-
1
-
-
38749140677
-
Linkage, association, and geneexpression analyses identify CNTNAP2 as an autism-susceptibility gene
-
doi:10.1016/j.ajhg.2007.09.005
-
Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., et al. (2008). Linkage, association, and geneexpression analyses identify CNT-NAP2 as an autism-susceptibility gene. Am. J. Hum. Genet. 82, 150-159. doi:10.1016/j.ajhg.2007.09.005
-
(2008)
Am. J. Hum. Genet
, vol.82
, pp. 150-159
-
-
Alarcón, M.1
Abrahams, B.S.2
Stone, J.L.3
Duvall, J.A.4
Perederiy, J.V.5
Bomar, J.M.6
-
2
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
doi:10.1093/hmg/ddq307
-
Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., et al. (2010). A genome-wide scan for common alleles affecting risk for autism. Hum. Mol. Genet. 19, 4072-4082. doi:10.1093/hmg/ddq307
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 4072-4082
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Regan, R.4
Conroy, J.5
Magalhaes, T.R.6
-
3
-
-
84867796651
-
Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling
-
doi:10.1523/JNEUROSCI.2215-12.2012
-
Arons, M. H., Thynne, C. J., Grabrucker, M., Li, D., Schoen, M., Cheyne, J. E., et al. (2012). Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling. J. Neurosci. 32, 14966-14978. doi:10.1523/JNEUROSCI.2215-12.2012
-
(2012)
J. Neurosci
, vol.32
, pp. 14966-14978
-
-
Arons, M.H.1
Thynne, C.J.2
Grabrucker, M.3
Li, D.4
Schoen, M.5
Cheyne, J.E.6
-
4
-
-
77951152163
-
ProbABEL package for genome-wide association analysis of imputed data
-
doi:10.1186/1471-2105-11-134
-
Aulchenko, Y. S., Struchalin, M. V., and van Duijn, C. M. (2010). ProbABEL package for genome-wide association analysis of imputed data. BMC Bioinformatics 11:134. doi:10.1186/1471-2105-11-134
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 134
-
-
Aulchenko, Y.S.1
Struchalin, M.V.2
van Duijn, C.M.3
-
5
-
-
10144233458
-
Personality correlates of the broader autism phenotype as assessed by the Autism Spectrum Quotient (AQ)
-
doi:10.1016/j.paid.2004.04.022
-
Austin, E. J. (2005). Personality correlates of the broader autism phenotype as assessed by the Autism Spectrum Quotient (AQ). Pers. Individ. Dif. 38, 451-460. doi:10.1016/j.paid.2004.04.022
-
(2005)
Pers. Individ. Dif
, vol.38
, pp. 451-460
-
-
Austin, E.J.1
-
6
-
-
0032837157
-
The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: A large scale study
-
doi:10.1017/S003329179900896X
-
Baron-Cohen, S., Scahill, V. L., Izaguirre, J., Hornsey, H., and Robertson, M. M. (1999). The prevalence of Gilles de la Tourette syndrome in children and adolescents with autism: a large scale study. Psychol. Med. 29, 1151-1159. doi:10.1017/S003329179900896X
-
(1999)
Psychol. Med
, vol.29
, pp. 1151-1159
-
-
Baron-Cohen, S.1
Scahill, V.L.2
Izaguirre, J.3
Hornsey, H.4
Robertson, M.M.5
-
7
-
-
0035261154
-
The autismspectrum quotient (AQ): Evidence from Asperger syndrome/highfunctioning autism, males and females, scientists and mathematicians
-
doi:10.1023/A:1005653411471
-
