Hagerman R - Search Results

1

Plasma Biomarkers for Monitoring Brain Pathophysiology in FMR1 Premutation Carriers.

Giulivi C, Napoli E, Tassone F, Halmai J, Hagerman R. Giulivi C, et al. Among authors: hagerman r. Front Mol Neurosci. 2016 Aug 12;9:71. doi: 10.3389/fnmol.2016.00071. eCollection 2016. Front Mol Neurosci. 2016. PMID: 27570505 Free PMC article.

2

Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome.

Taylor AK, Tassone F, Dyer PN, Hersch SM, Harris JB, Greenough WT, Hagerman RJ. Taylor AK, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):233-9. Am J Med Genet. 1999. PMID: 10331599

3

Tassone F, Hagerman RJ, Gane LW, Taylor AK. Tassone F, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):240-4. Am J Med Genet. 1999. PMID: 10331600

4

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Hum Genet. 2000 Jan;66(1):6-15. doi: 10.1086/302720. Am J Hum Genet. 2000. PMID: 10631132 Free PMC article.

5

Clinical involvement and protein expression in individuals with the FMR1 premutation.

Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Mar 13;91(2):144-52. doi: 10.1002/(sici)1096-8628(20000313)91:2<144::aid-ajmg14>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10748416

6

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

7

A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. J Med Genet. 2001 Jul;38(7):453-6. doi: 10.1136/jmg.38.7.453. J Med Genet. 2001. PMID: 11432964 Free PMC article.

8

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

Hagerman RJ, Leehey M, Heinrichs W, Tassone F, Wilson R, Hills J, Grigsby J, Gage B, Hagerman PJ. Hagerman RJ, et al. Among authors: hagerman pj. Neurology. 2001 Jul 10;57(1):127-30. doi: 10.1212/wnl.57.1.127. Neurology. 2001. PMID: 11445641

9

Transcription of the FMR1 gene in individuals with fragile X syndrome.

Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Fall;97(3):195-203. doi: 10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R. Am J Med Genet. 2000. PMID: 11449488

10

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers.

Greco CM, Hagerman RJ, Tassone F, Chudley AE, Del Bigio MR, Jacquemont S, Leehey M, Hagerman PJ. Greco CM, et al. Among authors: hagerman pj, hagerman rj. Brain. 2002 Aug;125(Pt 8):1760-71. doi: 10.1093/brain/awf184. Brain. 2002. PMID: 12135967

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