-
2
-
-
66349136495
-
Parent ratings of behavioral effects of biomedical interventions
-
Autism Research Institute
-
Autism Research Institute. (2008). Parent ratings of behavioral effects of biomedical interventions. Autism Research Review International, vol.34.
-
(2008)
Autism Research Review International
, vol.34
-
-
-
3
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey, A., LeCouteur, A., Gottesman, I., Bolton, P., Simonoff, E., 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
LeCouteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
-
4
-
-
34249680737
-
Autism: Highly heritable but not inherited
-
DOI 10.1038/nm0507-534, PII NM0507534
-
Beaudet, A.L. (2007). Autism: highly heritable but not inherited. Nature and Medicine, 13, 534-536. (Pubitemid 46828472)
-
(2007)
Nature Medicine
, vol.13
, Issue.5
, pp. 534-536
-
-
Beaudet, A.L.1
-
5
-
-
29544433072
-
Associaton of MTHFR gene variants with autism
-
Boris, M., Goldblatt, A., Galanko, J., & James, S.J. (2004). Associaton of MTHFR gene variants with autism. Journal of American Physicians and Surgeons, 9, 106-108.
-
(2004)
Journal of American Physicians and Surgeons
, vol.9
, pp. 106-108
-
-
Boris, M.1
Goldblatt, A.2
Galanko, J.3
James, S.J.4
-
6
-
-
21244472348
-
Specific genetic disorders and autism: Clinical contribution towards their identification
-
DOI 10.1007/s10803-004-1038-2
-
Cohen, D., Pichard, N., Tordjman, S., Baumann, C., Burglen, L., et al. (2005). Specific genetic disorders and autism: clinical contribution towards their identification. Journal of Autism and Developmental Disorders, 35, 103-116. (Pubitemid 40883082)
-
(2005)
Journal of Autism and Developmental Disorders
, vol.35
, Issue.1
, pp. 103-116
-
-
Cohen, D.1
Pichard, N.2
Tordjman, S.3
Baumann, C.4
Burglen, L.5
Excoffier, E.6
Lazar, G.7
Mazet, P.8
Pinquier, C.9
Verloes, A.10
Heron, D.11
-
7
-
-
0038975320
-
Multiplicity considerations in the design and analysis of clinical trials
-
Cook, R.J., & Farewell, V.T. (1996). Multiplicity considerations in the design and analysis of clinical trials. Journal of the Royal Statistical Society, 159, 93-110. (Pubitemid 126331636)
-
(1996)
Journal of the Royal Statistical Society. Series A: Statistics in Society
, vol.159
, Issue.1
, pp. 93-110
-
-
Cook, R.J.1
Farewell, V.T.2
-
9
-
-
0029049553
-
A candidate genetic risk factor for vascular-disease: A common mutation in methyltenetetrahydrofolate reductase
-
Frosst, P., Blom, H.J., Milos, R., Goyette, P., Sheppard, C.A., et al. (1995). A candidate genetic risk factor for vascular-disease: a common mutation in methyltenetetrahydrofolate reductase. Nature Genetics, 10, 111-113.
-
(1995)
Nature Genetics
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
-
10
-
-
0029864121
-
Autism and medical disorders: A review of the literature
-
Gillberg, C., & Coleman, M. (1996). Autism and medical disorders: a review of the literature. Developmental Medicine and Child Neurology, 38, 191-202. (Pubitemid 26083690)
-
(1996)
Developmental Medicine and Child Neurology
, vol.38
, Issue.3
, pp. 191-202
-
-
Gillberg, C.1
Coleman, M.2
-
11
-
-
84993808194
-
Congenital versus regressive onset of autism spectrum disorders: Parents' beliefs about causes
-
Goin-Kochel, R.P., & Myers, B. (2005). Congenital versus regressive onset of autism spectrum disorders: parents' beliefs about causes. Focus on Autism and Other Developmental Disabilities, 20, 169-179.
