-
1
-
-
0004235298
-
-
American Psychiatric Association. (3rd edn, DSM-III). Washington, DC: American Psychiatric Association
-
American Psychiatric Association. (1987). Diagnostic and statistical manual of mental disorders (3rd edn, DSM-III). Washington, DC: American Psychiatric Association.
-
(1987)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
2
-
-
0004235298
-
-
American Psychiatric Association. (4th edn, DSM-IV). Washington, DC: American Psychiatric Association
-
American Psychiatric Association. (1994). Diagnostic and statistical manual of mental disorders (4th edn, DSM-IV). Washington, DC: American Psychiatric Association.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
3
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangement
-
The Autism Genome Project Consortium
-
The Autism Genome Project Consortium. (2007). Mapping autism risk loci using genetic linkage and chromosomal rearrangement. Nature Genetics, 39, 319-328.
-
(2007)
Nature Genetics
, vol.39
, pp. 319-328
-
-
-
4
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey, A., Le Couteur, A., Gottesman, I., Bolton, P., Simonoff, E., Yuzda, E., & Rutter, M. (1995). Autism as a strongly genetic disorder: Evidence from a British twin study. Psychological Medicine, 25, 63-77.
-
(1995)
Psychological Medicine
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
5
-
-
0029872978
-
Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
DOI 10.1111/j.1469-7610.1996.tb01381.x
-
Bailey, A., Phillips, W., & Rutter, M. (1996). Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. Journal of Child Psychology and Psychiatry, 37, 89-126. (Pubitemid 26090588)
-
(1996)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, vol.37
, Issue.1
, pp. 89-126
-
-
Bailey, A.1
Phillips, W.2
Rutter, M.3
-
6
-
-
0342699760
-
Early development, temperament, and functional impairment in autism and fragile X syndrome
-
DOI 10.1023/A:1005412111706
-
Bailey, D.B., Hatton, D.D., Mesibov, G., Ament, N., & Skinner, M. (2000). Early development, temperament, and functional impairment in autism and fragile X syndrome. Journal of Autism and Developmental Disorders, 30, 49-59. (Pubitemid 30216633)
-
(2000)
Journal of Autism and Developmental Disorders
, vol.30
, Issue.1
, pp. 49-59
-
-
Bailey Jr., D.B.1
Hatton, D.D.2
Mesibov, G.3
Ament, N.4
Skinner, M.5
-
7
-
-
6544270937
-
Autistic behavior in young boys with fragile X syndrome
-
DOI 10.1023/A:1026048027397
-
Bailey, D.B., Mesibov, G.B., Hatton, D.D., Clark, R.D., Roberts, J.E., & Mayhew, L. (1998). Autistic behavior in young boys with fragile X syndrome. Journal of Autism and Developmental Disorders, 28, 499-508. (Pubitemid 29062059)
-
(1998)
Journal of Autism and Developmental Disorders
, vol.28
, Issue.6
, pp. 499-508
-
-
Bailey Jr., D.B.1
Mesibov, G.B.2
Hatton, D.D.3
Clark, R.D.4
Roberts, J.E.5
Mayhew, L.6
-
8
-
-
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, CD., Moseley, M., & Reiss, A.L. (2003). White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging. American Journal of Medical Genetics, 118B, 81-88. (Pubitemid 37064081)
-
(2003)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, 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
Reiss, A.L.7
-
9
-
-
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
-
10
-
-
0034122498
-
Inverse correlation between frontal lobe and cerebellum in children with autism
-
Carper, R.A., & Courchesne, E. (2000). Inverse correlation between frontal lobe and cerebellum in children with autism. Brain, 123, 836-844.
-
(2000)
Brain
, vol.123
, pp. 836-844
-
-
Carper, R.A.1
Courchesne, E.2
-
11
-
-
34147129139
-
Autism spectrum phenotype in males and females with fragile X full mutation and premutation
-
DOI 10.1007/s10803-006-0205-z
-
Clifford, S., Dissanayake, C., Bui, Q.M., Huggins, R.M., Taylor, A.K., & Loesch, D.Z. (2007). Autism spectrum phenotype in males and females with fragile X full mutation and premutation. Journal of Autism and Developmental Disorders, 37, 738-747. (Pubitemid 46571729)
-
(2007)
Journal of Autism and Developmental Disorders
, vol.37
, Issue.4
, pp. 738-747
-
-
Clifford, S.1
Dissanayake, C.2
Bui, Q.M.3
Huggins, R.4
Taylor, A.K.5
Loesch, D.Z.6
-
12
-
-
0030986183
-
Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits
-
Comery, T.A., Harris, J.B., Willems, P.J., Oostra, B.A., Irwin, S.A., Weiler, I.J., & Greenough, W.T. (1997). Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits. Proceedings of the National Academy of Science, 94, 5401-5404.
