-
1
-
-
0030879482
-
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
Albrecht U, Sutcliffe J, Cattanach B, et al. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nature Genet 1997;17: 75-78.
-
(1997)
Nature Genet
, vol.17
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.2
Cattanach, B.3
-
2
-
-
0027263256
-
Autism and megalencephaly
-
Bailey A, Luthert P, Bolton P, et al. Autism and megalencephaly. Lancet 1993;341:1225-1226.
-
(1993)
Lancet
, vol.341
, pp. 1225-1226
-
-
Bailey, A.1
Luthert, P.2
Bolton, P.3
-
3
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I, et al. Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med 1995;25:63-78.
-
(1995)
Psychol Med
, vol.25
, pp. 63-78
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
-
4
-
-
0029872978
-
Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
Bailey A, Philips W, Rutter M. Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. J Child Psychol Psychiatry 1996;37:89-126.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 89-126
-
-
Bailey, A.1
Philips, W.2
Rutter, M.3
-
5
-
-
0027934165
-
Duplication of chromosome 15q11-13 in two individuals with autistic disorder
-
Baker P, Piven J, Schwartz S, et al. Duplication of chromosome 15q11-13 in two individuals with autistic disorder. J Autism Dev Disord 1994;24:529-535.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 529-535
-
-
Baker, P.1
Piven, J.2
Schwartz, S.3
-
6
-
-
0021343570
-
A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus
-
Bell G, Horita S, Karam J. A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus. Diabetes 1984;33:176-183.
-
(1984)
Diabetes
, vol.33
, pp. 176-183
-
-
Bell, G.1
Horita, S.2
Karam, J.3
-
7
-
-
0029790129
-
Asperger syndrome associated with dystrophia myotonica of Steinert
-
Blondis T, Cook E, Koza-Taylor P, et al. Asperger syndrome associated with dystrophia myotonica of Steinert. Dev Med Child Neurol 1996;38:840-847.
-
(1996)
Dev Med Child Neurol
, vol.38
, pp. 840-847
-
-
Blondis, T.1
Cook, E.2
Koza-Taylor, P.3
-
9
-
-
0030904115
-
Family history of cognitive disabilities in first-degree relatives of autistic and mentally retarded children
-
Boutin P, Maziade M, Merette C, et al. Family history of cognitive disabilities in first-degree relatives of autistic and mentally retarded children. J Autism Dev Disord 1997;27:165-176.
-
(1997)
J Autism Dev Disord
, vol.27
, pp. 165-176
-
-
Boutin, P.1
Maziade, M.2
Merette, C.3
-
10
-
-
0031444629
-
Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations
-
Browne CE, Dennis NR, Maher E, et al. Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations. Am J Hum Genet 1997;61:1342-1352.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1342-1352
-
-
Browne, C.E.1
Dennis, N.R.2
Maher, E.3
-
11
-
-
0031459373
-
Genomewide transmission/disequilibrium testing-consideration of the genotypic relative risks at disease loci
-
Camp NJ. Genomewide transmission/disequilibrium testing-consideration of the genotypic relative risks at disease loci. Am J Hum Genet 1997;61:1424-1430.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1424-1430
-
-
Camp, N.J.1
-
12
-
-
0031974209
-
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
-
Charlier C, Singh N, Ryan S, et al. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nature Genet 1998;18:53-55.
-
(1998)
Nature Genet
, vol.18
, pp. 53-55
-
-
Charlier, C.1
Singh, N.2
Ryan, S.3
-
13
-
-
0030824236
-
Altered serotonin synthesis in the dentatothalamocortical pathway in autistic boys
-
Chugani DC, Muzik O, Rothermel R, et al. Altered serotonin synthesis in the dentatothalamocortical pathway in autistic boys. Ann Neurol 1997;42:666-669.
-
(1997)
Ann Neurol
, vol.42
, pp. 666-669
-
-
Chugani, D.C.1
Muzik, O.2
Rothermel, R.3
-
15
-
-
0025925207
-
The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders
-
Comings DE, Comings BG, Muhleman D, et al. The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders. JAMA 1991;266:1793-1800.
-
(1991)
JAMA
, vol.266
, pp. 1793-1800
-
-
Comings, D.E.1
Comings, B.G.2
Muhleman, D.3
-
16
-
-
0028934286
-
No association of a tyrosine hydroxylase gene tetranucleotide repeat polymorphism in autism, Tourette syndrome, or ADHD
-
Comings D, Gade R, Muhleman D, et al. No association of a tyrosine hydroxylase gene tetranucleotide repeat polymorphism in autism, Tourette syndrome, or ADHD. Biol Psychiatry 1995;37:484-486.
