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

Year Number of Results
1982 3
1983 8
1984 3
1985 5
1986 13
1987 8
1988 9
1989 8
1990 16
1991 16
1992 31
1993 29
1994 30
1995 35
1996 29
1997 29
1998 22
1999 25
2000 27
2001 27
2002 35
2003 33
2004 35
2005 39
2006 43
2007 37
2008 38
2009 45
2010 44
2011 57
2012 52
2013 56
2014 67
2015 54
2016 58
2017 53
2018 50
2019 39
2020 42
2021 41
2022 34
2023 38
2024 17

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1,273 results

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Page 1
Fragile X syndrome: clinical presentation, pathology and treatment.
Salcedo-Arellano MJ, Hagerman RJ, Martínez-Cerdeño V. Salcedo-Arellano MJ, et al. Gac Med Mex. 2020;156(1):60-66. doi: 10.24875/GMM.19005275. Gac Med Mex. 2020. PMID: 32026885 Free article. Review. English.
Fragile X syndrome is the monogenetic condition that produces more cases of autism and intellectual disability. ...Hispanic countries such as Colombia, Chile and Spain report high prevalence of fragile X syndrome and have created fragile
Fragile X syndrome is the monogenetic condition that produces more cases of autism and intellectual disability. ...Hisp
Fragile X syndrome.
Hagerman RJ, Berry-Kravis E, Hazlett HC, Bailey DB Jr, Moine H, Kooy RF, Tassone F, Gantois I, Sonenberg N, Mandel JL, Hagerman PJ. Hagerman RJ, et al. Nat Rev Dis Primers. 2017 Sep 29;3:17065. doi: 10.1038/nrdp.2017.65. Nat Rev Dis Primers. 2017. PMID: 28960184 Review.
Fragile X syndrome (FXS) is the leading inherited form of intellectual disability and autism spectrum disorder, and patients can present with severe behavioural alterations, including hyperactivity, impulsivity and anxiety, in addition to poor language develo
Fragile X syndrome (FXS) is the leading inherited form of intellectual disability and autism spectrum disorder, and pat
Fragile X syndrome: a review of clinical and molecular diagnoses.
Ciaccio C, Fontana L, Milani D, Tabano S, Miozzo M, Esposito S. Ciaccio C, et al. Ital J Pediatr. 2017 Apr 19;43(1):39. doi: 10.1186/s13052-017-0355-y. Ital J Pediatr. 2017. PMID: 28420439 Free PMC article. Review.
BACKGROUND: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndrome and the most prevalent cause of intellectual disability in males, affecting 1:5000-7000 men and 1:4000-6000 women. ...
BACKGROUND: Fragile X Syndrome (FXS) is the second cause of intellectual disability after Down syndrome and the most pr …
A Synaptic Perspective of Fragile X Syndrome and Autism Spectrum Disorders.
Bagni C, Zukin RS. Bagni C, et al. Neuron. 2019 Mar 20;101(6):1070-1088. doi: 10.1016/j.neuron.2019.02.041. Neuron. 2019. PMID: 30897358 Free PMC article. Review.
Altered synaptic structure and function is a major hallmark of fragile X syndrome (FXS), autism spectrum disorders (ASDs), and other intellectual disabilities (IDs), which are therefore classified as synaptopathies. ...
Altered synaptic structure and function is a major hallmark of fragile X syndrome (FXS), autism spectrum disorders (ASD …
Epidemiology of fragile X syndrome: a systematic review and meta-analysis.
Hunter J, Rivero-Arias O, Angelov A, Kim E, Fotheringham I, Leal J. Hunter J, et al. Am J Med Genet A. 2014 Jul;164A(7):1648-58. doi: 10.1002/ajmg.a.36511. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700618 Review.
Prevalence estimates for fragile X syndrome vary considerably. This systematic review and meta-analysis was conducted to provide an accurate prevalence estimate for this disorder using primary publications in PubMed, Embase, and the Cochrane library. ...Preva …
Prevalence estimates for fragile X syndrome vary considerably. This systematic review and meta-analysis was conducted t …
Fragile X syndrome.
Saldarriaga W, Tassone F, González-Teshima LY, Forero-Forero JV, Ayala-Zapata S, Hagerman R. Saldarriaga W, et al. Colomb Med (Cali). 2014 Dec 30;45(4):190-8. eCollection 2014 Oct-Dec. Colomb Med (Cali). 2014. PMID: 25767309 Free PMC article. Review.
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutation (greater than 200 CGG repeats), in the fragile X mental retardation 1 gene locus Xq27.3; which leads to an hypermethylated region in the gene promoter ther
Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutation (greater than 2
Rare FMR1 gene mutations causing fragile X syndrome: A review.
Sitzmann AF, Hagelstrom RT, Tassone F, Hagerman RJ, Butler MG. Sitzmann AF, et al. Am J Med Genet A. 2018 Jan;176(1):11-18. doi: 10.1002/ajmg.a.38504. Epub 2017 Nov 27. Am J Med Genet A. 2018. PMID: 29178241 Free PMC article. Review.
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability, typically due to CGG-repeat expansions in the FMR1 gene leading to lack of expression. ...
Fragile X syndrome (FXS) is the most common inherited form of intellectual disability, typically due to CGG-repeat expa
Fragile X Syndrome: From Molecular Aspect to Clinical Treatment.
Protic DD, Aishworiya R, Salcedo-Arellano MJ, Tang SJ, Milisavljevic J, Mitrovic F, Hagerman RJ, Budimirovic DB. Protic DD, et al. Int J Mol Sci. 2022 Feb 9;23(4):1935. doi: 10.3390/ijms23041935. Int J Mol Sci. 2022. PMID: 35216055 Free PMC article. Review.
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by the full mutation as well as highly localized methylation of the fragile X mental retardation 1 (FMR1) gene on the long arm of the X chromosome. ...
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by the full mutation as well as highly localized methy
The molecular biology of FMRP: new insights into fragile X syndrome.
Richter JD, Zhao X. Richter JD, et al. Nat Rev Neurosci. 2021 Apr;22(4):209-222. doi: 10.1038/s41583-021-00432-0. Epub 2021 Feb 19. Nat Rev Neurosci. 2021. PMID: 33608673 Free PMC article. Review.
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation 1 gene (FMR1), a gene that - when epigenetically inactivated by a triplet nucleotide repeat expansion - causes the neurodevelopmental disorder fragile X syndrome (F …
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation 1 gene (FMR1), a gene that - when epigenetica …
1,273 results