Mylène Béri

1.2k total citations
8 papers, 175 citations indexed

About

Mylène Béri is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mylène Béri has authored 8 papers receiving a total of 175 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mylène Béri's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Mylène Béri is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Mylène Béri collaborates with scholars based in France. Mylène Béri's co-authors include Philippe Jonveaux, Céline Bonnet, Christophe Philippe, Bruno Leheup, Mylène Valduga, B. Foliguet, Christophe Némos, O. Thiébaugeorges, Asma Ali Khan and Juliette Piard and has published in prestigious journals such as European Journal of Human Genetics, Clinical Immunology and Prenatal Diagnosis.

In The Last Decade

Mylène Béri

8 papers receiving 175 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mylène Béri France	7	150	79	65	13	11	8	175
Mylène Valduga France	8	169 1.1×	76 1.0×	90 1.4×	11 0.8×	18 1.6×	17	213
Ornella Galesi Italy	9	155 1.0×	107 1.4×	42 0.6×	14 1.1×	22 2.0×	17	198
Hannaleena Kokkonen Finland	8	173 1.2×	152 1.9×	83 1.3×	10 0.8×	11 1.0×	20	238
Gyri Aasland Gradek Norway	5	76 0.5×	58 0.7×	32 0.5×	13 1.0×	12 1.1×	5	151
Jessica Sebastian United States	6	92 0.6×	64 0.8×	21 0.3×	12 0.9×	6 0.5×	11	146
Ilse M. van der Werf Belgium	7	111 0.7×	79 1.0×	32 0.5×	9 0.7×	12 1.1×	8	155
Л. П. Назаренко Russia	10	155 1.0×	141 1.8×	38 0.6×	11 0.8×	55 5.0×	45	244
James M.J. Lawlor United States	9	95 0.6×	60 0.8×	16 0.2×	11 0.8×	8 0.7×	16	176
Carmen Esmer Mexico	5	157 1.0×	116 1.5×	33 0.5×	7 0.5×	17 1.5×	16	225
Fernanda T. Bellucco Brazil	9	140 0.9×	107 1.4×	43 0.7×	10 0.8×	56 5.1×	24	233

Countries citing papers authored by Mylène Béri

Since Specialization

Citations

This map shows the geographic impact of Mylène Béri'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 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 more than expected).

Fields of papers citing papers by Mylène Béri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mylène Béri

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

All Works

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8 of 8 papers shown

Landais, Emilie, Pascale Kleinfinger, Christine Piètrement, et al.. (2015). A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction. American Journal of Medical Genetics Part A. 167(6). 1275–1284. 2 indexed citations

Chehadeh, Salima El, Céline Bonnet, Patrick Callier, et al.. (2014). Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic Markers. JIMD Reports. 20. 45–55. 9 indexed citations

Bonnet, Céline, Asma Ali Khan, Emmanuel Bresso, et al.. (2013). Extended spectrum of MBD5 mutations in neurodevelopmental disorders. European Journal of Human Genetics. 21(12). 1457–1461. 30 indexed citations

Démurger, Florence, Laurent Pasquier, Christèle Dubourg, et al.. (2013). Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis. Molecular Syndromology. 4(6). 267–272. 11 indexed citations

Piard, Juliette, Christophe Philippe, Claire Bénéteau, et al.. (2010). Clinical and molecular characterization of a large family with an interstitial 15q11q13 duplication. American Journal of Medical Genetics Part A. 152A(8). 1933–1941. 25 indexed citations

Valduga, Mylène, Christophe Philippe, O. Thiébaugeorges, et al.. (2010). A retrospective study by oligonucleotide array‐CGH analysis in 50 fetuses with multiple malformations. Prenatal Diagnosis. 30(4). 333–341. 57 indexed citations

Bonnet, Céline, et al.. (2009). Aberrant GRIA3 transcripts with multi‐exon duplications in a family with X‐linked mental retardation. American Journal of Medical Genetics Part A. 149A(6). 1280–1289. 30 indexed citations

Daguindau, Nicolas, Véronique Decot, Rosine Nzietchueng, et al.. (2008). Immune constitution monitoring after PBMC transplantation in complete DiGeorge syndrome: An eight-year follow-up. Clinical Immunology. 128(2). 164–171. 11 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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