-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
doi:10.1038/nrg2346
-
Abrahams, B. S., & Geschwind, D. H. (2008). Advances in autism genetics: On the threshold of a new neurobiology. Nature Reviews Genetics, 9(5), 341-355. doi:10.1038/nrg2346.
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.5
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
84874541980
-
-
Agency for Healthcare Research and Quality. U.S. Department of Health and Human Services Agency for Healthcare Research and Quality. Retrieved January 12, 2012, from
-
Agency for Healthcare Research and Quality. (2011). Therapies for children with autism spectrum disorders: A review of the research for parents and caregivers. U.S. Department of Health and Human Services Agency for Healthcare Research and Quality. Retrieved January 12, 2012, from http://effectivehealthcare.ahrq.gov/ehc/products/106/709/autism_consumer.pdf.
-
(2011)
Therapies for children with autism spectrum disorders: A review of the research for parents and caregivers
-
-
-
3
-
-
84870469320
-
-
American Psychiatric Association. (1952, 1968, 1980, 1987, 1994, revisions I-IV). Washington, DC: Author
-
American Psychiatric Association. (1952, 1968, 1980, 1987, 1994, 2000). Diagnostic and statistical manual of mental disorders (revisions I-IV). Washington, DC: Author.
-
(2000)
Diagnostic and statistical manual of mental disorders
-
-
-
4
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., & Zoghbi, H. Y. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics, 23, 185-188.
-
(1999)
Nature Genetics
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
5
-
-
78549271649
-
Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders
-
doi:10.1007/s10803-010-1006-y
-
Atladottir, H. O., Thorsen, P., Ostergaard, L., Schendel, D. E., Lemcke, S., Abdallah, M., & Parner, E. T. (2010). Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. Journal of Autism and Developmental Disorders, 40(12), 1423-1430. doi:10.1007/s10803-010-1006-y.
-
(2010)
Journal of Autism and Developmental Disorders
, vol.40
, Issue.12
, pp. 1423-1430
-
-
Atladottir, H.O.1
Thorsen, P.2
Ostergaard, L.3
Schendel, D.E.4
Lemcke, S.5
Abdallah, M.6
Parner, E.T.7
-
6
-
-
82555196668
-
Mutations causing syndromic autism define an axis of synaptic pathophysiology
-
Auerbach, B. D., Osterweil, E. K., & Bear, M. F. (2011). Mutations causing syndromic autism define an axis of synaptic pathophysiology. Nature, 480(7375), 63-68.
-
(2011)
Nature
, vol.480
, Issue.7375
, pp. 63-68
-
-
Auerbach, B.D.1
Osterweil, E.K.2
Bear, M.F.3
-
7
-
-
78049388092
-
American Journal of Medical Genetics
-
The behavioral phenotype of the idic (15) syndrome.
-
Battaglia, A., Parrini, B., & Tancredi, R. (2010). The behavioral phenotype of the idic (15) syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 154C(4), 448-455.
-
(2010)
Part C, Seminars in Medical Genetics
, vol.154 C
, Issue.4
, pp. 448-455
-
-
Battaglia, A.1
Parrini, B.2
Tancredi, R.3
-
8
-
-
80052827372
-
Autism, language and communication in children with sex chromosome trisomies
-
Bishop, D. V. M., Jacobs, P. A., Lachlan, K., Wellesley, D., Barnicoat, A., Boyd, P. A., Scerif, G. (2011). Autism, language and communication in children with sex chromosome trisomies. Archives of Disabilities in Children, 96(10), 954-959.
-
(2011)
Archives of Disabilities in Children
, vol.96
, Issue.10
, pp. 954-959
-
-
Bishop, D.V.M.1
Jacobs, P.A.2
Lachlan, K.3
Wellesley, D.4
Barnicoat, A.5
Boyd, P.A.6
Scerif, G.7
-
9
-
-
0022462350
-
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
-
Butler, M. G., Meaney, F. J., & Palmer, C. G. (1986). Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. American Journal of Medical Genetics, 23(3), 793-809.
