Items where Author is "Schellenberg, GD"

Beecham, GW and Hamilton, K and Naj, AC and Martin, ER and Huentelman, M and Myers, AJ and Corneveaux, JJ and Hardy, J and Vonsattel, JP and Younkin, SG and Bennett, DA and De Jager, PL and Larson, EB and Crane, PK and Kamboh, MI and Kofler, JK and Mash, DC and Duque, L and Gilbert, JR and Gwirtsman, H and Buxbaum, JD and Kramer, P and Dickson, DW and Farrer, LA and Frosch, MP and Ghetti, B and Haines, JL and Hyman, BT and Kukull, WA and Mayeux, RP and Pericak-Vance, MA and Schneider, JA and Trojanowski, JQ and Reiman, EM and Schellenberg, GD and Montine, TJ (2014) Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias. PLoS Genetics, 10 (9). ISSN 1553-7390

He, X and Sanders, SJ and Liu, L and De Rubeis, S and Lim, ET and Sutcliffe, JS and Schellenberg, GD and Gibbs, RA and Daly, MJ and Buxbaum, JD and State, MW and Devlin, B and Roeder, K (2013) Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes. PLoS Genetics, 9 (8). ISSN 1553-7390

Liu, L and Sabo, A and Neale, BM and Nagaswamy, U and Stevens, C and Lim, E and Bodea, CA and Muzny, D and Reid, JG and Banks, E and Coon, H and DePristo, M and Dinh, H and Fennel, T and Flannick, J and Gabriel, S and Garimella, K and Gross, S and Hawes, A and Lewis, L and Makarov, V and Maguire, J and Newsham, I and Poplin, R and Ripke, S and Shakir, K and Samocha, KE and Wu, Y and Boerwinkle, E and Buxbaum, JD and Cook, EH and Devlin, B and Schellenberg, GD and Sutcliffe, JS and Daly, MJ and Gibbs, RA and Roeder, K (2013) Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls. PLoS Genetics, 9 (4). ISSN 1553-7390

Bucan, M and Abrahams, BS and Wang, K and Glessner, JT and Herman, EI and Sonnenblick, LI and Alvarez Retuerto, AI and Imielinski, M and Hadley, D and Bradfield, JP and Kim, C and Gidaya, NB and Lindquist, I and Hutman, T and Sigman, M and Kustanovich, V and Lajonchere, CM and Singleton, A and Kim, J and Wassink, TH and McMahon, WM and Owley, T and Sweeney, JA and Coon, H and Nurnberger, JI and Li, M and Cantor, RM and Minshew, NJ and Sutcliffe, JS and Cook, EH and Dawson, G and Buxbaum, JD and Grant, SFA and Schellenberg, GD and Geschwind, DH and Hakonarson, H (2009) Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genetics, 5 (6). ISSN 1553-7390