Children and Chronic Sorrow: Reconceptualizing the Emotional Impact of Parental Rejection and Its Treatment von McADAMS III, CHARLES R., DEWELL, JOHN A., HOLMAN, ANGELA R.

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This One’s for the Boys: How Gendered Political Socialization Limits Girls’ Political Ambition and Interest von BOS, ANGELA L., GREENLEE, JILL S., HOLMAN, MIRYA R., OXLEY, ZOE M., LAY, J. CELESTE

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Tim-3 is an inducible human natural killer cell receptor that enhances interferon gamma production in response to galectin-9 von Gleason, Michelle K., Lenvik, Todd R., McCullar, Valarie, Felices, Martin, O'Brien, M. Shea, Cooley, Sarah A., Verneris, Michael R., Cichocki, Frank, Holman, Carol J., Panoskaltsis-Mortari, Angela, Niki, Toshiro, Hirashima, Mitsuomi, Blazar, Bruce R., Miller, Jeffrey S.

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Are the cardiovascular properties of GLP-1 receptor agonists differentially modulated by sulfonylureas? Insights from post-hoc analysis of EXSCEL von Gooding, Kim M., Stevens, Susanna, Lokhnygina, Yuliya, Giczewska, Anna, Shore, Angela C., Holman, Rury R.

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Partisanship on the Playground: Expressive Party Politics Among Children von Lay, J. Celeste, Holman, Mirya R., Greenlee, Jill S., Oxley, Zoe M., Bos, Angela L.

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Generating human artery and vein cells from pluripotent stem cells highlights the arterial tropism of Nipah and Hendra viruses von Ang, Lay Teng, Nguyen, Alana T, Liu, Kevin J, Chen, Angela, Xiong, Xiaochen, Curtis, Matthew, Martin, Renata M, Raftry, Brian C, Ng, Chun Yi, Vogel, Uwe, Lander, Angelika, Lesch, Benjamin J, Fowler, Jonas L, Holman, Alyssa R, Chai, Timothy, Vijayakumar, Siva, Suchy, Fabian P, Nishimura, Toshinobu, Bhadury, Joydeep, Porteus, Matthew H, Nakauchi, Hiromitsu, Cheung, Christine, George, Steven C, Red-Horse, Kristy, Prescott, Joseph B, Loh, Kyle M

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Children’s Views of the American Presidency von Oxley, Zoe M, Holman, Mirya R, Greenlee, Jill S, Bos, Angela L, Lay, J Celeste

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SCORE2-Diabetes: 10-year cardiovascular risk estimation in type 2 diabetes in Europe von Pennells, Lisa, Kaptoge, Stephen, Østergaard, Helena Bleken, Read, Stephanie H, Carinci, Fabrizio, Franch-Nadal, Josep, Petitjean, Carmen, Taylor, Owen, Hageman, Steven H J, Xu, Zhe, Shi, Fanchao, Spackman, Sarah, Gualdi, Stefano, Holman, Naomi, Da Providencia E Costa, Rui Bebiano, Bonnet, Fabrice, Brenner, Hermann, Gillum, Richard F, Kiechl, Stefan, Lawlor, Deborah A, Potier, Louis, Schöttker, Ben, Sofat, Reecha, Völzke, Henry, Willeit, Johann, Baltane, Zane, Fava, Stephen, Janos, Sandor, Lavens, Astrid, Pildava, Santa, Poljicanin, Tamara, Pristas, Ivan, Rossing, Peter, Sascha, Reiff, Scheidt-Nave, Christa, Stotl, Iztok, Tibor, Gail, Urbančič-Rovan, Vilma, Vanherwegen, An-Sofie, Vistisen, Dorte, Du, Yong, Walker, Matthew R, Willeit, Peter, Ference, Brian, De Bacquer, Dirk, Halle, Martin, Huculeci, Radu, McEvoy, John William, Timmis, Adam, Vardas, Panagiotis, Dorresteijn, Jannick A N, Graham, Ian, Wood, Angela, Eliasson, Björn, Herrington, William, Danesh, John, Mauricio, Dídac, Benedetti, Massimo Massi, Sattar, Naveed, Visseren, Frank L J, Wild, Sarah, Di Angelantonio, Emanuele, Balkau, Beverley, Bonnet, Fabrice, Fumeron, Frederic, Stocker, Hannah, Holleczek, Bernd, Schipf, Sabine, Schmidt, Carsten Oliver, Dörr, Marcus, Tilg, Herbert, Leitner, Christoph, Notdurfter, Marlene, Taylor, Julie, Dale, Caroline, Prieto-Merino, David, Buble, Tamara, Ivanko, Pero, Rossing, Peter, Carstensen, Bendix, Heidemann, Christin, Gall, Tibor, Sandor, Janos, Lepiksone, Jana, Magri, Caroline J, Azzopardi, Joseph, Real, Jordi, Vlacho, Bogdan, Mata-Cases, Manel

