I Maire

1.9k total citations
85 papers, 1.2k citations indexed

About

I Maire is a scholar working on Physiology, Molecular Biology and Rheumatology. According to data from OpenAlex, I Maire has authored 85 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Physiology, 23 papers in Molecular Biology and 23 papers in Rheumatology. Recurrent topics in I Maire's work include Lysosomal Storage Disorders Research (42 papers), Glycogen Storage Diseases and Myoclonus (22 papers) and Metabolism and Genetic Disorders (13 papers). I Maire is often cited by papers focused on Lysosomal Storage Disorders Research (42 papers), Glycogen Storage Diseases and Myoclonus (22 papers) and Metabolism and Genetic Disorders (13 papers). I Maire collaborates with scholars based in France, Tunisia and United Kingdom. I Maire's co-authors include Roseline Froissart, Nathalie Guffon, P Guibaud, M. Mathieu, G Souillet, Dominique Bozon, J. Straczek, Monique Piraud, Alexey V. Pshezhetsky and Helena Poupětová and has published in prestigious journals such as The EMBO Journal, Neurology and Biochemical Journal.

In The Last Decade

I Maire

83 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
I Maire France	17	785	341	287	279	228	85	1.2k
Elisabeth Young United Kingdom	22	1.1k 1.4×	392 1.1×	274 1.0×	440 1.6×	286 1.3×	46	1.4k
Irène Maire France	21	950 1.2×	351 1.0×	379 1.3×	387 1.4×	285 1.3×	42	1.5k
C B Whitley United States	17	556 0.7×	287 0.8×	209 0.7×	214 0.8×	102 0.4×	30	970
Clare Beesley United Kingdom	17	607 0.8×	288 0.8×	241 0.8×	262 0.9×	240 1.1×	29	980
Barbara Czartoryska Poland	21	980 1.2×	292 0.9×	247 0.9×	496 1.8×	257 1.1×	67	1.2k
R J Desnick United States	12	778 1.0×	245 0.7×	212 0.7×	309 1.1×	198 0.9×	20	941
Brady Ro United States	19	1.1k 1.5×	594 1.7×	212 0.7×	264 0.9×	326 1.4×	44	1.6k
J. E. Wraith United Kingdom	20	692 0.9×	381 1.1×	434 1.5×	242 0.9×	105 0.5×	35	1.3k
Müge Güçsavaş‐Çalıkoğlu United States	7	797 1.0×	232 0.7×	277 1.0×	415 1.5×	142 0.6×	10	1.1k
Ai-Chu Huang Taiwan	11	608 0.8×	290 0.9×	337 1.2×	195 0.7×	179 0.8×	15	940

Countries citing papers authored by I Maire

Since Specialization

Citations

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

Fields of papers citing papers by I Maire

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I Maire

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

All Works

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20 of 20 papers shown

Piraud, Monique, I Maire, & Roseline Froissart. (2010). Intérêt du dosage du globotriaosylcéramide urinaire pour le diagnostic et le suivi du traitement de la maladie de Fabry. La Revue de Médecine Interne. 31. S270–S274. 4 indexed citations

Mousson, B., Jean-Marc Collombet, H Carrier, et al.. (2009). An abnormal exercise test response revealing a respiratory chain complex III deficiency. Acta Neurologica Scandinavica. 91(6). 488–493. 6 indexed citations

Guillot, Max, et al.. (2008). Mucopolysaccharidose de type I : intérêt d’un diagnostic et d’une enzymothérapie substitutive précoces. À propos d’un cas. Archives de Pédiatrie. 15(1). 45–49. 3 indexed citations

Pavic, Michel, P. Petiot, Nathalie Streichenberger, et al.. (2003). Maladie de Mac Ardle diagnostiquée après 30 ans : à propos de 12 cas. La Revue de Médecine Interne. 24(11). 716–720. 6 indexed citations

Souillet, G, Nathalie Guffon, I Maire, et al.. (2003). Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources. Bone Marrow Transplantation. 31(12). 1105–1117. 153 indexed citations

Froissart, Roseline, et al.. (2002). Mucopolysaccharidosis type II – genotype/phenotype aspects. Acta Paediatrica. 91(s439). 82–87. 43 indexed citations

Turpin, Christophe, et al.. (2002). Autisme de l’enfant lié à une mucopolysaccharidose. Annales Médico-psychologiques revue psychiatrique. 160(5-6). 421–426. 4 indexed citations

Bruni, N, et al.. (1999). Enzymatic characterization of four new mutations in the glucose‐6 phosphatase (G6PC) gene which cause glycogen storage disease type 1a. Annals of Human Genetics. 63(2). 141–146. 23 indexed citations

Guffon, Nathalie, G Souillet, I Maire, J. Straczek, & P Guibaud. (1998). Follow-up of nine patients with Hurler syndrome after bone marrow transplantation. The Journal of Pediatrics. 133(1). 119–125. 108 indexed citations

10.

Millat, Gilles, Roseline Froissart, I Maire, & Dominique Bozon. (1997). IDS Transfer from Overexpressing Cells to IDS-Deficient Cells. Experimental Cell Research. 230(2). 362–367. 16 indexed citations

11.

Birot, Anne‐Marie, et al.. (1996). A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patient. Human Mutation. 7(3). 266–268. 21 indexed citations

12.

Bozon, Dominique, et al.. (1996). Mutation analysis in 24 French patients with glycogen storage disease type 1a.. Journal of Medical Genetics. 33(5). 358–360. 42 indexed citations

13.

Bouton, Olivier, et al.. (1995). A deletion polymorphism in intron 4 of the IDUA gene. Molecular and Cellular Probes. 9(2). 143–143. 1 indexed citations

14.

Piraud, Monique, Sylvie Boyer, M. Mathieu, & I Maire. (1993). Diagnosis of mucopolysaccharidoses in a clinically selected population by urinary glycosaminoglycan analysis: A study of 2,000 urine samples. Clinica Chimica Acta. 221(1-2). 171–181. 48 indexed citations

15.

Mousson, B., et al.. (1991). Les cytopathies mitochondriales. La Revue de Médecine Interne. 12(3). 219–226. 3 indexed citations

16.

Dupond, J.L., et al.. (1991). [Another etiology of intermittent claudication of the jaw: Mac Ardle's disease (muscular glycogenosis type V)].. PubMed. 142(7). 556–7. 1 indexed citations

17.

Carrier, H, et al.. (1990). Myopathic evolution of an exertional muscle pain syndrome with phosphorylase b kinase deficiency. Acta Neuropathologica. 81(1). 84–88. 10 indexed citations

18.

Piraud, Monique & I Maire. (1990). Interference of amikacin in thin-layer chromatographic screening of urine for oligosaccharidosis. Clinical Chemistry. 36(5). 809–809. 3 indexed citations

19.

Sann, L, et al.. (1988). Prevention of neonatal hypoglycaemia by oral lipid supplementation in low birth weight infants. European Journal of Pediatrics. 147(2). 158–161. 12 indexed citations

20.

Mousson, B., et al.. (1988). [Recurrent rhabdomyolysis and deficiency of carnitine palmityl transferase. Evidence of the responsibility of a mutant in 2 brothers].. PubMed. 17(41). 2187–90. 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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