Stéphanie Valence

2.3k total citations
22 papers, 407 citations indexed

About

Stéphanie Valence is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Stéphanie Valence has authored 22 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Stéphanie Valence's work include Fetal and Pediatric Neurological Disorders (8 papers), Congenital heart defects research (3 papers) and Microtubule and mitosis dynamics (3 papers). Stéphanie Valence is often cited by papers focused on Fetal and Pediatric Neurological Disorders (8 papers), Congenital heart defects research (3 papers) and Microtubule and mitosis dynamics (3 papers). Stéphanie Valence collaborates with scholars based in France, United Kingdom and United States. Stéphanie Valence's co-authors include Nadia Bahi‐Buisson, Jamel Chelly, Karine Poirier, Yoann Saillour, Franck J. Fourniol, Nathalie Boddaert, Isabelle Souville, Chérif Beldjord, Nicolas Lebrun and Marie Hully and has published in prestigious journals such as Brain, Neurology and Epilepsia.

In The Last Decade

Stéphanie Valence

19 papers receiving 401 citations

Peers

Stéphanie Valence
Renske Oegema Netherlands
Jillian M. Felie United States
Danielle Gleason United States
Kristin Petras United States
Sébastien Moutton France
Sanne M. C. Savelberg Netherlands
Denia Ramirez‐Montealegre United States
Tatjana Bierhals Germany
Marc D’Hooghe Belgium
Antonio Vitobello France
Renske Oegema Netherlands
Stéphanie Valence
Citations per year, relative to Stéphanie Valence Stéphanie Valence (= 1×) peers Renske Oegema

Countries citing papers authored by Stéphanie Valence

Since Specialization
Citations

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

Fields of papers citing papers by Stéphanie Valence

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Valence

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

All Works

20 of 20 papers shown
1.
2.
Valence, Stéphanie, Saskia Vande Perre, Ferdinand Dhombres, et al.. (2024). Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up. Prenatal Diagnosis. 44(1). 35–48. 1 indexed citations
3.
Garel, Cathérine, Z. Leibovitz, Stéphanie Valence, et al.. (2023). Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation. American Journal of Neuroradiology. 44(3). 334–340.
4.
Lefebvre, Mathilde, A. Gélot, Solveig Heide, et al.. (2023). First reports of fetal SMARCC1 related hydrocephalus. European Journal of Medical Genetics. 66(8). 104797–104797. 1 indexed citations
5.
Valence, Stéphanie, Lucie Guilbaud, Marie‐Laure Moutard, et al.. (2022). Prenatal diagnosis of vermian cyst: a new type of posterior fossa cyst. Pediatric Radiology. 53(3). 461–469. 2 indexed citations
6.
Patat, Olivier, Sandra Whalen, Lionel Arnaud, et al.. (2021). Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome. Journal of Medical Genetics. 59(5). 505–510. 8 indexed citations
7.
Taytard, Jessica, Stéphanie Valence, Chiara Siléo, et al.. (2020). Severe central apnea secondary to cerebellar dysplasia in a child: look past Joubert syndrome. Journal of Clinical Sleep Medicine. 16(12). 2113–2116. 5 indexed citations
8.
Titheradge, Hannah, Nicola Cooper, Frances Elmslie, et al.. (2020). Expanding the genotype–phenotype correlation ofde novoheterozygous missense variants inYWHAGas a cause of developmental and epileptic encephalopathy. American Journal of Medical Genetics Part A. 182(4). 713–720. 14 indexed citations
9.
Valence, Stéphanie, Hélène Maurey, Sarah Weckhuysen, et al.. (2019). Three novel patients with epileptic encephalopathy due to biallelic mutations in the PLCB1 gene. Clinical Genetics. 97(3). 477–482. 11 indexed citations
10.
Fiévet, Alice, Dorine Bellanger, Stéphanie Valence, et al.. (2019). Three new cases of ataxia‐telangiectasia‐like disorder: No impairment of the ATM pathway, but S‐phase checkpoint defect. Human Mutation. 40(10). 1690–1699. 18 indexed citations
11.
Titheradge, Hannah, Nicola Cooper, Frances Elmslie, et al.. (2019). De novo, heterozygous missense variants in YWHAG as a novel cause of developmental and epileptic encephalopathy. White Rose Research Online (University of Leeds, The University of Sheffield, University of York). 1 indexed citations
12.
Halbertsma, Feico J. J., Francjan J. van Spronsen, Roelineke J. Lunsing, et al.. (2018). Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?. European Journal of Paediatric Neurology. 22(4). 662–666. 11 indexed citations
13.
Blondiaux, Éléonore, Stéphanie Valence, Stéphanie Friszer, et al.. (2017). Prenatal Imaging Findings of Pontine Tegmental Cap Dysplasia: Report of Four Cases. Fetal Diagnosis and Therapy. 45(3). 197–204. 12 indexed citations
14.
Blondiaux, Éléonore, Lydia Chougar, A. Gélot, et al.. (2017). Developmental patterns of fetal fat and corresponding signal on T1-weighted magnetic resonance imaging. Pediatric Radiology. 48(3). 317–324. 13 indexed citations
15.
Guët, Agnès, Névéna Danékova, Stéphanie Valence, et al.. (2017). Poor tolerance of ketogenic diet for suspicion of PDH deficiency: What about another diagnosis?. European Journal of Paediatric Neurology. 21. e134–e134. 2 indexed citations
16.
Valence, Stéphanie, Cathérine Garel, Annick Toutain, et al.. (2016). RELN and VLDLR mutations underlie two distinguishable clinico‐radiological phenotypes. Clinical Genetics. 90(6). 545–549. 22 indexed citations
17.
Poirier, Karine, Jelena Martinović, A. Laquérrière, et al.. (2015). Rare ACTG1 variants in fetal microlissencephaly. European Journal of Medical Genetics. 58(8). 416–418. 22 indexed citations
18.
Bahi‐Buisson, Nadia, Karine Poirier, Franck J. Fourniol, et al.. (2014). The wide spectrum of tubulinopathies: what are the key features for the diagnosis?. Brain. 137(6). 1676–1700. 190 indexed citations
19.
Valence, Stéphanie, Karine Poirier, Nicolas Lebrun, et al.. (2013). Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria. Neurogenetics. 14(3-4). 215–224. 21 indexed citations
20.
Poirier, Karine, Yoann Saillour, Franck J. Fourniol, et al.. (2012). Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria. European Journal of Human Genetics. 21(4). 381–385. 50 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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