Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 55

1.

Females in the Juvenile Justice System: Who Are They and How Do They Fare?

Bright CL, Kohl PL, Jonson-Reid M.

Crime Delinq. 2014 Feb 1;60(1):106-125.

PMID:
24683203
[PubMed]
Free PMC Article
2.

Autism risk factors: genes, environment, and gene-environment interactions.

Chaste P, Leboyer M.

Dialogues Clin Neurosci. 2012 Sep;14(3):281-92. Review.

PMID:
23226953
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

Sharma JR, Arieff Z, Gameeldien H, Davids M, Kaur M, van der Merwe L.

Genet Test Mol Biomarkers. 2013 Feb;17(2):93-8. doi: 10.1089/gtmb.2012.0212. Epub 2012 Dec 5.

PMID:
23216241
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Comparison of Methods for Identifying Phenotype Subgroups Using Categorical Features Data With Application to Autism Spectrum Disorder.

Gebregziabher M, Shotwell MS, Charles JM, Nicholas JS.

Comput Stat Data Anal. 2012 Jan 1;56(1):114-125.

PMID:
21927523
[PubMed]
Free PMC Article
5.

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders.

Schaaf CP, Sabo A, Sakai Y, Crosby J, Muzny D, Hawes A, Lewis L, Akbar H, Varghese R, Boerwinkle E, Gibbs RA, Zoghbi HY.

Hum Mol Genet. 2011 Sep 1;20(17):3366-75. doi: 10.1093/hmg/ddr243. Epub 2011 May 30.

PMID:
21624971
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders.

Kim SJ, Silva RM, Flores CG, Jacob S, Guter S, Valcante G, Zaytoun AM, Cook EH, Badner JA.

Mol Autism. 2011 May 24;2(1):8. doi: 10.1186/2040-2392-2-8.

PMID:
21609426
[PubMed]
Free PMC Article
7.

The pathophysiology of restricted repetitive behavior.

Lewis M, Kim SJ.

J Neurodev Disord. 2009 Jun;1(2):114-32. doi: 10.1007/s11689-009-9019-6. Epub 2009 Jun 16.

PMID:
21547711
[PubMed]
Free PMC Article
8.

Glyoxalase I polymorphism rs2736654 causing the Ala111Glu substitution modulates enzyme activity--implications for autism.

Barua M, Jenkins EC, Chen W, Kuizon S, Pullarkat RK, Junaid MA.

Autism Res. 2011 Aug;4(4):262-70. doi: 10.1002/aur.197. Epub 2011 Apr 12.

PMID:
21491613
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Mutations in the TSGA14 gene in families with autism spectrum disorders.

Korvatska O, Estes A, Munson J, Dawson G, Bekris LM, Kohen R, Yu CE, Schellenberg GD, Raskind WH.

Am J Med Genet B Neuropsychiatr Genet. 2011 Apr;156B(3):303-11. doi: 10.1002/ajmg.b.31162. Epub 2011 Jan 13.

PMID:
21438139
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Neurobehavioral abnormalities in first-degree relatives of individuals with autism.

Mosconi MW, Kay M, D'Cruz AM, Guter S, Kapur K, Macmillan C, Stanford LD, Sweeney JA.

Arch Gen Psychiatry. 2010 Aug;67(8):830-40. doi: 10.1001/archgenpsychiatry.2010.87. Erratum in: Arch Gen Psychiatry. 2011 Jan;68(1):60.

PMID:
20679591
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Candidate gene study of HOXB1 in autism spectrum disorder.

Muscarella LA, Guarnieri V, Sacco R, Curatolo P, Manzi B, Alessandrelli R, Giana G, Militerni R, Bravaccio C, Lenti C, Saccani M, Schneider C, Melmed R, D'Agruma L, Persico AM.

Mol Autism. 2010 May 25;1(1):9. doi: 10.1186/2040-2392-1-9.

PMID:
20678259
[PubMed]
Free PMC Article
12.

Overlaps between autism and language impairment: phenomimicry or shared etiology?

Bishop DV.

Behav Genet. 2010 Sep;40(5):618-29. doi: 10.1007/s10519-010-9381-x. Epub 2010 Jul 18.

PMID:
20640915
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Pharmacology and genetics of autism: implications for diagnosis and treatment.

Brkanac Z, Raskind WH, King BH.

Per Med. 2008 Nov;5(6):599-607.

PMID:
19727434
[PubMed]
Free PMC Article
14.

Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.

Ma DQ, Rabionet R, Konidari I, Jaworski J, Cukier HN, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA, Martin ER.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):477-83. doi: 10.1002/ajmg.b.31003.

PMID:
19588468
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.

Sykes NH, Toma C, Wilson N, Volpi EV, Sousa I, Pagnamenta AT, Tancredi R, Battaglia A, Maestrini E, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC).

Eur J Hum Genet. 2009 Oct;17(10):1347-53. doi: 10.1038/ejhg.2009.47. Epub 2009 Apr 22.

PMID:
19384346
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Density of cerebellar basket and stellate cells in autism: evidence for a late developmental loss of Purkinje cells.

Whitney ER, Kemper TL, Rosene DL, Bauman ML, Blatt GJ.

J Neurosci Res. 2009 Aug 1;87(10):2245-54. doi: 10.1002/jnr.22056.

PMID:
19301429
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

The role of rare structural variants in the genetics of autism spectrum disorders.

Kusenda M, Sebat J.

Cytogenet Genome Res. 2008;123(1-4):36-43. doi: 10.1159/000184690. Epub 2009 Mar 11.

PMID:
19287137
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.

Newbury DF, Warburton PC, Wilson N, Bacchelli E, Carone S; International Molecular Genetic Study of Autism Consortium, Lamb JA, Maestrini E, Volpi EV, Mohammed S, Baird G, Monaco AP.

Am J Med Genet A. 2009 Feb 15;149A(4):588-97. doi: 10.1002/ajmg.a.32704.

PMID:
19267418
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Examination of association of genes in the serotonin system to autism.

Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Neurogenetics. 2009 Jul;10(3):209-16. doi: 10.1007/s10048-009-0171-7. Epub 2009 Jan 28.

PMID:
19184136
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Association of common variants in the Joubert syndrome gene (AHI1) with autism.

Alvarez Retuerto AI, Cantor RM, Gleeson JG, Ustaszewska A, Schackwitz WS, Pennacchio LA, Geschwind DH.

Hum Mol Genet. 2008 Dec 15;17(24):3887-96. doi: 10.1093/hmg/ddn291. Epub 2008 Sep 9.

PMID:
18782849
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk