A Potent Activator of Melanogenesis Identified from Small‐Molecule Screening von McNaughton, Brian R., Gareiss, Peter C., Jacobs, Stacey E., Fricke, Alex F., Scott, Glynis A., Miller, Benjamin L.

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sPLA2-X Stimulates Cutaneous Melanocyte Dendricity and Pigmentation Through a Lysophosphatidylcholine-Dependent Mechanism von Scott, Glynis A., Jacobs, Stacey E., Pentland, Alice P.

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Lysophosphatidylcholine Mediates Melanocyte Dendricity through PKCζ Activation von Scott, Glynis A., Arioka, Manubu, Jacobs, Stacey E.

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sPLA2-X Stimulates Cutaneous Melanocyte Dendricity and Pigmentation Through a Lysophosphatidylcholine-Dependent Mechanism von Scott, Glynis A., Jacobs, Stacey E., Pentland, Alice P.

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Lysophosphatidylcholine Mediates Melanocyte Dendricity through PKC Activation von Scott, Glynis A, Arioka, Manubu, Jacobs, Stacey E

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Lysophosphatidylcholine mediates melanocyte dendricity through PKCzeta activation von Scott, Glynis A, Arioka, Manubu, Jacobs, Stacey E

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Performance and Implementation Evaluation of the Abbott BinaxNOW Rapid Antigen Test in a High-Throughput Drive-Through Community Testing Site in Massachusetts von Pollock, Nira R, Jacobs, Jesica R, Tran, Kristine, Cranston, Amber E, Smith, Sita, O'Kane, Claire Y, Roady, Tyler J, Moran, Anne, Scarry, Alison, Carroll, Melissa, Volinsky, Leila, Perez, Gloria, Patel, Pinal, Gabriel, Stacey, Lennon, Niall J, Madoff, Lawrence C, Brown, Catherine, Smole, Sandra C

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Enhancing the incorporation of lysine derivatives into proteins with methylester forms of unnatural amino acids von Zhou, Han, Cheung, Jenny W., Carpenter, Tomaya, Jones, Stacey K., Luong, Nhu H., Tran, Nhi C., Jacobs, Savannah E., Galbada Liyanage, Sahan A., Cropp, T. Ashton, Yin, Jun

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First known person-to-person transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the USA von Ghinai, Isaac, McPherson, Tristan D, Hunter, Jennifer C, Kirking, Hannah L, Christiansen, Demian, Joshi, Kiran, Rubin, Rachel, Morales-Estrada, Shirley, Black, Stephanie R, Pacilli, Massimo, Fricchione, Marielle J, Chugh, Rashmi K, Walblay, Kelly A, Ahmed, N Seema, Stoecker, William C, Hasan, Nausheen F, Burdsall, Deborah P, Reese, Heather E, Wallace, Megan, Wang, Chen, Moeller, Darcie, Korpics, Jacqueline, Novosad, Shannon A, Benowitz, Isaac, Jacobs, Max W, Dasari, Vishal S, Patel, Megan T, Kauerauf, Judy, Charles, E Matt, Ezike, Ngozi O, Chu, Victoria, Midgley, Claire M, Rolfes, Melissa A, Gerber, Susan I, Lu, Xiaoyan, Lindstrom, Stephen, Verani, Jennifer R, Layden, Jennifer E, Brister, Sarah, Goldesberry, Kristin, Hoferka, Stacey, Jovanov, Dejan, Nims, Dawn, Saathoff-Huber, Lori, Hoskin Snelling, Chantel, Adil, Hira, Ali, Raabiah, Andreychak, Elaina, Bemis, Kelley, Frias, Mabel, Quartey-Kumapley, Pearl, Baskerville, Kristin, Murphy, Elizabeth, Murskyj, Emily, Noffsinger, Zach, Vercillo, Janice, Elliott, Apryll, Onwuta, Uche S., Burck, Danielle, Abedi, Glen, Burke, Rachel M., Fagan, Ryan, Farrar, Jennifer, Fry, Alicia M., Hall, Aron J., Haynes, Amber, Hoff, Connor, Kamili, Shifaq, Killerby, Marie E., Kim, Lindsay, Kujawski, Stephanie A., Kuhar, David T., Lynch, Brian, Malapati, Lakshmi, Marlow, Mariel, Murray, Janná R., Rha, Brian, Sakthivel, Senthil Kumar K., Smith-Jeffcoat, Sarah E., Soda, Elizabeth, Wang, Lijuan, Whitaker, Brett L., Uyeki, Timothy M.

