Mylène Béri
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
-
- Congenital heart defects research 3
- Glycosylation and Glycoproteins Research 2
- Advanced biosensing and bioanalysis techniques 1
- Co-authors
- Philippe Jonveaux (6 shared papers)Céline Bonnet (5 shared papers)Christophe Philippe (4 shared papers)Bruno Leheup (4 shared papers)Mylène Valduga (2 shared papers)Christophe Némos (1 shared paper)B. Foliguet (1 shared paper)O. Thiébaugeorges (1 shared paper)
- Journals
- Clinical Immunology (1 paper)European Journal of Human Genetics (1 paper)Prenatal Diagnosis (1 paper)American Journal of Medical Genetics Part A (3 papers)Molecular Syndromology (1 paper)
- Partner nations
- France
In The Last Decade
Mylène Béri
8 papers receiving 175 citations
Peers
Comparison fields: 5 of 31
- Genetics 150
- Pediatrics, Perinatology and Child Health 65
- Molecular Biology 79
- Genetics 10
- Cellular and Molecular Neuroscience 13
Countries citing papers authored by Mylène Béri
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
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-authors
The 25 scholars most cited alongside Mylène Béri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 57 | |
| 2 | 2013 | 30 | |
| 3 | 2009 | 30 | |
| 4 | 2010 | 25 | |
| 5 | 2013 | 11 | |
| 6 | 2008 | 11 | |
| 7 | 2014 | 9 | |
| 8 | 2015 | 2 |
About Mylène Béri
Mylène Béri is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Epidemiology, having authored 8 papers that have together received 175 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (3 papers), Genomics and Rare Diseases (2 papers), Glycosylation and Glycoproteins Research (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers) and Advanced biosensing and bioanalysis techniques (1 paper). The work is most often cited by research in Genetics (150 citations), Pediatrics, Perinatology and Child Health (65 citations), Molecular Biology (79 citations), Genetics (10 citations) and Cellular and Molecular Neuroscience (13 citations). Mylène Béri has collaborated with scholars based in France. Frequent co-authors include Philippe Jonveaux, Céline Bonnet, Christophe Philippe, Bruno Leheup, Mylène Valduga, Christophe Némos, B. Foliguet, O. Thiébaugeorges, Virginie Roth and Claire Bénéteau. Their work appears in journals such as Clinical Immunology, European Journal of Human Genetics, Prenatal Diagnosis, American Journal of Medical Genetics Part A and Molecular Syndromology.
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.