-
(1986)
American Journal of Medical Genetics
, vol.23
, Issue.3
, pp. 793-809
-
-
Butler, M.G.1
Meaney, F.J.2
Palmer, C.G.3
-
10
-
-
45549104497
-
Autism spectrum disorders: Clinical and research frontiers RID D-5265-2009
-
doi:10.1136/adc.2006.115337
-
Caronna, E. B., Milunsky, J. M., & Tager-Flusberg, H. (2008). Autism spectrum disorders: Clinical and research frontiers RID D-5265-2009. Archives of Disease in Childhood, 93(6), 518-523. doi:10.1136/adc.2006.115337.
-
(2008)
Archives of Disease in Childhood
, vol.93
, Issue.6
, pp. 518-523
-
-
Caronna, E.B.1
Milunsky, J.M.2
Tager-Flusberg, H.3
-
11
-
-
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. Morbidity and Mortality Weekly Report Surveillance Summary, 61(3), 1-19.
-
(2012)
Morbidity and Mortality Weekly Report Surveillance Summary
, vol.61
, Issue.3
, pp. 1-19
-
-
-
12
-
-
79954571673
-
The quantitative nature of autistic social impairment
-
Constantino, J. N. (2011). The quantitative nature of autistic social impairment. Pediatric Research, 69(5, Pt 2), 55R-62R.
-
(2011)
Pediatric Research
, vol.69
, Issue.5 PART 2
-
-
Constantino, J.N.1
-
13
-
-
17344364660
-
Linkage disequilibrium mapping of autistic spectrum disorders, with 15q11-13 markers
-
Cook, E. H., Courchesne, E., Cox, N. J., Lord, C., Gonen, D., Guter, S. J., & Courchesne, E. (1998). Linkage disequilibrium mapping of autistic spectrum disorders, with 15q11-13 markers. American Journal of Human Genetics, 62, 1077-1083.
-
(1998)
American Journal of Human Genetics
, vol.62
, pp. 1077-1083
-
-
Cook, E.H.1
Courchesne, E.2
Cox, N.J.3
Lord, C.4
Gonen, D.5
Guter, S.J.6
Courchesne, E.7
-
14
-
-
33847308551
-
Fragile X syndrome and autism: Common developmental pathways
-
Cornish, K., Turk, J., & Levitas, A. (2007). Fragile X syndrome and autism: Common developmental pathways Current Pediatric Reviews, 3, 61-68.
-
(2007)
Current Pediatric Reviews
, vol.3
, pp. 61-68
-
-
Cornish, K.1
Turk, J.2
Levitas, A.3
-
15
-
-
49649118165
-
Tuberous sclerosis
-
Curatolo, P., Bombardieri, R., & Jozwiak, S. (2008). Tuberous sclerosis. Lancet, 372, 657-668.
-
(2008)
Lancet
, vol.372
, pp. 657-668
-
-
Curatolo, P.1
Bombardieri, R.2
Jozwiak, S.3
-
16
-
-
33845889998
-
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
-
Durand, C. M., Betancur, C., Boeckers, T. M., Bockmann, J., Chaste, P., Fauchereau, F., Boureron, T. (2007). Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nature Genetics, 39, 25-27.
-
(2007)
Nature Genetics
, vol.39
, pp. 25-27
-
-
Durand, C.M.1
Betancur, C.2
Boeckers, T.M.3
Bockmann, J.4
Chaste, P.5
Fauchereau, F.6
Boureron, T.7
-
17
-
-
49949152048
-
Head circumference as an early predictor of autism symptoms in younger siblings of children with autism spectrum disorder
-
doi:10.1007/s10803-007-0495-9
-
Elder, L. M., Dawson, G., Toth, K., Fein, D., & Munson, J. (2008). Head circumference as an early predictor of autism symptoms in younger siblings of children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 38(6), 1104-1111. doi:10.1007/s10803-007-0495-9.
