-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
DOI 10.1038/nrg2346, PII NRG2346
-
Abrahams, B. S., & Geschwind, D. H. (2008). Advances in autism genetics: On the threshold of a new neurobiology. Nature Reviews Genetics, 9, 341-355. doi:10.1038/nrg2346. (Pubitemid 351556064)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
84855431813
-
-
American Psychiatric Association - DSM-5 Development American Psychiatric Association Accessed February 01 2011
-
American Psychiatric Association - DSM-5 Development (2011). 299.00 Autistic Disorder. In: American Psychiatric Association. http://www.dsm5.org/ ProposedRevisions/Pages/proposedrevision.aspx?rid=94 Accessed February 01 2011.
-
(2011)
299.00 Autistic Disorder
-
-
-
3
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey, A., et al. (1995). Autism as a strongly genetic disorder: Evidence from a British twin study. Psychological Medicine, 25, 63-77.
-
(1995)
Psychological Medicine
, vol.25
, pp. 63-77
-
-
Bailey, A.1
-
4
-
-
84889237300
-
How meaningful are heritability estimates of liability?
-
doi:10.1007/s00439-013-1334-z
-
Benchek, P. H., & Morris, N. J. (2013). How meaningful are heritability estimates of liability? Human Genetics, 132, 1351-1360. doi:10.1007/s00439-013-1334-z.
-
(2013)
Human Genetics
, vol.132
, pp. 1351-1360
-
-
Benchek, P.H.1
Morris, N.J.2
-
5
-
-
66049113617
-
Prenatal, perinatal, and neonatal factors associated with autism spectrum disorders
-
doi:10.1542/peds.2008-0927
-
Bilder, D., Pinborough-Zimmerman, J., Miller, J., & McMahon, W. (2009). Prenatal, perinatal, and neonatal factors associated with autism spectrum disorders. Pediatrics, 123, 1293-1300. doi:10.1542/peds.2008-0927.
-
(2009)
Pediatrics
, vol.123
, pp. 1293-1300
-
-
Bilder, D.1
Pinborough-Zimmerman, J.2
Miller, J.3
McMahon, W.4
-
6
-
-
0032961701
-
The epidemiology of multiple births
-
DOI 10.1093/humupd/5.2.179
-
Bortolus, R., Parazzini, F., Chatenoud, L., Benzi, G., Bianchi, M. M., & Marini, A. (1999). The epidemiology of multiple births. Hum Reprod Update, 5, 179-187. (Pubitemid 29201887)
-
(1999)
Human Reproduction Update
, vol.5
, Issue.2
, pp. 179-187
-
-
Bortolus, R.1
Parazzini, F.2
Chatenoud, L.3
Benzi, G.4
Bianchi, M.M.5
Marini, A.6
-
7
-
-
40849109768
-
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles
-
doi:10.1016/j.ajhg.2007.12.011
-
Bruder, C. E., et al. (2008). Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. American Journal of Human Genetics, 82, 763-771. doi:10.1016/j.ajhg.2007.12.011.
-
(2008)
American Journal of Human Genetics
, vol.82
, pp. 763-771
-
-
Bruder, C.E.1
-
8
-
-
84859394070
-
Prevalence of autism spectrum disorders - Autism and developmental disabilities monitoring network, 14 Sites, United States, 2008
-
Centers for Disease Control and Prevention
-
Centers for Disease Control and Prevention. (2012). Prevalence of autism spectrum disorders - autism and developmental disabilities monitoring network, 14 Sites, United States, 2008. MMWR, 61, 1-19.
-
(2012)
MMWR
, vol.61
, pp. 1-19
-
-
-
9
-
-
34648846248
-
Validation of the Social Communication Questionnaire in a population cohort of children with autism spectrum disorders
-
DOI 10.1097/chi.0b013e31812f7d8d, PII 0000458320071000000011
-
Chandler, S., et al. (2007). Validation of the social communication questionnaire in a population cohort of children with autism spectrum disorders. Journal of the American Academy of Child and Adolescent Psychiatry, 46, 1324-1332. doi:10.1097/chi.0b013e31812f7d8d. (Pubitemid 47462191)
-
(2007)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.46
, Issue.10
, pp. 1324-1332
-
-
Chandler, S.1
Charman, T.2
Baird, G.3
Simonoff, E.4
Loucas, T.5
Meldrum, D.6
Scott, M.7
Pickles, A.8
-
10
-
-
70449588984
-
A prospective study of toddlers with ASD: Short-term diagnostic and cognitive outcomes
-
doi:10.1111/j.1469-7610.2009.02101.x
-
Chawarska, K., Klin, A., Paul, R., Macari, S., & Volkmar, F. (2009). A prospective study of toddlers with ASD: Short-term diagnostic and cognitive outcomes. Journal of Child Psychology and Psychiatry, 50, 1235-1245. doi:10.1111/j.1469-7610.2009.02101.x.
-
(2009)
Journal of Child Psychology and Psychiatry
, vol.50
, pp. 1235-1245
-
-
Chawarska, K.1
Klin, A.2
Paul, R.3
Macari, S.4
Volkmar, F.5
-
11
-
-
0026622871
-
Multiple regression analysis of twin data: A model-fitting approach
-
Cherney, S. S., DeFries, J. C., & Fulker, D. W. (1992). Multiple regression analysis of twin data: A model-fitting approach. Behavior Genetics, 22, 489-497.
