-
1
-
-
84863988574
-
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders
-
22726847 1:CAS:528:DC%2BC38XptVKqsrk%3D
-
Luo R et al (2012) Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. Am J Hum Genet 91(1):38-55
-
(2012)
Am J Hum Genet
, vol.91
, Issue.1
, pp. 38-55
-
-
Luo, R.1
-
2
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
21658581 10.1016/j.neuron.2011.05.002 1:CAS:528:DC%2BC3MXnsVyrt7Y%3D
-
Sanders SJ et al (2011) Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 70:863-885
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
-
3
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
20663923 10.1093/hmg/ddq307 1:CAS:528:DC%2BC3cXht1eqtL3F
-
Anney R et al (2010) A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet 19(20):4072-82
-
(2010)
Hum Mol Genet
, vol.19
, Issue.20
, pp. 4072-4082
-
-
Anney, R.1
-
4
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
18179893 10.1016/j.ajhg.2007.09.005 1:CAS:528:DC%2BD1cXhsFOksL8%3D
-
Alarcon M et al (2008) Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet 82(1):150-9
-
(2008)
Am J Hum Genet
, vol.82
, Issue.1
, pp. 150-159
-
-
Alarcon, M.1
-
5
-
-
80051944739
-
Genetic heritability and shared environmental factors among twin pairs with autism
-
21727249 10.1001/archgenpsychiatry.2011.76
-
Hallmayer J et al (2011) Genetic heritability and shared environmental factors among twin pairs with autism. Arch Gen Psychiatry 68:1095-1102
-
(2011)
Arch Gen Psychiatry
, vol.68
, pp. 1095-1102
-
-
Hallmayer, J.1
-
6
-
-
0024336203
-
The UCLA-University of Utah epidemiologic survey of autism: Recurrence risk estimates and genetic counseling
-
2750975 1:STN:280:DyaL1MzitVyhug%3D%3D
-
Ritvo ER et al (1989) The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling. Am J Psychiatry 146(8):1032-6
-
(1989)
Am J Psychiatry
, vol.146
, Issue.8
, pp. 1032-1036
-
-
Ritvo, E.R.1
-
7
-
-
0035958295
-
Pervasive developmental disorders in preschool children
-
11427137 10.1001/jama.285.24.3093 1:STN:280:DC%2BD3Mzotl2qtQ%3D%3D
-
Chakrabarti S, Fombonne E (2001) Pervasive developmental disorders in preschool children. JAMA 285(24):3093-9
-
(2001)
JAMA
, vol.285
, Issue.24
, pp. 3093-3099
-
-
Chakrabarti, S.1
Fombonne, E.2
-
8
-
-
80052366179
-
Recurrence risk for autism spectrum disorders: A Baby Siblings Research Consortium study
-
21844053
-
Ozonoff S et al (2011) Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study. Pediatrics 128(3):e488-95
-
(2011)
Pediatrics
, vol.128
, Issue.3
, pp. 488-495
-
-
Ozonoff, S.1
-
9
-
-
0033913088
-
The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: A family history study
-
10946750 10.1111/1469-7610.00644 1:STN:280:DC%2BD3M%2Fks1WgtQ%3D%3D
-
Szatmari P et al (2000) The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study. J Child Psychol Psychiatry 41(5):579-86
-
(2000)
J Child Psychol Psychiatry
, vol.41
, Issue.5
, pp. 579-586
-
-
Szatmari, P.1
-
10
-
-
33645004634
-
Autistic social impairment in the siblings of children with pervasive developmental disorders
-
16449484 10.1176/appi.ajp.163.2.294
-
Constantino JN et al (2006) Autistic social impairment in the siblings of children with pervasive developmental disorders. Am J Psychiatry 163(2):294-6
-
(2006)
Am J Psychiatry
, vol.163
, Issue.2
, pp. 294-296
-
-
Constantino, J.N.1
-
11
-
-
45149111189
-
Defining key features of the broad autism phenotype: A comparison across parents of multiple- and single-incidence autism families
-
17948871 10.1002/ajmg.b.30612
-
Losh M et al (2008) Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families. Am J Med Genet B Neuropsychiatr Genet 147B(4):424-33
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, Issue.4
, pp. 424-433
-
-
Losh, M.1
-
12
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
17363630 10.1126/science.1138659 1:CAS:528:DC%2BD2sXktlSkuro%3D
-
Sebat J et al (2007) Strong association of de novo copy number mutations with autism. Science 316:445-449
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
-
13
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
22495311 10.1038/nature11011 1:CAS:528:DC%2BC38XmtVerurs%3D
-
Neale BM et al (2012) Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 485:242-245
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
-
14
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
20531469 10.1038/nature09146 1:CAS:528:DC%2BC3cXntF2msbk%3D
-
