Fiona Francis - Publications

Institut du Fer-à-Moulin  

26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Romero DM, Zaidi D, Cifuentes-Diaz C, Maillard C, Grannec G, Selloum M, Birling MC, Bahi-Buisson N, Francis F. A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture. Neurobiology of Disease. 180: 106085. PMID 36933672 DOI: 10.1016/j.nbd.2023.106085  0.321
2022 Zaidi D, Chinnappa K, Francis F. Primary Cilia Influence Progenitor Function during Cortical Development. Cells. 11. PMID 36139475 DOI: 10.3390/cells11182895  0.529
2022 Romero DM, Poirier K, Belvindrah R, Moutkine I, Houllier A, LeMoing AG, Petit F, Boland A, Collins SC, Soiza-Reilly M, Yalcin B, Chelly J, Deleuze JF, Bahi-Buisson N, Francis F. Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development. Nature Communications. 13: 2746. PMID 35585091 DOI: 10.1038/s41467-022-30443-z  0.372
2022 Jabali A, Hoffrichter A, Uzquiano A, Marsoner F, Wilkens R, Siekmann M, Bohl B, Rossetti AC, Horschitz S, Koch P, Francis F, Ladewig J. Human cerebral organoids reveal progenitor pathology in EML1-linked cortical malformation. Embo Reports. e54027. PMID 35289477 DOI: 10.15252/embr.202154027  0.338
2021 Penisson M, Jin M, Wang S, Hirotsune S, Francis F, Belvindrah R. Lis1 mutation prevents basal radial glia-like cell production in the mouse. Human Molecular Genetics. PMID 34635911 DOI: 10.1093/hmg/ddab295  0.335
2021 Klingler E, Francis F, Jabaudon D, Cappello S. Mapping the molecular and cellular complexity of cortical malformations. Science (New York, N.Y.). 371. PMID 33479124 DOI: 10.1126/science.aba4517  0.383
2020 Ferent J, Zaidi D, Francis F. Extracellular Control of Radial Glia Proliferation and Scaffolding During Cortical Development and Pathology. Frontiers in Cell and Developmental Biology. 8: 578341. PMID 33178693 DOI: 10.3389/fcell.2020.578341  0.47
2020 Francis F, Cappello S. Neuronal migration and disorders - an update. Current Opinion in Neurobiology. 66: 57-68. PMID 33096394 DOI: 10.1016/j.conb.2020.10.002  0.43
2020 Ferent J, Zaidi D, Francis F. Extracellular Control of Radial Glia Proliferation and Scaffolding During Cortical Development and Pathology Frontiers in Cell and Developmental Biology. 8. DOI: 10.3389/fcell.2020.578341  0.463
2019 Penisson M, Ladewig J, Belvindrah R, Francis F. Genes and Mechanisms Involved in the Generation and Amplification of Basal Radial Glial Cells. Frontiers in Cellular Neuroscience. 13: 381. PMID 31481878 DOI: 10.3389/fncel.2019.00381  0.368
2019 Uzquiano A, Cifuentes-Diaz C, Jabali A, Romero DM, Houllier A, Dingli F, Maillard C, Boland A, Deleuze JF, Loew D, Mancini GMS, Bahi-Buisson N, Ladewig J, Francis F. Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia. Cell Reports. 28: 1596-1611.e10. PMID 31390572 DOI: 10.1016/j.celrep.2019.06.096  0.36
2019 Collins SC, Uzquiano A, Selloum M, Wendling O, Gaborit M, Osipenko M, Birling MC, Yalcin B, Francis F. The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia. Journal of Anatomy. PMID 31173351 DOI: 10.1111/joa.13013  0.345
2018 Uzquiano A, Gladwyn-Ng I, Nguyen L, Reiner O, Götz M, Matsuzaki F, Francis F. Cortical progenitor biology: key features mediating proliferation versus differentiation. Journal of Neurochemistry. PMID 29570795 DOI: 10.1111/Jnc.14338  0.445
