Heightened vulnerability and increased risk-taking among adolescent chat room users: Results from a statewide school Survey von BEEBE, Timothy J, ASCHE, Stephen E, HARRISON, Patricia A, QUINLAN, Kathryn B

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Matched and Mismatched Interventions With Young Adult Smokers: Testing a Stage Theory von Quinlan, Kathryn B, McCaul, Kevin D

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Heightened vulnerability and increased risk-taking among adolescent chat room users: results from a statewide school survey von Beebe, Timothy J., Asche, Stephen E., Harrison, Patricia A., Quinlan, Kathryn B.

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A descriptive study of breast cancer worry von MCCAUL, K. D, BRANSTETTER, A. D, O'DONNELL, S. M, JACOBSON, K, QUINLAN, K. B

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Mail surveys resulted in more reports of substance use than telephone surveys von Beebe, Timothy J., McRae, James A., Harrison, Patricia A., Davern, Michael E., Quinlan, Kathryn B.

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Evacetrapib and Cardiovascular Outcomes in High-Risk Vascular Disease von Lincoff, A. Michael, Nicholls, Stephen J, Riesmeyer, Jeffrey S, Barter, Philip J, Brewer, H. Bryan, Fox, Keith A.A, Gibson, C. Michael, Granger, Christopher, Menon, Venu, Montalescot, Gilles, Rader, Daniel, Tall, Alan R, McErlean, Ellen, Wolski, Kathy, Ruotolo, Giacomo, Vangerow, Burkhard, Weerakkody, Govinda, Goodman, Shaun G, Conde, Diego, McGuire, Darren K, Nicolau, Jose C, Leiva-Pons, Jose L, Pesant, Yves, Li, Weimin, Kandath, David, Kouz, Simon, Tahirkheli, Naeem, Mason, Denise, Nissen, Steven E

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Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder von An, Joon-Yong, Lin, Kevin, Zhu, Lingxue, Werling, Donna M, Dong, Shan, Brand, Harrison, Wang, Harold Z, Zhao, Xuefang, Schwartz, Grace B, Collins, Ryan L, Currall, Benjamin B, Dastmalchi, Claudia, Dea, Jeanselle, Duhn, Clif, Gilson, Michael C, Klei, Lambertus, Liang, Lindsay, Markenscoff-Papadimitriou, Eirene, Pochareddy, Sirisha, Ahituv, Nadav, Buxbaum, Joseph D, Coon, Hilary, Daly, Mark J, Kim, Young Shin, Marth, Gabor T, Neale, Benjamin M, Quinlan, Aaron R, Rubenstein, John L, Sestan, Nenad, State, Matthew W, Willsey, A Jeremy, Talkowski, Michael E, Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J

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An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder von Werling, Donna M., Brand, Harrison, An, Joon-Yong, Stone, Matthew R., Zhu, Lingxue, Glessner, Joseph T., Collins, Ryan L., Dong, Shan, Layer, Ryan M., Markenscoff-Papadimitriou, Eirene, Farrell, Andrew, Schwartz, Grace B., Wang, Harold Z., Currall, Benjamin B., Zhao, Xuefang, Dea, Jeanselle, Duhn, Clif, Erdman, Carolyn A., Gilson, Michael C., Yadav, Rachita, Handsaker, Robert E., Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D., Nowakowski, Tomasz J., Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F., Waterman, Matthew J., He, Xin, Kriegstein, Arnold R., Rubenstein, John L., Sestan, Nenad, McCarroll, Steven A., Neale, Benjamin M., Coon, Hilary, Willsey, A. Jeremy, Buxbaum, Joseph D., Daly, Mark J., State, Matthew W., Quinlan, Aaron R., Marth, Gabor T., Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E., Sanders, Stephan J.

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Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy von Yuen, Michaela, Sandaradura, Sarah A, Dowling, James J, Kostyukova, Alla S, Moroz, Natalia, Quinlan, Kate G, Lehtokari, Vilma-Lotta, Ravenscroft, Gianina, Todd, Emily J, Ceyhan-Birsoy, Ozge, Gokhin, David S, Maluenda, Jérome, Lek, Monkol, Nolent, Flora, Pappas, Christopher T, Novak, Stefanie M, D'Amico, Adele, Malfatti, Edoardo, Thomas, Brett P, Gabriel, Stacey B, Gupta, Namrata, Daly, Mark J, Ilkovski, Biljana, Houweling, Peter J, Davidson, Ann E, Swanson, Lindsay C, Brownstein, Catherine A, Gupta, Vandana A, Medne, Livija, Shannon, Patrick, Martin, Nicole, Bick, David P, Flisberg, Anders, Holmberg, Eva, Van den Bergh, Peter, Lapunzina, Pablo, Waddell, Leigh B, Sloboda, Darcée D, Bertini, Enrico, Chitayat, David, Telfer, William R, Laquerrière, Annie, Gregorio, Carol C, Ottenheijm, Coen A C, Bönnemann, Carsten G, Pelin, Katarina, Beggs, Alan H, Hayashi, Yukiko K, Romero, Norma B, Laing, Nigel G, Nishino, Ichizo, Wallgren-Pettersson, Carina, Melki, Judith, Fowler, Velia M, MacArthur, Daniel G, North, Kathryn N, Clarke, Nigel F

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Rapid whole-genome mutational profiling using next-generation sequencing technologies von Smith, Douglas R, Quinlan, Aaron R, Peckham, Heather E, Makowsky, Kathryn, Tao, Wei, Woolf, Betty, Shen, Lei, Donahue, William F, Tusneem, Nadeem, Stromberg, Michael P, Stewart, Donald A, Zhang, Lu, Ranade, Swati S, Warner, Jason B, Lee, Clarence C, Coleman, Brittney E, Zhang, Zheng, McLaughlin, Stephen F, Malek, Joel A, Sorenson, Jon M, Blanchard, Alan P, Chapman, Jarrod, Hillman, David, Chen, Feng, Rokhsar, Daniel S, McKernan, Kevin J, Jeffries, Thomas W, Marth, Gabor T, Richardson, Paul M

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Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy von Yuen, Michaela, Sandaradura, Sarah A, Dowling, James J, Kostyukova, Alla S, Moroz, Natalia, Quinlan, Kate G, Lehtokari, Vilma-Lotta, Ravenscroft, Gianina, Todd, Emily J, Ceyhan-Birsoy, Ozge, Gokhin, David S, Maluenda, Jérome, Lek, Monkol, Nolent, Flora, Pappas, Christopher T, Novak, Stefanie M, D'Amico, Adele, Malfatti, Edoardo, Thomas, Brett P, Gabriel, Stacey B, Gupta, Namrata, Daly, Mark J, Ilkovski, Biljana, Houweling, Peter J, Davidson, Ann E, Swanson, Lindsay C, Brownstein, Catherine A, Gupta, Vandana A, Medne, Livija, Shannon, Patrick, Martin, Nicole, Bick, David P, Flisberg, Anders, Holmberg, Eva, Van den Bergh, Peter, Lapunzina, Pablo, Waddell, Leigh B, Sloboda, Darcée D, Bertini, Enrico, Chitayat, David, Telfer, William R, Laquerrière, Annie, Gregorio, Carol C, Ottenheijm, Coen A C, Bönnemann, Carsten G, Pelin, Katarina, Beggs, Alan H, Hayashi, Yukiko K, Romero, Norma B, Laing, Nigel G, Nishino, Ichizo, Wallgren-Pettersson, Carina, Melki, Judith, Fowler, Velia M, MacArthur, Daniel G, North, Kathryn N, Clarke, Nigel F

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