Yoann Saillour
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Explore the profile of Yoann Saillour including associated specialties, affiliations and a list of published articles.
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39
Citations
1548
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Recent Articles
1.
Riva M, Ferreira S, Hayashi K, Saillour Y, Medvedeva V, Honda T, et al.
J Clin Invest
. 2024 Jul;
134(16).
PMID: 38980724
Reelin (RELN) is a secreted glycoprotein essential for cerebral cortex development. In humans, recessive RELN variants cause cortical and cerebellar malformations, while heterozygous variants were associated with epilepsy, autism, and...
2.
Moreau M, Saillour Y, Elorriaga V, Bouloudi B, Delberghe E, Deutsch Guerrero T, et al.
Dev Cell
. 2023 Jun;
58(15):1365-1382.e6.
PMID: 37321213
Cajal-Retzius cells (CRs) are key players in cerebral cortex development, and they display a unique transcriptomic identity. Here, we use scRNA-seq to reconstruct the differentiation trajectory of mouse hem-derived CRs,...
3.
Moreau M, Saillour Y, Cwetsch A, Pierani A, Causeret F
Development
. 2021 Jun;
148(14).
PMID: 34170322
In the developing cerebral cortex, how progenitors that seemingly display limited diversity end up producing a vast array of neurons remains a puzzling question. The prevailing model suggests that temporal...
4.
Ben Miled S, Loeuillet L, Duong van Huyen J, Bessieres B, Sekour A, Leroy B, et al.
Am J Obstet Gynecol
. 2020 Apr;
223(2):256.e1-256.e9.
PMID: 32283072
Background: Despite undisputable benefits, midtrimester prenatal surgery is not a cure for myelomeningocele (MMC): residual intracranial and motor deficits leading to lifelong handicap question the timing of prenatal surgery. Indeed,...
5.
Pillet L, Cresto N, Saillour Y, Ghezali G, Bemelmans A, Livet J, et al.
Glia
. 2020 Feb;
68(9):1729-1742.
PMID: 32073702
Astrocytes are involved in several aspects of neuronal development and properties which are altered in intellectual disability (ID). Oligophrenin-1 is a RhoGAP protein implicated in actin cytoskeleton regulation, and whose...
6.
Arai Y, Cwetsch A, Coppola E, Cipriani S, Nishihara H, Kanki H, et al.
Cell Rep
. 2019 Oct;
29(3):645-658.e5.
PMID: 31618633
Changes in transcriptional regulation through cis-regulatory elements are thought to drive brain evolution. However, how this impacts the identity of primate cortical neurons is still unresolved. Here, we show that...
7.
Broix L, Asselin L, Silva C, Ivanova E, Tilly P, Gilet J, et al.
Hum Mol Genet
. 2017 Oct;
27(2):224-238.
PMID: 29077851
Genetic findings reported by our group and others showed that de novo missense variants in the KIF2A gene underlie malformations of brain development called pachygyria and microcephaly. Though KIF2A is...
8.
Montani C, Ramos-Brossier M, Ponzoni L, Gritti L, Cwetsch A, Braida D, et al.
J Neurosci
. 2017 Jun;
37(28):6606-6627.
PMID: 28576939
Mutations and deletions of the () gene, located on the X chromosome, are associated with intellectual disability (ID) and autism spectrum disorder (ASD). IL1RAPL1 protein is located at the postsynaptic...
9.
Broix L, Jagline H, Ivanova E, Schmucker S, Drouot N, Clayton-Smith J, et al.
Nat Genet
. 2016 Oct;
48(11):1349-1358.
PMID: 27694961
Neurodevelopmental disorders with periventricular nodular heterotopia (PNH) are etiologically heterogeneous, and their genetic causes remain in many cases unknown. Here we show that missense mutations in NEDD4L mapping to the...
10.
Laquerriere A, Gonzales M, Saillour Y, Cavallin M, Joye N, Quelin C, et al.
Eur J Med Genet
. 2016 Jan;
59(4):249-56.
PMID: 26732629
Tubulinopathies are increasingly emerging major causes underlying complex cerebral malformations, particularly in case of microlissencephaly often associated with hypoplastic or absent corticospinal tracts. Fetal akinesia deformation sequence (FADS) refers to...