-
1
-
-
34347258541
-
Altered neocortical cell density and layer thickness in serotonin transporter knockout mice: a quantitation study
-
Altamura C., Dell'acqua M., Moessner R., Murphy D., Lesch K., and Pérsico A.M. Altered neocortical cell density and layer thickness in serotonin transporter knockout mice: a quantitation study. Cereb. Cortex 17 6 (2007) 1394-1401
-
(2007)
Cereb. Cortex
, vol.17
, Issue.6
, pp. 1394-1401
-
-
Altamura, C.1
Dell'acqua, M.2
Moessner, R.3
Murphy, D.4
Lesch, K.5
Pérsico, A.M.6
-
3
-
-
0004235298
-
-
American Psychological Association, American Psychological Association, Washington, D.C.
-
American Psychological Association. Diagnostic and Statistical Manual of Mental Disorders (1994), American Psychological Association, Washington, D.C.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
4
-
-
0027950817
-
The mouse 5-hydroxytryptamine1B receptor is localized predominantly on axon terminals
-
Boschert U., Amara D.A., Segu L., and Hen R. The mouse 5-hydroxytryptamine1B receptor is localized predominantly on axon terminals. Neuroscience. 58 1 (1994) 167-182
-
(1994)
Neuroscience.
, vol.58
, Issue.1
, pp. 167-182
-
-
Boschert, U.1
Amara, D.A.2
Segu, L.3
Hen, R.4
-
5
-
-
0033809813
-
Clorgyline treatment elevates cortical serotonin and temporarily disrupts the vibrissae-related pattern in rat somatosensory cortex
-
Boylan C.B., Bennett-Clarke C.A., Crissman R.S., Mooney R.D., and Rhoades R.W. Clorgyline treatment elevates cortical serotonin and temporarily disrupts the vibrissae-related pattern in rat somatosensory cortex. J. Comp. Neurol. 427 (2000) 139-149
-
(2000)
J. Comp. Neurol.
, vol.427
, pp. 139-149
-
-
Boylan, C.B.1
Bennett-Clarke, C.A.2
Crissman, R.S.3
Mooney, R.D.4
Rhoades, R.W.5
-
6
-
-
33845296559
-
Modeling early cortical serotonergic deficits in autism
-
Boylan C.B., Blue M.E., and Hohmann C.F. Modeling early cortical serotonergic deficits in autism. Behav. Brain Res. 176 1 (2007) 94-108
-
(2007)
Behav. Brain Res.
, vol.176
, Issue.1
, pp. 94-108
-
-
Boylan, C.B.1
Blue, M.E.2
Hohmann, C.F.3
-
7
-
-
41849117712
-
Interactions between integrin alphaIIbbeta3 and the serotonin transporter regulate serotonin transport and platelet aggregation in mice and humans
-
Carneiro A.M., Cook E.H., Murphy D.L., and Blakely R.D. Interactions between integrin alphaIIbbeta3 and the serotonin transporter regulate serotonin transport and platelet aggregation in mice and humans. J. Clin. Invest. 118 4 (2008) 1544-1552
-
(2008)
J. Clin. Invest.
, vol.118
, Issue.4
, pp. 1544-1552
-
-
Carneiro, A.M.1
Cook, E.H.2
Murphy, D.L.3
Blakely, R.D.4
-
8
-
-
18944365556
-
Replication of autism linkage: fine-mapping peak at 17q21
-
Cantor R.M., Kono N., Duvall J.A., Stone J.L., Nelson S.F., Geschwind D.H., et al. Replication of autism linkage: fine-mapping peak at 17q21. Am. J. Hum. Genet. 76 6 (2005) 1050-1056
-
(2005)
Am. J. Hum. Genet.
, vol.76
, Issue.6
, pp. 1050-1056
-
-
Cantor, R.M.1
Kono, N.2
Duvall, J.A.3
Stone, J.L.4
Nelson, S.F.5
Geschwind, D.H.6
-
9
-
-
20044390596
-
Pervasive developmental disorders in preschool children: confirmation of high prevalence
-
Chakrabarti S., and Fombonne E. Pervasive developmental disorders in preschool children: confirmation of high prevalence. Am. J. Psychiatry 162 (2005) 1133-1141
-
(2005)
Am. J. Psychiatry
, vol.162
, pp. 1133-1141
-
-
Chakrabarti, S.1
Fombonne, E.2
-
10
-
-
33749254952
-
En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder
-
Cheh M.A., Millonig J.H., Roselli L.M., Ming X., Kamdar S., Wagner G.C., et al. En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder. Brain Res. 1116 1 (2006) 166-176
-
(2006)
Brain Res.
