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For: Romaniello R, Arrigoni F, Fry AE, Bassi MT, Rees MI, Borgatti R, Pilz DT, Cushion TD. Tubulin genes and malformations of cortical development. Eur J Med Genet 2018;61:744-54. [PMID: 30016746 DOI: 10.1016/j.ejmg.2018.07.012] [Cited by in Crossref: 59] [Cited by in F6Publishing: 62] [Article Influence: 14.8] [Reference Citation Analysis]
Number Citing Articles
1 Clark LN, Gao Y, Wang GT, Hernandez N, Ashley-koch A, Jankovic J, Ottman R, Leal SM, Rodriguez SMB, Louis ED. Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. eBioMedicine 2022;85:104290. [DOI: 10.1016/j.ebiom.2022.104290] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Khalaf-nazzal R, Fasham J, Inskeep KA, Blizzard LE, Leslie JS, Wakeling MN, Ubeyratna N, Mitani T, Griffith JL, Baker W, Al-hijawi F, Keough KC, Gezdirici A, Pena L, Spaeth CG, Turnpenny PD, Walsh JR, Ray R, Neilson A, Kouranova E, Cui X, Curiel DT, Pehlivan D, Akdemir ZC, Posey JE, Lupski JR, Dobyns WB, Stottmann RW, Crosby AH, Baple EL. Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. The American Journal of Human Genetics 2022. [DOI: 10.1016/j.ajhg.2022.09.012] [Reference Citation Analysis]
3 Zhang C, Qin Q, Liu Z, Xu X, Lan M, Xie Y, Wang Z, Li J, Liu Z. Identification of the key proteins associated with different hair types in sheep and goats. Front Genet 2022;13:993192. [DOI: 10.3389/fgene.2022.993192] [Reference Citation Analysis]
4 Maillard C, Roux CJ, Charbit-Henrion F, Steffann J, Laquerriere A, Quazza F, Buisson NB. Tubulin mutations in human neurodevelopmental disorders. Semin Cell Dev Biol 2022:S1084-9521(22)00238-5. [PMID: 35915025 DOI: 10.1016/j.semcdb.2022.07.009] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Hung K, Lu J, Su D, Hsu S, Wang L. Tubulinopathy Presenting as Developmental and Epileptic Encephalopathy. Children 2022;9:1105. [DOI: 10.3390/children9081105] [Reference Citation Analysis]
6 Chu G, Li P, Wen J, Zheng G, Zhao Y, He R. Copy Number Variation Analysis of 5p Deletion Provides Accurate Prenatal Diagnosis and Reveals Candidate Pathogenic Genes. Front Med 2022;9. [DOI: 10.3389/fmed.2022.883565] [Reference Citation Analysis]
7 Bera A, Gupta ML. Microtubules in Microorganisms: How Tubulin Isotypes Contribute to Diverse Cytoskeletal Functions. Front Cell Dev Biol 2022;10:913809. [DOI: 10.3389/fcell.2022.913809] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Hernandez S, Serrano AG, Solis Soto LM. The Role of Nerve Fibers in the Tumor Immune Microenvironment of Solid Tumors. Adv Biol (Weinh) 2022;:e2200046. [PMID: 35751462 DOI: 10.1002/adbi.202200046] [Reference Citation Analysis]
9 Chun Fang G, Kaiwei D, Lingkong Z, Xuwei T. Diaphragmatic paralysis in a neonate with circumferential skin creases Kunze type. Mol Genet Genomic Med 2022;:e2003. [PMID: 35747986 DOI: 10.1002/mgg3.2003] [Reference Citation Analysis]
10 Atkins M, Nicol X, Fassier C. Microtubule remodelling as a driving force of axon guidance and pruning. Semin Cell Dev Biol 2022:S1084-9521(22)00199-9. [PMID: 35710759 DOI: 10.1016/j.semcdb.2022.05.030] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
11 Weber M, Jaber D, Encha-Razavi F, Julien E, Grevoul-Fesquet J, Steffann J, Melki J, Martinovic J. Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita. Am J Med Genet A 2022. [PMID: 35686685 DOI: 10.1002/ajmg.a.62866] [Reference Citation Analysis]
12 Musante L, Faletra F, Meier K, Tomoum H, Najarzadeh Torbati P, Blair E, North S, Gärtner J, Diegmann S, Beiraghi Toosi M, Ashrafzadeh F, Ghayoor Karimiani E, Murphy D, Murru FM, Zanus C, Magnolato A, La Bianca M, Feresin A, Girotto G, Gasparini P, Costa P, Carrozzi M. TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition. Am J Med Genet A 2022. [PMID: 35670379 DOI: 10.1002/ajmg.a.62852] [Reference Citation Analysis]
