-
1
-
-
0004235298
-
-
APA, 4th edition. Washington, DC, US: American Psychiatric Publishing, Inc. xxvii, 886 p
-
APA. 1994. Diagnostic and statistical manual of mental disorders, 4th edition. Washington, DC, US: American Psychiatric Publishing, Inc. xxvii, 886 p.
-
(1994)
Diagnostic and statistical manual of mental disorders
-
-
-
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, Rutter M. 1995. Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med 25(1):63-77.
-
(1995)
Psychol Med
, vol.25
, Issue.1
, 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
-
-
31044455614
-
Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology
-
Bittel DC, Butler MG. 2005. Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med 7(14):1-20.
-
(2005)
Expert Rev Mol Med
, vol.7
, Issue.14
, pp. 1-20
-
-
Bittel, D.C.1
Butler, M.G.2
-
5
-
-
0033797682
-
Varieties of repetitive behavior in autism: Comparisons to mental retardation
-
Bodfish JW, Symons FJ, Parker DE, Lewis MH. 2000. Varieties of repetitive behavior in autism: Comparisons to mental retardation. J Autism Dev Disord 30(3):237-243.
-
(2000)
J Autism Dev Disord
, vol.30
, Issue.3
, pp. 237-243
-
-
Bodfish, J.W.1
Symons, F.J.2
Parker, D.E.3
Lewis, M.H.4
-
6
-
-
0035829969
-
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders
-
Bolton PF, Dennis NR, Browne CE, Thomas NS, Veltman MW, Thompson RJ, Jacobs P. 2001. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders. Am J Med Genet 105(8):675-685.
-
(2001)
Am J Med Genet
, vol.105
, Issue.8
, pp. 675-685
-
-
Bolton, P.F.1
Dennis, N.R.2
Browne, C.E.3
Thomas, N.S.4
Veltman, M.W.5
Thompson, R.J.6
Jacobs, P.7
-
7
-
-
4644315735
-
Chromosome 15q 11-13abnormalities and other medical conditions in individuals with autism spectrum disorders
-
Bolton PF, Veltman MW, Weisblatt E, Holmes JR, Thomas NS, Youings SA, Thompson RJ, Roberts SE, Dennis NR, Browne CE, et al. 2004. Chromosome 15q 11-13abnormalities and other medical conditions in individuals with autism spectrum disorders. Psychiatr Genet 14(3):131-137.
-
(2004)
Psychiatr Genet
, vol.14
, Issue.3
, pp. 131-137
-
-
Bolton, P.F.1
Veltman, M.W.2
Weisblatt, E.3
Holmes, J.R.4
Thomas, N.S.5
Youings, S.A.6
Thompson, R.J.7
Roberts, S.E.8
Dennis, N.R.9
Browne, C.E.10
-
8
-
-
0031444629
-
Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations
-
Browne CE, Dennis NR, Maher E, Long FL, Nicholson JC, Sillibourne J, Barber JC. 1997. Inherited interstitial duplications of proximal 15q: Genotype-phenotype correlations. Am J Hum Genet 61(6):1342-1352.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.6
, pp. 1342-1352
-
-
Browne, C.E.1
Dennis, N.R.2
Maher, E.3
Long, F.L.4
Nicholson, J.C.5
Sillibourne, J.6
Barber, J.C.7
-
9
-
-
33846317078
-
5-HTTLPR genotype-specific phenotype in children and adolescents with autism
-
Brune CW, Kim SJ, Salt J, Leventhal BL, Lord C, Cook EH Jr. 2006. 5-HTTLPR genotype-specific phenotype in children and adolescents with autism. Am J Psychiatry 163(12):2148-2156.
-
(2006)
Am J Psychiatry
, vol.163
, Issue.12
, pp. 2148-2156
-
-
Brune, C.W.1
Kim, S.J.2
Salt, J.3
Leventhal, B.L.4
Lord, C.5
Cook Jr., E.H.6
-
10
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E, Lawlor BA, Fitzgerald M, Greenberg DA, Davis KL. 2001. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet 68(6):1514-1520.