-
(1997)
Proceedings of the National Academy of Science
, vol.94
, pp. 5401-5404
-
-
Comery, T.A.1
Harris, J.B.2
Willems, P.J.3
Oostra, B.A.4
Irwin, S.A.5
Weiler, I.J.6
Greenough, W.T.7
-
13
-
-
33846519358
-
Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder
-
DOI 10.1016/j.eurpsy.2006.05.002, PII S0924933806001210
-
Delorme, R., Gousse, V., Roy, I., Trandafir, A., Mathieu, F., Mouren-Simeoni, M.C, Betancue, C., & Leboyer, M. (2007). Shared executive functions in unaffected relatives of patients with autism and obsessivecompulsive disorder. European Psychiatry, 22, 32-38. (Pubitemid 46162177)
-
(2007)
European Psychiatry
, vol.22
, Issue.1
, pp. 32-38
-
-
Delorme, R.1
Gousse, V.2
Roy, I.3
Trandafir, A.4
Mathieu, F.5
Mouren-Simeoni, M.-C.6
Betancur, C.7
Leboyer, M.8
-
14
-
-
0011048214
-
Developmental issues in fragile X syndrome
-
R.M. Hodapp, J.A. Burack, & E. Zigler (Eds.), Cambridge: Cambridge University Press
-
Dykens, E., & Leckman, J. (1990). Developmental issues in fragile X syndrome. In R.M. Hodapp, J.A. Burack, & E. Zigler (Eds.), Issues in the developmental approach to mental retardation. Cambridge: Cambridge University Press.
-
(1990)
Issues in the Developmental Approach to Mental Retardation
-
-
Dykens, E.1
Leckman, J.2
-
15
-
-
0002986754
-
Medical conditions associated with autism
-
D.J. Cohen & F.R. Volkmar (Eds.), 2nd edn, New York: Wiley
-
Dykens, E.M., & Volkmar, F.R. (1997). Medical conditions associated with autism. In D.J. Cohen & F.R. Volkmar (Eds.), Handbook of autism and pervasive developmental disorders (2nd edn, pp. 388-410). New York: Wiley.
-
(1997)
Handbook of Autism and Pervasive Developmental Disorders
, pp. 388-410
-
-
Dykens, E.M.1
Volkmar, F.R.2
-
16
-
-
0024420299
-
Autism is not associated with the fragile X syndrome
-
Einfeld, S., Molony, H., & Hall, W. (1989). Autism is not associated with the fragile X syndrome. American Journal of Medical Genetics, 34, 187-193. (Pubitemid 19257633)
-
(1989)
American Journal of Medical Genetics
, vol.34
, Issue.2
, pp. 187-193
-
-
Einfeld, S.1
Molony, H.2
Hall, W.3
-
17
-
-
33750079257
-
High frequency of neurexin 1β signal peptide structural variants in patients with autism
-
DOI 10.1016/j.neulet.2006.08.017, PII S0304394006008172
-
Feng, J., Schroer, R., Yan, J., Song, W., Yang, C., Bockholt, A., Cook, E.H. Jr, Skinner, C., Schwartz, C.E., & Sommer, S.S. (2006). High frequency of neurexin 1β signal peptide structural variants in patients with autism. Neuroscience Letters, 409, 10-13. (Pubitemid 44585112)
-
(2006)
Neuroscience Letters
, vol.409
, Issue.1
, pp. 10-13
-
-
Feng, J.1
Schroer, R.2
Yan, J.3
Song, W.4
Yang, C.5
Bockholt, A.6
Cook Jr., E.H.7
Skinner, C.8
Schwartz, C.E.9
Sommer, S.S.10
-
18
-
-
0023789411
-
Screening developmentally disabled male populations for fragile X: The effect of sample size
-
Fisch, G.S., Cohen, I.L., Jenkins, E.C., & Brown, W.T. (1988). Screening developmentally disabled male populations for fragile X: The effect of sample size. American Journal of Medical Genetics., 30, 655-663.
