Irène Maire

2.2k total citations
42 papers, 1.5k citations indexed

About

Irène Maire is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Irène Maire has authored 42 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Physiology, 13 papers in Cell Biology and 11 papers in Molecular Biology. Recurrent topics in Irène Maire's work include Lysosomal Storage Disorders Research (25 papers), Cellular transport and secretion (10 papers) and Carbohydrate Chemistry and Synthesis (10 papers). Irène Maire is often cited by papers focused on Lysosomal Storage Disorders Research (25 papers), Cellular transport and secretion (10 papers) and Carbohydrate Chemistry and Synthesis (10 papers). Irène Maire collaborates with scholars based in France, United States and Germany. Irène Maire's co-authors include Roseline Froissart, Nathalie Desmaris, Dominique Bozon, Cyril Mignot, Thierry Billette de Villemeur, Isabel Moreira da Silva, Robert J. Desnick, Gilles Millat, Jean‐Michel Heard and Makiko Yasuda and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Irène Maire

42 papers receiving 1.4k citations

Peers

Irène Maire
Patricia Dickson United States
Otto P. van Diggelen Netherlands
I Maire France
Merry Passage United States
J. L. M. Keulemans Netherlands
Francyne Kubaski United States
Marianne Hoogeveen‐Westerveld Netherlands
G. T. N. Besley United Kingdom
Amparo Chabás Spain
Brady Ro United States
Patricia Dickson United States
Irène Maire
Citations per year, relative to Irène Maire Irène Maire (= 1×) peers Patricia Dickson

Countries citing papers authored by Irène Maire

Since Specialization
Citations

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

Fields of papers citing papers by Irène Maire

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irène Maire

This figure shows the co-authorship network connecting the top 25 collaborators of Irène Maire. A scholar is included among the top collaborators of Irène 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 Irène Maire. Irène Maire 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.
Maire, Irène. (2012). Le système lysosomial dans la protéolyse : panorama des maladies lysosomiales. Bulletin de l Académie Nationale de Médecine. 196(8). 1561–1574. 1 indexed citations
2.
Héron, Bénédicte, Yann Mikaeloff, Roseline Froissart, et al.. (2010). Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece. American Journal of Medical Genetics Part A. 155(1). 58–68. 128 indexed citations
3.
Iurisci, Ida, Elisabeth Filipski, Francis Harper, et al.. (2009). LIVER CIRCADIAN CLOCK, A PHARMACOLOGIC TARGET OF CYCLIN-DEPENDENT KINASE INHIBITOR SELICICLIB. Chronobiology International. 26(6). 1169–1188. 29 indexed citations
4.
Cheillan, David, Jérôme Ausseil, Sandrine Vitry, et al.. (2008). Abnormal expression of truncated CRMP-1 protein in the brain cortex of MPSIIIB mice. Molecular Genetics and Metabolism. 94(1). 135–138. 1 indexed citations
5.
Maire, Irène. (2007). [Lysosomal storage diseases: functional classification and treatment principles].. PubMed. 36 Spec No 1. 1S88–95. 2 indexed citations
6.
Maire, Irène. (2007). Maladies de surcharge lysosomale : classification fonctionnelle et principes thérapeutiques. La Presse Médicale. 36. 1 indexed citations
7.
Froissart, Roseline, Isabel Moreira da Silva, & Irène Maire. (2007). Mucopolysaccharidosis type II: an update on mutation spectrum. Acta Paediatrica. 96(s455). 71–77. 75 indexed citations
8.
Tomatsu, Shunji, Kazuko Sukegawa, Mónica Gutiérrez, et al.. (2006). Differences in methylation patterns in the methylation boundary region of IDS gene in hunter syndrome patients: implications for CpG hot spot mutations. European Journal of Human Genetics. 14(7). 838–845. 12 indexed citations
9.
Latour, Philippe, Pierre‐Marie Gonnaud, Elisabeth Ollagnon, et al.. (2006). SIMPLE mutation analysis in dominant demyelinating Charcot‐Marie‐Tooth disease: three novel mutations. Journal of the Peripheral Nervous System. 11(2). 148–155. 43 indexed citations
10.
Schiff, Manuel, Irène Maire, Yves Bertrand, Pierre Cochat, & Nathalie Guffon. (2005). Long-term follow-up of metachronous marrow-kidney transplantation in severe type II sialidosis: what does success mean?. Nephrology Dialysis Transplantation. 20(11). 2563–2565. 11 indexed citations
11.
Cressant, Arnaud, Nathalie Desmaris, Lucie Vérot, et al.. (2004). Improved Behavior and Neuropathology in the Mouse Model of Sanfilippo Type IIIB Disease after Adeno-Associated Virus-Mediated Gene Transfer in the Striatum. Journal of Neuroscience. 24(45). 10229–10239. 112 indexed citations
12.
Díaz, George A., Bruce D. Gelb, Neil Risch, et al.. (2000). Gaucher Disease: The Origins of the Ashkenazi Jewish N370S and 84GG Acid β-Glucosidase Mutations. The American Journal of Human Genetics. 66(6). 1821–1832. 52 indexed citations
13.
Froissart, Roseline, et al.. (1999). The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signals. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1447(1). 35–42. 8 indexed citations
14.
Froissart, Roseline, Irène Maire, Gilles Millat, et al.. (1998). Identification of iduronate sulfatase gene alterations in 70 unrelated Hunter patients. Clinical Genetics. 53(5). 362–368. 44 indexed citations
15.
Vervoort, R., R Gitzelmann, N. U. Bosshard, et al.. (1998). Low β-glucuronidase enzyme activity and mutations in the human β-glucuronidase gene in mild mucopolysaccharidosis type VII, pseudodeficiency and a heterozygote. Human Genetics. 102(1). 69–78. 26 indexed citations
16.
Roubertie, Agathe, et al.. (1998). McArdle's disease in childhood: Report of a new case. European Journal of Paediatric Neurology. 2(5). 269–273. 4 indexed citations
17.
Veiga‐da‐Cunha, Maria, Isabelle Gerin, Yuan‐Tsong Chen, et al.. (1998). A Gene on Chromosome 11q23 Coding for a Putative Glucose- 6-Phosphate Translocase Is Mutated in Glycogen-Storage Disease Types Ib and Ic. The American Journal of Human Genetics. 63(4). 976–983. 89 indexed citations
18.
Tylki‐Szymańska, Anna, Gilles Millat, Irène Maire, & Barbara Czartoryska. (1996). Types I and III Gaucher Disease inPoland: Incidence of the MostCommon Mutations andPhenotypic Manifestations. European Journal of Human Genetics. 4(6). 334–337. 22 indexed citations
19.
Birot, Anne‐Marie, Olivier Bouton, Roseline Froissart, Irène Maire, & Dominique Bozon. (1996). IDS gene-pseudogene exchange responsible for an intragenic deletion in a hunter patient. Human Mutation. 8(1). 44–50. 24 indexed citations
20.
Lessinger, Jean‐Marc, G Férard, Dominique Labbé, et al.. (1995). Usefulness of Reference Materials in Calibration of Enzyme Activities. Clinical Chemistry and Laboratory Medicine (CCLM). 33(11). 859–864. 10 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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