-
(2001)
Am J Hum Genet
, vol.68
, Issue.6
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
Hollander, E.6
Lawlor, B.A.7
Fitzgerald, M.8
Greenberg, D.A.9
Davis, K.L.10
-
11
-
-
85047700330
-
Association between a GABRB3 polymorphism and autism
-
Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH Jr, Fang Y, Song CY, Vitale R. 2002. Association between a GABRB3 polymorphism and autism. Mol Psychiatry 7(3):311-316.
-
(2002)
Mol Psychiatry
, vol.7
, Issue.3
, pp. 311-316
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Greenberg, D.A.4
Kilifarski, M.5
Reichert, J.6
Cook Jr, E.H.7
Fang, Y.8
Song, C.Y.9
Vitale, R.10
-
12
-
-
20044390596
-
Pervasive developmental disorders in preschool children: Confirmation of high prevalence
-
Chakrabarti S, Fombonne E. 2005. Pervasive developmental disorders in preschool children: Confirmation of high prevalence. Am J Psychiatry 162(6):1133-1141.
-
(2005)
Am J Psychiatry
, vol.162
, Issue.6
, pp. 1133-1141
-
-
Chakrabarti, S.1
Fombonne, E.2
-
13
-
-
33847300921
-
Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios
-
Cho IH, Yoo HJ, Park M, Lee YS, Kim SA. 2007. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. Brain Res 1139:34-41.
-
(2007)
Brain Res
, vol.1139
, pp. 34-41
-
-
Cho, I.H.1
Yoo, H.J.2
Park, M.3
Lee, Y.S.4
Kim, S.A.5
-
14
-
-
2942517830
-
An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene interactions on risk of myocardial infarction: The importance of model validation
-
Coffey CS, Hebert PR, Ritchie MD, Krumholz HM, Gaziano JM, Ridker PM, Brown NJ, Vaughan DE, Moore JH. 2004. An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene interactions on risk of myocardial infarction: The importance of model validation. BMC Bioinformatics 5:49.
-
(2004)
BMC Bioinformatics
, vol.5
, pp. 49
-
-
Coffey, C.S.1
Hebert, P.R.2
Ritchie, M.D.3
Krumholz, H.M.4
Gaziano, J.M.5
Ridker, P.M.6
Brown, N.J.7
Vaughan, D.E.8
Moore, J.H.9
-
15
-
-
0027281184
-
Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder
-
Cook EH Jr, Arora RC, Anderson GM, Berry-Kravis EM, Yan SY, Yeoh HC, Sklena PJ, Charak DA, Leventhal BL. 1993. Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder. Life Sci 52(25):2005-2015.
-
(1993)
Life Sci
, vol.52
, Issue.25
, pp. 2005-2015
-
-
Cook Jr, E.H.1
Arora, R.C.2
Anderson, G.M.3
Berry-Kravis, E.M.4
Yan, S.Y.5
Yeoh, H.C.6
Sklena, P.J.7
Charak, D.A.8
Leventhal, B.L.9
-
16
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook EH Jr, Lindgren V, Leventhal BL, Courchesne R, Lincoln A, Shulman C, Lord C, Courchesne E. 1997. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 60(4):928-934.
-
(1997)
Am J Hum Genet
, vol.60
, Issue.4
, pp. 928-934
-
-
Cook Jr, E.H.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
Lincoln, A.5
Shulman, C.6
Lord, C.7
Courchesne, E.8
-
17
-
-
17344364660
-
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
-
Cook EH Jr, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, et al. 1998. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Hum Genet 62(5):1077-1083.
-
(1998)
Am J Hum Genet
, vol.62
, Issue.5
, pp. 1077-1083
-
-
Cook Jr, E.H.1
Courchesne, R.Y.2
Cox, N.J.3
Lord, C.4
Gonen, D.5
Guter, S.J.6
Lincoln, A.7
Nix, K.8
Haas, R.9
Leventhal, B.L.10
-
18
-
-
1842483890
-
Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects
-
Cordell HJ, Barratt BJ, Clayton DG. 2004. Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects. Genet Epidemiol 26(3):167-185.
