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For: Hofman J, Hutny M, Sztuba K, Paprocka J. Corpus Callosum Agenesis: An Insight into the Etiology and Spectrum of Symptoms. Brain Sci 2020;10:E625. [PMID: 32916978 DOI: 10.3390/brainsci10090625] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Tsuji Y, Kerever A, Furukawa T, Kamagata K, Saito Y, Aoki S, Hata J, Okano H, Kobayashi K, Okada T, Miya K, Keino-masu K, Masu M, Arikawa-hirasawa E. Diffusion magnetic resonance tractography-based evaluation of commissural fiber abnormalities in a heparan sulfate endosulfatase-deficient mouse brain. Magnetic Resonance Imaging 2022. [DOI: 10.1016/j.mri.2022.01.017] [Reference Citation Analysis]
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5 Cingoz S, Soydemir D, Oner TO, Karaca E, Ozden B, Kurul SH, Bayram E, Coe BP, Nickerson DA, Eichler EE. Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations. European Journal of Medical Genetics 2022. [DOI: 10.1016/j.ejmg.2022.104497] [Reference Citation Analysis]
6 Wang X, Habet V, Aboian M, Leelatian N, McGuone D, Morotti R, Kandil S, Darbinyan A. Neuropathology of Chiari Malformation II with Chromosome X Alterations: An Autopsy Study in a 17-Month-Old and Review of Literature. J Neuropathol Exp Neurol 2022:nlab137. [PMID: 35139536 DOI: 10.1093/jnen/nlab137] [Reference Citation Analysis]
7 Pavinato L, Trajkova S, Grosso E, Giorgio E, Bruselles A, Radio FC, Pippucci T, Dimartino P, Tartaglia M, Petlichkovski A, De Rubeis S, Buxbaum J, Ferrero GB, Keller R, Brusco A. Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review. Am J Med Genet A 2021;185:1712-20. [PMID: 33675273 DOI: 10.1002/ajmg.a.62157] [Reference Citation Analysis]
8 Pomar L, Baert J, Mchirgui A, Lambert V, Carles G, Hcini N, Baud D, Vial Y. Comparison between Two-Dimensional and Three-Dimensional Assessments of the Fetal Corpus Callosum: Reproducibility of Measurements and Acquisition Time. Journal of Pediatric Neurology 2021;19:312-20. [DOI: 10.1055/s-0041-1722854] [Reference Citation Analysis]
9 Duncan AR, Polovitskaya MM, Gaitán-Peñas H, Bertelli S, VanNoy GE, Grant PE, O'Donnell-Luria A, Valivullah Z, Lovgren AK, England EM, Agolini E, Madden JA, Schmitz-Abe K, Kritzer A, Hawley P, Novelli A, Alfieri P, Colafati GS, Wieczorek D, Platzer K, Luppe J, Koch-Hogrebe M, Abou Jamra R, Neira-Fresneda J, Lehman A, Boerkoel CF, Seath K, Clarke L, van Ierland Y, Argilli E, Sherr EH, Maiorana A, Diel T, Hempel M, Bierhals T, Estévez R, Jentsch TJ, Pusch M, Agrawal PB; CAUSES Study. Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders. Am J Hum Genet 2021;108:1450-65. [PMID: 34186028 DOI: 10.1016/j.ajhg.2021.06.003] [Reference Citation Analysis]
10 Bertacchi M, Tocco C, Schaaf CP, Studer M. Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental Syndrome. Cells 2022;11:1260. [DOI: 10.3390/cells11081260] [Reference Citation Analysis]