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Results: 1 to 20 of 404

1.

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
[PubMed - indexed for MEDLINE]
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.

Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.

SLI Consortium (SLIC).

Am J Hum Genet. 2004 Jun;74(6):1225-38. Epub 2004 May 3.

PMID:
15133743
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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]
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
12192642
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Two-stage genome-wide linkage scan in keratoconus sib pair families.

Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Hu M, Yang H.

Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3791-5.

PMID:
16936089
[PubMed - indexed for MEDLINE]
Free Article
10.

Linkage analysis of high myopia susceptibility locus in 26 families.

Paget S, Julia S, Vitezica ZG, Soler V, Malecaze F, Calvas P.

Mol Vis. 2008;14:2566-74. Epub 2008 Dec 30.

PMID:
19122830
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

Badner JA, Gershon ES.

Mol Psychiatry. 2002;7(1):56-66.

PMID:
11803446
[PubMed - indexed for MEDLINE]
Free Article
12.

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

Bakker SC, van der Meulen EM, Buitelaar JK, Sandkuijl LA, Pauls DL, Monsuur AJ, van 't Slot R, Minderaa RB, Gunning WB, Pearson PL, Sinke RJ.

Am J Hum Genet. 2003 May;72(5):1251-60. Epub 2003 Apr 4.

PMID:
12679898
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
13680528
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Replication of autism linkage: fine-mapping peak at 17q21.

Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcón M, Nelson SF, Geschwind DH.

Am J Hum Genet. 2005 Jun;76(6):1050-6. Epub 2005 Apr 1.

PMID:
15877280
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Suggestive genetic linkage to chromosome 11p11.2-q12.2 in hereditary prostate cancer families with primary kidney cancer.

Johanneson B, Deutsch K, McIntosh L, Friedrichsen-Karyadi DM, Janer M, Kwon EM, Iwasaki L, Hood L, Ostrander EA, Stanford JL.

Prostate. 2007 May 15;67(7):732-42.

PMID:
17372923
[PubMed - indexed for MEDLINE]
16.

An autosomal genomic screen for autism.

Collaborative Linkage Study of Autism.

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

PMID:
11811142
[PubMed - indexed for MEDLINE]
17.

A genome wide scan for early onset primary hypertension in Scandinavians.

von Wowern F, Bengtsson K, Lindgren CM, Orho-Melander M, Fyhrquist F, Lindblad U, Råstam L, Forsblom C, Kanninen T, Almgren P, Burri P, Katzman P, Groop L, Hulthén UL, Melander O.

Hum Mol Genet. 2003 Aug 15;12(16):2077-81.

PMID:
12913078
[PubMed - indexed for MEDLINE]
Free Article
18.

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.

PMID:
11741194
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

Alarcón M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH.

Mol Psychiatry. 2005 Aug;10(8):747-57.

PMID:
15824743
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]

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