-
(2005)
Focus on Autism and Other Developmental Disabilities
, vol.20
, pp. 169-179
-
-
Goin-Kochel, R.P.1
Myers, B.2
-
12
-
-
15244348759
-
Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism
-
James, S.J., Cutler, P., Melnyk, S., Jernigan, S., Janak, L., et al. (2004). Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism. American Journal of Clinical Nutrition, 80, 1611-1617. (Pubitemid 41103861)
-
(2004)
American Journal of Clinical Nutrition
, vol.80
, Issue.6
, pp. 1611-1617
-
-
James, S.J.1
Cutler, P.2
Melnyk, S.3
Jernigan, S.4
Janak, L.5
Gaylor, D.W.6
Neubrander, J.A.7
-
13
-
-
33845438146
-
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism
-
DOI 10.1002/ajmg.b.30366
-
James, S.J., Melnyk, S., Jernigan, S., Cleves, M.A., Halsted, C.H., et al. (2006). Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism. American Journal of Medical Genetics Part B, 141B, 947-956. (Pubitemid 44905454)
-
(2006)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.141
, Issue.8
, pp. 947-956
-
-
James, S.J.1
Melnyk, S.2
Jernigan, S.3
Cleves, M.A.4
Halsted, C.H.5
Wong, D.H.6
Cutler, P.7
Bock, K.8
Boris, M.9
Bradstreet, J.J.10
Baker, S.M.11
Gaylor, D.W.12
-
14
-
-
3442890774
-
Epigenetics and human disease
-
DOI 10.1146/annurev.genom.5.061903.180014
-
Jiang, Y., Bressler, J., & Beaudet, A.L. (2004). Epigenetics and human disease. Annual Review of Genomics and Human Genetic, 5, 479-510. (Pubitemid 39362754)
-
(2004)
Annual Review of Genomics and Human Genetics
, vol.5
, pp. 479-510
-
-
Jiang, Y.-H.1
Bressler, J.2
Beaudet, A.L.3
-
15
-
-
5444246895
-
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A
-
DOI 10.1002/ajmg.a.30297
-
Jiang, Y.H., Sahoo, T., Michaelis, R.C., Bercovich, D., Bressler, J., et al. (2004). A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A. American Journal of Medical Genetics, 131A, 1-10. (Pubitemid 39434788)
-
(2004)
American Journal of Medical Genetics
, vol.131 A
, Issue.1
, pp. 1-10
-
-
Jiang, Y.-H.1
Sahoo, T.2
Michaelis, R.C.3
Bercovich, D.4
Bressler, J.5
Kashork, C.D.6
Liu, Q.7
Shaffer, L.G.8
Schroer, R.J.9
Stockton, D.W.10
Spielman, R.S.11
Stevenson, R.E.12
Beaudet, A.L.13
-
16
-
-
66349111618
-
Twin concordance for the autism spectrum based on community diagnoses and screening of a birth cohort.
-
Abstract
-
Kees, E.K., Hefter, R.L., Klaver, J., Schweigert, S.A., Arneson, C.L., et al. (2005). Twin concordance for the autism spectrum based on community diagnoses and screening of a birth cohort. [Abstract]. Behavior Genetics, 35, 808.
-
(2005)
Behavior Genetics
, vol.35
, pp. 808
-
-
Kees, E.K.1
Hefter, R.L.2
Klaver, J.3
Schweigert, S.A.4
Arneson, C.L.5
-
17
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
DOI 10.1007/BF02172145
-
Lord, C., Rutter, M., & LeCouteur, A. (1994). Autism Diagnostic Interview-Revised: A revised version of the diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. Journal of Autism and Developmental Disorders, 24, 659-685. (Pubitemid 24309810)
-
(1994)
Journal of Autism and Developmental Disorders
, vol.24
, Issue.5
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Couteur, A.L.3
-
18
-
-
0003428096
-
-
Austin, TX: The Psychological Corporation
-
Lord, C., Rutter, M., & DiLavore, P. (2001). Autism Diagnostic Observation Schedule - Generic (ADOS-G). Austin, TX: The Psychological Corporation.
-
(2001)
Autism Diagnostic Observation Schedule - Generic (ADOS-G)
-
-
Lord, C.1
Rutter, M.2
DiLavore, P.3
-
19
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall, C.R., Noor, A., Vincent, J.B., Lionel, A.C., Feuk, L., et al. (2008). Structural variation of chromosomes in autism spectrum disorder. American Journal of Human Genetics, 82, 477-488.
