| 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 |
0.527 |
|
| 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 |
0.371 |
|
| 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 |
0.337 |
|
| 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 |
0.334 |
|
| 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 |
0.471 |
|
| 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 |
0.429 |
|
| 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 |
0.464 |
|
| 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 |
0.367 |
|
| 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 |
0.359 |
|
| 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 |
0.444 |
|
| 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 |
0.4 |
|
| 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 |
0.39 |
|
| 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 |
0.322 |
|
| 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 |
0.403 |
|
| 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 |
0.316 |
|
| 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 |
0.46 |
|
| 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 |
0.459 |
|
| 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 |
0.342 |
|
| 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 |
0.502 |
|
| 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 |
0.357 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2015 |
Bourgeois F, Messéant J, Kordeli E, Petit JM, Delers P, Bahi-Buisson N, Bernard V, Sigoillot SM, Gitiaux C, Stouffer M, Francis F, Legay C. A critical and previously unsuspected role for doublecortin at the neuromuscular junction in mouse and human. Neuromuscular Disorders : Nmd. 25: 461-73. PMID 25817838 DOI: 10.1016/j.nmd.2015.01.012 |
0.299 |
|
| 2013 |
Khalaf-Nazzal R, Bruel-Jungerman E, Rio JP, Bureau J, Irinopoulou T, Sumia I, Roumegous A, Martin E, Olaso R, Parras C, Cifuentes-Diaz C, Francis F. Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice. Plos One. 8: e72622. PMID 24023755 DOI: 10.1371/journal.pone.0072622 |
0.287 |
|
| 2023 |
Vermoyal JC, Hardy D, Goirand-Lopez L, Vinck A, Silvagnoli L, Fortoul A, Francis F, Cappello S, Bureau I, Represa A, Cardoso C, Watrin F, Marissal T, Manent JB. Grey matter heterotopia subtypes show specific morpho-electric signatures and network dynamics. Brain : a Journal of Neurology. PMID 37724593 DOI: 10.1093/brain/awad318 |
0.285 |
|
| 2014 |
Kielar M, Tuy FP, Bizzotto S, Lebrand C, de Juan Romero C, Poirier K, Oegema R, Mancini GM, Bahi-Buisson N, Olaso R, Le Moing AG, Boutourlinsky K, Boucher D, Carpentier W, Berquin P, ... ... Francis F, et al. Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human. Nature Neuroscience. 17: 923-33. PMID 24859200 DOI: 10.1038/Nn.3729 |
0.285 |
|
| 2017 |
Broix L, Asselin L, Silva CG, Ivanova EL, Tilly P, Gilet JG, Lebrun N, Jagline H, Muraca G, Saillour Y, Drouot N, Reilly ML, Francis F, Benmerah A, Bahi-Buisson N, et al. Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development. Human Molecular Genetics. PMID 29077851 DOI: 10.1093/Hmg/Ddx384 |
0.279 |
|
| 2008 |
Fallet-Bianco C, Loeuillet L, Poirier K, Loget P, Chapon F, Pasquier L, Saillour Y, Beldjord C, Chelly J, Francis F. Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A. Brain : a Journal of Neurology. 131: 2304-20. PMID 18669490 DOI: 10.1093/brain/awn155 |
0.275 |
|
| 2013 |