-
(1992)
Behavior Genetics
, vol.22
, pp. 489-497
-
-
Cherney, S.S.1
DeFries, J.C.2
Fulker, D.W.3
-
12
-
-
60449084081
-
How continua converge in nature: Cognition, social competence, and autistic syndromes
-
doi:10.1097/CHI.0b013e318193069e
-
Constantino, J. N. (2009). How continua converge in nature: Cognition, social competence, and autistic syndromes. Journal of the American Academy of Child and Adolescent Psychiatry, 48, 97-98. doi:10.1097/CHI.0b013e318193069e.
-
(2009)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.48
, pp. 97-98
-
-
Constantino, J.N.1
-
15
-
-
0037629077
-
Autistic traits in the general population: A twin study
-
DOI 10.1001/archpsyc.60.5.524
-
Constantino, J. N., & Todd, R. D. (2003). Autistic traits in the general population: A twin study. Archives of General Psychiatry, 60, 524-530. (Pubitemid 36539062)
-
(2003)
Archives of General Psychiatry
, vol.60
, Issue.5
, pp. 524-530
-
-
Constantino, J.N.1
Todd, R.D.2
-
16
-
-
15744390996
-
Intergenerational transmission of subthreshold autistic traits in the general population
-
DOI 10.1016/j.biopsych.2004.12.014
-
Constantino, J. N., & Todd, R. D. (2005). Intergenerational transmission of subthreshold autistic traits in the general population. Biological Psychiatry, 57, 655-660. (Pubitemid 40409704)
-
(2005)
Biological Psychiatry
, vol.57
, Issue.6
, pp. 655-660
-
-
Constantino, J.N.1
Todd, R.D.2
-
17
-
-
13244275092
-
Maternal autoimmune diseases, asthma and allergies, and childhood autism spectrum disorders: A case-control study
-
DOI 10.1001/archpedi.159.2.151
-
Croen, L. A., Grether, J. K., Yoshida, C. K., Odouli, R., & Van de Water, J. (2005). Maternal autoimmune diseases, asthma and allergies, and childhood autism spectrum disorders: A case-control study. Archives of Pediatrics and Adolescent Medicine, 159, 151-157. doi:10.1001/archpedi.159.2. 151. (Pubitemid 40194181)
-
(2005)
Archives of Pediatrics and Adolescent Medicine
, vol.159
, Issue.2
, pp. 151-157
-
-
Croen, L.A.1
Grether, J.K.2
Yoshida, C.K.3
Odouli, R.4
De Water, J.V.5
-
18
-
-
0018417902
-
The 'singles' method for segregation analysis under incomplete ascertainment
-
Davie, A. M. (1979). The 'singles' method for segregation analysis under incomplete ascertainment. Annals of Human Genetics, 42, 507-512.
-
(1979)
Annals of Human Genetics
, vol.42
, pp. 507-512
-
-
Davie, A.M.1
-
19
-
-
0022396848
-
Multiple regression analysis of twin data
-
DOI 10.1007/BF01066239
-
DeFries, J. C., & Fulker, D. W. (1985). Multiple regression analysis of twin data. Behavior Genetics, 15, 467-473. (Pubitemid 16168923)
-
(1985)
Behavior Genetics
, vol.15
, Issue.5
, pp. 467-473
-
-
DeFries, J.C.1
Fulker, D.W.2
-
20
-
-
0024247881
-
Multiple regression analysis of twin data: Etiology of deviant scores versus individual differences
-
DeFries, J. C., & Fulker, D. W. (1988). Multiple regression analysis of twin data: Etiology of deviant scores versus individual differences. Acta Geneticae Medicae et Gemellologiae: Twin Research, 37, 205-216. (Pubitemid 20091864)
-
(1988)
Acta Geneticae Medicae et Gemellologiae
, vol.37
, Issue.3-4
, pp. 205-216
-
-
DeFries, J.C.1
Fulker, D.W.2
-
22
-
-
77955233281
-
Autism spectrum disorders as a qualitatively distinct category from typical behavior in a large, clinically ascertained sample
-
doi:10.1177/1073191109356534
-
Frazier, T. W., et al. (2010). Autism spectrum disorders as a qualitatively distinct category from typical behavior in a large, clinically ascertained sample. Assessment, 17, 308-320. doi:10.1177/1073191109356534.
-
(2010)
Assessment
, vol.17
, pp. 308-320
-
-
Frazier, T.W.1
-
23
-
-
83755198671
-
Validation of proposed DSM-5 criteria for autism spectrum disorder
-
doi:10.1016/j.jaac.2011.09.021
-
Frazier, T. W., et al. (2012). Validation of proposed DSM-5 criteria for autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 51 (28-40), e3. doi:10.1016/j.jaac.2011.09.021.
-
(2012)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.51
, Issue.28-40
-
-
Frazier, T.W.1
-
24
-
-
80051539002
-
Perinatal and neonatal risk factors for autism: A comprehensive meta-analysis
-
doi:10.1542/peds.2010-1036
-
Gardener, H., Spiegelman, D., & Buka, S. L. (2011). Perinatal and neonatal risk factors for autism: A comprehensive meta-analysis. Pediatrics, 128, 344-355. doi:10.1542/peds.2010-1036.
-
(2011)
Pediatrics
, vol.128
, pp. 344-355
-
-
Gardener, H.1
Spiegelman, D.2
Buka, S.L.3
-
25
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
doi:10.1038/nature07953
-
Glessner, J. T., et al. (2009). Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature, 459, 569-573. doi:10.1038/ nature07953.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
-
26
-
-
71149104488
-
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
-
doi:10.1186/1741-7015-7-62
-
Gregory, S. G., et al. (2009). Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Medicine, 7, 62. doi:10.1186/1741-7015-7-62.
