Mylène Valduga

810 total citations
17 papers, 213 citations indexed

About

Mylène Valduga is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mylène Valduga has authored 17 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mylène Valduga's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Mylène Valduga is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Mylène Valduga collaborates with scholars based in France and United Kingdom. Mylène Valduga's co-authors include Philippe Jonveaux, Christophe Philippe, Céline Bonnet, Mylène Béri, B. Foliguet, Juliette Piard, Christophe Némos, O. Thiébaugeorges, Lionel Van Maldergem and Bruno Leheup and has published in prestigious journals such as Frontiers in Immunology, Frontiers in Genetics and Journal of Clinical Medicine.

In The Last Decade

Mylène Valduga

15 papers receiving 201 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 Valduga France 8 169 90 76 19 18 17 213
María Ángeles Mori Spain 10 205 1.2× 136 1.5× 109 1.4× 46 2.4× 19 1.1× 17 280
Julie Scuffins United States 5 215 1.3× 126 1.4× 123 1.6× 18 0.9× 11 0.6× 10 348
Holly Feret United States 8 133 0.8× 37 0.4× 100 1.3× 16 0.8× 12 0.7× 8 200
Fernando Santos Spain 9 228 1.3× 84 0.9× 193 2.5× 23 1.2× 21 1.2× 13 325
Radu Harbuz France 7 140 0.8× 32 0.4× 93 1.2× 7 0.4× 16 0.9× 11 221
Beth A. Torchia United States 7 281 1.7× 177 2.0× 139 1.8× 35 1.8× 71 3.9× 11 369
Erika Carter United States 10 268 1.6× 82 0.9× 118 1.6× 26 1.4× 54 3.0× 15 338
M B Katznelson Israel 12 185 1.1× 71 0.8× 80 1.1× 52 2.7× 10 0.6× 24 324
Patricia Mowery‐Rushton United States 9 167 1.0× 74 0.8× 109 1.4× 11 0.6× 35 1.9× 13 242
Kimiaki Uetake Japan 7 88 0.5× 40 0.4× 61 0.8× 8 0.4× 15 0.8× 16 175

Countries citing papers authored by Mylène Valduga

Since Specialization
Citations

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

Fields of papers citing papers by Mylène Valduga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mylène Valduga

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

All Works

17 of 17 papers shown
1.
Benazra, Marion, Pascale Kleinfinger, Mylène Valduga, et al.. (2024). Optical genome mapping identifies a homozygous deletion in the non-coding region of the SCN9A gene in individuals from the same family with congenital insensitivity to pain. Frontiers in Genetics. 15. 1375770–1375770.
2.
Kleinfinger, Pascale, Armelle Luscan, Detlef Trost, et al.. (2022). Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome. Frontiers in Genetics. 13. 926290–926290.
3.
Kleinfinger, Pascale, Armelle Luscan, Stéphane Serero, et al.. (2022). Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin. Genes. 13(11). 2027–2027. 5 indexed citations
4.
Kleinfinger, Pascale, Armelle Luscan, Detlef Trost, et al.. (2020). Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies. Journal of Clinical Medicine. 9(8). 2466–2466. 18 indexed citations
5.
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
6.
Mottet, Nicolas, Christelle Cabrol, Francine Arbez‐Gindre, et al.. (2018). Autopsy findings of ectodermal dysplasia and sex development disorder in a fetus with 19q12q13 microdeletion. European Journal of Medical Genetics. 62(9). 103539–103539. 2 indexed citations
7.
Lambert, Laëtitia, et al.. (2017). Syndrome de microdélétion 22q11.2 : analyse du parcours patient avant le diagnostic génétique. Archives de Pédiatrie. 24(11). 1067–1075. 5 indexed citations
8.
Valduga, Mylène, et al.. (2015). WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period. Journal of Human Genetics. 60(5). 267–271. 26 indexed citations
9.
Piard, Juliette, A Czorny, Marion Lenoir, et al.. (2015). TCF12 microdeletion in a 72‐year‐old woman with intellectual disability. American Journal of Medical Genetics Part A. 167(8). 1897–1901. 11 indexed citations
10.
Piard, Juliette, Brigitte Mignot, Francine Arbez‐Gindre, et al.. (2014). Severe sex differentiation disorder in a boy with a 3.8 Mb 10q25.3–q26.12 microdeletion encompassing EMX2. American Journal of Medical Genetics Part A. 164(10). 2618–2622. 32 indexed citations
11.
Collet, Agnès, Mikaël Agopiantz, Mylène Valduga, et al.. (2014). An adult patient with 49, XXXXY syndrome: further clinical and biological delineation. Annales de biologie clinique. 72(3). 371–377. 1 indexed citations
12.
Mosca‐Boidron, Anne‐Laure, Mylène Valduga, Christel Thauvin‐Robinet, et al.. (2013). Additional evidence to support the role of the 20q13.33 region in susceptibility to autism. American Journal of Medical Genetics Part A. 161(6). 1505–1507. 1 indexed citations
13.
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
14.
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
15.
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
16.
Valduga, Mylène, C. Philippe, Serge Romana, et al.. (2007). Prenatal diagnosis of mosaicism for 11q terminal deletion. European Journal of Medical Genetics. 50(6). 475–481. 8 indexed citations
17.
Mosca, A.L., Patrick Callier, Bruno Leheup, et al.. (2007). Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri‐du‐chat syndrome. American Journal of Medical Genetics Part A. 143A(12). 1342–1347. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by María Ángeles Mori Breakdown of academic impact, for papers by Julie Scuffins Breakdown of academic impact, for papers by Holly Feret Breakdown of academic impact, for papers by Fernando Santos Breakdown of academic impact, for papers by Radu Harbuz Breakdown of academic impact, for papers by Beth A. Torchia Breakdown of academic impact, for papers by Erika Carter Breakdown of academic impact, for papers by M B Katznelson Breakdown of academic impact, for papers by Patricia Mowery‐Rushton Breakdown of academic impact, for papers by Kimiaki Uetake
Rankless by CCL
2026