-
1
-
-
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
-
2
-
-
0027232138
-
Acute tryptophan depletion in autistic disorder: A controlled case study
-
McDougle CJ, Naylor ST, Goodman WK, Volkmar FR, Cohen DJ, Price LH. Acute tryptophan depletion in autistic disorder: a controlled case study. Biol Psychiatr 1993; 33: 547-550.
-
(1993)
Biol Psychiatr
, vol.33
, pp. 547-550
-
-
McDougle, C.J.1
Naylor, S.T.2
Goodman, W.K.3
Volkmar, F.R.4
Cohen, D.J.5
Price, L.H.6
-
3
-
-
0032987647
-
Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children
-
Chugani DC, Muzik O, Behen M, Rothermel R, Janisse JJ, Lee J et al. Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children. Ann Neurol 1999; 45: 287-295.
-
(1999)
Ann Neurol
, vol.45
, pp. 287-295
-
-
Chugani, D.C.1
Muzik, O.2
Behen, M.3
Rothermel, R.4
Janisse, J.J.5
Lee, J.6
-
4
-
-
0029803880
-
A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder
-
McDougle C, Naylor S, Cohen D, Volkmar F, Heninger G, Price L. A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder. Arch Gen Psychiatr 1996; 53: 1001-1008.
-
(1996)
Arch Gen Psychiatr
, vol.53
, pp. 1001-1008
-
-
McDougle, C.1
Naylor, S.2
Cohen, D.3
Volkmar, F.4
Heninger, G.5
Price, L.6
-
5
-
-
0027281184
-
Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder
-
Cook Jr EH, Arora RC, Anderson GH, Berry-Kravis EM, Yan S, Yeoh HC et al. Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder. Life Sci 1993; 52: 2005-2015.
-
(1993)
Life Sci
, vol.52
, pp. 2005-2015
-
-
Cook Jr., E.H.1
Arora, R.C.2
Anderson, G.H.3
Berry-Kravis, E.M.4
Yan, S.5
Yeoh, H.C.6
-
6
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EH, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A et al. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatr 1997; 2: 247-250.
-
(1997)
Mol Psychiatr
, 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
-
7
-
-
0006463359
-
Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region
-
Lesch KP, Bengel D, Heils A, Sabol SZ, Greenberg BD, Petri S et al. Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science 1996; 274: 1527-1531.
-
(1996)
Science
, vol.274
, pp. 1527-1531
-
-
Lesch, K.P.1
Bengel, D.2
Heils, A.3
Sabol, S.Z.4
Greenberg, B.D.5
Petri, S.6
-
8
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants asociated with autism
-
Klauck SM, Poustka F, Benner A, Lesch K-P, Poustka A. Serotonin transporter (5-HTT) gene variants asociated with autism. Hum Mol Genet 1997; 13: 2233-2238.
-
(1997)
Hum Mol Genet
, vol.13
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.-P.4
Poustka, A.5
-
9
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes
-
Philippe A, Martinez M, Guilloudbataille M, Gillberg C, Rastam M, Sponheim E et al. Genome-wide scan for autism susceptibility genes. Hum Mol Genet 1999; 8: 805-812.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloudbataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
-
10
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J et al. A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet 1999; 65: 493-507.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nouri, N.4
Hinds, D.5
Hallmayer, J.6
-
11
-
-
0033573212
-
An autosomal genomic screen for autism
-
Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL et al. An autosomal genomic screen for autism. Am J Med Genet 1999; 88: 609-615.
-
(1999)
Am J Med Genet
, vol.88
, pp. 609-615
-
-
Barrett, S.1
Beck, J.C.2
Bernier, R.3
Bisson, E.4
Braun, T.A.5
Casavant, T.L.6
-
12
-
-
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 et al. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet 2001; 68: 1514-1520.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
Hollander, E.6
-
13
-
-
0036138102
-
Evidence for a language quantitative trait locus on chromosome 7q in multiplex families
-
Alarcon M, Cantor RM, Liu J, Gilliam TC, the Autism Genetic Resource Exchange Consortium, Geschwind DH. Evidence for a language quantitative trait locus on chromosome 7q in multiplex families. Am J Hum Genet 2002; 70: 60-71.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 60-71
-
-
Alarcon, M.1
Cantor, R.M.2
Liu, J.3
Gilliam, T.C.4
Geschwind, D.H.5
-
14
-
-
0036780698
-
A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-oja T et al. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet 2002; 71: 777-790.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
Ayers, K.4
Kempas, E.5
Ylisaukko-oja, T.6
-
15
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
International Molecular Genetic Study Group of Autism Consortium (IMGSAC). A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 2001; 69: 570-581.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 570-581
-
-
-
16
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan AL, Alarcon M, Cheng R, Magnusson PKE, Spence SJ, Palmer AA et al. A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet 2003; 73: 886-897.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.E.4
Spence, S.J.5
Palmer, A.A.6
-
17
-
-
2142645125
-
Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism
-
McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD et al. Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism. Am J Med Genet 2004; 127B: 104-112.