-
(2009)
BMC Medicine
, vol.7
, pp. 62
-
-
Gregory, S.G.1
-
27
-
-
72049102124
-
Risk of autism and increasing maternal and paternal age in a large north American population
-
doi:10.1093/aje/kwp247
-
Grether, J. K., Anderson, M. C., Croen, L. A., Smith, D., & Windham, G. C. (2009). Risk of autism and increasing maternal and paternal age in a large north American population. American Journal of Epidemiology, 170, 1118-1126. doi:10.1093/aje/kwp247.
-
(2009)
American Journal of Epidemiology
, vol.170
, pp. 1118-1126
-
-
Grether, J.K.1
Anderson, M.C.2
Croen, L.A.3
Smith, D.4
Windham, G.C.5
-
28
-
-
80051944739
-
Genetic heritability and shared environmental factors among twin pairs with autism
-
doi:10.1001/archgenpsychiatry.2011.76
-
Hallmayer, J., et al. (2011). Genetic heritability and shared environmental factors among twin pairs with autism. Archives of General Psychiatry, 68, 1095-1102. doi:10.1001/archgenpsychiatry.2011.76.
-
(2011)
Archives of General Psychiatry
, vol.68
, pp. 1095-1102
-
-
Hallmayer, J.1
-
29
-
-
34147174531
-
Heritability of autistic traits in the general population
-
DOI 10.1001/archpedi.161.4.372
-
Hoekstra, R. A., Bartels, M., Verweij, C. J., & Boomsma, D. I. (2007). Heritability of autistic traits in the general population. Archives of Pediatrics and Adolescent Medicine, 161, 372-377. doi:10.1001/archpedi.161.4. 372. (Pubitemid 46556368)
-
(2007)
Archives of Pediatrics and Adolescent Medicine
, vol.161
, Issue.4
, pp. 372-377
-
-
Hoekstra, R.A.1
Bartels, M.2
Verweij, C.J.H.3
Boomsma, D.I.4
-
30
-
-
0041694381
-
Reduced levels of mercury in first baby haircuts of autistic children
-
DOI 10.1080/10915810305120
-
Holmes, A. S., Blaxill, M. F., & Haley, B. E. (2003). Reduced levels of mercury in first baby haircuts of autistic children. International Journal of Toxicology, 22, 277-285. (Pubitemid 37075365)
-
(2003)
International Journal of Toxicology
, vol.22
, Issue.4
, pp. 277-285
-
-
Holmes, A.S.1
Blaxill, M.F.2
Haley, B.E.3
-
31
-
-
33746858084
-
Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes
-
doi:10.1186/1471-2164-7-118
-
Hu, V. W., Frank, B. C., Heine, S., Lee, N. H., & Quackenbush, J. (2006). Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes. BMC Genomics, 7, 118. doi:10.1186/1471-2164-7- 118.
-
(2006)
BMC Genomics
, vol.7
, pp. 118
-
-
Hu, V.W.1
Frank, B.C.2
Heine, S.3
Lee, N.H.4
Quackenbush, J.5
-
32
-
-
42649116478
-
Defining autism subgroups: A taxometric solution
-
doi:10.1007/s10803-007-0469-y
-
Ingram, D. G., Takahashi, T. N., & Miles, J. H. (2008). Defining autism subgroups: A taxometric solution. Journal of Autism and Developmental Disorders, 38, 950-960. doi:10.1007/s10803-007-0469-y.
-
(2008)
Journal of Autism and Developmental Disorders
, vol.38
, pp. 950-960
-
-
Ingram, D.G.1
Takahashi, T.N.2
Miles, J.H.3
-
33
-
-
84860297457
-
De novo gene disruptions in children on the autistic spectrum
-
doi:10.1016/j.neuron.2012.04.009
-
Iossifov, I., et al. (2012). De novo gene disruptions in children on the autistic spectrum. Neuron, 74, 285-299. doi:10.1016/j.neuron.2012.04.009.
-
(2012)
Neuron
, vol.74
, pp. 285-299
-
-
Iossifov, I.1
-
34
-
-
4544251808
-
Mercury exposure in children with autistic spectrum disorder: Case-control study
-
Ip, P., Wong, V., Ho, M., Lee, J., & Wong, W. (2004). Mercury exposure in children with autistic spectrum disorder: Case-control study. Journal of Child Neurology, 19, 431-434. (Pubitemid 39232334)
-
(2004)
Journal of Child Neurology
, vol.19
, Issue.6
, pp. 431-434
-
-
Ip, P.1
Wong, V.2
Ho, M.3
Lee, J.4
Wong, W.5
-
35
-
-
84881664021
-
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing
-
doi:10.1016/j.ajhg.2013.06.012
-
Jiang, Y. H., et al. (2013). Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. American Journal of Human Genetics, 93, 249. doi:10.1016/j.ajhg.2013.06.012.
-
(2013)
American Journal of Human Genetics
, vol.93
, pp. 249
-
-
Jiang, Y.H.1
-
36
-
-
0015711827
-
An analysis of the genetics of schizophrenia
-
Kidd, K. K., & Cavalli-Sforza, L. L. (1973). An analysis of the genetics of schizophrenia. Social Biology, 20, 254-265.
