Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

por Delahanty, Ryan J., Kang, Jingqiong, Brune, Camille W., Kistner, Emily O., Courchesne, Eric, Cox, Nancy J., Cook, Edwin H., Macdonald, Robert L., Sutcliffe, James S.
Publicado 2009

Interaction of Prenatal Exposure to Cigarettes and MAOA Genotype in Pathways to Youth Antisocial Behavior

por Wakschlag, Lauren S., Kistner, Emily O., Pine, Daniel S., Biesecker, Gretchen, Pickett, Kate E., Skol, Andrew, Dukic, Vanja, Blair, R. James, Leventhal, Bennett L., Cox, Nancy, Burns, James, Kasza, Kristen E., Wright, Rosalind J., Cook, Edwin H.
Publicado 2009

Reprogramming of CTLs into natural killer–like cells in celiac disease

por Meresse, Bertrand, Curran, Shane A., Ciszewski, Cezary, Orbelyan, Gerasim, Setty, Mala, Bhagat, Govind, Lee, Leanne, Tretiakova, Maria, Semrad, Carol, Kistner, Emily, Winchester, Robert J., Braud, Veronique, Lanier, Lewis L., Geraghty, Daniel E., Green, Peter H., Guandalini, Stefano, Jabri, Bana
Publicado 2006

Ulcerative colitis loci on chromosomes 1p36 and 12q15 identified by genome-wide association study

por Silverberg, Mark S., Cho, Judy H., Rioux, John D., McGovern, Dermot P.B., Wu, Jing, Annese, Vito, Achkar, Jean-Paul, Goyette, Philippe, Scott, Regan, Xu, Wei, Barmada, M. Michael, Klei, Lambertus, Daly, Mark J., Abraham, Clara, Bayless, Theodore M., Bossa, Fabrizio, Griffiths, Anne M., Ippoliti, Andrew F., Lahaie, Raymond G., Latiano, Anna, Paré, Pierre, Proctor, Deborah D., Regueiro, Miguel D., Steinhart, A. Hillary, Targan, Stephan R., Schumm, L. Philip, Kistner, Emily O., Lee, Annette T., Gregersen, Peter K., Rotter, Jerome I., Brant, Steven R., Taylor, Kent D., Roeder, Kathryn, Duerr, Richard H.
Publicado 2009