-
(1988)
American Journal of Medical Genetics
, vol.30
, pp. 655-663
-
-
Fisch, G.S.1
Cohen, I.L.2
Jenkins, E.C.3
Brown, W.T.4
-
19
-
-
0344329866
-
Predictors of cognitive test patterns in autism families
-
DOI 10.1017/S0021963099004461
-
Folstein, S.E., Santangelo, S.L., Gilman, S.E., Piven, J., Landa, R., Lainhart, J., et al. (1999). Predictors of cognitive test patterns in autism families. Journal of Child Psychology and Psychiatry, 40, 1117-1128. (Pubitemid 29481617)
-
(1999)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, vol.40
, Issue.7
, pp. 1117-1128
-
-
Folstein, S.E.1
Santangelo, S.L.2
Gilman, S.E.3
Piven, J.4
Landa, R.5
Lainhart, J.6
Hein, J.7
Wzorek, M.8
-
21
-
-
0030821680
-
A family study of autism: Cognitive patterns and levels in parents and siblings
-
Fombonne, E., Bolton, P., Prior, J., Jordon, H., & Rutter, M. (1997). A family study of autism: Cognitive patterns and levels in parents and siblings. Journal of Child Psychology and Psychiatry, 38, 667-684.
-
(1997)
Journal of Child Psychology and Psychiatry
, vol.38
, pp. 667-684
-
-
Fombonne, E.1
Bolton, P.2
Prior, J.3
Jordon, H.4
Rutter, M.5
-
22
-
-
0034639286
-
Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study
-
DOI 10.1002/1096-8628(20001211)95:4<307::AID-AJMG3>3.0.CO;2-3
-
Gould, E., Loesch, D.Z., Martin, M.J., Hagerman, R.J., Armstrong, S.M., & Huggins, R.M. (2000). Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study. American Journal of Medical Genetics, 95, 307-315. (Pubitemid 30954281)
-
(2000)
American Journal of Medical Genetics
, vol.95
, Issue.4
, pp. 307-315
-
-
Gould, E.L.1
Loesch, D.Z.2
Martin, M.J.3
Hagerman, R.J.4
Armstrong, S.M.5
Huggins, R.M.6
-
23
-
-
33749598639
-
The genetics of autism spectrum disorders
-
Grice, D.E., & Buxbaum, J.D. (2006). The genetics of autism spectrum disorders. Neuromolecular Medicine, 8, 451-460.
-
(2006)
Neuromolecular Medicine
, vol.8
, pp. 451-460
-
-
Grice, D.E.1
Buxbaum, J.D.2
-
24
-
-
1542576340
-
Cognition in autism: One deficit or many?
-
Happé, F. (2003). Cognition in autism: One deficit or many? Novartis Foundation Symposia, 251, 198-207.
-
(2003)
Novartis Foundation Symposia
, vol.251
, pp. 198-207
-
-
Happé, F.1
-
25
-
-
0001966753
-
The physical and behavioural phenotype
-
R.J. Hagerman & P.J. Hagerman (Eds.), Baltimore: John Hopkins
-
Hagerman, R.J. (2002). The physical and behavioural phenotype. In R.J. Hagerman & P.J. Hagerman (Eds.), Fragile X syndrome: Diagnosis, treatment and research (pp. 3-109). Baltimore: John Hopkins.