Baron-Cohen, S., Wheelwright, S., Skinner, R., Martin, J., and Clubley, E. (2001). The autismspectrum quotient (AQ): evidence from Asperger syndrome/highfunctioning autism, males and females, scientists and mathematicians. J. Autism Dev. Disord. 31, 5-17. doi:10.1023/A:1005653411471
-
(2001)
J. Autism Dev. Disord
, vol.31
, pp. 5-17
-
-
Baron-Cohen, S.1
Wheelwright, S.2
Skinner, R.3
Martin, J.4
Clubley, E.5
-
8
-
-
84865712382
-
Annotation of functional variation in personal genomes using RegulomeDB
-
doi:10.1101/gr.137323.112
-
Boyle, A. P., Hong, E. L., Hariharan, M., Cheng, Y., Schaub, M. A., Kasowski, M., et al. (2012). Annotation of functional variation in personal genomes using RegulomeDB. Genome Res. 22, 1790-1797. doi:10.1101/gr.137323.112
-
(2012)
Genome Res
, vol.22
, pp. 1790-1797
-
-
Boyle, A.P.1
Hong, E.L.2
Hariharan, M.3
Cheng, Y.4
Schaub, M.A.5
Kasowski, M.6
-
9
-
-
33750962208
-
A genetic variant that disrupts MET transcription is associated with autism
-
doi:10.1073/pnas.0605296103
-
Campbell, D. B., Sutcliffe, J. S., Ebert, P. J., Militerni, R., Bravaccio, C., Trillo, S., et al. (2006). A genetic variant that disrupts MET transcription is associated with autism. Proc. Natl. Acad. Sci. U.S.A. 103, 16834-16839. doi:10.1073/pnas.0605296103
-
(2006)
Proc. Natl. Acad. Sci. U.S.A
, vol.103
, pp. 16834-16839
-
-
Campbell, D.B.1
Sutcliffe, J.S.2
Ebert, P.J.3
Militerni, R.4
Bravaccio, C.5
Trillo, S.6
-
10
-
-
67651213461
-
Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome
-
doi: 10.1002/aur.80
-
Chakrabarti, B., Dudbridge, F., Kent, L., Wheelwright, S., Hill-Cawthorne, G., Allison, C., et al. (2009). Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome. Autism Res. 2, 157-177. doi: 10.1002/aur.80
-
(2009)
Autism Res
, vol.2
, pp. 157-177
-
-
Chakrabarti, B.1
Dudbridge, F.2
Kent, L.3
Wheelwright, S.4
Hill-Cawthorne, G.5
Allison, C.6
-
11
-
-
34249997024
-
Replicating genotype-phenotype associations
-
doi:10.1038/447655a
-
Chanock, S., Manolio, T., Boehnke, M., Boerwinkle, E., Hunter, D., Thomas, G., et al. (2007). Replicating genotype-phenotype associations. Nature 447, 655-660. doi:10.1038/447655a
-
(2007)
Nature
, vol.447
, pp. 655-660
-
-
Chanock, S.1
Manolio, T.2
Boehnke, M.3
Boerwinkle, E.4
Hunter, D.5
Thomas, G.6
-
12
-
-
84874440957
-
Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism
-
doi:10.1038/tp.2012.75
-
Clarke, R. A., Lee, S., and Eapen, V. (2012). Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism. Transl. Psychiatry 2, e158. doi:10.1038/tp.2012.75
-
(2012)
Transl. Psychiatry
, vol.2
-
-
Clarke, R.A.1
Lee, S.2
Eapen, V.3
-
13
-
-
0037629077
-
Autistic traits in the general population: A twin study
-
doi:10.1001/archpsyc.60.5.524
-
Constantino, J., and Todd, R. (2003). Autistic traits in the general population: a twin study. Arch. Gen. Psychiatry 60, 524-530. doi:10.1001/archpsyc.60.5.524
-
(2003)
Arch. Gen. Psychiatry
, vol.60
, pp. 524-530
-
-
Constantino, J.1
Todd, R.2
-
14
-
-
84894589405
-
Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system
-
et al, doi:10.1038/mp.2013.16
-