Poirier K, Lebrun N, Broix L, Tian G, Saillour Y, Boscheron C, Parrini E, Valence S, Pierre BS, Oger M, Lacombe D, Geneviève D, Fontana E, Darra F, Cances C, ... ... Francis F, et al. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. Nature Genetics. 45: 639-47. PMID 23603762 DOI: 10.1038/Ng.2613 |
0.274 |
|
| 2018 |
Francis F, Belvindrah R. Tubulin diversity and neuronal migration. Cell Cycle (Georgetown, Tex.). 1-5. PMID 29460664 DOI: 10.1080/15384101.2018.1439822 |
0.274 |
|
| 2005 |
Friocourt G, Kappeler C, Saillour Y, Fauchereau F, Rodriguez MS, Bahi N, Vinet MC, Chafey P, Poirier K, Taya S, Wood SA, Dargemont C, Francis F, Chelly J. Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes. Molecular and Cellular Neurosciences. 28: 153-64. PMID 15607950 DOI: 10.1016/j.mcn.2004.09.005 |
0.27 |
|
| 2013 |
Khalaf-Nazzal R, Francis F. Hippocampal development - old and new findings. Neuroscience. 248: 225-42. PMID 23756184 DOI: 10.1016/j.neuroscience.2013.05.061 |
0.262 |
|
| 2016 |
Khalaf-Nazzal R, Stouffer MA, Olaso R, Muresan L, Roumegous A, Lavilla V, Carpentier W, Moutkine I, Dumont S, Albaud B, Cagnard N, Roest Crollius H, Francis F. Early born neurons are abnormally positioned in the doublecortin knockout hippocampus. Human Molecular Genetics. PMID 28007902 DOI: 10.1093/hmg/ddw370 |
0.259 |
|
| 2013 |
Poirier K, Lebrun N, Broix L, Tian G, Saillour Y, Boscheron C, Parrini E, Valence S, Pierre BS, Oger M, Lacombe D, Geneviève D, Fontana E, Darra F, Cances C, ... ... Francis F, et al. Erratum: Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly (Nature Genetics (2013) 45 (639-647)) Nature Genetics. 45. DOI: 10.1038/Ng0813-962B |
0.258 |
|
| 2012 |
Bazelot M, Simonnet J, Dinocourt C, Bruel-Jungerman E, Miles R, Fricker D, Francis F. Cellular anatomy, physiology and epileptiform activity in the CA3 region of Dcx knockout mice: a neuronal lamination defect and its consequences. The European Journal of Neuroscience. 35: 244-56. PMID 22250815 DOI: 10.1111/J.1460-9568.2011.07962.X |
0.254 |
|
| 2006 |
Moores CA, Perderiset M, Kappeler C, Kain S, Drummond D, Perkins SJ, Chelly J, Cross R, Houdusse A, Francis F. Distinct roles of doublecortin modulating the microtubule cytoskeleton. The Embo Journal. 25: 4448-57. PMID 16957770 DOI: 10.1038/Sj.Emboj.7601335 |
0.252 |
|
| 2022 |
Brault JB, Bardin S, Lampic M, Carpentieri JA, Coquand L, Penisson M, Lachuer H, Victoria GS, Baloul S, El Marjou F, Boncompain G, Miserey-Lenkei S, Belvindrah R, Fraisier V, Francis F, et al. RAB6 and dynein drive post-Golgi apical transport to prevent neuronal progenitor delamination. Embo Reports. e54605. PMID 35979738 DOI: 10.15252/embr.202254605 |
0.252 |
|
| 2015 |
Dhaliwal J, Xi Y, Bruel-Jungerman E, Germain J, Francis F, Lagace DC. Doublecortin (DCX) is not Essential for Survival and Differentiation of Newborn Neurons in the Adult Mouse Dentate Gyrus. Frontiers in Neuroscience. 9: 494. PMID 26793044 DOI: 10.3389/Fnins.2015.00494 |
0.251 |
|
| 2002 |
des Portes V, Abaoub L, Joannard A, Souville I, Francis F, Pinard JM, Chelly J, Beldjord C, Jouk PS. So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation. Seizure. 11: 273-7. PMID 12027577 DOI: 10.1053/seiz.2001.0607 |
0.251 |
|
| 2004 |
Moores CA, Perderiset M, Francis F, Chelly J, Houdusse A, Milligan RA. Mechanism of microtubule stabilization by doublecortin. Molecular Cell. 14: 833-9. PMID 15200960 DOI: 10.1016/J.Molcel.2004.06.009 |
0.243 |
|
| 2010 |
Tian G, Jaglin XH, Keays DA, Francis F, Chelly J, Cowan NJ. Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway. Human Molecular Genetics. 19: 3599-613. PMID 20603323 DOI: 10.1093/Hmg/Ddq276 |
0.237 |
