-
1
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U. and Zohbi, H. Y. (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet, 23: 185-188.
-
(1999)
Nat Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zohbi, H.Y.6
-
2
-
-
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. and Rutter, M. (1995) Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med, 25: 63-77.
-
(1995)
Psychol Med
, 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
-
3
-
-
14644432508
-
Three autism candidate genes: A synthesis of human genetic analysis with other disciplines
-
Bartlett, C. W., Gharani, N., Millonig, J. H. and Brzustowicz, L. M. (2005) Three autism candidate genes: A synthesis of human genetic analysis with other disciplines. Int J Devl Neuroscience, 23: 221-234.
-
(2005)
Int J Devl Neuroscience
, vol.23
, pp. 221-234
-
-
Bartlett, C.W.1
Gharani, N.2
Millonig, J.H.3
Brzustowicz, L.M.4
-
4
-
-
0022617471
-
Fragile X and autism: A multicenter survey
-
Brown, W. T., Jenkins, E. C., Krawczun, M. S., Wisniewski, K., Rudelli, R., Cohen, I. L., Fisch, G. S., Wolf-Schein, E. G., Miezejeski, C. and Dobkin, C. (1986) Fragile X and autism: A multicenter survey. Am J Med Genet, 23: 341-352.
-
(1986)
Am J Med Genet
, vol.23
, pp. 341-352
-
-
Brown, W.T.1
Jenkins, E.C.2
Krawczun, M.S.3
Wisniewski, K.4
Rudelli, R.5
Cohen, I.L.6
Fisch, G.S.7
Wolf-Schein, E.G.8
Miezejeski, C.9
Dobkin, C.10
-
5
-
-
0033943538
-
Social amnesia in mice lacking the oxytocin gene
-
Ferguson, J. N., Young, L. J., Hearn, E. F., Matzuk, M. M., Insel, T. R. and Winslow, J. T. (2000) Social amnesia in mice lacking the oxytocin gene. Nat Genet, 25: 284-287.
-
(2000)
Nat Genet
, vol.25
, pp. 284-287
-
-
Ferguson, J.N.1
Young, L.J.2
Hearn, E.F.3
Matzuk, M.M.4
Insel, T.R.5
Winslow, J.T.6
-
6
-
-
0025778539
-
Etiology of autism: Genetic influences
-
Folstein, S. E. and Piven, J. (1991) Etiology of autism: Genetic influences. Pediatrics, 87: 767-773.
-
(1991)
Pediatrics
, vol.87
, pp. 767-773
-
-
Folstein, S.E.1
Piven, J.2
-
7
-
-
0017337957
-
Genetic influences and infantile autism
-
Folstein, S. and Rutter, M. (1977) Genetic influences and infantile autism. Nature, 265: 726-728.
-
(1977)
Nature
, vol.265
, pp. 726-728
-
-
Folstein, S.1
Rutter, M.2
-
8
-
-
0023950384
-
Autism: Familial aggregation and genetic implication
-
Folstein, S. E. and Rutter, M. L. (1988) Autism: Familial aggregation and genetic implication. J Autism Dev Disord, 18: 3-30.
-
(1988)
J Autism Dev Disord
, vol.18
, pp. 3-30
-
-
Folstein, S.E.1
Rutter, M.L.2
-
9
-
-
0032804766
-
The epidemiology of autism: A review
-
Fombonne, E. (1999) The epidemiology of autism: A review. Psychol Med, 29: 769-786.
-
(1999)
Psychol Med
, vol.29
, pp. 769-786
-
-
Fombonne, E.1
-
10
-
-
11244334274
-
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
-
Gauthier, J., Bonnel, A., St-Onge, J., Karemera, L., Laurent, S., Mottron, L., Fembonne, E., Joober, R. and Rouleau, G. A. (2005) NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. Am J Med Genet, 132B: 74-75.
