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Items: 1 to 20 of 152

1.

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

Molloy CA, Keddache M, Martin LJ.

Mol Psychiatry. 2005 Aug;10(8):741-6.

PMID:
15940295
2.
3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

Response to paper by Molloy et al.: linkage on 21q and 7q in autism subset with regression.

Parr JR, Lamb JA, Bailey AJ, Monaco AP.

Mol Psychiatry. 2006 Jul;11(7):617-9; author reply 619. No abstract available.

PMID:
16801976
6.

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.

Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E, Lawlor BA, Fitzgerald M, Greenberg DA, Davis KL.

Am J Hum Genet. 2001 Jun;68(6):1514-20. Epub 2001 May 14. Erratum in: Am J Hum Genet 2001 Aug;69(2):470.

7.

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.

Alarcón M, Cantor RM, Liu J, Gilliam TC, Geschwind DH; Autism Genetic Research Exchange Consortium.

Am J Hum Genet. 2002 Jan;70(1):60-71. Epub 2001 Dec 6.

8.

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.

9.

Ordered-subset analysis of savant skills in autism for 15q11-q13.

Ma DQ, Jaworski J, Menold MM, Donnelly S, Abramson RK, Wright HH, Delong GR, Gilbert JR, Pericak-Vance MA, Cuccaro ML.

Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):38-41.

PMID:
15756693
10.

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
11.

An autosomal genomic screen for autism.

Collaborative Linkage Study of Autism.

Am J Med Genet. 2001 Dec 8;105(8):609-15.

PMID:
11811142
12.

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.

Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, Abramson RK, Wright HH, DeLong GR, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2003 Mar;72(3):539-48. Epub 2003 Feb 3.

13.

Incorporating language phenotypes strengthens evidence of linkage to autism.

Collaborative Linkage Study of Autism.

Am J Med Genet. 2001 Dec 8;105(8):539-47.

PMID:
11811141
14.

Incorporating language phenotypes strengthens evidence of linkage to autism.

Bradford Y, Haines J, Hutcheson H, Gardiner M, Braun T, Sheffield V, Cassavant T, Huang W, Wang K, Vieland V, Folstein S, Santangelo S, Piven J.

Am J Med Genet. 2001 Aug 8;105(6):539-47. Erratum in: Am J Med Genet. 2001 Dec 8;105(8):805. Corrected and republished in: Am J Med Genet. 2001 Dec 8;105(8):539-47.

PMID:
11496372
15.

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
16.

An autosomal genomic screen for autism. Collaborative linkage study of autism.

Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL, Childress D, Folstein SE, Garcia M, Gardiner MB, Gilman S, Haines JL, Hopkins K, Landa R, Meyer NH, Mullane JA, Nishimura DY, Palmer P, Piven J, Purdy J, Santangelo SL, Searby C, Sheffield V, Singleton J, Slager S, et al.

Am J Med Genet. 1999 Dec 15;88(6):609-15. Erratum in: Am J Med Genet. 2001 Dec 8;105(8):805. Corrected and republished in: Am J Med Genet. 2001 Dec 8;105(8):609-15.

PMID:
10581478
17.

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.

Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, Sinsheimer JS, Peltonen L, Järvelä I.

Am J Hum Genet. 2002 Oct;71(4):777-90. Epub 2002 Aug 21.

18.

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].

19.

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.

PMID:
16880825
20.

Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.

BMC Med Genet. 2007 Dec 6;8:74.

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