-
1
-
-
0017138765
-
The genetics, if any, of infantile autism and childhood schizophrenia
-
Hanson DR, Gottesman I. The genetics, if any, of infantile autism and childhood schizophrenia. J Autism Dev Disord 1976; 6:209-34.
-
(1976)
J Autism Dev Disord
, vol.6
, pp. 209-234
-
-
Hanson, D.R.1
Gottesman, I.2
-
2
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Folstein S, Rutter M. Infantile autism: a genetic study of 21 twin pairs. J Child Psychol Psychiatry 1977;18:297-321.
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
5
-
-
0027101923
-
Is Rett syndrome a subtype of pervasive developmental disorder?
-
Tsai LY. Is Rett syndrome a subtype of pervasive developmental disorder? J Autism Dev Disord 1992;22:551-61.
-
(1992)
J Autism Dev Disord
, vol.22
, pp. 551-561
-
-
Tsai, L.Y.1
-
6
-
-
0027080250
-
Childhood disintegrate disorder: Issues for DSM-IV
-
Volkmar FR. Childhood disintegrate disorder: issues for DSM-IV. J Autism Dev Disord 1992;22:625-42.
-
(1992)
J Autism Dev Disord
, vol.22
, pp. 625-642
-
-
Volkmar, F.R.1
-
7
-
-
0027101924
-
The validity of autistic spectrum disorders: A literature review
-
Szatmari P.The validity of autistic spectrum disorders: a literature review. J Autism Dev Disord 1992;22:583-600.
-
(1992)
J Autism Dev Disord
, vol.22
, pp. 583-600
-
-
Szatmari, P.1
-
8
-
-
0039936043
-
Epidemiological surveys of autism
-
Volkmar FCUP. New York: Cambridge University Press
-
Fombonne E. Epidemiological surveys of autism. In: Volkmar FCUP. Monograph on autism. New York: Cambridge University Press; 1998.
-
(1998)
Monograph on Autism
-
-
Fombonne, E.1
-
10
-
-
0027501283
-
The epidemiology of Asperger syndrome: A total population study
-
Ehlers S, Gillberg C. The epidemiology of Asperger syndrome: a total population study. J Child Psychol Psychiatry 1993;34:1327-50.
-
(1993)
J Child Psychol Psychiatry
, vol.34
, pp. 1327-1350
-
-
Ehlers, S.1
Gillberg, C.2
-
13
-
-
0029944752
-
Brief report: Genetic, prenatal, and immunologic factors
-
Smalley SL, Collins F. Brief report: genetic, prenatal, and immunologic factors. J Autism Dev Disord 1996;26:195-8.
-
(1996)
J Autism Dev Disord
, vol.26
, pp. 195-198
-
-
Smalley, S.L.1
Collins, F.2
-
14
-
-
0028359950
-
A case-control family history study of autism
-
Bolton P, MacDonald H, Pickles A, Rios P, Goode S, Crowson M, et al. A case-control family history study of autism. J Child Psychol Psychiatry 1994;35:877-900.
-
(1994)
J Child Psychol Psychiatry
, vol.35
, pp. 877-900
-
-
Bolton, P.1
MacDonald, H.2
Pickles, A.3
Rios, P.4
Goode, S.5
Crowson, M.6
-
15
-
-
0024203213
-
Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease
-
DeLong RG, Dwyer JT. Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease. J Autism Dm Disord 1988;18:593-600.
-
(1988)
J Autism Dm Disord
, vol.18
, pp. 593-600
-
-
DeLong, R.G.1
Dwyer, J.T.2
-
16
-
-
0026596805
-
Siblings and parents of children with autism: A controlled population-based study
-
Gillberg C, Gillberg IC, Steffenberg S. Siblings and parents of children with autism: a controlled population-based study. Dev Med Child Neurol 1992;34:389-98.
-
(1992)
Dev Med Child Neurol
, vol.34
, pp. 389-398
-
-
Gillberg, C.1
Gillberg, I.C.2
Steffenberg, S.3
-
17
-
-
0027438546
-
Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders
-
Szatmari P, Jones MB, Tuff L, Bartolucci G, Fisman S, Mahoney W. Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders. J Am Acad Child Adolesc Psychiatry 1993;32:1264-73.
