Items where Author is "Devlin, B"

Dong, S and Walker, MF and Carriero, NJ and DiCola, M and Willsey, AJ and Ye, AY and Waqar, Z and Gonzalez, LE and Overton, JD and Frahm, S and Keaney, JF and Teran, NA and Dea, J and Mandell, JD and HusBal, V and Sullivan, CA and DiLullo, NM and Khalil, RO and Gockley, J and Yuksel, Z and Sertel, SM and Ercan-Sencicek, AG and Gupta, AR and Mane, SM and Sheldon, M and Brooks, AI and Roeder, K and Devlin, B and State, MW and Wei, L and Sanders, SJ (2014) De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. Cell Reports, 9 (1). 16 - 23.

Liu, L and Lei, J and Sanders, SJ and Willsey, AJ and Kou, Y and Cicek, AE and Klei, L and Lu, C and He, X and Li, M and Muhle, RA and Ma'Ayan, A and Noonan, JP and Šestan, N and McFadden, KA and State, MW and Buxbaum, JD and Devlin, B and Roeder, K (2014) DAWN: A framework to identify autism genes and subnetworks using gene expression and genetics. Molecular Autism, 5 (1).

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

Klei, L and Sanders, SJ and Murtha, MT and Hus, V and Lowe, JK and Willsey, AJ and Moreno-De-Luca, D and Yu, TW and Fombonne, E and Geschwind, D and Grice, DE and Ledbetter, DH and Lord, C and Mane, SM and Martin, CL and Martin, DM and Morrow, EM and Walsh, CA and Melhem, NM and Chaste, P and Sutcliffe, JS and State, MW and Cook, EH and Roeder, K and Devlin, B (2012) Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism, 3 (1).

Melhem, N and Devlin, B (2010) Shedding new light on genetic dark matter. Genome Medicine, 2 (10).