|
| 2003 |
Friocourt G, Koulakoff A, Chafey P, Boucher D, Fauchereau F, Chelly J, Francis F. Doublecortin functions at the extremities of growing neuronal processes. Cerebral Cortex (New York, N.Y. : 1991). 13: 620-6. PMID 12764037 |
0.235 |
|
| 2014 |
Belvindrah R, Nosten-Bertrand M, Francis F. Neuronal migration and its disorders affecting the CA3 region. Frontiers in Cellular Neuroscience. 8: 63. PMID 24624057 DOI: 10.3389/fncel.2014.00063 |
0.224 |
|
| 1998 |
des Portes V, Francis F, Pinard JM, Desguerre I, Moutard ML, Snoeck I, Meiners LC, Capron F, Cusmai R, Ricci S, Motte J, Echenne B, Ponsot G, Dulac O, Chelly J, et al. doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH). Human Molecular Genetics. 7: 1063-70. PMID 9618162 DOI: 10.1093/hmg/7.7.1063 |
0.221 |
|
| 2007 |
Kappeler C, Dhenain M, Phan Dinh Tuy F, Saillour Y, Marty S, Fallet-Bianco C, Souville I, Souil E, Pinard JM, Meyer G, Encha-Razavi F, Volk A, Beldjord C, Chelly J, Francis F. Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. The Journal of Comparative Neurology. 500: 239-54. PMID 17111359 DOI: 10.1002/Cne.21170 |
0.207 |
|
| 2014 |
Kielar M, Phan Dinh Tuy F, Bizzotto S, Belvindrah R, Croquelois A, Francis F. [Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human]. MéDecine Sciences : M/S. 30: 1087-90. PMID 25537038 DOI: 10.1051/medsci/20143012011 |
0.199 |
|
| 2022 |
Atherton J, Stouffer M, Francis F, Moores CA. Visualising the cytoskeletal machinery in neuronal growth cones using cryo-electron tomography. Journal of Cell Science. 135. PMID 35383828 DOI: 10.1242/jcs.259234 |
0.189 |
|
| 2008 |
Tuy FP, Saillour Y, Kappeler C, Chelly J, Francis F. Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout mice. Developmental Neuroscience. 30: 171-86. PMID 18075264 DOI: 10.1159/000109861 |
0.179 |
|
| 2002 |
Bienvenu T, Poirier K, Friocourt G, Bahi N, Beaumont D, Fauchereau F, Ben Jeema L, Zemni R, Vinet MC, Francis F, Couvert P, Gomot M, Moraine C, van Bokhoven H, Kalscheuer V, et al. ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation. Human Molecular Genetics. 11: 981-91. PMID 11971879 |
0.176 |
|
| 2018 |
Atherton J, Stouffer M, Francis F, Moores CA. Microtubule architecture in vitro and in cells revealed by cryo-electron tomography. Acta Crystallographica. Section D, Structural Biology. 74: 572-584. PMID 29872007 DOI: 10.1107/S2059798318001948 |
0.172 |
|
| 2011 |
Fourniol F, Sindelar CV, Amigues B, Clare DK, Thomas G, Perderiset M, Francis F, Houdusse A, Moores CA. Template-Free 13-Protofilament Microtubule-Map Assembly Visualised at 8Å Resolution Biophysical Journal. 100: 4-9. DOI: 10.1016/J.Bpj.2010.12.2644 |
0.168 |
|
| 2010 |
Fourniol FJ, Sindelar CV, Amigues B, Clare DK, Thomas G, Perderiset M, Francis F, Houdusse A, Moores CA. Template-free 13-protofilament microtubule-MAP assembly visualized at 8 A resolution. The Journal of Cell Biology. 191: 463-70. PMID 20974813 DOI: 10.1083/Jcb.201007081 |
0.166 |
|
| 2019 |
Oegema R, McGillivray G, Leventer R, Le Moing AG, Bahi-Buisson N, Barnicoat A, Mandelstam S, Francis D, Francis F, Mancini GMS, Savelberg S, van Haaften G, Mankad K, Lequin MH. EML1-associated brain overgrowth syndrome with ribbon-like heterotopia. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 31710781 DOI: 10.1002/ajmg.c.31751 |
0.165 |
|
| 2007 |
Poirier K, Keays DA, Francis F, Saillour Y, Bahi N, Manouvrier S, Fallet-Bianco C, Pasquier L, Toutain A, Tuy FP, Bienvenu T, Joriot S, Odent S, Ville D, Desguerre I, et al. Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). Human Mutation. 28: 1055-64. PMID 17584854 DOI: 10.1002/humu.20572 |
