Mylène Béri‐Dexheimer

1.0k total citations
8 papers, 159 citations indexed

About

Mylène Béri‐Dexheimer is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Mylène Béri‐Dexheimer has authored 8 papers receiving a total of 159 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Mylène Béri‐Dexheimer's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). Mylène Béri‐Dexheimer is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). Mylène Béri‐Dexheimer collaborates with scholars based in France and Italy. Mylène Béri‐Dexheimer's co-authors include Jean‐Louis Guéant, Céline Bonnet, Philippe Jonveaux, Bruno Leheup, Christophe Philippe, Thomas Lecompte, Pierre Bordigoni, Véronique Latger‐Cannard, Marie‐José Gregoire and Virginie Roth and has published in prestigious journals such as Frontiers in Immunology, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Mylène Béri‐Dexheimer

8 papers receiving 159 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mylène Béri‐Dexheimer France 6 54 54 45 34 29 8 159
Kristin Johnson United States 6 12 0.2× 32 0.6× 89 2.0× 51 1.5× 6 0.2× 10 158
Gordon J. Hildick-Smith United States 7 15 0.3× 33 0.6× 121 2.7× 22 0.6× 3 0.1× 9 204
Andrei M. Vacaru United States 8 18 0.3× 18 0.3× 121 2.7× 28 0.8× 5 0.2× 16 196
Sebastian Shterental United States 3 19 0.4× 112 2.1× 129 2.9× 37 1.1× 21 0.7× 3 224
Mieko Matsuyama United States 6 17 0.3× 15 0.3× 143 3.2× 6 0.2× 7 0.2× 10 203
Katayoon Shirneshan Germany 10 57 1.1× 82 1.5× 118 2.6× 30 0.9× 2 0.1× 21 271
Jessica Goodman United States 5 43 0.8× 97 1.8× 65 1.4× 88 2.6× 6 217
Boris Skrobek France 2 48 0.9× 51 0.9× 63 1.4× 37 1.1× 2 0.1× 2 140
Manoussos N. Papadakis Greece 10 85 1.6× 139 2.6× 105 2.3× 203 6.0× 5 0.2× 22 301

Countries citing papers authored by Mylène Béri‐Dexheimer

Since Specialization
Citations

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

Fields of papers citing papers by Mylène Béri‐Dexheimer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mylène Béri‐Dexheimer. 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 Mylène Béri‐Dexheimer. The network helps show where Mylène Béri‐Dexheimer may publish in the future.

Co-authorship network of co-authors of Mylène Béri‐Dexheimer

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

All Works

8 of 8 papers shown
1.
Sorlin, Arthur, Mylène Valduga, Mylène Béri‐Dexheimer, et al.. (2019). Deletion of chr7p22 and chr15q11: Two Familial Cases of Immune Deficiency: Extending the Phenotype Toward Dysimmunity. Frontiers in Immunology. 10. 1871–1871. 4 indexed citations
2.
Auger, Julie, Céline Bonnet, Mylène Valduga, et al.. (2013). De novo complex X chromosome rearrangement unmasking maternally inherited CSF2RA deletion in a girl with pulmonary alveolar proteinosis. American Journal of Medical Genetics Part A. 161(10). 2594–2599. 11 indexed citations
3.
Béri‐Dexheimer, Mylène, Céline Bonnet, Myriam Bronner, et al.. (2012). RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability. American Journal of Medical Genetics Part A. 158A(7). 1782–1784. 5 indexed citations
4.
Bénéteau, Claire, Emilie Landais, C. Philippe, et al.. (2011). Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability. Journal of Medical Genetics. 48(9). 635–639. 9 indexed citations
5.
Béri‐Dexheimer, Mylène, Véronique Latger‐Cannard, Christophe Philippe, et al.. (2008). Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions. European Journal of Human Genetics. 16(8). 1014–1018. 72 indexed citations
6.
Béri‐Dexheimer, Mylène, et al.. (2007). Cobalamin Potentiates Vinblastine Cytotoxicity Through Downregulation of mdr-1 Gene Expression in HepG2 Cells. Cellular Physiology and Biochemistry. 20(6). 967–976. 22 indexed citations
7.
Guéant‐Rodriguez, Rosa‐Maria, Antonino Romano, Mylène Béri‐Dexheimer, et al.. (2006). Gene–gene interactions of IL13 and IL4RA variants in immediate allergic reactions to betalactam antibiotics. Pharmacogenetics and Genomics. 16(10). 713–719. 34 indexed citations
8.
Béri‐Dexheimer, Mylène, et al.. (2006). L'hybridation génomique comparative sur microréseau d'ADN (puces à ADN) en pathologie chromosomique constitutionnelle. Pathologie Biologie. 55(1). 13–18. 2 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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