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For: Chandrasekar G, Vesterlund L, Hultenby K, Tapia-Páez I, Kere J. The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function. PLoS One 2013;8:e63123. [PMID: 23650548 DOI: 10.1371/journal.pone.0063123] [Cited by in Crossref: 45] [Cited by in F6Publishing: 36] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 McKnight I, Hart C, Park IH, Shim JW. Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions. Exp Neurol 2021;335:113523. [PMID: 33157092 DOI: 10.1016/j.expneurol.2020.113523] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
2 Costa-Martins AG, Lima L, Alves JMP, Serrano MG, Buck GA, Camargo EP, Teixeira MMG. Genome-wide identification of evolutionarily conserved Small Heat-Shock and eight other proteins bearing α-crystallin domain-like in kinetoplastid protists. PLoS One 2018;13:e0206012. [PMID: 30346990 DOI: 10.1371/journal.pone.0206012] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
3 Tarkar A, Loges NT, Slagle CE, Francis R, Dougherty GW, Tamayo JV, Shook B, Cantino M, Schwartz D, Jahnke C, Olbrich H, Werner C, Raidt J, Pennekamp P, Abouhamed M, Hjeij R, Köhler G, Griese M, Li Y, Lemke K, Klena N, Liu X, Gabriel G, Tobita K, Jaspers M, Morgan LC, Shapiro AJ, Letteboer SJ, Mans DA, Carson JL, Leigh MW, Wolf WE, Chen S, Lucas JS, Onoufriadis A, Plagnol V, Schmidts M, Boldt K, Roepman R, Zariwala MA, Lo CW, Mitchison HM, Knowles MR, Burdine RD, Loturco JJ, Omran H; UK10K. DYX1C1 is required for axonemal dynein assembly and ciliary motility. Nat Genet 2013;45:995-1003. [PMID: 23872636 DOI: 10.1038/ng.2707] [Cited by in Crossref: 184] [Cited by in F6Publishing: 160] [Article Influence: 20.4] [Reference Citation Analysis]
4 Schueler M, Braun DA, Chandrasekar G, Gee HY, Klasson TD, Halbritter J, Bieder A, Porath JD, Airik R, Zhou W, LoTurco JJ, Che A, Otto EA, Böckenhauer D, Sebire NJ, Honzik T, Harris PC, Koon SJ, Gunay-Aygun M, Saunier S, Zerres K, Bruechle NO, Drenth JP, Pelletier L, Tapia-Páez I, Lifton RP, Giles RH, Kere J, Hildebrandt F. DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. Am J Hum Genet 2015;96:81-92. [PMID: 25557784 DOI: 10.1016/j.ajhg.2014.12.002] [Cited by in Crossref: 64] [Cited by in F6Publishing: 52] [Article Influence: 8.0] [Reference Citation Analysis]
5 Ito-Amano M, Nakamura Y, Morisaki M, He X, Hayashi M, Watanapokasin R, Kato H. Temporal and spatial expression patterns of bone morphogenetic protein 3 in developing zebrafish. Open Rheumatol J 2014;8:69-72. [PMID: 25328556 DOI: 10.2174/1874312901408010069] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
6 Mehjabin R, Xiong L, Huang R, Yang C, Chen G, He L, Liao L, Zhu Z, Wang Y. Full-Length Transcriptome Sequencing and the Discovery of New Transcripts in the Unfertilized Eggs of Zebrafish (Danio rerio). G3 (Bethesda) 2019;9:1831-8. [PMID: 30872328 DOI: 10.1534/g3.119.200997] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
7 Bieder A, Yoshihara M, Katayama S, Krjutškov K, Falk A, Kere J, Tapia-Páez I. Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation. Mol Neurobiol 2020;57:2944-58. [PMID: 32445086 DOI: 10.1007/s12035-020-01905-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Gialluisi A, Visconti A, Willcutt EG, Smith SD, Pennington BF, Falchi M, DeFries JC, Olson RK, Francks C, Fisher SE. Investigating the effects of copy number variants on reading and language performance. J Neurodev Disord 2016;8:17. [PMID: 27186239 DOI: 10.1186/s11689-016-9147-8] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