-
(2008)
Journal of Autism and Developmental Disorders
, vol.38
, Issue.6
, pp. 1104-1111
-
-
Elder, L.M.1
Dawson, G.2
Toth, K.3
Fein, D.4
Munson, J.5
-
18
-
-
84891861407
-
Deletion on chromosome 2 linked to epilepsy, autism
-
Elsea, S., & Eikler, E. (2011). Deletion on chromosome 2 linked to epilepsy, autism. American Journal of Human Genetics, 89, 551-563.
-
(2011)
American Journal of Human Genetics
, vol.89
, pp. 551-563
-
-
Elsea, S.1
Eikler, E.2
-
19
-
-
24044515278
-
Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome
-
Fine, S. E., Weissman, A., Gerdes, M., Pinto-Martin, J., Zackai, E. H., McDonald-McGinn, D. M., & Emaneul, B. S. (2005). Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome. Journal of Autism and Developmental Disorder, 35(4), 461-470.
-
(2005)
Journal of Autism and Developmental Disorder
, vol.35
, Issue.4
, pp. 461-470
-
-
Fine, S.E.1
Weissman, A.2
Gerdes, M.3
Pinto-Martin, J.4
Zackai, E.H.5
McDonald-McGinn, D.M.6
Emaneul, B.S.7
-
20
-
-
67049118065
-
Epidemiology of pervasive developmental disorders
-
Fombonne, E. (2009). Epidemiology of pervasive developmental disorders. Pediatric Research, 65, 591-598.
-
(2009)
Pediatric Research
, vol.65
, pp. 591-598
-
-
Fombonne, E.1
-
21
-
-
77950864908
-
Genetics of autistic disorders: Review and clinical implications
-
doi:10.1007/s00787-009-0076-x
-
Freitag, C. M., Staal, W., Klauck, S. M., Duketis, E., & Waltes, R. (2010). Genetics of autistic disorders: Review and clinical implications. European Child & Adolescent Psychiatry, 19(3), 169-178. doi:10.1007/s00787-009-0076-x.
-
(2010)
European Child & Adolescent Psychiatry
, vol.19
, Issue.3
, pp. 169-178
-
-
Freitag, C.M.1
Staal, W.2
Klauck, S.M.3
Duketis, E.4
Waltes, R.5
-
22
-
-
33644836511
-
Intervention pilot for parents of children with autism spectrum disorder
-
Giarelli, E., Sounders, M., Pinto-Martin, J., Bloch, J., & Levy, S. (2005). Intervention pilot for parents of children with autism spectrum disorder. Pediatric Nursing, 31(5), 389-399.
-
(2005)
Pediatric Nursing
, vol.31
, Issue.5
, pp. 389-399
-
-
Giarelli, E.1
Sounders, M.2
Pinto-Martin, J.3
Bloch, J.4
Levy, S.5
-
23
-
-
0021815213
-
Rett's syndrome: Prevalence and impact on progressive severe mental retardation in girls
-
Hagberg, B. (1985). Rett's syndrome: Prevalence and impact on progressive severe mental retardation in girls. Acta Paediatrica Scandinavia, 74, 405-408.
-
(1985)
Acta Paediatrica Scandinavia
, vol.74
, pp. 405-408
-
-
Hagberg, B.1
-
24
-
-
80051944739
-
Genetic heritability and shared environmental factors among twin pairs with autism
-
Hallmayer, J., Cleveland, S., Torres, A., Philips, J., Cohen, B., Torigoe, T., Risch, N. (2011). Genetic heritability and shared environmental factors among twin pairs with autism. Archives of General Psychiatry, 68(11), 1095-1102.
-
(2011)
Archives of General Psychiatry
, vol.68
, Issue.11
, pp. 1095-1102
-
-
Hallmayer, J.1
Cleveland, S.2
Torres, A.3
Philips, J.4
Cohen, B.5
Torigoe, T.6
Risch, N.7
-
25
-
-
79952323516
-
Autism spectrum diagnoses in neurogenetic syndromes
-
E. Hollander, A. Kolevzon, & J. T. Coyle (Eds.), Washington, DC: American Psychiatric Publishing Co
-
Harris, J. C. (2011). Autism spectrum diagnoses in neurogenetic syndromes. In E. Hollander, A. Kolevzon, & J. T. Coyle (Eds.), Textbook of autism spectrum disorders (pp. 223-235). Washington, DC: American Psychiatric Publishing Co.
