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For: Klingler E, Francis F, Jabaudon D, Cappello S. Mapping the molecular and cellular complexity of cortical malformations. Science 2021;371:eaba4517. [PMID: 33479124 DOI: 10.1126/science.aba4517] [Cited by in Crossref: 33] [Cited by in F6Publishing: 33] [Article Influence: 16.5] [Reference Citation Analysis]
Number Citing Articles
1 Hippenmeyer S. Principles of neural stem cell lineage progression: Insights from developing cerebral cortex. Curr Opin Neurobiol 2023;79:102695. [PMID: 36842274 DOI: 10.1016/j.conb.2023.102695] [Reference Citation Analysis]
2 Pilaz LJ, Liu J, Joshi K, Tsunekawa Y, Musso CM, D'Arcy BR, Suzuki IK, Alsina FC, Kc P, Sethi S, Vanderhaeghen P, Polleux F, Silver DL. Subcellular mRNA localization and local translation of Arhgap11a in radial glial progenitors regulates cortical development. Neuron 2023;111:839-856.e5. [PMID: 36924763 DOI: 10.1016/j.neuron.2023.02.023] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Vaid S, Heikinheimo O, Namba T. Embryonic mouse medial neocortex as a model system for studying the radial glial scaffold in fetal human neocortex. J Neural Transm (Vienna) 2023;130:185-94. [PMID: 36450874 DOI: 10.1007/s00702-022-02570-w] [Reference Citation Analysis]
4 Dekker J, Schot R, Bongaerts M, de Valk WG, van Veghel-Plandsoen MM, Monfils K, Douben H, Elfferich P, Kasteleijn E, van Unen LMA, Geeven G, Saris JJ, van Ierland Y, Verheijen FW, van der Sterre MLT, Sadeghi Niaraki F, Smits DJ, Huidekoper HH, Williams M, Wilke M, Verhoeven VJM, Joosten M, Kievit AJA, van de Laar IMBH, Hoefsloot LH, Hoogeveen-Westerveld M, Nellist M, Mancini GMS, van Ham TJ. Web-accessible application for identifying pathogenic transcripts with RNA-seq: Increased sensitivity in diagnosis of neurodevelopmental disorders. Am J Hum Genet 2023;110:251-72. [PMID: 36669495 DOI: 10.1016/j.ajhg.2022.12.015] [Reference Citation Analysis]
5 Vermaercke B, Iwata R, Weirda K, Boubakar L, Rodriguez P, Ditkowska M, Bonin V, Vanderhaeghen P. SYNGAP1 deficiency disrupts neoteny in human cortical neurons in vivo.. [DOI: 10.1101/2023.01.14.524054] [Reference Citation Analysis]
6 Schütze TM, Bölicke N, Sameith K, Albert M. Profiling Cell Type-Specific Gene Regulatory Regions in Human Cortical Organoids. Neuromethods 2023. [DOI: 10.1007/978-1-0716-2720-4_2] [Reference Citation Analysis]
7 Staiger JF, Sachkova A, Möck M, Guy J, Witte M. Repetitively burst-spiking neurons in reeler mice show conserved but also highly variable morphological features of layer Vb-fated “thick-tufted” pyramidal cells. Front Neuroanat 2022;16. [DOI: 10.3389/fnana.2022.1000107] [Reference Citation Analysis]
8 Damianidou E, Mouratidou L, Kyrousi C. Research models of neurodevelopmental disorders: The right model in the right place. Front Neurosci 2022;16:1031075. [DOI: 10.3389/fnins.2022.1031075] [Reference Citation Analysis]
9 Fleck JS, Jansen SMJ, Wollny D, Zenk F, Seimiya M, Jain A, Okamoto R, Santel M, He Z, Camp JG, Treutlein B. Inferring and perturbing cell fate regulomes in human brain organoids. Nature 2022. [PMID: 36198796 DOI: 10.1038/s41586-022-05279-8] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 7.0] [Reference Citation Analysis]
10 Li C, Fleck JS, Martins-costa C, Burkard TR, Stuempflen M, Vertesy Á, Peer AM, Esk C, Elling U, Kasprian G, Corsini NS, Treutlein B, Knoblich JA. Single-cell brain organoid screening identifies developmental defects in autism.. [DOI: 10.1101/2022.09.15.508118] [Reference Citation Analysis]