-
(1973)
Social Biology
, vol.20
, pp. 254-265
-
-
Kidd, K.K.1
Cavalli-Sforza, L.L.2
-
37
-
-
0030758262
-
Comorbidity of mathematics and reading deficits: Evidence for a genetic etiology
-
DOI 10.1023/A:1025622400239
-
Knopik, V. S., Alarcon, M., & DeFries, J. C. (1997). Comorbidity of mathematics and reading deficits: Evidence for a genetic etiology. Behavior Genetics, 27, 447-453. (Pubitemid 27426335)
-
(1997)
Behavior Genetics
, vol.27
, Issue.5
, pp. 447-453
-
-
Knopik, V.S.1
Alarcon, M.2
DeFries, J.C.3
-
38
-
-
77956128856
-
Accuracy of phenotyping of autistic children based on internet implemented parent report
-
doi:10.1002/ajmg.b.31103
-
Lee, H., et al. (2010). Accuracy of phenotyping of autistic children based on internet implemented parent report. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B, 1119-1126. doi:10.1002/ajmg.b.31103.
-
(2010)
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
, vol.153 B
, pp. 1119-1126
-
-
Lee, H.1
-
39
-
-
79958032110
-
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
-
doi:10.1016/j.neuron.2011.05.015
-
Levy, D., et al. (2011). Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron, 70, 886-897. doi:10.1016/j.neuron.2011.05.015.
-
(2011)
Neuron
, vol.70
, pp. 886-897
-
-
Levy, D.1
-
40
-
-
78349293844
-
The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood
-
doi:10.1176/appi.ajp.2010.10020223
-
Lichtenstein, P., Carlstrom, E., Rastam, M., Gillberg, C., & Anckarsater, H. (2010). The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood. American Journal of Psychiatry, 167, 1357-1363. doi:10.1176/appi.ajp.2010.10020223.
-
(2010)
American Journal of Psychiatry
, vol.167
, pp. 1357-1363
-
-
Lichtenstein, P.1
Carlstrom, E.2
Rastam, M.3
Gillberg, C.4
Anckarsater, H.5
-
41
-
-
84860683127
-
Heritability across the distribution: An application of quantile regression
-
doi:10.1007/s10519-011-9497-7
-
Logan, J. A., et al. (2012). Heritability across the distribution: An application of quantile regression. Behavior Genetics, 42, 256-267. doi:10.1007/s10519-011-9497-7.
-
(2012)
Behavior Genetics
, vol.42
, pp. 256-267
-
-
Logan, J.A.1
-
42
-
-
33744909414
-
Autism from 2 to 9 years of age
-
DOI 10.1001/archpsyc.63.6.694
-
Lord, C., Risi, S., DiLavore, P. S., Shulman, C., Thurm, A., & Pickles, A. (2006). Autism from 2 to 9 years of age. Archives of General Psychiatry, 63, 694-701. doi:10.1001/archpsyc.63.6.694. (Pubitemid 43848301)
-
(2006)
Archives of General 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
-
43
-
-
65549157376
-
Neuropsychological profile of autism and the broad autism phenotype
-
doi:10.1001/archgenpsychiatry.2009.34
-
Losh, M., et al. (2009). Neuropsychological profile of autism and the broad autism phenotype. Archives of General Psychiatry, 66, 518-526. doi:10.1001/archgenpsychiatry.2009.34.
-
(2009)
Archives of General Psychiatry
, vol.66
, pp. 518-526
-
-
Losh, M.1
-
44
-
-
84855331271
-
Autism spectrum disorders and autistic like traits: Similar etiology in the extreme end and the normal variation
-
doi:10.1001/archgenpsychiatry.2011.144
-
Lundstrom, S., et al. (2012). Autism spectrum disorders and autistic like traits: Similar etiology in the extreme end and the normal variation. Archives of General Psychiatry, 69, 46-52. doi:10.1001/archgenpsychiatry.2011.144.
-
(2012)
Archives of General Psychiatry
, vol.69
, pp. 46-52
-
-
Lundstrom, S.1
-
45
-
-
83755176896
-
Testing the construct validity of proposed criteria for DSM-5 autism spectrum disorder
-
doi:10.1016/j.jaac.2011.10.013
-
Mandy, W. P., Charman, T., & Skuse, D. H. (2012). Testing the construct validity of proposed criteria for DSM-5 autism spectrum disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 51, 41-50. doi:10.1016/j.jaac.2011.10.013.
-
(2012)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.51
, pp. 41-50
-
-
Mandy, W.P.1
Charman, T.2
Skuse, D.H.3
-
46
-
-
84860694964
-
-
Hyattsville, MD: National Center for Health Statistics
-
Martin, J. A., Hamilton, B. E., & Osterman, M. J. K. (2012). Three decades of twin births in the United States, 1980-2009. NCHS data brief., vol 80. Hyattsville, MD: National Center for Health Statistics.
-
(2012)
Three Decades of Twin Births in the United States, 1980-2009. NCHS Data Brief
, vol.80
-
-
Martin, J.A.1
Hamilton, B.E.2
Osterman, M.J.K.3
-
47
-
-
84867846381
-
Parental occupational exposures and autism spectrum disorder
-
doi:10.1007/s10803-012-1468-1
-
McCanlies, E. C., et al. (2012). Parental occupational exposures and autism spectrum disorder. Journal of Autism and Developmental Disorders, 42, 2323. doi:10.1007/s10803-012-1468-1.
