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Results: 1 to 20 of 140

1.

A high-density SNP genome-wide linkage scan in a large autism extended pedigree.

Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, Krasny L, Pingree C, Lainhart J, Leppert M, McMahon WM, Coon H.

Mol Psychiatry. 2009 Jun;14(6):590-600. doi: 10.1038/mp.2008.14. Epub 2008 Feb 19.

PMID:
18283277
[PubMed - indexed for MEDLINE]
2.

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.

McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS.

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):51-9.

PMID:
15389768
[PubMed - indexed for MEDLINE]
3.

Support for schizophrenia susceptibility locus on chromosome 2q detected in a Swedish isolate using a dense map of microsatellites and SNPs.

Aberg K, Axelsson E, Saetre P, Jiang L, Wetterberg L, Pettersson U, Lindholm E, Jazin E.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1238-44. doi: 10.1002/ajmg.b.30762.

PMID:
18449909
[PubMed - indexed for MEDLINE]
4.

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.

Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS.

Mol Psychiatry. 2003 Jun;8(6):624-34, 570.

PMID:
12851639
[PubMed - indexed for MEDLINE]
5.

A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba.

Marcheco-Teruel B, Flint TJ, Wikman FP, Torralbas M, González L, Blanco L, Tan Q, Ewald H, Orntoft T, Kruse TA, Børglum AD, Mors O.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):833-43.

PMID:
16917938
[PubMed - indexed for MEDLINE]
6.

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]
7.

Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.

Guhathakurta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Gangopadhyay PK, Usha R.

Brain Res. 2008 Nov 13;1240:12-21. doi: 10.1016/j.brainres.2008.08.063. Epub 2008 Sep 4.

PMID:
18804097
[PubMed - indexed for MEDLINE]
8.

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.

Hutcheson HB, Olson LM, Bradford Y, Folstein SE, Santangelo SL, Sutcliffe JS, Haines JL.

BMC Med Genet. 2004 May 5;5:12.

PMID:
15128462
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

High density SNP association study of a major autism linkage region on chromosome 17.

Stone JL, Merriman B, Cantor RM, Geschwind DH, Nelson SF.

Hum Mol Genet. 2007 Mar 15;16(6):704-15. Epub 2007 Mar 21.

PMID:
17376794
[PubMed - indexed for MEDLINE]
Free Article
10.

Evidence supporting WNT2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Huang J, Swiderski RE, Pietila J, Braun T, Beck G, Folstein SE, Haines JL, Sheffield VC.

Am J Med Genet. 2001 Jul 8;105(5):406-13.

PMID:
11449391
[PubMed - indexed for MEDLINE]
11.

Genome-wide linkage scan for nicotine dependence in European Americans and its converging results with African Americans in the Mid-South Tobacco Family sample.

Li MD, Ma JZ, Payne TJ, Lou XY, Zhang D, Dupont RT, Elston RC.

Mol Psychiatry. 2008 Apr;13(4):407-16. Epub 2007 Jun 19.

PMID:
17579606
[PubMed - indexed for MEDLINE]
12.

A heterogeneity-based genome search meta-analysis for autism-spectrum disorders.

Trikalinos TA, Karvouni A, Zintzaras E, Ylisaukko-oja T, Peltonen L, Järvelä I, Ioannidis JP.

Mol Psychiatry. 2006 Jan;11(1):29-36.

PMID:
16189507
[PubMed - indexed for MEDLINE]
13.

No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.

Nabi R, Zhong H, Serajee FJ, Huq AH.

Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):98-101.

PMID:
12707945
[PubMed - indexed for MEDLINE]
14.

Lack of association between autism and SLC25A12.

Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Am J Psychiatry. 2006 May;163(5):929-31.

PMID:
16648338
[PubMed - indexed for MEDLINE]
15.

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
16.

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
[PubMed - indexed for MEDLINE]
Free Article
17.

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.

Li H, Li Y, Shao J, Li R, Qin Y, Xie C, Zhao Z.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):194-200.

PMID:
17955477
[PubMed - indexed for MEDLINE]
18.

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.

Philippi A, Roschmann E, Tores F, Lindenbaum P, Benajou A, Germain-Leclerc L, Marcaillou C, Fontaine K, Vanpeene M, Roy S, Maillard S, Decaulne V, Saraiva JP, Brooks P, Rousseau F, Hager J.

Mol Psychiatry. 2005 Oct;10(10):950-60.

PMID:
16027742
[PubMed - indexed for MEDLINE]
19.
20.

Evaluation of FOXP2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, Sheffield VC.

Am J Med Genet. 2002 Jul 8;114(5):566-9.

PMID:
12116195
[PubMed - indexed for MEDLINE]

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