-
(2004)
Genet Epidemiol
, vol.26
, Issue.3
, pp. 167-185
-
-
Cordell, H.J.1
Barratt, B.J.2
Clayton, D.G.3
-
19
-
-
33947114826
-
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels
-
Coutinho AM, Sousa I, Martins M, Correia C, Morgadinho T, Bento C, Marques C, Ataide A, Miguel TS, Moore JH, et al. 2007. Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. Hum Genet 121(2):243-256.
-
(2007)
Hum Genet
, vol.121
, Issue.2
, pp. 243-256
-
-
Coutinho, A.M.1
Sousa, I.2
Martins, M.3
Correia, C.4
Morgadinho, T.5
Bento, C.6
Marques, C.7
Ataide, A.8
Miguel, T.S.9
Moore, J.H.10
-
20
-
-
0043193924
-
Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R
-
Cuccaro ML, Shao Y, Grubber J, Slifer M, Wolpert CM, Donnelly SL, Abramson RK, Ravan SA, Wright HH, DeLong GR, et al. 2003. Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R. Child Psychiatry Hum Dev 34(1):3-17.
-
(2003)
Child Psychiatry Hum Dev
, vol.34
, Issue.1
, pp. 3-17
-
-
Cuccaro, M.L.1
Shao, Y.2
Grubber, J.3
Slifer, M.4
Wolpert, C.M.5
Donnelly, S.L.6
Abramson, R.K.7
Ravan, S.A.8
Wright, H.H.9
DeLong, G.R.10
-
21
-
-
23044490896
-
An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder
-
Part B
-
Curran S, Roberts S, Thomas S, Veltman M, Browne J, Medda E, Pickles A, Sham P, Bolton PF. 2005. An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder. Am J Med Genet Part B 137B(1):25-28.
-
(2005)
Am J Med Genet
, vol.137 B
, Issue.1
, pp. 25-28
-
-
Curran, S.1
Roberts, S.2
Thomas, S.3
Veltman, M.4
Browne, J.5
Medda, E.6
Pickles, A.7
Sham, P.8
Bolton, P.F.9
-
22
-
-
32444434874
-
Autism and the serotonin transporter: The long and short of it
-
Devlin B, Cook EH Jr, Coon H, Dawson G, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, et al. 2005. Autism and the serotonin transporter: The long and short of it. Mol Psychiatry 10(12):1110-1116.
-
(2005)
Mol Psychiatry
, vol.10
, Issue.12
, pp. 1110-1116
-
-
Devlin, B.1
Cook Jr, E.H.2
Coon, H.3
Dawson, G.4
Grigorenko, E.L.5
McMahon, W.6
Minshew, N.7
Pauls, D.8
Smith, M.9
Spence, M.A.10
-
23
-
-
0029093668
-
The pre-linguistic autism diagnostic observation schedule
-
DiLavore PC, Lord C, Rutter M. 1995. The pre-linguistic autism diagnostic observation schedule. J Autism Dev Disord 25(4):355-379.
-
(1995)
J Autism Dev Disord
, vol.25
, Issue.4
, pp. 355-379
-
-
DiLavore, P.C.1
Lord, C.2
Rutter, M.3
-
24
-
-
0037220764
-
Psychiatric disorders in Prader-Willi syndrome: Epidemiology and management
-
Dykens E, Shah B. 2003. Psychiatric disorders in Prader-Willi syndrome: Epidemiology and management. CNS Drugs 17(3):167-178.
-
(2003)
CNS Drugs
, vol.17
, Issue.3
, pp. 167-178
-
-
Dykens, E.1
Shah, B.2
-
25
-
-
0032858626
-
Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy
-
Dykens EM, Cassidy SB, King BH. 1999. Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy. Am J Ment Retard 104(1):67-77.
-
(1999)
Am J Ment Retard
, vol.104
, Issue.1
, pp. 67-77
-
-
Dykens, E.M.1
Cassidy, S.B.2
King, B.H.3
-
26
-
-
0035653670
-
Genetics of autism: Complex aetiology for a heterogeneous disorder
-
Folstein SE, Rosen-Sheidley B. 2001. Genetics of autism: Complex aetiology for a heterogeneous disorder. Nat Rev Genet 2(12):943-955.