9 Guidi LG, Velayos-Baeza A, Martinez-Garay I, Monaco AP, Paracchini S, Bishop DVM, Molnár Z. The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on. Eur J Neurosci 2018;48:3212-33. [PMID: 30218584 DOI: 10.1111/ejn.14149] [Cited by in Crossref: 23] [Cited by in F6Publishing: 22] [Article Influence: 5.8] [Reference Citation Analysis]
10 Wang S, Dong Z. Primary cilia and kidney injury: current research status and future perspectives. Am J Physiol Renal Physiol 2013;305:F1085-98. [PMID: 23904226 DOI: 10.1152/ajprenal.00399.2013] [Cited by in Crossref: 30] [Cited by in F6Publishing: 27] [Article Influence: 3.3] [Reference Citation Analysis]
11 Kumar V, Umair Z, Kumar S, Goutam RS, Park S, Kim J. The regulatory roles of motile cilia in CSF circulation and hydrocephalus. Fluids Barriers CNS 2021;18:31. [PMID: 34233705 DOI: 10.1186/s12987-021-00265-0] [Reference Citation Analysis]
12 Bieder A, Einarsdottir E, Matsson H, Nilsson HE, Eisfeldt J, Dragomir A, Paucar M, Granberg T, Li TQ, Lindstrand A, Kere J, Tapia-Páez I. Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report. BMC Med Genet 2020;21:87. [PMID: 32357925 DOI: 10.1186/s12881-020-01020-2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Osinka A, Poprzeczko M, Zielinska MM, Fabczak H, Joachimiak E, Wloga D. Ciliary Proteins: Filling the Gaps. Recent Advances in Deciphering the Protein Composition of Motile Ciliary Complexes. Cells 2019;8:E730. [PMID: 31319499 DOI: 10.3390/cells8070730] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 5.0] [Reference Citation Analysis]
14 Johnson JL. Mutations in Hsp90 Cochaperones Result in a Wide Variety of Human Disorders. Front Mol Biosci 2021;8:787260. [PMID: 34957217 DOI: 10.3389/fmolb.2021.787260] [Reference Citation Analysis]
15 Yamamoto R, Obbineni JM, Alford LM, Ide T, Owa M, Hwang J, Kon T, Inaba K, James N, King SM, Ishikawa T, Sale WS, Dutcher SK. Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms. PLoS Genet 2017;13:e1006996. [PMID: 28892495 DOI: 10.1371/journal.pgen.1006996] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
16 Fassad MR, Shoemark A, le Borgne P, Koll F, Patel M, Dixon M, Hayward J, Richardson C, Frost E, Jenkins L, Cullup T, Chung EMK, Lemullois M, Aubusson-Fleury A, Hogg C, Mitchell DR, Tassin AM, Mitchison HM. C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia. Am J Hum Genet 2018;102:956-72. [PMID: 29727692 DOI: 10.1016/j.ajhg.2018.03.024] [Cited by in Crossref: 33] [Cited by in F6Publishing: 32] [Article Influence: 8.3] [Reference Citation Analysis]
17 Xie S, Jin J, Xu Z, Huang Y, Zhang W, Zhao L, Lo LJ, Peng J, Liu W, Wang F, Shu Q, Zhou T. Centrosomal protein FOR20 is essential for cilia-dependent development in zebrafish embryos. FASEB J 2019;33:3613-22. [PMID: 30475641 DOI: 10.1096/fj.201801235RR] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
18 Kumar D, Thomason RT, Yankova M, Gitlin JD, Mains RE, Eipper BA, King SM. Microvillar and ciliary defects in zebrafish lacking an actin-binding bioactive peptide amidating enzyme. Sci Rep 2018;8:4547. [PMID: 29540787 DOI: 10.1038/s41598-018-22732-9] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
19 Darki F, Peyrard-Janvid M, Matsson H, Kere J, Klingberg T. DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development. J Neurosci 2014;34:14455-62. [PMID: 25339756 DOI: 10.1523/JNEUROSCI.1216-14.2014] [Cited by in Crossref: 26] [Cited by in F6Publishing: 15] [Article Influence: 3.7] [Reference Citation Analysis]