13 Chaudhari BP, Ho M. Congenital brain malformations: an integrated diagnostic approach. Seminars in Pediatric Neurology 2022. [DOI: 10.1016/j.spen.2022.100973] [Reference Citation Analysis]
14 Wethekam LC, Moore JK. Asymmetric requirement for α-tubulin over β-tubulin.. [DOI: 10.1101/2022.02.17.480930] [Reference Citation Analysis]
15 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]
16 Bogatcheva NV, Machado RF. Cytoskeletal Proteins. Encyclopedia of Respiratory Medicine 2022. [DOI: 10.1016/b978-0-12-801238-3.11678-2] [Reference Citation Analysis]
17 Di Bella DJ, Habibi E. Genetics of Cortical Development. Reference Module in Biomedical Sciences 2022. [DOI: 10.1016/b978-0-12-818872-9.00108-4] [Reference Citation Analysis]
18 Sánchez-Huertas C, Herrera E. With the Permission of Microtubules: An Updated Overview on Microtubule Function During Axon Pathfinding. Front Mol Neurosci 2021;14:759404. [PMID: 34924953 DOI: 10.3389/fnmol.2021.759404] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
19 Dekker J, Diderich KEM, Schot R, Husen SC, Dremmen MHG, Go ATJI, Weerts MJA, van Slegtenhorst MA, Mancini GMS. A novel family illustrating the mild phenotypic spectrum of TUBB2B variants. Eur J Paediatr Neurol 2021;35:35-9. [PMID: 34592644 DOI: 10.1016/j.ejpn.2021.09.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Gavazzi F, Charsar BA, Williams C, Shults J, Alves CA, Adang L, Vanderver A. Acquisition of Developmental Milestones in Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy. J Child Neurol 2021;36:805-11. [PMID: 34514881 DOI: 10.1177/08830738211000977] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, Sekhara T, Van Coster R, Van Den Ende J, Van der Aa N, Van Esch H, Vanakker O, Verhelst H, Vilain C, Weckhuysen S, Passemard S, Verloes A, Aeby A, Deconinck N, Van Bogaert P, Pirson I, Abramowicz M. Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy. Mol Genet Genomic Med 2021;9:e1768. [PMID: 34402213 DOI: 10.1002/mgg3.1768] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Watanabe K, Nakashima M, Kumada S, Mashimo H, Enokizono M, Yamada K, Kato M, Saitsu H. Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review. J Hum Genet 2021. [PMID: 34211110 DOI: 10.1038/s10038-021-00956-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
23 Alhassen W, Chen S, Vawter M, Robbins BK, Nguyen H, Myint TN, Saito Y, Schulmann A, Nauli SM, Civelli O, Baldi P, Alachkar A. Patterns of cilia gene dysregulations in major psychiatric disorders. Progress in Neuro-Psychopharmacology and Biological Psychiatry 2021;109:110255. [DOI: 10.1016/j.pnpbp.2021.110255] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 9.0] [Reference Citation Analysis]
24 Fine AL, Wong‐kisiel LC, Sheth RD. Genetics of Epilepsy. Epilepsy 2021. [DOI: 10.1002/9781119431893.ch4] [Reference Citation Analysis]
25 Gavazzi F, Charsar BA, Williams C, Shults J, Alves CA, Adang L, Vanderver A. Acquisition of Developmental Milestones in Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy. J Child Neurol 2021;:883073821000977. [PMID: 33843299 DOI: 10.1177/0883073821000977] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Shen R, Zhang Z, Zhuang Y, Yang X, Duan L. A novel TUBG1 mutation with neurodevelopmental disorder caused by malformations of cortical development. Biomed Res Int 2021;2021:6644274. [PMID: 33728335 DOI: 10.1155/2021/6644274] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Severino M, Geraldo AF, Utz N, Tortora D, Pogledic I, Klonowski W, Triulzi F, Arrigoni F, Mankad K, Leventer RJ, Mancini GMS, Barkovich JA, Lequin MH, Rossi A. Definitions and classification of malformations of cortical development: practical guidelines. Brain 2020;143:2874-94. [PMID: 32779696 DOI: 10.1093/brain/awaa174] [Cited by in Crossref: 67] [Cited by in F6Publishing: 71] [Article Influence: 67.0] [Reference Citation Analysis]
