Coastal dunes as a sink and secondary source of marine plastics: A study at Perran Beach, southwest England von Turner, Andrew, Amos, Sara L., Williams, Tracey

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A high-stringency blueprint of the human proteome von Adhikari, Subash, Nice, Edouard C., Deutsch, Eric W., Lane, Lydie, Omenn, Gilbert S., Pennington, Stephen R., Paik, Young-Ki, Overall, Christopher M., Corrales, Fernando J., Cristea, Ileana M., Van Eyk, Jennifer E., Uhlén, Mathias, Lindskog, Cecilia, Chan, Daniel W., Bairoch, Amos, Waddington, James C., Justice, Joshua L., LaBaer, Joshua, Rodriguez, Henry, He, Fuchu, Kostrzewa, Markus, Ping, Peipei, Gundry, Rebekah L., Stewart, Peter, Srivastava, Sanjeeva, Srivastava, Sudhir, Nogueira, Fabio C. S., Domont, Gilberto B., Vandenbrouck, Yves, Lam, Maggie P. Y., Wennersten, Sara, Vizcaino, Juan Antonio, Wilkins, Marc, Schwenk, Jochen M., Lundberg, Emma, Bandeira, Nuno, Marko-Varga, Gyorgy, Weintraub, Susan T., Pineau, Charles, Kusebauch, Ulrike, Moritz, Robert L., Ahn, Seong Beom, Palmblad, Magnus, Snyder, Michael P., Aebersold, Ruedi, Baker, Mark S.

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Germline mutations in shelterin complex genes are associated with familial glioma von Bainbridge, Matthew N, Armstrong, Georgina N, Gramatges, M Monica, Bertuch, Alison A, Jhangiani, Shalini N, Doddapaneni, Harsha, Lewis, Lora, Tombrello, Joseph, Tsavachidis, Spyros, Liu, Yanhong, Jalali, Ali, Plon, Sharon E, Lau, Ching C, Parsons, Donald W, Claus, Elizabeth B, Barnholtz-Sloan, Jill, Il'yasova, Dora, Schildkraut, Joellen, Ali-Osman, Francis, Sadetzki, Siegal, Johansen, Christoffer, Houlston, Richard S, Jenkins, Robert B, Lachance, Daniel, Olson, Sara H, Bernstein, Jonine L, Merrell, Ryan T, Wrensch, Margaret R, Walsh, Kyle M, Davis, Faith G, Lai, Rose, Shete, Sanjay, Aldape, Kenneth, Amos, Christopher I, Thompson, Patricia A, Muzny, Donna M, Gibbs, Richard A, Melin, Beatrice S, Bondy, Melissa L

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome von Heron, Sarah E., Grinton, Bronwyn E., Kivity, Sara, Afawi, Zaid, Zuberi, Sameer M., Hughes, James N., Pridmore, Clair, Hodgson, Bree L., Iona, Xenia, Sadleir, Lynette G., Pelekanos, James, Herlenius, Eric, Goldberg-Stern, Hadassa, Bassan, Haim, Haan, Eric, Korczyn, Amos D., Gardner, Alison E., Corbett, Mark A., Gécz, Jozef, Thomas, Paul Q., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E., Dibbens, Leanne M.

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Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study von Zhang, Chenan, Doherty, Jennifer A, Burgess, Stephen, Hung, Rayjean J, Lindström, Sara, Kraft, Peter, Gong, Jian, Amos, Christopher I, Sellers, Thomas A, Monteiro, Alvaro N A, Chenevix-Trench, Georgia, Bickeböller, Heike, Risch, Angela, Brennan, Paul, Mckay, James D, Houlston, Richard S, Landi, Maria Teresa, Timofeeva, Maria N, Wang, Yufei, Heinrich, Joachim, Kote-Jarai, Zsofia, Eeles, Rosalind A, Muir, Ken, Wiklund, Fredrik, Grönberg, Henrik, Berndt, Sonja I, Chanock, Stephen J, Schumacher, Fredrick, Haiman, Christopher A, Henderson, Brian E, Amin Al Olama, Ali, Andrulis, Irene L, Hopper, John L, Chang-Claude, Jenny, John, Esther M, Malone, Kathleen E, Gammon, Marilie D, Ursin, Giske, Whittemore, Alice S, Hunter, David J, Gruber, Stephen B, Knight, Julia A, Hou, Lifang, Le Marchand, Loic, Newcomb, Polly A, Hudson, Thomas J, Chan, Andrew T, Li, Li, Woods, Michael O, Ahsan, Habibul, Pierce, Brandon L