Cristino, A. S., Williams, S. M., Hawi, Z., An, J. Y., Bellgrove, M. A., Schwartz, C. E., et al. (2013). Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system. Mol. Psychiatry doi:10.1038/mp.2013.16
-
(2013)
Mol. Psychiatry
-
-
Cristino, A.S.1
Williams, S.M.2
Hawi, Z.3
An, J.Y.4
Bellgrove, M.A.5
Schwartz, C.E.6
-
15
-
-
84862160222
-
Global prevalence of autism and other pervasive developmental disorders
-
doi:10.1002/aur.239
-
Elsabbagh, M., Divan, G., Koh, Y.-J., Kim, Y. S., Kauchali, S., Marcin, C., et al. (2012). Global prevalence of autism and other pervasive developmental disorders. Autism Res. 5, 160-179. doi:10.1002/aur.239
-
(2012)
Autism Res
, vol.5
, pp. 160-179
-
-
Elsabbagh, M.1
Divan, G.2
Koh, Y.-J.3
Kim, Y.S.4
Kauchali, S.5
Marcin, C.6
-
16
-
-
84858737859
-
Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
-
doi:10.1016/j.biopsych.2011.09.034
-
Fernandez, T. V., Sanders, S. J., Yurkiewicz, I. R., Ercan-Sencicek, A. G., Kim, Y. S., Fishman, D. O., et al. (2012). Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biol. Psychiatry 71,392-402. doi:10.1016/j.biopsych.2011.09.034
-
(2012)
Biol. Psychiatry
, vol.71
, pp. 392-402
-
-
Fernandez, T.V.1
Sanders, S.J.2
Yurkiewicz, I.R.3
Ercan-Sencicek, A.G.4
Kim, Y.S.5
Fishman, D.O.6
-
17
-
-
0036499241
-
Sample size requirements for association studies of gene-gene interactions
-
doi:10.1093/aje/155.5.478
-
Gauderman, W. J. (2002). Sample size requirements for association studies of gene-gene interactions. Am. J. Epidemiol. 155, 478-484. doi:10.1093/aje/155.5.478
-
(2002)
Am. J. Epidemiol
, vol.155
, pp. 478-484
-
-
Gauderman, W.J.1
-
18
-
-
0026897662
-
The Emanuel Miller Memorial Lecture 1991. Autism and autistic-like conditions: Subclasses among disorders of empathy
-
doi:10.1111/j.1469-7610.1992.tb01959.x
-
Gillberg, C. L. (1992). The Emanuel Miller Memorial Lecture 1991. Autism and autistic-like conditions: subclasses among disorders of empathy. J. Child Psychol. Psychiatry 33,813-842. doi:10.1111/j.1469-7610.1992.tb01959.x
-
(1992)
J. Child Psychol. Psychiatry
, vol.33
, pp. 813-842
-
-
Gillberg, C.L.1
-
19
-
-
66849097781
-
Failure to replicate a genetic association may provide important clues about genetic architecture
-
doi:10.1371/journal.pone.0005639
-
Greene, C. S., Penrod, N. M., Williams, S. M., and Moore, J. H. (2009). Failure to replicate a genetic association may provide important clues about genetic architecture. PLoS ONE 4:e5639. doi:10.1371/journal.pone.0005639
-
(2009)
PLoS ONE
, vol.4
-
-
Greene, C.S.1
Penrod, N.M.2
Williams, S.M.3
Moore, J.H.4
-
20
-
-
0037464828
-
Obsessive-compulsive behaviors in parents of multiplex autism families
-
doi:10.1016/S0165-1781(02)00304-9
-
Hollander, E., King, A., Delaney, K., Smith, C. J., and Silverman, J. M. (2003). Obsessive-compulsive behaviors in parents of multiplex autism families. Psychiatry Res. 117, 11-16. doi:10.1016/S0165-1781(02)00304-9
-
(2003)
Psychiatry Res
, vol.117
, pp. 11-16
-
-
Hollander, E.1
King, A.2
Delaney, K.3
Smith, C.J.4
Silverman, J.M.5
-
21
-
-
70350366111
-
A critical assessment of the factors affecting reporter gene assays for promoter SNP function: A reassessment of -308 TNF polymorphism function using a novel integrated reporter system