, vol.1116
, Issue.1
, pp. 166-176
-
-
Cheh, M.A.1
Millonig, J.H.2
Roselli, L.M.3
Ming, X.4
Kamdar, S.5
Wagner, G.C.6
-
11
-
-
33847300921
-
Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios
-
Cho I.H., Yoo H.J., Park M., Lee Y.S., and Kim S.A. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. Brain Res. 1139 (2007) 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
-
12
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
Clayton D. A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am. J. Hum. Genet. 65 (1999) 1170-1177
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
13
-
-
2342520299
-
Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population
-
Conroy J., Meally E., Kearney G., Fitzgerald M., Gill M., and Gallagher L. Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population. Mol. Psychiatry 9 (2004) 587-593
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 587-593
-
-
Conroy, J.1
Meally, E.2
Kearney, G.3
Fitzgerald, M.4
Gill, M.5
Gallagher, L.6
-
14
-
-
20244374414
-
Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2)
-
Coon H., Dunn D., Lainhart J., Miller J., Hamil C., McMahon W., et al. Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2). Am. J. Med. Genet B Neuropsychiatr. Genet. 135 (2005) 42-46
-
(2005)
Am. J. Med. Genet B Neuropsychiatr. Genet.
, vol.135
, pp. 42-46
-
-
Coon, H.1
Dunn, D.2
Lainhart, J.3
Miller, J.4
Hamil, C.5
McMahon, W.6
-
15
-
-
11144358488
-
Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism
-
Coutinho A.M., Oliveira G., Fesel C., Miguel T., Borges L., Vicente A.M., et al. Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism. Mol. Psychiatry 9 (2004) 264-271
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 264-271
-
-
Coutinho, A.M.1
Oliveira, G.2
Fesel, C.3
Miguel, T.4
Borges, L.5
Vicente, A.M.6
-
16
-
-
33947114826
-
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels
-
Coutinho A.M., Sousa I., Martins M., Correia C., Morgadinho T., Vicente A.M., et al. Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. Hum. Genet 121 2 (2007) 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
Vicente, A.M.6
-
17
-
-
36949000858
-
Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism
-
Cross S., Kim S.J., Weiss L.A., Sutcliffe J.S., Cook E.H., and Veenstra-Vanderweele J. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Neuropsychopharmacology 33 2 (2008) 353-360
-
(2008)
Neuropsychopharmacology
, vol.33
, Issue.2
, pp. 353-360
-
-
Cross, S.1
Kim, S.J.2
Weiss, L.A.3
Sutcliffe, J.S.4
Cook, E.H.5
Veenstra-Vanderweele, J.6
-
18
-
-
0242637425
-
Polymorphisms in the 5′-unstranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression
-
Duan J., Sanders A.R., Mowry B.J., Levinson D.F., Silverman J.M., Gejman P.V., et al. Polymorphisms in the 5′-unstranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression. Mol. Psychiatry 8 (2003) 901-910
-
(2003)
Mol. Psychiatry
, vol.8
, pp. 901-910
-
-
Duan, J.1
Sanders, A.R.2
Mowry, B.J.3
Levinson, D.F.4
Silverman, J.M.5
Gejman, P.V.6
-
19
-
-
0000497985
-
PS power and sample size program available for free on the internet
-
Dupont W.D., and Plummer W.S. PS power and sample size program available for free on the internet. Controlled Clin. Trials 18 (1997) 274
-
(1997)
Controlled Clin. Trials
, vol.18
, pp. 274
-
-
Dupont, W.D.1
Plummer, W.S.2
-
20
-
-
0035653670
-
Genetics of autism: complex aetiology for a heterogeneous disorder
-
Folstein S.E., and Rosen-Sheidley B. Genetics of autism: complex aetiology for a heterogeneous disorder. Nat. Rev. Genet. 2 (2001) 943-955
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 943-955
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
-
21
-
-
54949116893
-
Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal
-
Guhathakurta S., Sinha S., Ghosh S., Chatterjee A., Ahmed S., Gangopadhyay P.K., and Usha R. Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal. Brain Res. 1240 (2008) 12-21
-
(2008)
Brain Res.