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Partitioned glioma heritability shows subtype-specific enrichment in immune cells von Ostrom, Quinn T, Edelson, Jacob, Byun, Jinyoung, Han, Younghun, Kinnersley, Ben, Melin, Beatrice, Houlston, Richard S, Monje, Michelle, Walsh, Kyle M, Amos, Christopher I, Bondy, Melissa L

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Approaching a Scientific Consensus on the Association between Allergies and Glioma Risk: A Report from the Glioma International Case-Control Study von Amirian, E Susan, Zhou, Renke, Wrensch, Margaret R, Olson, Sara H, Scheurer, Michael E, Il'yasova, Dora, Lachance, Daniel, Armstrong, Georgina N, McCoy, Lucie S, Lau, Ching C, Claus, Elizabeth B, Barnholtz-Sloan, Jill S, Schildkraut, Joellen, Ali-Osman, Francis, Sadetzki, Siegal, Johansen, Christoffer, Houlston, Richard S, Jenkins, Robert B, Bernstein, Jonine L, Merrell, Ryan T, Davis, Faith G, Lai, Rose, Shete, Sanjay, Amos, Christopher I, Melin, Beatrice S, Bondy, Melissa L

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Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects von Simon, Amos J, Lev, Atar, Zhang, Yong, Weiss, Batia, Rylova, Anna, Eyal, Eran, Kol, Nitzan, Barel, Ortal, Cesarkas, Keren, Soudack, Michalle, Greenberg-Kushnir, Noa, Rhodes, Michele, Wiest, David L, Schiby, Ginette, Barshack, Iris, Katz, Shulamit, Pras, Elon, Poran, Hana, Reznik-Wolf, Haike, Ribakovsky, Elena, Simon, Carlos, Hazou, Wadi, Sidi, Yechezkel, Lahad, Avishay, Katzir, Hagar, Sagie, Shira, Aqeilan, Haifa A, Glousker, Galina, Amariglio, Ninette, Tzfati, Yehuda, Selig, Sara, Rechavi, Gideon, Somech, Raz

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Multilingual markers of depression in remotely collected speech samples: A preliminary analysis von Cummins, Nicholas, Dineley, Judith, Conde, Pauline, Matcham, Faith, Siddi, Sara, Lamers, Femke, Carr, Ewan, Lavelle, Grace, Leightley, Daniel, White, Katie M., Oetzmann, Carolin, Campbell, Edward L., Simblett, Sara, Bruce, Stuart, Haro, Josep Maria, Penninx, Brenda W.J.H., Ranjan, Yatharth, Rashid, Zulqarnain, Stewart, Callum, Folarin, Amos A., Bailón, Raquel, Schuller, Björn W., Wykes, Til, Vairavan, Srinivasan, Dobson, Richard J.B., Narayan, Vaibhav A., Hotopf, Matthew

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Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study von Dimitrakopoulou, Vasiliki I, Tsilidis, Konstantinos K, Haycock, Philip C, Dimou, Niki L, Al-Dabhani, Kawthar, Martin, Richard M, Lewis, Sarah J, Gunter, Marc J, Mondul, Alison, Shui, Irene M, Theodoratou, Evropi, Nimptsch, Katharina, Lindström, Sara, Albanes, Demetrius, Kühn, Tilman, Key, Timothy J, Travis, Ruth C, Vimaleswaran, Karani Santhanakrishnan, Kraft, Peter, Pierce, Brandon L, Schildkraut, Joellen M