28 Ragoussis V, Pagnamenta AT, Haines RL, Giacopuzzi E, McClatchey MA, Sampson JR, Suri M, Gardham A, Cobben JM, Osio D, Fry AE, Taylor JC; Genomics England Research Consortium. Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation. J Med Genet 2021:jmedgenet-2020-107528. [PMID: 33547136 DOI: 10.1136/jmedgenet-2020-107528] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 Kolbjer S, Martin DA, Pettersson M, Dahlin M, Anderlid BM. Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects. Eur J Paediatr Neurol 2021;30:71-81. [PMID: 33453472 DOI: 10.1016/j.ejpn.2020.12.011] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 12.0] [Reference Citation Analysis]
30 Geraldo AF, Rossi A, Severino M. Malformations of Cortical Development. Pediatric Neuroradiology 2021. [DOI: 10.1007/978-3-662-46258-4_6-1] [Reference Citation Analysis]
31 Smith M. Brain, early development cortices, architecture, cell types, connectivity, networks. Mechanisms and Genetics of Neurodevelopmental Cognitive Disorders 2021. [DOI: 10.1016/b978-0-12-821913-3.00013-5] [Reference Citation Analysis]
32 Lee HMT, Sayegh NY, Gayek AS, Jao SLJ, Chalfie M, Zheng C. Epistatic, synthetic, and balancing interactions among tubulin missense mutations affecting neurite growth in Caenorhabditis elegans. Mol Biol Cell 2021;32:331-47. [PMID: 33378215 DOI: 10.1091/mbc.E20-07-0492] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
33 Gungor S, Oktay Y, Hiz S, Aranguren-Ibáñez Á, Kalafatcilar I, Yaramis A, Karaca E, Yis U, Sonmezler E, Ekinci B, Aslan M, Yilmaz E, Özgör B, Balaraju S, Szabo N, Laurie S, Beltran S, MacArthur DG, Hathazi D, Töpf A, Roos A, Lochmuller H, Vernos I, Horvath R. Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease. iScience 2021;24:101948. [PMID: 33458610 DOI: 10.1016/j.isci.2020.101948] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
34 Xie L, Huang J, Dai L, Luo J, Zhang J, Peng Q, Sun J, Zhang W. Loss-of-Function Plays a Major Role in Early Neurogenesis of Tubulin α-1 A (TUBA1A) Mutation-Related Brain Malformations. Mol Neurobiol 2021;58:1291-302. [PMID: 33165829 DOI: 10.1007/s12035-020-02193-w] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
35 Fourel G, Boscheron C. Tubulin mutations in neurodevelopmental disorders as a tool to decipher microtubule function. FEBS Lett 2020;594:3409-38. [PMID: 33064843 DOI: 10.1002/1873-3468.13958] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
36 Schröter J, Döring JH, Garbade SF, Hoffmann GF, Kölker S, Ries M, Syrbe S. Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies. Genet Med 2021;23:516-23. [PMID: 33082561 DOI: 10.1038/s41436-020-01001-z] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
37 Francis F, Cappello S. Neuronal migration and disorders - an update. Curr Opin Neurobiol 2021;66:57-68. [PMID: 33096394 DOI: 10.1016/j.conb.2020.10.002] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 7.0] [Reference Citation Analysis]
38 Sferra A, Nicita F, Bertini E. Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases. Int J Mol Sci 2020;21:E7354. [PMID: 33027950 DOI: 10.3390/ijms21197354] [Cited by in Crossref: 28] [Cited by in F6Publishing: 32] [Article Influence: 14.0] [Reference Citation Analysis]