-
(1995)
Biol Psychiatry
, vol.37
, pp. 484-486
-
-
Comings, D.1
Gade, R.2
Muhleman, D.3
-
17
-
-
0030602650
-
Studies of the c-Harvey-Ras gene in psychiatric disorders
-
Comings DE, Wu SJ, Chiu C, et al. Studies of the c-Harvey-Ras gene in psychiatric disorders. Psychiatry Res 1996;63:25-32.
-
(1996)
Psychiatry Res
, vol.63
, pp. 25-32
-
-
Comings, D.E.1
Wu, S.J.2
Chiu, C.3
-
18
-
-
0028946270
-
Pediatric psychopharmacology II: Autistic disorder and other pervasive developmental disorders
-
Cook E, Leventhal B. Pediatric psychopharmacology II: Autistic disorder and other pervasive developmental disorders. Child Adolesc Psychiatr Chn North Am 1995;4:381-399.
-
(1995)
Child Adolesc Psychiatr Chn North Am
, vol.4
, pp. 381-399
-
-
Cook, E.1
Leventhal, B.2
-
19
-
-
10544234621
-
The serotonin system in autism
-
Cook E, Leventhal B. The serotonin system in autism. Curr Opin Pediatr 1996;8:348-354.
-
(1996)
Curr Opin Pediatr
, vol.8
, pp. 348-354
-
-
Cook, E.1
Leventhal, B.2
-
20
-
-
0028365630
-
Depressive and obsessive-compulsive symptoms in hyperserotonemic parents of children with autistic disorder
-
Cook EH, Charak DA, Arida J, et al. Depressive and obsessive-compulsive symptoms in hyperserotonemic parents of children with autistic disorder. Psychiatr Res 1994;52:25-33.
-
(1994)
Psychiatr Res
, vol.52
, pp. 25-33
-
-
Cook, E.H.1
Charak, D.A.2
Arida, J.3
-
21
-
-
0028987091
-
Association of attention deficit disorder and the dopamine transporter gene
-
Cook E, Stein M, Krasowski M, et al. Association of attention deficit disorder and the dopamine transporter gene. Am J Hum Genet 1995;56: 993-998.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 993-998
-
-
Cook, E.1
Stein, M.2
Krasowski, M.3
-
22
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook E, Courchesne R, Lord C, et al. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry 1997a;2:247-250.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247-250
-
-
Cook, E.1
Courchesne, R.2
Lord, C.3
-
23
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook E, Lindgren V, Leventhal B, et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 1997b;60:928-934.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 928-934
-
-
Cook, E.1
Lindgren, V.2
Leventhal, B.3
-
24
-
-
17344364660
-
Linkage disequilibrium mapping with 15q11-13 markers in autistic disorder
-
Cook EH, Courchesne R, Cox NJ, et al. Linkage disequilibrium mapping with 15q11-13 markers in autistic disorder. Am J Hum Genet 1998;62:1077-1083.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1077-1083
-
-
Cook, E.H.1
Courchesne, R.2
Cox, N.J.3
-
25
-
-
0023906645
-
Hypoplasia of cerebellar vermal lobules VI and VII in autism
-
Courchesne E, Yeung CR, Press GA, Hypoplasia of cerebellar vermal lobules VI and VII in autism. N Engl J Med 1988;318:1349-1354.
-
(1988)
N Engl J Med
, vol.318
, pp. 1349-1354
-
-
Courchesne, E.1
Yeung, C.R.2
Press, G.A.3
-
26
-
-
0028821373
-
Supernumerary marker 15 chromosomes: A clinical, molecular and FISH approach to diagnosis and prognosis
-
Crolla J, Harvey J, Sitch F, et al. Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis. Hum Genet 1995;95:161-170.
-
(1995)
Hum Genet
, vol.95
, pp. 161-170
-
-
Crolla, J.1
Harvey, J.2
Sitch, F.3
-
27
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies J, Kawaguchi Y, Bennett S, et al. A genome-wide search for human type 1 diabetes susceptibility genes. Nature 1994;371: 130-136.