-
(2002)
Fragile X Syndrome: Diagnosis, Treatment and Research
, pp. 3-109
-
-
Hagerman, R.J.1
-
26
-
-
0022612801
-
An analysis of autism in fifty males with the fragile X syndrome
-
Hagerman, R.J., Jackson, A.W., Levitas, A., Rimland, B., & Braden, M. (1986). An analysis of autism in fifty males with the fragile X syndrome. American Journal of Medical Genetics, 23, 359-374. (Pubitemid 16139741)
-
(1986)
American Journal of Medical Genetics
, vol.23
, Issue.1-2
, pp. 359-374
-
-
Hagerman, R.J.1
Jackson III, A.W.2
Levitas, A.3
-
27
-
-
1642283099
-
Localization of White Matter Volume Increase in Autism and Developmental Language Disorder
-
DOI 10.1002/ana.20032
-
Herbert, M.R., Ziegler, D.A., Makris, N., Makris, N., Filipek, P.A., Kemper, T.L., Normandin, J.J., Sanders, H.A., Kennedy, D.N., & Caviness, V.S. Jr (2004). Localization of white matter volume increase in autism and developmental language disorder. Annals of Neurology, 55, 530-540. (Pubitemid 38391970)
-
(2004)
Annals of Neurology
, vol.55
, Issue.4
, pp. 530-540
-
-
Herbert, M.R.1
Ziegler, D.A.2
Makris, N.3
Filipek, P.A.4
Kemper, T.L.5
Normandin, J.J.6
Sanders, H.A.7
Kennedy, D.N.8
Caviness Jr., V.S.9
-
28
-
-
84990493873
-
On the robust analysis of pedigree data
-
Huggins, R.M. (1993). On the robust analysis of pedigree data. Australian Journal of Statistics, 35, 43-57.
-
(1993)
Australian Journal of Statistics
, vol.35
, pp. 43-57
-
-
Huggins, R.M.1
-
29
-
-
0034222555
-
Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation
-
DOI 10.1006/nlme.1999.3914
-
Irwin, S.A, Swain, R.A., Christmon, C.A., Chakravarti, A., Weiler, I.J., & Greenough, W.T. (2000). Evidence for altered fragile-X mental retardation protein expression in response to behavioral stimulation. Neurobiology of Learning and Memory, 73, 87-93. (Pubitemid 30167121)
-
(2000)
Neurobiology of Learning and Memory
, vol.73
, Issue.1
, pp. 87-93
-
-
Irwin, S.A.1
Swain, R.A.2
Christmon, C.A.3
Chakravarti, A.4
Weiler, I.J.5
Greenough, W.T.6
-
30
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Jamain, S., Quach, H., Betancur, C., Rastam, M., Colineaux, C., Gillberg, I.C, Söderström, H., Giros, B., Leboyer, M., Gillberg, C., & Bourgeron, T. (2003). Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nature Genetics, 34, 27-29.
-
(2003)
Nature Genetics
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Rastam, M.4
Colineaux, C.5
Gillberg, I.C.6
Söderström, H.7
Giros, B.8
Leboyer, M.9
Gillberg, C.10
Bourgeron, T.11
-
31
-
-
4043138783
-
Cortical activation and synchronization during sentence comprehension in high-functioning autism: Evidence of underconnectivity
-
Just, M.A., Cherkassky, V.L., Keller, T.A., & Minshew, N.J. (2004). Cortical activation and synchronization during sentence comprehension in high-functioning autism: Evidence of underconnectivity. Brain, 127, 1811-1821.
-
(2004)
Brain
, vol.127
, pp. 1811-1821
-
-
Just, M.A.1
Cherkassky, V.L.2
Keller, T.A.3
Minshew, N.J.4
-
32
-
-
4444322917
-
Autism spectrum disorder in fragile X syndrome: Communication, social interaction, and specific behaviors
-
Kaufmann, W.E., Cortell, R., Kau, A., Bukelis, I., Tierney, E., Gray, R.M., Cox, C., Capone, G.T., & Stanard, P. (2004). Autism spectrum disorder in fragile X syndrome: Communication, social interaction, and specific behaviors. American Journal of Medical Genetics, 129, 225-234.
