Selected Publications
Petrie EC, Cross D, Galasko D, Schellenberg GD, Raskind MA, Peskind ER, Minoshima S.: Preclinical evidence of Alzheimer's changes: convergent cerbrospinal fluid biomarker and fluorodeoxyglucose positron emission tomography findings. Arch. Neurol. (in press) [in press], 2009.
Guthrie C, Schellenberg GD, Kraemer BC.: SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans. Hum. Molec. Genet. (in press) 2009.
Little DM, Crooks VC, Petitti DB, Chiu V, Schellenber GD, Jacobsen SJ.: Mortality, dementia, and Apolipoprotein E genotype in elderly white women in the United States. J. Am. Geriat. Soc. (in press) [in press], 2009.
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune C, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman P, 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 C, Davis LK, Miller J, Posey D, Michaels S, Bernier R, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger Jr JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SFA, Bucan M, Cook Jr EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H.: Autism genome wise copy number variation reveals ubiquitin and neuronal genes. Nature (in press) in press, 2009.
Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes N, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Reichert J, Cai G, Buxbaum JD, Schellenberg GD, de Bildt A, Minderaa RB, Mulder EJ, Tancredi R, Battaglia A, Bailey AJ, Morris AP, Monaco AP, IMGSAAC.: High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicates the IMMP2L-DOCK4 gene region in autism susceptibility. Hum. Molec. Genet. (in press) in press, 2009.
Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards EL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H.: LRRK2 mutations and risk variants in Japanese patients with Parkinson's Disease. Mov. Disord. (in press) in press, 2009.
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PMA, Kim CE, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Retuerto AIA, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor R, Bernier R, Gilbert JR< Cuccaro ML, Wassink TH, McMahon WM, Coon H, Miller J, Nurnberger Jr JI, State MW, Haines JL, Levy SE, SutcliffeJS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SFA, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.: Common genetic variation in the intergenic region between CDH10 and CDH9 is associated with susceptibility to autism spectrum disorders. Nature (in press) 2009.
Jayadev S, Steinbart EJ, Chi YY, Kukull WA, Schellenberg GD, Bird TD.: Conjugal Alzheimer's disease: risk in children when both parents have Alzheimer's disease. Arch Neurol 65: 373-378, 2008.
Crawford DC, Nord AS, Badzioch MD, Ranchalis J, McKinstry LA, Ahearn M, Bertucci C, Shephard C, Wong M, Rieder MJ, Schellenberg GD, Nickerson DA, Heagerty PJ, Wijsman EM, Jarvik GP.: VLDLR common genetic variation and interaction with APOE is associated with carotid artery disease. J Lipid Res 49: 588-596, 2008.
Mata IF, Samii A, Schneer SH, Roberts JW, Griffith A, Leis BC, Schellenberg GD, Sidransky E, Bird TD, Leverenz JB, Tsuang D, Zabetian CP.: Glucocerebrosidase gene mutations: a putative risk factor for Parkinson disease. Arch Neurol 65: 379-382, 2008.
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Last updated: 03/23/2009
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