Double differential fragmentation cross-section measurements of 95 MeV/u 12C on thin targets for hadrontherapy von Dudouet, J., Juliani, D., Angélique, J.C., Braunn, B., Colin, J., Cussol, D., Finck, Ch, Fontbonne, J.M., Gu Erin, H., Henriquet, P., Krimmer, J., Labalme, M., Rousseau, Marc, Saint-Laurent, M.G., Salvador, S. Samuel

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Double di ffential fragmentation cross sections measurements of 95 MeV/u 12C on thin targets for hadrontherapy von Dudouet, J, Juliani, D, Ang elique, J C, Braunn, B, Colin, J, Cussol, D, Finck, Ch, Fontbonne, J M, H Gu erin, Henriquet, P, Krimmer, J, Labalme, M, Rousseau, M, Saint-Laurent, M G, Salvador, S

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure von Henry, Albert, Roselli, Carolina, Sveinbjörnsson, Garðar, Fatemifar, Ghazaleh, Hedman, Åsa K., Morley, Michael P., Helgadottir, Anna, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Andersson, Charlotte, Backman, Joshua D., Biggs, Mary L., Brandimarto, Jeffrey, Buckbinder, Leonard, Carey, David J., Chasman, Daniel I., Chen, Xu, Chung, Jonathan, Cook, James P., Delgado, Graciela E., Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C., Esko, Tõnu, Finan, Chris, Gottdiener, John S., Gross, Stefan, Guðbjartsson, Daníel F., Gutmann, Rebecca, Haggerty, Christopher M., Hyde, Craig L., Ingelsson, Erik, Jukema, J. Wouter, Kavousi, Maryam, Khaw, Kay-Tee, Kleber, Marcus E., Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, Lotta, Luca A., Luan, Jian’an, März, Winfried, Melander, Olle, Mordi, Ify R., Morgan, Thomas, Morris, Andrew D., Morris, Andrew P., Morrison, Alanna C., Nelson, Christopher P., Niessner, Alexander, Niiranen, Teemu, O’Donoghue, Michelle L., Owens, Anjali T., Parry, Helen M., Perola, Markus, Rice, Kenneth M., Ridker, Paul M., Rotter, Jerome I., Salo, Perttu, Salomaa, Veikko, Smelser, Diane T., Stender, Steen, Stott, David J., Tammesoo, Mari-Liis, Taylor, Kent D., Teder-Laving, Maris, Thorsteinsdottir, Unnur, Torp-Pedersen, Christian, Trompet, Stella, Tyl, Benoit, Uitterlinden, Andre G., Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A., Wareham, Nicholas J., Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L., Yerges-Armstrong, Laura M., Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, McMurray, John J. V., Yang, Jian, Visscher, Peter M., Malarstig, Anders, Holm, Hilma, Sattar, Naveed, Holmes, Michael V., Cappola, Thomas P., Hingorani, Aroon D., Kuchenbaecker, Karoline, Ellinor, Patrick T., Smith, J. Gustav, Vasan, Ramachandran S., Swerdlow, Daniel I., Lumbers, R. Thomas

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Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes von Mansour Aly, Dina, Dwivedi, Om Prakash, Prasad, Rashmi B., Käräjämäki, Annemari, Hjort, Rebecka, Thangam, Manonanthini, Åkerlund, Mikael, Mahajan, Anubha, Udler, Miriam S., Florez, Jose C., McCarthy, Mark I., Brosnan, Julia, Melander, Olle, Carlsson, Sofia, Hansson, Ola, Tuomi, Tiinamaija, Groop, Leif, Ahlqvist, Emma

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Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank von Jurgens, Sean J., Choi, Seung Hoan, Morrill, Valerie N., Chaffin, Mark, Pirruccello, James P., Halford, Jennifer L., Weng, Lu-Chen, Nauffal, Victor, Roselli, Carolina, Hall, Amelia W., Oetjens, Matthew T., Lagerman, Braxton, vanMaanen, David P., Aragam, Krishna G., Lunetta, Kathryn L., Haggerty, Christopher M., Lubitz, Steven A., Ellinor, Patrick T.