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Genetic epilepsy with febrile seizures plus: Refining the spectrum von Zhang, Yue-Hua, Burgess, Rosemary, Malone, Jodie P, Glubb, Georgie C, Helbig, Katherine L, Vadlamudi, Lata, Kivity, Sara, Afawi, Zaid, Bleasel, Andrew, Grattan-Smith, Padraic, Grinton, Bronwyn E, Bellows, Susannah T, Vears, Danya F, Damiano, John A, Goldberg-Stern, Hadassa, Korczyn, Amos D, Dibbens, Leanne M, Ruzzo, Elizabeth K, Hildebrand, Michael S, Berkovic, Samuel F, Scheffer, Ingrid E

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Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case–control study von Berntsson, Shala G., Merrell, Ryan T., Amirian, E. Susan, Armstrong, Georgina N., Lachance, Daniel, Smits, Anja, Zhou, Renke, Jacobs, Daniel I., Wrensch, Margaret R., Olson, Sara H., Il’yasova, Dora, Claus, Elizabeth B., Barnholtz-Sloan, Jill S., Schildkraut, Joellen, Sadetzki, Siegal, Johansen, Christoffer, Houlston, Richard S., Jenkins, Robert B., Bernstein, Jonine L., Lai, Rose, Shete, Sanjay, Amos, Christopher I., Bondy, Melissa L., Melin, Beatrice S.

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Radiotherapy to the primary tumour for newly diagnosed, metastatic prostate cancer (STAMPEDE): a randomised controlled phase 3 trial von Parker, Christopher C, James, Nicholas D, Brawley, Christopher D, Clarke, Noel W, Hoyle, Alex P, Ali, Adnan, Ritchie, Alastair W S, Attard, Gerhardt, Chowdhury, Simon, Cross, William, Dearnaley, David P, Gillessen, Silke, Gilson, Clare, Jones, Robert J, Langley, Ruth E, Malik, Zafar I, Mason, Malcolm D, Matheson, David, Millman, Robin, Russell, J Martin, Thalmann, George N, Amos, Claire L, Alonzi, Roberto, Bahl, Amit, Birtle, Alison, Din, Omar, Douis, Hassan, Eswar, Chinnamani, Gale, Joanna, Gannon, Melissa R, Jonnada, Sai, Khaksar, Sara, Lester, Jason F, O'Sullivan, Joe M, Parikh, Omi A, Pedley, Ian D, Pudney, Delia M, Sheehan, Denise J, Srihari, Narayanan Nair, Tran, Anna T H, Parmar, Mahesh K B, Sydes, Matthew R

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Mendelian randomization study of adiposity-related traits and risk of breast, ovarian, prostate, lung and colorectal cancer von Gao, Chi, Patel, Chirag J, Michailidou, Kyriaki, Peters, Ulrike, Gong, Jian, Schildkraut, Joellen, Schumacher, Fredrick R, Zheng, Wei, Boffetta, Paolo, Stucker, Isabelle, Willett, Walter, Gruber, Stephen, Easton, Douglas F, Hunter, David J, Sellers, Thomas A, Haiman, Christopher, Henderson, Brian E, Hung, Rayjean J, Amos, Christopher, Pierce, Brandon L, Lindström, Sara, Kraft, Peter

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Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics von Ostrom, Quinn T., Egan, Kathleen M., Nabors, L. Burt, Gerke, Travis, Thompson, Reid C., Olson, Jeffrey J., LaRocca, Renato, Chowdhary, Sajeel, Eckel‐Passow, Jeanette E., Armstrong, Georgina, Wiencke, John K., Bernstein, Jonine L., Claus, Elizabeth B., Il'yasova, Dora, Johansen, Christoffer, Lachance, Daniel H., Lai, Rose K., Merrell, Ryan T., Olson, Sara H., Sadetzki, Siegal, Schildkraut, Joellen M., Shete, Sanjay, Houlston, Richard S., Jenkins, Robert B., Wrensch, Margaret R., Melin, Beatrice, Amos, Christopher I., Huse, Jason T., Barnholtz‐Sloan, Jill S., Bondy, Melissa L.

