Changing tides: A vascular surgery trainee perspective on the #MedBikini Campaign and a call for action by DiLosa, Kathryn, Drudi, Laura M., Drudi, Laura M., Hata, Kai, Devrome, Andrea N., Yang, Yang, Shraga, Sarrina, Blakely, Channa, Zaza, Sarah, Kinio, Anna, Kim, Gloria Y., Andraska, Elizabeth, Phillips, Amanda R., Summers, Kelli, Sethi, Danielle, Kim, Joyce J., Rojas, Elianne, Newhall, Karina, Thayer, Angelyn, MacCallum, Katherine, Lubitz, Andrea L., Liao, Jane, Kochubey, Mariya, Pappas, Georgina M., Concha-Moore, Kirsten, Gonzalez, Kathy, Rea, Jessica Nicole, Grafmuller, Leanne, Ilyas, Sadia, Scully, Rebecca, Jones, Melissa, Boudreau, Catherine, Strauss, Shira, Keller, Melissa R., Story, Lauren, Loh, Sarah, George, Elizabeth L., Ho, Vy Thuy, Brathwaite, Shayna, Jokisch, Christine, Lee Fierro, Allegra, Dunphy, Kaitlyn, Kumar, Shivani, Powell, Chloé, Dufresne, Laurence, Raju, Sneha, Balogun, Yetunde, Minisandram, Aarathi, Lee, Mary, Peng, Kate, Mai, Trinh, Beliveau, Lauren, Kenney, Kevin P., Doonan, R.J., Ayeed, Saad Bin, Schroeder, Andrew C., Fortin, William, Locham, Satinderjit S., Balceniuk, Mark D., Kanna, Sreedharan, Davidson, Anders J., Hanna, Paul, Donde, Nikunj N., Kim, Young, Jacob-Brassard, Jean, Robinson, Scott, Desai, Kash, Braet, Drew, Audu, Chris, Hemingway, Jake, Nkansah, Reginald

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Incidence of venous thromboembolism in coronavirus disease 2019: An experience from a single large academic center by Rali, Parth, O'Corragain, Oisin, Ali, Nadia, Lakhter, Vladimir, Caricchio, Roberto, Gupta, Rohit, Rao, A. Koneti, Mishkin, Aaron, Rastogi, Abhinav, Diamond, Adam, Satti, Aditi, Soliman, Ahmed, Goldberg, Amy, Kambo, Amy, Gangemi, Andrew, Vaidya, Anjali, Basil, Anuj, Bakhos, Charles T., Cornwell, Bill, Sanguily, Brianna, Corso, Brittany, Myers, Catherine, Bakhos, Charles, Reddy Mandapati, Chenna Kesava, Erkmen, Cherie, Crabbe, Deborah, Simon, Daniele, Ciccolella, David, Fehrle, Dolores, Cronin, Edmund, Dominguez, Eduardo, Hamad, Eman, Male, Eneida, Narewski, Erin, Jaffe, Frederic, Galli, Jonathan, Garfield, Jamie, D'Alonzo, Gilbert, Millio, Gregory, Simborio, Hannah, Alvarado, Hernan, Oriaku, Ifeoma, Brown, James, Garfield, Jamie L., Stewart, Jeffrey, Murray, Jenna, Travaline, John M., Cooper, Joshua, Song, Jun, Loukmane, Karim, Brennan, Kathleen, Johnson, Keith, Carney, Kevin, Miller, Lauren, Samuels, Llera A., Kerper, Margaret, Marcinkienwicz, Mariola, Aksoy, Mark, Wolfson, Marla, Marron, Robert, Patel, Maulin, Navaro, Melissa, Brisco-Bacik, Meredith A., Gannon, Michael, Kaur, Navjot, Nadpara, Neil, Desai, Nicole, Mills, Nicole, Sheriff, Omar, Abramian, Osheen, Mulhall, Patrick, Varghe, Priju, Dubal, Puja, Alashram, Rami, Armbruster, Rebecca A., Caricchio, Roberto, Soans, Rohit, Pettigrew, Samantha, Wallace, Samantha, Sehgal, Sameep, Krachman, Samuel, Hoang, Sarah, Duffy, Sean, Weaver, Sheila, George, Sheril, Brictson, Stephanie, Priest, Stephen, Codella, Steve, Kelsen, Steven G., Verga, Steven, Bolla, Sudhir, Karhadkar, Sunil, Shariff, Tahseen, Hooper, Thomas, Sajjan, Uma, Cabey, Whitney, Chatila, Wissam, Li, Wuyan, Dorey-Stein, Zachariah, Repanshek, Zachary D.

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Genetic Factors Influencing Warfarin Dose in Black‐African Patients: A Systematic Review and Meta‐Analysis by Asiimwe, Innocent G., Zhang, Eunice J., Osanlou, Rostam, Krause, Amanda, Dillon, Chrisly, Suarez‐Kurtz, Guilherme, Zhang, Honghong, Perini, Jamila A., Renta, Jessicca Y., Duconge, Jorge, Cavallari, Larisa H., Marcatto, Leiliane R., Beasly, Mark T., Perera, Minoli A., Limdi, Nita A., Santos, Paulo C.J.L., Kimmel, Stephen E., Lubitz, Steven A., Scott, Stuart A., Kawai, Vivian K., Jorgensen, Andrea L., Pirmohamed, Munir

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The mutational constraint spectrum quantified from variation in 141,456 humans by Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

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The histone 3 lysine 4 methyltransferase, Mll2, is only required briefly in development and spermatogenesis by Glaser, Stefan, Lubitz, Sandra, Loveland, Kate L, Ohbo, Kazu, Robb, Lorraine, Schwenk, Frieder, Seibler, Jost, Roellig, Daniela, Kranz, Andrea, Anastassiadis, Konstantinos, Stewart, A Francis

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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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Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans by Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

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Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans by Gudmundsson, Sanna, Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

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Author Correction: 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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