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Evolutionary history of transformation from chronic lymphocytic leukemia to Richter syndrome von Parry, Erin M., Leshchiner, Ignaty, Guièze, Romain, Johnson, Connor, Tausch, Eugen, Parikh, Sameer A., Lemvigh, Camilla, Broséus, Julien, Hergalant, Sébastien, Messer, Conor, Utro, Filippo, Levovitz, Chaya, Rhrissorrakrai, Kahn, Li, Liang, Rosebrock, Daniel, Yin, Shanye, Deng, Stephanie, Slowik, Kara, Jacobs, Raquel, Huang, Teddy, Li, Shuqiang, Fell, Geoff, Redd, Robert, Lin, Ziao, Knisbacher, Binyamin A., Livitz, Dimitri, Schneider, Christof, Ruthen, Neil, Elagina, Liudmila, Taylor-Weiner, Amaro, Persaud, Bria, Martinez, Aina, Fernandes, Stacey M., Purroy, Noelia, Anandappa, Annabelle J., Ma, Jialin, Hess, Julian, Rassenti, Laura Z., Kipps, Thomas J., Jain, Nitin, Wierda, William, Cymbalista, Florence, Feugier, Pierre, Kay, Neil E., Livak, Kenneth J., Danysh, Brian P., Stewart, Chip, Neuberg, Donna, Davids, Matthew S., Brown, Jennifer R., Parida, Laxmi, Stilgenbauer, Stephan, Getz, Gad, Wu, Catherine J.

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Association of a Low-Frequency Variant in HNF1A With Type 2 Diabetes in a Latino Population von Estrada, Karol, Aukrust, Ingvild, Bjørkhaug, Lise, Burtt, Noël P, Mercader, Josep M, García-Ortiz, Humberto, Huerta-Chagoya, Alicia, Moreno-Macías, Hortensia, Walford, Geoffrey, Flannick, Jason, Williams, Amy L, Gómez-Vázquez, María J, Fernandez-Lopez, Juan C, Martínez-Hernández, Angélica, Centeno-Cruz, Federico, Mendoza-Caamal, Elvia, Revilla-Monsalve, Cristina, Islas-Andrade, Sergio, Córdova, Emilio J, Soberón, Xavier, González-Villalpando, María E, Henderson, E, Wilkens, Lynne R, Le Marchand, Loic, Arellano-Campos, Olimpia, Ordóñez-Sánchez, Maria L, Rodríguez-Torres, Maribel, Rodríguez-Guillén, Rosario, Riba, Laura, Najmi, Laeya A, Jacobs, Suzanne B.R, Fennell, Timothy, Gabriel, Stacey, Fontanillas, Pierre, Hanis, Craig L, Lehman, Donna M, Jenkinson, Christopher P, Abboud, Hanna E, Bell, Graeme I, Cortes, Maria L, Boehnke, Michael, González-Villalpando, Clicerio, Orozco, Lorena, Haiman, Christopher A, Tusié-Luna, Teresa, Aguilar-Salinas, Carlos A, Altshuler, David, Njølstad, Pål R, Florez, Jose C, MacArthur, Daniel G

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Randomized study combining interferon and glatiramer acetate in multiple sclerosis von Lublin, Fred D., Cofield, Stacey S., Cutter, Gary R., Conwit, Robin, Narayana, Ponnada A., Nelson, Flavia, Salter, Amber R., Gustafson, Tarah, Wolinsky, Jerry S.

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

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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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Burnout and engagement among resident doctors in the Netherlands: a national study von Prins, Jelle T, Hoekstra-Weebers, Josette E H M, Gazendam-Donofrio, Stacey M, Dillingh, Gea S, Bakker, Arnold B, Huisman, Mark, Jacobs, Bram, Van Der Heijden, Frank M M A

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Randomized Trial of Endoscopic or Open Vein-Graft Harvesting for Coronary-Artery Bypass von Zenati, Marco A, Bhatt, Deepak L, Bakaeen, Faisal G, Stock, Eileen M, Biswas, Kousick, Gaziano, J. Michael, Kelly, Rosemary F, Tseng, Elaine E, Bitondo, Jerene, Quin, Jacquelyn A, Almassi, G. Hossein, Haime, Miguel, Hattler, Brack, DeMatt, Ellen, Scrymgeour, Alexandra, Huang, Grant D

