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A Nurr1 agonist causes neuroprotection in a Parkinson's disease lesion model primed with the toll-like receptor 3 dsRNA inflammatory stimulant poly(I:C) von Smith, Gaynor A, Rocha, Emily M, Rooney, Thomas, Barneoud, Pascal, McLean, Jesse R, Beagan, Jonathan, Osborn, Teresia, Coimbra, Madeleine, Luo, Yongyi, Hallett, Penelope J, Isacson, Ole

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Adapt to more wildfire in western North American forests as climate changes von Schoennagel, Tania, Balch, Jennifer K., Brenkert-Smith, Hannah, Dennison, Philip E., Harvey, Brian J., Krawchuk, Meg A., Mietkiewicz, Nathan, Morgan, Penelope, Moritz, Max A., Rasker, Ray, Turner, Monica G., Whitlock, Cathy

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Subtypes of EGFR- and HER2-Mutant Metastatic NSCLC Influence Response to Immune Checkpoint Inhibitors von Lau, Sally C.M., Fares, Aline Fusco, Le, Lisa W., Mackay, Kate M., Soberano, Spencer, Chan, Sze Wah, Smith, Elliot, Ryan, Malcolm, Tsao, Ming Sound, Bradbury, Penelope A., Pal, Prodipto, Shepherd, Frances A., Liu, Geoffrey, Leighl, Natasha B., Sacher, Adrian G.

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Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight von Tyrrell, Jessica, Richmond, Rebecca C, Palmer, Tom M, Feenstra, Bjarke, Rangarajan, Janani, Metrustry, Sarah, Cavadino, Alana, Paternoster, Lavinia, Armstrong, Loren L, De Silva, N. Maneka G, Wood, Andrew R, Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Bradfield, Jonathan P, Kreiner-Møller, Eskil, Huikari, Ville, Painter, Jodie N, Hottenga, Jouke-Jan, Allard, Catherine, Berry, Diane J, Bouchard, Luigi, Das, Shikta, Evans, David M, Hakonarson, Hakon, Hayes, M. Geoffrey, Heikkinen, Jani, Hofman, Albert, Knight, Bridget, Lind, Penelope A, McCarthy, Mark I, McMahon, George, Medland, Sarah E, Melbye, Mads, Morris, Andrew P, Nodzenski, Michael, Reichetzeder, Christoph, Ring, Susan M, Sebert, Sylvain, Sengpiel, Verena, Sørensen, Thorkild I. A, Willemsen, Gonneke, de Geus, Eco J. C, Martin, Nicholas G, Spector, Tim D, Power, Christine, Järvelin, Marjo-Riitta, Bisgaard, Hans, Grant, Struan F. A, Nohr, Ellen A, Jaddoe, Vincent W, Jacobsson, Bo, Murray, Jeffrey C, Hocher, Berthold, Hattersley, Andrew T, Scholtens, Denise M, Davey Smith, George, Hivert, Marie-France, Felix, Janine F, Hyppönen, Elina, Lowe, William L, Frayling, Timothy M, Lawlor, Debbie A, Freathy, Rachel M

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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects von Howe, Laurence J., Nivard, Michel G., Morris, Tim T., Hansen, Ailin F., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., Palviainen, Teemu, van der Zee, Matthijs D., Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M., Bielak, Lawrence F., Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A., Reynolds, Chandra A., Balbona, Jared V., Andreassen, Ole A., Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth, Dahm, Christina C., Dokuru, Deepika R., Evans, Luke M., de Geus, Eco J. C., Giddaluru, Sudheer, Gordon, Scott D., Harden, K. Paige, Hill, W. David, Hughes, Amanda, Kerr, Shona M., Kim, Yongkang, Kweon, Hyeokmoon, Latvala, Antti, Lawlor, Deborah A., Li, Liming, Lin, Kuang, Magnus, Per, Magnusson, Patrik K. E., Mallard, Travis T., Martikainen, Pekka, Mills, Melinda C., Njølstad, Pål Rasmus, Overton, John D., Pedersen, Nancy L., Porteous, David J., Reid, Jeffrey, Silventoinen, Karri, Southey, Melissa C., Stoltenberg, Camilla, Tucker-Drob, Elliot M., Wright, Margaret J., Hewitt, John K., Keller, Matthew C., Stallings, Michael C., Lee, James J., Christensen, Kaare, Kardia, Sharon L. R., Peyser, Patricia A., Smith, Jennifer A., Wilson, James F., Hopper, John L., Hägg, Sara, Spector, Tim D., Pingault, Jean-Baptiste, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G., Oskarsson, Sven, Justice, Anne E., Millwood, Iona Y., Hveem, Kristian, Naess, Øyvind, Willer, Cristen J., Åsvold, Bjørn Olav, Koellinger, Philipp D., Kaprio, Jaakko, Medland, Sarah E., Walters, Robin G., Benjamin, Daniel J., Turley, Patrick, Evans, David M., Davey Smith, George, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil M.

