Josette Mancini

1.8k total citations
29 papers, 1.2k citations indexed

About

Josette Mancini is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Josette Mancini has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Josette Mancini's work include Genetics and Neurodevelopmental Disorders (7 papers), Epilepsy research and treatment (5 papers) and Epigenetics and DNA Methylation (4 papers). Josette Mancini is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Epilepsy research and treatment (5 papers) and Epigenetics and DNA Methylation (4 papers). Josette Mancini collaborates with scholars based in France, United States and Germany. Josette Mancini's co-authors include Anne Moncla, Laurent Villard, Jean‐Christophe Roux, B. Chabrol, P. Divry, Marie-Odile Livet, K. Michael Gibson, G. Léna, Sébastien Zanella and Jean‐Charles Viemari and has published in prestigious journals such as Journal of Neuroscience, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Josette Mancini

29 papers receiving 1.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Josette Mancini 484 454 305 224 185 29 1.2k
Alessandra Murgia 724 1.5× 638 1.4× 254 0.8× 110 0.5× 70 0.4× 76 1.6k
Dawna D. Armstrong 730 1.5× 754 1.7× 510 1.7× 167 0.7× 195 1.1× 33 1.6k
Izabela Kuchna 507 1.0× 541 1.2× 518 1.7× 147 0.7× 148 0.8× 37 1.5k
Ryoichi Sakuta 841 1.7× 408 0.9× 256 0.8× 359 1.6× 299 1.6× 59 1.7k
E Peeters 447 0.9× 220 0.5× 205 0.7× 650 2.9× 560 3.0× 46 1.7k
Bernd Wilken 345 0.7× 96 0.2× 118 0.4× 147 0.7× 124 0.7× 36 1.0k
Chiara Pantaleoni 496 1.0× 335 0.7× 221 0.7× 352 1.6× 292 1.6× 84 1.5k
Michael A. Nigro 618 1.3× 211 0.5× 112 0.4× 180 0.8× 139 0.8× 36 1.4k
Leland Allen 659 1.4× 739 1.6× 95 0.3× 130 0.6× 135 0.7× 13 1.4k
Edvige Veneselli 190 0.4× 210 0.5× 236 0.8× 352 1.6× 149 0.8× 41 1.1k

Countries citing papers authored by Josette Mancini

Since Specialization
Citations

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

Fields of papers citing papers by Josette Mancini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Josette Mancini. 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 Josette Mancini. The network helps show where Josette Mancini may publish in the future.

Co-authorship network of co-authors of Josette Mancini

This figure shows the co-authorship network connecting the top 25 collaborators of Josette Mancini. A scholar is included among the top collaborators of Josette Mancini 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 Josette Mancini. Josette Mancini 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.
Riant, Florence, Josette Mancini, Mathieu Milh, et al.. (2015). Severe phenotypic spectrum of biallelic mutations inPRRT2gene. Journal of Neurology Neurosurgery & Psychiatry. 86(7). 782–785. 58 indexed citations
2.
Jover, Marianne, et al.. (2013). Motor disorders in dyslexic children: a review and perspectives. Enfance. 4(4). 323–347. 4 indexed citations
3.
Milh, Mathieu, Nathalie Villeneuve, F. Chapon, et al.. (2010). New onset refractory convulsive status epilepticus associated with serum neuropil auto-antibodies in a school aged child. Brain and Development. 33(8). 687–691. 9 indexed citations
4.
Jennesson, Mélanie, Mathieu Milh, Nathalie Villeneuve, et al.. (2010). Posterior glucose hypometabolism in Lafora disease: Early and late FDG‐PET assessment. Epilepsia. 51(4). 708–711. 12 indexed citations
5.
Santos, Andréia, et al.. (2009). Does preterm birth affect global and configural processing differently?. Developmental Medicine & Child Neurology. 52(3). 293–298. 10 indexed citations
6.
Minkin, Krasimir, Olivier Klein, Josette Mancini, & G. Léna. (2008). Surgical strategies and seizure control in pediatric patients with dysembryoplastic neuroepithelial tumors: a single-institution experience. Journal of Neurosurgery Pediatrics. 1(3). 206–210. 55 indexed citations
7.
Roux, Jean‐Christophe, et al.. (2007). Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome. European Journal of Neuroscience. 25(7). 1915–1922. 107 indexed citations
8.
Santos, Andréia, Cécilie Rondan, Josette Mancini, & Christine Deruelle. (2007). Behavioural indexes of callosal functioning in Williams syndrome. Journal of Neuropsychology. 1(2). 189–200. 2 indexed citations
9.
Bienvenu, Thierry, Christophe Philippe, Nicolás de Roux, et al.. (2006). The Incidence of Rett Syndrome in France. Pediatric Neurology. 34(5). 372–375. 41 indexed citations
10.
Viemari, Jean‐Charles, Jean‐Christophe Roux, Andrew K. Tryba, et al.. (2005). Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice. Journal of Neuroscience. 25(50). 11521–11530. 233 indexed citations
11.
Schonen, Scania de, et al.. (2005). Early brain lesions and face‐processing development. Developmental Psychobiology. 46(3). 184–208. 18 indexed citations
12.
Deruelle, Christine, et al.. (2005). Global and local music perception in children with Williams syndrome. Neuroreport. 16(6). 631–634. 36 indexed citations
13.
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
14.
Mikaeloff, Yann, Anne de Saint Martin, Josette Mancini, et al.. (2003). Topiramate: efficacy and tolerability in children according to epilepsy syndromes. Epilepsy Research. 53(3). 225–232. 70 indexed citations
15.
Moncla, Anne, Arlette Kpebe, Chantal Missirian, Josette Mancini, & Laurent Villard. (2002). Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling. European Journal of Human Genetics. 10(1). 86–89. 28 indexed citations
16.
Hinson, Debra D., Skaidrite K. Krisans, Joanne Shaw, et al.. (1999). Identification of a Mutation Cluster in Mevalonate Kinase Deficiency, Including a New Mutation in a Patient of Mennonite Ancestry. The American Journal of Human Genetics. 65(2). 327–335. 35 indexed citations
17.
Chabrol, B., Sabine Sigaudy, Jean‐François Pellissier, et al.. (1997). Stüve-Wiedemann syndrome and defects of the mitochondrial respiratory chain. American Journal of Medical Genetics. 72(2). 222–226. 20 indexed citations
18.
Léna, G., Thierry Dufour, Danielle Gambarellï, B. Chabrol, & Josette Mancini. (1994). Choristoma of the intracranial maxillary nerve in a child. Journal of neurosurgery. 81(5). 788–791. 17 indexed citations
19.
Mancini, Josette, Nicole Philip, B. Chabrol, et al.. (1993). Mevalonic aciduria in 3 siblings: A new recognizable metabolic encephalopathy. Pediatric Neurology. 9(3). 243–246. 19 indexed citations
20.
Confort‐Gouny, Sylviane, B. Chabrol, Jean Vion‐Dury, Josette Mancini, & Patrick J. Cozzone. (1993). MRI and localized proton MRS in early infantile form of neuronal ceroid-lipofuscinosis. Pediatric Neurology. 9(1). 57–60. 26 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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