Publications - Fragile X
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A Role for APP and beta-Amyloid in Fragile X Syndrome. Westmark, C. FRAXXA Investigators Meeting 2008. [abstract]
A converging-methods approach to Fragile X syndrome. Churchill, J.D., Grossman, A.W., Irwin, S.A., Galvez, R., Klintsova, A.Y., Weiler, I.J. and Greenough, W.T. Developmental Psychobiology 40: 323-328, 2002. [paper]
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with Fragile-X syndrome: a quantitative examination. Irwin, S.A., Patel, B., Idupulapati, M., Harris, J.B., Crisostomo, R.A., Larsen, B.P., Kooy, F., Willems, P.J., Cras, P. Kozlowski, P.B., Swain, R.A., Weiler, I.J. and Greenough, W.T. Amer. J. Med. Gen. 98:161-167, 2001. [paper]
Abnormal dendritic spine morphology in Fragile-X syndrome: a role for the Fragile-X mental retardation protein in spine maturation and pruning. Comery, T.A., Irwin, S.A., Patel, B.A., Gilbert, M.E., Kooy, R.F., Willems, P.J., Oostra, B.A. and Greenough, W.T. Soc. of Neuroscience, 1997. [abstract]
Abnormal dentritic and dendritic spine characteristics in Fragile-X patients and the mouse model of Fragile-X syndrome. Irwin, S.A., Idupulapati, M., Mehta, A.B., Crisostomo, R.A., Rogers, E.J., Larsen, B.P., Alcantara, C.J., Harris, J.B., Patel, B.A., Gilbert, M.E., Chakravarti, A., Swain, R.A., Kooy, R.F., Kozlowski, P.B., Weiler, I.J. and Greenough, W.T. Soc. of Neuroscience, 1999. [abstract]
Brain structure and the functions of FMRP. (Chapter in Fragioe XSsyndrome: Diagnosis, Treatment,and Research", 3rd edition) Irwin, S.A., Galvez, R., Weiler, I.J., Beckel-Mitchener, A. and Greenough, W.T. Johns Hopins University Press, 2002. [paper]
Dendritic spine and dendritic field characteristics in Fragile X patients and Fragile X knockout mice: quantitative examination. Greenough, W.T., Irwin, S.A., Rogers, E., Idupulapati, M., Mehta, A., Crisostomo, R., Larson, B., Alcantrara, C. and Weiler, I.J. 9th Intern. Workshop on Fragile X syndrome, 1999. [abstract]
Dendritic spine structural anomalies in Fragile-X mental retardation syndrome. Irwin, S.A., Galvez, R. and Greenough, W.T. Cerebral Cortex 10:1038-1044, 2000. [paper]
Differential impact of the FMR1 gene on visual processing in Fragile X syndrome. Kogan, C., Boutet, I., Cornish, K., Zangenehpour, S., Mullen, K., Holden, J., Der Kaloustian, V., Andermann, E. and Chaudhuri, A. Brain 127: 591-601, 2004. [paper]
Effects of Fragile X syndrome and an Fmr1 knockout mouse model on forebrain neuronal cell biology. Churchill, J.D., Beckel-Mitchener, A., Weiler, I.J., and Greenough, W.T. Microscopy Research and Technique 57:156:158, 2002. [paper]
FXTAS (Fragile X tremor ataxia syndrome): neuropathological and neuroradiologic analysis of eight cases in male premutation carriers. Greco, C.M., Brunber, J.A., Tassone, F., Hagerman, R.J., Jacquemont, S., Johl, J., Schwartz, P.H. and Hagerman, P.J. XLMR conference, 2003. [abstract]
FXTAS (Fragile X-associated tremor/ataxia syndrome): postmortem neuropahtological analysis of eight male and three female premutation carriers. Greco, C.M., Tassone, F., Hagerman, R.J., Berman, R.F., Schwartz, P.H. and Hagerman, P.J. National Fragile X Foundation Conference, 2004. [abstract]
