Marie-Odile Livet

912 total citations
20 papers, 631 citations indexed

About

Marie-Odile Livet is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Developmental Neuroscience. According to data from OpenAlex, Marie-Odile Livet has authored 20 papers receiving a total of 631 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 5 papers in Genetics and 5 papers in Developmental Neuroscience. Recurrent topics in Marie-Odile Livet's work include Williams Syndrome Research (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Syndromes and Imprinting (2 papers). Marie-Odile Livet is often cited by papers focused on Williams Syndrome Research (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Syndromes and Imprinting (2 papers). Marie-Odile Livet collaborates with scholars based in France, Italy and United States. Marie-Odile Livet's co-authors include Christine Deruelle, Julien Mancini, Catherine Cassé‐Perrot, Scania de Schonen, Josette Mancini, B. Chabrol, Anne Moncla, Marie‐Antoinette Voelckel, Jean-François Mattéi and Nicole Philip and has published in prestigious journals such as Blood, Epilepsia and Journal of Medical Genetics.

In The Last Decade

Marie-Odile Livet

19 papers receiving 608 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marie-Odile Livet France 13 257 182 161 127 122 20 631
Monique Gingold United States 9 271 1.1× 187 1.0× 131 0.8× 295 2.3× 11 0.1× 14 749
Gilles Lyon Belgium 13 45 0.2× 119 0.7× 109 0.7× 160 1.3× 64 0.5× 18 515
C. Nuttin France 11 79 0.3× 189 1.0× 95 0.6× 97 0.8× 8 0.1× 12 527
Ignacio Pascual Castroviejo Spain 11 216 0.8× 170 0.9× 236 1.5× 182 1.4× 6 0.0× 67 600
A. C. Warren United States 9 222 0.9× 286 1.6× 85 0.5× 61 0.5× 21 0.2× 15 611
M Dambska Poland 13 73 0.3× 127 0.7× 51 0.3× 318 2.5× 54 0.4× 47 608
Raffaello Canapicchi Italy 12 59 0.2× 120 0.7× 161 1.0× 253 2.0× 8 0.1× 20 628
Eulália Calado Portugal 14 217 0.8× 176 1.0× 266 1.7× 150 1.2× 8 0.1× 21 615
Clotilde Mircher France 12 150 0.6× 146 0.8× 60 0.4× 124 1.0× 8 0.1× 22 613
Shin Okazaki Japan 12 160 0.6× 243 1.3× 148 0.9× 66 0.5× 50 0.4× 79 620

Countries citing papers authored by Marie-Odile Livet

Since Specialization
Citations

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

Fields of papers citing papers by Marie-Odile Livet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie-Odile Livet. 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 Marie-Odile Livet. The network helps show where Marie-Odile Livet may publish in the future.

Co-authorship network of co-authors of Marie-Odile Livet

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

All Works

20 of 20 papers shown
1.
Cignetti, Fabien, Marianne Vaugoyeau, Marianne Jover, et al.. (2018). Feedforward motor control in developmental dyslexia and developmental coordination disorder: Does comorbidity matter?. Research in Developmental Disabilities. 76. 25–34. 19 indexed citations
2.
Depienne, Christel, Oriane Trouillard, Isabelle Gourfinkel‐An, et al.. (2010). Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome. Journal of Medical Genetics. 47(6). 404–410. 117 indexed citations
3.
Milh, Mathieu, Nathalie Villeneuve, F. Chapon, et al.. (2009). Transient Brain Magnetic Resonance Imaging Hyperintensity in Basal Ganglia and Brain Stem of Epileptic Infants Treated With Vigabatrin. Journal of Child Neurology. 24(3). 305–315. 25 indexed citations
4.
Mancini, Julien, Catherine Pech‐Georgel, Frédéric Brun, et al.. (2008). EVAL MATER : proposition d’une évaluation pédiatrique des compétences langagières et psychomotrices lors du 1er bilan de santé en école maternelle. Archives de Pédiatrie. 15(4). 397–405. 7 indexed citations
5.
Rondan, Cécilie, et al.. (2008). Global and Local processing in Williams Syndrome: Drawing versus Perceiving. Child Neuropsychology. 14(3). 237–248. 8 indexed citations
6.
Mathey, C., et al.. (2007). Stagnation pondérale et régression psychomotrice révélant une carence en vitamine B12 chez 3 nourrissons. Archives de Pédiatrie. 14(5). 467–471. 16 indexed citations
7.
Mancini, Julien, Cécilie Rondan, Marie-Odile Livet, B. Chabrol, & Christine Deruelle. (2006). Reconnaissance des visages chez les enfants porteurs du syndrome de Williams. Neuropsychiatrie de l Enfance et de l Adolescence. 54(3). 159–164. 1 indexed citations
8.
Deruelle, Christine, Cécilie Rondan, Josette Mancini, & Marie-Odile Livet. (2005). Do children with Williams syndrome fail to process visual configural information?. Research in Developmental Disabilities. 27(3). 243–253. 19 indexed citations
9.
Billard, C., et al.. (2002). BREV: une batterie rapide clinique d'évaluation des fonctions cognitives chez les enfants d'âge scolaire et préscolaire.. Revue Neurologique. 158(2). 1 indexed citations
10.
Portes, V. des, Marie-Odile Livet, & Louis Vallée. (2002). Démarche diagnostique devant une déficience mentale de l’enfant en 2002. Archives de Pédiatrie. 9(7). 709–725. 10 indexed citations
11.
12.
Livet, Marie-Odile, et al.. (2000). Phénotypes neuropsychologiques des génopathies. Archives de Pédiatrie. 7. 112s–113s. 1 indexed citations
13.
Moncla, Anne, Perrine Malzac, Marie‐Antoinette Voelckel, et al.. (1999). Phenotype–genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients. European Journal of Human Genetics. 7(2). 131–139. 78 indexed citations
14.
Deruelle, Christine, Julien Mancini, Marie-Odile Livet, Catherine Cassé‐Perrot, & Scania de Schonen. (1999). Configural and Local Processing of Faces in Children with Williams Syndrome. Brain and Cognition. 41(3). 276–298. 121 indexed citations
15.
Moncla, Anne, Perrine Malzac, Marie-Odile Livet, et al.. (1999). Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling. Journal of Medical Genetics. 36(7). 554–560. 51 indexed citations
16.
Mancini, Josette, Nadine Girard, B. Chabrol, et al.. (1997). Ischemic Cerebrovascular Disease in Children: Retrospective Study of 35 Patients. Journal of Child Neurology. 12(3). 193–199. 49 indexed citations
17.
Cieuta, Cécile, et al.. (1996). Early Clinical and EEG Features of Infantile Spasms in Down Syndrome. Epilepsia. 37(10). 977–982. 42 indexed citations
18.
Divry, P., C. Jakobs, Christine Vianey‐Saban, et al.. (1993). l‐2‐Hydroxyglutaric aciduria: Two further cases. Journal of Inherited Metabolic Disease. 16(3). 505–507. 27 indexed citations
19.
Guerrini, Renzo, R. Canapicchi, C Raybaud, et al.. (1992). Risonanza magnetica nella sindrome opercolare congenita. Rivista di Neuroradiologia. 5(1_suppl). 79–83.
20.
Raybaud, Charles, Marie-Odile Livet, Mohamed Jiddane, & N Pinsard. (1985). Radiology of ischemic strokes in children. Neuroradiology. 27(6). 567–578. 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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