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Engineered Cardiac Pacemaker Nodes Created by TBX18 Gene Transfer Overcome Source–Sink Mismatch von Grijalva, Sandra I., Gu, Jin‐mo, Li, Jun, Fernandez, Natasha, Fan, Jinqi, Sung, Jung Hoon, Lee, Seung Yup, Herndon, Conner, Buckley, Erin M., Park, Sung‐Jin, Fenton, Flavio H., Cho, Hee Cheol

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Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline von Li, Yong, Wuttke, Matthias, Winkler, Thomas W., Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Tin, Adrienne, Tayo, Bamidele O., Bakker, Stephan J.L., Banas, Bernhard, Biggs, Mary L., Bottinger, Erwin P., Brenner, Hermann, Chalmers, John, Chee, Miao-Ling, Degenhardt, Frauke, Eckardt, Kai-Uwe, Ghanbari, Mohsen, Gieger, Christian, Hofer, Edith, Xian Foo, Valencia Hui, Hutri-Kähönen, Nina, Ikram, M. Arfan, Kähönen, Mika, Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, Bernhard K., Kühnel, Brigitte, Lange, Leslie A., Franke, Lude, van der Harst, Pim, Navis, Gerjan, Snieder, Harold, Swertz, Morris, Wolffenbuttel, Bruce H.R., Wijmenga, Cisca, Abecasis, Goncalo, Baras, Aris, Coppola, Giovanni, Economides, Aris, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Beechert, Christina, Forsythe, Caitlin, Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Toledo, Karina, Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Barnard, Leland, Blumenfeld, Andrew, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Mitnaul, Lyndon J., Loos, Ruth J.F., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mychaleckyj, Josyf C., Nikus, Kjell, Nolte, Ilja M., O’Donoghue, Michelle L., Pendergrass, Sarah A., Penninx, Brenda W.J.H., Preuss, Michael H., Psaty, Bruce M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Sedaghat, Sanaz, Taylor, Kent D., Tremblay, Johanne, Völker, Uwe, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Snieder, Harold, Böger, Carsten A., Köttgen, Anna, Heid, Iris M.

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High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease von Tcheandjieu, Catherine, Xiao, Ke, Tejeda, Helio, Lynch, Julie A., Ruotsalainen, Sanni, Bellomo, Tiffany, Palnati, Madhuri, Judy, Renae, Klarin, Derek, Kember, Rachel L., Verma, Shefali, Palotie, Aarno, Daly, Mark, Ritchie, Marylyn, Rader, Daniel J., Rivas, Manuel A., Assimes, Themistocles, Tsao, Philip, Damrauer, Scott, Priest, James R.

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ALG9 Mutation Carriers Develop Kidney and Liver Cysts von Besse, Whitney, Chang, Alex R, Luo, Jonathan Z, Triffo, William J, Moore, Bryn S, Gulati, Ashima, Hartzel, Dustin N, Mane, Shrikant, Torres, Vicente E, Somlo, Stefan, Mirshahi, Tooraj

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Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals von Kember, Rachel L., Merikangas, Alison K., Verma, Shefali S., Verma, Anurag, Judy, Renae, Abecasis, Goncalo, Baras, Aris, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Lotta, Luca, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Schleicher, Thomas D., Padilla, Maria Sotiropoulos, Toledo, Karina, Widom, Louis, Wolf, Sarah E., Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Balasubramanian, Suganthi, Barnard, Leland, Blumenfeld, Andrew, Eom, Gisu, Habegger, Lukas, Hahn, Young, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Staples, Jeffrey C., Yadav, Ashish, Jones, Marcus B., Mitnaul, Lyndon J., Damrauer, Scott M., Ritchie, Marylyn D., Rader, Daniel J., Bućan, Maja

