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Items: 1 to 20 of 159

1.

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.

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

Neurosci Lett. 2004 Dec 6;372(3):209-14.

PMID:
15542242
2.

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.

3.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
4.

An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.

Ramoz N, Cai G, Reichert JG, Silverman JM, Buxbaum JD.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1152-8. doi: 10.1002/ajmg.b.30739.

PMID:
18348195
5.

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
6.

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
7.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Jenkins L, Frantz R, Bartlett CW, Goedken R, Childress D, Spence MA, Smith M, Sheffield VC.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):36-44.

PMID:
15892143
8.

GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss.

Addington AM, Gornick M, Duckworth J, Sporn A, Gogtay N, Bobb A, Greenstein D, Lenane M, Gochman P, Baker N, Balkissoon R, Vakkalanka RK, Weinberger DR, Rapoport JL, Straub RE.

Mol Psychiatry. 2005 Jun;10(6):581-8.

PMID:
15505639
9.

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.

10.

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.

11.

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.

Conroy J, Cochrane L, Anney RJ, Sutcliffe JS, Carthy P, Dunlop A, Mullarkey M, O'hici B, Green AJ, Ennis S, Gill M, Gallagher L.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):535-44. doi: 10.1002/ajmg.b.30854.

PMID:
18846500
12.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
13.

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.

Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N.

Am J Med Genet. 1999 Oct 15;88(5):551-6.

PMID:
10490715
14.

Linkage and association of the glutamate receptor 6 gene with autism.

Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T; Paris Autism Research International Sibpair (PARIS) Study.

Mol Psychiatry. 2002;7(3):302-10.

15.

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
16.

Defining the autism minimum candidate gene region on chromosome 7.

Hutcheson HB, Bradford Y, Folstein SE, Gardiner MB, Santangelo SL, Sutcliffe JS, Haines JL.

Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):90-6.

PMID:
12555242
17.

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.

18.

An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.

Curran S, Roberts S, Thomas S, Veltman M, Browne J, Medda E, Pickles A, Sham P, Bolton PF.

Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):25-8.

PMID:
15952184
19.

Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31.

Evans JC, Frayling TM, Ellard S, Gutowski NJ.

Hum Genet. 2000 Jun;106(6):636-8.

PMID:
10942112
20.

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.

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