Fragile X Syndrome Research Today is a free monthly online journal that collates and summarizes the latest research about Fragile X Syndrome, including details on symptoms, treatment, heritability, diagnosis.

Volume 7 (2011), Issue 1 (January)

1. BDNF and TrkB in neuronal differentiation of Fmr1-knockout mouse.
   Neurobiol Dis, 41(2): 469-80. [Abstract] [Full-text]
2. BDNF and TrkB in neuronal differentiation of Fmr1-knockout mouse.
   Neurobiol Dis, 41(2): 469-80. [Abstract] [Full-text]
3. BDNF and TrkB in neuronal differentiation of Fmr1-knockout mouse.
   Neurobiol Dis, 41(2): 469-80. [Abstract] [Full-text]
4. Status epilepticus in fragile X syndrome.
   Epilepsia, 51(12): 2470-3. [Abstract] [Full-text]
5. Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056.
   Sci Transl Med, 3(64): 64ra1. [Abstract] [Full-text]
6. Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.
   Sci Transl Med, 3(64): 64ra1. [Abstract] [Full-text]
7. Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.
   Sci Transl Med, 3(64): 64ra1. [Abstract] [Full-text]
8. Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology.
   Res Dev Disabil. [Abstract] [Full-text]
9. Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology.
   Res Dev Disabil. [Abstract] [Full-text]
10. Behavioral features of Williams Beuren syndrome compared to Fragile X syndrome and subjects with intellectual disability without defined etiology.
    Res Dev Disabil. [Abstract] [Full-text]
11. Molecular mechanisms of cognitive and behavioral comorbidities of epilepsy in children.
    Epilepsia, 52: 13-20. [Abstract] [Full-text]
12. FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States.
    Genet Med, 13(1): 39-45. [Abstract] [Full-text]
13. Molecular mechanisms of cognitive and behavioral comorbidities of epilepsy in children.
    Epilepsia, 52: 13-20. [Abstract] [Full-text]
14. FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States.
    Genet Med, 13(1): 39-45. [Abstract] [Full-text]
15. Toward fulfilling the promise of molecular medicine in fragile X syndrome.
    Annu Rev Med, 62: 411-29. [Abstract] [Full-text]
16. Toward fulfilling the promise of molecular medicine in fragile X syndrome.
    Annu Rev Med, 62: 411-29. [Abstract] [Full-text]
17. Toward fulfilling the promise of molecular medicine in fragile X syndrome.
    Annu Rev Med, 62: 411-29. [Abstract] [Full-text]
18. Large-scale population screening for spinal muscular atrophy: Clinical implications.
    Genet Med. [Abstract] [Full-text]
19. Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.
    Am J Med Genet A. [Abstract] [Full-text]
20. Genetic deletion of regulator of G-protein signaling 4 (RGS4) rescues a subset of fragile X related phenotypes in the FMR1 knockout mouse.
    Mol Cell Neurosci. [Abstract] [Full-text]
21. Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.
    Am J Med Genet A. [Abstract] [Full-text]
22. Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.
    Am J Med Genet A. [Abstract] [Full-text]
23. Aetiology of intellectual disability in paediatric outpatients in Northern India.
    Dev Med Child Neurol, 53(2): 167-72. [Abstract] [Full-text]
24. Brief report: Sensorimotor gating in idiopathic autism and autism associated with fragile X syndrome.
    J Autism Dev Disord, 41(2): 248-53. [Abstract] [Full-text]
25. Aetiology of intellectual disability in paediatric outpatients in Northern India.
    Dev Med Child Neurol, 53(2): 167-72. [Abstract] [Full-text]
26. Brief report: Sensorimotor gating in idiopathic autism and autism associated with fragile X syndrome.
    J Autism Dev Disord, 41(2): 248-53. [Abstract] [Full-text]
27. Aetiology of intellectual disability in paediatric outpatients in Northern India.
    Dev Med Child Neurol, 53(2): 167-72. [Abstract] [Full-text]
28. Brief report: Sensorimotor gating in idiopathic autism and autism associated with fragile X syndrome.