-
(2004)
American Journal of Medical Genetics
, vol.129
, pp. 225-234
-
-
Kaufmann, W.E.1
Cortell, R.2
Kau, A.3
Bukelis, I.4
Tierney, E.5
Gray, R.M.6
Cox, C.7
Capone, G.T.8
Stanard, P.9
-
34
-
-
0028297411
-
Aberrant behaviors of young boys with fragile X syndrome
-
Lachiewicz, A., Spiridigliozzi, G., Gullion, C., Ransford, S., & Rao, K. (1994). Aberrant behaviors of young boys with fragile X syndrome. American Journal of Mental Retardation, 98, 567-579. (Pubitemid 24096753)
-
(1994)
American Journal on Mental Retardation
, vol.98
, Issue.5
, pp. 567-579
-
-
Lachiewicz, A.M.1
Spiridigliozzi, G.A.2
Gullion, C.M.3
Ransford, S.N.4
Rao, K.5
-
35
-
-
12144291350
-
X-Linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
-
DOI 10.1086/382137
-
Laumonnier, F., Bonnet-Brilhault, F., Gomot, M., Blanc, R., David, A., Moizard, M.P., Raynaud, M., Ronce, N., Lemonnier, E., Calvas, P., Laudier, B., Chelly, J., Fryns, J.P., Ropers, H.H., Hamel, B.C., Andres, C., Barthélémy, C., Moraine, C., & Briault, S. (2004). X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. American Journal of Human Genetics, 74, 552-557. (Pubitemid 38325925)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.3
, pp. 552-557
-
-
Laumonnier, F.1
Bonnet-Brilhault, F.2
Gomot, M.3
Blanc, R.4
David, A.5
Moizard, M.-P.6
Raynaud, M.7
Ronce, N.8
Lemonnier, E.9
Calvas, P.10
Laudier, B.11
Chelly, J.12
Fryns, J.-P.13
Ropers, H.-H.14
Hamel, B.C.J.15
Andres, C.16
Barthelemy, C.17
Moraine, C.18
Briault, S.19
-
36
-
-
33846899670
-
Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X
-
DOI 10.1016/j.neubiorev.2006.09.007, PII S0149763406001114
-
Loesch, D.Z., Bui, Q.M., Dissanayake, C., Clifford, S., Gould, E., Bulhak-Paterson, D., Tassone, F., Taylor, A.K., Hessl, D., Hagerman, R., & Huggins, R.M. (2007). Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X. Neuroscience and Biobehavioural Reviews, 31, 315-326. (Pubitemid 46241448)
-
(2007)
Neuroscience and Biobehavioral Reviews
, vol.31
, Issue.3
, pp. 315-326
-
-
Loesch, D.Z.1
Bui, Q.M.2
Dissanayake, C.3
Clifford, S.4
Gould, E.5
Bulhak-Paterson, D.6
Tassone, F.7
Taylor, A.K.8
Hessl, D.9
Hagerman, R.10
Huggins, R.M.11
-
37
-
-
0242467602
-
Effect of the fragile X status categories and the FMRP levels on executive functioning in fragile X males and females
-
Loesch, D.Z., Bui, Q.M., Grigsby, J., Butler, E., Epstein, J., Huggins, R.M., Taylor, A.K., & Hagerman, R.J. (2003a). Effect of the fragile X status categories and the FMRP levels on executive functioning in fragile X males and females. Neuropsychology, 17, 646-657.
-
(2003)
Neuropsychology
, vol.17
, pp. 646-657
-
-
Loesch, D.Z.1
Bui, Q.M.2
Grigsby, J.3
Butler, E.4
Epstein, J.5
Huggins, R.M.6
Taylor, A.K.7
Hagerman, R.J.8
-
38
-
-
0023187798
-
Phenotypic variation in male transmitted fragile X: Genetic inferences
-
Loesch, D.Z., Hay, D.A., Sutherland, G.R., Halliday, J., Judge, C., & Webb, G.C. (1987). Phenotypic variation in male transmitted fragile X: Genetic inferences. American Journal of Medical Genetics, 22, 401.
-
(1987)
American Journal of Medical Genetics
, vol.22
, pp. 401
-
-
Loesch, D.Z.1
Hay, D.A.2
Sutherland, G.R.3
Halliday, J.4
Judge, C.5
Webb, G.C.6
-
39
-
-
71949125317
-
Effect of the fragile X status categories on cognitive profiles of fragile X males and females assessed by robust pedigree analysis
-
Loesch, D.Z., Huggins, R.M., Butler, E., Taylor, A., & Hagerman, R.J. (2003b). Effect of the fragile X status categories on cognitive profiles of fragile X males and females assessed by robust pedigree analysis. American Journal of Medical Genetics, 23, 416-422.
-
(2003)
American Journal of Medical Genetics
, vol.23
, pp. 416-422
-
-
Loesch, D.Z.1
Huggins, R.M.2
Butler, E.3
Taylor, A.4
Hagerman, R.J.5
-
40
-
-
0027246074
-
Effect of fragile X on physical and intellectual traits estimated by pedigree analysis
-
Loesch, D.Z., Huggins, R.M., & Chin, W.F. (1993). Effect of fragile X on physical and intellectual traits estimated by pedigree analysis. American Journal of Medical Genetics, 46, 415-422. (Pubitemid 23149684)
-
(1993)
American Journal of Medical Genetics
, vol.46
, Issue.4
, pp. 415-422
-
-
Loesch, D.Z.1
Huggins, R.M.2
Chin, W.F.3
-
41
-
-
1642316414
-
Phenotypic variation and FMRP levels in fragile X
-
Loesch, D.Z., Huggins, R.M., & Hagerman, R.J. (2004). Phenotypic variation and FMRP levels in fragile X. Mental Retardation and Developmental Disability Research Reviews, 10, 31-41.
