-
2
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I et al. (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
-
3
-
-
0023683047
-
First report of a Canadian epidemiological study of autistic syndromes
-
Bryson SE, Clark BS, Smith IM (1988), First report of a Canadian epidemiological study of autistic syndromes. J Child Psychol Psychiatry 29:433-445
-
(1988)
J Child Psychol Psychiatry
, vol.29
, pp. 433-445
-
-
Bryson, S.E.1
Clark, B.S.2
Smith, I.M.3
-
4
-
-
0029948203
-
Clinical similarities in siblings with schizophrenia
-
Burke JG, Murphy BM, Bray JC, Walsh D, Kendler KS (1996), Clinical similarities in siblings with schizophrenia. Am J Med Genet 67:239-243
-
(1996)
Am J Med Genet
, vol.67
, pp. 239-243
-
-
Burke, J.G.1
Murphy, B.M.2
Bray, J.C.3
Walsh, D.4
Kendler, K.S.5
-
5
-
-
0019369245
-
Developing criteria for establishing interrater reliability of specific items in a given inventory
-
Cicchetti DV, Sparrow SS (1981), Developing criteria for establishing interrater reliability of specific items in a given inventory. Am J Ment Defic 86:127-137
-
(1981)
Am J Ment Defic
, vol.86
, pp. 127-137
-
-
Cicchetti, D.V.1
Sparrow, S.S.2
-
6
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EH Jr, Courchesne R, Lord C et al. (1997), Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry 2:247-250
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247-250
-
-
Cook Jr., E.H.1
Courchesne, R.2
Lord, C.3
-
7
-
-
0027501283
-
The epidemiology of Asperger syndrome: A total population study
-
Ehlers S, Gillberg C (1993), The epidemiology of Asperger syndrome: a total population study. J Autism Dev Disord 34:1327-1350
-
(1993)
J Autism Dev Disord
, vol.34
, pp. 1327-1350
-
-
Ehlers, S.1
Gillberg, C.2
-
8
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Holstein S, Rutter M (1977), Infantile autism: a genetic study of 21 twin pairs. J Child Psychol Psychiatry 18:297-321
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Holstein, S.1
Rutter, M.2
-
10
-
-
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. J Child Psychol Psychiatry 38:667-683
-
(1997)
J Child Psychol Psychiatry
, vol.38
, pp. 667-683
-
-
Fombonne, E.1
Bolton, P.2
Prior, J.3
Jordon, H.4
Rutter, M.5
-
11
-
-
0030050286
-
Clinical and pathological correlates of apolipoprotein E epsilon 4 in Alzheimer's disease
-
Gonez-Isla T, West HL, Rebek GW et al. (1996), Clinical and pathological correlates of apolipoprotein E epsilon 4 in Alzheimer's disease. Ann Neurol 39:62-70
-
(1996)
Ann Neurol
, vol.39
, pp. 62-70
-
-
Gonez-Isla, T.1
West, H.L.2
Rebek, G.W.3
-
13
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium (1998), A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 7:571-578
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
14
-
-
0031029394
-
Resemblance of psychotic symptoms and syndromes in affected sibling pairs from the Irish Study of High-Density Schizophrenia Families: Evidence for possible etiologic heterogeneity
-
Kendler KS, Karkowski-Shuman L, O'Neill FA, Straub RE, MacLean CJ, Walsh D (1997), Resemblance of psychotic symptoms and syndromes in affected sibling pairs from the Irish Study of High-Density Schizophrenia Families: evidence for possible etiologic heterogeneity. Am J Psychiatry 154:191-198
-
(1997)
Am J Psychiatry
, vol.154
, pp. 191-198
-
-
Kendler, K.S.1
Karkowski-Shuman, L.2
O'Neill, F.A.3
Straub, R.E.4
MacLean, C.J.5
Walsh, D.6
-
15
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauk SM, Poustka BA, Lesch KP, Poustka A (1997), Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet 6:2233-2238
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233-2238
-
-
Klauk, S.M.1
Poustka, B.A.2
Lesch, K.P.3
Poustka, A.4
-
16
-
-
0029959476
-
A broader phenotype of autism: The clinical spectrum in twins
-
Le Couteur A, Bailey A, Goode S et al. (1996), A broader phenotype of autism: the clinical spectrum in twins. J Child Psychol Psychiatry 37:785-801
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 785-801
-
-
Le Couteur, A.1
Bailey, A.2
Goode, S.3
-
17
-
-
0024430952
-
Autism Diagnostic Interview a standardized investigator-based interview
-
Le Couteur A, Rutter M, Lord C et al. (1989), Autism Diagnostic Interview a standardized investigator-based interview. J Autism Dev Disord 19:363-387
-
(1989)
J Autism Dev Disord
, vol.19
, pp. 363-387
-
-
Le Couteur, A.1
Rutter, M.2
Lord, C.3
-
18
-
-
0024369122
-
Autism Diagnostic Observation Schedule: A standardized observation of communication and social behavior
-
Lord C, Rutter M, Goode S et al. (1989), Autism Diagnostic Observation Schedule: a standardized observation of communication and social behavior. J Autism Dev Disord 19:185-212
-
(1989)
J Autism Dev Disord
, vol.19
, pp. 185-212
-
-
Lord, C.1
Rutter, M.2
Goode, S.3
-
19
-
-
0027997172
-
Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorder
-
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 disorder. J Autism Dev Disord 24:659-685