-
doi:10.1038/ejhg.2009.80
-
Karimi, M., Goldie, L. C., Cruickshank, M. N., Moses, E. K., and Abraham, L. J. (2009). A critical assessment of the factors affecting reporter gene assays for promoter SNP function: a reassessment of -308 TNF polymorphism function using a novel integrated reporter system. Eur. J. Hum. Genet. 17, 1454-1462. doi:10.1038/ejhg.2009.80
-
(2009)
Eur. J. Hum. Genet
, vol.17
, pp. 1454-1462
-
-
Karimi, M.1
Goldie, L.C.2
Cruickshank, M.N.3
Moses, E.K.4
Abraham, L.J.5
-
22
-
-
84898771680
-
Molecular prioritisation strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1
-
doi:10.1038/ejhg.2013.208
-
Kaskow, B. J., Diepeveen, L. A., Proffitt, J. M., Rea, A. J., Ulgiati, D., Blangero, J., et al. (2013). Molecular prioritisation strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1. Eur. J. Hum. Genet. doi:10.1038/ejhg.2013.208
-
(2013)
Eur. J. Hum. Genet
-
-
Kaskow, B.J.1
Diepeveen, L.A.2
Proffitt, J.M.3
Rea, A.J.4
Ulgiati, D.5
Blangero, J.6
-
23
-
-
84864087818
-
Genes associated with autism spectrum disorder
-
doi:10.1016/j.brainresbull.2012.05.017
-
Li, X., Zou, H., and Brown, W. T. (2012). Genes associated with autism spectrum disorder. Brain Res. Bull. 88, 543-552. doi:10.1016/j.brainresbull.2012.05.017
-
(2012)
Brain Res. Bull
, vol.88
, pp. 543-552
-
-
Li, X.1
Zou, H.2
Brown, W.T.3
-
24
-
-
37549064336
-
Mach 1.0: Rapid haplotype reconstruction and missing genotype inference
-
Li, Y., and Abecasis, G. (2006). Mach 1.0: rapid haplotype reconstruction and missing genotype inference. Am. J. Hum. Genet. 79, 2290.
-
(2006)
Am. J. Hum. Genet
, vol.79
, pp. 2290
-
-
Li, Y.1
Abecasis, G.2
-
25
-
-
67649387094
-
Involvement of the PRKCB1 gene in autistic disorder: Significant genetic association and reduced neocortical gene expression
-
doi:10.1038/mp.2008.21
-
Lintas, C., Sacco, R., Garbett, K., Mirnics, K., Militerni, R., Bravaccio, C., et al. (2009). Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression. Mol. Psychiatry 14, 705-718. doi:10.1038/mp.2008.21
-
(2009)
Mol. Psychiatry
, vol.14
, pp. 705-718
-
-
Lintas, C.1
Sacco, R.2
Garbett, K.3
Mirnics, K.4
Militerni, R.5
Bravaccio, C.6
-
26
-
-
84855331271
-
Autism spectrum disorders and autistic like traits: Similar etiology in the extreme end and the normal variation
-
doi:10.1001/, archgenpsychiatry.2011.144
-
Lundström, S., Chang, Z., Rastam, M., Gillberg, C., Larsson, H., Anckarsater, H., et al. (2012). Autism spectrum disorders and autistic like traits: similar etiology in the extreme end and the normal variation. Arch. Gen. Psychiatry 69, 46-52. doi:10.1001/archgenpsychiatry.2011.144
-
(2012)
Arch. Gen. Psychiatry
, vol.69
, pp. 46-52
-
-
Lundström, S.1
Chang, Z.2
Rastam, M.3
Gillberg, C.4
Larsson, H.5
Anckarsater, H.6
-
27
-
-
0031976356
-
The prevalence of Tourette syndrome in a mainstream school population
-
Mason, A., Banerjee, S., Eapen, V., Zeitlin, H., and Robertson, M. M. (1998). The prevalence of Tourette syndrome in a mainstream school population. Dev. Med. Child Neurol. 40, 292-296.
