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Items: 1 to 20 of 103


Neurodevelopmental disabilities in children with intermediate and premutation range fragile X cytosine-guanine-guanine expansions.

Renda MM, Voigt RG, Babovic-Vuksanovic D, Highsmith WE, Vinson SS, Sadowski CM, Hagerman RJ.

J Child Neurol. 2014 Mar;29(3):326-30. doi: 10.1177/0883073812469723. Epub 2012 Dec 23.


Unstable mutations in the FMR1 gene and the phenotypes.

Loesch D, Hagerman R.

Adv Exp Med Biol. 2012;769:78-114. Review.


Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: a controlled study.

Kogan CS, Turk J, Hagerman RJ, Cornish KM.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):859-72. doi: 10.1002/ajmg.b.30685.


Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation.

Farzin F, Perry H, Hessl D, Loesch D, Cohen J, Bacalman S, Gane L, Tassone F, Hagerman P, Hagerman R.

J Dev Behav Pediatr. 2006 Apr;27(2 Suppl):S137-44.


Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms.

Loesch DZ, Godler DE, Khaniani M, Gould E, Gehling F, Dissanayake C, Burgess T, Tassone F, Huggins R, Slater H, Choo KH.

Am J Med Genet A. 2009 Oct;149A(10):2306-10. doi: 10.1002/ajmg.a.32990. No abstract available.


Size bias of fragile X premutation alleles in late-onset movement disorders.

Jacquemont S, Leehey MA, Hagerman RJ, Beckett LA, Hagerman PJ.

J Med Genet. 2006 Oct;43(10):804-9. Epub 2006 May 24.


Fragile X-associated disorders: a clinical overview.

Gallagher A, Hallahan B.

J Neurol. 2012 Mar;259(3):401-13. doi: 10.1007/s00415-011-6161-3. Epub 2011 Jul 12. Review.


A neuropsychological investigation of male premutation carriers of fragile X syndrome.

Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG.

Neuropsychologia. 2004;42(14):1934-47.


FMR1 gray-zone alleles: association with Parkinson's disease in women?

Hall DA, Berry-Kravis E, Zhang W, Tassone F, Spector E, Zerbe G, Hagerman PJ, Ouyang B, Leehey MA.

Mov Disord. 2011 Aug 15;26(10):1900-6. doi: 10.1002/mds.23755. Epub 2011 May 12.


Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome.

Hagerman R, Hagerman P.

Lancet Neurol. 2013 Aug;12(8):786-98. doi: 10.1016/S1474-4422(13)70125-X. Review.


Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.

Wang JY, Hessl D, Schneider A, Tassone F, Hagerman RJ, Rivera SM.

JAMA Neurol. 2013 Aug;70(8):1022-9. doi: 10.1001/jamaneurol.2013.2934.


An assessment of screening strategies for fragile X syndrome in the UK.

Pembrey ME, Barnicoat AJ, Carmichael B, Bobrow M, Turner G.

Health Technol Assess. 2001;5(7):1-95. Review.


Fragile X analysis of 1112 prenatal samples from 1991 to 2010.

Nolin SL, Glicksman A, Ding X, Ersalesi N, Brown WT, Sherman SL, Dobkin C.

Prenat Diagn. 2011 Oct;31(10):925-31. doi: 10.1002/pd.2815. Epub 2011 Jun 30.


No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.

Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL.

Am J Hum Genet. 2008 Dec;83(6):692-702. doi: 10.1016/j.ajhg.2008.10.021. Epub 2008 Nov 20.


Clinical features of boys with fragile X premutations and intermediate alleles.

Aziz M, Stathopulu E, Callias M, Taylor C, Turk J, Oostra B, Willemsen R, Patton M.

Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):119-27.


Enhanced asynchronous Ca(2+) oscillations associated with impaired glutamate transport in cortical astrocytes expressing Fmr1 gene premutation expansion.

Cao Z, Hulsizer S, Cui Y, Pretto DL, Kim KH, Hagerman PJ, Tassone F, Pessah IN.

J Biol Chem. 2013 May 10;288(19):13831-41. doi: 10.1074/jbc.M112.441055. Epub 2013 Apr 3.


Newborn, carrier, and early childhood screening recommendations for fragile X.

Abrams L, Cronister A, Brown WT, Tassone F, Sherman SL, Finucane B, McConkie-Rosell A, Hagerman R, Kaufmann WE, Picker J, Coffey S, Skinner D, Johnson V, Miller R, Berry-Kravis E.

Pediatrics. 2012 Dec;130(6):1126-35. doi: 10.1542/peds.2012-0693. Epub 2012 Nov 5. Review.


Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS.

Kogan CS, Cornish KM.

Brain Cogn. 2010 Aug;73(3):236-43. doi: 10.1016/j.bandc.2010.05.008. Epub 2010 Jun 22.


Selective executive markers of at-risk profiles associated with the fragile X premutation.

Cornish KM, Hocking DR, Moss SA, Kogan CS.

Neurology. 2011 Aug 16;77(7):618-22. doi: 10.1212/WNL.0b013e3182299e59. Epub 2011 Jul 20.

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