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A genome scan for loci shared by autism spectrum disorder and language impairment.

Bartlett CW, Hou L, Flax JF, Hare A, Cheong SY, Fermano Z, Zimmerman-Bier B, Cartwright C, Azaro MA, Buyske S, Brzustowicz LM.

Am J Psychiatry. 2014 Jan;171(1):72-81. doi: 10.1176/appi.ajp.2013.12081103.


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.


Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS.

BMC Med Genet. 2005 Jan 12;6:1.


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].


The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.


Autism and specific language impairment: to know what we see, or how your sample determines what you observe.

Kim YS.

Am J Psychiatry. 2014 Jan;171(1):5-8. doi: 10.1176/appi.ajp.2013.13101379. No abstract available.


Brief report: do the nature of communication impairments in autism spectrum disorders relate to the broader autism phenotype in parents?

Taylor LJ, Maybery MT, Wray J, Ravine D, Hunt A, Whitehouse AJ.

J Autism Dev Disord. 2013 Dec;43(12):2984-9. doi: 10.1007/s10803-013-1838-3.


A quantitative trait locus analysis of social responsiveness in multiplex autism families.

Duvall JA, Lu A, Cantor RM, Todd RD, Constantino JN, Geschwind DH.

Am J Psychiatry. 2007 Apr;164(4):656-62. Erratum in: Am J Psychiatry. 2007 Jun;164(6):980.


Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.

Ryu S, Won HH, Oh S, Kim JW, Park T, Cho EY, Cho Y, Park DY, Lee YS, Kwon JS, Hong KS.

Psychiatry Res. 2013 Dec 30;210(3):756-60. doi: 10.1016/j.psychres.2013.08.015. Epub 2013 Sep 12.


Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.

Liu XQ, Georgiades S, Duku E, Thompson A, Devlin B, Cook EH, Wijsman EM, Paterson AD, Szatmari P.

J Am Acad Child Adolesc Psychiatry. 2011 Jul;50(7):687-696.e13. doi: 10.1016/j.jaac.2011.05.002.


Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.

Chen GK, Kono N, Geschwind DH, Cantor RM.

Mol Psychiatry. 2006 Feb;11(2):214-20.


QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders.

Lu AT, Yoon J, Geschwind DH, Cantor RM.

Mol Psychiatry. 2013 Feb;18(2):226-35. doi: 10.1038/mp.2011.155. Epub 2011 Nov 22.


Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8.

Lowe JK, Werling DM, Constantino JN, Cantor RM, Geschwind DH.

Am J Psychiatry. 2015 Mar 1;172(3):266-75. doi: 10.1176/appi.ajp.2014.14050576. Epub 2014 Nov 7.


Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.

Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, DeMille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR.

Hum Genet. 2016 Dec;135(12):1329-1341. Epub 2016 Aug 17.


Autism spectrum and obsessive-compulsive disorders: OC behaviors, phenotypes and genetics.

Jacob S, Landeros-Weisenberger A, Leckman JF.

Autism Res. 2009 Dec;2(6):293-311. doi: 10.1002/aur.108. Review.


Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder.

Vardarajan BN, Eran A, Jung JY, Kunkel LM, Wall DP.

Transl Psychiatry. 2013 May 28;3:e262. doi: 10.1038/tp.2013.38.


A genomewide scan identifies two novel loci involved in specific language impairment.

SLI Consortium.

Am J Hum Genet. 2002 Feb;70(2):384-98. Epub 2002 Jan 4.


Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive-compulsive disorder: Results from the OCD Collaborative Genetics Study.

Samuels J, Shugart YY, Wang Y, Grados MA, Bienvenu OJ, Pinto A, Rauch SL, Greenberg BD, Knowles JA, Fyer AJ, Piacentini J, Pauls DL, Cullen B, Rasmussen SA, Stewart SE, Geller DA, Maher BS, Goes FS, Murphy DL, McCracken JT, Riddle MA, Nestadt G.

Am J Med Genet B Neuropsychiatr Genet. 2014 Jun;165B(4):326-36. doi: 10.1002/ajmg.b.32235. Epub 2014 May 4.


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