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Items: 1 to 20 of 121

1.

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.

Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM.

Hum Genet. 2011 Jan;129(1):59-70. doi: 10.1007/s00439-010-0899-z. Epub 2010 Oct 21.

2.

Evidence for multiple loci from a genome scan of autism kindreds.

Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.

Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. Epub 2006 Aug 1.

3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.

Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP.

J Med Genet. 2011 Jan;48(1):48-54. doi: 10.1136/jmg.2010.079426. Epub 2010 Oct 23.

5.

Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.

Field LL, Shumansky K, Ryan J, Truong D, Swiergala E, Kaplan BJ.

Genes Brain Behav. 2013 Feb;12(1):56-69. doi: 10.1111/gbb.12003. Epub 2012 Dec 7.

6.

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.

7.

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

Liu XQ, Paterson AD, Szatmari P; Autism Genome Project Consortium.

Biol Psychiatry. 2008 Oct 1;64(7):561-70. doi: 10.1016/j.biopsych.2008.05.023. Epub 2008 Jul 16.

8.

Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample.

Dick DM, Aliev F, Bierut L, Goate A, Rice J, Hinrichs A, Bertelsen S, Wang JC, Dunn G, Kuperman S, Schuckit M, Nurnberger J Jr, Porjesz B, Beglieter H, Kramer J, Hesselbrock V.

Behav Genet. 2006 Jan;36(1):77-86. Epub 2005 Dec 10.

PMID:
16341907
9.
10.

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.

11.

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
12.

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.

Posthuma D, Luciano M, Geus EJ, Wright MJ, Slagboom PE, Montgomery GW, Boomsma DI, Martin NG.

Am J Hum Genet. 2005 Aug;77(2):318-26. Epub 2005 Jul 1.

13.

Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.

Kilpinen H, Ylisaukko-oja T, Rehnström K, Gaál E, Turunen JA, Kempas E, von Wendt L, Varilo T, Peltonen L.

Hum Mol Genet. 2009 Aug 1;18(15):2912-21. doi: 10.1093/hmg/ddp229. Epub 2009 May 19.

14.

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Råstam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M.

Hum Mol Genet. 1999 May;8(5):805-12. Erratum in: Hum Mol Genet 1999 Jul;8(7):1353. van Malldergerme L [corrected to Van Maldergem L].

PMID:
10196369
15.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.

Mol Psychiatry. 2007 Apr;12(4):376-84. Epub 2006 Dec 19.

PMID:
17179998
16.

The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.

Hippolyte L, Maillard AM, Rodriguez-Herreros B, Pain A, Martin-Brevet S, Ferrari C, Conus P, Macé A, Hadjikhani N, Metspalu A, Reigo A, Kolk A, Männik K, Barker M, Isidor B, Le Caignec C, Mignot C, Schneider L, Mottron L, Keren B, David A, Doco-Fenzy M, Gérard M, Bernier R, Goin-Kochel RP, Hanson E, Green Snyder L; 16p11.2 European Consortium, Simons Variation in Individuals Project Consortium, Ramus F, Beckmann JS, Draganski B, Reymond A, Jacquemont S.

Biol Psychiatry. 2016 Jul 15;80(2):129-39. doi: 10.1016/j.biopsych.2015.10.021. Epub 2015 Nov 10.

17.

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.

Auranen M, Nieminen T, Majuri S, Vanhala R, Peltonen L, Järvelä I.

Mol Psychiatry. 2000 May;5(3):320-2.

PMID:
10889536
18.

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

International Molecular Genetic Study of Autism Consortium (IMGSAC).

Am J Hum Genet. 2001 Sep;69(3):570-81. Epub 2001 Jul 30.

19.

A genomewide screen of 345 families for autism-susceptibility loci.

Yonan AL, Alarcón M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC.

Am J Hum Genet. 2003 Oct;73(4):886-97. Epub 2003 Sep 17.

20.

Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.

Fradin D, Cheslack-Postava K, Ladd-Acosta C, Newschaffer C, Chakravarti A, Arking DE, Feinberg A, Fallin MD.

PLoS One. 2010 Sep 2;5(9). pii: e12513. doi: 10.1371/journal.pone.0012513.

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