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Results: 1 to 20 of 92

1.

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.

PMID:
21125004
[PubMed]
Free PMC Article
2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
15647115
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
19997522
[PubMed]
Free PMC Article
5.

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.

PMID:
24093601
[PubMed]
Free PMC Article
6.

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.

Bartlett CW, Flax JF, Logue MW, Smith BJ, Vieland VJ, Tallal P, Brzustowicz LM.

Hum Hered. 2004;57(1):10-20.

PMID:
15133308
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

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.

PMID:
21484201
[PubMed]
Free PMC Article
8.

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.

PMID:
24533643
[PubMed]
Free PMC Article
9.

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.

PMID:
16752361
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

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.

PMID:
24170272
[PubMed - indexed for MEDLINE]
11.

A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism.

Talebizadeh Z, Arking DE, Hu VW.

PLoS One. 2013 Jun 26;8(6):e67569. Print 2013.

PMID:
23840741
[PubMed - as supplied by publisher]
Free PMC Article
12.

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.

PMID:
17403980
[PubMed - indexed for MEDLINE]
13.

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.

PMID:
16288458
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
20678246
[PubMed]
Free PMC Article
15.

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.

PMID:
11424991
[PubMed - indexed for MEDLINE]
16.

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N, Reichert JG.

Mol Psychiatry. 2004 Feb;9(2):144-50.

PMID:
14699429
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
21703496
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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.

PMID:
15108191
[PubMed - indexed for MEDLINE]
19.

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families.

Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H.

Autism Res. 2010 Apr;3(2):47-52. doi: 10.1002/aur.119.

PMID:
20437600
[PubMed - indexed for MEDLINE]
20.

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79. Epub 2005 Jul 1.

PMID:
15995945
[PubMed - indexed for MEDLINE]
Free PMC Article

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