-
2
-
-
20244383946
-
Early developmental trajectories of males with fragile X syndrome
-
Bailey, D.B. Jr, Hatton, D.D., & Skinner, M. (1998). Early developmental trajectories of males with fragile X syndrome. American Journal ofMental Retardation, 103, 29-39.
-
(1998)
American Journal ofMental Retardation
, vol.103
, pp. 29-39
-
-
Bailey Jr, D.B.1
Hatton, D.D.2
Skinner, M.3
-
3
-
-
0038417101
-
White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging
-
Barnea-Goraly, N., Eliez, S., Hedeus, M., Menon, V., White, C.D., Moseley, M., et al. (2003). White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging. American Journal ofMedical Genetics B: Neuropsychiatric Gen- etetics, 118B, 81-88.
-
(2003)
American Journal ofMedical Genetics B: Neuropsychiatric Gen- etetics
, vol.118 B
, pp. 81-88
-
-
Barnea-Goraly, N.1
Eliez, S.2
Hedeus, M.3
Menon, V.4
White, C.D.5
Moseley, M.6
-
4
-
-
36749009300
-
-
Berry-Kravis, E., Abrams, L., Coffey, S.M., Hall, D.A., Greco, C., Gane, L.W., et al. (2007). Fragile X-asso- ciated tremor/ataxia syndrome: Clinical features,genetics, and testing guidelines. Movement Disorders, 22, 2018-2030, quiz 2140. Berry-Kravis, E., Krause, S.E., Block, S.S., Guter, S., Wuu, J., Leurgans, S., et al. (2006). Effect of CX516, an AMPA-modulating compound, on cognition and behavior in fragile X syndrome: A controlled trial. Journal ofChild and Adolescent Psychopharmacology, 16, 525-540.
-
Berry-Kravis, E., Abrams, L., Coffey, S.M., Hall, D.A., Greco, C., Gane, L.W., et al. (2007). Fragile X-asso- ciated tremor/ataxia syndrome: Clinical features,genetics, and testing guidelines. Movement Disorders, 22, 2018-2030, quiz 2140. Berry-Kravis, E., Krause, S.E., Block, S.S., Guter, S., Wuu, J., Leurgans, S., et al. (2006). Effect of CX516, an AMPA-modulating compound, on cognition and behavior in fragile X syndrome: A controlled trial. Journal ofChild and Adolescent Psychopharmacology, 16, 525-540.
-
-
-
-
5
-
-
35648978121
-
The story of Rett syndrome: From clinic to neurobiology
-
Chahrour, M., & Zoghbi, H.Y. (2007). The story of Rett syndrome: From clinic to neurobiology. Neuron, 56,422-437.
-
(2007)
Neuron
, vol.56
, pp. 422-437
-
-
Chahrour, M.1
Zoghbi, H.Y.2
-
6
-
-
34748831111
-
MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number
-
Chao, H.T., Zoghbi, H.Y., & Rosenmund, C. (2007). MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number. Neuron, 56,58-65.
-
(2007)
Neuron
, vol.56
, pp. 58-65
-
-
Chao, H.T.1
Zoghbi, H.Y.2
Rosenmund, C.3
-
7
-
-
64149127881
-
-
Costa Lima, M.A., & Pimentel, M.M. (2004). Dynamic
-
Costa Lima, M.A., & Pimentel, M.M. (2004). Dynamic
-
-
-
-
8
-
-
1442280669
-
-
mutation and human disorders: The spinocerebellar ataxias (review). International Journal of Molecular Medicine, 13, 299-302.
-
mutation and human disorders: The spinocerebellar ataxias (review). International Journal of Molecular Medicine, 13, 299-302.
-
-
-
-
9
-
-
0035746538
-
FMR1 and the fragile X syndrome: Human genome epidemiology review
-
Crawford, D.C., Acuna, J.M., & Sherman, S.L. (2001). FMR1 and the fragile X syndrome: Human genome epidemiology review. Genetics in Medicine, 3, 359371.