-
(2011)
Textbook of autism spectrum disorders
, pp. 223-235
-
-
Harris, J.C.1
-
26
-
-
77954893211
-
Parental beliefs about cause and course of their child's autism and outcomes of their beliefs: A review of the literature
-
Hebert, E. B., & Koulouglioti, C. (2010). Parental beliefs about cause and course of their child's autism and outcomes of their beliefs: A review of the literature. Issues in Comprehensive Pediatric Nursing, 33, 149-163.
-
(2010)
Issues in Comprehensive Pediatric Nursing, 33
, pp. 149-163
-
-
Hebert, E.B.1
Koulouglioti, C.2
-
27
-
-
0033667613
-
Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders
-
Ingram, J. L., Stodgell, C. J., Hyman, S. L., Figlewicz, D. A., Weitkamp, L. R., & Rodier, P. M. (2000). Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders. Teratology, 62, 393-405.
-
(2000)
Teratology
, vol.62
, pp. 393-405
-
-
Ingram, J.L.1
Stodgell, C.J.2
Hyman, S.L.3
Figlewicz, D.A.4
Weitkamp, L.R.5
Rodier, P.M.6
-
28
-
-
62649088108
-
Population analysis of large copy number variants and hotspots of human genetic disease
-
Itsara, A., Cooper, G. M., Baker, C., Girirajan, S., Li, J., Absher, D., Eichler, E. E. (2009). Population analysis of large copy number variants and hotspots of human genetic disease. American Journal of Human Genetics, 84, 148-161.
-
(2009)
American Journal of Human Genetics
, vol.84
, pp. 148-161
-
-
Itsara, A.1
Cooper, G.M.2
Baker, C.3
Girirajan, S.4
Li, J.5
Absher, D.6
Eichler, E.E.7
-
29
-
-
36048931014
-
Identification and evaluation of children with autism spectrum disorders
-
doi:10.1542/peds.2007-2361
-
Johnson, C. P., & Myers, S. (2007). Identification and evaluation of children with autism spectrum disorders. Pediatrics, 120(5), 1183-1215. doi:10.1542/peds.2007-2361.
-
(2007)
Pediatrics
, vol.120
, Issue.5
, pp. 1183-1215
-
-
Johnson, C.P.1
Myers, S.2
-
30
-
-
51449090505
-
Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders
-
Jones, J. R., Skinner, C. E., Friez, M. J., Schwartz, C. E., & Stevenson, R. E. (2008). Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders. American Journal of Medical Genetics, 146A(17), 2213-2220.
-
(2008)
American Journal of Medical Genetics
, vol.146 A
, Issue.17
, pp. 2213-2220
-
-
Jones, J.R.1
Skinner, C.E.2
Friez, M.J.3
Schwartz, C.E.4
Stevenson, R.E.5
-
31
-
-
0000984981
-
Autistic disturbances of affective contact
-
Kanner, L. (1943). Autistic disturbances of affective contact. Nervous Child, 2, 217-250.
-
(1943)
Nervous Child
, vol.2
, pp. 217-250
-
-
Kanner, L.1
-
32
-
-
79958258583
-
Prevalence of autism spectrum disorders in a total population sample
-
Kim, Y. S., Leventhal, B. L., Koh, Y. J, Fombonne, E., Laska, E., Lim, E. C., Grinker, R. R. (2011). Prevalence of autism spectrum disorders in a total population sample. American Journal of Psychiatry, 168, 904-912.