    J Autism Dev Disord, 41(2): 248-53. [Abstract] [Full-text]
29. TMS: Using the Theta-Burst Protocol to Explore Mechasnism of Plasticity in Individuals with Fragile X Syndrome and Autism.
    J Vis Exp. [Abstract] [Full-text]
30. TMS: using the theta-burst protocol to explore mechanism of plasticity in individuals with Fragile X syndrome and autism.
    J Vis Exp. [Abstract] [Full-text]
31. Distribution of CGG/GCC Repeats at the FMR1 and FMR2 Genes in Indian Population with Mental Retardation of Unknown etiology.
    Genet Test Mol Biomarkers. [Abstract] [Full-text]
32. Distribution of CGG/GCC Repeats at the FMR1 and FMR2 Genes in Indian Population with Mental Retardation of Unknown etiology.
    Genet Test Mol Biomarkers. [Abstract] [Full-text]
33. Distribution of CGG/GCC Repeats at the FMR1 and FMR2 Genes in Indian Population with Mental Retardation of Unknown etiology.
    Genet Test Mol Biomarkers. [Abstract] [Full-text]
34. Cognitive dysfunction and prefrontal synaptic abnormalities in a mouse model of fragile X syndrome.
    Proc Natl Acad Sci U S A. [Abstract] [Full-text]
35. Four sisters compound heterozygotes for the pre- and full mutation in fragile X syndrome and a complete inactivation of X-functional chromosome: implications for genetic counseling.
    J Hum Genet, 56(1): 87-90. [Abstract] [Full-text]
36. Four sisters compound heterozygotes for the pre- and full mutation in fragile X syndrome and a complete inactivation of X-functional chromosome: implications for genetic counseling.
    J Hum Genet, 56(1): 87-90. [Abstract] [Full-text]
37. Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses.
    Autism Res. [Abstract] [Full-text]
38. Reliability of Eye Tracking and Pupillometry Measures in Individuals with Fragile X Syndrome.
    J Autism Dev Disord. [Abstract] [Full-text]
39. A nonsense mutation in FMR1 causing fragile X syndrome.
    Eur J Hum Genet. [Abstract] [Full-text]
40. Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses.
    Autism Res. [Abstract] [Full-text]
41. Reliability of Eye Tracking and Pupillometry Measures in Individuals with Fragile X Syndrome.
    J Autism Dev Disord. [Abstract] [Full-text]
42. A nonsense mutation in FMR1 causing fragile X syndrome.
    Eur J Hum Genet. [Abstract] [Full-text]
43. Reliability of Eye Tracking and Pupillometry Measures in Individuals with Fragile X Syndrome.
    J Autism Dev Disord. [Abstract] [Full-text]
44. A nonsense mutation in FMR1 causing fragile X syndrome.
    Eur J Hum Genet. [Abstract] [Full-text]
45. FMRP Regulates the Transition from Radial Glial Cells to Intermediate Progenitor Cells during Neocortical Development.
    J Neurosci, 31(4): 1427-39. [Abstract] [Full-text]
46. Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.
    Am J Med Genet A, 155(2): 343-8. [Abstract] [Full-text]
47. FMRP regulates the transition from radial glial cells to intermediate progenitor cells during neocortical development.
    J Neurosci, 31(4): 1427-39. [Abstract] [Full-text]
48. Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.
    Am J Med Genet A, 155(2): 343-8. [Abstract] [Full-text]
49. Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.
    Am J Med Genet A, 155(2): 343-8. [Abstract] [Full-text]
50. New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS).
    Neurogenetics. [Abstract] [Full-text]
51. Genetic deletion of regulator of G-protein signaling 4 (RGS4) rescues a subset of fragile X related phenotypes in the FMR1 knockout mouse.
    Mol Cell Neurosci. [Abstract] [Full-text]
52. New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS).
    Neurogenetics. [Abstract] [Full-text]
53. New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS).
    Neurogenetics. [Abstract] [Full-text]

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