-
(1993)
J Am Acad Child Adolesc 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
-
18
-
-
0025997752
-
Complex segregation analysis of autism
-
Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, et al. Complex segregation analysis of autism. Am J Hum Genet 1991 49:932-8.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 932-938
-
-
Jorde, L.B.1
Hasstedt, S.J.2
Ritvo, E.R.3
Mason-Brothers, A.4
Freeman, B.J.5
Pingree, C.6
-
19
-
-
0029134874
-
Latent class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
-
Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim C H, et al. Latent class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet 1995;57:717-26.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
Bailey, A.4
Le Couteur, A.5
Sim, C.H.6
-
20
-
-
0029116940
-
Parents and collateral relatives of children with pervasive developmental disorders: A family history study
-
Szatmari P, Jones MB, Fisman S, Tuff L, Bartolucci G, Mahoney WJ, et al. Parents and collateral relatives of children with pervasive developmental disorders: a family history study. Am J Med Genet 1995;60:282-9.
-
(1995)
Am J Med Genet
, vol.60
, pp. 282-289
-
-
Szatmari, P.1
Jones, M.B.2
Fisman, S.3
Tuff, L.4
Bartolucci, G.5
Mahoney, W.J.6
-
21
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg I, Jakobsson G et al.A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 1989; 30:405-16.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
Andersson, L.4
Gillberg, I.5
Jakobsson, G.6
-
22
-
-
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, et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med 1995;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
-
23
-
-
0021960916
-
Concordance for the syndrome of autism in 40 pairs of affected twins
-
Ritvo ER, Freeman BJ, Mason-Brothers A, Mo A, Ritvo AM. Concordance for the syndrome of autism in 40 pairs of affected twins. Am J Psychiatry 1985;142:74-7.
-
(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
-
25
-
-
0001937842
-
Methods in psychiatric genetics
-
Tsuang MT, Tohen M, Zahner GEP, editors. New York: Wiley-Liss
-
Faraone SV, Tsuang MT. Methods in psychiatric genetics. In: Tsuang MT, Tohen M, Zahner GEP, editors. Textbook in psychiatric epidemiology. New York: Wiley-Liss; 1995. p. 81-134.
-
(1995)
Textbook in Psychiatric Epidemiology
, pp. 81-134
-
-
Faraone, S.V.1
Tsuang, M.T.2
-
27
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch H, Merikangas KR. The future of genetic studies of complex human diseases. Science 1996;173:1516-7.
-
(1996)
Science
, vol.173
, pp. 1516-1517
-
-
Risch, H.1
Merikangas, K.R.2
-
28
-
-
0027367005
-
Genotype relative risks: Methods for design and analysis of candidate-gene association studies
-
Schaid DJ, Sommer SS. Genotype relative risks: methods for design and analysis of candidate-gene association studies. Am J Hum Genet 1993;53:1114-26.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1114-1126
-
-
Schaid, D.J.1
Sommer, S.S.2
-
29
-
-
0025355888
-
Genetic linkage and complex diseases, with special reference to psychiatric disorders
-
Risch N. Genetic linkage and complex diseases, with special reference to psychiatric disorders. Genet Epidemiol 1990;7:3-45.
-
(1990)
Genet Epidemiol
, vol.7
, pp. 3-45
-
-
Risch, N.1
-
31
-
-
0020684781
-
The development of sex differences in infantile autism
-
Tsai LY, Beisler JM. The development of sex differences in infantile autism. Br J Psychiatry 1983;42:373-8.
-
(1983)
Br J Psychiatry
, vol.42
, pp. 373-378
-
-
Tsai, L.Y.1
Beisler, J.M.2
-
32
-
-
0021839624
-
Differences in sex ratios in autism as a function of measured intelligence
-
Lord C, Schopler E. Differences in sex ratios in autism as a function of measured intelligence. J Autism Dev Disord 1985; 15:185-193.
-
(1985)
J Autism Dev Disord
, vol.15
, pp. 185-193
-
-
Lord, C.1
Schopler, E.2
-
34
-
-
0027191543
-
Sex differences in higher functioning people with autism
-
McLennan JD, Lord C, Schopler E. Sex differences in higher functioning people with autism. J Autism Dev Disord 1993;23: 217-27.