-
(2001)
Genetics in Medicine
, vol.3
, pp. 359371
-
-
Crawford, D.C.1
Acuna, J.M.2
Sherman, S.L.3
-
10
-
-
0033837083
-
Practice parameter: Screening and diagnosis of autism: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society
-
Filipek, P.A., Accardo, P.J., Ashwal, S., Baranek, G.T., Cook, E.H. Jr, Dawson, G., et al. (2000). Practice parameter: Screening and diagnosis of autism: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society. Neurology, 55, 468-479.
-
(2000)
Neurology
, vol.55
, pp. 468-479
-
-
Filipek, P.A.1
Accardo, P.J.2
Ashwal, S.3
Baranek, G.T.4
Cook Jr, E.H.5
Dawson, G.6
-
11
-
-
44449084899
-
Fragile X syndrome
-
Garber, K.B., Visootsak, J., & Warren, S.T. (2008). Fragile X syndrome. European Journal of Human Genetics, 16, 666-672.
-
(2008)
European Journal of Human Genetics
, vol.16
, pp. 666-672
-
-
Garber, K.B.1
Visootsak, J.2
Warren, S.T.3
-
12
-
-
39049094764
-
Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP)
-
Gothelf, D., Furfaro, J.A., Hoeft, F., Eckert, M.A., Hall, S.S., O'Hara, R., etal. (2008). Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP). Annals ofNeurology, 63, 40-51.
-
(2008)
Annals ofNeurology
, vol.63
, pp. 40-51
-
-
Gothelf, D.1
Furfaro, J.A.2
Hoeft, F.3
Eckert, M.A.4
Hall, S.S.5
O'Hara, R.6
-
13
-
-
0035127846
-
Developmental dyslexia: An update on genes, brains, and environments
-
Grigorenko, E.L. (2001). Developmental dyslexia: An update on genes, brains, and environments. Journal of Child Psychology and Psychiatry, 42, 91-125.
-
(2001)
Journal of Child Psychology and Psychiatry
, vol.42
, pp. 91-125
-
-
Grigorenko, E.L.1
-
14
-
-
33846614076
-
Recent advances in the genetics of autism
-
Gupta, A.R., & State, M.W. (2007). Recent advances in the genetics of autism. Biological Psychiatry, 61,429-437.
-
(2007)
Biological Psychiatry
, vol.61
, pp. 429-437
-
-
Gupta, A.R.1
State, M.W.2
-
15
-
-
38949147825
-
Compulsive, self-injurious, and autistic behavior in children and adolescents with fragile X syndrome
-
Hall, S.S., Lightbody, A.A., & Reiss, A.L. (2008). Compulsive, self-injurious, and autistic behavior in children and adolescents with fragile X syndrome. American Journal ofMental Retardation, 113, 44-53.
-
(2008)
American Journal ofMental Retardation
, vol.113
, pp. 44-53
-
-
Hall, S.S.1
Lightbody, A.A.2
Reiss, A.L.3
-
16
-
-
33749032127
-
Time to give up on a single explanation for autism
-
Happé, F., Ronald, A., & Plomin, R. (2006). Time to give up on a single explanation for autism. Nature Neuro- science, 9, 1218-1220.
-
(2006)
Nature Neuro- science
, vol.9
, pp. 1218-1220
-
-
Happé, F.1
Ronald, A.2
Plomin, R.3
-
17
-
-
33748295575
-
Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP
-
Hatton, D.D., Sideris, J., Skinner, M., Mankowski, J., Bailey, D.B. Jr, Roberts, J., et al. (2006). Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP. American Journal of Medical Genetics A, 140A, 1804-1813.
-
(2006)
American Journal of Medical Genetics A
, vol.140 A
, pp. 1804-1813
-
-
Hatton, D.D.1
Sideris, J.2
Skinner, M.3
Mankowski, J.4
Bailey Jr, D.B.5
Roberts, J.6
-
18
-
-
10744231868
-
Adaptive behavior in children with fragile X syndrome
-
Hatton, D.D., Wheeler, A.C., Skinner, M.L., Bailey, D.B., Sullivan, K.M., Roberts, J.E., et al. (2003). Adaptive behavior in children with fragile X syndrome. American Journal of Mental Retardation, 108,373-390.