11 Kirschner M, Paquola C, Khundrakpam BS, Vainik U, Bhutani N, Hodzic-santor B, Georgiadis F, Al-sharif NB, Misic B, Bernhardt B, Evans AC, Dagher A. Schizophrenia polygenic risk during typical development reflects multiscale cortical organization. Biological Psychiatry Global Open Science 2022. [DOI: 10.1016/j.bpsgos.2022.08.003] [Reference Citation Analysis]
12 Qu Y, An O, Yang H, Toh Y, En JCJ. FEZ1 participates in human embryonic brain development by modulating neuronal progenitor subpopulation specification and migration.. [DOI: 10.1101/2022.07.11.499073] [Reference Citation Analysis]
13 Saha S, Jungas T, Ohayon D, Audouard C, Ye T, Fawal M, Davy A. DHFR metabolic activity controls neurogenic transitions in the developing Human and mouse neocortex.. [DOI: 10.1101/2022.06.22.497156] [Reference Citation Analysis]
14 Dekker J, Schot R, Bongaerts M, de Valk WG, van Veghel-plandsoen MM, Monfils K, Douben H, Elfferich P, Kasteleijn E, van Unen LM, Geeven G, Saris JJ, van Ierland Y, Verheijen FW, van der Sterre ML, Niaraki FS, Huidekoper HH, Williams M, Wilke M, Verhoeven VJ, Joosten M, Kievit AJ, van de Laar IM, Hoefsloot LH, Hoogeveen-westerveld M, Nellist M, Mancini GM, van Ham TJ. RNA-sequencing improves diagnosis for neurodevelopmental disorders by identifying pathogenic non-coding variants and reinterpretation of coding variants.. [DOI: 10.1101/2022.06.05.22275956] [Reference Citation Analysis]
15 Sapir T, Sela-donenfeld D, Karlinski M, Reiner O. Brain Organization and Human Diseases. Cells 2022;11:1642. [DOI: 10.3390/cells11101642] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
16 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 Rep 2022;23:e54027. [PMID: 35289477 DOI: 10.15252/embr.202154027] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
17 Carabalona A, Kallo H, Andriichuk L, Gonzalez M, Elomaa E, Molinari F, Fragkou C, Lappalainen P, Wessels M, Saarikangas J, Rivera C. Identification of novel microcephaly-linked protein ABBA that mediates cortical progenitor cell division and corticogenesis through NEDD9-RhoA.. [DOI: 10.1101/2022.03.28.22272122] [Reference Citation Analysis]
18 Poeta L, Malacarne M, Padula A, Drongitis D, Verrillo L, Lioi MB, Chiariello AM, Bianco S, Nicodemi M, Piccione M, Salzano E, Coviello D, Miano MG. Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability. IJMS 2022;23:3084. [DOI: 10.3390/ijms23063084] [Reference Citation Analysis]
19 Ferreira A, Bressan C, Hardy SV, Saghatelyan A. Deciphering heterogeneous populations of migrating cells based on the computational assessment of their dynamic properties. Stem Cell Reports 2022:S2213-6711(22)00100-X. [PMID: 35303437 DOI: 10.1016/j.stemcr.2022.02.011] [Reference Citation Analysis]
20 Ossola C, Kalebic N. Roots of the Malformations of Cortical Development in the Cell Biology of Neural Progenitor Cells. Front Neurosci 2021;15:817218. [PMID: 35069108 DOI: 10.3389/fnins.2021.817218] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Gonzalez-Bohorquez D, Gallego López IM, Jaeger BN, Pfammatter S, Bowers M, Semenkovich CF, Jessberger S. FASN-dependent de novo lipogenesis is required for brain development. Proc Natl Acad Sci U S A 2022;119. [PMID: 34996870 DOI: 10.1073/pnas.2112040119] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
22 Becker T, Cappel C, Di Matteo F, Sonsalla G, Kaminska E, Spada F, Cappello S, Damme M, Kielkowski P. AMPylation profiling during neuronal differentiation reveals extensive variation on lysosomal proteins. iScience 2021;24:103521. [PMID: 34917898 DOI: 10.1016/j.isci.2021.103521] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
