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Items: 1 to 20 of 62

1.

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

International Molecular Genetic Study of Autism Consortium (IMGSAC)..

Hum Mol Genet. 2001 Apr 15;10(9):973-82.

PMID:
11392322
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.

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.

Persico AM, D'Agruma L, Maiorano N, Totaro A, Militerni R, Bravaccio C, Wassink TH, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Conciatori M, Marino R, Quattrocchi CC, Baldi A, Zelante L, Gasparini P, Keller F; Collaborative Linkage Study of Autism..

Mol Psychiatry. 2001 Mar;6(2):150-9.

4.

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.

Lord C, Risi S, Lambrecht L, Cook EH Jr, Leventhal BL, DiLavore PC, Pickles A, Rutter M.

J Autism Dev Disord. 2000 Jun;30(3):205-23.

PMID:
11055457
5.

Genetic studies in autistic disorder and chromosome 15.

Bass MP, Menold MM, Wolpert CM, Donnelly SL, Ravan SA, Hauser ER, Maddox LO, Vance JM, Abramson RK, Wright HH, Gilbert JR, Cuccaro ML, DeLong GR, Pericak-Vance MA.

Neurogenetics. 2000 Mar;2(4):219-26.

PMID:
10983717
6.

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP.

Am J Hum Genet. 2000 Aug;67(2):357-68. Epub 2000 Jul 5.

7.

Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32.

Hayashida S, Yamasaki K, Asada Y, Soeda E, Niikawa N, Kishino T.

Genomics. 2000 Jun 1;66(2):221-5.

PMID:
10860668
8.

Genetic clues to the biological basis of autism.

Turner M, Barnby G, Bailey A.

Mol Med Today. 2000 Jun;6(6):238-44. Review.

PMID:
10840382
9.

Variable expression of the autism broader phenotype: findings from extended pedigrees.

Pickles A, Starr E, Kazak S, Bolton P, Papanikolaou K, Bailey A, Goodman R, Rutter M.

J Child Psychol Psychiatry. 2000 May;41(4):491-502.

PMID:
10836679
10.

Plexin/neuropilin complexes mediate repulsion by the axonal guidance signal semaphorin 3A.

Rohm B, Ottemeyer A, Lohrum M, Püschel AW.

Mech Dev. 2000 May;93(1-2):95-104.

11.

The impact of transmission-ratio distortion on allele sharing in affected sibling pairs.

Greenwood CM, Morgan K.

Am J Hum Genet. 2000 Jun;66(6):2001-4. Epub 2000 Apr 20.

12.

Autism: recent molecular genetic advances.

Lamb JA, Moore J, Bailey A, Monaco AP.

Hum Mol Genet. 2000 Apr 12;9(6):861-8. Review. Erratum in: Hum Mol Genet 2000 May 22;9(9):1461.

PMID:
10767308
13.

A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.

Douglas JA, Boehnke M, Lange K.

Am J Hum Genet. 2000 Apr;66(4):1287-97. Epub 2000 Mar 28.

14.

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples.

Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M, Damiani V, Baldi A, Keller F.

Am J Med Genet. 2000 Feb 7;96(1):123-7.

PMID:
10686565
15.

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA.

Am J Med Genet. 2000 Feb 7;96(1):43-8.

PMID:
10686550
16.

Physical and cDNA mapping in the DBH region of human chromosome 9q34.

Gilbert JR, Kumar A, Newey S, Rao N, Ioannou P, Qiu H, Lin D, Xu P, Pettenati MJ, Pericak-Vance MA.

Hum Hered. 2000 May-Jun;50(3):151-7.

PMID:
10686491
17.

A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx genes in the embryonic forebrain.

Zerucha T, Stühmer T, Hatch G, Park BK, Long Q, Yu G, Gambarotta A, Schultz JR, Rubenstein JL, Ekker M.

J Neurosci. 2000 Jan 15;20(2):709-21.

18.
19.

Association study of the NF1 gene and autistic disorder.

Mbarek O, Marouillat S, Martineau J, Barthélémy C, Müh JP, Andres C.

Am J Med Genet. 1999 Dec 15;88(6):729-32.

PMID:
10581497
20.

Transmission ratio distortion in females on chromosome 10p11-p15.

Paterson AD, Petronis A.

Am J Med Genet. 1999 Dec 15;88(6):657-61.

PMID:
10581486

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