-
4
-
-
0028223951
-
A behavioral neurogenetics approach to developmental disabilities: Gene-brain-behavior associations
-
Baumgardner, T. L., Green, K. E., & Reiss, A. L. (1994). A behavioral neurogenetics approach to developmental disabilities: gene-brain-behavior associations. Current Opinion in Neurology, 7, 172-178.
-
(1994)
Current Opinion in Neurology
, vol.7
, pp. 172-178
-
-
Baumgardner, T.L.1
Green, K.E.2
Reiss, A.L.3
-
5
-
-
0020327807
-
Autism is associated with the fragile-X syndrome
-
Brown W. T., Jenkins E. C., Friedman, E., Brooks, J., Wisniewski, K., Raguthu, S., & French, J. (1982). Autism is associated with the fragile-X syndrome. Journal of Autism and Developmental Disorders, 12, 303-308.
-
(1982)
Journal of Autism and Developmental Disorders
, vol.12
, pp. 303-308
-
-
Brown, W.T.1
Jenkins, E.C.2
Friedman, E.3
Brooks, J.4
Wisniewski, K.5
Raguthu, S.6
French, J.7
-
6
-
-
0022446695
-
The genetics of Rett syndrome: The consequences of a disorder where every case is a new mutation
-
Comings, D. (1990). The genetics of Rett syndrome: The consequences of a disorder where every case is a new mutation. American Journal of Medical Genetics, 36, 383-388.
-
(1990)
American Journal of Medical Genetics
, vol.36
, pp. 383-388
-
-
Comings, D.1
-
7
-
-
0023906645
-
Hypoplasia of cerebellar vermal lobules VI and VII in autism
-
Courchesne, E., Young-Courchesne, R., Press, G. A., Hesselink, J. R., & Jernigan, T. L. (1988). Hypoplasia of cerebellar vermal lobules VI and VII in autism. New England Journal of Medicine, 318, 1349-1354.
-
(1988)
New England Journal of Medicine
, vol.318
, pp. 1349-1354
-
-
Courchesne, E.1
Young-Courchesne, R.2
Press, G.A.3
Hesselink, J.R.4
Jernigan, T.L.5
-
8
-
-
0028234806
-
Is fragile X syndrome a pervasive developmental disability? Cognitive ability and adaptive behavior in males with the full mutation
-
Fisch, G. S., Holden, J. J., Simensen, R., Carpenter, N., Howard, P. P., Maddalena, A., Sandgrund, A., Jacques, J. R., & McGann, B. (1994). Is fragile X syndrome a pervasive developmental disability? Cognitive ability and adaptive behavior in males with the full mutation. American Journal of Medical Genetics, 51, 346-52.
-
(1994)
American Journal of Medical Genetics
, vol.51
, pp. 346-352
-
-
Fisch, G.S.1
Holden, J.J.2
Simensen, R.3
Carpenter, N.4
Howard, P.P.5
Maddalena, A.6
Sandgrund, A.7
Jacques, J.R.8
McGann, B.9
-
11
-
-
0023752882
-
Morphological evidence of brainstem involvement in infantile autism
-
Gaffney, G., Kuperman, S., Tsai, L., & Minchin, S. (1988). Morphological evidence of brainstem involvement in infantile autism. Biological Psychiatry, 24, 545-586.
-
(1988)
Biological Psychiatry
, vol.24
, pp. 545-586
-
-
Gaffney, G.1
Kuperman, S.2
Tsai, L.3
Minchin, S.4
-
12
-
-
0023508495
-
Cerebellar structure in autism
-
Gaffney, G., Tsai, L., Kuperman, S., & Minchin, S. (1987). Cerebellar structure in autism. American Journal of Diseases in Childhood, 141, 1330-1332.
-
(1987)
American Journal of Diseases in Childhood
, vol.141
, pp. 1330-1332
-
-
Gaffney, G.1
Tsai, L.2
Kuperman, S.3
Minchin, S.4
-
13
-
-
0023608401
-
Autistic behaviors in Rett syndrome: The first two years according to mother reports
-
Gillberg, C. (1987). Autistic behaviors in Rett syndrome: The first two years according to mother reports. Brain and Development, 9, 499-501.
-
(1987)
Brain and Development
, vol.9
, pp. 499-501
-
-
Gillberg, C.1
-
14
-
-
0024852414
-
The borderland of autism and Rett syndrome: Five case histories to highlight diagnostic difficulties
-
Gillberg, C. (1989). The borderland of autism and Rett syndrome: Five case histories to highlight diagnostic difficulties. Journal of Autism and Developmental Disorders, 19, 545-559.
-
(1989)
Journal of Autism and Developmental Disorders
, vol.19
, pp. 545-559
-
-
Gillberg, C.1
-
15
-
-
0001966753
-
Physical and behavioral phenotype
-
R. J. Hagerman & A. C. Cronister (Eds.), Baltimore: Johns Hopkins University Press
-
Hagerman, R. J. (1996). Physical and behavioral phenotype. In R. J. Hagerman & A. C. Cronister (Eds.), Fragile X syndrome (pp. 3-87). Baltimore: Johns Hopkins University Press.