-
(2011)
American Journal of Psychiatry
, vol.168
, pp. 904-912
-
-
Kim, Y.S.1
Leventhal, B.L.2
Koh, Y.J.3
Fombonne, E.4
Laska, E.5
Lim, E.C.6
Grinker, R.R.7
-
33
-
-
52049113008
-
Prenatal stress and risk for autism
-
doi:10.1016/j.neubiorev.2008.06.004
-
Kinney, D. K., Munir, K. M., Crowley, D. J., & Miller, A. M. (2008). Prenatal stress and risk for autism. Neuroscience and Biobehavioral Reviews, 32(8), 1519-1532. doi:10.1016/j.neubiorev.2008.06.004.
-
(2008)
Neuroscience and Biobehavioral Reviews
, vol.32
, Issue.8
, pp. 1519-1532
-
-
Kinney, D.K.1
Munir, K.M.2
Crowley, D.J.3
Miller, A.M.4
-
34
-
-
64649104580
-
Genetics of autism spectrum disorders
-
doi:10.1007/s11910-009-0029-2
-
Kumar, R. A., & Christian, S. L. (2009). Genetics of autism spectrum disorders. Current Neurology and Neuroscience Reports, 9(3), 188-197. doi:10.1007/s11910-009-0029-2.
-
(2009)
Current Neurology and Neuroscience Reports
, vol.9
, Issue.3
, pp. 188-197
-
-
Kumar, R.A.1
Christian, S.L.2
-
35
-
-
0035807360
-
A forkhead-domain gene is mutated in severe speech and language disorder
-
Lai, C.S.L., Fisher, S.E., Hurst, J.A., Vargha-Khadem, F., & Monaco, A.P. (2001). A forkhead-domain gene is mutated in severe speech and language disorder. Nature, 413, 519-523.
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.L.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
36
-
-
78049410034
-
Autism spectrum features in Smith-Magenis syndrome
-
Laje, G., Morse, R., Richter, W., Ball, J., Pao, M., & Smith, A. C. M. (2010). Autism spectrum features in Smith-Magenis syndrome. American Journal of Medical Genetics Part C, 154C, 456-462.
-
(2010)
American Journal of Medical Genetics Part C
, vol.154 C
, pp. 456-462
-
-
Laje, G.1
Morse, R.2
Richter, W.3
Ball, J.4
Pao, M.5
Smith, A.C.M.6
-
37
-
-
84870543830
-
-
Lister Hill Center for Biomedical Communication. Retrieved from
-
Lister Hill Center for Biomedical Communication. (2012). Genetics home reference. Retrieved from http://ghr.nlm.nih.gov/gene/SLC6A4.
-
(2012)
Genetics home reference
-
-
-
38
-
-
0003428096
-
-
Retrieved from
-
Lord, C., Rutter, M., DiLavore, P. E., & Risi, S. (2012). Autism Diagnostic Observation Schedule (ADOS). Retrieved from http://www.mhs.com/product.aspx?gr=edu&prod=ados&id=overview.
-
(2012)
Autism Diagnostic Observation Schedule (ADOS)
-
-
Lord, C.1
Rutter, M.2
DiLavore, P.E.3
Risi, S.4
-
39
-
-
84862269651
-
Fertility therapies, infertility and autism spectrum disorders in the Nurses' Health Study II
-
doi:10.1111/j.1365-3016.2012.01294.x
-
Lyall, K., Pauls, D. L., Spiegelman, D., Santangelo, S. L., & Ascherio, A. (2012). Fertility therapies, infertility and autism spectrum disorders in the Nurses' Health Study II. Paediatric Perinatal Epidemiology, 26(4), 361-372. doi:10.1111/j.1365-3016.2012.01294.x.
-
(2012)
Paediatric Perinatal Epidemiology
, vol.26
, Issue.4
, pp. 361-372
-
-
Lyall, K.1
Pauls, D.L.2
Spiegelman, D.3
Santangelo, S.L.4
Ascherio, A.5
-
40
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall, C. R., Noor, A., Vincent, J. B., Lionel, A. C., Feuk, L., Skaug, J., Scherer, S. W. (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
Skaug, J.6
Scherer, S.W.7
-
41
-
-
32444436499
-
Genetic counseling and ethical issues for autism
-
McMahon, W. M., Baty, B. J., & Botkin, J. (2006). Genetic counseling and ethical issues for autism. American Journal of Medical Genetics Part C, 142C, 52-57.