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.1
Kawaguchi, Y.2
Bennett, S.3
-
29
-
-
0342601394
-
Low medial prefrontal dopaminergic activity in autistic children
-
Ernst M, Zametkin AJ, Matochik JA, et al. Low medial prefrontal dopaminergic activity in autistic children [letter]. Lancet 1997;350:638.
-
(1997)
Lancet
, vol.350
, pp. 638
-
-
Ernst, M.1
Zametkin, A.J.2
Matochik, J.A.3
-
30
-
-
0031469678
-
Genomic imprinting: A chromatin connection
-
Feil R, Kelsey G. Genomic imprinting: A chromatin connection. Am J Hum Genet 1997;61: 1213-1219.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1213-1219
-
-
Feil, R.1
Kelsey, G.2
-
31
-
-
0005088916
-
The status of the dopamine D2 receptor (DRD2) locus as a susceptibility factor in autism: Family association studies
-
Flanagan S, Cook E, Courchesne E, et al. The status of the dopamine D2 receptor (DRD2) locus as a susceptibility factor in autism: Family association studies. Soc Neurosci Abstr 1995; 21.2053.
-
(1995)
Soc Neurosci Abstr
, vol.21
, pp. 2053
-
-
Flanagan, S.1
Cook, E.2
Courchesne, E.3
-
32
-
-
0030070898
-
Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation
-
Flejter WL, Bennett-Baker PE, Ghaziuddin M, et al. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. Am J Med Genet 1996;61:182-187.
-
(1996)
Am J Med Genet
, vol.61
, pp. 182-187
-
-
Flejter, W.L.1
Bennett-Baker, P.E.2
Ghaziuddin, M.3
-
34
-
-
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 1977b;18:297-321.
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
35
-
-
0023950384
-
Autism: Familial aggregation and genetic implications
-
Folstein SE, Rutter ML. Autism: Familial aggregation and genetic implications. J Autism Dev Disord 1988;18:3-30.
-
(1988)
J Autism Dev Disord
, vol.18
, pp. 3-30
-
-
Folstein, S.E.1
Rutter, M.L.2
-
36
-
-
0030821680
-
A family study of autism: Cognitive patterns and levels in parents and siblings
-
Fombonne E, Bolton P, Prior J, et al. A family study of autism: cognitive patterns and levels in parents and siblings. J Child Psychol Psychiatry 1997;38:667-683.
-
(1997)
J Child Psychol Psychiatry
, vol.38
, pp. 667-683
-
-
Fombonne, E.1
Bolton, P.2
Prior, J.3
-
38
-
-
0027304995
-
Abnormalities of chromosome 18 in a girl with mental retardation and autistic disorder
-
Ghaziuddin M, Sheldon S, Tsai LY, et al. Abnormalities of chromosome 18 in a girl with mental retardation and autistic disorder. J Intellect Disabil Res 1993;37:313-317.
-
(1993)
J Intellect Disabil Res
, vol.37
, pp. 313-317
-
-
Ghaziuddin, M.1
Sheldon, S.2
Tsai, L.Y.3
-
39
-
-
0030844034
-
Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism
-
Gill M, Daly G, Heron S, et al. Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism. Mol Psychiatry 1997;2:311-313.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 311-313
-
-
Gill, M.1
Daly, G.2
Heron, S.3
-
40
-
-
0021932002
-
Chromosome abnormalities in infantile autism and other childhood psychoses: A population study of 66 cases
-
Gillberg C, Wahlstrom J. Chromosome abnormalities in infantile autism and other childhood psychoses: A population study of 66 cases. Dev Med Child Neurol 1985;27:293-294.
-
(1985)
Dev Med Child Neurol
, vol.27
, pp. 293-294
-
-
Gillberg, C.1
Wahlstrom, J.2
-
42
-
-
0027158571
-
A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder
-
Gordon C, State R, Nelson J, et al. A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder. Arch Gen Psychiatry 1993;50:441-447.
