Learning organizational roles for negotiated search in a multiagent system von PRASAD, M.V.N., LESSER, VICTOR R., LANDER, SUSAN E.

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Designing Integrated Engineering Environments: Blackboard-Based Integration of Design and Analysis Tools von Lander, Susan E., Corkill, Daniel D., Staley, Scott M.

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The Application of Multiagent Systems to Concurrent Engineeering von Brown, David C., Lander, Susan E., Petrie, Charles J.

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Sharing metainformation to guide cooperative search among heterogeneous reusable agents von Lander, S.E., Lesser, V.R.

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Retrieval and Reasoning in Distributed Case Bases1 von Prasad, M.V.Nagendra, Lesser, Victor R., Lander, Susan E.

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Issues in multiagent design systems von Lander, S.E.

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Knowledge-based conflict resolution for cooperation among expert agents von Lander, Susan E., Lesser, Victor R., Connell, Margaret E.

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Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1 von Barbie, David A., Tamayo, Pablo, Boehm, Jesse S., Kim, So Young, Moody, Susan E., Dunn, Ian F., Schinzel, Anna C., Sandy, Peter, Meylan, Etienne, Scholl, Claudia, Fröhling, Stefan, Chan, Edmond M., Sos, Martin L., Michel, Kathrin, Mermel, Craig, Silver, Serena J., Weir, Barbara A., Reiling, Jan H., Sheng, Qing, Gupta, Piyush B., Wadlow, Raymond C., Le, Hanh, Hoersch, Sebastian, Wittner, Ben S., Ramaswamy, Sridhar, Livingston, David M., Sabatini, David M., Meyerson, Matthew, Thomas, Roman K., Lander, Eric S., Mesirov, Jill P., Root, David E., Gilliland, D. Gary, Jacks, Tyler, Hahn, William C.

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Assessing improvement in detection of breast cancer with three-dimensional automated breast US in women with dense breast tissue: the SomoInsight Study von Brem, Rachel F, Tabár, László, Duffy, Stephen W, Inciardi, Marc F, Guingrich, Jessica A, Hashimoto, Beverly E, Lander, Marla R, Lapidus, Robert L, Peterson, Mary Kay, Rapelyea, Jocelyn A, Roux, Susan, Schilling, Kathy J, Shah, Biren A, Torrente, Jessica, Wynn, Ralph T, Miller, Dave P

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Massively parallel base editing to map variant effects in human hematopoiesis von Martin-Rufino, Jorge D., Castano, Nicole, Pang, Michael, Grody, Emanuelle I., Joubran, Samantha, Caulier, Alexis, Wahlster, Lara, Li, Tongqing, Qiu, Xiaojie, Riera-Escandell, Anna Maria, Newby, Gregory A., Al’Khafaji, Aziz, Chaudhary, Santosh, Black, Susan, Weng, Chen, Munson, Glen, Liu, David R., Wlodarski, Marcin W., Sims, Kacie, Oakley, Jamie H., Fasano, Ross M., Xavier, Ramnik J., Lander, Eric S., Klein, Daryl E., Sankaran, Vijay G.

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction von Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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The variant call format and VCFtools von Danecek, Petr, Auton, Adam, Abecasis, Goncalo, Albers, Cornelis A., Banks, Eric, DePristo, Mark A., Handsaker, Robert E., Lunter, Gerton, Marth, Gabor T., Sherry, Stephen T., McVean, Gilean, Durbin, Richard

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Donor Human Milk for the High-Risk Infant: Preparation, Safety, and Usage Options in the United States von Daniels, Stephen, Corkins, Mark, de Ferranti, Sarah, Golden, Neville H., Kim, Jae H., Magge, Sheela N., Schwarzenberg, Sarah Jane, Meek, Joan Younger, Johnston, Margreete G., O’Connor, Mary Ellen, Stellwagen, Lisa M., Thomas, Jennifer Peelen, Ware, Julie L., Schanler, Richard J., Watterberg, Kristi L., Aucott, Susan Wright, Benitz, William E., Cummings, James J., Eichenwald, Eric C., Goldsmith, Jay P., Poindexter, Brenda B., Puopolo, Karen M., Stewart, Dan L.

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals von Natarajan, Pradeep, Peloso, Gina M., Zekavat, Seyedeh Maryam, Montasser, May, Ganna, Andrea, Chaffin, Mark, Khera, Amit V., Zhou, Wei, Bloom, Jonathan M., Engreitz, Jesse M., Ernst, Jason, O’Connell, Jeffrey R., Ruotsalainen, Sanni E., Alver, Maris, Manichaikul, Ani, Johnson, W. Craig, Perry, James A., Poterba, Timothy, Seed, Cotton, Surakka, Ida L., Esko, Tonu, Ripatti, Samuli, Salomaa, Veikko, Correa, Adolfo, Vasan, Ramachandran S., Kellis, Manolis, Neale, Benjamin M., Lander, Eric S., Abecasis, Goncalo, Mitchell, Braxton, Rich, Stephen S., Wilson, James G., Cupples, L. Adrienne, Rotter, Jerome I., Willer, Cristen J., Kathiresan, Sekar

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Hospitalized Patients with 2009 H1N1 Influenza in the United States, April–June 2009 von Jain, Seema, Kamimoto, Laurie, Bramley, Anna M, Schmitz, Ann M, Benoit, Stephen R, Louie, Janice, Sugerman, David E, Druckenmiller, Jean K, Ritger, Kathleen A, Chugh, Rashmi, Jasuja, Supriya, Deutscher, Meredith, Chen, Sanny, Walker, John D, Duchin, Jeffrey S, Lett, Susan, Soliva, Susan, Wells, Eden V, Swerdlow, David, Uyeki, Timothy M, Fiore, Anthony E, Olsen, Sonja J, Fry, Alicia M, Bridges, Carolyn B, Finelli, Lyn