-
(2006)
American Journal of Medical Genetics Part C
, vol.142 C
, pp. 52-57
-
-
McMahon, W.M.1
Baty, B.J.2
Botkin, J.3
-
42
-
-
84857434829
-
Genomics, intellectual disability, and autism
-
Mefford, H. C., Batshaw, M. L., & Hoffman, E. P. (2012). Genomics, intellectual disability, and autism. New England Journal of Medicine, 366, 733-743.
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 733-743
-
-
Mefford, H.C.1
Batshaw, M.L.2
Hoffman, E.P.3
-
43
-
-
77954915671
-
What is a meaningful result? Disclosing the results of genomic research in autism to research participants
-
Miller, F. A., Hayeems, R. Z., & Bytautas, J. P. (2010). What is a meaningful result? Disclosing the results of genomic research in autism to research participants. European Journal of Human Genetics, 18, 867-871.
-
(2010)
European Journal of Human Genetics
, vol.18
, pp. 867-871
-
-
Miller, F.A.1
Hayeems, R.Z.2
Bytautas, J.P.3
-
44
-
-
78249281977
-
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
-
SGENE Consortium, Simons Simplex Collection Genetics Consortium
-
Moreno-De-Luca, D., SGENE Consortium, Mulle, J. G., Simons Simplex Collection Genetics Consortium, Kaminsky, E. B., Sanders, S. J., Uhas, K. (2010). Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. American Journal of Human Genetics, 87, 618-630.
-
(2010)
American Journal of Human Genetics
, vol.87
, pp. 618-630
-
-
Moreno-De-Luca, D.1
Mulle, J.G.2
Kaminsky, E.B.3
Sanders, S.J.4
Uhas, K.5
-
45
-
-
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
-
46
-
-
79952254931
-
A population genetic approach to mapping neurological disorder genes using deep resequencing
-
doi:10.1371/journal.pgen.1001318
-
Myers, R. A., Casals, F., Gauthier, J., Hamdan, F. F., Keebler, J., Boyko, A. R., Awadalla, P. (2011). A population genetic approach to mapping neurological disorder genes using deep resequencing. Plos Genetics, 7(2), e1001318. doi:10.1371/journal.pgen.1001318.
-
(2011)
Plos Genetics
, vol.7
, Issue.2
-
-
Myers, R.A.1
Casals, F.2
Gauthier, J.3
Hamdan, F.F.4
Keebler, J.5
Boyko, A.R.6
Awadalla, P.7
-
48
-
-
0035417396
-
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families
-
Nurmi, E. L., Bradford, Y., Chen, Y. H., Hall, J., Arnone, B., Gardiner, M. B., Sutcliffe, J. S. (2001). Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics, 77(1-2), 105-113.
-
(2001)
Genomics
, vol.77
, Issue.1-2
, pp. 105-113
-
-
Nurmi, E.L.1
Bradford, Y.2
Chen, Y.H.3
Hall, J.4
Arnone, B.5
Gardiner, M.B.6
Sutcliffe, J.S.7
-
50
-
-
0028439064
-
Smith-Lemli-Opitz (RSH) syndrome bibliography: 1964-1993
-
Opitz, J. M., Penchaszadeh, V. B., Holt, M. C., Spano, L. M., & Smith, V. L. (1994). Smith-Lemli-Opitz (RSH) syndrome bibliography: 1964-1993. American Journal of Human Genetics, 50, 339-343.
-
(1994)
American Journal of Human Genetics
, vol.50
, pp. 339-343
-
-
Opitz, J.M.1
Penchaszadeh, V.B.2
Holt, M.C.3
Spano, L.M.4
Smith, V.L.5
-
51
-
-
79957589237
-
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
-
doi:10.1038/ng.835
-
O'Roak, B. J., Deriziotis, P., Lee, C., Vives, L., Schwartz, J. J., Girirajan, S., Eichler, E. E. (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
Deriziotis, P.2
Lee, C.3
Vives, L.4
Schwartz, J.J.5
Girirajan, S.6
Eichler, E.E.7
-
52
-
-
80052366179
-
Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study
-
Retrieved from
-
Ozonoff, S., Young, G. S., Carter, A., Messinger, D., Yirmiya, N., Zwaigenbaum, L., Stone, W. L. (2011). Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study. Pediatrics, 128(3), e488-e495. Retrieved from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164092/.