-
(2005)
Am J Med Genet
, vol.132 B
, pp. 74-75
-
-
Gauthier, J.1
Bonnel, A.2
St-Onge, J.3
Karemera, L.4
Laurent, S.5
Mottron, L.6
Fembonne, E.7
Joober, R.8
Rouleau, G.A.9
-
11
-
-
0037656313
-
-
Jamain, S., Quach, H., Betancur, C., Rastam, M., Colineaux, C., Gillberg, I. C., Soderstrom, H., Giros, B., Leboter, M., Gillberg, C., Bourgeron, T. and Paris Autism Research International Sibpair Study (2003) Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet, 34: 27-29.
-
Jamain, S., Quach, H., Betancur, C., Rastam, M., Colineaux, C., Gillberg, I. C., Soderstrom, H., Giros, B., Leboter, M., Gillberg, C., Bourgeron, T. and Paris Autism Research International Sibpair Study (2003) Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet, 34: 27-29.
-
-
-
-
12
-
-
0025318908
-
The UCLA-University of Utah epidemiologic survey of autism: Genealogical analysis of familial aggregation
-
Jorde, L. B., Mason-Brothers, A., Waldmann, R., Ritvo, E. R., Freeman, B. J., Pingree, C., McMahon, W. M., Petersen, B., Jenson, W. R. and Mo, A. (1990) The UCLA-University of Utah epidemiologic survey of autism: Genealogical analysis of familial aggregation. Am J Med Genet, 36: 85-88.
-
(1990)
Am J Med Genet
, vol.36
, pp. 85-88
-
-
Jorde, L.B.1
Mason-Brothers, A.2
Waldmann, R.3
Ritvo, E.R.4
Freeman, B.J.5
Pingree, C.6
McMahon, W.M.7
Petersen, B.8
Jenson, W.R.9
Mo, A.10
-
13
-
-
0000984981
-
Autistic disturbances of affective contact
-
Kanner, L. (1943) Autistic disturbances of affective contact. Nerv Child, 2: 217-250.
-
(1943)
Nerv Child
, vol.2
, pp. 217-250
-
-
Kanner, L.1
-
14
-
-
12144291350
-
X-linked mental retardation and autism are associated with a mutation in the NLGL4 gene, a member of the neuroligin family
-
Laumonnier, F., Bonnet-Brilhault, F., Gomet, 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. J., Andres, C., Barthelemy, C., Moraine, C. and Briault, S. (2004) X-linked mental retardation and autism are associated with a mutation in the NLGL4 gene, a member of the neuroligin family. Am J Hum Genet, 74: 552-557.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 552-557
-
-
Laumonnier, F.1
Bonnet-Brilhault, F.2
Gomet, 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
-
15
-
-
0038064292
-
Heritable and nonheritable risk factors for autism spectrum disorders
-
Newschaffer, C. J., Fallin, D. and Lee, N. L. (2002) Heritable and nonheritable risk factors for autism spectrum disorders. Epidemiol Rev, 24: 137-153.
-
(2002)
Epidemiol Rev
, vol.24
, pp. 137-153
-
-
Newschaffer, C.J.1
Fallin, D.2
Lee, N.L.3
-
16
-
-
0021960916
-
Concordance for the syndrome of autism in 40 pairs of afflicted twins
-
Ritvo, E. R., Freeman, B. J., Mason-Brothers, A., Mo, A. and Ritvo, A. M. (1985) Concordance for the syndrome of autism in 40 pairs of afflicted twins. Am J Psychiatry, 142: 74-77.
-
(1985)
Am J Psychiatry
, vol.142
, pp. 74-77
-
-
Ritvo, E.R.1
Freeman, B.J.2
Mason-Brothers, A.3
Mo, A.4
Ritvo, A.M.5
-
17
-
-
37649026213
-
Genomic screen and follow-up analysis for autistic disorder
-
Shao, Y., Wolpert, C. M., Raiford, K. L., Menold, M. M., Donnelly, S. L., Ravan, S. A., Bass, M. P., McClain, C., von Wendt, L., Vance, J. M., Abramson, R. H., Wright, H. H., Ashley-Koch, A., Gilbert, J. R., DeLong, R. G., Cuccaro, M. L. and Pericak-Vance, M. A. (2002) Genomic screen and follow-up analysis for autistic disorder. Am J Med Genet, 114: 99-105.