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Proteomic Analysis of Lupin Seed Proteins To Identify Conglutin β as an Allergen, Lup an 1 von Goggin, Danica E., Mir, Gisela, Smith, William B., Stuckey, Martin, Smith, Penelope M. C.

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Protein Intake and Physical Activity Levels as Determinants of Sarcopenia Risk in Community-Dwelling Older Adults von Stoodley, Isobel L, Berthon, Bronwyn S, Scott, Hayley A, Williams, Evan J, Baines, Penelope J, Knox, Hannah, Wood, Sophie, Paradzayi, Beauty, Cameron-Smith, David, Wood, Lisa G

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Homogeneous analysis of globular clusters from the APOGEE survey with the BACCHUS code – II. The Southern clusters and overview von Mészáros, Szabolcs, Masseron, Thomas, García-Hernández, D A, Allende Prieto, Carlos, Beers, Timothy C, Bizyaev, Dmitry, Chojnowski, Drew, Cohen, Roger E, Cunha, Katia, Dell’Agli, Flavia, Ebelke, Garrett, Fernández-Trincado, José G, Frinchaboy, Peter, Geisler, Doug, Hasselquist, Sten, Hearty, Fred, Holtzman, Jon, Johnson, Jennifer, Lane, Richard R, Lacerna, Ivan, Longa-Peña, Penelopé, Majewski, Steven R, Martell, Sarah L, Minniti, Dante, Nataf, David, Nidever, David L, Pan, Kaike, Schiavon, Ricardo P, Shetrone, Matthew, Smith, Verne V, Sobeck, Jennifer S, Stringfellow, Guy S, Szigeti, László, Tang, Baitian, Wilson, John C, Zamora, Olga

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Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults: A 2-Sample Mendelian Randomization Study von Choi, Karmel W, Chen, Chia-Yen, Stein, Murray B, Klimentidis, Yann C, Wang, Min-Jung, Koenen, Karestan C, Smoller, Jordan W

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors von Beaumont, Robin N., Day, Felix R., Peng, Shouneng, Hao, Ke, Feenstra, Bjarke, Qiao, Zhen, Moen, Gunn-Helen, Marsit, Carmen J., Nodzenski, Michael, Bradfield, Jonathan P., Grarup, Niels, Kooijman, Marjolein N., Li-Gao, Ruifang, Ahluwalia, Tarunveer S., Paternoster, Lavinia, Rueedi, Rico, Huikari, Ville, Metrustry, Sarah, Thiering, Elisabeth, Wang, Carol A., Joshi, Peter K., Myhre, Ronny, Pitkänen, Niina, van Leeuwen, Elisabeth M., Lagou, Vasiliki, Richmond, Rebecca C., Espinosa, Ana, Inskip, Hazel M., Holloway, John W., Santa-Marina, Loreto, Estivill, Xavier, Hocher, Berthold, Hivert, Marie-France, Muglia, Louis J., Heikkinen, Jani, van Kampen, Antoine H. C., van Schaik, Barbera D. C., Luan, Jian’an, Scott, Robert A., Zhao, Jing Hua, Ring, Susan M., Fernandez-Tajes, Juan, van Zuydam, Natalie R., Medina-Gomez, Carolina, de Haan, Hugoline G., Müller-Nurasyid, Martina, Fonvig, Cilius E., van Beijsterveldt, Catharina E. M., Bustamante, Mariona, Bonas-Guarch, Sílvia, Hougaard, David M., Mercader, Josep M., Linneberg, Allan, Knight, Bridget A., Bartels, Meike, Willems, Sara M., Chawes, Bo L., Kovacs, Peter, Prokopenko, Inga, Tuke, Marcus A., Yaghootkar, Hanieh, Loh, Po-Ru, Murray, Anna, Tönjes, Anke, Michaelsen, Kim F., Körner, Antje, Niinikoski, Harri, Pahkala, Katja, Jacobsson, Bo, Dedoussis, George V., Vrijkotte, Tanja G. M., Vrijheid, Martine, de Geus, Eco J. C. N., Kadarmideen, Haja N., Beilin, Lawrence J., Heinrich, Joachim, Borja, Judith B., Widén, Elisabeth E., Hattersley, Andrew T., Lehtimäki, Terho, Vollenweider, Peter, Sørensen, Thorkild I. A., Melbye, Mads, Rivadeneira, Fernando, Jaddoe, Vincent W. V., Hansen, Torben, Pisinger, Charlotta, Vaag, Allan A., Pedersen, Oluf, Uitterlinden, André G., Hyppönen, Elina, Scholtens, Denise M., Lowe, William L., Timpson, Nicholas J., Wareham, Nicholas J., Hakonarson, Hakon, Lawlor, Debbie A., Johansson, Stefan, Ong, Ken K., Evans, David M.