0.161 |
|
| 1999 |
Horesh D, Sapir T, Francis F, Wolf SG, Caspi M, Elbaum M, Chelly J, Reiner O. Doublecortin, a stabilizer of microtubules. Human Molecular Genetics. 8: 1599-610. PMID 10441322 DOI: 10.1093/Hmg/8.9.1599 |
0.158 |
|
| 2000 |
Zemni R, Bienvenu T, Vinet MC, Sefiani A, Carrié A, Billuart P, McDonell N, Couvert P, Francis F, Chafey P, Fauchereau F, Friocourt G, des Portes V, Cardona A, Frints S, et al. A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Nature Genetics. 24: 167-70. PMID 10655063 DOI: 10.1038/72829 |
0.155 |
|
| 2013 |
Kremer T, Jagasia R, Herrmann A, Matile H, Borroni E, Francis F, Kuhn HG, Czech C. Analysis of adult neurogenesis: evidence for a prominent "non-neurogenic" DCX-protein pool in rodent brain. Plos One. 8: e59269. PMID 23690918 DOI: 10.1371/journal.pone.0059269 |
0.155 |
|
| 2008 |
Nosten-Bertrand M, Kappeler C, Dinocourt C, Denis C, Germain J, Phan Dinh Tuy F, Verstraeten S, Alvarez C, Métin C, Chelly J, Giros B, Miles R, Depaulis A, Francis F. Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus. Plos One. 3: e2473. PMID 18575605 DOI: 10.1371/Journal.Pone.0002473 |
0.152 |
|
| 2013 |
Poirier K, Saillour Y, Fourniol F, Francis F, Souville I, Valence S, Desguerre I, Marie Lepage J, Boddaert N, Line Jacquemont M, Beldjord C, Chelly J, Bahi-Buisson N. Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria. European Journal of Human Genetics : Ejhg. 21: 381-5. PMID 22948023 DOI: 10.1038/ejhg.2012.195 |
0.151 |
|
| 2000 |
Sapir T, Horesh D, Caspi M, Atlas R, Burgess HA, Wolf SG, Francis F, Chelly J, Elbaum M, Pietrokovski S, Reiner O. Doublecortin mutations cluster in evolutionarily conserved functional domains. Human Molecular Genetics. 9: 703-12. PMID 10749977 DOI: 10.1093/Hmg/9.5.703 |
0.14 |
|
| 2019 |
Penisson M, Ladewig J, Belvindrah R, Francis F. Corrigendum: Genes and Mechanisms Involved in the Generation and Amplification of Basal Radial Glial Cells. Frontiers in Cellular Neuroscience. 13: 462. PMID 31695596 DOI: 10.3389/fncel.2019.00462 |
0.14 |
|
| 2013 |
Germain J, Bruel-Jungerman E, Grannec G, Denis C, Lepousez G, Giros B, Francis F, Nosten-Bertrand M. Doublecortin knockout mice show normal hippocampal-dependent memory despite CA3 lamination defects. Plos One. 8: e74992. PMID 24073232 DOI: 10.1371/Journal.Pone.0074992 |
0.136 |
|
| 2014 |
Hamelin S, Pouyatos B, Khalaf-Nazzal R, Chabrol T, Francis F, David O, Depaulis A. Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse. Neurobiology of Disease. 69: 156-68. PMID 24874545 DOI: 10.1016/J.Nbd.2014.05.025 |
0.12 |
|
| 2024 |
Francis FT, Burke L, Marliave J, Schultz J, Borden L, Weltman A, Dunham A. Fishing damage to cloud sponges may lead to losses in associated fish communities in Pacific Canada. Marine Environmental Research. 197: 106448. PMID 38518407 DOI: 10.1016/j.marenvres.2024.106448 |
0.12 |
|
| 2003 |
Moores CA, Francis F, Perderiset M, Houdusse A. A double-take on MAPs. Nature Structural Biology. 10: 314-6. PMID 12714997 DOI: 10.1038/Nsb0503-314 |
0.119 |
|
| 2013 |
Bahi-Buisson N, Souville I, Fourniol FJ, Toussaint A, Moores CA, Houdusse A, Lemaitre JY, Poirier K, Khalaf-Nazzal R, Hully M, Leger PL, Elie C, Boddaert N, Beldjord C, Chelly J, ... Francis F, et al. New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum. Brain : a Journal of Neurology. 136: 223-44. PMID 23365099 DOI: 10.1093/Brain/Aws323 |
0.118 |
|
| 2006 |