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 441-447
-
-
Gordon, C.1
State, R.2
Nelson, J.3
-
43
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
-
Grigorenko EL, Wood FB, Mcyer MS, et al. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet 1997,60:27-39.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 27-39
-
-
Grigorenko, E.L.1
Wood, F.B.2
Mcyer, M.S.3
-
44
-
-
0028171490
-
Molecular analysis and test of linkage between the FMR-I gene and infantile autism in multiplex families
-
Hallmayer J, Pintado E, Lotspeich L, et al. Molecular analysis and test of linkage between the FMR-I gene and infantile autism in multiplex families. Am J Hum Genet 1994;55: 951-959.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 951-959
-
-
Hallmayer, J.1
Pintado, E.2
Lotspeich, L.3
-
45
-
-
85008560109
-
Autism and the X chromosome: Multipoint sib-pair analysis
-
Hallmayer J, Hebert J, Spiker D, et al. Autism and the X chromosome: Multipoint sib-pair analysis. Arch Gen Psychiatry 1996a;53:985-989.
-
(1996)
Arch Gen Psychiatry
, vol.53
, pp. 985-989
-
-
Hallmayer, J.1
Hebert, J.2
Spiker, D.3
-
46
-
-
0029935737
-
Male-to-male transmission in extended pedigrees with multiple cases of autism
-
Hallmayer J, Spiker D, Lotspeich L, et al. Male-to-male transmission in extended pedigrees with multiple cases of autism. Am J Med Genet 1996b;67:13-18.
-
(1996)
Am J Med Genet
, vol.67
, pp. 13-18
-
-
Hallmayer, J.1
Spiker, D.2
Lotspeich, L.3
-
47
-
-
0027419999
-
Possible association of c-Harvey-Ras-1 (HR-AS-1) marker with autism
-
Hérault J, Perrot A, Barthélémy C, et al. Possible association of c-Harvey-Ras-1 (HR-AS-1) marker with autism. Psychiatry Res 1993;46: 261-267.
-
(1993)
Psychiatry Res
, vol.46
, pp. 261-267
-
-
Hérault, J.1
Perrot, A.2
Barthélémy, C.3
-
48
-
-
0029116939
-
Autism and genetics: Clinical approach and association study with two markers of HRAS gene
-
Hérault J, Petit E, Martineau J, et al. Autism and genetics: Clinical approach and association study with two markers of HRAS gene. Am J Med Genet (Neuropsychiatr Genet) 1997;60: 276-281.
-
(1997)
Am J Med Genet (Neuropsychiatr Genet)
, vol.60
, pp. 276-281
-
-
Hérault, J.1
Petit, E.2
Martineau, J.3
-
49
-
-
0028959478
-
A case of autism associated with partial tetrasomy 15
-
Hotof M, Bolton P. A case of autism associated with partial tetrasomy 15. J Autism Dev Disord 1995;25:41-49.
-
(1995)
J Autism Dev Disord
, vol.25
, pp. 41-49
-
-
Hotof, M.1
Bolton, P.2
-
50
-
-
0027223683
-
A prevalence study of autism in tuberous sclerosis
-
Hunt A, Shepherd C. A prevalence study of autism in tuberous sclerosis. J Autism Dev Disord 1993;23:323-339.
-
(1993)
J Autism Dev Disord
, vol.23
, pp. 323-339
-
-
Hunt, A.1
Shepherd, C.2
-
51
-
-
0030795260
-
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene
-
Ishikawa-Brush Y, Powell J, Bolton P, et al. Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. Hum Mol Genet 1997;6:1241-1250.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1241-1250
-
-
Ishikawa-Brush, Y.1
Powell, J.2
Bolton, P.3
-
52
-
-
0025997752
-
Complex segregation analysis of autism
-
Jorde L, Hasstedt S, Ritvo E, et al. Complex segregation analysis of autism. Am J Hum Genet 1991;49:932-938.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 932-938
-
-
Jorde, L.1
Hasstedt, S.2
Ritvo, E.3
-
53
-
-
0000984981
-
Autistic disturbances of affective contact
-
Kanner L. Autistic disturbances of affective contact. Nerv Child 1943;2:217-250.
-
(1943)
Nerv Child
, vol.2
, pp. 217-250
-
-
Kanner, L.1
-
54
-
-
1842288542
-
Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients
-
Klauck SM, Munstermann E, Bieber-Martig B, et al. Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients. Hum Genet 1997a;100:224-229.
-
(1997)
Hum Genet
, vol.100
, pp. 224-229
-
-
Klauck, S.M.1
Munstermann, E.2
Bieber-Martig, B.3
-
55
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck SM, Poustka F, Benner A, et al. Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet 1997b;6:2233-2238.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
-
56
-
-
0030861903
-
The use of a genetic map of biallelic markers in linkage studies
-
Kruglyak L. The use of a genetic map of biallelic markers in linkage studies. Nature Genet 1997;17:21-24.
