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Page 1
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial Endpoints.
Valluripalli Soorya L, Brune CW, Farmer CA, Ocampo EV, Berger NI, Pearson DA, Busch RM, Klaas P, Siper P, Currans K, Gulsrud AC, Phillips JM, Filip-Dhima R, O'Kelley SE, Frazier TW, Levy T, Wainer AL, Buxbaum JD, Powell CM, Bernstein JA, Warfield SK, Krueger DA, Bebin EM, Northrup H, Jeste SS, Kolevzon A, Berry-Kravis E, Sahin M, Srivastava S, Thurm A; Developmental Synaptopathies Consortium. Valluripalli Soorya L, et al. Among authors: brune cw. Am J Intellect Dev Disabil. 2025 Sep 1;130(5):414-437. doi: 10.1352/1944-7558-130.5.414. Am J Intellect Dev Disabil. 2025. PMID: 40858308
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.
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. Glessner JT, et al. Among authors: brune cw. Nature. 2009 May 28;459(7246):569-73. doi: 10.1038/nature07953. Epub 2009 Apr 28. Nature. 2009. PMID: 19404257 Free PMC article.
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.
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. Wang K, et al. Among authors: brune cw. Nature. 2009 May 28;459(7246):528-33. doi: 10.1038/nature07999. Epub 2009 Apr 28. Nature. 2009. PMID: 19404256 Free PMC article.
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.
17 results