-
(2012)
Journal of Autism and Developmental Disorders
, vol.42
, pp. 2323
-
-
McCanlies, E.C.1
-
48
-
-
49949152363
-
Stability of the autism diagnostic interview-revised from pre-school to elementary school age in children with autism spectrum disorders
-
doi:10.1007/s10803-007-0487-9
-
Moss, J., Magiati, I., Charman, T., & Howlin, P. (2008). Stability of the autism diagnostic interview-revised from pre-school to elementary school age in children with autism spectrum disorders. Journal of Autism and Developmental Disorders, 38, 1081-1091. doi:10.1007/s10803-007-0487-9.
-
(2008)
Journal of Autism and Developmental Disorders
, vol.38
, pp. 1081-1091
-
-
Moss, J.1
Magiati, I.2
Charman, T.3
Howlin, P.4
-
49
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
doi:10.1038/nature11011
-
Neale, B. M., et al. (2012). Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature, 485, 242. doi:10.1038/ nature11011.
-
(2012)
Nature
, vol.485
, pp. 242
-
-
Neale, B.M.1
-
50
-
-
0038064292
-
Heritable and nonheritable risk factors for autism spectrum disorders
-
DOI 10.1093/epirev/mxf010
-
Newschaffer, C. J., Fallin, D., & Lee, N. L. (2002). Heritable and nonheritable risk factors for autism spectrum disorders. Epidemiologic Reviews, 24, 137-153. (Pubitemid 36553836)
-
(2002)
Epidemiologic Reviews
, vol.24
, Issue.2
, pp. 137-153
-
-
Newschaffer, C.J.1
Fallin, D.2
Lee, N.L.3
-
51
-
-
34249735268
-
The epidemiology of autism spectrum disorders
-
DOI 10.1146/annurev.publhealth.28.021406.144007
-
Newschaffer, C. J., et al. (2007). The epidemiology of autism spectrum disorders. Annual Review of Public Health, 28, 235-258. doi:10.1146/annurev. publhealth.28.021406.144007. (Pubitemid 46833342)
-
(2007)
Annual Review of Public Health
, vol.28
, pp. 235-258
-
-
Newschaffer, C.J.1
Croen, L.A.2
Daniels, J.3
Giarelli, E.4
Grether, J.K.5
Levy, S.E.6
Mandell, D.S.7
Miller, L.A.8
Pinto-Martin, J.9
Reaven, J.10
Reynolds, A.M.11
Rice, C.E.12
Schendel, D.13
Windham, G.C.14
-
52
-
-
79957589237
-
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
-
doi:10.1038/ng.835
-
O'Roak, B. J., et al. (2011). Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature Genetics, 43, 585-589. doi:10.1038/ng.835.
-
(2011)
Nature Genetics
, vol.43
, pp. 585-589
-
-
O'Roak, B.J.1
-
53
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
doi:10.1038/nature10989
-
O'Roak, B. J., et al. (2012). Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature, 485, 246. doi:10.1038/nature10989.
-
(2012)
Nature
, vol.485
, pp. 246
-
-
O'Roak, B.J.1
-
54
-
-
80052366179
-
Recurrence risk for autism spectrum disorders: A baby siblings research consortium study
-
doi:10.1542/peds.2010-2825
-
Ozonoff, S., et al. (2011). Recurrence risk for autism spectrum disorders: A baby siblings research consortium study. Pediatrics, 128, e488-e495. doi:10.1542/peds.2010-2825.
-
(2011)
Pediatrics
, vol.128
-
-
Ozonoff, S.1
-
55
-
-
0037762731
-
A model-fitting implementation of the DeFries-Fulker model for selected twin data
-
DOI 10.1023/A:1023494408079
-
Purcell, S., & Sham, P. C. (2003). A model-fitting implementation of the DeFries-Fulker model for selected twin data. Behavior Genetics, 33, 271-278. (Pubitemid 36637998)
-
(2003)
Behavior Genetics
, vol.33
, Issue.3
, pp. 271-278
-
-
Purcell, S.1
Sham, P.C.2
-
56
-
-
33748297511
-
Advancing paternal age and autism
-
DOI 10.1001/archpsyc.63.9.1026
-
Reichenberg, A., et al. (2006). Advancing paternal age and autism. Archives of General Psychiatry, 63, 1026-1032. doi:10.1001/archpsyc.63.9.1026. (Pubitemid 44330462)
-
(2006)
Archives of General Psychiatry
, vol.63
, Issue.9
, pp. 1026-1032
-
-
Reichenberg, A.1
Gross, R.2
Weiser, M.3
Bresnahan, M.4
Silverman, J.5
Harlap, S.6
Rabinowitz, J.7
Shulman, C.8
Malaspina, D.9
Lubin, G.10
Knobler, H.Y.11
Davidson, M.12
Susser, E.13
-
57
-
-
73149102059
-
Prevalence of autism spectrum disorders - Autism and developmental disabilities monitoring network, United States, 2006
-
Rice, C. (2009). Prevalence of autism spectrum disorders - autism and developmental disabilities monitoring network, United States, 2006. MMWR Surveill Summ, 58, 1-20.
-
(2009)
MMWR Surveill Summ
, vol.58
, pp. 1-20
-
-
Rice, C.1
-
58
-
-
0033789771
-
Zygosity diagnosis in young twins by parental report
-
Rietveld, M. J., van Der Valk, J. C., Bongers, I. L., Stroet, T. M., Slagboom, P. E., & Boomsma, D. I. (2000). Zygosity diagnosis in young twins by parental report. Twin Research, 3, 134-141.