-
(2003)
American Journal of Mental Retardation
, vol.108
, pp. 373-390
-
-
Hatton, D.D.1
Wheeler, A.C.2
Skinner, M.L.3
Bailey, D.B.4
Sullivan, K.M.5
Roberts, J.E.6
-
19
-
-
0035511650
-
The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome
-
Hessl, D., Dyer-Friedman, J., Glaser, B., Wisbeck, J., Barajas, R.G., Taylor, A., et al. (2001). The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome. Pediatrics, 108, E88.
-
(2001)
Pediatrics
, vol.108
-
-
Hessl, D.1
Dyer-Friedman, J.2
Glaser, B.3
Wisbeck, J.4
Barajas, R.G.5
Taylor, A.6
-
20
-
-
1642291847
-
The neuroanatomy and neuroendocrinology of fragile X syndrome
-
Hessl, D., Rivera, S.M., & Reiss, A.L. (2004). The neuroanatomy and neuroendocrinology of fragile X syndrome. Mental Retardation and Developmental Disabilities Research Reviews, 10, 17-24.
-
(2004)
Mental Retardation and Developmental Disabilities Research Reviews
, vol.10
, pp. 17-24
-
-
Hessl, D.1
Rivera, S.M.2
Reiss, A.L.3
-
21
-
-
34249804167
-
Fronto-striatal dysfunction and potential compensatory mechanisms in male adolescents with fragile X syndrome
-
Hoeft, F., Hernandez, A., Parthasarathy, S., Watson,C.L., Hall, S.S., & Reiss, A.L. (2007). Fronto-striatal dysfunction and potential compensatory mechanisms in male adolescents with fragile X syndrome. Human Brain Mapping, 28, 543-554.
-
(2007)
Human Brain Mapping
, vol.28
, pp. 543-554
-
-
Hoeft, F.1
Hernandez, A.2
Parthasarathy, S.3
Watson, C.L.4
Hall, S.S.5
Reiss, A.L.6
-
22
-
-
39049123212
-
Executive functions in young males with fragile X syndrome in comparison to mental age-matched controls: Baseline findings from a longitudinal study
-
Hooper, S.R., Hatton, D., Sideris, J., Sullivan, K., Hammer, J., Schaaf, J., et al. (2008). Executive functions in young males with fragile X syndrome in comparison to mental age-matched controls: Baseline findings from a longitudinal study. Neuropsychology,22, 36-47.
-
(2008)
Neuropsychology
, vol.22
, pp. 36-47
-
-
Hooper, S.R.1
Hatton, D.2
Sideris, J.3
Sullivan, K.4
Hammer, J.5
Schaaf, J.6
-
23
-
-
0035500835
-
Neurobehavioral phenotype in carriers of the fragile X premutation
-
Johnston, C., Eliez, S., Dyer-Friedman, J., Hessl, D., Glaser, B., Blasey, C., et al. (2001). Neurobehavioral phenotype in carriers of the fragile X premutation. American Journal ofMedical Genetics, 103, 314-319.
-
(2001)
American Journal ofMedical Genetics
, vol.103
, pp. 314-319
-
-
Johnston, C.1
Eliez, S.2
Dyer-Friedman, J.3
Hessl, D.4
Glaser, B.5
Blasey, C.6
-
24
-
-
64149083756
-
Cholinergic dysfunction in males with fragile X syndrome and potential pharmacological intervention: A preliminary 1H MRS study
-
in press
-
Kesler, S.R., Lightbody, A.A., & Reiss, A.L. (in press). Cholinergic dysfunction in males with fragile X syndrome and potential pharmacological intervention: A preliminary 1H MRS study. American Journal ofMedical Genetics A.