39 Oegema R, Barakat TS, Wilke M, Stouffs K, Amrom D, Aronica E, Bahi-Buisson N, Conti V, Fry AE, Geis T, Andres DG, Parrini E, Pogledic I, Said E, Soler D, Valor LM, Zaki MS, Mirzaa G, Dobyns WB, Reiner O, Guerrini R, Pilz DT, Hehr U, Leventer RJ, Jansen AC, Mancini GMS, Di Donato N. International consensus recommendations on the diagnostic work-up for malformations of cortical development. Nat Rev Neurol 2020;16:618-35. [PMID: 32895508 DOI: 10.1038/s41582-020-0395-6] [Cited by in Crossref: 28] [Cited by in F6Publishing: 31] [Article Influence: 14.0] [Reference Citation Analysis]
40 Hecher L, Johannsen J, Bierhals T, Buhk JH, Hempel M, Denecke J. The Clinical Picture of a Bilateral Perisylvian Syndrome as the Initial Symptom of Mega-Corpus-Callosum Syndrome due to a MAST1-Gene Mutation. Neuropediatrics 2020;51:435-9. [PMID: 32818970 DOI: 10.1055/s-0040-1710588] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
41 Ramos SI, Makeyev EV, Salierno M, Kodama T, Kawakami Y, Sahara S. Tuba8 Drives Differentiation of Cortical Radial Glia into Apical Intermediate Progenitors by Tuning Modifications of Tubulin C Termini. Dev Cell 2020;52:477-491.e8. [PMID: 32097653 DOI: 10.1016/j.devcel.2020.01.036] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
42 Accogli A, Severino M, Riva A, Madia F, Balagura G, Iacomino M, Carlini B, Baldassari S, Giacomini T, Croci C, Pisciotta L, Messana T, Boni A, Russo A, Bilo L, Tonziello R, Coppola A, Filla A, Mecarelli O, Casalone R, Pisani F, Falsaperla R, Marino S, Parisi P, Ferretti A, Elia M, Luchetti A, Milani D, Vanadia F, Silvestri L, Rebessi E, Parente E, Vatti G, Mancardi MM, Nobili L, Capra V, Salpietro V, Striano P, Zara F. Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations. Seizure 2020;80:145-52. [DOI: 10.1016/j.seizure.2020.05.023] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
43 Kamal MA, Al-zahrani MH, Khan SH, Khan MH, Al-subhi HA, Kuerban A, Aslam M, Al-abbasi FA, Anwar F. Tubulin Proteins in Cancer Resistance: A Review. CDM 2020;21:178-85. [DOI: 10.2174/1389200221666200226123638] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
44 Brock S, Vanderhasselt T, Vermaning S, Keymolen K, Régal L, Romaniello R, Wieczorek D, Storm TM, Schaeferhoff K, Hehr U, Kuechler A, Krägeloh-Mann I, Haack TB, Kasteleijn E, Schot R, Mancini GMS, Webster R, Mohammad S, Leventer RJ, Mirzaa G, Dobyns WB, Bahi-Buisson N, Meuwissen M, Jansen AC, Stouffs K. Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet 2021;58:33-40. [PMID: 32571897 DOI: 10.1136/jmedgenet-2019-106740] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
45 Woodbury-Smith M, Zarrei M, Wei J, Thiruvahindrapuram B, O'Connor I, Paterson AD, Yuen RKC, Dastan J, Stavropoulos DJ, Howe JL, Thompson A, Parlier M, Fernandez B, Piven J, Anagnostou E, Scherer SW, Vieland VJ, Szatmari P. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees. Am J Med Genet B Neuropsychiatr Genet 2020;183:268-76. [PMID: 32372567 DOI: 10.1002/ajmg.b.32785] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
46 Abdel Aleem A, Elsaid MF, Chalhoub N, Chakroun A, Mohamed KAS, AlShami R, Kuzu O, Mohamed RB, Ibrahim K, AlMudheki N, Osman O, Ross ME, ELalamy O. Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variant. Neuromuscul Disord 2020;30:457-71. [PMID: 32444167 DOI: 10.1016/j.nmd.2020.03.009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
47 Çitli Ş, Serdaroglu E. Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings. Fetal Pediatr Pathol 2020;:1-11. [PMID: 32281916 DOI: 10.1080/15513815.2020.1753270] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
