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Items: 1 to 20 of 163

1.

Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors.

Sakurai T, Ramoz N, Reichert JG, Corwin TE, Kryzak L, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.

Psychiatr Genet. 2006 Dec;16(6):251-7.

PMID:
17106428
2.

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism.

Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Sasaki T, Kato N.

Int J Neuropsychopharmacol. 2009 Feb;12(1):1-10. doi: 10.1017/S1461145708009127. Epub 2008 Jul 30. Erratum in: Int J Neuropsychopharmacol. 2009 Apr;12(3):439. Sasaki, Tsukasa [added].

PMID:
18664314
3.

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.

4.

Family-based association study of TPH1 and TPH2 polymorphisms in autism.

Ramoz N, Cai G, Reichert JG, Corwin TE, Kryzak LA, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):861-7.

PMID:
16958027
5.

Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism.

Ramoz N, Reichert JG, Corwin TE, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.

Biol Psychiatry. 2006 Jul 15;60(2):186-91. Epub 2006 Apr 17.

PMID:
16616719
6.
7.

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
8.

Obsessive-compulsive behaviors in parents of multiplex autism families.

Hollander E, King A, Delaney K, Smith CJ, Silverman JM.

Psychiatry Res. 2003 Jan 25;117(1):11-6.

PMID:
12581816
9.

Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.

Sacco R, Papaleo V, Hager J, Rousseau F, Moessner R, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Curatolo P, Manzi B, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM.

BMC Med Genet. 2007 Mar 8;8:11.

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.

A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.

Stewart SE, Platko J, Fagerness J, Birns J, Jenike E, Smoller JW, Perlis R, Leboyer M, Delorme R, Chabane N, Rauch SL, Jenike MA, Pauls DL.

Arch Gen Psychiatry. 2007 Feb;64(2):209-14.

PMID:
17283288
12.

Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.

Dickel DE, Veenstra-VanderWeele J, Cox NJ, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL.

Arch Gen Psychiatry. 2006 Jul;63(7):778-85.

PMID:
16818867
13.

The relationship between restrictive and repetitive behaviors in individuals with autism and obsessive compulsive symptoms in parents.

Abramson RK, Ravan SA, Wright HH, Wieduwilt K, Wolpert CM, Donnelly SA, Pericak-Vance MA, Cuccaro ML.

Child Psychiatry Hum Dev. 2005 Winter;36(2):155-65.

PMID:
16228144
14.

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
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.

16.

Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.

Lerer E, Levi S, Salomon S, Darvasi A, Yirmiya N, Ebstein RP.

Mol Psychiatry. 2008 Oct;13(10):980-8. Epub 2007 Sep 25.

PMID:
17893705
17.

Genetic susceptibility to obsessive-compulsive hoarding: the contribution of neurotrophic tyrosine kinase receptor type 3 gene.

Alonso P, Gratacòs M, Menchón JM, Segalàs C, González JR, Labad J, Bayés M, Real E, de Cid R, Pertusa A, Escaramís G, Vallejo J, Estivill X.

Genes Brain Behav. 2008 Oct;7(7):778-85. doi: 10.1111/j.1601-183X.2008.00418.x. Epub 2008 Jul 28.

18.

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
19.

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.

Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):628-36. doi: 10.1002/ajmg.b.30655.

PMID:
18205172
20.

Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study.

Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, Sasaki T.

Brain Dev. 2007 Sep;29(8):510-3. Epub 2007 Mar 21.

PMID:
17376622
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