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Serajee FJ, Nabi R, Zhong H, Mahbubul Huq AH.
Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism.
PMID:14627686
J Med Genet. 2003 Nov;40(11):e119.

Yonan AL, Alarcon M, Cheng R, Magnusson PK, Spence SJ, Palmer AA, Grunn A, Juo SH, Terwilliger JD, Liu J, Cantor RM, Geschwind DH, Gilliam TC.
A genomewide screen of 345 families for autism-susceptibility loci.
PMID:13680528
Am J Hum Genet. 2003 Oct;73(4):886-97. Epub 2003 Sep 17.

Yonan AL, Palmer AA, Smith KC, Feldman I, Lee HK, Yonan JM, Fischer SG, Pavlidis P, Gilliam TC.
Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction.
PMID:14606695
Genes Brain Behav. 2003 Oct;2(5):303-20.

Nabi R, Zhong H, Serajee FJ, Huq AH.
No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.
PMID:12707945
Am J Med Genet 2003 May 15;119B(1):98-101.

Serajee FJ, Zhong H, Nabi R, Huq AH.
The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism.
PMID:12676915
J Med Genet 2003 Apr;40(4):e42.

Cisternas FA, Vincent JB, Scherer SW, Ray PN.
Cloning and characterization of human CADPS and CADPS2, new members of the Ca(2+)-dependent activator for secretion protein family.
PMID:12659812
Genomics 2003 Mar;81(3):279-91.

Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH.
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
PMID:12610651
Mol Psychiatry 2003 Feb;8(2):186-94.

Zhong H, Serajee FJ, Nabi R, Huq AH.
No association between the EN2 gene and autistic disorder.
PMID:12525552
J Med Genet 2003 Jan;40(1):e4.