48 Guedes-Dias P, Holzbaur ELF. Axonal transport: Driving synaptic function. Science 2019;366:eaaw9997. [PMID: 31601744 DOI: 10.1126/science.aaw9997] [Cited by in Crossref: 126] [Cited by in F6Publishing: 128] [Article Influence: 63.0] [Reference Citation Analysis]
49 Wilton KM, Morales-Rosado JA, Selcen D, Muthusamy K, Ewing S, Agre K, Nickels K, Klee EW, Ho ML, Morava E. Developmental brain abnormalities and acute encephalopathy in a patient with myopathy with extrapyramidal signs secondary to pathogenic variants in MICU1. JIMD Rep 2020;53:22-8. [PMID: 32395406 DOI: 10.1002/jmd2.12114] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
50 Cai S, Li J, Wu Y, Jiang Y. De novo mutations of TUBB2A cause infantile-onset epilepsy and developmental delay. J Hum Genet 2020;65:601-8. [PMID: 32203252 DOI: 10.1038/s10038-020-0739-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
51 Blumkin L, Leibovitz Z, Krajden-Haratz K, Arad A, Yosovich K, Gindes L, Zerem A, Ben-Sira L, Lev D, Nissenkorn A, Kidron D, Dobyns WB, Malinger G, Bahi-Buisson N, Leventer RJ, Lerman-Sagie T. Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. Eur J Paediatr Neurol 2020;26:46-60. [PMID: 32169460 DOI: 10.1016/j.ejpn.2020.03.001] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
52 De Pasquale V, Costanzo M, Siciliano RA, Mazzeo MF, Pistorio V, Bianchi L, Marchese E, Ruoppolo M, Pavone LM, Caterino M. Proteomic Analysis of Mucopolysaccharidosis IIIB Mouse Brain. Biomolecules 2020;10:E355. [PMID: 32111039 DOI: 10.3390/biom10030355] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 10.0] [Reference Citation Analysis]
53 Sferra A, Petrini S, Bellacchio E, Nicita F, Scibelli F, Dentici ML, Alfieri P, Cestra G, Bertini ES, Zanni G. TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics. Int J Mol Sci 2020;21:E1385. [PMID: 32085672 DOI: 10.3390/ijms21041385] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
54 Lossi L, Castagna C, Granato A, Merighi A. The Reeler Mouse: A Translational Model of Human Neurological Conditions, or Simply a Good Tool for Better Understanding Neurodevelopment? J Clin Med 2019;8:E2088. [PMID: 31805691 DOI: 10.3390/jcm8122088] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 3.7] [Reference Citation Analysis]
55 Liskovykh M, Goncharov NV, Petrov N, Aksenova V, Pegoraro G, Ozbun LL, Reinhold WC, Varma S, Dasso M, Kumeiko V, Masumoto H, Earnshaw WC, Larionov V, Kouprina N. A novel assay to screen siRNA libraries identifies protein kinases required for chromosome transmission. Genome Res 2019;29:1719-32. [PMID: 31515286 DOI: 10.1101/gr.254276.119] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
56 Stoll C, Dott B, Roth MP. Associated anomalies in cases with agenesis of the corpus callosum. Am J Med Genet A 2019;179:2101-11. [PMID: 31444900 DOI: 10.1002/ajmg.a.61330] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
57 Romaniello R, Zucca C, Arrigoni F, Bonanni P, Panzeri E, Bassi MT, Borgatti R. Epilepsy in Tubulinopathy: Personal Series and Literature Review. Cells 2019;8:E669. [PMID: 31269740 DOI: 10.3390/cells8070669] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 5.3] [Reference Citation Analysis]
58 Hakanen J, Ruiz-Reig N, Tissir F. Linking Cell Polarity to Cortical Development and Malformations. Front Cell Neurosci 2019;13:244. [PMID: 31213986 DOI: 10.3389/fncel.2019.00244] [Cited by in Crossref: 26] [Cited by in F6Publishing: 30] [Article Influence: 8.7] [Reference Citation Analysis]
59 Yuen YTK, Guella I, Roland E, Sargent M, Boelman C. Case reports: novel TUBG1 mutations with milder neurodevelopmental presentations. BMC Med Genet 2019;20:95. [PMID: 31151415 DOI: 10.1186/s12881-019-0827-6] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]