-
(2004)
Mental Retardation and Developmental Disability Research Reviews
, vol.10
, pp. 31-41
-
-
Loesch, D.Z.1
Huggins, R.M.2
Hagerman, R.J.3
-
42
-
-
0028802715
-
Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring
-
Loesch, D.Z., Huggins, R., Petrovic, V., & Slater, H. (1995). Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring. American Journal of Human Genetics, 57, 1408-1413.
-
(1995)
American Journal of Human Genetics
, vol.57
, pp. 1408-1413
-
-
Loesch, D.Z.1
Huggins, R.2
Petrovic, V.3
Slater, H.4
-
43
-
-
0037079905
-
Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome
-
Loesch, D.Z., Huggins, R.M., & Taylor, A.K. (2002). Application of robust pedigree analysis in studies of complex genotype-phenotype relationships in fragile X syndrome. American Journal of Human Genetics, 107, 136-142.
-
(2002)
American Journal of Human Genetics
, vol.107
, pp. 136-142
-
-
Loesch, D.Z.1
Huggins, R.M.2
Taylor, A.K.3
-
44
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
DOI 10.1007/BF02172145
-
Lord, C., Rutter, M., & Le Couteur, A. (1994). Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. Journal of Autism and Developmental Disorders, 24, 659-685. (Pubitemid 24309810)
-
(1994)
Journal of Autism and Developmental Disorders
, vol.24
, Issue.5
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Couteur, A.L.3
-
45
-
-
0003428096
-
-
Los Angeles, CA: Western Psychological Services
-
Lord, C., Rutter, M., DiLavore, P., & Risi, S. (1999). Autism Diagnostic Observation Schedule-WPS Edition. Los Angeles, CA: Western Psychological Services.
-
(1999)
Autism Diagnostic Observation Schedule-WPS Edition
-
-
Lord, C.1
Rutter, M.2
Dilavore, P.3
Risi, S.4
-
46
-
-
18544371505
-
Technical standards and guidelines for fragile X: The first series of disease-specific supplements to the standards and guidelines for clinical genetic laboratories of the white American college of medical genetics
-
Quality Assurance Subcommittee of the Laboratory Practice Committee
-
Maddalena, A., Richards, C.S., McGinnis, M.J., Brothman, A., Desnick, R.J., Grier, R.E., et al. (2001). Technical standards and guidelines for fragile X: The first series of disease-specific supplements to the Standards and Guidelines for Clinical Genetic Laboratories of the White American College of Medical Genetics. Quality Assurance Subcommittee of the Laboratory Practice Committee. Genetics in Medicine, 3, 200-205.
-
(2001)
Genetics in Medicine
, vol.3
, pp. 200-205
-
-
Maddalena, A.1
Richards, C.S.2
McGinnis, M.J.3
Brothman, A.4
Desnick, R.J.5
Grier, R.E.6
-
47
-
-
33750687891
-
Constitutional downregulation of SEMA5A expression in autism
-
DOI 10.1159/000096040
-
Melin, M., Carlsson, B., Anckarsater, H., Rastam, M., Betancur, C., Isaksson, A., Gillberg, C., & Dahl, N. (2006). Constitutional downregulation of SEMA5A expression in autism. Neuropsychobiology, 54, 64-69. (Pubitemid 44699463)
-
(2006)
Neuropsychobiology
, vol.54
, Issue.1
, pp. 64-69
-
-
Melin, M.1
Carlsson, B.2
Anckarsater, H.3
Rastam, M.4
Betancur, C.5
Isaksson, A.6
Gillberg, C.7
Dahl, N.8
-
48
-
-
0033515516
-
Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report
-
DOI 10.1002/(SICI)1096-8628(19990402)83:4<268::AID-AJMG7>3.0.CO;2-K
-
Miller, L.J., Mcintosh, D.N., McGrath, J., Shyu, V., Lampe, M., Taylor, A.K., Tassone, F., Neitzel, K., Stackhouse, T., & Hagerman, R.J. (1999). Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report. American Journal of Medical Genetics, 83, 268-279. (Pubitemid 29162627)
-
(1999)
American Journal of Medical Genetics
, vol.83
, Issue.4
, pp. 268-279
-
-
Miller, L.J.1
McIntosh, D.N.2
McGrath, J.3
Shyu, V.4
Lampe, M.5
Taylor, A.K.6
Tassone, F.7
Neitzel, K.8
Stackhouse, T.9
Hagerman, R.J.10
-
49
-
-
0029584732
-
Brief report: Circadian melatonin, thyroid stimulating hormone, prolactin and Cortisol levels in serum in young adults with autism
-
Nir, I., Meir, D., Zilber, N., Knobler, H., Hadjez, J., Lerner, Y., et al. (1995). Brief report: Circadian melatonin, thyroid stimulating hormone, prolactin and Cortisol levels in serum in young adults with autism. Journal of Autism and Developmental Disorders, 25, 641-654.