-
(1998)
Dev. Med. Child Neurol
, vol.40
, pp. 292-296
-
-
Mason, A.1
Banerjee, S.2
Eapen, V.3
Zeitlin, H.4
Robertson, M.M.5
-
28
-
-
84864160745
-
-
National Human Genome Research Institute, Bethesda, MD. Available at, accessed 2012
-
National Human Genome Research Institute. (2012). A Catalog of Genome-Wide Association Studies [Online]. Bethesda, MD. Available at: http://www.genome.gov/26525384 (accessed 2012).
-
(2012)
A Catalog of Genome-Wide Association Studies [Online]
-
-
-
29
-
-
84886435468
-
-
NCBI, Bethesda: National Center for Biotechnology Information
-
NCBI. (2012). PRKCB Protein Kinase C, Beta [Online]. Bethesda: National Center for Biotechnology Information.
-
(2012)
PRKCB Protein Kinase C, Beta [Online]
-
-
-
30
-
-
0027379214
-
Effects of frequent ultrasound during pregnancy: A randomised controlled trial
-
doi:10.1016/0140-6736(93)91944-H
-
Newnham, J. P., Evans, S. F., Michael, C. A., Stanley, F. J., and Landau, L. I. (1993). Effects of frequent ultrasound during pregnancy: a randomised controlled trial. Lancet 342, 887-891. doi:10.1016/0140-6736(93)91944-H
-
(1993)
Lancet
, vol.342
, pp. 887-891
-
-
Newnham, J.P.1
Evans, S.F.2
Michael, C.A.3
Stanley, F.J.4
Landau, L.I.5
-
31
-
-
84863338087
-
What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations
-
doi:10.1093/ije/dyr178
-
Panagiotou, O. A., and Ioannidis, J. P. A. (2011). What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations. Int. J. Epidemiol. 41,273-286. doi:10.1093/ije/dyr178
-
(2011)
Int. J. Epidemiol
, vol.41
, pp. 273-286
-
-
Panagiotou, O.A.1
Ioannidis, J.P.A.2
-
32
-
-
27144517182
-
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism
-
doi:10.1038/sj.mp.4001704
-
Philippi, A., Roschmann, E., Tores, G., Lindenbaum, P., Benajou, A., Germain-Leclerc, L., et al. (2005). Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. Mol. Psychiatry 10, 950-960. doi:10.1038/sj.mp.4001704
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 950-960
-
-
Philippi, A.1
Roschmann, E.2
Tores, G.3
Lindenbaum, P.4
Benajou, A.5
Germain-Leclerc, L.6
-
33
-
-
33645893472
-
Autistic features in a total population of 7-9-yearold children assessed by the ASSQ (Autism Spectrum Screening Questionnaire)
-
doi:10.1111/j.1469-7610.2005.01462.x
-
Posserud, M.-B., Lundervold, A. J., and Gillberg, C. (2006). Autistic features in a total population of 7-9-yearold children assessed by the ASSQ (Autism Spectrum Screening Questionnaire). J. Child Psychol. Psychiatry 47,167-175. doi:10.1111/j.1469-7610.2005.01462.x
-
(2006)
J. Child Psychol. Psychiatry
, vol.47
, pp. 167-175
-
-
Posserud, M.-B.1
Lundervold, A.J.2
Gillberg, C.3
-
34
-
-
77956586071
-
LocusZoom: Regional visualization of genomewide association scan results
-
doi:10.1093/bioinformatics/btq419
-
Pruim, R. J., Welch, R. P., Sanna, S., Teslovich, T. M., Chines, P. S., Gliedt, T. P., et al. (2010). LocusZoom: regional visualization of genomewide association scan results. Bioinformatics 26, 2336-2337. doi:10.1093/bioinformatics/btq419
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
Gliedt, T.P.6
-
35
-
-
48549086424
-
-
R Development Core Team, Vienna: R Foundation for Statistical Computing
-
R Development Core Team. (2008). R: ALanguageandEnvironmentforStatistical Computing. Vienna: R Foundation for Statistical Computing.