-
(1997)
Nature Genet
, vol.17
, pp. 21-24
-
-
Kruglyak, L.1
-
58
-
-
0025930895
-
Spontaneous narrative-discourse performance of parents of autistic individuals
-
Landa R, Polstein SE, Isaacs C. Spontaneous narrative-discourse performance of parents of autistic individuals. J Speech Hear Res 1991;34:1339-1345.
-
(1991)
J Speech Hear Res
, vol.34
, pp. 1339-1345
-
-
Landa, R.1
Polstein, S.E.2
Isaacs, C.3
-
59
-
-
0026519362
-
Social language use in parents of autistic individuals
-
Landa R, Piven J, Wzorek MM, et al. Social language use in parents of autistic individuals. Psychol Med 1992;22:245-254.
-
(1992)
Psychol Med
, vol.22
, pp. 245-254
-
-
Landa, R.1
Piven, J.2
Wzorek, M.M.3
-
60
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander E, Schork N. Genetic dissection of complex traits. Science 1994;265:2037-2048.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.1
Schork, N.2
-
62
-
-
0029959476
-
A broader phenotype of autism: The clinical spectrum in twins
-
Le Couteur A, Bailey A, Goode S, 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
-
63
-
-
0028205957
-
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications
-
Leana-Cox J, Jenkins L, Palmer C, et al. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: Clinical implications. Am J Hum Genet 1994;54:748-756.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 748-756
-
-
Leana-Cox, J.1
Jenkins, L.2
Palmer, C.3
-
64
-
-
0030866899
-
Social interaction and sensorimotor gating abnormalities in mice lacking Dv11
-
Lijam N, Paylor R, McDonald M, et al. Social interaction and sensorimotor gating abnormalities in mice lacking Dv11. Cell 1997;90:895-905.
-
(1997)
Cell
, vol.90
, pp. 895-905
-
-
Lijam, N.1
Paylor, R.2
McDonald, M.3
-
65
-
-
0031586148
-
Polymorphism of FXR1 showing lack of association with autism
-
Limprasert P, Zhong N, Dobkin C, et al. Polymorphism of FXR1 showing lack of association with autism [letter]. Am J Med Genet 1997;74:453-454.
-
(1997)
Am J Med Genet
, vol.74
, pp. 453-454
-
-
Limprasert, P.1
Zhong, N.2
Dobkin, C.3
-
66
-
-
0027351015
-
The neurobiology and genetics of infantile autism
-
Lotspeich LJ, Ciaranello RD. The neurobiology and genetics of infantile autism. Int Rev Neurobiol 1993;35:87-129.
-
(1993)
Int Rev Neurobiol
, vol.35
, pp. 87-129
-
-
Lotspeich, L.J.1
Ciaranello, R.D.2
-
68
-
-
0029803880
-
A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder
-
McDougle C, Naylor S, Cohen D, et al. A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder. Arch Gen Psychiatry 1996;53:1001-1008.
-
(1996)
Arch Gen Psychiatry
, vol.53
, pp. 1001-1008
-
-
McDougle, C.1
Naylor, S.2
Cohen, D.3
-
69
-
-
0030753926
-
Interstitial deletion of 20p: New candidate region for Hirschprung disease and autism?
-
Michaelis R, Skinner S, Deason R, et al. Interstitial deletion of 20p: New candidate region for Hirschprung disease and autism? Am J Med Genet 1997,71:298-304.
-
(1997)
Am J Med Genet
, vol.71
, pp. 298-304
-
-
Michaelis, R.1
Skinner, S.2
Deason, R.3
-
70
-
-
0024536523
-
Statistical properties of the haplotype relative risk
-
Ott J. Statistical properties of the haplotype relative risk. Genet Epidemiol 1989;6:127-130.
-
(1989)
Genet Epidemiol
, vol.6
, pp. 127-130
-
-
Ott, J.1
-
72
-
-
0029789619
-
Autosomal chromosome disorders and autism
-
Pearl P, Coleman M. Autosomal chromosome disorders and autism. Dev Brain Dysfunction 1996;9.224-229.
-
(1996)
Dev Brain Dysfunction
, vol.9
, pp. 224-229
-
-
Pearl, P.1
Coleman, M.2
-
73
-
-
0001777849
-
Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT)
-
Pericak-Vance M, Wolpert C, Menold M, et al. Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT). Am J Hum Genet 1997;61:A40.