-
(1995)
Journal of Autism and Developmental Disorders
, vol.25
, pp. 641-654
-
-
Nir, I.1
Meir, D.2
Zilber, N.3
Knobler, H.4
Hadjez, J.5
Lerner, Y.6
-
50
-
-
0024360491
-
The fragile X marker and autism in perspective: Case study
-
Payton, J.B., Steele, M.W., Wenger, S.L., & Minshew, N.J. (1989). The fragile X marker and autism in perspective: Case study. Journal of the American Academy of Child and Adolescent Psychiatry, 28, 417-421.
-
(1989)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.28
, pp. 417-421
-
-
Payton, J.B.1
Steele, M.W.2
Wenger, S.L.3
Minshew, N.J.4
-
51
-
-
0025833298
-
Absence of expression of the FMR-1 gene in fragile X syndrome
-
Pieretti, M., Zhang, F.P., Fu, Y.H., Warren, S.T., Oostra, B.A., Caskey, C.T., & Nelson, D.L. (1991). Absence of expression of the FMR-1 gene in fragile X syndrome. Cell, 66, 817-822. (Pubitemid 121001715)
-
(1991)
Cell
, vol.66
, Issue.4
, pp. 817-822
-
-
Pieretti, M.1
Zhang, F.2
Fu, Y.-H.3
Warren, S.T.4
Oostra, B.A.5
Caskey, C.T.6
Nelson, D.L.7
-
52
-
-
0035825185
-
The broad autism phenotype: A complimentary strategy for molecular genetic studies of autism
-
Piven, J. (2001). The broad autism phenotype: A complimentary strategy for molecular genetic studies of autism. American Journal of Medical Genetics, 105, 34-35.
-
(2001)
American Journal of Medical Genetics
, vol.105
, pp. 34-35
-
-
Piven, J.1
-
53
-
-
0033839568
-
Brain imaging in neurogenetic conditions: Realizing the potential of behavioral neurogenetics research
-
DOI 10.1002/1098-2779(2000)6:3<186::AID-MRDD6>3.0.CO;2-9
-
Reiss, A.L., Eliez, S., Schmitt, J.E., Patwardhan, A., Haberecht, M., et al. (2000). Brain imaging in neurogenetic conditions: Realizing the potential of behavioural neurogenetics research. Mental Retardation and Developmental Disability Research Reviews, 6, 186-197. (Pubitemid 30679661)
-
(2000)
Mental Retardation and Developmental Disabilities Research Reviews
, vol.6
, Issue.3
, pp. 186-197
-
-
Reiss, A.L.1
Eliez, S.2
Schmitt, J.E.3
Patwardhan, A.4
Haberecht, M.5
-
54
-
-
0035675794
-
The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders
-
Rogers, S.J., Wehner, E., & Hagerman, R.J. (2001). The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. Journal of Developmental and Behavioural Paediatrics, 22, 409-417. (Pubitemid 34026944)
-
(2001)
Journal of Developmental and Behavioral Pediatrics
, vol.22
, Issue.6
, pp. 409-417
-
-
Rogers, S.J.1
Wehner, E.A.2
Hagerman, R.3
-
55
-
-
2342520066
-
Understanding orbitofrontal contributions to theory-of-mind reasoning: Implications for autism
-
Sabbagh, M.A. (2004). Understanding orbitofrontal contributions to theory-of-mind reasoning: Implications for autism. Brain and Cognition, 55, 209-219.