, vol.1240
, pp. 12-21
-
-
Guhathakurta, S.1
Sinha, S.2
Ghosh, S.3
Chatterjee, A.4
Ahmed, S.5
Gangopadhyay, P.K.6
Usha, R.7
-
22
-
-
0036364966
-
Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample
-
Hawi Z., Dring M., Kirley A., Foley D., Kent L., Craddock N., Asherson P., Curran S., Gould A., Richards S., Lawson D., Pay H., Turic D., Langley K., Owen M., O'Donovan M., Thapar A., Fitzgerald M., and Gill M. Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Mol. Psychiatry 7 7 (2002) 718-725
-
(2002)
Mol. Psychiatry
, vol.7
, Issue.7
, pp. 718-725
-
-
Hawi, Z.1
Dring, M.2
Kirley, A.3
Foley, D.4
Kent, L.5
Craddock, N.6
Asherson, P.7
Curran, S.8
Gould, A.9
Richards, S.10
Lawson, D.11
Pay, H.12
Turic, D.13
Langley, K.14
Owen, M.15
O'Donovan, M.16
Thapar, A.17
Fitzgerald, M.18
Gill, M.19
-
23
-
-
13444310798
-
Serotonergic paradoxes of autism replicated in a simple mathematical model
-
Janusonis S. Serotonergic paradoxes of autism replicated in a simple mathematical model. Med. Hypotheses 64 4 (2005) 742-750
-
(2005)
Med. Hypotheses
, vol.64
, Issue.4
, pp. 742-750
-
-
Janusonis, S.1
-
24
-
-
33750044558
-
Ontogeny of brain and blood serotonin levels in 5-HT receptor knockout mice: potential relevance to the neurobiology of autism
-
Janusonis S., Anderson G.M., Shifrovich I., and Rakic P. Ontogeny of brain and blood serotonin levels in 5-HT receptor knockout mice: potential relevance to the neurobiology of autism. J. Neurochem. 99 (2006) 1019-1031
-
(2006)
J. Neurochem.
, vol.99
, pp. 1019-1031
-
-
Janusonis, S.1
Anderson, G.M.2
Shifrovich, I.3
Rakic, P.4
-
25
-
-
33748687580
-
Association between polymorphisms in serotonin 2C receptor gene and attention-deficit/hyperactivity disorder in Han Chinese subjects
-
Li J., Wang Y., Zhou R., Zhang H., Yang L., Wang B., and Faraone S.V. Association between polymorphisms in serotonin 2C receptor gene and attention-deficit/hyperactivity disorder in Han Chinese subjects. Neurosci. Lett. 407 2 (2006) 107-111
-
(2006)
Neurosci. Lett.
, vol.407
, Issue.2
, pp. 107-111
-
-
Li, J.1
Wang, Y.2
Zhou, R.3
Zhang, H.4
Yang, L.5
Wang, B.6
Faraone, S.V.7
-
26
-
-
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., and 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. 24 (1994) 659-685
-
(1994)
J. Autism Dev. Disord.
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
27
-
-
34548329722
-
HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study
-
Massat I., Lerer B., Souery D., Blackwood D., Muir W., Kaneva R., Nöthen M.M., Oruc L., Papadimitriou G.N., Dikeos D., Serretti A., Bellivier F., Golmard J.L., Milanova V., Del-Favero J., Van Broeckhoven C., and Mendlewicz J. HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study. Mol. Psychiatry 12 9 (2007) 797-798
-
(2007)
Mol. Psychiatry
, vol.12
, Issue.9
, pp. 797-798
-
-
Massat, I.1
Lerer, B.2
Souery, D.3
Blackwood, D.4
Muir, W.5
Kaneva, R.6
Nöthen, M.M.7
Oruc, L.8
Papadimitriou, G.N.9
Dikeos, D.10
Serretti, A.11
Bellivier, F.12
Golmard, J.L.13
Milanova, V.14
Del-Favero, J.15
Van Broeckhoven, C.16
Mendlewicz, J.17
-
28
-
-
2142645125
-
Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism
-
McCauley J.L., Olson L.M., Dowd M., Folstein S.E., Haines J.L., Sutcliffe J.S., et al. Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism. Am. J. Med. Genet. B Neuropsychiatr. Genet. 127 1 (2004) 104-112
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.127
, Issue.1
, pp. 104-112
-
-
McCauley, J.L.1
Olson, L.M.2
Dowd, M.3
Folstein, S.E.4
Haines, J.L.5
Sutcliffe, J.S.6
-
29
-
-
33847128627
-
Pharmacological treatments
-
Moldin S.O., and Rubenstein J.L.R. (Eds), CRC Press, Taylor and Francis Group
-
McDougle C.J., Posey D.J., and Sigler K.A. Pharmacological treatments. In: Moldin S.O., and Rubenstein J.L.R. (Eds). Understanding Autism (2006), CRC Press, Taylor and Francis Group 417-442
-
(2006)
Understanding Autism
, pp. 417-442
-
-
McDougle, C.J.1
Posey, D.J.2
Sigler, K.A.3
-
30
-
-
0942279743
-
Association of tryptophan 2,3 dioxygenase gene polymorphism with autism
-
Nabi R., Serajee F.J., Chugani D.C., Zhong H., Huq A.H., et al. Association of tryptophan 2,3 dioxygenase gene polymorphism with autism. Am. J. Med. Genet. B Neuropsychiatr Genet. 125 1 (2004) 63-68
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr Genet.