-
(2001)
Nat Rev Genet
, vol.2
, Issue.12
, pp. 943-955
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
-
28
-
-
33846441661
-
Structure of the autism symptom phenotype: A proposed multidimensional model
-
Georgiades S, Szatmari P, Zwaigenbaum L, Duku E, Bryson S, Roberts W, Goldberg J, Mahoney W. 2007. Structure of the autism symptom phenotype: A proposed multidimensional model. J Am Acad Child Adolesc Psychiatry 46(2):188-196.
-
(2007)
J Am Acad Child Adolesc Psychiatry
, vol.46
, Issue.2
, pp. 188-196
-
-
Georgiades, S.1
Szatmari, P.2
Zwaigenbaum, L.3
Duku, E.4
Bryson, S.5
Roberts, W.6
Goldberg, J.7
Mahoney, W.8
-
29
-
-
0032454027
-
Chromosomal disorders and autism
-
Gillberg C. 1998. Chromosomal disorders and autism. J Autism Dev Disord 28(5):415-425.
-
(1998)
J Autism Dev Disord
, vol.28
, Issue.5
, pp. 415-425
-
-
Gillberg, C.1
-
30
-
-
34147123692
-
The autism diagnostic observation schedule: Revised algorithms for improved diagnostic validity
-
Gotham K, Risi S, Pickles A, Lord C. 2007. The autism diagnostic observation schedule: Revised algorithms for improved diagnostic validity. J Autism Dev Disord 37(4):613-627.
-
(2007)
J Autism Dev Disord
, vol.37
, Issue.4
, pp. 613-627
-
-
Gotham, K.1
Risi, S.2
Pickles, A.3
Lord, C.4
-
31
-
-
33646489612
-
A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorder
-
Guerini FR, Manca S, Sotgiu S, Tremolada S, Zanzottera M, Agliardi C, Zanetta L, Saresella M, Mancuso R, De Silvestri A, et al. 2006. A family based linkage analysis of HLA and 5-HTTLPR gene polymorphisms in Sardinian children with autism spectrum disorder. Hum Immunol 67(1-2):108-117.
-
(2006)
Hum Immunol
, vol.67
, Issue.1-2
, pp. 108-117
-
-
Guerini, F.R.1
Manca, S.2
Sotgiu, S.3
Tremolada, S.4
Zanzottera, M.5
Agliardi, C.6
Zanetta, L.7
Saresella, M.8
Mancuso, R.9
De Silvestri, A.10
-
32
-
-
34247170891
-
15q 11-13GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders
-
Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM. 2007. 15q 11-13GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. Hum Mol Genet 16(6):691-703.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.6
, pp. 691-703
-
-
Hogart, A.1
Nagarajan, R.P.2
Patzel, K.A.3
Yasui, D.H.4
Lasalle, J.M.5
-
33
-
-
35348999630
-
Hyperserotonemia in adults with autistic disorder
-
Hranilovic D, Bujas-Petkovic Z, Vragovic R, Vuk T, Hock K, Jernej B. 2007. Hyperserotonemia in adults with autistic disorder. J Autism Dev Disord 37(10):1934-1940.
-
(2007)
J Autism Dev Disord
, vol.37
, Issue.10
, pp. 1934-1940
-
-
Hranilovic, D.1
Bujas-Petkovic, Z.2
Vragovic, R.3
Vuk, T.4
Hock, K.5
Jernej, B.6
-
34
-
-
33846641608
-
Using the autism diagnostic interview-revised to increase phenotypic homogeneity in genetic studies of autism
-
Hus V, Pickles A, Cook EH Jr, Risi S, Lord C. 2007. Using the autism diagnostic interview-revised to increase phenotypic homogeneity in genetic studies of autism. Biol Psychiatry 61(4):438-448.
-
(2007)
Biol Psychiatry
, vol.61
, Issue.4
, pp. 438-448
-
-
Hus, V.1
Pickles, A.2
Cook Jr, E.H.3
Risi, S.4
Lord, C.5
-
35
-
-
0025997752
-
Complex segregation analysis of autism
-
Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, McMahon WM, Petersen B, Jenson WR, Mo A. 1991. Complex segregation analysis of autism. Am J Hum Genet 49(5):932-938.