-
(1996)
Fragile X Syndrome
, pp. 3-87
-
-
Hagerman, R.J.1
-
16
-
-
0022610146
-
Autism in fragile X females
-
Hagerman, R. J., Chudley, A. E., Knoll, J. H., Jackson, A., Kemper, M., & Ahmad, R. (1986). Autism in fragile X females. American Journal of Medical Genetics, 23, 375-380.
-
(1986)
American Journal of Medical Genetics
, vol.23
, pp. 375-380
-
-
Hagerman, R.J.1
Chudley, A.E.2
Knoll, J.H.3
Jackson, A.4
Kemper, M.5
Ahmad, R.6
-
17
-
-
0027397622
-
Epidemiology of Rett syndrome: A population based registry
-
Kozinetz, C. A., Skender, M. L., MacNaughton, N., Almes, M. J., Schultz, R. J., Percy, A. K., & Glaze, D. G. (1993). Epidemiology of Rett syndrome: A population based registry. Pediatrics, 91, 445-449.
-
(1993)
Pediatrics
, vol.91
, pp. 445-449
-
-
Kozinetz, C.A.1
Skender, M.L.2
MacNaughton, N.3
Almes, M.J.4
Schultz, R.J.5
Percy, A.K.6
Glaze, D.G.7
-
18
-
-
0021037652
-
Autism and the fragile X syndrome
-
Levitas, A., Hagerman, R. J., Braden, M., Rimland, B., McBogg, P., & Matus, I. (1983). Autism and the fragile X syndrome. Journal of Developmental and Behavioral Pediatrics, 4, 151-158.
-
(1983)
Journal of Developmental and Behavioral Pediatrics
, vol.4
, pp. 151-158
-
-
Levitas, A.1
Hagerman, R.J.2
Braden, M.3
Rimland, B.4
McBogg, P.5
Matus, I.6
-
19
-
-
0030857615
-
Autistic behavior among girls with fragile X syndrome
-
Mazzocco, M. M. M., Kates, W. R., Baumgardner, T., Freund, L. S., & Reiss, A. L. (1997). Autistic behavior among girls with fragile X syndrome. Journal of Autism and Developmental Disorders, 27, 415-436.
-
(1997)
Journal of Autism and Developmental Disorders
, vol.27
, pp. 415-436
-
-
Mazzocco, M.M.M.1
Kates, W.R.2
Baumgardner, T.3
Freund, L.S.4
Reiss, A.L.5
-
21
-
-
0028902950
-
Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome
-
Migeon, B., Dunn, M., Thomas, G., Schmeckpeper, B., & Naidu, S. (1995). Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome. American Journal of Human Genetics, 56, 647-653.
-
(1995)
American Journal of Human Genetics
, vol.56
, pp. 647-653
-
-
Migeon, B.1
Dunn, M.2
Thomas, G.3
Schmeckpeper, B.4
Naidu, S.5
-
22
-
-
0026750186
-
Cerebellar and cerebral abnormalities in Rett syndrome
-
Murakami, J., Courchesne, E., Haas, R., Press, G., & Young-Courchesne, R. (1992). Cerebellar and cerebral abnormalities in Rett syndrome. American Journal of Roentgenology, 159, 177-183.
-
(1992)
American Journal of Roentgenology
, vol.159
, pp. 177-183
-
-
Murakami, J.1
Courchesne, E.2
Haas, R.3
Press, G.4
Young-Courchesne, R.5
-
23
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
-
Oberle, I., Rousseau, F., Heitz, D., Kretz, C., Devys, D., Hanauer, A., Boue, J., Bertheas, M. F., & Mandel, J. L. (1991). Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science, 252, 1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberle, I.1
Rousseau, F.2
Heitz, D.3
Kretz, C.4
Devys, D.5
Hanauer, A.6
Boue, J.7
Bertheas, M.F.8
Mandel, J.L.9
-
24
-
-
0023388643
-
Autism and Rett syndrome: Behavioral investigations and differential diagnosis
-
Olsson, B., & Rett, A. (1987). Autism and Rett syndrome: Behavioral investigations and differential diagnosis. Developmental Medicine and Child Neurology, 29, 429-441.
-
(1987)
Developmental Medicine and Child Neurology
, vol.29
, pp. 429-441
-
-
Olsson, B.1
Rett, A.2
-
25
-
-
0025041274
-
Rett syndrome and the autistic disorders
-
Percy, A., Gillberg, C., Hagberg, B., & Witt-Engerstrom, I. (1990). Rett syndrome and the autistic disorders. Neurologic Clinics, 8, 659-676.
-
(1990)
Neurologic Clinics
, vol.8
, pp. 659-676
-
-
Percy, A.1
Gillberg, C.2
Hagberg, B.3
Witt-Engerstrom, I.4
-
26
-
-
0028838676
-
Contribution of the FMRI gene mutation to human intellectual dysfunction
-
Reiss, A., Baumgardner, T., Freund, L., Abrams, M., & Denckla, M. (1995). Contribution of the FMRI gene mutation to human intellectual dysfunction. Nature Genetics, 11, 331-334.