-
(2004)
Brain and Cognition
, vol.55
, pp. 209-219
-
-
Sabbagh, M.A.1
-
56
-
-
0003451164
-
-
Los Angeles, CA: Western Psychological Services
-
Schopler, E., Reichler, R.J., & Renner, B.R. (1988). The Childhood Autism Rating Scale. Los Angeles, CA: Western Psychological Services.
-
(1988)
The Childhood Autism Rating Scale
-
-
Schopler, E.1
Reichler, R.J.2
Renner, B.R.3
-
57
-
-
0343283416
-
-
STATA Statistical Software. College Station, TX: Stata Corporation
-
STATA Statistical Software. (1997) Release 5.0. College Station, TX: Stata Corporation.
-
(1997)
Release 5.0
-
-
-
58
-
-
0027438546
-
Lack of cognitive impairment in first degree relatives of children with pervasive developmental disorders
-
Szatmari, P., Jones, M.B., Tuff, L., Bartolucci, G., Fisman, S., & Mahoney, W. (1993). Lack of cognitive impairment in first degree relatives of children with pervasive developmental disorders. Journal of the American Academy of Child and Adolescent Psychiatry, 32, 1264-1273.
-
(1993)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.32
, pp. 1264-1273
-
-
Szatmari, P.1
Jones, M.B.2
Tuff, L.3
Bartolucci, G.4
Fisman, S.5
Mahoney, W.6
-
59
-
-
84942951309
-
Molecular predictors of cognitive involvement in female carriers of fragile X syndrome
-
DOI 10.1001/jama.271.7.507
-
Taylor, A.K., Safanda, J.F., Fall, M.Z., Quince, C., Lang, K.A., Hull, C.E., Carpenter, I., Staley, L.W., & Hagerman, R.J. (1994). Molecular predictors of cognitive involvement in female carriers of fragile X syndrome. Journal of the American Medical Association, 271, 507-514. (Pubitemid 24050314)
-
(1994)
Journal of the American Medical Association
, vol.271
, Issue.7
, pp. 507-514
-
-
Taylor, A.K.1
Safanda, J.F.2
Fall, M.Z.3
Quince, C.4
Lang, K.A.5
Hull, C.E.6
Carpenter, I.7
Staley, L.W.8
Hagerman, R.J.9
-
60
-
-
0000501087
-
Fragile X syndrome, autism and autistic features
-
Turk, J., & Graham, P. (1997). Fragile X syndrome, autism, and autistic features. Autism, 1, 175-197. (Pubitemid 127708488)
-
(1997)
Autism
, vol.1
, Issue.2
, pp. 175-197
-
-
Turk, J.1
Graham, P.2
-
61
-
-
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., & Zhang, F.P. (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. (Pubitemid 121001321)
-
(1991)
Cell
, vol.65
, Issue.5
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhl, D.P.A.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.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..
-
62
-
-
0003441705
-
-
(3rd edn). San Antonio, TX: The Psychological Corporation
-
Wechsler, D. (1997). Wechsler Adult Intelligence Scale (3rd edn). San Antonio, TX: The Psychological Corporation.
-
(1997)
Wechsler Adult Intelligence Scale
-
-
Wechsler, D.1
-
65
-
-
0033515497
-
Synaptic synthesis of the fragile X protein: Possible involvement in synapse maturation and elimination
-
Weiler, I.J., & Greenough, W.T. (1999). Synaptic synthesis of the fragile X protein: Possible involvement in synapse maturation and elimination. American Journal of Medical Genetics, 83, 248-252.
-
(1999)
American Journal of Medical Genetics
, vol.83
, pp. 248-252
-
-
Weiler, I.J.1
Greenough, W.T.2
-
66
-
-
38449096091
-
Epigenetics and neural developmental disorders
-
Zhao, X., Park, C., Smrt, R.D., & Jin, P. (2007). Epigenetics and neural developmental disorders. Epigenetics, 2, 126-134.
-
(2007)
Epigenetics
, vol.2
, pp. 126-134
-
-
Zhao, X.1
Park, C.2
Smrt, R.D.3
Jin, P.4
|