-
(1991)
Am J Hum Genet
, vol.49
, Issue.5
, 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
McMahon, W.M.7
Petersen, B.8
Jenson, W.R.9
Mo, A.10
-
36
-
-
85047695697
-
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder
-
Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH Jr. 2002. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatry 7(3):278-288.
-
(2002)
Mol Psychiatry
, vol.7
, Issue.3
, pp. 278-288
-
-
Kim, S.J.1
Cox, N.2
Courchesne, R.3
Lord, C.4
Corsello, C.5
Akshoomoff, N.6
Guter, S.7
Leventhal, B.L.8
Courchesne, E.9
Cook Jr., E.H.10
-
37
-
-
33847748974
-
Association of GABRB3 Polymorphisms with Autism Spectrum Disorders in Korean Trios
-
Kim SA, Kim JH, Park M, Cho IH, Yoo HJ. 2007. Association of GABRB3 Polymorphisms with Autism Spectrum Disorders in Korean Trios. Neuropsychobiology 54(3):160-165.
-
(2007)
Neuropsychobiology
, vol.54
, Issue.3
, pp. 160-165
-
-
Kim, S.A.1
Kim, J.H.2
Park, M.3
Cho, I.H.4
Yoo, H.J.5
-
38
-
-
30844442607
-
The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C
-
Kishore S, Stamm S. 2006. The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C. Science 311(5758):230-232.
-
(2006)
Science
, vol.311
, Issue.5758
, pp. 230-232
-
-
Kishore, S.1
Stamm, S.2
-
39
-
-
33645754287
-
Selective serotonin reuptake inhibitors in autism: A review of efficacy and tolerability
-
Kolevzon A, Mathewson KA, Hollander E. 2006. Selective serotonin reuptake inhibitors in autism: A review of efficacy and tolerability. J Clin Psychiatry 67(3):407-414.
-
(2006)
J Clin Psychiatry
, vol.67
, Issue.3
, pp. 407-414
-
-
Kolevzon, A.1
Mathewson, K.A.2
Hollander, E.3
-
40
-
-
0033814928
-
Implementing a unified approach to family-based tests of association
-
Laird NM, Horvath S, Xu X. 2000. Implementing a unified approach to family-based tests of association. Genet Epidemiol 19 (Suppl 1):S36-S42.
-
(2000)
Genet Epidemiol
, vol.19
, Issue.SUPPL. 1
-
-
Laird, N.M.1
Horvath, S.2
Xu, X.3
-
42
-
-
0034920299
-
A genomewide screen for autism susceptibility loci
-
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, et al. 2001. A genomewide screen for autism susceptibility loci. Am J Hum Genet 69(2):327-340.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.2
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
Parano, E.4
Pavone, P.5
Geschwind, D.6
Lord, C.7
Iversen, P.8
Hoh, J.9
Ott, J.10
-
43
-
-
0027997172
-
Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
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. J Autism Dev Disord 24(5):659-685.
-
(1994)
J Autism Dev Disord
, vol.24
, Issue.5
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
44
-
-
0033802632
-
The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
-
Lord C, Risi S, Lambrecht L, Cook EH Jr, Leventhal BL, DiLavore PC, Pickles A, Rutter M. 2000. The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord 30(3):205-223.
-
(2000)
J Autism Dev Disord
, vol.30
, Issue.3
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
Cook Jr, E.H.4
Leventhal, B.L.5
DiLavore, P.C.6
Pickles, A.7
Rutter, M.8
-
45
-
-
33744909414
-
Autism from 2 to 9 years of age
-
Lord C, Risi S, DiLavore PS, Shulman C, Thurm A, Pickles A. 2006. Autism from 2 to 9 years of age. Arch Gen Psychiatry 63(6):694-701.
-
(2006)
Arch Gen Psychiatry
, vol.63
, Issue.6
, pp. 694-701
-
-
Lord, C.1
Risi, S.2
DiLavore, P.S.3
Shulman, C.4
Thurm, A.5
Pickles, A.6
-
46
-
-
23944444250
-
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism
-
Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, et al. 2005. Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. Am J Hum Genet 77(3):377-388.