Pinto D et al (2010) Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466:368-372
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
-
15
-
-
84864335157
-
Autism genetics: Searching for specificity and convergence
-
22849751 10.1186/gb-2012-13-7-247
-
Berg JM, Geschwind DH (2012) Autism genetics: searching for specificity and convergence. Genome Biol 13(7):247
-
(2012)
Genome Biol
, vol.13
, Issue.7
, pp. 247
-
-
Berg, J.M.1
Geschwind, D.H.2
-
16
-
-
84870821992
-
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders
-
23227143 10.1371/journal.pone.0049475 1:CAS:528:DC%2BC38XhvVyhurnM
-
Kong SW et al (2012) Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders. PLoS One 7(12):e49475
-
(2012)
PLoS One
, vol.7
, Issue.12
, pp. 49475
-
-
Kong, S.W.1
-
17
-
-
84865277288
-
Blood-based gene expression signatures of infants and toddlers with autism
-
22917206 10.1016/j.jaac.2012.07.007 e2
-
Glatt SJ et al (2012) Blood-based gene expression signatures of infants and toddlers with autism. J Am Acad Child Adolesc Psychiatry 51(9):934-44 e2
-
(2012)
J Am Acad Child Adolesc Psychiatry
, vol.51
, Issue.9
, pp. 934-944
-
-
Glatt, S.J.1
-
18
-
-
56949100252
-
Altered gene expression and function of peripheral blood natural killer cells in children with autism
-
18762240 10.1016/j.bbi.2008.08.001 1:CAS:528:DC%2BD1cXhsVCntbvM
-
Enstrom AM et al (2009) Altered gene expression and function of peripheral blood natural killer cells in children with autism. Brain Behav Immun 23(1):124-33
-
(2009)
Brain Behav Immun
, vol.23
, Issue.1
, pp. 124-133
-
-
Enstrom, A.M.1
-
19
-
-
66349137661
-
Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: Evidence for circadian rhythm dysfunction in severe autism
-
19418574 10.1002/aur.73
-
Hu VW et al (2009) Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism. Autism Res 2(2):78-97
-
(2009)
Autism Res
, vol.2
, Issue.2
, pp. 78-97
-
-
Hu, V.W.1
-
20
-
-
66349087284
-
Gene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: Altered pathways in neuronal development and steroid biosynthesis
-
19492049 10.1371/journal.pone.0005775
-
Hu VW et al (2009) Gene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: altered pathways in neuronal development and steroid biosynthesis. PLoS One 4(6):e5775
-
(2009)
PLoS One
, vol.4
, Issue.6
, pp. 5775
-
-
Hu, V.W.1
-
21
-
-
37349002507
-
Gene expression changes in children with autism
-
18006270 10.1016/j.ygeno.2007.09.003 1:CAS:528:DC%2BD2sXhsVGltbbF
-
Gregg JP et al (2008) Gene expression changes in children with autism. Genomics 91(1):22-9
-
(2008)
Genomics
, vol.91
, Issue.1
, pp. 22-29
-
-
Gregg, J.P.1
-
22
-
-
34547731978
-
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways
-
17519220 10.1093/hmg/ddm116 1:CAS:528:DC%2BD2sXosFektLc%3D
-
Nishimura Y et al (2007) Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. Hum Mol Genet 16(14):1682-98
-
(2007)
Hum Mol Genet
, vol.16
, Issue.14
, pp. 1682-1698
-
-
Nishimura, Y.1
-
23
-
-
33845906332
-
Utilization of lymphoblastoid cell lines as a system for the molecular modeling of autism
-
16845580 10.1007/s10803-006-0134-x
-
Baron CA et al (2006) Utilization of lymphoblastoid cell lines as a system for the molecular modeling of autism. J Autism Dev Disord 36(8):973-82
-
(2006)
J Autism Dev Disord
, vol.36
, Issue.8
, pp. 973-982
-
-
Baron, C.A.1
-
24
-
-
0042424602
-
Statistical significance for genomewide studies
-
12883005 10.1073/pnas.1530509100 1:CAS:528:DC%2BD3sXmtlyktbY%3D
-
Storey JD, Tibshirani R (2003) Statistical significance for genomewide studies. Proc Natl Acad Sci U S A 100(16):9440-5
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, Issue.16
, pp. 9440-9445
-
-
Storey, J.D.1
Tibshirani, R.2
-
25
-
-
27844521293
-
A shrinkage approach to large-scale covariance matrix estimation and implications for functional genomics
-
Schäfer J, Strimmer K (2005) A shrinkage approach to large-scale covariance matrix estimation and implications for functional genomics. Statist Appl Genet Mol Biol 4:(32)
-
(2005)
Statist Appl Genet Mol Biol
, vol.4
, Issue.32
-
-
Schäfer, J.S.1
-
26
-
-
33646361583
-
GenePattern 2.0
-
16642009 10.1038/ng0506-500 1:CAS:528:DC%2BD28XjvVGksLo%3D
-
Reich M et al (2006) GenePattern 2.0. Nat Genet 38(5):500-1
-
(2006)
Nat Genet
, vol.38
, Issue.5
, pp. 500-501
-
-
Reich, M.1
-
27
-
-
78349291914
-
Sibling recurrence and the genetic epidemiology of autism
-