-
(2004)
Am J Med Genet
, vol.127 B
, pp. 104-112
-
-
McCauley, J.L.1
Olson, L.M.2
Dowd, M.3
Amin, T.4
Steele, A.5
Blakely, R.D.6
-
18
-
-
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 et al. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatr 2002; 7: 278-288.
-
(2002)
Mol Psychiatr
, vol.7
, pp. 278-288
-
-
Kim, S.J.1
Cox, N.2
Courchesne, R.3
Lord, C.4
Corsello, C.5
Akshoomoff, N.6
-
19
-
-
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. Autism diagnostic interview revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 1994; 24: 659-685.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
20
-
-
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, Leventhal BL, DiLavore P et al. The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord 2000; 30: 205-223.
-
(2000)
J Autism Dev Disord
, vol.30
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
Cook, E.H.4
Leventhal, B.L.5
DiLavore, P.6
-
21
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63: 259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
22
-
-
0038449167
-
Evolutionary-based association analysis using haplotype data
-
Seltman H, Roeder K, Devlin B. Evolutionary-based association analysis using haplotype data. Genet Epidemiol 2003; 25: 48-58.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 48-58
-
-
Seltman, H.1
Roeder, K.2
Devlin, B.3
-
23
-
-
0034054165
-
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
-
Rabinowitz D, Laird N. A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered 2000; 50: 211-223.
-
(2000)
Hum Hered
, vol.50
, pp. 211-223
-
-
Rabinowitz, D.1
Laird, N.2
-
24
-
-
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
-
25
-
-
0034098774
-
Allegro, a new computer program for multipoint linkage analysis
-
Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 2000; 25: 12-13.
-
(2000)
Nat Genet
, vol.25
, pp. 12-13
-
-
Gudbjartsson, D.F.1
Jonasson, K.2
Frigge, M.L.3
Kong, A.4
-
26
-
-
0036668724
-
On a general class of conditional tests for family-based association studies in genetics: The asymptotic distribution, the conditional power, and optimality considerations
-
Lange C, Laird NM. On a general class of conditional tests for family-based association studies in genetics: the asymptotic distribution, the conditional power, and optimality considerations. Genet Epidemiol 2002; 23: 165-180.
-
(2002)
Genet Epidemiol
, vol.23
, pp. 165-180
-
-
Lange, C.1
Laird, N.M.2
-
27
-
-
0036724540
-
Power calculations for a general class of family-based association tests: Dichotomous traits
-
Lange C, Laird NM. Power calculations for a general class of family-based association tests: dichotomous traits. Am J Hum Genet 2002; 71: 575-584.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 575-584
-
-
Lange, C.1
Laird, N.M.2
-
28
-
-
0029564413
-
The TDT reveals linkage and linkage disequilibrium in a rare disease
-
McGinnis RE, Ewens WJ, Spielman RS. The TDT reveals linkage and linkage disequilibrium in a rare disease. Genet Epidemiol 1995; 12: 637-640.
-
(1995)
Genet Epidemiol
, vol.12
, pp. 637-640
-
-
McGinnis, R.E.1
Ewens, W.J.2
Spielman, R.S.3
-
29
-
-
8844244724
-
Evidence for sex-specific risk alleles in autism spectrum disorder
-
Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH et al. Evidence for sex-specific risk alleles in autism spectrum disorder. Am J Hum Genet 2004; 75: 1117-1123.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1117-1123
-
-
Stone, J.L.1
Merriman, B.2
Cantor, R.M.3
Yonan, A.L.4
Gilliam, T.C.5
Geschwind, D.H.6
-
30
-
-
0036373349
-
Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children
-
Persico AM, Pascucci T, Puglisi-Allegra S, Militerni R, Bravaccio C, Schneider C et al. Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children. Mol Psychiatr 2002; 7: 795-800.
-
(2002)
Mol Psychiatr
, vol.7
, pp. 795-800
-
-
Persico, A.M.1
Pascucci, T.2
Puglisi-Allegra, S.3
Militerni, R.4
Bravaccio, C.5
Schneider, C.6
-
31
-
-
11144358488
-
Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism
-
Coutinho AM, Oliveira G, Morgadinho T, Fesel C, Macedo TR, Bento C et al. Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism. Mol Psychiatr 2004; 9: 264-271.
-
(2004)
Mol Psychiatr
, vol.9
, pp. 264-271
-
-
Coutinho, A.M.1
Oliveira, G.2
Morgadinho, T.3
Fesel, C.4
Macedo, T.R.5
Bento, C.6
-
32
-
-
85047695651
-
Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder
-
Betancur C, Corbex M, Spielewoy C, Philippe A, Laplanche JL, Launay JM et al. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder. Mol Psychiatr 2002; 7: 67-71.
-
(2002)
Mol Psychiatr
, vol.7
, pp. 67-71
-
-
Betancur, C.1
Corbex, M.2
Spielewoy, C.3
Philippe, A.4
Laplanche, J.L.5
Launay, J.M.6
-
33
-
-
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
-
34
-
-
0031959051
-
Autism, affective and other psychiatric disorders: Patterns of familial aggregation
-
Bolton PF, Pickles A, Murphy M, Rutter M. Autism, affective and other psychiatric disorders: patterns of familial aggregation. Psychol Med 1998; 28: 385-395.