-
(2008)
American Journal of Human Genetics
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
Lionel, A.C.4
Feuk, L.5
-
20
-
-
1842630333
-
Matching Strategies in Cognitive Research with Individuals with High-Functioning Autism: Current Practices, Instrument Biases, and Recommendations
-
DOI 10.1023/B:JADD.0000018070.88380.83
-
Mottron, L. (2004). Matching strategies in cognitive research with individuals with high-functioning autism: current practices, instrument biases, and recommendations. Journal of Autism and Developmental Disorders, 34, 19-27. (Pubitemid 38468636)
-
(2004)
Journal of Autism and Developmental Disorders
, vol.34
, Issue.1
, pp. 19-27
-
-
Mottron, L.1
-
21
-
-
3442894480
-
The genetics of autism
-
Muhle, R., Trentacoste, S.V., & Rapin, I. (2004). The genetics of autism. Pediatrics, 113, e472-e486.
-
(2004)
Pediatrics
, vol.113
-
-
Muhle, R.1
Trentacoste, S.V.2
Rapin, I.3
-
22
-
-
0006471913
-
Autistic disorder
-
Mash EJ, Terdal LG, editors. New York: Guilford
-
Newsom, C., & Hovanitz, C.A. (1997). Autistic disorder. In: Mash EJ, Terdal LG, editors. Assessment of childhood disorders, 3e. New York: Guilford, pp 408-452.
-
(1997)
Assessment of Childhood Disorders, 3e
, pp. 408-452
-
-
Newsom, C.1
Hovanitz, C.A.2
-
23
-
-
0141524027
-
The genetics of autistic disorder
-
Plomin R, Defries JC, Craig IW, McGuffin P, editors. Washington, DC: American Psychological Association
-
Pericak-Vance, M.A. (2003). The genetics of autistic disorder. In: Plomin R, Defries JC, Craig IW, McGuffin P, editors. Behavioral genetics in the postgenomic era. Washington, DC: American Psychological Association, pp 267-288.
-
(2003)
Behavioral Genetics in the Postgenomic Era
, pp. 267-288
-
-
Pericak-Vance, M.A.1
-
25
-
-
84878710785
-
-
SAS Institute. (2004). SAS. Cary, NC: SAS Institute
-
SAS Institute. (2004). SAS. Cary, NC: SAS Institute.
-
-
-
-
26
-
-
33749007122
-
Epigenetics of autism spectrum disorders
-
DOI 10.1093/hmg/ddl213
-
Schanen, N.C. (2006). Epigenetics of autism spectrum disorders. Human Molecular Genetics, 15, R138-R150. (Pubitemid 44446787)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.SUPPL. 2
-
-
Schanen, N.C.1
-
27
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
DOI 10.1126/science.1138659
-
Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., 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..
-
29
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
DOI 10.1111/j.1469-7610.1989.tb00254.x
-
Steffenburg, S., Gillberg, C., Hellgren, I., Andersson, L., Gillberg, I.C., Jakobsson, G., & Bohman, M. (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
-
30
-
-
0041326346
-
Geographical and ethnic variation of the 677C>T allele of 5, 10 methylenetetrahydrofolate reductase (MTHFR): Findings from over 7000 newborns from 16 areas world wide
-
Wilcken, B., Bamforth, F., Li, Z., et al. (2003). Geographical and ethnic variation of the 677C-T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7,000 newborns from 16 areas world wide. Journal of Medical Genetics, 40, 619-625. (Pubitemid 37046918)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.8
, pp. 619-625
-
-
Wilcken, B.1
Bamforth, F.2
Li, Z.3
Zhu, H.4
Ritvanen, A.5
Redlund, M.6
Stoll, C.7
Alembik, Y.8
Dott, B.9
Czeizel, A.E.10
Gelman-Kohan, Z.11
Scarano, G.12
Bianca, S.13
Ettore, G.14
Tenconi, R.15
Bellato, S.16
Scala, I.17
Mutchinick, O.M.18
Lopez, M.A.19
De Walle, H.20
Hofstra, R.21
Joutchenko, L.22
Kavteladze, L.23
Bermejo, E.24
Martinez-Frias, M.L.25
Gallagher, M.26
Erickson, J.D.27
Vollset, S.E.28
Mastroiacovo, P.29
Andria, G.30
Botto, L.D.31
more..
|