-
(1993)
J Autism Dev Disord
, vol.23
, pp. 217-227
-
-
McLennan, J.D.1
Lord, C.2
Schopler, E.3
-
35
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families
-
Narod SA, Ford D, Devilee P, Barkardottir RB, Lynch HT, Smith SA, et al. An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Am J Hum Genet 1995:56:254-64.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 254-264
-
-
Narod, S.A.1
Ford, D.2
Devilee, P.3
Barkardottir, R.B.4
Lynch, H.T.5
Smith, S.A.6
-
36
-
-
0025179972
-
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder
-
St. George-Hyslop P, Haines J, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature 1990;347:194-7.
-
(1990)
Nature
, vol.347
, pp. 194-197
-
-
St. George-Hyslop, P.1
Haines, J.2
Farrer, L.A.3
Polinsky, R.4
Van Broeckhoven, C.5
Goate, A.6
-
37
-
-
0028012565
-
Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families
-
Spiker D, Lotspeich L, Kraemer HC, Hallmayer J, McMahon W, Petersen PB, et al. Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families. Am J Med Genet 1994;54:27-35.
-
(1994)
Am J Med Genet
, vol.54
, pp. 27-35
-
-
Spiker, D.1
Lotspeich, L.2
Kraemer, H.C.3
Hallmayer, J.4
McMahon, W.5
Petersen, P.B.6
-
38
-
-
0029959476
-
A broader phenotype of autism: The clinical spectrum in twins
-
Le Couteur A, Bailey A, Goode S, Pickles A, Robertson S, Gottesman I, et al. A broader phenotype of autism: the clinical spectrum in twins. J Child Psychol Psychiatry 1996 37:785-801.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 785-801
-
-
Le Couteur, A.1
Bailey, A.2
Goode, S.3
Pickles, A.4
Robertson, S.5
Gottesman, I.6
-
39
-
-
0024336203
-
The UCLA-University of Utah epidemiologic survey of autism: Recurrence risk estimates and genetic counselling
-
Ritvo ER, Jorde LB, Mason-Brothers A, Freeman BJ, Pingree C, Jones MB, et al. The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counselling. Am J Psychiatry 1989;146:1032-6.
-
(1989)
Am J Psychiatry
, vol.146
, pp. 1032-1036
-
-
Ritvo, E.R.1
Jorde, L.B.2
Mason-Brothers, A.3
Freeman, B.J.4
Pingree, C.5
Jones, M.B.6
-
40
-
-
0039343806
-
Familial factors influence the severity of pervasive developmental disorders; evidence for possible genetic heterogeneity
-
In press
-
MacLean JE, Szatmari P, Jones MB, Bryson SE, Mahoney WJ, Bartolucci G, et al. Familial factors influence the severity of pervasive developmental disorders; evidence for possible genetic heterogeneity. J Am Acad Child Adolesc Psychiatry. In press.
-
J Am Acad Child Adolesc Psychiatry
-
-
MacLean, J.E.1
Szatmari, P.2
Jones, M.B.3
Bryson, S.E.4
Mahoney, W.J.5
Bartolucci, G.6
-
41
-
-
0031035019
-
Broader autism phenotype: Evidence from a family history study of multiple-incidence autism families
-
Piven J, Palmer P, Jacobi D, Childress D, Arndt S. Broader autism phenotype: evidence from a family history study of multiple-incidence autism families. Am J Psychiatry 1997;154: 185-90.
-
(1997)
Am J Psychiatry
, vol.154
, pp. 185-190
-
-
Piven, J.1
Palmer, P.2
Jacobi, D.3
Childress, D.4
Arndt, S.5
-
42
-
-
8244234472
-
Evidence of linkage between the serotonin transporster and autistic disorder
-
Cook EH, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, et al. Evidence of linkage between the serotonin transporster and autistic disorder. Mol Psychiatry 1997;2:247-50.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247-250
-
-
Cook, E.H.1
Courchesne, R.2
Lord, C.3
Cox, N.J.4
Yan, S.5
Lincoln, A.6
-
43
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 1998;7(:3):571-8.
-
(1998)
Hum Mol Genet
, vol.7
, Issue.3
, pp. 571-578
-
-
-
44
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck SM, Poutstka F, Benner A, Lesch KP, Poustka A. Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet 1997;6(13):2233-8.
-
(1997)
Hum Mol Genet
, vol.6
, Issue.13
, pp. 2233-2238
-
-
Klauck, S.M.1
Poutstka, F.2
Benner, A.3
Lesch, K.P.4
Poustka, A.5
|