-
(2000)
Twin Research
, vol.3
, pp. 134-141
-
-
Rietveld, M.J.1
Van Der Valk, J.C.2
Bongers, I.L.3
Stroet, T.M.4
Slagboom, P.E.5
Boomsma, D.I.6
-
59
-
-
0036596190
-
Analytic approaches to twin data using structural equation models
-
Rijsdijk, F. V., & Sham, P. C. (2002). Analytic approaches to twin data using structural equation models. Brief Bioinformatics, 3, 119-133.
-
(2002)
Brief Bioinformatics
, vol.3
, pp. 119-133
-
-
Rijsdijk, F.V.1
Sham, P.C.2
-
60
-
-
0021960916
-
Concordance for the syndrome of autism in 40 pairs of afflicted twins
-
Ritvo, E. R., Freeman, B. J., Mason-Brothers, A., Mo, A., & Ritvo, A. M. (1985). Concordance for the syndrome of autism in 40 pairs of afflicted twins. American Journal of Psychiatry, 142, 74-77. (Pubitemid 15189523)
-
(1985)
American Journal of Psychiatry
, vol.142
, Issue.1
, pp. 74-77
-
-
Ritvo, E.R.1
Freeman, B.J.2
Mason-Brothers, A.3
-
61
-
-
80755185186
-
Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%)
-
doi:10.1001/archgenpsychiatry.2011.119
-
Robinson, E. B., et al. (2011). Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%). Archives of General Psychiatry, 68, 1113-1121. doi:10.1001/archgenpsychiatry.2011.119.
-
(2011)
Archives of General Psychiatry
, vol.68
, pp. 1113-1121
-
-
Robinson, E.B.1
-
62
-
-
84860651207
-
A multivariate twin study of autistic traits in 12-year-olds: Testing the fractionable autism triad hypothesis
-
doi:10.1007/s10519-011-9500-3
-
Robinson, E. B., et al. (2012). A multivariate twin study of autistic traits in 12-year-olds: testing the fractionable autism triad hypothesis. Behavior Genetics, 42, 245-255. doi:10.1007/s10519-011-9500-3.
-
(2012)
Behavior Genetics
, vol.42
, pp. 245-255
-
-
Robinson, E.B.1
-
63
-
-
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., & Plomin, R. (2005). The genetic relationship between individual differences in social and nonsocial behaviours characteristic of autism. Developmental Science, 8, 444-458. doi:10.1111/j.1467-7687.2005. 00433.x. (Pubitemid 41137417)
-
(2005)
Developmental Science
, vol.8
, Issue.5
, pp. 444-458
-
-
Ronald, A.1
Happe, F.2
Plomin, R.3
-
64
-
-
33749076052
-
Phenotypic and genetic overlap between autistic traits at the extremes of the general population
-
DOI 10.1097/01.chi.0000230165.54117.41, PII 0000458320061000000008
-
Ronald, A., Happe, F., Price, T. S., Baron-Cohen, S., Plomin, R., et al. (2006a). Phenotypic and genetic overlap between autistic traits at the extremes of the general population. Journal of the American Academy of Child and Adolescent Psychiatry, 45, 1206-1214. doi:10.1097/01.chi.0000230165.54117.41. (Pubitemid 44465641)
-
(2006)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.45
, Issue.10
, pp. 1206-1214
-
-
Ronald, A.1
Happe, F.2
Price, T.S.3
Baron-Cohen, S.4
Plomin, R.5
-
66
-
-
41849124886
-
Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample
-
DOI 10.1111/j.1469-7610.2007.01857.x
-
Ronald, A., Simonoff, E., Kuntsi, J., Asherton, P., & Plomin, R. (2008). Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample. Journal of Child Psychology and Psychiatry, 49, 535-542. (Pubitemid 351503093)
-
(2008)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, vol.49
, Issue.5
, pp. 535-542
-
-
Ronald, A.1
Simonoff, E.2
Kuntsi, J.3
Asherson, P.4
Plomin, R.5
-
67
-
-
33744821617
-
Genetic heterogeneity between the three components of the autism spectrum: A twin study
-
DOI 10.1097/01.chi.0000215325.13058.9d, PII 0000458320060600000010
-
Ronald, A., et al. (2006b). Genetic heterogeneity between the three components of the autism spectrum: A twin study. Journal of the American Academy of Child and Adolescent Psychiatry, 45, 691-699. (Pubitemid 43833102)
-
(2006)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.45
, Issue.6
, pp. 691-699
-
-
Ronald, A.1
Happe, F.2
Bolton, P.3
Butcher, L.M.4
Price, T.S.5
Wheelwright, S.6
Baron-Cohen, S.7
Plomin, R.8
-
68
-
-
70349753233
-
Characteristics and concordance of autism spectrum disorders among 277 twin pairs
-
doi:10.1001/archpediatrics.2009.98
-
Rosenberg, R. E., Law, J. K., Yenokyan, G., McGready, J., Kaufmann, W. E., & Law, P. A. (2009). Characteristics and concordance of autism spectrum disorders among 277 twin pairs. Archives of Pediatrics and Adolescent Medicine, 163, 907-914. doi:10.1001/archpediatrics.2009.98.