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Human and mouse essentiality screens as a resource for disease gene discovery von Cacheiro, Pilar, Muñoz-Fuentes, Violeta, Murray, Stephen A., Dickinson, Mary E., Bucan, Maja, Nutter, Lauryl M. J., Peterson, Kevin A., Haselimashhadi, Hamed, Flenniken, Ann M., Morgan, Hugh, Westerberg, Henrik, Konopka, Tomasz, Hsu, Chih-Wei, Christiansen, Audrey, Lanza, Denise G., Beaudet, Arthur L., Heaney, Jason D., Fuchs, Helmut, Gailus-Durner, Valerie, Sorg, Tania, Prochazka, Jan, Novosadova, Vendula, Lelliott, Christopher J., Wardle-Jones, Hannah, Wells, Sara, Teboul, Lydia, Cater, Heather, Stewart, Michelle, Hough, Tertius, Wurst, Wolfgang, Sedlacek, Radislav, Adams, David J., Seavitt, John R., Tocchini-Valentini, Glauco, Mammano, Fabio, Braun, Robert E., McKerlie, Colin, Herault, Yann, de Angelis, Martin Hrabě, Mallon, Ann-Marie, Lloyd, K. C.  Kent, Brown, Steve D. M., Parkinson, Helen, Meehan, Terrence F., Smedley, Damian

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TIME for Kids to Learn Gender Stereotypes: Analysis of Gender and Political Leadership in a Common Social Studies Resource for Children von Lay, J. Celeste, Holman, Mirya R., Bos, Angela L., Greenlee, Jill S., Oxley, Zoe M., Buffett, Allison

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A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage von Zou, Xueqing, Koh, Gene Ching Chiek, Nanda, Arjun Scott, Degasperi, Andrea, Urgo, Katie, Roumeliotis, Theodoros I, Agu, Chukwuma A, Badja, Cherif, Momen, Sophie, Young, Jamie, Amarante, Tauanne Dias, Side, Lucy, Brice, Glen, Perez-Alonso, Vanesa, Rueda, Daniel, Gomez, Celine, Bushell, Wendy, Harris, Rebecca, Choudhary, Jyoti S, Jiricny, Josef, Skarnes, William C, Nik-Zainal, Serena

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100 Years of Suffrage and Girls Still Struggle to Find their “Fit” in Politics von Bos, Angela L., Holman, Mirya R., Greenlee, Jill S., Oxley, Zoe M., Lay, J. Celeste

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Perceived Benefits and Barriers of a COVID-19 Test to Stay Program in a School District Serving Black or African American People With Low Income, December 2021 von Kamitani, Emiko, Holman, Emily J., Philpott, David, Parasram, Vidisha D., Ruth, Laird J., Onyeuku, Chisom, Carter, Brittani, Gwynn, Eugenia, Beck, Timothy W., Regan, Kelly, Hagler, LaVerne R., Clark, Angela, Shelley, Gene, Thomas, Ebony S.

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Spectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma von Jones, Christine L., Degasperi, Andrea, Grandi, Vieri, Amarante, Tauanne D., Mitchell, Tracey J., Nik-Zainal, Serena, Whittaker, Sean J.

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Omega-6 DPA and its 12-lipoxygenase–oxidized lipids regulate platelet reactivity in a nongenomic PPARα-dependent manner von Yeung, Jennifer, Adili, Reheman, Yamaguchi, Adriana, Freedman, Cody J., Chen, Angela, Shami, Ryan, Das, Aditi, Holman, Theodore R., Holinstat, Michael

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An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy von Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O'Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry

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The initial noncovalent binding of glucose to human hemoglobin in nonenzymatic glycation von Clark, Shelley L D, Santin, Angela E, Bryant, Priscilla A, Holman, Rw, Rodnick, Kenneth J