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Discovery of a potent and selective Aurora kinase inhibitor von Oslob, Johan D., Romanowski, Michael J., Allen, Darin A., Baskaran, Subramanian, Bui, Minna, Elling, Robert A., Flanagan, William M., Fung, Amy D., Hanan, Emily J., Harris, Shannon, Heumann, Stacey A., Hoch, Ute, Jacobs, Jeffrey W., Lam, Joni, Lawrence, Chris E., McDowell, Robert S., Nannini, Michelle A., Shen, Wang, Silverman, Jeffrey A., Sopko, Michelle M., Tangonan, Bradley T., Teague, Juli, Yoburn, Josh C., Yu, Chul H., Zhong, Min, Zimmerman, Kristin M., O’Brien, Tom, Lew, Willard

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Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol von Lange, Leslie A., Schmidt, Ellen M., Bizon, Chris, Jun, Goo, Auer, Paul, Li, Kuo-ping, Locke, Adam, Rivas, Manuel A., Feitosa, Mary F., Zhang, Qunyuan, Huffman, Jennifer E., Crosby, Jacy, Robinson, Jennifer G., Crosslin, David R., Rosenthal, Elisabeth A., Tsai, Michael, Rieder, Mark J., Fox, Ervin R., van Duijn, Cornelia M., Taylor, Herman A., Loos, Ruth J.F., Ballantyne, Christie M., Reiner, Alexander P., Cupples, L. Adrienne, Kang, Hyun Min, Lettre, Guillaume, Rader, Daniel J., Reilly, Muredach P., Stoletzki, Nina, Barr, R. Graham, Benjamin, Emelia J., Carr, Jeff, Dupuis, Josée, Ellis, Jaclyn, Fornage, Myriam, Goff, David, Grody, Wayne, Heard-Costa, Nancy L., Levy, Daniel, Li, Dalin, Loria, Cay, Mackey, Rachel, Quinlan, Aaron R., Rice, Kenneth, Sanders, Jill P., Tracy, Russell P., Tsai, Michael Y., Wassel, Chrstina L., Watson, Karol, Wilson, Gregory, Wilson, James G., Zakai, Neil A., Nalls, Michael, Bamshad, Michael J., Accurso, Frank, Beaty, Terri, Caplan, Daniel, Chidekel, Aaron, Christiani, David C., De Paula, Alicia, Gutierrez, Hector, Hassoun, Paul M., Hiatt, Peter, Hummer, Laura K., Kim, Yoonhee, Lin, Xihong, Louie, Tin L., Mathias, Rasika A., McNamara, John, McNamara, Sharon, Nielson, Dennis, Orenstein, David, O’Sullivan, Brian, Passero, Mary Ann, Perkett, Elizabeth, Spencer, Terry, Tabor, Holly K., Weiss, Robert, Wigley, Fred, Wise, Robert A., Wurfel, Mark M., Eichler, Evan E., Fu, Wenqing, Smith, Joshua D., Tennessen, Jacob A., Peters, Ulrike, Brzyski, Robert, Curb, J. David, Eaton, Charles B., Heiss, Gerardo, Johnson, Karen C., Lasser, Norman, Lin, Dan-Yu, Logsdon, Benjamin A., Manson, JoAnn E., Martin, Lisa, Stein, Evan, Applebaum-Bowden, Deborah, Paltoo, Dina N., Sturcke, Anne

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TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome von Boileau, Catherine, Guo, Dong-Chuan, Hanna, Nadine, Regalado, Ellen S, Detaint, Delphine, Gong, Limin, Varret, Mathilde, Prakash, Siddharth K, Li, Alexander H, d'Indy, Hyacintha, Braverman, Alan C, Grandchamp, Bernard, Kwartler, Callie S, Gouya, Laurent, Santos-Cortez, Regie Lyn P, Abifadel, Marianne, Leal, Suzanne M, Muti, Christine, Shendure, Jay, Gross, Marie-Sylvie, Rieder, Mark J, Vahanian, Alec, Nickerson, Deborah A, Michel, Jean Baptiste, Jondeau, Guillaume, Milewicz, Dianna M

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Glaucoma-Related Adverse Events in the First 5 Years After Unilateral Cataract Removal in the Infant Aphakia Treatment Study von Freedman, Sharon F, Lynn, Michael J, Beck, Allen D, Bothun, Erick D, Örge, Faruk H, Lambert, Scott R

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