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Items: 16

1.

Parent-of-origin effects of the serotonin transporter gene associated with autism.

Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH Jr.

Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):139-44. doi: 10.1002/ajmg.b.31146. Epub 2010 Dec 8.

2.

Family-based association testing of glutamate transporter genes in autism.

Jacob S, Brune CW, Badner JA, Ernstrom K, Courchesne E, Lord C, Leventhal BL, Cook EH, Kim SJ.

Psychiatr Genet. 2011 Aug;21(4):212-3. doi: 10.1097/YPG.0b013e328341a323. No abstract available.

3.

A pharmacogenetic study of escitalopram in autism spectrum disorders.

Owley T, Brune CW, Salt J, Walton L, Guter S, Ayuyao N, Gibbons RD, Leventhal BL, Cook EH.

Autism Res. 2010 Feb;3(1):1-7. doi: 10.1002/aur.109.

4.

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.

Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH Jr, Macdonald RL, Sutcliffe JS.

Mol Psychiatry. 2011 Jan;16(1):86-96. doi: 10.1038/mp.2009.118. Epub 2009 Nov 24.

5.

A genome-wide linkage and association scan reveals novel loci for autism.

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A.

Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490.

6.

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.

7.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):569-73. doi: 10.1038/nature07953. Epub 2009 Apr 28.

8.

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):528-33. doi: 10.1038/nature07999. Epub 2009 Apr 28.

9.

Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample.

Brune CW, Kim SJ, Hanna GL, Courchesne E, Lord C, Leventhal BL, Cook EH.

Autism Res. 2008 Apr;1(2):108-13. doi: 10.1002/aur.11.

10.

Association and mutation analyses of 16p11.2 autism candidate genes.

Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL.

PLoS One. 2009;4(2):e4582. doi: 10.1371/journal.pone.0004582. Epub 2009 Feb 26.

11.

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

Christian SL, Brune CW, Sudi J, Kumar RA, Liu S, Karamohamed S, Badner JA, Matsui S, Conroy J, McQuaid D, Gergel J, Hatchwell E, Gilliam TC, Gershon ES, Nowak NJ, Dobyns WB, Cook EH Jr.

Biol Psychiatry. 2008 Jun 15;63(12):1111-7. doi: 10.1016/j.biopsych.2008.01.009. Epub 2008 Mar 28.

12.

Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.

Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1116-25. doi: 10.1002/ajmg.b.30733.

13.

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A.

Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015.

14.

Heterogeneous association between engrailed-2 and autism in the CPEA network.

Brune CW, Korvatska E, Allen-Brady K, Cook EH Jr, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):187-93.

PMID:
17948868
15.

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism.

Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH Jr.

Neurosci Lett. 2007 Apr 24;417(1):6-9. Epub 2007 Feb 3.

16.

5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism.

Brune CW, Kim SJ, Salt J, Leventhal BL, Lord C, Cook EH Jr.

Am J Psychiatry. 2006 Dec;163(12):2148-56.

PMID:
17151167

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