Brune CW - Search Results

1

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. Arking DE, et al. Among authors: brune cw. Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015. Am J Hum Genet. 2008. PMID: 18179894 Free PMC article.

2

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. Weiss LA, et al. Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490. Nature. 2009. PMID: 19812673 Free PMC article.

3

Recurrent 16p11.2 microdeletions in autism.

Kumar RA, KaraMohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH Jr, Dobyns WB, Christian SL. Kumar RA, et al. Hum Mol Genet. 2008 Feb 15;17(4):628-38. doi: 10.1093/hmg/ddm376. Epub 2007 Dec 21. Hum Mol Genet. 2008. PMID: 18156158

4

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. Kim SJ, et al. Among authors: brune cw. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1116-25. doi: 10.1002/ajmg.b.30733. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18361419 Free PMC article.

5

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. Kistner-Griffin E, et al. Among authors: brune cw. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):139-44. doi: 10.1002/ajmg.b.31146. Epub 2010 Dec 8. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302342 Free PMC article.

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. Kumar RA, et al. Among authors: brune cw. J Med Genet. 2010 Feb;47(2):81-90. doi: 10.1136/jmg.2008.065821. Epub 2009 Jun 21. J Med Genet. 2010. PMID: 19546099 Free PMC article.

7

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

Brune CW, Kim SJ, Salt J, Leventhal BL, Lord C, Cook EH Jr. Brune CW, et al. Am J Psychiatry. 2006 Dec;163(12):2148-56. doi: 10.1176/ajp.2006.163.12.2148. Am J Psychiatry. 2006. PMID: 17151167

8

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. Jacob S, et al. Among authors: brune cw. Neurosci Lett. 2007 Apr 24;417(1):6-9. doi: 10.1016/j.neulet.2007.02.001. Epub 2007 Feb 3. Neurosci Lett. 2007. PMID: 17383819 Free PMC article.

9

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. Brune CW, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):187-93. doi: 10.1002/ajmg.b.30585. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17948868

10

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. Jacob S, et al. Among authors: brune cw. Psychiatr Genet. 2011 Aug;21(4):212-3. doi: 10.1097/YPG.0b013e328341a323. Psychiatr Genet. 2011. PMID: 21085054 Free PMC article. No abstract available.

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