-
American Journal ofMedical Genetics A
-
-
Kesler, S.R.1
Lightbody, A.A.2
Reiss, A.L.3
-
26
-
-
33745795152
-
Chronological age, but not FMRP levels, predicts neuro- psychological performance in girls with fragile X syndrome
-
Lightbody, A.A., Hall, S.S., & Reiss, A.L. (2006). Chronological age, but not FMRP levels, predicts neuro- psychological performance in girls with fragile X syndrome. American Journal ofMedical Genetics B: Neuropsychiatric Genetics, 141B, 468-472.
-
(2006)
American Journal ofMedical Genetics B: Neuropsychiatric Genetics
, vol.141 B
, pp. 468-472
-
-
Lightbody, A.A.1
Hall, S.S.2
Reiss, A.L.3
-
28
-
-
33847022974
-
Determining treatment outcome in early intervention programs for autism spectrum disorders: A critical analysis of measurement issues in learning based interventions
-
Matson, J.L. (2007). Determining treatment outcome in early intervention programs for autism spectrum disorders: A critical analysis of measurement issues in learning based interventions. Research in Developmental Disabilities, 28, 207-218.
-
(2007)
Research in Developmental Disabilities
, vol.28
, pp. 207-218
-
-
Matson, J.L.1
-
29
-
-
1542723394
-
Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression
-
Menon, V., Leroux, J., White, C.D., & Reiss, A.L. (2004). Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression. Proceedings ofthe National Academy ofSciences U S A, 101, 3615-3620.
-
(2004)
Proceedings ofthe National Academy ofSciences U S A
, vol.101
, pp. 3615-3620
-
-
Menon, V.1
Leroux, J.2
White, C.D.3
Reiss, A.L.4
-
30
-
-
0344420060
-
Dystrophin and mutations: One gene, several proteins, multiple phenotypes
-
Muntoni, F., Torelli, S., & Ferlini, A. (2003). Dystrophin and mutations: One gene, several proteins, multiple phenotypes. Lancet Neurology, 2, 731-740.
-
(2003)
Lancet Neurology
, vol.2
, pp. 731-740
-
-
Muntoni, F.1
Torelli, S.2
Ferlini, A.3
-
31
-
-
10744223120
-
Clinical variability in Rett syndrome
-
Naidu, S., Bibat, G., Kratz, L., Kelley, R.I., Pevsner, J., Hoffman, E., et al. (2003). Clinical variability in Rett syndrome. Journal ofChild Neurology, 18, 662668.
-
(2003)
Journal ofChild Neurology
, vol.18
, pp. 662668
-
-
Naidu, S.1
Bibat, G.2
Kratz, L.3
Kelley, R.I.4
Pevsner, J.5
Hoffman, E.6
-
32
-
-
1642367538
-
Rett syndrome: A prototypical neurodevelopmental disorder
-
Neul, J.L., & Zoghbi, H.Y. (2004). Rett syndrome: A prototypical neurodevelopmental disorder. Neuro- scientist, 10, 118-128.
-
(2004)
Neuro- scientist
, vol.10
, pp. 118-128
-
-
Neul, J.L.1
Zoghbi, H.Y.2
-
33
-
-
0036637040
-
Dyslexia: Nature and nurture
-
Olson, R.K. (2002). Dyslexia: Nature and nurture. Dyslexia, 8, 143-159.
-
(2002)
Dyslexia
, vol.8
, pp. 143-159
-
-
Olson, R.K.1
-
35
-
-
0031943325
-
Schizophrenia as a developmental disorder of the cerebral cortex
-
Raedler, T.J., Knable, M.B., & Weinberger, D.R. (1998). Schizophrenia as a developmental disorder of the cerebral cortex. Current Opinion in Neurobiology, 8,157-161.
-
(1998)
Current Opinion in Neurobiology
, vol.8
, pp. 157-161
-
-
Raedler, T.J.1
Knable, M.B.2
Weinberger, D.R.3
-
36
-
-
64149114342
-
-
Paper presented at the The Convergence of Neuroscience, Behavioral Science, Neurology, and Psychiatry
-
Reiss, A. (2005). Childhood developmental disorders. Paper presented at the The Convergence of Neuroscience, Behavioral Science, Neurology, and Psychiatry.