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Genome-wide and fine-resolution association analysis of malaria in West Africa von Jallow, Muminatou, Teo, Yik Ying, Small, Kerrin S, Rockett, Kirk A, Deloukas, Panos, Clark, Taane G, Kivinen, Katja, Bojang, Kalifa A, Conway, David J, Pinder, Margaret, Sirugo, Giorgio, Sisay-Joof, Fatou, Usen, Stanley, Auburn, Sarah, Bumpstead, Suzannah J, Campino, Susana, Coffey, Alison, Dunham, Andrew, Fry, Andrew E, Green, Angela, Gwilliam, Rhian, Hunt, Sarah E, Inouye, Michael, Jeffreys, Anna E, Mendy, Alieu, Palotie, Aarno, Potter, Simon, Ragoussis, Jiannis, Rogers, Jane, Rowlands, Kate, Somaskantharajah, Elilan, Whittaker, Pamela, Widden, Claire, Donnelly, Peter, Howie, Bryan, Marchini, Jonathan, Morris, Andrew, SanJoaquin, Miguel, Achidi, Eric Akum, Agbenyega, Tsiri, Allen, Angela, Amodu, Olukemi, Corran, Patrick, Djimde, Abdoulaye, Dolo, Amagana, Doumbo, Ogobara K, Drakeley, Chris, Dunstan, Sarah, Evans, Jennifer, Farrar, Jeremy, Fernando, Deepika, Hien, Tran Tinh, Horstmann, Rolf D, Ibrahim, Muntaser, Karunaweera, Nadira, Kokwaro, Gilbert, Koram, Kwadwo A, Lemnge, Martha, Makani, Julie, Marsh, Kevin, Michon, Pascal, Modiano, David, Molyneux, Malcolm E, Mueller, Ivo, Parker, Michael, Peshu, Norbert, Plowe, Christopher V, Puijalon, Odile, Reeder, John, Reyburn, Hugh, Riley, Eleanor M, Sakuntabhai, Anavaj, Singhasivanon, Pratap, Sirima, Sodiomon, Tall, Adama, Taylor, Terrie E, Thera, Mahamadou, Troye-Blomberg, Marita, Williams, Thomas N, Wilson, Michael, Kwiatkowski, Dominic P

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Genome-wide association study identifies eight loci associated with blood pressure von Newton-Cheh, Christopher, Johnson, Toby, Gateva, Vesela, Tobin, Martin D, Coin, Lachlan, Zhao, Jing Hua, Zhang, Feng, Farrall, Martin, Tanaka, Toshiko, Wallace, Chris, Chambers, John C, Khaw, Kay-Tee, van der Harst, Pim, Polidoro, Silvia, Elliott, Katherine S, Teumer, Alexander, Luan, Jian'an, Kuusisto, Johanna, Hadley, David, McArdle, Wendy L, Dominiczak, Anna, Samani, Nilesh J, Webster, John, Beckmann, Jacques S, Bergmann, Sven, Lim, Noha, Song, Kijoung, Vollenweider, Peter, Waeber, Gerard, Waterworth, Dawn M, Yuan, Xin, Orho-Melander, Marju, Allione, Alessandra, Di Gregorio, Alessandra, Guarrera, Simonetta, Panico, Salvatore, Barroso, Inês, Sandhu, Manjinder S, Luben, Robert N, Crawford, Gabriel J, Jousilahti, Pekka, Perola, Markus, Bonnycastle, Lori L, Collins, Francis S, Jackson, Anne U, Stringham, Heather M, Valle, Timo T, Bergman, Richard N, Gieger, Christian, Illig, Thomas, Kathiresan, Sekar, O'Donnell, Christopher J, Subirana, Isaac, Freimer, Nelson B, O'Reilly, Paul F, Peltonen, Leena, Pouta, Anneli, de Jong, Paul E, Snieder, Harold, van Gilst, Wiek H, Clarke, Robert, Hamsten, Anders, Peden, John F, Seedorf, Udo, Lakatta, Edward G, Sanna, Serena, Scuteri, Angelo, Dörr, Marcus, Ernst, Florian, Felix, Stephan B, Homuth, Georg, Gut, Ivo G, Lathrop, G Mark, Zelenika, Diana, Deloukas, Panos, Soranzo, Nicole, Williams, Frances M, Salomaa, Veikko, Laakso, Markku, Elosua, Roberto, Forouhi, Nita G, Völzke, Henry, Uiterwaal, Cuno S, van der Schouw, Yvonne T, Matullo, Giuseppe, Navis, Gerjan, Berglund, Göran, Kooner, Jaspal S, Bandinelli, Stefania, Watkins, Hugh, Tuomilehto, Jaakko, Altshuler, David, Laan, Maris, Meneton, Pierre, Jarvelin, Marjo-Riitta, Mooser, Vincent, Melander, Olle, Elliott, Paul, Caulfield, Mark, Munroe, Patricia B

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Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia von Chen, Zhongbo, Tucci, Arianna, Cipriani, Valentina, Gustavsson, Emil K, Ibañez, Kristina, Reynolds, Regina H, Zhang, David, Vestito, Letizia, García, Alejandro Cisterna, Sethi, Siddharth, Brenton, Jonathan W, García-Ruiz, Sonia, Fairbrother-Browne, Aine, Gil-Martinez, Ana-Luisa, Wood, Nick, Hardy, John A, Smedley, Damian, Houlden, Henry, Botía, Juan, Ryten, Mina

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