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Items: 1 to 20 of 218

1.

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Castermans D, Vermeesch JR, Fryns JP, Steyaert JG, Van de Ven WJ, Creemers JW, Devriendt K.

Eur J Hum Genet. 2007 Apr;15(4):422-31. Epub 2007 Feb 7.

2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
3.

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

Castermans D, Wilquet V, Steyaert J, Van de Ven W, Fryns JP, Devriendt K.

Autism. 2004 Jun;8(2):141-61. Review.

PMID:
15165431
4.

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.

Castermans D, Volders K, Crepel A, Backx L, De Vos R, Freson K, Meulemans S, Vermeesch JR, Schrander-Stumpel CT, De Rijk P, Del-Favero J, Van Geet C, Van De Ven WJ, Steyaert JG, Devriendt K, Creemers JW.

Hum Mol Genet. 2010 Apr 1;19(7):1368-78. doi: 10.1093/hmg/ddq013. Epub 2010 Jan 12.

5.

Identification and characterization of TRIP8 gene in silico.

Katoh M, Katoh M.

Int J Mol Med. 2003 Nov;12(5):817-21.

PMID:
14533015
6.

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.

7.

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.

Ramanathan S, Woodroffe A, Flodman PL, Mays LZ, Hanouni M, Modahl CB, Steinberg-Epstein R, Bocian ME, Spence MA, Smith M.

BMC Med Genet. 2004 Apr 16;5:10.

8.

The creatine transporter gene paralogous at 16p11.2 is expressed in human brain.

Bayou N, M'rad R, Belhaj A, Daoud H, Zemni R, Briault S, Helayem MB, Ben Jemaa L, Chaabouni H.

Comp Funct Genomics. 2008:609684. doi: 10.1155/2008/609684.

9.

Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders.

Vorsanova SG, Yurov IY, Demidova IA, Voinova-Ulas VY, Kravets VS, Solov'ev IV, Gorbachevskaya NL, Yurov YB.

Neurosci Behav Physiol. 2007 Jul;37(6):553-8.

PMID:
17657425
10.

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
11.

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.

Vincent JB, Herbrick JA, Gurling HM, Bolton PF, Roberts W, Scherer SW.

Am J Hum Genet. 2000 Aug;67(2):510-4. Epub 2000 Jul 7.

12.

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
13.

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.

Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K.

Genet Couns. 2004;15(3):293-301.

PMID:
15517821
14.

Autism-associated familial microdeletion of Xp11.22.

Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, Lewis ME.

Clin Genet. 2008 Aug;74(2):134-44. doi: 10.1111/j.1399-0004.2008.01028.x. Epub 2008 May 21.

PMID:
18498374
15.

An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.

Vincent JB, Horike SI, Choufani S, Paterson AD, Roberts W, Szatmari P, Weksberg R, Fernandez B, Scherer SW.

J Med Genet. 2006 May;43(5):429-34. Epub 2006 Mar 23.

16.

Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.

Vincent JB, Noor A, Windpassinger C, Gianakopoulos PJ, Schwarzbraun T, Alfred SE, Stachowiak B, Scherer SW, Roberts W, Wagner K, Kroisel PM, Petek E.

Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):817-26. doi: 10.1002/ajmg.b.30903.

PMID:
19086034
17.

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.

Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, Yen M, Nowak NJ, Cook EH, Christian SL, Dobyns WB.

J Med Genet. 2010 Feb;47(2):81-90. doi: 10.1136/jmg.2008.065821. Epub 2009 Jun 21.

18.

Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.

Floris C, Rassu S, Boccone L, Gasperini D, Cao A, Crisponi L.

Eur J Hum Genet. 2008 Jun;16(6):696-704. doi: 10.1038/ejhg.2008.7. Epub 2008 Feb 13.

19.

Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction.

Yonan AL, Palmer AA, Smith KC, Feldman I, Lee HK, Yonan JM, Fischer SG, Pavlidis P, Gilliam TC.

Genes Brain Behav. 2003 Oct;2(5):303-20.

20.

Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility.

Cukier HN, Skaar DA, Rayner-Evans MY, Konidari I, Whitehead PL, Jaworski JM, Cuccaro ML, Pericak-Vance MA, Gilbert JR.

Autism Res. 2009 Oct;2(5):258-66. doi: 10.1002/aur.96.

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