-
(2011)
Pediatrics
, vol.128
, Issue.3
-
-
Ozonoff, S.1
Young, G.S.2
Carter, A.3
Messinger, D.4
Yirmiya, N.5
Zwaigenbaum, L.6
Stone, W.L.7
-
53
-
-
79955950305
-
The changing prevalence of the autism spectrum disorders
-
Rice, C. E. (2011). The changing prevalence of the autism spectrum disorders. American Family Physician, 83(5), 515-520.
-
(2011)
American Family Physician
, vol.83
, Issue.5
, pp. 515-520
-
-
Rice, C.E.1
-
54
-
-
70349753233
-
Characteristics and concordance of autism spectrum disorders among 277 twin pairs
-
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 Pediatric Adolescent Medicine, 163, 907-914.
-
(2009)
Archives of Pediatric 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
-
55
-
-
84860780495
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
-
doi:10.1038/nature10945
-
Sanders, S. J., Murtha, M. T., Gupta, A. R., Murdoch, J. D., Raubeson, M. J., Willsey, A. J., State, M. W. (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
Murtha, M.T.2
Gupta, A.R.3
Murdoch, J.D.4
Raubeson, M.J.5
Willsey, A.J.6
State, M.W.7
-
56
-
-
84864137096
-
Genomic architecture of autism spectrum disorder
-
A. Hollancer, A. Kolevzon, & J. Coyle (Eds.), Washington, DC: American Psychiatric Publishing, Inc
-
Sakurai, T., Cai, G., Grice, D., & Buxbaum, J. D. (2011). Genomic architecture of autism spectrum disorder. In A. Hollancer, A. Kolevzon, & J. Coyle (Eds.), Textbook of autism spectrum disorders (pp. 281-298). Washington, DC: American Psychiatric Publishing, Inc.
-
(2011)
Textbook of autism spectrum disorders
, pp. 281-298
-
-
Sakurai, T.1
Cai, G.2
Grice, D.3
Buxbaum, J.D.4
-
57
-
-
80855144716
-
Have secular changes in perinatal risk factors contributed to the recent autism prevalence increase? Development and application of a mathematical assessment model
-
Schieve, L. A., Rice, C., Devine, O., Maenner, M. J., Lee, L., Fitzgerald, R., Durkin, M. (2011). Have secular changes in perinatal risk factors contributed to the recent autism prevalence increase? Development and application of a mathematical assessment model. Annals of Epidemiology, 21(12), 930-945.
-
(2011)
Annals of Epidemiology
, vol.21
, Issue.12
, pp. 930-945
-
-
Schieve, L.A.1
Rice, C.2
Devine, O.3
Maenner, M.J.4
Lee, L.5
Fitzgerald, R.6
Durkin, M.7
-
58
-
-
79955569025
-
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
-
Schumann, G., Coin, L. J., Lourdusamy, A., Charoen, P., Berger, K. A., Stacey, D., Elliott, P. (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Science, 108, 7119-7124.
-
(2011)
Proceedings of the National Academy of Science
, vol.108
, pp. 7119-7124
-
-
Schumann, G.1
Coin, L.J.2
Lourdusamy, A.3
Charoen, P.4
Berger, K.A.5
Stacey, D.6
Elliott, P.7
-
59
-
-
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., Walsh, T., Wigler, M. (2007). Strong association of de novo copy number mutations with autism. Science, 316(5823), 445-449. doi:10.1126/science.1138659.
-
(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
Wigler, M.7
-
60
-
-
84864120951
-
Tipping the balance of autism risk: Potential mechanisms linking pesticides and autism
-
Shelton, J. F., Hertz-Picciotto, I., & Pessah, I. N. (2012). Tipping the balance of autism risk: Potential mechanisms linking pesticides and autism. Environmental Health Perspectives, 120(7), 944-951.