-
(1997)
Am J Hum Genet
, vol.61
-
-
Pericak-Vance, M.1
Wolpert, C.2
Menold, M.3
-
74
-
-
0029169674
-
Association study with two markers of a human homeogene in infantile autism
-
Perit E, Hérault J, Martineau J, et al. Association study with two markers of a human homeogene in infantile autism. J Med Genet 1995;32;269-274.
-
(1995)
J Med Genet
, vol.32
, pp. 269-274
-
-
Perit, E.1
Hérault, J.2
Martineau, J.3
-
76
-
-
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. 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;57:717-726.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
-
77
-
-
0030734602
-
Cognitive deficits in parents from multiple-incidence autism families
-
Piven J, Palmer P. Cognitive deficits in parents from multiple-incidence autism families. J Child Psychol Psychiatry 1997;38:1011-1021.
-
(1997)
J Child Psychol Psychiatry
, vol.38
, pp. 1011-1021
-
-
Piven, J.1
Palmer, P.2
-
78
-
-
0025239714
-
A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals
-
Piven J, Gayle J, Chase GA, et al. A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals. J Am Acad Child Adolesc Psychiatry 1990;29:177-183.
-
(1990)
J Am Acad Child Adolesc Psychiatry
, vol.29
, pp. 177-183
-
-
Piven, J.1
Gayle, J.2
Chase, G.A.3
-
80
-
-
0025973054
-
Platelet serotonin, a possible marker for familial autism
-
Piven J, Tsai G, Nehme E, et al. Platelet serotonin, a possible marker for familial autism. J Autism Dev Disord 1991b;21:51-59.
-
(1991)
J Autism Dev Disord
, vol.21
, pp. 51-59
-
-
Piven, J.1
Tsai, G.2
Nehme, E.3
-
81
-
-
0028074514
-
Personality characteristics of the parents of autistic individuals
-
Piven J, Wzorek M, Landa R, et al. Personality characteristics of the parents of autistic individuals. Psychol Med 1994;24:783-796.
-
(1994)
Psychol Med
, vol.24
, pp. 783-796
-
-
Piven, J.1
Wzorek, M.2
Landa, R.3
-
82
-
-
0029111597
-
An MRI study of brain size in autism
-
Piven J, Arndt S, Bailey J, et al. An MRI study of brain size in autism. Am J Psychiatry 1995;152: 1145-1149.
-
(1995)
Am J Psychiatry
, vol.152
, pp. 1145-1149
-
-
Piven, J.1
Arndt, S.2
Bailey, J.3
-
83
-
-
0031035019
-
Broader autism phenotype: Evidence from a family history study of multiple-incidence autism families
-
Piven J, Palmer P, Jacobi D, et al. Broader autism phenotype: Evidence from a family history study of multiple-incidence autism families. Am J Psychiatry 1997a;154:185-190.
-
(1997)
Am J Psychiatry
, vol.154
, pp. 185-190
-
-
Piven, J.1
Palmer, P.2
Jacobi, D.3
-
84
-
-
0030799999
-
Personality and language characteristics in parents from multiple- incidence autism families
-
Piven J, Palmer P, Landa R, et al. Personality and language characteristics in parents from multiple- incidence autism families. Am J Med Genet 1997b;74:398-411.
-
(1997)
Am J Med Genet
, vol.74
, pp. 398-411
-
-
Piven, J.1
Palmer, P.2
Landa, R.3
-
85
-
-
0025201932
-
Fragile X syndrome, DSM-III-R, and autism
-
Reiss AL, Freund L, Fragile X syndrome, DSM-III-R, and autism. J Am Acad Child Adolesc Psychiatry 1990;29:885-891.
-
(1990)
J Am Acad Child Adolesc Psychiatry
, vol.29
, pp. 885-891
-
-
Reiss, A.L.1
Freund, L.2
-
86
-
-
0026649793
-
Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children
-
Reiss AL, Freund L. Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children. Am J Med Genet 1992;43:35-46.
-
(1992)
Am J Med Genet
, vol.43
, pp. 35-46
-
-
Reiss, A.L.1
Freund, L.2
-
87
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science 1996;273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
88
-
-
0021960916
-
Concordance for the syndrome of autism in 40 pairs of afflicted twins
-
Ritvo ER, Freeman BJ, Mason-Brothers A, et al. Concordance for the syndrome of autism in 40 pairs of afflicted twins. Am J Psychiatry 1985a;142:74-77.