-
(2009)
Archives of Pediatrics and Adolescent Medicine
, vol.163
, pp. 907-914
-
-
Rosenberg, R.E.1
Law, J.K.2
Yenokyan, G.3
McGready, J.4
Kaufmann, W.E.5
Law, P.A.6
-
69
-
-
0842297288
-
-
CA, Western Psychological Services: Los Angeles
-
Rutter, M., Bailey, A., & Lord, C. (2003). The social communication questionnaire manual. CA, Western Psychological Services: Los Angeles.
-
(2003)
The Social Communication Questionnaire Manual
-
-
Rutter, M.1
Bailey, A.2
Lord, C.3
-
70
-
-
79958074870
-
Multiple recurrent De Novo CNVs, including duplications of the 7q11.23 Williams syndrome region. Are strongly associated with autism
-
doi:10.1016/j.neuron.2011.05.002
-
Sanders, S. J., et al. (2011a). Multiple recurrent De Novo CNVs, including duplications of the 7q11.23 Williams syndrome region. Are strongly associated with autism. Neuron, 70, 863-885. doi:10.1016/j.neuron.2011.05.002.
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
-
71
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
doi:10.1016/j.neuron.2011.05.002
-
Sanders, S. J., et al. (2011b). Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron, 70, 863-885. doi:10.1016/j.neuron.2011.05.002.
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
-
72
-
-
84860780495
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
-
doi:10.1038/nature10945
-
Sanders, S. J., et al. (2012). De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature, 485, 237-241. doi:10.1038/nature10945.
-
(2012)
Nature
, vol.485
, pp. 237-241
-
-
Sanders, S.J.1
-
73
-
-
84860223780
-
Advancing maternal age is associated with increasing risk for autism: A review and meta-analysis
-
doi:10.1016/j.jaac.2012.02.018
-
Sandin, S., Hultman, C. M., Kolevzon, A., Gross, R., MacCabe, J. H., & Reichenberg, A. (2012). Advancing maternal age is associated with increasing risk for autism: A review and meta-analysis. Journal of the American Academy of Child and Adolescent Psychiatry, 51(477-486), e1. doi:10.1016/j.jaac.2012.02.018.
-
(2012)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.51
, Issue.477-486
-
-
Sandin, S.1
Hultman, C.M.2
Kolevzon, A.3
Gross, R.4
MacCabe, J.H.5
Reichenberg, A.6
-
74
-
-
80051674258
-
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders
-
doi:10.1093/hmg/ddr243
-
Schaaf, C. P., et al. (2011). Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders. Human Molecular Genetics, 20, 3366-3375. doi:10.1093/hmg/ddr243.
-
(2011)
Human Molecular Genetics
, vol.20
, pp. 3366-3375
-
-
Schaaf, C.P.1
-
75
-
-
84863600970
-
Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study
-
doi:10.3945/ajcn.110.004416
-
Schmidt, R. J., et al. (2012). Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study. American Journal of Clinical Nutrition, 96, 80-89. doi:10.3945/ajcn.110. 004416.
-
(2012)
American Journal of Clinical Nutrition
, vol.96
, pp. 80-89
-
-
Schmidt, R.J.1
-
76
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
DOI 10.1126/science.1138659
-
Sebat, J., et al. (2007). Strong association of de novo copy number mutations with autism. Science, 316, 445-449. (Pubitemid 46651493)
-
(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
Leotta, A.11
Pai, D.12
Zhang, R.13
Lee, Y.-H.14
Hicks, J.15
Spence, S.J.16
Lee, A.T.17
Puura, K.18
Lehtimaki, T.19
Ledbetter, D.20
Gregersen, P.K.21
Bregman, J.22
Sutcliffe, J.S.23
Jobanputra, V.24
Chung, W.25
Warburton, D.26
King, M.-C.27
Skuse, D.28
Geschwind, D.H.29
Gilliam, T.C.30
Ye, K.31
Wigler, M.32
more..
-
77
-
-
77249095480
-
Independent and dependent contributions of advanced maternal and paternal ages to autism risk
-
doi:10.1002/aur.116
-
Shelton, J. F., Tancredi, D. J., & Hertz-Picciotto, I. (2010). Independent and dependent contributions of advanced maternal and paternal ages to autism risk. Autism Research, 3, 30-39. doi:10.1002/aur.116.
-
(2010)
Autism Research
, vol.3
, pp. 30-39
-
-
Shelton, J.F.1
Tancredi, D.J.2
Hertz-Picciotto, I.3
-
78
-
-
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., & Scourfield, J. (2005). Measuring autistic traits: heritability, reliability and validity of the social and communication disorders checklist. British Journal of Psychiatry, 187, 568-572. doi:10.1192/bjp.187.6.568. (Pubitemid 41752747)
-
(2005)
British Journal of Psychiatry
, vol.187
, Issue.DEC.
, pp. 568-572
-
-
Skuse, D.H.1
Mandy, W.P.L.2
Scourfield, J.3
-
79
-
-
3142779092
-
The genetic and environmental origins of language disability and ability
-
DOI 10.1111/j.1467-8624.2004.00685.x
-
Spinath, F. M., Price, T. S., Dale, P. S., & Plomin, R. (2004). The genetic and environmental origins of language disability and ability. Child Development, 75, 445-454. doi:10.1111/j.1467-8624.2004.00685.x. (Pubitemid 39080066)
-
(2004)
Child Development
, vol.75
, Issue.2
, pp. 445-454
-
-
Spinath, F.M.1
Price, T.S.2
Dale, P.S.3
Plomin, R.4
-
80
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
DOI 10.1111/j.1469-7610.1989.tb00254.x
-
Steffenburg, S., et al. (1989). A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. Journal of Child Psychology and Psychiatry, 30, 405-416. (Pubitemid 19131643)
-
(1989)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, 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
-
81
-
-
0026653516
-
Evidence for a genetic etiology in hyperactivity in children
-
Stevenson, J. (1992). Evidence for a genetic etiology in hyperactivity in children. Behavior Genetics, 22, 337-344.