-
(1998)
Psychol Med
, vol.28
, pp. 385-395
-
-
Bolton, P.F.1
Pickles, A.2
Murphy, M.3
Rutter, M.4
-
35
-
-
0033766345
-
Personality traits of the relative of autistic probands
-
Murphy M, Bolton PF, Pickles A, Fombonne E, Piven J, Rutter M. Personality traits of the relative of autistic probands. Psychol Med 2000; 30: 1411-1424.
-
(2000)
Psychol Med
, vol.30
, pp. 1411-1424
-
-
Murphy, M.1
Bolton, P.F.2
Pickles, A.3
Fombonne, E.4
Piven, J.5
Rutter, M.6
-
36
-
-
2142817209
-
Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits
-
Sen S, Burmeister M, Ghosh D. Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits. Am J Med Genet 2004; 127B: 85-89.
-
(2004)
Am J Med Genet
, vol.127 B
, pp. 85-89
-
-
Sen, S.1
Burmeister, M.2
Ghosh, D.3
-
37
-
-
0031802343
-
Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder
-
McDougle CJ, Epperson CN, Price LH, Gelernter J. Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder. Mol Psychiatr 1998; 3: 270-273.
-
(1998)
Mol Psychiatr
, vol.3
, pp. 270-273
-
-
McDougle, C.J.1
Epperson, C.N.2
Price, L.H.3
Gelernter, J.4
-
38
-
-
0034987571
-
Role of the serotonin transporter gene in the behavioral expression of autism
-
Tordjman S, Gutknecht L, Carlier M, Spitz E, Antoine C, Slama F et al. Role of the serotonin transporter gene in the behavioral expression of autism. Mol Psychiatr 2001; 6: 434-439.
-
(2001)
Mol Psychiatr
, vol.6
, pp. 434-439
-
-
Tordjman, S.1
Gutknecht, L.2
Carlier, M.3
Spitz, E.4
Antoine, C.5
Slama, F.6
-
39
-
-
2342520299
-
Serotonin transporter gene and autism: A haplotype analysis in an Irish autistic population
-
Conroy J, Meally E, Kearney G, Fitzgerald M, Gill M, Gallagher L. Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population. Mol Psychiatr 2004; 9: 587-593.
-
(2004)
Mol Psychiatr
, vol.9
, pp. 587-593
-
-
Conroy, J.1
Meally, E.2
Kearney, G.3
Fitzgerald, M.4
Gill, M.5
Gallagher, L.6
-
40
-
-
0034615162
-
Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples
-
Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M et al. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. Am J Med Genet 2000; 96: 123-127.
-
(2000)
Am J Med Genet
, vol.96
, pp. 123-127
-
-
Persico, A.M.1
Militerni, R.2
Bravaccio, C.3
Schneider, C.4
Melmed, R.5
Conciatori, M.6
-
41
-
-
0033569931
-
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta 3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families
-
Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A et al. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta 3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. Am J Med Genet 1999; 88: 492-496.
-
(1999)
Am J Med Genet
, vol.88
, pp. 492-496
-
-
Maestrini, E.1
Lai, C.2
Marlow, A.3
Matthews, N.4
Wallace, S.5
Bailey, A.6
-
42
-
-
0035826536
-
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
-
Yirmiya N, Pilowsky T, Nemanov L, Arbelle S, Feinsilver T, Fried I et al. Evidence for an association with the serotonin transporter promoter region polymorphism and autism. Am J Med Genet 2001; 105: 381-386.
-
(2001)
Am J Med Genet
, vol.105
, pp. 381-386
-
-
Yirmiya, N.1
Pilowsky, T.2
Nemanov, L.3
Arbelle, S.4
Feinsilver, T.5
Fried, I.6
-
43
-
-
0029895783
-
Allelic variation of human serotonin transporter gene expression
-
Heils A, Teufel A, Petri S, Stober G, Riederer P, Bengel D et al. Allelic variation of human serotonin transporter gene expression. J Neurochem 1996; 66: 2621-2624.
-
(1996)
J Neurochem
, vol.66
, pp. 2621-2624
-
-
Heils, A.1
Teufel, A.2
Petri, S.3
Stober, G.4
Riederer, P.5
Bengel, D.6
-
44
-
-
0028174014
-
Organization of the human serotonin transporter gene
-
Lesch K-P, Balling U, Gross J, Strauss K, Wolozin BL, Murphy DL et al. Organization of the human serotonin transporter gene. J Neural Trans Gen Sect 1994; 95: 157-162.
-
(1994)
J Neural Trans Gen Sect
, vol.95
, pp. 157-162
-
-
Lesch, K.-P.1
Balling, U.2
Gross, J.3
Strauss, K.4
Wolozin, B.L.5
Murphy, D.L.6
|