Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx

Por Wang, Jiebiao, Gamazon, Eric R., Pierce, Brandon L., Stranger, Barbara E., Im, Hae Kyung, Gibbons, Robert D., Cox, Nancy J., Nicolae, Dan L., Chen, Lin S.
Publicado no Am J Hum Genet (2016)

A Non-Degenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk

Por Blair, David R., Lyttle, Christopher S., Mortensen, Jonathan M., Bearden, Charles F., Jensen, Anders Boeck, Khiabanian, Hossein, Melamed, Rachel, Rabadan, Raul, Bernstam, Elmer V., Brunak, Søren, Jensen, Lars Juhl, Nicolae, Dan, Shah, Nigam H., Grossman, Robert L., Cox, Nancy J., White, Kevin P., Rzhetsky, Andrey
Publicado em 2013

LPA variants are associated with residual cardiovascular risk in patients receiving statins

Por Wei, Wei-Qi, Li, Xiaohui, Feng, Qiping, Kubo, Michiaki, Kullo, Iftikhar J, Peissig, Peggy L., Karlson, Elizabeth W., Jarvik, Gail P., Lee, Ming Ta Michael, Shang, Ning, Larson, Eric A., Edwards, Todd, Shaffer, Christian, Mosley, Jonathan D., Maeda, Shiro, Horikoshi, Momoko, Ritchie, Marylyn, Williams, Marc S., Larson, Eric B., Crosslin, David R., Bland, Sarah T., Pacheco, Jennifer A., Rasmussen-Torvik, Laura J, Cronkite, David, Hripcsak, George, Cox, Nancy J., Wilke, Russell A, Michael Stein, C., Rotter, Jerome I., Momozawa, Yukihide, Roden, Dan M., Krauss, Ronald M., Denny, Joshua C.
Publicado no Circulation (2018)

Genome-wide Ancestry Association Testing Identifies a Common European Variant on 6q14.1 as a Risk Factor for Asthma in African Americans

Por Torgerson, Dara G., Capurso, Daniel, Ampleford, Elizabeth J., Li, Xingnan, Moore, Wendy C., Gignoux, Christopher R., Hu, Donglei, Eng, Celeste, Mathias, Rasika A., Busse, William W., Castro, Mario, Erzurum, Serpil C., Fitzpatrick, Anne M., Gaston, Benjamin, Israel, Elliot, Jarjour, Nizar N., Teague, W. Gerald, Wenzel, Sally E., Rodríguez-Santana, José R., Rodríguez-Cintrón, William, Avila, Pedro C., Ford, Jean G., Barnes, Kathleen C., Burchard, Esteban G., Howard, Timothy D., Bleecker, Eugene R., Meyers, Deborah A., Cox, Nancy J., Ober, Carole, Nicolae, Dan L.
Publicado em 2012

Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette Syndrome and Obsessive-Compulsive Disorder

Por Yu, Dongmei, Mathews, Carol A., Scharf, Jeremiah M., Neale, Benjamin M., Davis, Lea K., Gamazon, Eric R., Derks, Eske M., Evans, Patrick, Edlund, Christopher K., Crane, Jacquelyn, Fagerness, Jesen A., Osiecki, Lisa, Gallagher, Patience, Gerber, Gloria, Haddad, Stephen, Illmann, Cornelia, McGrath, Lauren M., Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L., Bellodi, Laura, Benarroch, Fortu, Berrió, Gabriel Bedoya, Bienvenu, O. Joseph, Black, Donald, Bloch, Michael H., Brentani, Helena, Bruun, Ruth D., Budman, Cathy L., Camarena, Beatriz, Campbell, Desmond D., Cappi, Carolina, Cardona Silgado, Julio C., Cavallini, Maria C., Chavira, Denise A., Chouinard, Sylvain, Cook, Edwin H., Cookson, M. R., Coric, Vladimir, Cullen, Bernadette, Cusi, Daniele, Delorme, Richard, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Falkai, Peter, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Gilbert, Donald, Girard, Simon L., Grabe, Hans J., Grados, Marco A., Greenberg, Benjamin D., Gross-Tsur, Varda, Grünblatt, Edna, Hardy, John, Heiman, Gary A., Hemmings, Sian M.J., Herrera, Luis D., Hezel, Dianne M., Hoekstra, Pieter J., Jankovic, Joseph, Kennedy, James L., King, Robert A., Konkashbaev, Anuar I., Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F., Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L., Lupoli, Sara, Macciardi, Fabio, Maier, Wolfgang, Manunta, Paolo, Marconi, Maurizio, McCracken, James T., Mesa Restrepo, Sandra C., Moessner, Rainald, Moorjani, Priya, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Ochoa, William Cornejo, Ophoff, Roel A., Pakstis, Andrew J., Pato, Michele T., Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L., Renner, Tobias, Reus, Victor I., Richter, Margaret A., Riddle, Mark A., Robertson, Mary M., Romero, Roxana, Rosário, Maria C., Rosenberg, David, Ruhrmann, Stephan, Sabatti, Chiara, Salvi, Erika, Sampaio, Aline S., Samuels, Jack, Sandor, Paul, Service, Susan K., Sheppard, Brooke, Singer, Harvey S., Smit, Jan H., Stein, Dan J., Strengman, Eric, Tischfield, Jay A., Turiel, Maurizio, Valencia Duarte, Ana V., Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Walkup, John, Wang, Ying, Weale, Mike, Weiss, Robert, Wendland, Jens R., Westenberg, Herman G.M., Yao, Yin, Hounie, Ana G., Miguel, Euripedes C., Nicolini, Humberto, Wagner, Michael, Ruiz-Linares, Andres, Cath, Danielle C., McMahon, William, Posthuma, Danielle, Oostra, Ben A., Nestadt, Gerald, Rouleau, Guy A., Purcell, Shaun, Jenike, Michael A., Heutink, Peter, Hanna, Gregory L., Conti, David V., Arnold, Paul D., Freimer, Nelson, Stewart, S. Evelyn, Knowles, James A., Cox, Nancy J., Pauls, David L.
Publicado no Am J Psychiatry (2014)