Chelly J, Khelfaoui M, Francis F, Chérif B, Bienvenu T. Genetics and pathophysiology of mental retardation. European Journal of Human Genetics : Ejhg. 14: 701-13. PMID 16721406 DOI: 10.1038/sj.ejhg.5201595 |
0.116 |
|
| 2001 |
Friocourt G, Chafey P, Billuart P, Koulakoff A, Vinet MC, Schaar BT, McConnell SK, Francis F, Chelly J. Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous system. Molecular and Cellular Neurosciences. 18: 307-19. PMID 11591131 DOI: 10.1006/mcne.2001.1022 |
0.114 |
|
| 2019 |
Bose APH, Zayonc D, Avrantinis N, Ficzycz N, Fischer-Rush J, Francis FT, Gray S, Manning F, Robb H, Schmidt C, Spice C, Umedaly A, Warden J, Côté IM. Effects of handling and short-term captivity: a multi-behaviour approach using red sea urchins, . Peerj. 7: e6556. PMID 30918753 DOI: 10.7717/peerj.6556 |
0.113 |
|
| 2015 |
Gottfried C, Bambini-Junior V, Francis F, Riesgo R, Savino W. The Impact of Neuroimmune Alterations in Autism Spectrum Disorder. Frontiers in Psychiatry. 6: 121. PMID 26441683 DOI: 10.3389/fpsyt.2015.00121 |
0.107 |
|
| 2008 |
Leger PL, Souville I, Boddaert N, Elie C, Pinard JM, Plouin P, Moutard ML, des Portes V, Van Esch H, Joriot S, Renard JL, Chelly J, Francis F, Beldjord C, Bahi-Buisson N. The location of DCX mutations predicts malformation severity in X-linked lissencephaly. Neurogenetics. 9: 277-85. PMID 18685874 DOI: 10.1007/s10048-008-0141-5 |
0.107 |
|
| 2024 |
Klingler E, Govindan S, Francis F. Editorial: Advances and challenges in studying brain disorders: from development to aging. Frontiers in Neuroscience. 18: 1341410. PMID 38348132 DOI: 10.3389/fnins.2024.1341410 |
0.09 |
|
| 2003 |
Leneuve P, Colnot S, Hamard G, Francis F, Niwa-Kawakita M, Giovannini M, Holzenberger M. Cre-mediated germline mosaicism: a new transgenic mouse for the selective removal of residual markers from tri-lox conditional alleles. Nucleic Acids Research. 31: e21. PMID 12595570 DOI: 10.1093/Nar/Gng021 |
0.089 |
|
| 2019 |
Uzquiano A, Francis F. Rotatin' the phenotypes. Brain : a Journal of Neurology. 142: 834-838. PMID 30946475 DOI: 10.1093/brain/awz048 |
0.055 |
|
| 1999 |
Filisetti D, Ostermann G, von Bredow M, Strom T, Filler G, Ehrich J, Pannetier S, Garnier JM, Rowe P, Francis F, Julienne A, Hanauer A, Econs MJ, Oudet C. Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues. European Journal of Human Genetics : Ejhg. 7: 615-9. PMID 10439971 DOI: 10.1038/sj.ejhg.5200341 |
0.044 |
|
| 2013 |
Germain J, Bruel-Jungerman E, Grannec G, Denis C, Lepousez G, Giros B, Francis F, Nosten-Bertrand M. Abnormal social interaction and reduced aggressive behavior in the Dcx-KO mice. A/Spontaneous social interaction Plos One. DOI: 10.1371/Journal.Pone.0074992.G005 |
0.042 |
|
| 2005 |
Poirier K, Francis F, Hamel B, Moraine C, Fryns JP, Ropers HH, Chelly J, Bienvenu T. Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males [1] European Journal of Human Genetics. 13: 523-524. PMID 15770224 DOI: 10.1038/sj.ejhg.5201399 |
0.035 |
|
| 2005 |
Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, ... ... Francis F, et al. The DNA sequence of the human X chromosome. Nature. 434: 325-37. PMID 15772651 DOI: 10.1038/Nature03440 |
0.034 |
|
| 2019 |
Francis FT, Howard BR, Berchtold AE, Branch TA, Chaves LCT, Dunic JC, Favaro B, Jeffrey KM, Malpica-Cruz L, Maslowski N, Schultz JA, Smith NS, Côté IM. Shifting headlines? Size trends of newsworthy fishes. Peerj. 7: e6395. PMID 30783570 DOI: 10.7717/Peerj.6395 |
0.01 |
|
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