-
(2008)
R: ALanguageandEnvironmentforStaTistical Computing
-
-
-
36
-
-
77949309281
-
A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples
-
doi:10.1007/s10519-009-9308-6
-
Ronald, A., Butcher, L. M., Docherty, S., Davis, O. S. P., Schalkwyk, L., Craig, I. W., et al. (2010). A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples. Behav. Genet. 40, 31-45. doi:10.1007/s10519-009-9308-6
-
(2010)
Behav. Genet
, vol.40
, pp. 31-45
-
-
Ronald, A.1
Butcher, L.M.2
Docherty, S.3
Davis, O.S.P.4
Schalkwyk, L.5
Craig, I.W.6
-
37
-
-
23744468693
-
The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism
-
doi:10.1111/j.1467-7687.2005.00433.x
-
Ronald, A., Happe, F., and Plomin, R. (2005). The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism. Dev. Sci. 8, 444-458. doi:10.1111/j.1467-7687.2005.00433.x
-
(2005)
Dev. Sci
, vol.8
, pp. 444-458
-
-
Ronald, A.1
Happe, F.2
Plomin, R.3
-
38
-
-
79952597943
-
Autism spectrum disorders and autistic traits: A decade of new twin studies
-
doi:10.1002/ajmg.b.31159
-
Ronald, A., and Hoekstra, R. A. (2011). Autism spectrum disorders and autistic traits: a decade of new twin studies. Am. J. Med. Genet. B Neuropsychiatr. Genet. 156, 255-274. doi:10.1002/ajmg.b.31159
-
(2011)
Am. J. Med. Genet. B NeuRopsychiatr. Genet
, vol.156
, pp. 255-274
-
-
Ronald, A.1
Hoekstra, R.A.2
-
39
-
-
79955610369
-
Relationships between autistic-like and schizotypy traits: An analysis using the Autism Spectrum Quotient and Oxford-Liverpool Inventory of Feelings and Experiences
-
doi:10.1016/j.paid.2011.03.027
-
Russell-Smith, S. N., Maybery, M. T., and Bayliss, D. M. (2011). Relationships between autistic-like and schizotypy traits: an analysis using the Autism Spectrum Quotient and Oxford-Liverpool Inventory of Feelings and Experiences. Pers. Individ. Dif. 51,128-132. doi:10.1016/j.paid.2011.03.027
-
(2011)
Pers. Individ. Dif
, vol.51
, pp. 128-132
-
-
Russell-Smith, S.N.1
Maybery, M.T.2
Bayliss, D.M.3
-
40
-
-
34347408099
-
Problems with genome-wide association studies
-
doi:10.1126/science.316.5833.1840c
-
Shriner, D., Vaughan, L. K., Padilla, M. A., and Tiwari, H. K. (2007). Problems with genome-wide association studies. Science 316, 1840-1842. doi:10.1126/science.316.5833.1840c
-
(2007)
Science
, vol.316
, pp. 1840-1842
-
-
Shriner, D.1
Vaughan, L.K.2
Padilla, M.A.3
Tiwari, H.K.4
-
41
-
-
84886379473
-
-
Simons Foundation Autism Research Initiative, New York. Available at, (accessed June 4, 2012)
-
Simons Foundation Autism Research Initiative. (2012). SFARI Gene: A Modular Database for Autism Research [Online]. New York. Available at: https://gene.sfari.org/autdb/Welcome.do (accessed June 4, 2012).