-
(1995)
Nature Genetics
, vol.11
, pp. 331-334
-
-
Reiss, A.1
Baumgardner, T.2
Freund, L.3
Abrams, M.4
Denckla, M.5
-
27
-
-
0027308186
-
Neuroanatomy of Rett syndrome: A volumetric imaging study
-
Reiss, A. L., Faruque, F., Naidu, S., Abrams, M., Beaty, T., Bryan, R. N., & Moser, H. (1993). Neuroanatomy of Rett syndrome: A volumetric imaging study. Annals of Neurology, 34, 227-234.
-
(1993)
Annals of Neurology
, vol.34
, pp. 227-234
-
-
Reiss, A.L.1
Faruque, F.2
Naidu, S.3
Abrams, M.4
Beaty, T.5
Bryan, R.N.6
Moser, H.7
-
28
-
-
0025201932
-
Fragile X syndrome, DSM-III-R, and autism
-
Reiss, A. L., & Freund, L. (1990). Fragile X syndrome, DSM-III-R, and autism. Journal of the American Academy of Child and Adolescent Psychiatry, 29, 885-891.
-
(1990)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.29
, pp. 885-891
-
-
Reiss, A.L.1
Freund, L.2
-
29
-
-
0026649793
-
Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children
-
Reiss, A. L., & Freund, L. (1992). Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children. American Journal of Medical Genetics, 43, 35-46.
-
(1992)
American Journal of Medical Genetics
, vol.43
, pp. 35-46
-
-
Reiss, A.L.1
Freund, L.2
-
30
-
-
0027073075
-
Classification of pervasive developmental disorders: Some concepts and practical considerations
-
Rutter, M., & Schopler, E. (1992). Classification of pervasive developmental disorders: Some concepts and practical considerations. Journal of Autism and Developmental Disorders, 22, 459-482.
-
(1992)
Journal of Autism and Developmental Disorders
, vol.22
, pp. 459-482
-
-
Rutter, M.1
Schopler, E.2
-
31
-
-
0001784141
-
Epidemiology
-
R. J. Hagerman & A. C. Cronister (Eds.), Baltimore: Johns Hopkins University Press
-
Sherman, S. (1991). Epidemiology. In R. J. Hagerman & A. C. Cronister (Eds.), The fragile X syndrome (pp. 69-86). Baltimore: Johns Hopkins University Press.
-
(1991)
The Fragile X Syndrome
, pp. 69-86
-
-
Sherman, S.1
-
32
-
-
0023722983
-
Autism and genetics: A decade of research
-
Smalley, S. L., Asarnow, R. F., & Spence, M. A. (1988). Autism and genetics: A decade of research. Archives of General Psychiatry, 45, 953-961.
-
(1988)
Archives of General Psychiatry
, vol.45
, pp. 953-961
-
-
Smalley, S.L.1
Asarnow, R.F.2
Spence, M.A.3
-
33
-
-
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., Reiner, O., Richards, S., Victoria, M. F., Fuping Zhang, M. F. V., Eussen, B. E., van Ommen, G. J. B., Blonden, L. A. J., Riggins, G. J., Chastain, J. L., Kunst, C. B., Galjaard, H., Caskey, C. T., Nelson, D. L., Oostra, B. A., & Warren, S. T. (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
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Fuping Zhang, M.F.V.10
Eussen, B.E.11
Van Ommen, G.J.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
34
-
-
0027078810
-
Pervasive developmental disorders: From DSM-III to DSM-III-R
-
Waterhouse, L., Wing, L., Spitzer, R., & Siegel, B. (1992). Pervasive developmental disorders: From DSM-III to DSM-III-R. Journal of Autism and Developmental Disorders, 22, 525-549.
-
(1992)
Journal of Autism and Developmental Disorders
, vol.22
, pp. 525-549
-
-
Waterhouse, L.1
Wing, L.2
Spitzer, R.3
Siegel, B.4
-
38
-
-
0022249463
-
Fragile X syndrome: Associated neurological abnormalities and developmental disabilities
-
Wisniewski, K. E., French, J. H., Fernando, S., Brown, W. T., Jenkins, E. C., Friedman, E., Hill, A. L., & Miezejeski, C. M. (1985). Fragile X syndrome: Associated neurological abnormalities and developmental disabilities. Annals of Neurology, 18, 665-669.
-
(1985)
Annals of Neurology
, vol.18
, pp. 665-669
-
-
Wisniewski, K.E.1
French, J.H.2
Fernando, S.3
Brown, W.T.4
Jenkins, E.C.5
Friedman, E.6
Hill, A.L.7
Miezejeski, C.M.8
-
39
-
-
0024586488
-
Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome
-
Zoghbi, H., Milstein, S., Butler, I., Smith, E., Kaufman, S., Glaze, D., & Percy, A. (1989). Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome. Annals of Neurology, 25, 56-60.
-
(1989)
Annals of Neurology
, vol.25
, pp. 56-60
-
-
Zoghbi, H.1
Milstein, S.2
Butler, I.3
Smith, E.4
Kaufman, S.5
Glaze, D.6
Percy, A.7
|