-
(1992)
Behavior Genetics
, vol.22
, pp. 337-344
-
-
Stevenson, J.1
-
82
-
-
0027374527
-
Hyperactivity and spelling disability: Testing for shared genetic aetiology
-
Stevenson, J., Pennington, B. F., Gilger, J. W., DeFries, J. C., & Gillis, J. J. (1993). Hyperactivity and spelling disability: Testing for shared genetic aetiology. Journal of Child Psychology and Psychiatry, 34, 1137-1152. (Pubitemid 23288409)
-
(1993)
Journal of Child Psychology and Psychiatry and Allied Disciplines
, vol.34
, Issue.7
, pp. 1137-1152
-
-
Stevenson, J.1
Pennington, B.F.2
Gilger, J.W.3
Defries, J.C.4
Gillis, J.J.5
-
83
-
-
76749150349
-
Genetic variance for autism screening items in an unselected sample of toddler-age twins
-
Stilp, R. L., Gernsbacher, M. A., Schweigert, E. K., Arneson, C. L., & Goldsmith, H. H. (2010). Genetic variance for autism screening items in an unselected sample of toddler-age twins. Journal of the American Academy of Child and Adolescent Psychiatry, 49, 267-276.
-
(2010)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.49
, pp. 267-276
-
-
Stilp, R.L.1
Gernsbacher, M.A.2
Schweigert, E.K.3
Arneson, C.L.4
Goldsmith, H.H.5
-
84
-
-
83755163060
-
Sex differences in repetitive stereotyped behaviors in autism: Implications for genetic liability
-
doi:10.1002/ajmg.b.31238
-
Szatmari, P., et al. (2012). Sex differences in repetitive stereotyped behaviors in autism: Implications for genetic liability. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B, 5-12. doi:10.1002/ajmg.b.31238.
-
(2012)
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
, vol.159 B
, pp. 5-12
-
-
Szatmari, P.1
-
85
-
-
51449089853
-
Genetic influences on the broad spectrum of autism: Study of proband-ascertained twins
-
doi:10.1002/ajmg.b.30740
-
Taniai, H., Nishiyama, T., Miyachi, T., Imaeda, M., & Sumi, S. (2008). Genetic influences on the broad spectrum of autism: Study of proband-ascertained twins. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B, 844-849. doi:10.1002/ajmg.b.30740.
-
(2008)
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
, vol.147 B
, pp. 844-849
-
-
Taniai, H.1
Nishiyama, T.2
Miyachi, T.3
Imaeda, M.4
Sumi, S.5
-
86
-
-
84855829221
-
Rare deletions at the neurexin 3 locus in autism spectrum disorder
-
doi:10.1016/j.ajhg.2011.11.025
-
Vaags, A. K., et al. (2012). Rare deletions at the neurexin 3 locus in autism spectrum disorder. American Journal of Human Genetics, 90, 133-141. doi:10.1016/j.ajhg.2011.11.025.
-
(2012)
American Journal of Human Genetics
, vol.90
, pp. 133-141
-
-
Vaags, A.K.1
-
87
-
-
33748150467
-
Autism spectrum disorders in relation to distribution of hazardous air pollutants in the San Francisco Bay area
-
DOI 10.1289/ehp.9120
-
Windham, G. C., Zhang, L., Gunier, R., Croen, L. A., & Grether, J. K. (2006). Autism spectrum disorders in relation to distribution of hazardous air pollutants in the San Francisco bay area. Environmental Health Perspectives, 114, 1438-1444. (Pubitemid 44314771)
-
(2006)
Environmental Health Perspectives
, vol.114
, Issue.9
, pp. 1438-1444
-
-
Windham, G.C.1
Zhang, L.2
Gunier, R.3
Croen, L.A.4
Grether, J.K.5
-
88
-
-
80053620120
-
Assisted reproductive technology and risk for autism spectrum disorder
-
doi:10.1016/j.ridd.2011.05.007
-
Zachor, D. A., & Ben Itzchak, E. (2011). Assisted reproductive technology and risk for autism spectrum disorder. Research in Developmental Disabilities, 32, 2950-2956. doi:10.1016/j.ridd.2011.05.007.
-
(2011)
Research in Developmental Disabilities
, vol.32
, pp. 2950-2956
-
-
Zachor, D.A.1
Ben Itzchak, E.2
-
89
-
-
34547886497
-
A unified genetic theory for sporadic and inherited autism
-
DOI 10.1073/pnas.0705803104
-
Zhao, X., et al. (2007). A unified genetic theory for sporadic and inherited autism. Proceedings of the National Academy of Sciences, 104, 12831-12836. (Pubitemid 47255240)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.31
, pp. 12831-12836
-
-
Zhao, X.1
Leotta, A.2
Kustanovich, V.3
Lajonchere, C.4
Geschwind, D.H.5
Law, K.6
Law, P.7
Qiu, S.8
Lord, C.9
Sebat, J.10
Ye, K.11
Wigler, M.12
|