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For: Reiche L, Göttle P, Lane L, Duek P, Park M, Azim K, Schütte J, Manousi A, Schira-Heinen J, Küry P. C21orf91 Regulates Oligodendroglial Precursor Cell Fate-A Switch in the Glial Lineage? Front Cell Neurosci 2021;15:653075. [PMID: 33796011 DOI: 10.3389/fncel.2021.653075] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Price KM, Wigg KG, Eising E, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL, Abbondanza F, Allegrini AG, Andlauer TFM, Bates TC, Bernard M, Bonte M, Boomsma DI, Bourgeron T, Brandeis D, Carreiras M, Ceroni F, Csépe V, Dale PS, Defries JC, de Jong PF, Démonet JF, de Zeeuw EL, Franken MJ, Francks C, Gerritse M, Gialluisi A, Gordon SD, Gruen JR, Hayiou-thomas ME, Hernández-cabrera J, Hottenga J, Hulme C, Jansen PR, Kere J, Koomar T, Landerl K, Leonard GT, Liao Z, Luciano M, Lyytinen H, Martin NG, Martinelli A, Maurer U, Michaelson JJ, Mirza-schreiber N, Moll K, Monaco AP, Morgan AT, Müller-myhsok B, Newbury DF, Nöthen MM, Olson RK, Paracchini S, Paus T, Pausova Z, Pennell CE, Pennington BF, Plomin RJ, Ramus F, Reilly S, Richer L, Rimfeld K, Schulte-körne G, Shapland CY, Simpson NH, Smith SD, Snowling MJ, St Pourcain B, Stein JF, Talcott JB, Tiemeier H, Tomblin JB, Truong DT, van Bergen E, van der Schroeff MP, Van Donkelaar M, Verhoef E, Wang CA, Watkins KE, Whitehouse AJO, Willcutt EG, Wright MJ, Zhu G, Fisher SE, Lovett MW, Strug LJ, Barr CL, Quantitative Trait Working Group of the GenLang Consortium. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Transl Psychiatry 2022;12:495. [DOI: 10.1038/s41398-022-02250-z] [Reference Citation Analysis]
2 Fukami - Gartner A, Baburamani AA, Dimitrova R, Patkee PA, Alfageme OO, Bonthrone AF, Cromb D, Uus A, Counsell SJ, Hajnal JV, O’muircheartaigh J, Rutherford MA. Comprehensive volumetric phenotyping of the neonatal brain in Down syndrome.. [DOI: 10.1101/2022.09.30.510205] [Reference Citation Analysis]
3 Stagni F, Bartesaghi R. The Challenging Pathway of Treatment for Neurogenesis Impairment in Down Syndrome: Achievements and Perspectives. Front Cell Neurosci 2022;16:903729. [DOI: 10.3389/fncel.2022.903729] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Prutton KM, Marentette JO, Leifheit BA, Esquer H, Labarbera DV, Anderson CC, Maclean KN, Roede JR. Oxidative stress as a candidate mechanism for accelerated neuroectodermal differentiation due to trisomy 21. Free Radical Biology and Medicine 2022. [DOI: 10.1016/j.freeradbiomed.2022.04.015] [Reference Citation Analysis]
5 Hu H, Zhang R, Ma Y, Luo Y, Pan Y, Xu J, Jiang L, Wang D. Prenatal Diagnosis and Genetic Analysis of 21q21.1-q21.2 Aberrations in Seven Chinese Pedigrees. Front Genet 2021;12:731815. [PMID: 34992628 DOI: 10.3389/fgene.2021.731815] [Reference Citation Analysis]
6 Ishihara K. Genes Associated with Disturbed Cerebral Neurogenesis in the Embryonic Brain of Mouse Models of Down Syndrome. Genes (Basel) 2021;12:1598. [PMID: 34680993 DOI: 10.3390/genes12101598] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Mollo N, Esposito M, Aurilia M, Scognamiglio R, Accarino R, Bonfiglio F, Cicatiello R, Charalambous M, Procaccini C, Micillo T, Genesio R, Calì G, Secondo A, Paladino S, Matarese G, De Vita G, Conti A, Nitsch L, Izzo A. Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation. Biology (Basel) 2021;10:609. [PMID: 34209429 DOI: 10.3390/biology10070609] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]