20 Paracchini S, Diaz R, Stein J. Advances in Dyslexia Genetics—New Insights Into the Role of Brain Asymmetries. Elsevier; 2016. pp. 53-97. [DOI: 10.1016/bs.adgen.2016.08.003] [Cited by in Crossref: 38] [Cited by in F6Publishing: 25] [Article Influence: 6.3] [Reference Citation Analysis]
21 Georgitsi M, Dermitzakis I, Soumelidou E, Bonti E. The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder. Brain Sci 2021;11:631. [PMID: 34068951 DOI: 10.3390/brainsci11050631] [Reference Citation Analysis]
22 Gostic M, Martinelli A, Tucker C, Yang Z, Gasparoli F, Ewart JY, Dholakia K, Sillar KT, Tello JA, Paracchini S. The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration. J Comp Neurol 2019;527:2634-43. [PMID: 30950042 DOI: 10.1002/cne.24696] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
23 Wang J, Vesterlund L, Kere J, Jiao H. Identification of Novel Transcribed Regions in Zebrafish (Danio rerio) Using RNA-Sequencing. PLoS One 2016;11:e0160197. [PMID: 27462902 DOI: 10.1371/journal.pone.0160197] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
24 Newbury DF, Monaco AP, Paracchini S. Reading and language disorders: the importance of both quantity and quality. Genes (Basel) 2014;5:285-309. [PMID: 24705331 DOI: 10.3390/genes5020285] [Cited by in Crossref: 29] [Cited by in F6Publishing: 19] [Article Influence: 3.6] [Reference Citation Analysis]
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26 Carrion-castillo A, Franke B, Fisher SE. Molecular Genetics of Dyslexia: An Overview: Molecular Genetics of Dyslexia: An Overview. Dyslexia 2013;19:214-40. [DOI: 10.1002/dys.1464] [Cited by in Crossref: 89] [Cited by in F6Publishing: 73] [Article Influence: 9.9] [Reference Citation Analysis]
27 Brandler WM, Paracchini S. The genetic relationship between handedness and neurodevelopmental disorders. Trends Mol Med 2014;20:83-90. [PMID: 24275328 DOI: 10.1016/j.molmed.2013.10.008] [Cited by in Crossref: 85] [Cited by in F6Publishing: 69] [Article Influence: 9.4] [Reference Citation Analysis]
28 Lyons PJ, Sapio MR, Fricker LD. Zebrafish cytosolic carboxypeptidases 1 and 5 are essential for embryonic development. J Biol Chem 2013;288:30454-62. [PMID: 24022483 DOI: 10.1074/jbc.M113.497933] [Cited by in Crossref: 16] [Cited by in F6Publishing: 8] [Article Influence: 1.8] [Reference Citation Analysis]
29 Tammimies K, Bieder A, Lauter G, Sugiaman-Trapman D, Torchet R, Hokkanen ME, Burghoorn J, Castrén E, Kere J, Tapia-Páez I, Swoboda P. Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs. FASEB J 2016;30:3578-87. [PMID: 27451412 DOI: 10.1096/fj.201500124RR] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
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35 Trulioff A, Ermakov A, Malashichev Y. Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases. Genes (Basel) 2017;8:E48. [PMID: 28125008 DOI: 10.3390/genes8020048] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 4.2] [Reference Citation Analysis]
36 Kageyama H, Miyajima M, Ogino I, Nakajima M, Shimoji K, Fukai R, Miyake N, Nishiyama K, Matsumoto N, Arai H. Panventriculomegaly with a wide foramen of Magendie and large cisterna magna. J Neurosurg 2016;124:1858-66. [PMID: 26636390 DOI: 10.3171/2015.6.JNS15162] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
37 Falkenberg LG, Beckman SA, Ravisankar P, Dohn TE, Waxman JS. Ccdc103 promotes myeloid cell proliferation and migration independent of motile cilia. Dis Model Mech 2021;14:dmm048439. [PMID: 34028558 DOI: 10.1242/dmm.048439] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]