-
(1985)
Am J Psychiatry
, vol.142
, pp. 74-77
-
-
Ritvo, E.R.1
Freeman, B.J.2
Mason-Brothers, A.3
-
89
-
-
0021959586
-
Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism
-
Ritvo ER, Spence MA, Freeman BJ, et al. Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism. Am J Psychiatry 1985b;142:187-192.
-
(1985)
Am J Psychiatry
, vol.142
, pp. 187-192
-
-
Ritvo, E.R.1
Spence, M.A.2
Freeman, B.J.3
-
90
-
-
0025245438
-
The UCLA-University of Utah epidemiological survey of autism: The etiologic role of rare diseases
-
Ritvo ER, Mason-Brothers A, Freeman BJ, et al. The UCLA-University of Utah epidemiological survey of autism: The etiologic role of rare diseases. Am J Psychiatry 1990;147:1614-1621.
-
(1990)
Am J Psychiatry
, vol.147
, pp. 1614-1621
-
-
Ritvo, E.R.1
Mason-Brothers, A.2
Freeman, B.J.3
-
91
-
-
0027792161
-
Clinical and molecular analysis of five inv dup(15) patients
-
Robinson W, Binkert F, Giné R, et al. Clinical and molecular analysis of five inv dup(15) patients. Eur J Hum Genet 1993;1:37-50.
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 37-50
-
-
Robinson, W.1
Binkert, F.2
Giné, R.3
-
92
-
-
0029990539
-
Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei
-
Rodier PM, Ingram JL, Tisdale B, et al. Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei. J Comp Neurol 1996;370:247-261.
-
(1996)
J Comp Neurol
, vol.370
, pp. 247-261
-
-
Rodier, P.M.1
Ingram, J.L.2
Tisdale, B.3
-
93
-
-
0030765761
-
Minor malformations and physical measurements in autism: Data from Nova Scotia
-
Rodier PM, Bryson SE, Welch JP. Minor malformations and physical measurements in autism: data from Nova Scotia. Teratology 1997a;55: 319-325.
-
(1997)
Teratology
, vol.55
, pp. 319-325
-
-
Rodier, P.M.1
Bryson, S.E.2
Welch, J.P.3
-
94
-
-
0031104734
-
Linking etiologies in humans and animal models: Studies of autism
-
Rodier PM, Ingram JL, Tisdale B, et al. Linking etiologies in humans and animal models: Studies of autism. Reprod Toxicol 1997b;11: 417-422.
-
(1997)
Reprod Toxicol
, vol.11
, pp. 417-422
-
-
Rodier, P.M.1
Ingram, J.L.2
Tisdale, B.3
-
95
-
-
0000575788
-
Genetics of HLA disease associations. The use of the Haplotype Relative Risk (HRR) and the 'Haplo-Delta' (Dh) estimates in juvenile diabetes from three racial groups
-
Rubinstein P, Walker M, Carpenter C, et al. Genetics of HLA disease associations. The use of the Haplotype Relative Risk (HRR) and the 'Haplo-Delta' (Dh) estimates in juvenile diabetes from three racial groups. Hum Immunol 1981;3:384.
-
(1981)
Hum Immunol
, vol.3
, pp. 384
-
-
Rubinstein, P.1
Walker, M.2
Carpenter, C.3
-
96
-
-
0028089258
-
Autism and known medical conditions: Myth and substance
-
Rutter M, Bailey A, Bolton P, et al. Autism and known medical conditions: Myth and substance. J Child Psychol Psychiatry 1994;35: 311-322.
-
(1994)
J Child Psychol Psychiatry
, vol.35
, pp. 311-322
-
-
Rutter, M.1
Bailey, A.2
Bolton, P.3
-
98
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
-
Singh N, Charlier C, Stauffer D, et al. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Nature Genet 1998;18:25-29.
-
(1998)
Nature Genet
, vol.18
, pp. 25-29
-
-
Singh, N.1
Charlier, C.2
Stauffer, D.3
-
99
-
-
0030845381
-
Genetic factors in the etiology of child psychiatric disorders
-
Skuse D. Genetic factors in the etiology of child psychiatric disorders. Curr Opin Pediatr 1997;9:354-360.
-
(1997)
Curr Opin Pediatr
, vol.9
, pp. 354-360
-
-
Skuse, D.1
-
100
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse D, James R, Bishop D, et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997;387:705-708.