-
(2005)
Am J Hum Genet
, vol.77
, Issue.3
, pp. 377-388
-
-
Ma, D.Q.1
Whitehead, P.L.2
Menold, M.M.3
Martin, E.R.4
Ashley-Koch, A.E.5
Mei, H.6
Ritchie, M.D.7
Delong, G.R.8
Abramson, R.K.9
Wright, H.H.10
-
47
-
-
0034615152
-
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
-
Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, et al. 2000. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. Am J Med Genet 96(1):43-48.
-
(2000)
Am J Med Genet
, vol.96
, Issue.1
, pp. 43-48
-
-
Martin, E.R.1
Menold, M.M.2
Wolpert, C.M.3
Bass, M.P.4
Donnelly, S.L.5
Ravan, S.A.6
Zimmerman, A.7
Gilbert, J.R.8
Vance, J.M.9
Maddox, L.O.10
-
48
-
-
7644221741
-
-
GABA(A) receptor subunit cluster and association to autism. Am J Med Genet Part B
-
McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS. 2004. A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism. Am J Med Genet Part B 131B(1):51-59.
-
(2004)
A linkage disequilibrium map of the 1-Mb 15q12
, vol.131 B
, Issue.1
, pp. 51-59
-
-
McCauley, J.L.1
Olson, L.M.2
Delahanty, R.3
Amin, T.4
Nurmi, E.L.5
Organ, E.L.6
Jacobs, M.M.7
Folstein, S.E.8
Haines, J.L.9
Sutcliffe, J.S.10
-
49
-
-
10744229245
-
-
Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS. 2003a. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Mol Psychiatry 8(6):624-634, 570.
-
Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS. 2003a. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Mol Psychiatry 8(6):624-634, 570.
-
-
-
-
50
-
-
0042970462
-
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13
-
Nurmi EL, Dowd M, Tadevosyan-Leyfer O, Haines JL, Folstein SE, Sutcliffe JS. 2003b. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13. J Am Acad Child Adolesc Psychiatry 42(7):856-863.
-
(2003)
J Am Acad Child Adolesc Psychiatry
, vol.42
, Issue.7
, pp. 856-863
-
-
Nurmi, E.L.1
Dowd, M.2
Tadevosyan-Leyfer, O.3
Haines, J.L.4
Folstein, S.E.5
Sutcliffe, J.S.6
-
51
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Rastam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Van Maldergem L, et al. 1999. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet 8(5):805-812.
-
(1999)
Hum Mol Genet
, vol.8
, Issue.5
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
-
52
-
-
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 CH, Rutter M. 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(3):717-726.
-
(1995)
Am J Hum Genet
, vol.57
, Issue.3
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
Bailey, A.4
Le Couteur, A.5
Sim, C.H.6
Rutter, M.7
-
53
-
-
12244264435
-
Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC. 2003. Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19(1):149-150.
-
(2003)
Bioinformatics
, vol.19
, Issue.1
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
54
-
-
0034054165
-
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
-
Rabinowitz D, Laird N. 2000. A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered 50(4):211-223.
-
(2000)
Hum Hered
, vol.50
, Issue.4
, pp. 211-223
-
-
Rabinowitz, D.1
Laird, N.2
-
55
-
-
33745712342
-
Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism
-
Ramoz N, Reichert JG, Corwin TE, Smith CJ, Silverman JM, Hollander E, Buxbaum JD. 2006. Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism. Biol Psychiatry 60(2):186-191.
-
(2006)
Biol Psychiatry
, vol.60
, Issue.2
, pp. 186-191
-
-
Ramoz, N.1
Reichert, J.G.2
Corwin, T.E.3
Smith, C.J.4
Silverman, J.M.5
Hollander, E.6
Buxbaum, J.D.7
-
56
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, et al. 1999. A genomic screen of autism: Evidence for a multilocus etiology. Am J Hum Genet 65(2):493-507.
-
(1999)
Am J Hum Genet
, vol.65
, Issue.2
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nouri, N.4
Hinds, D.5
Hallmayer, J.6
Kalaydjieva, L.7
McCague, P.8
Dimiceli, S.9
Pitts, T.10
-
57
-
-
0021971395
-
The treatment of autistic children
-
Rutter M. 1985. The treatment of autistic children. J Child Psychol Psychiatry 26(2):193-214.