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Deliberately introduced dung beetles in Australia: 12 years of occurrence and abundance records from 2001 to 2022 von Berson, Jacob D., Edwards, Penelope B., Ridsdill‐Smith, T. James, Taylor, Christopher K., Anderson, Daniel J., Andrew, Nigel R., Barrow, Russell A., Cousins, David A., Emery, Robert N., Fagan, Laura L., Foster, Rhiannon M., Harwood, Lucas G., Hemmings, Zac, Lewis, Megan J., Lukehurst, Sherralee S., Manger, Jake, Matthiessen, John N., Vieira, Marcela D. C., Weston, Paul A., Didham, Raphael K., Evans, Theodore A.

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MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder von Heimer, Gali, Kerätär, Juha M., Riley, Lisa G., Balasubramaniam, Shanti, Eyal, Eran, Pietikäinen, Laura P., Hiltunen, J. Kalervo, Marek-Yagel, Dina, Hamada, Jeffrey, Gregory, Allison, Rogers, Caleb, Hogarth, Penelope, Nance, Martha A., Shalva, Nechama, Veber, Alvit, Tzadok, Michal, Nissenkorn, Andreea, Tonduti, Davide, Renaldo, Florence, Bamshad, Michael J., Leal, Suzanne M., Nickerson, Deborah A., Anderson, Peter, Annable, Marcus, Blue, Elizabeth Marchani, Buckingham, Kati J., Chin, Jennifer, Chong, Jessica X., Cornejo, Rodolfo, Davis, Colleen P., Frazar, Christopher, He, Zongxiao, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Kolar, Tom, Krauter, Stephanie A., Luksic, Daniel, Marvin, Colby T., McGee, Sean, McGoldrick, Daniel J., Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Robertson, Peggy D., Santos-Cortez, Regie, Shankar, Aditi, Slattery, Krystal, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Tackett, Monica, Wang, Gao, Wegener, Marc, Weiss, Jeffrey M., Wernick, Riana I., Wheeler, Marsha M., Yi, Qian, Kraoua, Ichraf, Panteghini, Celeste, Valletta, Lorella, Garavaglia, Barbara, Cowley, Mark J., Gayevskiy, Velimir, Roscioli, Tony, Silberstein, Jonathon M., Hoffmann, Chen, Raas-Rothschild, Annick, Tiranti, Valeria, Anikster, Yair, Christodoulou, John, Kastaniotis, Alexander J., Ben-Zeev, Bruria, Hayflick, Susan J.

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Progressive axonal transport and synaptic protein changes correlate with behavioral and neuropathological abnormalities in the heterozygous Q175 KI mouse model of Huntington's dise... von Smith, Gaynor A, Rocha, Emily M, McLean, Jesse R, Hayes, Melissa A, Izen, Sarah C, Isacson, Ole, Hallett, Penelope J

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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank von Coleman, Jonathan R. I., Peyrot, Wouter J., Purves, Kirstin L., Davis, Katrina A. S., Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A., Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M., Choi, Karmel W., Dunn, Erin C., Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J., Lewis, Cathryn M., O’Reilly, Paul F., McIntosh, Andrew M., Smith, Daniel J., Wray, Naomi R., Hotopf, Matthew, Eley, Thalia C., Breen, Gerome

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Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4) von Beach, Thomas G, Serrano, Geidy E, Kremer, Thomas, Canamero, Marta, Dziadek, Sebastian, Sade, Hadassah, Derkinderen, Pascal, Corbillé, Anne-Gaëlle, Letournel, Franck, Munoz, David G, White, Charles L, Schneider, Julie, Crary, John F, Sue, Lucia I, Adler, Charles H, Glass, Michael J, Intorcia, Anthony J, Walker, Jessica E, Foroud, Tatiana, Coffey, Christopher S, Ecklund, Dixie, Riss, Holly, Goßmann, Jennifer, König, Fatima, Kopil, Catherine M, Arnedo, Vanessa, Riley, Lindsey, Linder, Carly, Dave, Kuldip D, Jennings, Danna, Seibyl, John, Mollenhauer, Brit, Chahine, Lana

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Polymorphisms in MGMT and DNA repair genes and the risk of esophageal adenocarcinoma von Doecke, James, Zhao, Zhen Zhen, Pandeya, Nirmala, Sadeghi, Shahram, Stark, Mitchell, Green, Adèle C., Hayward, Nicholas K., Webb, Penelope M., Whiteman, David C.

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