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Page 1
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. Christian SL, et al. Among authors: brune cw. Biol Psychiatry. 2008 Jun 15;63(12):1111-7. doi: 10.1016/j.biopsych.2008.01.009. Epub 2008 Mar 28. Biol Psychiatry. 2008. PMID: 18374305 Free PMC article.
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
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. Kumar RA, et al. Among authors: brune cw. PLoS One. 2009;4(2):e4582. doi: 10.1371/journal.pone.0004582. Epub 2009 Feb 26. PLoS One. 2009. PMID: 19242545 Free PMC article.
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
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.
17 results