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.1
James, R.2
Bishop, D.3
-
101
-
-
0025898654
-
Genetic influences in autism
-
Smalley S. Genetic influences in autism. Psychiatr Clin North Am 1991;14:125-139.
-
(1991)
Psychiatr Clin North Am
, vol.14
, pp. 125-139
-
-
Smalley, S.1
-
102
-
-
0030977686
-
Genetic influences in childhood-onset psychiatric disorders: Autism and attention-deficit/hyperactivity disorder
-
Smalley S. Genetic influences in childhood-onset psychiatric disorders: Autism and attention-deficit/hyperactivity disorder. Am J Hum Genet 1997;60:1276-1282.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1276-1282
-
-
Smalley, S.1
-
103
-
-
0029944752
-
Brief report: Generic, prenatal, and immunologic factors
-
Smalley SL, Collins F. Brief report: generic, prenatal, and immunologic factors. J Autism Dev Disord 1996;26:195-198.
-
(1996)
J Autism Dev Disord
, vol.26
, pp. 195-198
-
-
Smalley, S.L.1
Collins, F.2
-
106
-
-
0028939441
-
Autism, affective disorders, and social phobia
-
Smalley SL, McCracken J, Tanguay P. Autism, affective disorders, and social phobia. Am J Med Genet 1995;60:19-26.
-
(1995)
Am J Med Genet
, vol.60
, pp. 19-26
-
-
Smalley, S.L.1
McCracken, J.2
Tanguay, P.3
-
107
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993;52:506-516.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
108
-
-
0028012565
-
Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families
-
Spiker D, Lotspeich L, Kraemer HC, 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
-
109
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L, et al. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 1989;30:405-416.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
-
111
-
-
0024539633
-
HLA and insulin-dependent diabetes: An overview
-
Svejgaard A, Ryder L. HLA and insulin-dependent diabetes: An overview. Genet Epidemiol 1989;6:1-14.
-
(1989)
Genet Epidemiol
, vol.6
, pp. 1-14
-
-
Svejgaard, A.1
Ryder, L.2
-
112
-
-
0026494911
-
A haplotype based 'Haplotype Relative Risk' approach to detecting allelic associations
-
Terwilliger J, Ott J. A haplotype based 'Haplotype Relative Risk' approach to detecting allelic associations. Hum Hered 1992;42:337-346.
-
(1992)
Hum Hered
, vol.42
, pp. 337-346
-
-
Terwilliger, J.1
Ott, J.2
-
113
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
The 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: 571-578.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
114
-
-
0003185660
-
Association of the dopamine transporter gene (DAT1) and attention deficit hyperactivity disorder
-
Waldman ID, Rowe DC, Abramowitz A, Kozel S, Mohr J, Sherman SL, Cleveland HH, Sanders ML, Stever C. Association of the dopamine transporter gene (DAT1) and attention deficit hyperactivity disorder. Am J Hum Genet 1996;59:A25.
-
(1996)
Am J Hum Genet
, vol.59
-
-
Waldman, I.D.1
Rowe, D.C.2
Abramowitz, A.3
Kozel, S.4
Mohr, J.5
Sherman, S.L.6
Cleveland, H.H.7
Sanders, M.L.8
Stever, C.9
-
115
-
-
0030200135
-
Strong association of the third hypervariable region of HLA-DR beta1 with autism
-
Warren RP, Odell JD, Warren WL, et al. Strong association of the third hypervariable region of HLA-DR beta1 with autism. J Neuroimmunol 1996;67:97-102.
-
(1996)
J Neuroimmunol
, vol.67
, pp. 97-102
-
-
Warren, R.P.1
Odell, J.D.2
Warren, W.L.3
-
116
-
-
0029921128
-
The expanding world of trinucleotide repeats
-
Warren S. The expanding world of trinucleotide repeats. Science 1996,271:1374-1375.
-
(1996)
Science
, vol.271
, pp. 1374-1375
-
-
Warren, S.1
-
117
-
-
0029778284
-
Head circumference in autism and other pervasive developmental disorders
-
Woodhouse W, Bailey A, Rutter M, et al. Head circumference in autism and other pervasive developmental disorders. J Child Psychol Psychiatry 1996;37:665-671.
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 665-671
-
-
Woodhouse, W.1
Bailey, A.2
Rutter, M.3
|