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von 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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The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium von Amirian, E Susan, Armstrong, Georgina N, Zhou, Renke, Lau, Ching C, Claus, Elizabeth B, Barnholtz-Sloan, Jill S, Il'yasova, Dora, Schildkraut, Joellen, Ali-Osman, Francis, Sadetzki, Siegal, Johansen, Christoffer, Houlston, Richard S, Jenkins, Robert B, Lachance, Daniel, Olson, Sara H, Bernstein, Jonine L, Merrell, Ryan T, Wrensch, Margaret R, Davis, Faith G, Lai, Rose, Shete, Sanjay, Amos, Christopher I, Scheurer, Michael E, Aldape, Kenneth, Alafuzoff, Irina, Brännström, Thomas, Broholm, Helle, Collins, Peter, Giannini, Caterina, Rosenblum, Marc, Tihan, Tarik, Melin, Beatrice S, Bondy, Melissa L

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Food environment research in Canada: a rapid review of methodologies and measures deployed between 2010 and 2021 von Vaillancourt, Caroline, Ahmed, Mavra, Kirk, Sara, Labonté, Marie-Ève, Laar, Amos, Mah, Catherine L, Minaker, Leia, Olstad, Dana Lee, Potvin Kent, Monique, Provencher, Véronique, Prowse, Rachel, Raine, Kim D, Schram, Ashley, Zavala-Mora, Daniela, Rancourt-Bouchard, Maryka, Vanderlee, Lana

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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1 von Carvill, Gemma L, Heavin, Sinéad B, Yendle, Simone C, McMahon, Jacinta M, O'Roak, Brian J, Cook, Joseph, Khan, Adiba, Dorschner, Michael O, Weaver, Molly, Calvert, Sophie, Malone, Stephen, Wallace, Geoffrey, Stanley, Thorsten, Bye, Ann M E, Bleasel, Andrew, Howell, Katherine B, Kivity, Sara, Mackay, Mark T, Rodriguez-Casero, Victoria, Webster, Richard, Korczyn, Amos, Afawi, Zaid, Zelnick, Nathanel, Lerman-Sagie, Tally, Lev, Dorit, Møller, Rikke S, Gill, Deepak, Andrade, Danielle M, Freeman, Jeremy L, Sadleir, Lynette G, Shendure, Jay, Berkovic, Samuel F, Scheffer, Ingrid E, Mefford, Heather C

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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture von Stevelink, Remi, Campbell, Ciarán, Chen, Siwei, Abou-Khalil, Bassel, Adesoji, Oluyomi M., Afawi, Zaid, Amadori, Elisabetta, Anderson, Alison, Anderson, Joseph, Andrade, Danielle M., Annesi, Grazia, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bast, Thomas, Baum, Larry, Baumgartner, Tobias, Baykan, Betül, Bebek, Nerses, Becker, Albert J., Becker, Felicitas, Bennett, Caitlin A., Berghuis, Bianca, Berkovic, Samuel F., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blatt, Ilan, Bobbili, Dheeraj R., Borggraefe, Ingo, Bosselmann, Christian, Braatz, Vera, Bradfield, Jonathan P., Brockmann, Knut, Brody, Lawrence C., Buono, Russell J., Busch, Robyn M., Caglayan, Hande, Campbell, Ellen, Canafoglia, Laura, Canavati, Christina, Cascino, Gregory D., Castellotti, Barbara, Catarino, Claudia B., Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherny, Stacey S., Cheung, Ching-Lung, Chinthapalli, Krishna, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Clark, Peggy O., Cole, Andrew J., Compston, Alastair, Coppola, Antonietta, Cosico, Mahgenn, Cossette, Patrick, Craig, John J., Cusick, Caroline, Daly, Mark J., Davis, Lea K., de Haan, Gerrit-Jan, Delanty, Norman, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Di Vito, Lidia, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Elger, Christian E., Ellis, Colin A., Eriksson, Johan G., Faucon, Annika, Feng, Yen-Chen A., Ferguson, Lisa, Ferraro, Thomas N., Ferri, Lorenzo, Feucht, Martha, Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, Franke, Andre, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Geller, Eric B., Giangregorio, Tania, Gjerstad, Leif

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