-
(2012)
SFARI Gene: A Modular Database For Autism Research [Online]
-
-
-
42
-
-
28644434111
-
Measuring autistic traits: Heritability, reliability and validity of the Social and Communication Disorders Checklist
-
doi:10.1192/bjp.187.6.568
-
Skuse, D. H., Mandy, W. P. L., and Scourfield, J. (2005). Measuring autistic traits: heritability, reliability and validity of the Social and Communication Disorders Checklist. Br. J. Psychiatry 187, 568-572. doi:10.1192/bjp.187.6.568
-
(2005)
Br. J. Psychiatry
, vol.187
, pp. 568-572
-
-
Skuse, D.H.1
Mandy, W.P.L.2
Scourfield, J.3
-
43
-
-
84874314770
-
-
SNAP, Cambridge. Available at, (accessed 2012)
-
SNAP. (2008). SNP Annotation and Proxy Search [Online]. Cambridge. Available at: http://www.broadinstitute.org/mpg/snap/ldsearch.php (accessed 2012).
-
(2008)
SNP Annotation and Proxy Search [Online]
-
-
-
44
-
-
78349233542
-
Association between a highrisk autism locus on 5p14 and social communication spectrum phenotypes in the general population
-
doi:10.1176/appi.ajp.2010.09121789
-
St Pourcain, B., Wang, K., Glessner, J., Golding, J., Steer, C., Ring, S., et al. (2010). Association between a highrisk autism locus on 5p14 and social communication spectrum phenotypes in the general population. Am. J. Psychiatry 167, 1364-1372. doi:10.1176/appi.ajp.2010.09121789
-
(2010)
Am. J. Psychiatry
, vol.167
, pp. 1364-1372
-
-
St Pourcain, B.1
Wang, K.2
Glessner, J.3
Golding, J.4
Steer, C.5
Ring, S.6
-
45
-
-
62249203986
-
The structure of the Autism-Spectrum Quotient (AQ): Evidence from a student sample in Scotland
-
doi: 10.1016/j.paid.2009.03.004
-
Stewart, M. E., and Austin, E. J. (2009). The structure of the Autism-Spectrum Quotient (AQ): evidence from a student sample in Scotland. Pers. Individ. Dif. 47, 224-228. doi: 10.1016/j.paid.2009.03.004
-
(2009)
Pers. Individ. Dif
, vol.47
, pp. 224-228
-
-
Stewart, M.E.1
Austin, E.J.2
-
46
-
-
77952503974
-
Tourette syndrome is associated with recurrent exonic copy number variants
-
doi: 10.1212/WNL.0b013e3181e0f147
-
Sundaram, S. K., Huq, A. M., Wilson, J., and Chugani, H. T. (2010). Tourette syndrome is associated with recurrent exonic copy number variants. Neurology 74, 1583-1590. doi: 10.1212/WNL.0b013e3181e0f147
-
(2010)
Neurology
, vol.74
, pp. 1583-1590
-
-
Sundaram, S.K.1
Huq, A.M.2
Wilson, J.3
Chugani, H.T.4
-
47
-
-
84886426476
-
-
UCSC Genome, Santa Cruz. Available at, [accessed 2012]
-
UCSC Genome. (2012). Bioinformatics, [Online]. Santa Cruz. Available at: http://genome.ucsc.edu/ [accessed 2012].
