M.O. Livet

453 total citations
14 papers, 349 citations indexed

About

M.O. Livet is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience. According to data from OpenAlex, M.O. Livet has authored 14 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Psychiatry and Mental health, 7 papers in Pediatrics, Perinatology and Child Health and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in M.O. Livet's work include Epilepsy research and treatment (7 papers), Neonatal and fetal brain pathology (3 papers) and Neuroscience and Neuropharmacology Research (3 papers). M.O. Livet is often cited by papers focused on Epilepsy research and treatment (7 papers), Neonatal and fetal brain pathology (3 papers) and Neuroscience and Neuropharmacology Research (3 papers). M.O. Livet collaborates with scholars based in France, Türkiye and Italy. M.O. Livet's co-authors include Michelle Bureau, Charlotte Dravet, Renzo Guerrini, Joseph Roger, Charles Raybaud, O. Robain, Agatino Battaglia, C. Billard, Danielle Gambarellï and Marie‐Anne Barthez and has published in prestigious journals such as Developmental Medicine & Child Neurology, Journal of Medical Genetics and Neuromuscular Disorders.

In The Last Decade

M.O. Livet

13 papers receiving 337 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.O. Livet France	8	224	166	96	95	59	14	349
Sue Harrison United Kingdom	8	249 1.1×	187 1.1×	68 0.7×	114 1.2×	34 0.6×	10	343
Hadassah Goldberg‐Stern Israel	12	255 1.1×	143 0.9×	91 0.9×	114 1.2×	79 1.3×	18	380
Alena Jahodová Czechia	10	184 0.8×	131 0.8×	75 0.8×	62 0.7×	57 1.0×	27	309
Véronique Davidoff Switzerland	6	303 1.4×	160 1.0×	112 1.2×	155 1.6×	51 0.9×	7	352
C. D. Ferrie United Kingdom	10	219 1.0×	153 0.9×	107 1.1×	51 0.5×	33 0.6×	11	305
Ana María Soprano Argentina	7	191 0.9×	95 0.6×	96 1.0×	84 0.9×	39 0.7×	11	264
Peronelle Richards United Kingdom	9	435 1.9×	312 1.9×	99 1.0×	71 0.7×	54 0.9×	10	500
Maria Paola Valenti France	9	194 0.9×	78 0.5×	105 1.1×	63 0.7×	45 0.8×	17	272
C Jalin France	12	446 2.0×	310 1.9×	208 2.2×	106 1.1×	40 0.7×	29	536
Monique M.J. van Schooneveld Netherlands	12	286 1.3×	279 1.7×	55 0.6×	77 0.8×	41 0.7×	17	402

Countries citing papers authored by M.O. Livet

Since Specialization

Citations

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

Fields of papers citing papers by M.O. Livet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.O. 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 M.O. Livet. The network helps show where M.O. Livet may publish in the future.

Co-authorship network of co-authors of M.O. Livet

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

All Works

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14 of 14 papers shown

1.

Pinton, Florence, B. Ducot, Jacques Motté, et al.. (2006). Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS). Epileptic Disorders. 8(1). 11–23. 96 indexed citations

2.

Billard, C., J. Motte, Mary E. Farmer, et al.. (2002). The BREV neuropsychological test: Part II. Results of validation in children with epilepsy. Developmental Medicine & Child Neurology. 44(6). 398–404. 8 indexed citations

3.

Billard, C., J. Motte, Mary E. Farmer, et al.. (2002). The BREV neuropsychological test: Part II. Results of validation in children with epilepsy. Developmental Medicine & Child Neurology. 44(6). 398–404. 8 indexed citations

4.

Billard, C., et al.. (2002). [BREV: a rapid clinical scale for cognitive function evaluation in preschool and school-age children].. PubMed. 158(2). 167–75. 4 indexed citations

5.

Billard, C., et al.. (2002). The BREV neuropsychological test: Part I. Results from 500 normally developing children. Developmental Medicine & Child Neurology. 44(6). 391–398. 15 indexed citations

6.

Çokar, Özlem, Philippe Gélisse, M.O. Livet, et al.. (2001). Startle response: epileptic or non‐epileptic? The case for “flash” SMA reflex seizures. Epileptic Disorders. 3(1). 7–11. 7 indexed citations

7.

Chabrol, B., et al.. (2000). Intérêt de la lamotrigine en pédiatrie. Étude rétrospective chez 32 enfants. Archives de Pédiatrie. 7(3). 234–242. 4 indexed citations

8.

Billard, C., et al.. (2000). BREV: une batterie de dépistage des déficits cognitifs chez l'enfant de 4 à 9 ans. Résultats de l'étude normative chez 500 enfants. Archives de Pédiatrie. 7. 128s–130s. 7 indexed citations

9.

Mancini, Julien, B. Chabrol, M.O. Livet, N. Philip, & N Pinsard. (1995). Démarche diagnostique pratique devant une déficience mentale. Archives de Pédiatrie. 2. S44–S48.

10.

Malzac, Perrine, A. Moncla, Marie‐Antoinette Voelckel, et al.. (1993). Prader-Willi syndrome: Diagnostic strategy with a cytogenetic and molecular approach. Neuromuscular Disorders. 3(5-6). 493–496. 1 indexed citations

11.

Guerrini, Renzo, Charlotte Dravet, Charles Raybaud, et al.. (1992). NEUROLOGICAL FINDINGS AND SEIZURE OUTCOME IN CHILDREN WITH BILATERAL OPERCULAR MACROGYRIC‐LIKE CHANGES DETECTED BY MRI. Developmental Medicine & Child Neurology. 34(8). 694–705. 63 indexed citations

12.

Guerrini, Renzo, Charlotte Dravet, Charles Raybaud, et al.. (1992). EPILEPSY AND FOCAL GYRAL ANOMALIES DETECTED BY MRI: ELECTROCLINICO‐MORPHOLOGICAL CORRELATIONS AND FOLLOW‐UP. Developmental Medicine & Child Neurology. 34(8). 706–718. 102 indexed citations

13.

Moncla, A., et al.. (1991). Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.. Journal of Medical Genetics. 28(9). 627–632. 32 indexed citations

14.

Livet, M.O., et al.. (1978). Céroide Lipofuscinose A Début Atypique. Revue d Electroencé phalographie et de Neurophysiologie Clinique. 8(1). 175–179. 2 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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