-
(1985)
J Child Psychol Psychiatry
, vol.26
, Issue.2
, pp. 193-214
-
-
Rutter, M.1
-
58
-
-
18344413881
-
Autism and maternally derived aberrations of chromosome 15q
-
Schroer RJ, Phelan MC, Michaelis RC, Crawford EC, Skinner SA, Cuccaro M, Simensen RJ, Bishop J, Skinner C, Fender D, et al. 1998. Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet 76(4):327-336.
-
(1998)
Am J Med Genet
, vol.76
, Issue.4
, pp. 327-336
-
-
Schroer, R.J.1
Phelan, M.C.2
Michaelis, R.C.3
Crawford, E.C.4
Skinner, S.A.5
Cuccaro, M.6
Simensen, R.J.7
Bishop, J.8
Skinner, C.9
Fender, D.10
-
59
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, et al. 2007. Strong association of de novo copy number mutations with autism. Science 316(5823):445-449.
-
(2007)
Science
, vol.316
, Issue.5823
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Yamrom, B.7
Yoon, S.8
Krasnitz, A.9
Kendall, J.10
-
60
-
-
18344374001
-
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
-
Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashley-Koch AA, Abramson RK, Wright HH, DeLong RG, Gilbert JR, et al. 2002a. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. Am J Hum Genet 70(4):1058-1061.
-
(2002)
Am J Hum Genet
, vol.70
, Issue.4
, pp. 1058-1061
-
-
Shao, Y.1
Raiford, K.L.2
Wolpert, C.M.3
Cope, H.A.4
Ravan, S.A.5
Ashley-Koch, A.A.6
Abramson, R.K.7
Wright, H.H.8
DeLong, R.G.9
Gilbert, J.R.10
-
61
-
-
37649026213
-
Genomic screen and follow-up analysis for autistic disorder
-
Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, et al. 2002b. Genomic screen and follow-up analysis for autistic disorder. Am JMed Genet 114(1):99-105.
-
(2002)
Am JMed Genet
, vol.114
, Issue.1
, 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
-
62
-
-
0037371673
-
Finemapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
-
Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, et al. 2003. Finemapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. Am J Hum Genet 72(3):539-548.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.3
, pp. 539-548
-
-
Shao, Y.1
Cuccaro, M.L.2
Hauser, E.R.3
Raiford, K.L.4
Menold, M.M.5
Wolpert, C.M.6
Ravan, S.A.7
Elston, L.8
Decena, K.9
Donnelly, S.L.10
-
63
-
-
33748922426
-
Stratification based on language-related endophenotypes in autism: Attempt to replicate reported linkage
-
Part B
-
Spence SJ, Cantor RM, Chung L, Kim S, Geschwind DH, Alarcon M. 2006. Stratification based on language-related endophenotypes in autism: Attempt to replicate reported linkage. Am J Med Genet Part B 141B(6):591-598.
-
(2006)
Am J Med Genet
, vol.141 B
, Issue.6
, pp. 591-598
-
-
Spence, S.J.1
Cantor, R.M.2
Chung, L.3
Kim, S.4
Geschwind, D.H.5
Alarcon, M.6
-
64
-
-
0034035398
-
Genetics of childhood disorders: XV. Prader-Willi syndrome: Genes, brain, and behavior
-
State MW, Dykens EM. 2000. Genetics of childhood disorders: XV. Prader-Willi syndrome: Genes, brain, and behavior. J Am Acad Child Adolesc Psychiatry 39(6):797-800.
-
(2000)
J Am Acad Child Adolesc Psychiatry
, vol.39
, Issue.6
, pp. 797-800
-
-
State, M.W.1
Dykens, E.M.2
-
65
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G, Bohman M. 1989. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 30(3):405-416.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, Issue.3
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
Andersson, L.4
Gillberg, I.C.5
Jakobsson, G.6
Bohman, M.7
-
66
-
-
33646739906
-
Investigating the structure of the restricted, repetitive behaviours and interests domain of autism
-
Szatmari P, Georgiades S, Bryson S, Zwaigenbaum L, Roberts W, Mahoney W, Goldberg J, Tuff L. 2006. Investigating the structure of the restricted, repetitive behaviours and interests domain of autism. J Child Psychol Psychiatry 47(6):582-590.