-
(2012)
Bioinformatics, [Online]
-
-
-
48
-
-
77953725365
-
Trans-synaptic interaction of GluRdelta2 and Neurexin through Cbln1 mediates synapse formation in the cerebellum
-
doi:10.1016/j.cell.2010.04.035
-
Uemura, T., Lee, S. J., Yasumura, M., Takeuchi, T., Yoshida, T., Ra, M., et al. (2010). Trans-synaptic interaction of GluRdelta2 and Neurexin through Cbln1 mediates synapse formation in the cerebellum. Cell 141, 1068-1079. doi:10.1016/j.cell.2010.04.035
-
(2010)
Cell
, vol.141
, pp. 1068-1079
-
-
Uemura, T.1
Lee, S.J.2
Yasumura, M.3
Takeuchi, T.4
Yoshida, T.5
Ra, M.6
-
49
-
-
5544306699
-
Autism as a paradigmatic complex genetic disorder
-
doi:10.1146/annurev.genom.5.061903.180050
-
Veenstra-VanderWeele, J., Christian, S. L., and Cook, E. H. (2004). Autism as a paradigmatic complex genetic disorder. Annu. Rev. Genomics Hum. Genet. 5, 379-405. doi:10.1146/annurev.genom.5.061903.180050
-
(2004)
Annu. Rev. Genomics Hum. Genet
, vol.5
, pp. 379-405
-
-
Veenstra-Vanderweele, J.1
Christian, S.L.2
Cook, E.H.3
-
50
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
doi:10.1038/nature07999
-
Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., et al. (2009). Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 459, 528-533. doi:10.1038/nature07999
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
Bucan, M.4
Glessner, J.T.5
Abrahams, B.S.6
-
51
-
-
79961136622
-
Are autistic traits in the general population stable across development?
-
doi:10.1371/journal.pone.0023029
-
Whitehouse, A. J. O., Hickey, M., and Ronald, A. (2011). Are autistic traits in the general population stable across development? PLoS ONE 6:e23029. doi:10.1371/journal.pone.0023029
-
(2011)
PLoS ONE
, vol.6
-
-
Whitehouse, A.J.O.1
Hickey, M.2
Ronald, A.3
-
52
-
-
34347408099
-
Problems with genome-wide association studies
-
doi:10.1126/science.316.5833.1840c
-
Williams, S. M., Canter, J. A., Crawford, C., Moore, J. H., Ritchie, M. D., and Haines, J. L. (2007). Problems with genome-wide association studies. Science 316, 1840-1842. doi:10.1126/science.316.5833.1840c
-
(2007)
Science
, vol.316
, pp. 1840-1842
-
-
Williams, S.M.1
Canter, J.A.2
Crawford, C.3
Moore, J.H.4
Ritchie, M.D.5
Haines, J.L.6
-
53
-
-
33845683734
-
Protein kinase Cbeta 1 gene variants are not associated with autism in the Irish population
-
doi: 10.1097/YPG.0b013e3280115428
-
Yang, M. S., Cochrane, L., Conroy, J., Hawi, Z., Fitzgerald, M., Gallagher, L., et al. (2007). Protein kinase Cbeta 1 gene variants are not associated with autism in the Irish population. Psychiatr. Genet. 17,39-41. doi: 10.1097/YPG.0b013e3280115428
-
(2007)
Psychiatr. Genet
, vol.17
, pp. 39-41
-
-
Yang, M.S.1
Cochrane, L.2
Conroy, J.3
Hawi, Z.4
Fitzgerald, M.5
Gallagher, L.6
-
54
-
-
33746494621
-
Autism, the superior temporal sulcus and social perception
-
doi:10.1016/j.tins.2006.06.004
-
Zilbovicius, M., Meresse, I., Chabane, N., Brunelle, F., Samson, Y., and Boddaert, N. (2006). Autism, the superior temporal sulcus and social perception. Trends Neurosci. 29, 359-366. doi:10.1016/j.tins.2006.06.004
-
(2006)
Trends Neurosci
, vol.29
, pp. 359-366
-
-
Zilbovicius, M.1
Meresse, I.2
Chabane, N.3
Brunelle, F.4
Samson, Y.5
Boddaert, N.6
|