Hagerman RJ - Search Results

1

A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome.

Hessl D, Nguyen DV, Green C, Chavez A, Tassone F, Hagerman RJ, Senturk D, Schneider A, Lightbody A, Reiss AL, Hall S. Hessl D, et al. Among authors: hagerman rj. J Neurodev Disord. 2009 Mar;1(1):33-45. doi: 10.1007/s11689-008-9001-8. J Neurodev Disord. 2009. PMID: 19865612 Free PMC article.

2

Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome.

Freund LS, Reiss AL, Hagerman R, Vinogradov S. Freund LS, et al. Arch Gen Psychiatry. 1992 Jan;49(1):54-60. doi: 10.1001/archpsyc.1992.01820010054007. Arch Gen Psychiatry. 1992. PMID: 1728251

3

Parental inheritance and psychological disability in fragile X females.

Reiss AL, Freund L, Vinogradov S, Hagerman R, Cronister A. Reiss AL, et al. Am J Hum Genet. 1989 Nov;45(5):697-705. Am J Hum Genet. 1989. PMID: 2816940 Free PMC article.

4

Psychiatric disability in female carriers of the fragile X chromosome.

Reiss AL, Hagerman RJ, Vinogradov S, Abrams M, King RJ. Reiss AL, et al. Among authors: hagerman rj. Arch Gen Psychiatry. 1988 Jan;45(1):25-30. doi: 10.1001/archpsyc.1988.01800250029005. Arch Gen Psychiatry. 1988. PMID: 3337608

5

Trajectories and profiles of adaptive behavior in males with fragile X syndrome: multicenter studies.

Dykens E, Ort S, Cohen I, Finucane B, Spiridigliozzi G, Lachiewicz A, Reiss A, Freund L, Hagerman R, O'Connor R. Dykens E, et al. J Autism Dev Disord. 1996 Jun;26(3):287-301. doi: 10.1007/BF02172475. J Autism Dev Disord. 1996. PMID: 8792261

6

Compound heterozygous female with fragile X syndrome.

Linden MG, Tassone F, Gane LW, Hills JL, Hagerman RJ, Taylor AK. Linden MG, et al. Among authors: hagerman rj. Am J Med Genet. 1999 Apr 2;83(4):318-21. Am J Med Genet. 1999. PMID: 10208169

7

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

8

FMRP expression as a potential prognostic indicator in fragile X syndrome.

Tassone F, Hagerman RJ, Iklé DN, Dyer PN, Lampe M, Willemsen R, Oostra BA, Taylor AK. Tassone F, et al. Among authors: hagerman rj. Am J Med Genet. 1999 May 28;84(3):250-61. Am J Med Genet. 1999. PMID: 10331602

9

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.

10

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

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