Yoann Saillour

3.8k total citations
35 papers, 1.5k citations indexed

About

Yoann Saillour is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Yoann Saillour has authored 35 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 19 papers in Genetics and 8 papers in Cell Biology. Recurrent topics in Yoann Saillour's work include Genetics and Neurodevelopmental Disorders (15 papers), RNA Research and Splicing (8 papers) and Microtubule and mitosis dynamics (7 papers). Yoann Saillour is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), RNA Research and Splicing (8 papers) and Microtubule and mitosis dynamics (7 papers). Yoann Saillour collaborates with scholars based in France, United Kingdom and Italy. Yoann Saillour's co-authors include Karine Poirier, Jamel Chelly, Nadia Bahi‐Buisson, Fiona Francis, Chérif Beldjord, Nathalie Boddaert, Jamel Chelly, Nicolas Lebrun, Isabelle Souville and Catherine Fallet‐Bianco and has published in prestigious journals such as Journal of Neuroscience, Brain and Development.

In The Last Decade

Yoann Saillour

34 papers receiving 1.5k citations

Peers

Yoann Saillour

GENET

CMN

Karine Poirier France

Marie Claude Vinet France

Carlos Cardoso France

Xavier H. Jaglin United States

Konstantinos Zarbalis United States

Gökhan Uyanık Germany

Christopher A. Walsh United States

José Manuel Morante‐Redolat Spain

Holden Higginbotham United States

Mark Zervas United States

Karine Poirier France

Yoann Saillour

1.2k ×1.4

698 ×1.3

778 ×1.5

GENET

414 ×1.1

CMN

229 ×0.9

Citations per year, relative to Yoann Saillour Yoann Saillour (= 1×) peers Karine Poirier

Countries citing papers authored by Yoann Saillour

Since Specialization

Citations

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

Fields of papers citing papers by Yoann Saillour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoann Saillour

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Saillour, Yoann, Rolf W. Stottmann, Nadia Bahi‐Buisson, et al.. (2025). Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis. Development. 152(9).

Saillour, Yoann, et al.. (2021). Single-cell transcriptomics of the early developing mouse cerebral cortex disentangle the spatial and temporal components of neuronal fate acquisition. Development. 148(14). 32 indexed citations

Cresto, Noémie, Yoann Saillour, Grégory Ghézali, et al.. (2020). The intellectual disability protein Oligophrenin‐1 controls astrocyte morphology and migration. Glia. 68(9). 1729–1742. 6 indexed citations

Montani, Caterina, Mariana Ramos-Brossier, Luisa Ponzoni, et al.. (2017). The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity. Journal of Neuroscience. 37(28). 6606–6627. 34 indexed citations

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

Toussaint, Aurélie, Chrystel Leroy, Nathalie Deburgrave, et al.. (2013). Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes. European Journal of Human Genetics. 21(9). 977–987. 14 indexed citations

Saillour, Yoann, Loïc Broix, Elodie Bruel‐Jungerman, et al.. (2013). Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown. Human Molecular Genetics. 23(6). 1516–1526. 39 indexed citations

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

Quēlin, Chloé, Yoann Saillour, Isabelle Souville, et al.. (2012). Mosaic DCX deletion causes subcortical band heterotopia in males. Neurogenetics. 13(4). 367–373. 11 indexed citations

10.

Quēlin, Chloé, Yoann Saillour, Karine Poirier, et al.. (2012). Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysis. European Journal of Medical Genetics. 55(10). 527–530. 6 indexed citations

11.

Boddaert, Nathalie, Isabelle Desguerre, Nadia Bahi‐Buisson, et al.. (2010). Posterior fossa imaging in 158 children with ataxia. Journal of Neuroradiology. 37(4). 220–230. 22 indexed citations

12.

Bahi‐Buisson, Nadia, Benôıt Girard, Agnès Gautier, et al.. (2009). Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 202–207. 20 indexed citations

13.

Poirier, Karine, Monika Eisermann, Anna Kamińska, et al.. (2008). Combination of infantile spasms, non-epileptic seizures and complex movement disorder: A new case of ARX-related epilepsy. Epilepsy Research. 80(2-3). 224–228. 26 indexed citations

14.

Bahi‐Buisson, Nadia, Nathalie Boddaert, Yoann Saillour, et al.. (2008). Malformations cérébrales et épilepsie : présentations radiocliniques et implications pour le diagnostic génétique. Revue Neurologique. 164(12). 995–1009. 7 indexed citations

15.

Saillour, Yoann, Mireille Cossée, France Leturcq, et al.. (2008). Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method. Human Mutation. 29(9). 1083–1090. 37 indexed citations

16.

Bahi‐Buisson, Nadia, Karine Poirier, Nathalie Boddaert, et al.. (2008). Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations. Journal of Medical Genetics. 45(10). 647–653. 85 indexed citations

17.

Kappeler, Caroline, Yoann Saillour, Jean‐Pierre Baudoin, et al.. (2006). Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice. Human Molecular Genetics. 15(9). 1387–1400. 125 indexed citations

18.

Kappeler, Caroline, Marc Dhénain, Françoise Phan Dinh Tuy, et al.. (2006). Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. The Journal of Comparative Neurology. 500(2). 239–254. 54 indexed citations

19.

Poirier, Karine, Hilde Van Esch, Gaëlle Friocourt, et al.. (2004). Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons. Molecular Brain Research. 122(1). 35–46. 74 indexed citations

20.

Friocourt, Gaëlle, Caroline Kappeler, Yoann Saillour, et al.. (2004). Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes. Molecular and Cellular Neuroscience. 28(1). 153–164. 33 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