Fragile X-associated tremor/ataxia syndrome (FXTAS). Hagerman, P.J., Iwahashi, C., Babineau, B., Yasui, D., Greco, C.M., Schwartz, P.H., Hagerman, R.J. XLMR conference, 2004. [abstract]
Fragile X-associated tremor/ataxia syndrome (FXTAS): a common heritable neuronal inclusion disorder. Hagerman, P.J., Iwahashi, C., Babineau, B., Yasui, D., Greco, C.M., Schwartz, P., Graw, S. and Hagerman, R.J. AAN conference 2004. [abstract]
Intranuclear inclustions in Fragile X-associated tremor/ataxia syndrome neuronal cells from five premutation carriers. Tassone, F., Hagerman, R.J., Garcia, D., Sahota, P.K., Khandjian, C.M., Greco, C.M. and Hagerman, P.J. ASHG, 2003. [abstract]
Molecular phenotype and neuropathology in a male with the Fragile X premutation. Tassone, F., Greco, C.M., Khandjian, E.W., Hagerman, R.J. and Hagerman, P.J. AAN Conference 2004. [abstract]
Morphological and biochemical changes in Fragile X syndrome. Singh, A., Wang, X., Siedlak,S.L., Zhu, X. Klann, E., Smith, M.A. Summer program in undergrauate research (SPUR), Case Western Reserve. [abstract]
Neuronal and non-neuronal plasticity in the developing and adult brain. (22nd International Neuroscience Summer School, "Plasticity in the Adult Brain: From Genes to Neurotherapy"). Greenough, W.T. Amsterdam, Holland, Aug. 20-23, 2001. [abstract]
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Greco, C.M., Hagerman, R.J., Tassone, F., Chudley, A.E., Del Bigio, M.R., Jacquemont, S., Leehey, M. and Hagerman, P.J. Brain 125: 1760-1771, 2002. [paper]
Neuronal intranuclear inclusions in a tremor/ataxia syndrome among fragile X premutation carriers. Hagerman, P.J., Greco, C.M., Hagerman, R.J., Tassone, F., Chudley, A.E., Del Bigio, M.R., Jacquemont, S., Gane, L and Leehey, M. ASHG, 2002. [abstract]
Pathological changes in the brains of indiviuals with Fragile X-associated tremor/ataxia syndrome (FXTAS). Greco, C.M., Brunberg, J.A., Randi, J., Hagerman, R.J., Schwartz, P.H., Bakhtiar, B., Johl, J. and Hagerman, P.J. 55th Annual Meeting of the American Academy of Neurology, 2004. [abstract]
Reversal of Fragile X phenotypes by manipulation of APP/AB levels. Westmark, C., Hays, S., Westmark, P., Hervey, C., Salamat, M., Stein, K., Ray, B., Stodola, L., Gibson, R., Tranfaglia, M., Berry-Kravis, E., Huber, K. and Malter, J. Presented 2010. [abstract]
Role of GABAa receptors in Fragile X - associated tremor/ataxia syndrome (FXTAS). Kumar, M., Hagerman, P. Berman, Rob., Willemsen, R., Kooy, F. and Tassone, F. presented 2010. [abstract]
Synaptic regulation of protein synthesis and the fragile X protein. Greenough, W.T., Kintsova, A.K., Irwin, S.A., Galvez, R., Bates, K.E., and Weiler, I.J. PNAS, 98: 7101-7106, 2001. [paper]
Visual perception deficits in fragile X syndrome: recent findings and their implications Kogan, C.S. and Chaudhuri, A. SFN, 2004, San Diego, CA. [abstract]
Whole genome microarray analysis of gene expression in subjects with fragile X syndrome. Bittel, D., Kibiyeva, N., and Butler, M. Genetics in Medicine 9: 1-10, 2007. [paper]