20889652 10.1176/appi.ajp.2010.09101470
-
Constantino JN et al (2010) Sibling recurrence and the genetic epidemiology of autism. Am J Psychiatry 167(11):1349-56
-
(2010)
Am J Psychiatry
, vol.167
, Issue.11
, pp. 1349-1356
-
-
Constantino, J.N.1
-
28
-
-
84858983547
-
KEGG for integration and interpretation of large-scale molecular data sets
-
22080510 10.1093/nar/gkr988 1:CAS:528:DC%2BC3MXhs12htbrO
-
Kanehisa M et al (2012) KEGG for integration and interpretation of large-scale molecular data sets. Nucleic Acids Res 40(Database issue):D109-14
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.DATABASE ISSUE
, pp. 109-114
-
-
Kanehisa, M.1
-
29
-
-
79958032110
-
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
-
21658582 10.1016/j.neuron.2011.05.015 1:CAS:528:DC%2BC3MXnsVyrt7c%3D
-
Levy D et al (2011) Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron 70(5):886-97
-
(2011)
Neuron
, vol.70
, Issue.5
, pp. 886-897
-
-
Levy, D.1
-
30
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
17322880 10.1038/ng1985 1:CAS:528:DC%2BD2sXitVOkt78%3D
-
Szatmari P et al (2007) Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet 39:319-328
-
(2007)
Nat Genet
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
-
31
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
18252227 10.1016/j.ajhg.2007.12.009 1:CAS:528:DC%2BD1cXit1Sisrs%3D
-
Marshall CR et al (2008) Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet 82:477-488
-
(2008)
Am J Hum Genet
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
-
32
-
-
11144230769
-
Neuroglial activation and neuroinflammation in the brain of patients with autism
-
15546155 10.1002/ana.20315 1:CAS:528:DC%2BD2MXpsFSktA%3D%3D
-
Vargas DL et al (2005) Neuroglial activation and neuroinflammation in the brain of patients with autism. Ann Neurol 57(1):67-81
-
(2005)
Ann Neurol
, vol.57
, Issue.1
, pp. 67-81
-
-
Vargas, D.L.1
-
33
-
-
33847292420
-
A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins
-
17189958 1:CAS:528:DC%2BD2sXitFCiur4%3D
-
Corbett BA et al (2007) A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins. Mol Psychiatry 12(3):292-306
-
(2007)
Mol Psychiatry
, vol.12
, Issue.3
, pp. 292-306
-
-
Corbett, B.A.1
-
34
-
-
43849112803
-
Immune transcriptome alterations in the temporal cortex of subjects with autism
-
18378158 10.1016/j.nbd.2008.01.012 1:CAS:528:DC%2BD1cXmtlSiu74%3D
-
Garbett K et al (2008) Immune transcriptome alterations in the temporal cortex of subjects with autism. Neurobiol Dis 30(3):303-11
-
(2008)
Neurobiol Dis
, vol.30
, Issue.3
, pp. 303-311
-
-
Garbett, K.1
-
35
-
-
84876296688
-
Identification of risk loci with shared effects on five major psychiatric disorders: A genome-wide analysis
-
Cross-Disorder Group of the Psychiatric Genomics, C
-
Cross-Disorder Group of the Psychiatric Genomics, C. (2013) Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Lancet
-
(2013)
Lancet
-
-
-
36
-
-
78649758904
-
Mitochondrial dysfunction in autism
-
21119085 10.1001/jama.2010.1706 1:CAS:528:DC%2BC3cXhsFaisrjK
-
Giulivi C et al (2010) Mitochondrial dysfunction in autism. JAMA 304(21):2389-96
-
(2010)
JAMA
, vol.304
, Issue.21
, pp. 2389-2396
-
-
Giulivi, C.1
-
37
-
-
84876293747
-
Downregulation of the expression of mitochondrial electron transport complex genes in autism brains
-
Anitha A et al (2012) Downregulation of the expression of mitochondrial electron transport complex genes in autism brains. Brain Pathol. 23(3):294-302
-
(2012)
Brain Pathol
, vol.23
, Issue.3
, pp. 294-302
-
-
Anitha, A.1
-
38
-
-
0033136483
-
Evidence of altered energy metabolism in autistic children
-
10390722 10.1016/S0278-5846(99)00022-6 1:CAS:528:DyaK1MXlvFynsLw%3D
-
Chugani DC et al (1999) Evidence of altered energy metabolism in autistic children. Prog Neuropsychopharmacol Biol Psychiatry 23(4):635-41
-
(1999)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.23
, Issue.4
, pp. 635-641
-
-
Chugani, D.C.1
-
39
-
-
0027337120
-
A preliminary 31P MRS study of autism: Evidence for undersynthesis and increased degradation of brain membranes
-
8373914 10.1016/0006-3223(93)90017-8 1:STN:280:DyaK3szosFaruw%3D%3D
-
Minshew NJ et al (1993) A preliminary 31P MRS study of autism: evidence for undersynthesis and increased degradation of brain membranes. Biol Psychiatry 33(11-12):762-73
-
(1993)
Biol Psychiatry
, vol.33
, Issue.11-12
, pp. 762-773
-
-
Minshew, N.J.1
|