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Cited by in F6Publishing
For: Usui D, Shimada S, Shimojima K, Sugawara M, Kawasaki H, Shigematu H, Takahashi Y, Inoue Y, Imai K, Yamamoto T. Interstitial duplication of 2q32.1-q33.3 in a patient with epilepsy, developmental delay, and autistic behavior. Am J Med Genet A. 2013;161A:1078-1084. [PMID: 23463730 DOI: 10.1002/ajmg.a.35679] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 1.9] [Reference Citation Analysis]
Number Citing Articles
1 Rudolf G, Lovrečić L, Tul N, Teran N, Peterlin B. The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy. Mol Genet Genomic Med 2019;7:e658. [PMID: 31004418 DOI: 10.1002/mgg3.658] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
2 Kashevarova AA, Lebedev IN. Genomic architecture of human chromosomal diseases. Russ J Genet 2016;52:447-62. [DOI: 10.1134/s1022795416040062] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
3 Toma K, Hanashima C. Switching modes in corticogenesis: mechanisms of neuronal subtype transitions and integration in the cerebral cortex. Front Neurosci 2015;9:274. [PMID: 26321900 DOI: 10.3389/fnins.2015.00274] [Cited by in Crossref: 29] [Cited by in F6Publishing: 33] [Article Influence: 4.1] [Reference Citation Analysis]
4 Teng X, Aouacheria A, Lionnard L, Metz KA, Soane L, Kamiya A, Hardwick JM. KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders. CNS Neurosci Ther 2019;25:887-902. [PMID: 31197948 DOI: 10.1111/cns.13156] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 9.5] [Reference Citation Analysis]
5 Li Y, Huang WY, Lv CY, Cong J, Jie W, Li SJ, Li JM. Satb2 ablation decreases PTZ-induced seizure susceptibility and pyramidal neuronal excitability. Brain Res 2018;1695:102-7. [PMID: 29750936 DOI: 10.1016/j.brainres.2018.05.006] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
6 Alvarez-Saavedra M, Yan K, De Repentigny Y, Hashem LE, Chaudary N, Sarwar S, Yang D, Ioshikhes I, Kothary R, Hirayama T, Yagi T, Picketts DJ. Snf2h Drives Chromatin Remodeling to Prime Upper Layer Cortical Neuron Development. Front Mol Neurosci 2019;12:243. [PMID: 31680852 DOI: 10.3389/fnmol.2019.00243] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
7 Gupta A, Yo J, Huang G, Soong L, Dong J. Developmental Defects Associated With DNA Copy Number Gain of Chromosome 2q33.1: A Case Report and Review of Literature. Lab Med 2018;49:160-4. [PMID: 29301000 DOI: 10.1093/labmed/lmx086] [Reference Citation Analysis]
8 Liedén A, Kvarnung M, Nilssson D, Sahlin E, Lundberg ES. Intragenic duplication--a novel causative mechanism for SATB2-associated syndrome. Am J Med Genet A 2014;164A:3083-7. [PMID: 25251319 DOI: 10.1002/ajmg.a.36769] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 3.0] [Reference Citation Analysis]
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10 Zhang Q, Huang Y, Zhang L, Ding YQ, Song NN. Loss of Satb2 in the Cortex and Hippocampus Leads to Abnormal Behaviors in Mice. Front Mol Neurosci. 2019;12:33. [PMID: 30809123 DOI: 10.3389/fnmol.2019.00033] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 5.0] [Reference Citation Analysis]
11 Silipigni R, Milani D, Tolva G, Monfrini E, Giacobbe A, Marchisio PG, Guerneri S. Complex genomic alterations and intellectual disability: an interpretative challenge. J Intellect Disabil Res 2021;65:113-24. [PMID: 33140510 DOI: 10.1111/jir.12797] [Reference Citation Analysis]
12 Gigek CO, Chen ES, Ota VK, Maussion G, Peng H, Vaillancourt K, Diallo AB, Lopez JP, Crapper L, Vasuta C, Chen GG, Ernst C. A molecular model for neurodevelopmental disorders. Transl Psychiatry 2015;5:e565. [PMID: 25966365 DOI: 10.1038/tp.2015.56] [Cited by in Crossref: 29] [Cited by in F6Publishing: 24] [Article Influence: 4.1] [Reference Citation Analysis]
13 Turovsky EA, Turovskaya MV, Fedotova EI, Babaev AA, Tarabykin VS, Varlamova EG. Role of Satb1 and Satb2 Transcription Factors in the Glutamate Receptors Expression and Ca2+ Signaling in the Cortical Neurons In Vitro. Int J Mol Sci 2021;22:5968. [PMID: 34073140 DOI: 10.3390/ijms22115968] [Reference Citation Analysis]
14 Domínguez MG, Rivera H, Aguilar-Lemarroy A, Jave-Suarez LF, Ramírez-Velazco A, González-Ramos IA, Barros-Núñez P, Partida-Pérez M, Gutiérrez-Amavizca BE, Brambila-Tapia AJ, Figuera LE. Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring. Clin Dysmorphol 2017;26:209-16. [PMID: 28737552 DOI: 10.1097/MCD.0000000000000191] [Reference Citation Analysis]
15 Gao K, Zhang Y, Zhang L, Kong W, Xie H, Wang J, Wu Y, Wu X, Liu X, Zhang Y, Zhang F, Yu AC, Jiang Y. Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis. In: Cheung-hoi Yu A, Li L, editors. Systems Neuroscience. Cham: Springer International Publishing; 2018. pp. 247-66. [DOI: 10.1007/978-3-319-94593-4_9] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
16 Yamamoto T, Shimada S, Shimojima K. Fiber-fluorescence in situ hybridization analyses as a diagnostic application for orientation of microduplications. World J Med Genet 2013; 3(2): 5-8 [DOI: 10.5496/wjmg.v3.i2.5] [Reference Citation Analysis]