Role of Tryptophan Oxidation in Peroxynitrite-Dependent Protein Chemiluminescence by Pollet, Eric, Martı́nez, J.Andrés, Metha, Binali, Watts, Benjamin P., Turrens, Julio F.

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Peroxynitrite-Dependent Chemiluminescence of Amino Acids, Proteins, and Intact Cells by Watts, B.P., Barnard, M., Turrens, J.F.

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Inhibition of Trypanosoma cruzi and T. brucei NADH fumarate reductase by benznidazole and anthelmintic imidazole derivatives by Turrens, Julio F., Watts, Benjamin P., Zhong, Li, Docampo, Roberto

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Achieving the triple bottom line in the face of inherent trade-offs among social equity, economic return, and conservation by Halpern, Benjamin S., Klein, Carissa J., Brown, Christopher J., Beger, Maria, Grantham, Hedley S., Mangubhai, Sangeeta, Ruckelshaus, Mary, Tulloch, Vivitskaia J., Watts, Matt, White, Crow, Possingham, Hugh P.

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Cross-tissue, single-cell stromal atlas identifies shared pathological fibroblast phenotypes in four chronic inflammatory diseases by Korsunsky, Ilya, Wei, Kevin, Pohin, Mathilde, Kim, Edy Y, Barone, Francesca, Major, Triin, Taylor, Emily, Ravindran, Rahul, Kemble, Samuel, Watts, Gerald F M, Jonsson, A Helena, Jeong, Yunju, Athar, Humra, Windell, Dylan, Kang, Joyce B, Friedrich, Matthias, Turner, Jason, Nayar, Saba, Fisher, Benjamin A, Raza, Karim, Marshall, Jennifer L, Croft, Adam P, Tamura, Tomoyoshi, Sholl, Lynette M, Vivero, Marina, Rosas, Ivan O, Bowman, Simon J, Coles, Mark, Frei, Andreas P, Lassen, Kara, Filer, Andrew, Powrie, Fiona, Buckley, Christopher D, Brenner, Michael B, Raychaudhuri, Soumya

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Deformation Microscopy for Dynamic Intracellular and Intranuclear Mapping of Mechanics with High Spatiotemporal Resolution by Ghosh, Soham, Seelbinder, Benjamin, Henderson, Jonathan T., Watts, Ryan D., Scott, Adrienne K., Veress, Alexander I., Neu, Corey P.

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A structural variation reference for medical and population genetics by Collins, Ryan L, Brand, Harrison, Karczewski, Konrad J, Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C, Khera, Amit V, Lowther, Chelsea, Gauthier, Laura D, Wang, Harold, Watts, Nicholas A, Solomonson, Matthew, O'Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W, Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R, Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M, Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D, Lin, Henry J, Rich, Stephen S, Post, Wendy S, Chen, Yii-Der Ida, Rotter, Jerome I, Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M, Kathiresan, Sekar, Daly, Mark J, Banks, Eric, MacArthur, Daniel G, Talkowski, Michael E

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Forest conservation delivers highly variable coral reef conservation outcomes by Klein, Carissa J, Jupiter, Stacy D, Selig, Elizabeth R, Watts, Matthew E, Halpern, Benjamin S, Kamal, Muhammad, Roelfsema, Chris, Possingham, Hugh P

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Rare coding variants in ten genes confer substantial risk for schizophrenia by Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D, Bigdeli, Tim B, Breen, Gerome, Buckley, Peter F, Bunney, William E, Bybjerg-Grauholm, Jonas, Chapman, Sinéad B, Chen, Wei J, Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M, DeLisi, Lynn, Dodge, Sheila, Eskelinen, Saana, Fanous, Ayman H, Faraone, Stephen V, Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B, Gage, Diane, Gagliano Taliun, Sarah A, Ganna, Andrea, Genovese, Giulio, Glahn, David C, Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O, Holi, Matti, Hougaard, David M, Howrigan, Daniel P, Huang, Hailiang, Kahn, René S, Kang, Hyun Min, Karczewski, Konrad J, Kirov, George, Knowles, James A, Lee, Francis S, Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R, McCarroll, Steven A, Medeiros, Helena, Milani, Lili, Morley, Christopher P, Morris, Derek W, Mortensen, Preben Bo, Myers, Richard M, Nordentoft, Merete, O'Brien, Niamh L, Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H, Palmer, Duncan S, Paunio, Tiina, Quested, Digby, Rapaport, Mark H, Rees, Elliott, Rollins, Brandi, Satterstrom, F Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J, Sharp, Sally I, Sklar, Pamela, Smoller, Jordan W, Sobell, Janet L, Solomonson, Matthew, Stahl, Eli A, Stevens, Christine R, Tiao, Grace, Watson, Stanley J, Watts, Nicholas A, Blackwood, Douglas H, Cohen, Bruce M, Corvin, Aiden P, Esko, Tõnu, Freimer, Nelson B, Glatt, Stephen J, Hultman, Christina M, McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N, Pato, Michele T, Pulver, Ann E, St Clair, David, Tsuang, Ming T, Vawter, Marquis P, Walters, James T, Werge, Thomas M, Ophoff, Roel A, Sullivan, Patrick F, Owen, Michael J, O'Donovan, Michael C, Neale, Benjamin M, Daly, Mark J

