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Items: 1 to 20 of 100

1.

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.

Robinson EB, Howrigan D, Yang J, Ripke S, Anttila V, Duncan LE, Jostins L, Barrett JC, Medland SE, MacArthur DG, Breen G, O'Donovan MC, Wray NR, Devlin B, Daly MJ, Visscher PM, Sullivan PF, Neale BM.

Mol Psychiatry. 2014 Aug;19(8):859-61. doi: 10.1038/mp.2013.125. Epub 2013 Oct 22. No abstract available.

2.

Population structure confounds autism genetic classifier.

Belgard TG, Jankovic I, Lowe JK, Geschwind DH.

Mol Psychiatry. 2014 Apr;19(4):405-7. doi: 10.1038/mp.2013.34. Epub 2013 Apr 2. No abstract available.

3.

Response to Robinson et al.

Skafidas E, Testa R, Zantomio D, Chana G, Everall IP, Pantelis C.

Mol Psychiatry. 2015 Jul;20(7):794. doi: 10.1038/mp.2015.15. Epub 2015 Mar 10. No abstract available.

PMID:
25754086
4.

Response to Belgard et al.

Skafidas E, Testa R, Zantomio D, Chana G, Everall IP, Pantelis C.

Mol Psychiatry. 2014 Apr;19(4):407-9. doi: 10.1038/mp.2013.186. Epub 2014 Jan 14. No abstract available. Erratum in: Mol Psychiatry. 2014 Jun;19(6):743-4.

5.

Predicting the diagnosis of autism spectrum disorder using gene pathway analysis.

Skafidas E, Testa R, Zantomio D, Chana G, Everall IP, Pantelis C.

Mol Psychiatry. 2014 Apr;19(4):504-10. doi: 10.1038/mp.2012.126. Epub 2012 Sep 11.

6.

Advances in our understanding of genetic risk factors for autism spectrum disorders.

Kendler KS.

Am J Psychiatry. 2010 Nov;167(11):1291-3. doi: 10.1176/appi.ajp.2010.10081160. No abstract available.

PMID:
21041249
7.

A detailed association analysis between the tryptophan hydroxylase 2 (TPH2) gene and autism spectrum disorders in a Japanese population.

Egawa J, Watanabe Y, Nunokawa A, Endo T, Kaneko N, Tamura R, Sugiyama T, Someya T.

Psychiatry Res. 2012 Apr 30;196(2-3):320-2. doi: 10.1016/j.psychres.2011.09.001. Epub 2012 Feb 22.

PMID:
22361444
8.

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood.

Lichtenstein P, Carlström E, Råstam M, Gillberg C, Anckarsäter H.

Am J Psychiatry. 2010 Nov;167(11):1357-63. doi: 10.1176/appi.ajp.2010.10020223. Epub 2010 Aug 4.

PMID:
20686188
9.

Association between peroxisomal biogenesis factor 7 and autism spectrum disorders in a Korean population.

Ro M, Park J, Nam M, Bang HJ, Yang J, Choi KS, Kim SK, Chung JH, Kwack K.

J Child Neurol. 2012 Oct;27(10):1270-5. Epub 2012 Feb 28.

PMID:
22378669
10.

No association of Val158Met variant in the COMT gene with autism spectrum disorder in Thai children.

Limprasert P, Maisrikhaw W, Sripo T, Wirojanan J, Hansakunachai T, Roongpraiwan R, Sombuntham T, Ruangdaraganon N, Guo X.

Psychiatr Genet. 2014 Oct;24(5):230-1. doi: 10.1097/YPG.0000000000000046. No abstract available.

PMID:
24912046
11.

Possible association between the oxytocin receptor gene and N-acetylaspartate of the right medial temporal lobe in autism spectrum disorders.

Egawa J, Watanabe Y, Endo T, Kitamura H, Someya T.

Psychiatry Clin Neurosci. 2014 Jan;68(1):83. doi: 10.1111/pcn.12087. Epub 2013 Oct 28. No abstract available.

12.

The genetics of Autism Spectrum Disorders--a guide for clinicians.

Heil KM, Schaaf CP.

Curr Psychiatry Rep. 2013 Jan;15(1):334. doi: 10.1007/s11920-012-0334-3. Review.

PMID:
23250815
13.

Association between OXTR and clinical phenotypes of autism spectrum disorders.

Egawa J, Watanabe Y, Endo T, Tamura R, Masuzawa N, Someya T.

Psychiatry Res. 2013 Jun 30;208(1):99-100. doi: 10.1016/j.psychres.2012.11.007. Epub 2012 Dec 7. No abstract available.

PMID:
23219106
14.

Associations between single-nucleotide polymorphism in the FNDC3A and autism spectrum disorder in a Korean population.

Ro M, Park J, Nam M, Bang HJ, Yang JW, Choi KS, Kim SK, Chung JH, Kwack K.

Psychiatry Res. 2013 Sep 30;209(2):246-8. doi: 10.1016/j.psychres.2013.02.028. Epub 2013 Apr 29.

PMID:
23639254
15.

[Genetic analyses for identifying molecular mechanisms in autism spectrum disorders].

Chiocchetti A, Klauck SM.

Z Kinder Jugendpsychiatr Psychother. 2011 Mar;39(2):101-11. doi: 10.1024/1422-4917/a000096. Review. German.

PMID:
21442598
16.

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population.

St Pourcain B, Wang K, Glessner JT, Golding J, Steer C, Ring SM, Skuse DH, Grant SF, Hakonarson H, Davey Smith G.

Am J Psychiatry. 2010 Nov;167(11):1364-72. doi: 10.1176/appi.ajp.2010.09121789. Epub 2010 Jul 15. Erratum in: Am J Psychiatry. 2010 Oct;167(10):1283. Smith, George D [corrected to Davey Smith, George].

17.

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.

Nijmeijer JS, Arias-Vásquez A, Rommelse NN, Altink ME, Anney RJ, Asherson P, Banaschewski T, Buschgens CJ, Fliers EA, Gill M, Minderaa RB, Poustka L, Sergeant JA, Buitelaar JK, Franke B, Ebstein RP, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sonuga-Barke EJ, Steinhausen HC, Faraone SV, Hartman CA, Hoekstra PJ.

J Am Acad Child Adolesc Psychiatry. 2010 Jul;49(7):675-85. doi: 10.1016/j.jaac.2010.03.015. Epub 2010 May 20.

18.

Copy number and sequence variants implicate APBA2 as an autism candidate gene.

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.

Autism Res. 2009 Dec;2(6):359-64. doi: 10.1002/aur.107.

PMID:
20029827
19.

Association with tryptophan hydroxylase 2 gene polymorphisms and autism spectrum disorders in Korean families.

Yang SY, Yoo HJ, Cho IH, Park M, Kim SA.

Neurosci Res. 2012 Aug;73(4):333-6. doi: 10.1016/j.neures.2012.05.012. Epub 2012 Jun 12.

PMID:
22698779
20.

A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma.

Ceroni F, Sagar A, Simpson NH, Gawthrope AJ, Newbury DF, Pinto D, Francis SM, Tessman DC, Cook EH, Monaco AP, Maestrini E, Pagnamenta AT, Jacob S.

Autism Res. 2014 Apr;7(2):254-63. doi: 10.1002/aur.1365. Epub 2014 Mar 13.

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