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Items: 1 to 20 of 147

1.

A genome-wide linkage and association scan reveals novel loci for autism.

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A.

Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490.

2.

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.

3.

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.

Cheng Y, Quinn JF, Weiss LA.

Hum Mol Genet. 2013 Jul 15;22(14):2960-72. doi: 10.1093/hmg/ddt150. Epub 2013 Apr 10.

4.

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.

Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, Martin ER, Hussman JP, Gilbert JR, Cuccaro ML, Haines JL, Pericak-Vance MA.

Ann Hum Genet. 2009 May;73(Pt 3):263-73. doi: 10.1111/j.1469-1809.2009.00523.x.

5.

Common genetic variants on 1p13.2 associate with risk of autism.

Xia K, Guo H, Hu Z, Xun G, Zuo L, Peng Y, Wang K, He Y, Xiong Z, Sun L, Pan Q, Long Z, Zou X, Li X, Li W, Xu X, Lu L, Liu Y, Hu Y, Tian D, Long L, Ou J, Liu Y, Li X, Zhang L, Pan Y, Chen J, Peng H, Liu Q, Luo X, Su W, Wu L, Liang D, Dai H, Yan X, Feng Y, Tang B, Li J, Miedzybrodzka Z, Xia J, Zhang Z, Luo X, Zhang X, St Clair D, Zhao J, Zhang F.

Mol Psychiatry. 2014 Nov;19(11):1212-9. doi: 10.1038/mp.2013.146. Epub 2013 Nov 5.

PMID:
24189344
6.

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.

7.

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.

Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD.

Am J Psychiatry. 2004 Apr;161(4):662-9.

PMID:
15056512
8.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
9.

A genomewide screen for autism susceptibility loci.

Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC; Autism Genetic Resource Exchange Consortium.

Am J Hum Genet. 2001 Aug;69(2):327-40. Epub 2001 Jul 10.

10.

Analysis of the RELN gene as a genetic risk factor for autism.

Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA.

Mol Psychiatry. 2005 Jun;10(6):563-71.

PMID:
15558079
11.

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
12.

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
13.

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.

Barnby G, Abbott A, Sykes N, Morris A, Weeks DE, Mott R, Lamb J, Bailey AJ, Monaco AP; International Molecular Genetics Study of Autism Consortium.

Am J Hum Genet. 2005 Jun;76(6):950-66. Epub 2005 Apr 13.

14.

Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families.

Ammar M, Bouchlaka-Souissi C, Helms CA, Zaraa I, Jordan CT, Anbunathan H, Bouhaha R, Kouidhi S, Doss N, Dhaoui R, Ben Osman A, Ben Ammar El Gaied A, Marrakchi R, Mokni M, Bowcock AM.

Br J Dermatol. 2013 Mar;168(3):583-7. doi: 10.1111/bjd.12050.

PMID:
23013406
15.

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA.

Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Review.

PMID:
19895225
16.

Defining the contribution of CNTNAP2 to autism susceptibility.

Sampath S, Bhat S, Gupta S, O'Connor A, West AB, Arking DE, Chakravarti A.

PLoS One. 2013 Oct 17;8(10):e77906. doi: 10.1371/journal.pone.0077906. eCollection 2013.

17.

Association of Reelin gene polymorphisms with autism.

Serajee FJ, Zhong H, Mahbubul Huq AH.

Genomics. 2006 Jan;87(1):75-83. Epub 2005 Nov 28.

18.

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):528-33. doi: 10.1038/nature07999. Epub 2009 Apr 28.

19.

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.

Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.

20.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

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