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Evaluating drug targets through human loss-of-function genetic variation by Minikel, Eric Vallabh, Karczewski, Konrad J, Martin, Hilary C, Cummings, Beryl B, Whiffin, Nicola, Rhodes, Daniel, Alföldi, Jessica, Trembath, Richard C, van Heel, David A, Daly, Mark J, Schreiber, Stuart L, MacArthur, Daniel G

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Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes by Karczewski, Konrad J., Solomonson, Matthew, Chao, Katherine R., Goodrich, Julia K., Tiao, Grace, Lu, Wenhan, Riley-Gillis, Bridget M., Tsai, Ellen A., Kim, Hye In, Zheng, Xiuwen, Rahimov, Fedik, Esmaeeli, Sahar, Grundstad, A. Jason, Reppell, Mark, Waring, Jeff, Jacob, Howard, Sexton, David, Bronson, Paola G., Chen, Xing, Hu, Xinli, Goldstein, Jacqueline I., King, Daniel, Vittal, Christopher, Poterba, Timothy, Palmer, Duncan S., Churchhouse, Claire, Howrigan, Daniel P., Zhou, Wei, Watts, Nicholas A., Nguyen, Kevin, Nguyen, Huy, Mason, Cara, Farnham, Christopher, Tolonen, Charlotte, Gauthier, Laura D., Gupta, Namrata, MacArthur, Daniel G., Rehm, Heidi L., Seed, Cotton, Philippakis, Anthony A., Daly, Mark J., Davis, J. Wade, Runz, Heiko, Miller, Melissa R., Neale, Benjamin M.

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Incoherent light imaging using an optical phased array by Clevenson, Hannah A., Spector, Steven J., Benney, Lucas, Moebius, Michael G., Brown, Julian, Hare, Alva, Huang, Alex, Mlynarczyk, Jacqueline, Poulton, Christopher V., Hosseini, Ehsan, Watts, Michael R., Dawson, Robin, Laine, J. P., Lane, Benjamin F.

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Sub-4 nm mapping of donor-acceptor organic semiconductor nanoparticle composition by Persson, Ingemar, Laval, Hugo, Chambon, Sylvain, Bonfante, Gwenael, Hirakawa, Kazuhiko, Wantz, Guillaume, Watts, Benjamin, Marcus, Matthew A, Xu, Xiaoxue, Ying, Lei, Lakhwani, Girish, Andersson, Mats R, Cairney, Julie M, Holmes, Natalie P

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Transcript expression-aware annotation improves rare variant interpretation by Cummings, Beryl B, Karczewski, Konrad J, Kosmicki, Jack A, Seaby, Eleanor G, Watts, Nicholas A, Singer-Berk, Moriel, Mudge, Jonathan M, Karjalainen, Juha, Satterstrom, F Kyle, O'Donnell-Luria, Anne H, Poterba, Timothy, Seed, Cotton, Solomonson, Matthew, Alföldi, Jessica, Daly, Mark J, MacArthur, Daniel G

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Metal-Mediated Catalytic Polarization Transfer from para Hydrogen to 3,5-Dihalogenated Pyridines by Tickner, Ben. J., Dennington, Marcus, Collins, Benjamin G., Gater, Callum A., Tanner, Theo F. N., Whitwood, Adrian C., Rayner, Peter J., Watts, Daniel P., Duckett, Simon B.

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Tundra wildfire triggers sustained lateral nutrient loss in Alaskan Arctic by Abbott, Benjamin W., Rocha, Adrian V., Shogren, Arial, Zarnetske, Jay P., Iannucci, Frances, Bowden, William B., Bratsman, Samuel P., Patch, Leika, Watts, Rachel, Fulweber, Randy, Frei, Rebecca J., Huebner, Amanda M., Ludwig, Sarah M., Carling, Gregory T., O’Donnell, Jonathan A.

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals by Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes by Wang, Qingbo, Pierce-Hoffman, Emma, Cummings, Beryl B, Alföldi, Jessica, Francioli, Laurent C, Gauthier, Laura D, Hill, Andrew J, O'Donnell-Luria, Anne H, Karczewski, Konrad J, MacArthur, Daniel G

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Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals by Whiffin, Nicola, Karczewski, Konrad J, Zhang, Xiaolei, Chothani, Sonia, Smith, Miriam J, Evans, D Gareth, Roberts, Angharad M, Quaife, Nicholas M, Schafer, Sebastian, Rackham, Owen, Alföldi, Jessica, O'Donnell-Luria, Anne H, Francioli, Laurent C, Cook, Stuart A, Barton, Paul J R, MacArthur, Daniel G, Ware, James S

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A genomic mutational constraint map using variation in 76,156 human genomes by Chen, Siwei, Francioli, Laurent C, Goodrich, Julia K, Collins, Ryan L, Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A, Vittal, Christopher, Gauthier, Laura D, Poterba, Timothy, Wilson, Michael W, Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T, Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O'Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R, Talkowski, Michael E, Rehm, Heidi L, Daly, Mark J, Tiao, Grace, Neale, Benjamin M, MacArthur, Daniel G, Karczewski, Konrad J

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