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
20
-
-
0031932927
-
Reliability and accuracy of differentiating pervasive developmental disorder subtypes
-
Mahoney WJ, Szatmari P, MacLean JE et al. (1998), Reliability and accuracy of differentiating pervasive developmental disorder subtypes. J Am Acad Child Adolesc Psychiatry 37:278-285
-
(1998)
J Am Acad Child Adolesc Psychiatry
, vol.37
, pp. 278-285
-
-
Mahoney, W.J.1
Szatmari, P.2
MacLean, J.E.3
-
21
-
-
0031051256
-
Did Asperger's cases have Asperger disorder? A research note
-
Miller JN, Ozonoff S (1997), Did Asperger's cases have Asperger disorder? A research note. J Child Psychol Psychiatry 38:247-251
-
(1997)
J Child Psychol Psychiatry
, vol.38
, pp. 247-251
-
-
Miller, J.N.1
Ozonoff, S.2
-
22
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families
-
Narod SA, Ford D, Devilee P et al. and the Breast Cancer Linkage Consortium (1995), An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Am J Hum Genet 56:254-264
-
(1995)
Am J Hum Genet
, vol.56
, pp. 254-264
-
-
Narod, S.A.1
Ford, D.2
Devilee, P.3
-
23
-
-
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 et al. (1995), 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 57:717-726
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
-
24
-
-
0021960916
-
Concordance for the syndrome of autism in 40 pairs of afflicted twins
-
Ritvo ER, Freeman BJ, Mason-Brothers A, Mo A, Ritvo AM (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
-
25
-
-
0030024492
-
Molecular genetics of neurofibromatosis type I (NFI)
-
Shen MH, Harper BS, Upadhyaya M (1996), Molecular genetics of neurofibromatosis type I (NFI). J Med Genet 33:2-17
-
(1996)
J Med Genet
, vol.33
, pp. 2-17
-
-
Shen, M.H.1
Harper, B.S.2
Upadhyaya, M.3
-
27
-
-
0028012565
-
Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families
-
Spiker D, Lotspeich L, Kraemer HC et al. (1994), Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families. Am J Med Genet 54:27-35
-
(1994)
Am J Med Genet
, vol.54
, pp. 27-35
-
-
Spiker, D.1
Lotspeich, L.2
Kraemer, H.C.3
-
28
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L et al. (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
Hellgren, L.3
-
29
-
-
0028884674
-
Asperger's syndrome and autism: Differences in behavior, cognition and adaptive functioning
-
Szatmari P, Archer L, Fisman S, Streiner DL, Wilson FJ (1995), Asperger's syndrome and autism: differences in behavior, cognition and adaptive functioning. J Am Acad Child Adolesc Psychiatry 34:1662-1671
-
(1995)
J Am Acad Child Adolesc Psychiatry
, vol.34
, pp. 1662-1671
-
-
Szatmari, P.1
Archer, L.2
Fisman, S.3
Streiner, D.L.4
Wilson, F.J.5
-
30
-
-
13044258318
-
The two-year outcome of preschool children with autism and Asperger syndrome
-
Toronto, October
-
Szatmari P, Bryson SE, Streiner DL, Wilson FJ, Ryerse C (1997), The two-year outcome of preschool children with autism and Asperger syndrome. Presented at the annual meeting of the American Academy of Child and Adolescent Psychiatry, Toronto, October
-
(1997)
Annual Meeting of the American Academy of Child and Adolescent Psychiatry
-
-
Szatmari, P.1
Bryson, S.E.2
Streiner, D.L.3
Wilson, F.J.4
Ryerse, C.5
-
32
-
-
0029813328
-
High phenotypic correlations among siblings with autism and pervasive developmental disorders (PDD)
-
Szatmari P, Jones MB, Holden J et al. (1996), High phenotypic correlations among siblings with autism and pervasive developmental disorders (PDD). Am J Med Genet 67:354-360
-
(1996)
Am J Med Genet
, vol.67
, pp. 354-360
-
-
Szatmari, P.1
Jones, M.B.2
Holden, J.3
-
33
-
-
0027438546
-
Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders
-
Szatmari P, Jones MB, Tuff LP, Bartolucci G, Fisman S, Mahoney WJ (1993), Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders. J Am Acad Child Adolesc Psychiatry 32:1264-1273
-
(1993)
J Am Acad Child Adolesc Psychiatry
, vol.32
, pp. 1264-1273
-
-
Szatmari, P.1
Jones, M.B.2
Tuff, L.P.3
Bartolucci, G.4
Fisman, S.5
Mahoney, W.J.6
-
34
-
-
0032462548
-
The genetics of autism: An overview and new directions
-
Szatmari P, Jones MB, Zwaigenbaum L, MacLean JE (1998), The genetics of autism: an overview and new directions. J Autism Dev Disord 28:351-368
-
(1998)
J Autism Dev Disord
, vol.28
, pp. 351-368
-
-
Szatmari, P.1
Jones, M.B.2
Zwaigenbaum, L.3
MacLean, J.E.4
-
35
-
-
0023114380
-
Social deficits in autism: An operational approach using the Vineland Adaptive Behavior Scales
-
Volkmar FR, Sparrow SS, Goudreau D, Cicchetti D, Paul R, Cohen DJ (1987), Social deficits in autism: an operational approach using the Vineland Adaptive Behavior Scales. J Am Acad Child Adolesc Psychiatry 26:156-161
-
(1987)
J Am Acad Child Adolesc Psychiatry
, vol.26
, pp. 156-161
-
-
Volkmar, F.R.1
Sparrow, S.S.2
Goudreau, D.3
Cicchetti, D.4
Paul, R.5
Cohen, D.J.6
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