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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 1
1949 2
1950 2
1951 1
1952 2
1953 2
1954 2
1957 3
1960 1
1961 1
1962 1
1964 2
1965 2
1966 1
1967 2
1970 1
1972 1
1973 1
1975 1
1985 1
2001 1
2004 2
2005 4
2007 3
2008 6
2009 2
2010 2
2011 5
2012 2
2013 3
2014 3
2015 1
2016 1
2017 1
2018 3
2019 9
2020 8
2021 10
2022 7
2023 5
2024 0

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101 results

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Page 1
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies.
Kang Y, Zhou Y, Li Y, Han Y, Xu J, Niu W, Li Z, Liu S, Feng H, Huang W, Duan R, Xu T, Raj N, Zhang F, Dou J, Xu C, Wu H, Bassell GJ, Warren ST, Allen EG, Jin P, Wen Z. Kang Y, et al. Among authors: allen eg. Nat Neurosci. 2021 Oct;24(10):1377-1391. doi: 10.1038/s41593-021-00913-6. Epub 2021 Aug 19. Nat Neurosci. 2021. PMID: 34413513 Free PMC article.
Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease.
Liu Q, Zhang K, Kang Y, Li Y, Deng P, Li Y, Tian Y, Sun Q, Tang Y, Xu K, Zhou Y, Wang JL, Guo J, Li JD, Xia K, Meng Q, Allen EG, Wen Z, Li Z, Jiang H, Shen L, Duan R, Yao B, Tang B, Jin P, Pan Y. Liu Q, et al. Among authors: allen eg. Sci Adv. 2022 Nov 25;8(47):eadd6391. doi: 10.1126/sciadv.add6391. Epub 2022 Nov 23. Sci Adv. 2022. PMID: 36417528 Free PMC article.
Metabolic Alterations in FMR1 Premutation Carriers.
Cao Y, Peng Y, Kong HE, Allen EG, Jin P. Cao Y, et al. Among authors: allen eg. Front Mol Biosci. 2020 Sep 18;7:571092. doi: 10.3389/fmolb.2020.571092. eCollection 2020. Front Mol Biosci. 2020. PMID: 33195417 Free PMC article. Review.
Epitranscriptomic dynamics in brain development and disease.
Shafik AM, Allen EG, Jin P. Shafik AM, et al. Among authors: allen eg. Mol Psychiatry. 2022 Sep;27(9):3633-3646. doi: 10.1038/s41380-022-01570-2. Epub 2022 Apr 26. Mol Psychiatry. 2022. PMID: 35474104 Free PMC article. Review.
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ. Tassone F, et al. Among authors: allen eg. Cells. 2023 Sep 21;12(18):2330. doi: 10.3390/cells12182330. Cells. 2023. PMID: 37759552 Free PMC article. Review.
Diverse and dynamic DNA modifications in brain and diseases.
Armstrong MJ, Jin Y, Allen EG, Jin P. Armstrong MJ, et al. Among authors: allen eg. Hum Mol Genet. 2019 Nov 21;28(R2):R241-R253. doi: 10.1093/hmg/ddz179. Hum Mol Genet. 2019. PMID: 31348493 Free PMC article. Review.
Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.
Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, Juncos J, Nelson DL, Epstein MP, Cutler DJ, Todd PK, Sherman SL, Warren ST, Jin P. Kong HE, et al. Among authors: allen eg. Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2118124119. doi: 10.1073/pnas.2118124119. Epub 2022 May 26. Proc Natl Acad Sci U S A. 2022. PMID: 35617426 Free PMC article.
Epidemiology of Down syndrome.
Sherman SL, Allen EG, Bean LH, Freeman SB. Sherman SL, et al. Among authors: allen eg. Ment Retard Dev Disabil Res Rev. 2007;13(3):221-7. doi: 10.1002/mrdd.20157. Ment Retard Dev Disabil Res Rev. 2007. PMID: 17910090 Review.
101 results