Stereovision monitoring system for cooking appliance von Ehrenbeck, Blake William, Wiatrak, Bruce, Daly, Michael Benjamin, Herndon, Seth Douglas, Gvozdjan, Milica

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STEREOVISION MONITORING SYSTEM FOR COOKING APPLIANCE von Ehrenbeck, Blake William, Wiatrak, Bruce, Daly, Michael Benjamin, Herndon, Seth Douglas, Gvozdjan, Milica

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STEREOVISION MONITORING SYSTEM FOR COOKING APPLIANCE von Ehrenbeck, Blake William, Wiatrak, Bruce, Daly, Michael Benjamin, Herndon, Seth Douglas, Gvozdjan, Milica

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STEREOVISION MONITORING SYSTEM FOR COOKING APPLIANCE von Ehrenbeck, Blake William, Wiatrak, Bruce, Daly, Michael Benjamin, Herndon, Seth Douglas, Gvozdjan, Milica

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DRAM for distilling microbial metabolism to automate the curation of microbiome function von Shaffer, Michael, Borton, Mikayla A., McGivern, Bridget B., Zayed, Ahmed A., La Rosa, Sabina Leanti, Solden, Lindsey M., Liu, Pengfei, Narrowe, Adrienne B., Rodriguez-Ramos, Josue, Bolduc, Benjamin, Gazitua, M. Consuelo, Daly, Rebecca A., Smith, Garrett J., Vik, Dean R., Pope, Phil B., Sullivan, Matthew B., Roux, Simon, Wrighton, Kelly C.

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Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies von Sohail, Mashaal, Maier, Robert M, Ganna, Andrea, Bloemendal, Alex, Martin, Alicia R, Turchin, Michael C, Chiang, Charleston Wk, Hirschhorn, Joel, Daly, Mark J, Patterson, Nick, Neale, Benjamin, Mathieson, Iain, Reich, David, Sunyaev, Shamil R

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Schizophrenia risk from complex variation of complement component 4 von Sekar, Aswin, Bialas, Allison R., de Rivera, Heather, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa, Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A.

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Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries von Talkowski, Michael E., Rosenfeld, Jill A., Blumenthal, Ian, Pillalamarri, Vamsee, Chiang, Colby, Heilbut, Adrian, Ernst, Carl, Hanscom, Carrie, Rossin, Elizabeth, Lindgren, Amelia M., Pereira, Shahrin, Ruderfer, Douglas, Kirby, Andrew, Ripke, Stephan, Harris, David J., Lee, Ji-Hyun, Ha, Kyungsoo, Kim, Hyung-Goo, Solomon, Benjamin D., Gropman, Andrea L., Lucente, Diane, Sims, Katherine, Ohsumi, Toshiro K., Borowsky, Mark L., Loranger, Stephanie, Quade, Bradley, Lage, Kasper, Miles, Judith, Wu, Bai-Lin, Shen, Yiping, Neale, Benjamin, Shaffer, Lisa G., Daly, Mark J., Morton, Cynthia C., Gusella, James F.

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An index to assess the health and benefits of the global ocean von Halpern, Benjamin S., Longo, Catherine, Hardy, Darren, McLeod, Karen L., Samhouri, Jameal F., Katona, Steven K., Kleisner, Kristin, Lester, Sarah E., O’Leary, Jennifer, Ranelletti, Marla, Rosenberg, Andrew A., Scarborough, Courtney, Selig, Elizabeth R., Best, Benjamin D., Brumbaugh, Daniel R., Chapin, F. Stuart, Crowder, Larry B., Daly, Kendra L., Doney, Scott C., Elfes, Cristiane, Fogarty, Michael J., Gaines, Steven D., Jacobsen, Kelsey I., Karrer, Leah Bunce, Leslie, Heather M., Neeley, Elizabeth, Pauly, Daniel, Polasky, Stephen, Ris, Bud, St Martin, Kevin, Stone, Gregory S., Sumaila, U. Rashid, Zeller, Dirk

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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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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis von Smoller, JW, Ripke, S, Lee, PH, Neale, B, Nurnberger, JI, Santangelo, S, Sullivan, PF, Perlis, RH, Purcell, SM, Fanous, A, Landén, Mikael

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The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders von Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Lehner, Thomas, Roeder, Kathryn, State, Matthew W.

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No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti... von Murdoch, John D, Gupta, Abha R, Sanders, Stephan J, Walker, Michael F, Keaney, John, Fernandez, Thomas V, Murtha, Michael T, Anyanwu, Samuel, Ober, Gordon T, Raubeson, Melanie J, DiLullo, Nicholas M, Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A Jeremy, Choe, So-Yeon, Neale, Benjamin M, Daly, Mark J, State, Matthew W

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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein von Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, McCauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-Chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J., Neale, Benjamin M.