-
(2012)
Environmental Health Perspectives
, vol.120
, Issue.7
, pp. 944-951
-
-
Shelton, J.F.1
Hertz-Picciotto, I.2
Pessah, I.N.3
-
61
-
-
84863247768
-
Epigenetic signatures of autism: Trimethylated H3K4 landscapes in prefrontal neurons
-
Shulha, H. P., Cheung, I., Whittle, C., Wang, J., Virgil, D., Lin, C. L., Akbarian, S. (2012). Epigenetic signatures of autism: Trimethylated H3K4 landscapes in prefrontal neurons. Archives of General Psychiatry, 69(3), 314-324.
-
(2012)
Archives of General Psychiatry
, vol.69
, Issue.3
, pp. 314-324
-
-
Shulha, H.P.1
Cheung, I.2
Whittle, C.3
Wang, J.4
Virgil, D.5
Lin, C.L.6
Akbarian, S.7
-
62
-
-
21244491530
-
Analysis of the RELN gene as a genetic risk factor for autism
-
Skaar, D. A., Shao, Y., Haines, J. L., Stenger, J. E., Jaworski, J., Martin, E. R., Pericak-Vance, M. A. (2005). Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry, 10, 563-571.
-
(2005)
Molecular Psychiatry
, vol.10
, pp. 563-571
-
-
Skaar, D.A.1
Shao, Y.2
Haines, J.L.3
Stenger, J.E.4
Jaworski, J.5
Martin, E.R.6
Pericak-Vance, M.A.7
-
63
-
-
34447278070
-
Array identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
-
Ullmann, R., Turner, G., Kirschhoff, M., Chen, W., Tonge, B., Rosenberg, C., Roepper, H. (2007). Array identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutations, 28, 674-682.
-
(2007)
Human Mutations
, vol.28
, pp. 674-682
-
-
Ullmann, R.1
Turner, G.2
Kirschhoff, M.3
Chen, W.4
Tonge, B.5
Rosenberg, C.6
Roepper, H.7
-
64
-
-
80053003849
-
In search of biomarkers for autism: Scientific, social and ethical challenges
-
Walsh, P. N., Elsabbagh, M., Bolton, P., & Singh, I. (2011). In search of biomarkers for autism: Scientific, social and ethical challenges. Nature Reviews-Neuroscience, 12, 603-612.
-
(2011)
Nature Reviews-Neuroscience
, vol.12
, pp. 603-612
-
-
Walsh, P.N.1
Elsabbagh, M.2
Bolton, P.3
Singh, I.4
-
65
-
-
39049163023
-
Association between microdeletion and microduplication at 16p11.2 and autism
-
Weiss, L. A., Shen, Y., Korn, J. M., Arking, D. E., Miller, D. T., Fossdal, R., Daly, M. (2008). Association between microdeletion and microduplication at 16p11.2 and autism. New England Journal of Medicine, 358, 667-675.
-
(2008)
New England Journal of Medicine
, vol.358
, pp. 667-675
-
-
Weiss, L.A.1
Shen, Y.2
Korn, J.M.3
Arking, D.E.4
Miller, D.T.5
Fossdal, R.6
Daly, M.7
-
67
-
-
29944441305
-
Search for autism loci by combined analysis of autism genetic resource exchange and Finnish families
-
Ylisaukko-Oja T., Alarcon, M., Cantor, R. M., Auranen, M., Vanhala, R., Kempas, M., Peltonen, L. (2006). Search for autism loci by combined analysis of autism genetic resource exchange and Finnish families. Annals of Neurology, 1, 145-155.
-
(2006)
Annals of Neurology
, vol.1
, pp. 145-155
-
-
Ylisaukko-Oja, T.1
Alarcon, M.2
Cantor, R.M.3
Auranen, M.4
Vanhala, R.5
Kempas, M.6
Peltonen, L.7
|