Manuèle Miné

979 total citations
27 papers, 612 citations indexed

About

Manuèle Miné is a scholar working on Molecular Biology, Immunology and Allergy and Neurology. According to data from OpenAlex, Manuèle Miné has authored 27 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 10 papers in Immunology and Allergy and 9 papers in Neurology. Recurrent topics in Manuèle Miné's work include Cell Adhesion Molecules Research (10 papers), Metabolism and Genetic Disorders (8 papers) and Cerebrovascular and genetic disorders (7 papers). Manuèle Miné is often cited by papers focused on Cell Adhesion Molecules Research (10 papers), Metabolism and Genetic Disorders (8 papers) and Cerebrovascular and genetic disorders (7 papers). Manuèle Miné collaborates with scholars based in France, United Kingdom and United States. Manuèle Miné's co-authors include C. Marsac, M. Brivet, Elisabeth Tournier‐Lasserve, Marc Abitbol, Johann Soret, Jamal Tazi, Mathieu Gabut, Hugues Chabriat, Mokhtar Zater and Paula J. Grabowski and has published in prestigious journals such as Journal of Biological Chemistry, Molecular and Cellular Biology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Manuèle Miné

27 papers receiving 604 citations

Peers

Manuèle Miné

NEURO

GENET

Ginat Narkis Israel

Alessandro Malandrini Italy

Xinghua Luan China

Kenji Nanao Japan

Sietske H. Kevelam Netherlands

Dayami Hernandez United States

R. M. Brown United Kingdom

Victor H. K. Yong Singapore

Aisha Al‐Shamsi United Arab Emirates

Erik Pearson United States

Ginat Narkis Israel

Manuèle Miné

528 ×1.5

72 ×0.5

NEURO

127 ×1.2

GENET

10 ×0.1

101 ×1.0

Citations per year, relative to Manuèle Miné Manuèle Miné (= 1×) peers Ginat Narkis

Countries citing papers authored by Manuèle Miné

Since Specialization

Citations

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

Fields of papers citing papers by Manuèle Miné

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuèle Miné

This figure shows the co-authorship network connecting the top 25 collaborators of Manuèle Miné. A scholar is included among the top collaborators of Manuèle Miné 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 Manuèle Miné. Manuèle Miné 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

Grangeon, Lou, Kévin Cassinari, Stéphane Rousseau, et al.. (2021). Early-Onset Cerebral Amyloid Angiopathy and Alzheimer Disease Related to an APP Locus Triplication. Neurology Genetics. 7(5). e609–e609. 20 indexed citations

Pichiecchio, Anna, Francesca Ormitti, Davide Tonduti, et al.. (2019). Cortical malformations and COL4A1 mutation: Three new cases. European Journal of Paediatric Neurology. 23(3). 410–417. 7 indexed citations

Cavallin, Mara, Manuèle Miné, Nathalie Boddaert, et al.. (2018). Further refinement of COL4A1 and COL4A2 related cortical malformations. European Journal of Medical Genetics. 61(12). 765–772. 23 indexed citations

Miné, Manuèle, Tibor Kovács, Dániel Bereczki, et al.. (2014). COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy. Journal of Neurology. 261(3). 500–503. 31 indexed citations

Carra‐Dallière, Clarisse, Xavier Ayrignac, Dimitri Renard, et al.. (2013). Isolated Lacunar Infarct: An Early Clinical Presentation of CADASIL?. Cerebrovascular Diseases. 35(3). 298–299. 4 indexed citations

Colin, Estelle, Manuèle Miné, Agnès Guichet, et al.. (2013). Fetal intracerebral hemorrhage and cataract: think COL4A1. Journal of Perinatology. 34(1). 75–77. 23 indexed citations

Corlobé, Astrid, Elisabeth Tournier‐Lasserve, Manuèle Miné, et al.. (2013). COL4A1 Mutation Revealed by an Isolated Brain Hemorrhage. Cerebrovascular Diseases. 35(6). 593–594. 14 indexed citations

Pichiecchio, Anna, Roberta La Piana, Daniel Doherty, et al.. (2012). COL4A1-Related Disease: Raised Creatine Kinase and Cerebral Calcification as Useful Pointers. Neuropediatrics. 43(5). 283–288. 16 indexed citations

Imbard, Apolline, Audrey Boutron, Mokhtar Zater, et al.. (2011). Molecular characterization of 82 patients with pyruvate dehydrogenase complex deficiency. Structural implications of novel amino acid substitutions in E1 protein. Molecular Genetics and Metabolism. 104(4). 507–516. 64 indexed citations

10.

Paquet, Claire, Éric Jouvent, Manuèle Miné, et al.. (2010). A cortical form of CADASIL with cerebral Aβ amyloidosis. Acta Neuropathologica. 120(6). 813–820. 13 indexed citations

11.

Fouillade, Charles, Hugues Chabriat, Florence Riant, et al.. (2008). Activating NOTCH3 mutation in a patient with small-vessel-disease of the Brain. Human Mutation. 29(3). 452–452. 48 indexed citations

12.

Miné, Manuèle, Jian‐Min Chen, M. Brivet, et al.. (2006). A large genomic deletion in thePDHX gene caused by the retrotranspositional insertion of a full-length LINE-1 element. Human Mutation. 28(2). 137–142. 45 indexed citations

13.

Miné, Manuèle, et al.. (2006). A novel gross deletion caused by non-homologous recombination of the PDHX gene in a patient with pyruvate dehydrogenase deficiency☆. Molecular Genetics and Metabolism. 89(1-2). 106–110. 10 indexed citations

14.

Schiff, Manuel, Manuèle Miné, M. Brivet, et al.. (2006). Leigh's disease due to a new mutation in the PDHX gene. Annals of Neurology. 59(4). 709–714. 24 indexed citations

15.

Brivet, M., et al.. (2005). First characterization of a large deletion of the PDHA1 gene. Molecular Genetics and Metabolism. 86(4). 456–461. 14 indexed citations

16.

Gabut, Mathieu, et al.. (2005). The SR Protein SC35 Is Responsible for Aberrant Splicing of the E1α Pyruvate Dehydrogenase mRNA in a Case of Mental Retardation with Lactic Acidosis. Molecular and Cellular Biology. 25(8). 3286–3294. 55 indexed citations

17.

Miné, Manuèle, M. Brivet, Guy Touati, et al.. (2003). Splicing Error in E1α Pyruvate Dehydrogenase mRNA Caused by Novel Intronic Mutation Responsible for Lactic Acidosis and Mental Retardation. Journal of Biological Chemistry. 278(14). 11768–11772. 41 indexed citations

18.

Dey, Runu, Manuèle Miné, Isabelle Desguerre, et al.. (2003). A new case of pyruvate dehydrogenase deficiency due to a novel mutation in the pdx1 gene. Annals of Neurology. 53(2). 273–277. 19 indexed citations

19.

Karges, Beate, Manuèle Miné, Leopold Ludwig, et al.. (2003). Mutation Ala¹⁷¹Thr Stabilizes the Gonadotropin-Releasing Hormone Receptor in Its Inactive Conformation, Causing Familial Hypogonadotropic Hypogonadism. The Journal of Clinical Endocrinology & Metabolism. 88(4). 1873–1879. 39 indexed citations

20.

Tóth, Petra, Bénédicte Sohm, Manuèle Miné, et al.. (2003). Proteomic Consequences of a Human Mitochondrial tRNA Mutation beyond the Frame of Mitochondrial Translation. Journal of Biological Chemistry. 278(27). 24314–24323. 24 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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