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Results: 1 to 20 of 28

Cited In for PubMed (Select 11803446)

1.

Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population.

Liang S, Wang XL, Zou MY, Wang H, Zhou X, Sun CH, Xia W, Wu LJ, Fujisawa TX, Tomoda A.

J Zhejiang Univ Sci B. 2014 Mar;15(3):264-71. doi: 10.1631/jzus.B1300133.

2.

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.

Cheng Y, Quinn JF, Weiss LA.

Hum Mol Genet. 2013 Jul 15;22(14):2960-72. doi: 10.1093/hmg/ddt150. Epub 2013 Apr 10.

4.

Comparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia.

Tang B, Thornton-Wells T, Askland KD.

PLoS One. 2011 Apr 29;6(4):e19073. doi: 10.1371/journal.pone.0019073.

5.

Mutations in the TSGA14 gene in families with autism spectrum disorders.

Korvatska O, Estes A, Munson J, Dawson G, Bekris LM, Kohen R, Yu CE, Schellenberg GD, Raskind WH.

Am J Med Genet B Neuropsychiatr Genet. 2011 Apr;156B(3):303-11. doi: 10.1002/ajmg.b.31162. Epub 2011 Jan 13.

6.

Data integration in genetics and genomics: methods and challenges.

Hamid JS, Hu P, Roslin NM, Ling V, Greenwood CM, Beyene J.

Hum Genomics Proteomics. 2009 Jan 12;2009. pii: 869093. doi: 10.4061/2009/869093.

7.

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.

Sousa I, Clark TG, Holt R, Pagnamenta AT, Mulder EJ, Minderaa RB, Bailey AJ, Battaglia A, Klauck SM, Poustka F, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Mol Autism. 2010 Mar 25;1(1):7. doi: 10.1186/2040-2392-1-7.

8.

Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds.

Panaitof SC, Abrahams BS, Dong H, Geschwind DH, White SA.

J Comp Neurol. 2010 Jun 1;518(11):1995-2018. doi: 10.1002/cne.22318.

9.

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.

Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S, Lowy E, Harold DH, Chapman JA, Klauck SM, Poustka F, Houben RH, Staal WG, Ophoff RA, O'Donovan MC, Williams J, Nöthen MM, Schulte-Körne G, Deloukas P, Ragoussis J, Bailey AJ, Maestrini E, Monaco AP; International Molecular Genetic Study Of Autism Consortium.

Biol Psychiatry. 2010 Aug 15;68(4):320-8. doi: 10.1016/j.biopsych.2010.02.002. Epub 2010 Mar 26.

10.

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.

Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes NH, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Minopoli F, Reichert J, Cai G, Buxbaum JD, Korvatska O, Schellenberg GD, Dawson G, de Bildt A, Minderaa RB, Mulder EJ, Morris AP, Bailey AJ, Monaco AP; IMGSAC.

Mol Psychiatry. 2010 Sep;15(9):954-68. doi: 10.1038/mp.2009.34. Epub 2009 Apr 28.

11.

A linkage search for joint panic disorder/bipolar genes.

Logue MW, Durner M, Heiman GA, Hodge SE, Hamilton SP, Knowles JA, Fyer AJ, Weissman MM.

Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1139-46. doi: 10.1002/ajmg.b.30939.

12.

MET and autism susceptibility: family and case-control studies.

Sousa I, Clark TG, Toma C, Kobayashi K, Choma M, Holt R, Sykes NH, Lamb JA, Bailey AJ, Battaglia A, Maestrini E, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Eur J Hum Genet. 2009 Jun;17(6):749-58. doi: 10.1038/ejhg.2008.215. Epub 2008 Nov 12.

13.

Autism: many genes, common pathways?

Geschwind DH.

Cell. 2008 Oct 31;135(3):391-5. doi: 10.1016/j.cell.2008.10.016.

14.

Association of common variants in the Joubert syndrome gene (AHI1) with autism.

Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA, Geschwind DH.

Hum Mol Genet. 2008 Dec 15;17(24):3887-96. doi: 10.1093/hmg/ddn291. Epub 2008 Sep 9.

15.

Advances in autism genetics: on the threshold of a new neurobiology.

Abrahams BS, Geschwind DH.

Nat Rev Genet. 2008 May;9(5):341-55. doi: 10.1038/nrg2346. Review. Erratum in: Nat Rev Genet. 2008 Jun;9(6):493.

16.

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.

Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.

17.

Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.

Rosenberger A, Sharma M, Müller-Myhsok B, Gasser T, Bickeböller H.

BMC Genet. 2007 Jul 2;8:44.

18.

Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage.

Spence SJ, Cantor RM, Chung L, Kim S, Geschwind DH, Alarcón M.

Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):591-8.

19.

Analysis of four DLX homeobox genes in autistic probands.

Hamilton SP, Woo JM, Carlson EJ, Ghanem N, Ekker M, Rubenstein JL.

BMC Genet. 2005 Nov 2;6:52.

20.

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene.

Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA, Schmeidler J, De Gasperi R, Sosa MA, Rabidou D, Santucci AC, Perl D, Morrisey E, Buxbaum JD.

Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9643-8. Epub 2005 Jun 27.

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