-
(2006)
J Child Psychol Psychiatry
, vol.47
, Issue.6
, pp. 582-590
-
-
Szatmari, P.1
Georgiades, S.2
Bryson, S.3
Zwaigenbaum, L.4
Roberts, W.5
Mahoney, W.6
Goldberg, J.7
Tuff, L.8
-
67
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, et al. 2007. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet 39(3):319-328.
-
(2007)
Nat Genet
, vol.39
, Issue.3
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
Roberts, W.4
Brian, J.5
Liu, X.Q.6
Vincent, J.B.7
Skaug, J.L.8
Thompson, A.P.9
Senman, L.10
-
68
-
-
0041968765
-
A principal components analysis of the Autism Diagnostic Interview-Revised
-
Tadevosyan-Leyfer O, Dowd M, Mankoski R, Winklosky B, Putnam S, McGrath L, Tager-Flusberg H, Folstein SE. 2003. A principal components analysis of the Autism Diagnostic Interview-Revised. J Am Acad Child Adolesc Psychiatry 42(7):864-872.
-
(2003)
J Am Acad Child Adolesc Psychiatry
, vol.42
, Issue.7
, pp. 864-872
-
-
Tadevosyan-Leyfer, O.1
Dowd, M.2
Mankoski, R.3
Winklosky, B.4
Putnam, S.5
McGrath, L.6
Tager-Flusberg, H.7
Folstein, S.E.8
-
69
-
-
0033191409
-
Annotation: Repetitive behaviour in autism: A review of psychological research
-
Turner M. 1999. Annotation: Repetitive behaviour in autism: A review of psychological research. J Child Psychol Psychiatry 40(6):839-849.
-
(1999)
J Child Psychol Psychiatry
, vol.40
, Issue.6
, pp. 839-849
-
-
Turner, M.1
-
71
-
-
33645733702
-
Autism spectrum disorders in Prader-Willi and Angelman syndromes: A systematic review
-
Veltman MW, Craig EE, Bolton PF. 2005. Autism spectrum disorders in Prader-Willi and Angelman syndromes: A systematic review. Psychiatr Genet 15(4):243-254.
-
(2005)
Psychiatr Genet
, vol.15
, Issue.4
, pp. 243-254
-
-
Veltman, M.W.1
Craig, E.E.2
Bolton, P.F.3
-
72
-
-
0033362236
-
Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
-
Weinberg CR. 1999. Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. Am J Hum Genet 65(1):229-235.
-
(1999)
Am J Hum Genet
, vol.65
, Issue.1
, pp. 229-235
-
-
Weinberg, C.R.1
-
73
-
-
0034615032
-
Autistic symptoms among children and young adults with isodicentric chromosome 15
-
Wolpert C, Pericak-Vance MA, Abramson RK, Wright HH, Cuccaro ML. 2000a. Autistic symptoms among children and young adults with isodicentric chromosome 15. Am J Med Genet 96(1):128-129.
-
(2000)
Am J Med Genet
, vol.96
, Issue.1
, pp. 128-129
-
-
Wolpert, C.1
Pericak-Vance, M.A.2
Abramson, R.K.3
Wright, H.H.4
Cuccaro, M.L.5
-
74
-
-
0034640701
-
Three probands with autistic disorder and isodicentric chromosome 15
-
Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, et al. 2000b. Three probands with autistic disorder and isodicentric chromosome 15. Am J Med Genet 96(3):365-372.
-
(2000)
Am J Med Genet
, vol.96
, Issue.3
, pp. 365-372
-
-
Wolpert, C.M.1
Menold, M.M.2
Bass, M.P.3
Qumsiyeh, M.B.4
Donnelly, S.L.5
Ravan, S.A.6
Vance, J.M.7
Gilbert, J.R.8
Abramson, R.K.9
Wright, H.H.10
|