23 Yin J, Ma G, Luo S, Luo X, He B, Liang C, Zuo X, Xu X, Chen Q, Xiong S, Tan Z, Fu J, Lv D, Dai Z, Wen X, Zhu D, Ye X, Lin Z, Lin J, Li Y, Chen W, Luo Z, Li K, Wang Y. Glyoxalase 1 Confers Susceptibility to Schizophrenia: From Genetic Variants to Phenotypes of Neural Function. Front Mol Neurosci 2021;14:739526. [PMID: 34790095 DOI: 10.3389/fnmol.2021.739526] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
24 Wilsch-Bräuninger M, Huttner WB. Primary Cilia and Centrosomes in Neocortex Development. Front Neurosci 2021;15:755867. [PMID: 34744618 DOI: 10.3389/fnins.2021.755867] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
25 Konner M. Nine Levels of Explanation : A Proposed Expansion of Tinbergen's Four-Level Framework for Understanding the Causes of Behavior. Hum Nat 2021;32:748-93. [PMID: 34739657 DOI: 10.1007/s12110-021-09414-8] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Tokariev A, Breakspear M, Videman M, Stjerna S, Scholtens LH, van den Heuvel MP, Cocchi L, Vanhatalo S. Impact of In Utero Exposure to Antiepileptic Drugs on Neonatal Brain Function. Cereb Cortex 2021:bhab338. [PMID: 34585721 DOI: 10.1093/cercor/bhab338] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
27 Massimo M, Long KR. Orchestrating human neocortex development across the scales; from micro to macro. Semin Cell Dev Biol 2021:S1084-9521(21)00242-1. [PMID: 34583893 DOI: 10.1016/j.semcdb.2021.09.007] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
28 Kalebic N, Namba T. Inheritance and flexibility of cell polarity: a clue for understanding human brain development and evolution. Development 2021;148:dev199417. [PMID: 34499710 DOI: 10.1242/dev.199417] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
29 Fleck JS, Jansen SM, Wollny D, Seimiya M, Zenk F, Santel M, He Z, Gray Camp J, Treutlein B. Inferring and perturbing cell fate regulomes in human cerebral organoids.. [DOI: 10.1101/2021.08.24.457460] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]
30 Kobow K, Baulac S, von Deimling A, Lee JH. Molecular diagnostics in drug-resistant focal epilepsy define new disease entities. Brain Pathol 2021;31:e12963. [PMID: 34196984 DOI: 10.1111/bpa.12963] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
31 Kirschner M, Paquola C, Khundrakpam BS, Vainik U, Bhutani N, Hodzic-santor B, Georgiadis F, Al-sharif NB, Misic B, Bernhardt B, Evans AC, Dagher A. Schizophrenia polygenic risk during typical development reflects multiscale cortical organization.. [DOI: 10.1101/2021.06.13.448243] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
32 Limoni G. Modelling and Refining Neuronal Circuits with Guidance Cues: Involvement of Semaphorins. Int J Mol Sci 2021;22:6111. [PMID: 34204060 DOI: 10.3390/ijms22116111] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
33 Riva M, Ferreira S, Medvedeva VP, Causeret F, Henry OJ, Roux C, Bellesme C, Freri E, Parrini E, Josifova D, Guerrini R, Bahi-buisson N, Pierani A. Functional characterization of RELN missense mutations involved in recessive and dominant forms of Neuronal Migration Disorders.. [DOI: 10.1101/2021.05.25.445586] [Reference Citation Analysis]
34 Gilardi C, Kalebic N. The Ferret as a Model System for Neocortex Development and Evolution. Front Cell Dev Biol 2021;9:661759. [PMID: 33996819 DOI: 10.3389/fcell.2021.661759] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
35 Becker T, Cappel C, Matteo FD, Sonsalla G, Kaminska E, Spada F, Cappello S, Damme M, Kielkowski P. AMPylation is a specific lysosomal protein posttranslational modification in neuronal maturation.. [DOI: 10.1101/2021.03.02.433531] [Reference Citation Analysis]