-
(2005)
Childhood developmental disorders
-
-
Reiss, A.1
-
37
-
-
0028898302
-
Neurodevelopmental effects of the FMR-1 full mutation in humans
-
Reiss, A.L., Abrams, M.T., Greenlaw, R., Freund, L., & Denckla, M.B. (1995). Neurodevelopmental effects of the FMR-1 full mutation in humans. Nature Medicine, 1, 159-167.
-
(1995)
Nature Medicine
, vol.1
, pp. 159-167
-
-
Reiss, A.L.1
Abrams, M.T.2
Greenlaw, R.3
Freund, L.4
Denckla, M.B.5
-
38
-
-
2442661885
-
The behavioral neur- ogenetics of fragile X syndrome: Analyzing gene- brain-behavior relationships in child developmental psychopathologies
-
Reiss, A.L., & Dant, C.C. (2003). The behavioral neur- ogenetics of fragile X syndrome: Analyzing gene- brain-behavior relationships in child developmental psychopathologies. Development and Psychopathol- ogy, 15, 927-968.
-
(2003)
Development and Psychopathol- ogy
, vol.15
, pp. 927-968
-
-
Reiss, A.L.1
Dant, C.C.2
-
41
-
-
34249291910
-
Management ofdyslexia, its rationale, and underlying neurobiology
-
viii
-
Shaywitz, S.E., Gruen, J.R., & Shaywitz, B.A. (2007). Management ofdyslexia, its rationale, and underlying neurobiology. Pediatric Clinics of North America, 54,609-623, viii.
-
(2007)
Pediatric Clinics of North America
, vol.54
, pp. 609-623
-
-
Shaywitz, S.E.1
Gruen, J.R.2
Shaywitz, B.A.3
-
42
-
-
10944226908
-
A perspective on the research literature related to early intensive behavioral intervention (Lovaas) for young children with autism
-
Shea, V. (2004). A perspective on the research literature related to early intensive behavioral intervention (Lovaas) for young children with autism. Autism, 8,349-367.
-
(2004)
Autism
, vol.8
, pp. 349-367
-
-
Shea, V.1
-
43
-
-
46649092318
-
Towards a neuroanatomy of autism: A systematic review and meta-analysis of structural magnetic resonance imaging studies
-
Stanfield, A.C., Mcintosh, A.M., Spencer, M.D., Philip, R., Gaur, S., & Lawrie, S.M. (2007). Towards a neuroanatomy of autism: A systematic review and meta-analysis of structural magnetic resonance imaging studies. European Psychiatry,23, 289-299.
-
(2007)
European Psychiatry
, vol.23
, pp. 289-299
-
-
Stanfield, A.C.1
Mcintosh, A.M.2
Spencer, M.D.3
Philip, R.4
Gaur, S.5
Lawrie, S.M.6
-
44
-
-
0037880419
-
Acquired epileptiform aphasia: A dimensional view of Landau-Kleffner syndrome and the relation to regressive autistic spectrum disorders
-
Stefanatos, G.A., Kinsbourne, M., & Wasserstein, J. (2002). Acquired epileptiform aphasia: A dimensional view of Landau-Kleffner syndrome and the relation to regressive autistic spectrum disorders. Child Neuro- psychology, 8, 195-228.
-
(2002)
Child Neuro- psychology
, vol.8
, pp. 195-228
-
-
Stefanatos, G.A.1
Kinsbourne, M.2
Wasserstein, J.3
-
45
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A.J., Pieretti, M., Sutcliffe, J.S., Fu, Y.H.,Kuhl, D.P., Pizzuti, A., et al. (1991). Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell, 65, 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
-
46
-
-
20944444232
-
Fragile X syndrome: An update and review for the primary pediatrician
-
Visootsak, J., Warren, S.T., Anido, A., & Graham, J.M. Jr (2005). Fragile X syndrome: An update and review for the primary pediatrician. Clinical Pediatrics, 44,371-381.
-
(2005)
Clinical Pediatrics
, vol.44
, pp. 371-381
-
-
Visootsak, J.1
Warren, S.T.2
Anido, A.3
Graham Jr, J.M.4
|