Jean-Marc Pinard

738 total citations
16 papers, 311 citations indexed

About

Jean-Marc Pinard is a scholar working on Physiology, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Jean-Marc Pinard has authored 16 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 7 papers in Molecular Biology and 4 papers in Psychiatry and Mental health. Recurrent topics in Jean-Marc Pinard's work include Epilepsy research and treatment (4 papers), Neuroscience of respiration and sleep (3 papers) and Sleep and Wakefulness Research (3 papers). Jean-Marc Pinard is often cited by papers focused on Epilepsy research and treatment (4 papers), Neuroscience of respiration and sleep (3 papers) and Sleep and Wakefulness Research (3 papers). Jean-Marc Pinard collaborates with scholars based in France, Switzerland and United Kingdom. Jean-Marc Pinard's co-authors include Martine Fohlen, Olivier Delalande, Catherine Chiron, Georg Dorfmüller, Sandrine de Ribaupierre, F. Chéliout-Héraut, Christine Ioos, Robert Carlier, B. Estournet and Marion Leboyer and has published in prestigious journals such as Radiology, Neurosurgery and European Journal of Human Genetics.

In The Last Decade

Jean-Marc Pinard

16 papers receiving 302 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean-Marc Pinard France	11	119	106	76	57	47	16	311
Takeshi Okinaga Japan	14	160 1.3×	69 0.7×	74 1.0×	58 1.0×	26 0.6×	27	411
Anne Roubergue France	9	125 1.1×	120 1.1×	55 0.7×	32 0.6×	41 0.9×	18	291
Federica Graziola Italy	13	175 1.5×	120 1.1×	122 1.6×	69 1.2×	85 1.8×	28	406
Andrea Hanson‐Kahn United States	11	131 1.1×	54 0.5×	128 1.7×	62 1.1×	35 0.7×	16	293
Clara DM van Karnebeek Canada	7	190 1.6×	39 0.4×	105 1.4×	49 0.9×	30 0.6×	7	349
M. A. Farnetani Italy	14	137 1.2×	59 0.6×	133 1.8×	56 1.0×	56 1.2×	24	447
Bouchra Ouled Amar Bencheikh Canada	9	105 0.9×	62 0.6×	79 1.0×	65 1.1×	39 0.8×	13	307
Magda Verdecchia Italy	10	77 0.6×	328 3.1×	133 1.8×	40 0.7×	46 1.0×	12	479
Louise Bier United States	9	90 0.8×	222 2.1×	152 2.0×	44 0.8×	161 3.4×	16	485
R Lahl Germany	10	164 1.4×	74 0.7×	76 1.0×	115 2.0×	67 1.4×	37	424

Countries citing papers authored by Jean-Marc Pinard

Since Specialization

Citations

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

Fields of papers citing papers by Jean-Marc Pinard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean-Marc Pinard. 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 Jean-Marc Pinard. The network helps show where Jean-Marc Pinard may publish in the future.

Co-authorship network of co-authors of Jean-Marc Pinard

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

All Works

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16 of 16 papers shown

Busa, Tiffany, Dominique P. Germain, Gwenaël Nadeau, et al.. (2017). The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability. European Journal of Human Genetics. 26(1). 143–148. 22 indexed citations

Pinard, Jean-Marc, et al.. (2012). Sleep-disordered breathing in children with congenital muscular dystrophies. European Journal of Paediatric Neurology. 16(6). 619–624. 14 indexed citations

Tabet, Anne‐Claude, Marion Pilorge, Richard Delorme, et al.. (2012). Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother. European Journal of Human Genetics. 20(5). 540–546. 33 indexed citations

Chéliout-Héraut, F., et al.. (2012). Sleep architecture impairment in epileptic children and putative role of anti epileptic drugs. Neurological Sciences. 34(1). 57–62. 7 indexed citations

Pinard, Jean-Marc, et al.. (2009). Sleep disorders in succinic semialdehyde dehydrogenase deficiency: A family report. European Journal of Paediatric Neurology. 14(3). 282–287. 3 indexed citations

Ribaupierre, Sandrine de, Georg Dorfmüller, Martine Fohlen, et al.. (2007). SUBEPENDYMAL GIANT-CELL ASTROCYTOMASIN PEDIATRIC TUBEROUS SCLEROSIS DISEASE. Neurosurgery. 60(1). 83–90. 88 indexed citations

Clavelou, Pierre, Gérard Besson, Jean-Marc Pinard, et al.. (2006). Manifestations neurologiques de la maladie de Fabry. Revue Neurologique. 162(5). 569–580. 12 indexed citations

Quijano‐Roy, Susana, Itxaso Martì, S. Makri, et al.. (2005). Brain MRI abnormalities in muscular dystrophy due to FKRP mutations. Brain and Development. 28(4). 232–242. 26 indexed citations

Portes, V. des, Fiona Francis, Jean-Marc Pinard, et al.. (2002). So-called ‘cryptogenic’ partial seizures resulting from a subtle cortical dysgenesis due to adoublecortin gene mutation. Seizure. 11(4). 273–277. 13 indexed citations

10.

Ioos, Christine, Brigitte Estournet-Mathiaud, Jean-Marc Pinard, & F. Chéliout-Héraut. (2001). Sleep Disorders Caused by Brainstem Tumor: Case Report. Journal of Child Neurology. 16(10). 767–770. 13 indexed citations

11.

Portes, V. des, Jean-Marc Pinard, Fiona Francis, et al.. (2000). Retard mental et troubles de la corticogenèse. Archives de Pédiatrie. 7. 109s–111s. 1 indexed citations

12.

Ioos, Christine, Martine Fohlen, Nathalie Villeneuve, et al.. (2000). Hot Water Epilepsy: A Benign and Unrecognized Form. Journal of Child Neurology. 15(2). 125–128. 26 indexed citations

13.

Pinard, Jean-Marc, C. Marsac, I. Desguerre, et al.. (1999). Syndrome de Leigh et leucodystrophie par déficit partiel en succinate déshydrogénase: régression sous riboflavine. Archives de Pédiatrie. 6(4). 421–426. 17 indexed citations

14.

Ioos, Christine, Nathalie Villeneuve, Martine Fohlen, et al.. (1999). L'épilepsie à l'eau chaude : une forme bénigne et méconnue. Archives de Pédiatrie. 6(7). 755–758. 5 indexed citations

15.

Carlier, Robert, Jean-Marc Pinard, D. Mompoint, et al.. (1998). Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.. Radiology. 206(3). 811–816. 28 indexed citations

16.

Coz, Pierre Le, M. T. Vanier, Françoise Goutières, et al.. (1994). [GM2-Gangliosidosis variant B1 disclosed during adolescence by an isolated multi-systemic involvement of the central and peripheral nervous systems].. PubMed. 150(1). 61–6. 3 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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