric Huet, Emmanuel Sapin, Francine Mugneret	2003	43
5	Linkage Analysis of Chromosome 12 Markers in Italian Families with Atopic Asthmatic Children American Journal of Respiratory and Critical Care Medicine ·Giovanni Malerba, Maria Camilla Lauciello, Titia Scherpbier, Elisabetta Trabetti, Roberta Galavotti, Véronica Cusin, Lydia Pescollderungg, Giovanna Zanoni, L. C. Martinati, ATTILIO L. BONER, Roy C. Levitt, Pier Franco Pignatti	2000	36
6	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 ·Valérie Biancalana, Chérif Beldjord, A. Taillandier, Sylvie Szpiro‐Tapia, Véronica Cusin, Fabienne Gerson, Christophe Philippe, Jean‐Louis Mandel, (unknown)	2004	29
7	Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome American Journal of Medical Genetics Part A ·Patrick Callier, Laurence Faivre, Véronica Cusin, Nathalie Marle, Christel Thauvin-Robinet, Dominique Sandre, Thierry Rousseau, Paul Sagot, Éric Lacombe, V. Faber, Francine Mugneret	2005	26
8	Clinical implications of CTNNA1 germline mutations in asymptomatic carriers Gastric Cancer ·Patrick R. Benusiglio, Chrystelle Colas, Erell Guillerm, Axelle Canard, Hélène Delhomelle, Mathilde Warcoin, J Bellanger, Mélanie Eyries, Mohamed Zizi, Jeanne Netter, Florent Soubrier, Yann Parc, Anne Mourrégot, Aurélie Maran Gonzalez, Véronica Cusin, Jérôme Alexandre Denis, Isabelle Coupier, Magali Svrcek, Florence Coulet	2018	26
9	Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population. Journal of Medical Genetics ·Elisabetta Trabetti, Véronica Cusin, Giovanni Malerba, L. C. Martinati, Alessandro Casartelli, A. L. Boner, П. Ф. Пигнатти	1998	21
10	SHOX gene mutations and deletions in dyschondrosteosis or Leri‐Weill syndrome Acta Paediatrica ·Valérie Cormier‐Daire, V Belin, Véronica Cusin, Géraldine Viot, Delphine Girlich, Annick Toutain, A. Moncla, Michel Vekemans, M. Le Merrer, Arnold Münnich	1999	20
11	Prenatal overgrowth and mosaic trisomy 15q25‐qter including the IGF1 receptor gene Prenatal Diagnosis ·Laurence Faivre, Thierry Rousseau, Nicole Laurent, Philippe Gosset, Damien Sanlaville, Christel Thauvin‐Robinet, Véronica Cusin, Stéphanie Lionnais, Patrick Callier, Philippe Khau Van Kien, Frédéric Huet, C Turleau, Paul Sagot, Francine Mugneret	2004	14
12	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 ·Louis Viollet, Mohammed Zarhrate, Isabelle Maystadt, Brigitte Estournet-Mathiaut, A Barois, Isabelle Desguerre, M. Mayer, B. Chabrol, Bruno Leheup, Véronica Cusin, Thierry Billette de Villemeur, Dominique Bonneau, Pascale Saugier-Véber, A. Touzery-de Villepin, Anne Delaubier, Jocelyne Kaplan, Marc Jeanpierre, Joshué Feingold, Arnold Münnich	2004	12
13	[Clinical spectrum of prenatal tetralogy of Fallot]. PubMed ·A. Azancot, Patrice Eydoux, E. Vuillard, Véronica Cusin, Christa Baumann, P Blot	2000	5

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 721 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), Asthma and respiratory diseases (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Genetics (309 citations), Developmental Biology (22 citations), Genetics (86 citations), Molecular Biology (443 citations) and Urology (37 citations). Véronica Cusin has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Arnold Münnich, Géraldine Viot, Michel Vekemans, Delphine Girlich, Valérie Cormier‐Daire, Annick Toutain, Martine Le Merrer, Anne Moncla, Laurence Faivre and Albert David. Their work appears in journals such as Human Mutation, Acta Paediatrica, The American Journal of Human Genetics, European Journal of Human Genetics and Nature Genetics.

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