-
(2002)
Am J Med Genet
, vol.114
, pp. 99-105
-
-
Shao, Y.1
Wolpert, C.M.2
Raiford, K.L.3
Menold, M.M.4
Donnelly, S.L.5
Ravan, S.A.6
Bass, M.P.7
McClain, C.8
von Wendt, L.9
Vance, J.M.10
Abramson, R.H.11
Wright, H.H.12
Ashley-Koch, A.13
Gilbert, J.R.14
DeLong, R.G.15
Cuccaro, M.L.16
Pericak-Vance, M.A.17
-
18
-
-
0032453497
-
Autism and tuberous sclerosis
-
Smalley, S. L. (1998) Autism and tuberous sclerosis. J Autism Dev Disord, 28: 407-414.
-
(1998)
J Autism Dev Disord
, vol.28
, pp. 407-414
-
-
Smalley, S.L.1
-
19
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway, and Sweden
-
Steffenburg, S., Gillberg, C., Hellgran, L., Andersson, L., Gillberg, I. C., Jakobsson, G. and Bohman, M. (1989) A twin study of autism in Denmark, Finland, Iceland, Norway, and Sweden. J Child Psychol Psychiatry, 30: 405-416.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgran, L.3
Andersson, L.4
Gillberg, I.C.5
Jakobsson, G.6
Bohman, M.7
-
20
-
-
0029916624
-
Autism in Angelman syndrome: A population-based study
-
Steffenburg, S., Gillberg, C. L., Steffenburg, U. and Kyllerman, M. (1996) Autism in Angelman syndrome: A population-based study. Pediatr Neurol, 14: 131-136.
-
(1996)
Pediatr Neurol
, vol.14
, pp. 131-136
-
-
Steffenburg, S.1
Gillberg, C.L.2
Steffenburg, U.3
Kyllerman, M.4
-
21
-
-
3342965856
-
Mutation screening of X-chromosomal neuroligin genes: No mutation in 196 autism probands
-
Vincent, J. B., Kolozsvari, D., Roberts, W. S., Bolton, P. F., Gurling, H. M. D. and Scherer, S. W. (2004) Mutation screening of X-chromosomal neuroligin genes: No mutation in 196 autism probands. Am J Med Genet, 129B: 82-84.
-
(2004)
Am J Med Genet
, vol.129 B
, pp. 82-84
-
-
Vincent, J.B.1
Kolozsvari, D.2
Roberts, W.S.3
Bolton, P.F.4
Gurling, H.M.D.5
Scherer, S.W.6
-
22
-
-
21344444796
-
Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population
-
Wu, S., Jia, M., Ruan, Y., Liu, J., Guo, Y., Shuang, M., Gong, X., Zhang, Y., Yang, X. and Zhang, D. (2005) Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population. Biol Psychciatry, 58: 74-77.
-
(2005)
Biol Psychciatry
, vol.58
, pp. 74-77
-
-
Wu, S.1
Jia, M.2
Ruan, Y.3
Liu, J.4
Guo, Y.5
Shuang, M.6
Gong, X.7
Zhang, Y.8
Yang, X.9
Zhang, D.10
-
23
-
-
20144389549
-
Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients
-
Yan, J., Oliveira, G., Coutinho, A., Yang, C., Feng, J., Katz, C., Sram, J., Bockholt, A., Jones, I. R., Craddock, N., Cook, Jr. E. H., Vicente, A. and Sommer, S. S. (2005) Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients. Mol Psychiatry, 10: 329-335.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 329-335
-
-
Yan, J.1
Oliveira, G.2
Coutinho, A.3
Yang, C.4
Feng, J.5
Katz, C.6
Sram, J.7
Bockholt, A.8
Jones, I.R.9
Craddock, N.10
Cook Jr., E.H.11
Vicente, A.12
Sommer, S.S.13
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