2017 Bizzotto S, Uzquiano A, Dingli F, Ershov D, Houllier A, Arras G, Richards M, Loew D, Minc N, Croquelois A, Houdusse A, Francis F. Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex. Scientific Reports. 7: 17308. PMID 29229923 DOI: 10.1038/S41598-017-15253-4  0.401
2017 Romero DM, Bahi-Buisson N, Francis F. Genetics and mechanisms leading to human cortical malformations. Seminars in Cell & Developmental Biology. PMID 28951247 DOI: 10.1016/j.semcdb.2017.09.031  0.391
2017 Belvindrah R, Natarajan K, Shabajee P, Bruel-Jungerman E, Bernard J, Goutierre M, Moutkine I, Jaglin XH, Savariradjane M, Irinopoulou T, Poncer JC, Janke C, Francis F. Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration. The Journal of Cell Biology. PMID 28687665 DOI: 10.1083/Jcb.201607074  0.323
2015 Stouffer MA, Golden JA, Francis F. Neuronal migration disorders: Focus on the cytoskeleton and epilepsy. Neurobiology of Disease. PMID 26299390 DOI: 10.1016/j.nbd.2015.08.003  0.39
2015 Bizzotto S, Francis F. Morphological and functional aspects of progenitors perturbed in cortical malformations. Frontiers in Cellular Neuroscience. 9: 30. PMID 25729350 DOI: 10.3389/fncel.2015.00030  0.404
2014 Cid E, Gomez-Dominguez D, Martin-Lopez D, Gal B, Laurent F, Ibarz JM, Francis F, Menendez de la Prida L. Dampened hippocampal oscillations and enhanced spindle activity in an asymptomatic model of developmental cortical malformations. Frontiers in Systems Neuroscience. 8: 50. PMID 24782720 DOI: 10.3389/fnsys.2014.00050  0.317
2014 Saillour Y, Broix L, Bruel-Jungerman E, Lebrun N, Muraca G, Rucci J, Poirier K, Belvindrah R, Francis F, Chelly J. Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown. Human Molecular Genetics. 23: 1516-26. PMID 24179174 DOI: 10.1093/hmg/ddt538  0.462
2011 Bruel-Jungerman E, Lucassen PJ, Francis F. Cholinergic influences on cortical development and adult neurogenesis. Behavioural Brain Research. 221: 379-88. PMID 21272598 DOI: 10.1016/J.Bbr.2011.01.021  0.461
2006 Kappeler C, Saillour Y, Baudoin JP, Tuy FP, Alvarez C, Houbron C, Gaspar P, Hamard G, Chelly J, Métin C, Francis F. Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice. Human Molecular Genetics. 15: 1387-400. PMID 16571605 DOI: 10.1093/Hmg/Ddl062  0.343
2006 Molnár Z, Métin C, Stoykova A, Tarabykin V, Price DJ, Francis F, Meyer G, Dehay C, Kennedy H. Comparative aspects of cerebral cortical development. The European Journal of Neuroscience. 23: 921-34. PMID 16519657 DOI: 10.1111/J.1460-9568.2006.04611.X  0.503
2006 Francis F, Meyer G, Fallet-Bianco C, Moreno S, Kappeler C, Socorro AC, Tuy FP, Beldjord C, Chelly J. Human disorders of cortical development: from past to present. The European Journal of Neuroscience. 23: 877-93. PMID 16519653 DOI: 10.1111/J.1460-9568.2006.04649.X  0.381
2004 Poirier K, Van Esch H, Friocourt G, Saillour Y, Bahi N, Backer S, Souil E, Castelnau-Ptakhine L, Beldjord C, Francis F, Bienvenu T, Chelly J. Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons. Brain Research. Molecular Brain Research. 122: 35-46. PMID 14992814 DOI: 10.1016/j.molbrainres.2003.11.021  0.311
1999 Francis F, Koulakoff A, Boucher D, Chafey P, Schaar B, Vinet MC, Friocourt G, McDonnell N, Reiner O, Kahn A, McConnell SK, Berwald-Netter Y, Denoulet P, Chelly J. Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons. Neuron. 23: 247-56. PMID 10399932 DOI: 10.1016/S0896-6273(00)80777-1  0.358
Show low-probability matches.