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Attitude toward cheating among Ghanaian undergraduate students: a parallel mediational analysis of personality, religiosity and mastery von Amponsah, Benjamin, Dey, Nutifafa Eugene Yaw, Oti-Boadi, Mabel

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COVID-19 in patients with lung cancer von Luo, J., Rizvi, H., Preeshagul, I.R., Egger, J.V., Hoyos, D., Bandlamudi, C., McCarthy, C.G., Falcon, C.J., Schoenfeld, A.J., Arbour, K.C., Chaft, J.E., Daly, R.M., Drilon, A., Eng, J., Iqbal, A., Lai, W.V., Li, B.T., Lito, P., Namakydoust, A., Ng, K., Offin, M., Paik, P.K., Riely, G.J., Rudin, C.M., Yu, H.A., Zauderer, M.G., Donoghue, M.T.A., Łuksza, M., Greenbaum, B.D., Kris, M.G., Hellmann, M.D.

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53. RARE CODING VARIATION ACROSS 149,356 INDIVIDUALS IDENTIFIES OVER 20 NOVEL GENES ASSOCIATED WITH BIPOLAR DISORDER von Liao, Calwing, Daly, Mark, Talkowski, Michael, Neale, Benjamin

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An anatomically comprehensive atlas of the adult human brain transcriptome von Hawrylycz, Michael J., Lein, Ed S., Guillozet-Bongaarts, Angela L., Shen, Elaine H., Ng, Lydia, Miller, Jeremy A., van de Lagemaat, Louie N., Smith, Kimberly A., Ebbert, Amanda, Riley, Zackery L., Abajian, Chris, Beckmann, Christian F., Bernard, Amy, Bertagnolli, Darren, Boe, Andrew F., Cartagena, Preston M., Chakravarty, M. Mallar, Chapin, Mike, Chong, Jimmy, Dalley, Rachel A., Daly, Barry David, Dang, Chinh, Datta, Suvro, Dee, Nick, Dolbeare, Tim A., Faber, Vance, Feng, David, Fowler, David R., Goldy, Jeff, Gregor, Benjamin W., Haradon, Zeb, Haynor, David R., Hohmann, John G., Horvath, Steve, Howard, Robert E., Jeromin, Andreas, Jochim, Jayson M., Kinnunen, Marty, Lau, Christopher, Lazarz, Evan T., Lee, Changkyu, Lemon, Tracy A., Li, Ling, Li, Yang, Morris, John A., Overly, Caroline C., Parker, Patrick D., Parry, Sheana E., Reding, Melissa, Royall, Joshua J., Schulkin, Jay, Sequeira, Pedro Adolfo, Slaughterbeck, Clifford R., Smith, Simon C., Sodt, Andy J., Sunkin, Susan M., Swanson, Beryl E., Vawter, Marquis P., Williams, Derric, Wohnoutka, Paul, Zielke, H. Ronald, Geschwind, Daniel H., Hof, Patrick R., Smith, Stephen M., Koch, Christof, Grant, Seth G. N., Jones, Allan R.

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Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion von Huyghe, Jeroen R, Jackson, Anne U, Fogarty, Marie P, Buchkovich, Martin L, Stančáková, Alena, Stringham, Heather M, Sim, Xueling, Yang, Lingyao, Fuchsberger, Christian, Cederberg, Henna, Chines, Peter S, Teslovich, Tanya M, Romm, Jane M, Ling, Hua, McMullen, Ivy, Ingersoll, Roxann, Pugh, Elizabeth W, Doheny, Kimberly F, Neale, Benjamin M, Daly, Mark J, Kuusisto, Johanna, Scott, Laura J, Kang, Hyun Min, Collins, Francis S, Abecasis, Gonçalo R, Watanabe, Richard M, Boehnke, Michael, Laakso, Markku, Mohlke, Karen L

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Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases von Yuan, Kai, Longchamps, Ryan J., Pardiñas, Antonio F., Yu, Mingrui, Chen, Tzu-Ting, Lin, Shu-Chin, Chen, Yu, Lam, Max, Liu, Ruize, Xia, Yan, Guo, Zhenglin, Shi, Wenzhao, Shen, Chengguo, Daly, Mark J., Neale, Benjamin M., Feng, Yen-Chen A., Lin, Yen-Feng, Chen, Chia-Yen, O’Donovan, Michael C., Ge, Tian, Huang, Hailiang

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