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Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells von Barclay, Jane, Balaguero, Nuria, Mione, Marina, Ackerman, Susan L, Letts, Verity A, Brodbeck, Jens, Canti, Carles, Meir, Alon, Page, Karen M, Kusumi, Kenro, Perez-Reyes, Edward, Lander, Eric S, Frankel, Wayne N, Gardiner, R. Mark, Dolphin, Annette C, Rees, Michele

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Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes von Weinstock, Joshua S., Nandakumar, Satish K., Bao, Erik L., Szeto, Mindy D., Liao, Xiaotian, Nasser, Joseph, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J., Lin, Amy E., Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D., Barnes, Kathleen C., Moscati, Arden, Redline, Susan, Psaty, Bruce M., Silverman, Edwin K., Weiss, Scott T., Palmer, Nicholette D., Vasan, Ramachandran S., He, Jiang, Kaplan, Robert C., Smith, Nicholas L., Arnett, Donna K., Schwartz, David A., Guo, Xiuqing, Konkle, Barbara A., Custer, Brian, Peralta, Juan M., Gui, Hongsheng, Meyers, Deborah A., McGarvey, Stephen T., Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Peyser, Patricia A., Broome, Jai G., Wang, Fei Fei, North, Kari E., Launer, Lenore J., Cade, Brian E., Bis, Joshua C., Cho, Michael H., Lasky-Su, Jessica, Bowden, Donald W., Cupples, L. Adrienne, Mak, Angel C. Y., Smith, Jennifer A., Kelly, Tanika N., Aslibekyan, Stella, Heckbert, Susan R., Tiwari, Hemant K., Yang, Ivana V., Heit, John A., Johnsen, Jill M., Curran, Joanne E., Wenzel, Sally E., Rao, Dabeeru C., Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P., Buth, Erin J., Rafaels, Nicholas, Loos, Ruth J. F., Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I., Levy, Daniel, Bielak, Lawrence F., Hixson, James E., Floyd, James S., Whitsel, Eric A., Ellinor, Patrick T., Irvin, Marguerite R., Fingerlin, Tasha E., Armasu, Sebastian M., Wheeler, Marsha M., Blangero, John, Williams, L. Keoki, Levy, Bruce D., Sheu, Wayne Huey-Herng, Roden, Dan M., Boerwinkle, Eric, Taylor, Kent D., Johnson, Andrew D., Auer, Paul L., Kooperberg, Charles, Laurie, Cathy C., Blackwell, Thomas W., Smith, Albert V., Lange, Ethan, Rotter, Jerome I., Kitzman, Jacob O., Lander, Eric S., Ebert, Benjamin L., Reiner, Alexander P., Jaiswal, Siddhartha, Kathiresan, Sekar

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Finishing the euchromatic sequence of the human genome von Human Genome Sequencing Consortium, International

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Inherited Causes of Clonal Haematopoiesis in 97,691 Whole Genomes von Bick, Alexander, Weinstock, Joshua S, Nandakumar, Satish K, Fulco, Charles P, Zekavat, Seyedeh M, Szeto, Mindy D, Liao, Xiaotian, Leventhal, Matthew J, Nasser, Joseph, Chang, Kyle, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J, Lin, Amy, Taub, Margaret A, Aguet, Francois, Mitchell, Braxton D, Barnes, Kathleen C, Moscati, Arden, Fornage, Myriam, Redline, Susan, Silverman, Edwin, Weiss, Scott, Palmer, Nicholette D, Kardia, Sharon L. R, He, Jiang, Kaplan, Robert C, Smith, Nicholas L, Arnett, Donna K, Correa, Adolfo, Guo, Xiuqing, Konkle, Barbara A, Custer, Brian, Peralta, Juan M, Meyers, Deborah A, McGarvey, Stephen T, Chen, Ida Yii-Der, Shoemaker, M. Benjamin, Wang, Fei Fei, Wong, Quenna, Daya, Michelle, Kenny, Eimear E, Launer, Lenore J, Cade, Brian, Bis, Joshua C, Cho, Michael, Cupples, L. Adrienne, Mak, Angel C. Y, Becker, Lewis C, Smith, Jennifer A, Heckbert, Susan R, Yang, Ivana V, Heit, John A, Lubitz, Steven, Johnsen, Jill M, Wenzel, Sally E, Weeks, Daniel E, Rao, Dabeeru C, Darbar, Dawood, Buth, Erin J, Rafaels, Nicholas, Loos, Ruth J. F, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I, Floyd, James S, Whitsel, Eric A, Ellinor, Patrick, Irvin, Marguerite R, Fingerlin, Tasha E, Raffield, Laura M, Armasu, Sebastian M, Wheeler, Marsha M, Sabino, Ester C, Blangero, John, Williams, L. Keoki, Levy, Bruce, Roden, Dan M, Manson, JoAnn, Mathias, Rasika A, Taylor, Kent D, Johnson, Andrew D, Auer, Paul L, Kooperberg, Charles, Laurie, Cathy C, Blackwell, Thomas W, Zhao, Hongyu, Lange, Ethan, Rotter, Jerome I, Wilson, James G, Scheet, Paul, Kitzman, Jacob O, Lander, Eric, Engreitz, Jesse, Ebert, Benjamin, Reiner, Alexander P, Abecasis, Gonçalo, Kathiresan, Sekar, Natarajan, Pradeep

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Pediatric Application of Coding and Valuation Systems von Kanter, David M, Lander, Richard, Molteni, Richard A

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