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Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.

Flax JF, Hare A, Azaro MA, Vieland VJ, Brzustowicz LM.

J Neurodev Disord. 2010 Dec;2(4):210-223. Epub 2010 Oct 12.


The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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


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.


Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.

Rice ML, Smith SD, Gayán J.

J Neurodev Disord. 2009 Dec;1(4):264-82. doi: 10.1007/s11689-009-9031-x. Epub 2009 Aug 26.


A molecular genetic study of autism and related phenotypes in extended pedigrees.

Piven J, Vieland VJ, Parlier M, Thompson A, O'Conner I, Woodbury-Smith M, Huang Y, Walters KA, Fernandez B, Szatmari P.

J Neurodev Disord. 2013 Oct 5;5(1):30. doi: 10.1186/1866-1955-5-30.


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.


Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder.

Werling DM, Lowe JK, Luo R, Cantor RM, Geschwind DH.

Mol Autism. 2014 Feb 17;5(1):13. doi: 10.1186/2040-2392-5-13.


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.


Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.

Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P; Autism Genome Project (AGP).

J Neurodev Disord. 2011 Jun;3(2):113-23. doi: 10.1007/s11689-011-9072-9. Epub 2011 Jan 19.


Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.

Ylisaukko-oja T, Alarcón M, Cantor RM, Auranen M, Vanhala R, Kempas E, von Wendt L, Järvelä I, Geschwind DH, Peltonen L.

Ann Neurol. 2006 Jan;59(1):145-55.


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.


High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.

Strom SP, Stone JL, Ten Bosch JR, Merriman B, Cantor RM, Geschwind DH, Nelson SF.

Mol Psychiatry. 2010 Oct;15(10):996-1005. doi: 10.1038/mp.2009.41. Epub 2009 May 19.


Quantifying the phenotype in autism spectrum disorders.

Lord C, Leventhal BL, Cook EH Jr.

Am J Med Genet. 2001 Jan 8;105(1):36-8.


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 analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders.

Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon H.

Mol Autism. 2010 Feb 22;1(1):3. doi: 10.1186/2040-2392-1-3.


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.


Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):104-12.


Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.

Woodbury-Smith M, Bilder DA, Morgan J, Jerominski L, Darlington T, Dyer T, Paterson AD, Coon H.

J Neurodev Disord. 2017 Feb 13;9:5. doi: 10.1186/s11689-017-9187-8. eCollection 2017.

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