, vol.125
, Issue.1
, pp. 63-68
-
-
Nabi, R.1
Serajee, F.J.2
Chugani, D.C.3
Zhong, H.4
Huq, A.H.5
-
31
-
-
12244292661
-
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder
-
Quist J.F., Barr C.L., Schachar R., Roberts W., Malone M., Tannock R., Basile V.S., Beitchman J., and Kennedy J.L. The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder. Mol. Psychiatry 8 1 (2003) 98-102
-
(2003)
Mol. Psychiatry
, vol.8
, Issue.1
, pp. 98-102
-
-
Quist, J.F.1
Barr, C.L.2
Schachar, R.3
Roberts, W.4
Malone, M.5
Tannock, R.6
Basile, V.S.7
Beitchman, J.8
Kennedy, J.L.9
-
32
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes
-
and the Paris Autism International Sibpair Study
-
Philippe A., Martinez M., Guilloud-Bataille M., Gillberg C., Leboyer M., and and the Paris Autism International Sibpair Study. Genome-wide scan for autism susceptibility genes. HMG 8 5 (1999) 805-812
-
(1999)
HMG
, vol.8
, Issue.5
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Leboyer, M.5
-
34
-
-
0000526929
-
Studies of 5 hydroxyindole metabolism in autistic and other mentally retarded children
-
Schain R., and Freedman D. Studies of 5 hydroxyindole metabolism in autistic and other mentally retarded children. J. Pediatr. 58 (1961) 315-320
-
(1961)
J. Pediatr.
, vol.58
, pp. 315-320
-
-
Schain, R.1
Freedman, D.2
-
36
-
-
8844244724
-
Evidence for sex-specific risk alleles in autism spectrum disorder
-
Stone J.L., Merriman B., Cantor R.M., Yonan A.L., Geschwind D.H., Nelson S.F., et al. Evidence for sex-specific risk alleles in autism spectrum disorder. Am. J. Hum. Genet. 75 6 (2004) 1117-1123
-
(2004)
Am. J. Hum. Genet.
, vol.75
, Issue.6
, pp. 1117-1123
-
-
Stone, J.L.1
Merriman, B.2
Cantor, R.M.3
Yonan, A.L.4
Geschwind, D.H.5
Nelson, S.F.6
-
37
-
-
0037041326
-
Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism
-
Veenstra-VanderWeele J., Kim S.J., Lord C., Courchesne R., Akshoomoff N., Cook E.H., et al. Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism. Am. J. Med. Genet. 114 3 (2002) 277-283
-
(2002)
Am. J. Med. Genet.
, vol.114
, Issue.3
, pp. 277-283
-
-
Veenstra-VanderWeele, J.1
Kim, S.J.2
Lord, C.3
Courchesne, R.4
Akshoomoff, N.5
Cook, E.H.6
-
38
-
-
33745682011
-
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility
-
Weiss L.A., Kosova G., Delahanty R.J., Cook E.H., Ober C., and Sutcliffe J.S. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. Eur. J. Hum. Genet 14 8 (2006) 923-931
-
(2006)
Eur. J. Hum. Genet
, vol.14
, Issue.8
, pp. 923-931
-
-
Weiss, L.A.1
Kosova, G.2
Delahanty, R.J.3
Cook, E.H.4
Ober, C.5
Sutcliffe, J.S.6
-
39
-
-
0032587196
-
Serotonin 5-HT1B and 5-HT1D receptors form homodimers when expressed alone and heterodimers when co-expressed
-
Xie Z., Lee S.P., O'Dowd B.F., and George S.R. Serotonin 5-HT1B and 5-HT1D receptors form homodimers when expressed alone and heterodimers when co-expressed. FEBS Lett. 456 1 (1999) 63-67
-
(1999)
FEBS Lett.
, vol.456
, Issue.1
, pp. 63-67
-
-
Xie, Z.1
Lee, S.P.2
O'Dowd, B.F.3
George, S.R.4
|