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Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes von Deaton, Aimee M., Parker, Margaret M., Ward, Lucas D., Flynn-Carroll, Alexander O., BonDurant, Lucas, Hinkle, Gregory, Akbari, Parsa, Lotta, Luca A., Baras, Aris, Nioi, Paul

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Causes of and Clinical Features Associated with Death in Tobacco Cigarette Users by Lung Function Impairment von Labaki, Wassim W, Gu, Tian, Murray, Susan, Curtis, Jeffrey L, Wells, J Michael, Bhatt, Surya P, Bon, Jessica, Diaz, Alejandro A, Hersh, Craig P, Wan, Emily S, Kim, Victor, Beaty, Terri H, Hokanson, John E, Bowler, Russell P, Arenberg, Douglas A, Kazerooni, Ella A, Martinez, Fernando J, Silverman, Edwin K, Crapo, James D, Make, Barry J, Regan, Elizabeth A, Han, MeiLan K

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GDF11 modulates NGN3+ islet progenitor cell number and promotes beta-cell differentiation in pancreas development von Harmon, Erin B, Apelqvist, Asa A, Smart, Nora G, Gu, Xueying, Osborne, Douglas H, Kim, Seung K

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Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes von Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste, Witt, Stephanie H., Binz, Tina M., McGrath, John, Hickie, Ian B., Hansell, Narelle K., Wright, Margaret J., Gillespie, Nathan A., Forstner, Andreas J., Schulze, Thomas G, Wüst, Stefan, Nöthen, Markus M., Baumgartner, Markus R., Walker, Brian R., Crawford, Andrew A., Colodro-Conde, Lucía, Medland, Sarah E., Martin, Nicholas G., Rietschel, Marcella

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Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study von Sun, Jiangming, Borné, Yan, Edsfeldt, Andreas, Wang, Yunpeng, Pan, Mengyu, Melander, Olle, Engström, Gunnar, Gonçalves, Isabel

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Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study von Manderstedt, Eric, Halldén, Christer, Lind‐Halldén, Christina, Elf, Johan, Svensson, Peter J., Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A., Zöller, Bengt, Abecasis, Goncalo, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Manoochehri, Kia, Overton, John D., Padilla, Maria Sotiropoulos, Pradhan, Manasi, Schleicher, Thomas D., Ulloa, Ricardo H., Widom, Louis, Wolf, Sarah E., Bai, Xiaodong, Balasubramanian, Suganthi, Blumenfeld, Andrew, Boutkov, Boris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Mansfield, Adam J., Maxwell, Evan K., Nafde, Mrunali, O’Keeffe, Sean, Orelus, Max, Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Reid, Jeffrey G., Salerno, William, Staples, Jeffrey C., Jones, Marcus B., Mighty, Jason, Mitnaul, Lyndon J.

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A Multi-Site Analysis of the Prevalence of Food Insecurity in the United States, before and during the COVID-19 Pandemic von Niles, Meredith T, Beavers, Alyssa W, Clay, Lauren A, Dougan, Marcelle M, Pignotti, Giselle A, Rogus, Stephanie, Savoie-Roskos, Mateja R, Schattman, Rachel E, Zack, Rachel M, Acciai, Francesco, Allegro, Deanne, Belarmino, Emily H, Bertmann, Farryl, Biehl, Erin, Birk, Nick, Bishop-Royse, Jessica, Bozlak, Christine, Bradley, Brianna, Brenton, Barrett P, Buszkiewicz, James, Cavaliere, Brittney N, Cho, Young, Clark, Eric M, Coakley, Kathryn, Coffin-Schmitt, Jeanne, Collier, Sarah M, Coombs, Casey, Dressel, Anne, Drewnowski, Adam, Evans, Tom, Feingold, Beth J, Fiechtner, Lauren, Fiorella, Kathryn J, Funderburk, Katie, Gadhoke, Preety, Gonzales-Pacheco, Diana, Safi, Amelia Greiner, Gu, Sen, Hanson, Karla L, Harley, Amy, Harper, Kaitlyn, Hosler, Akiko S, Ismach, Alan, Josephson, Anna, Laestadius, Linnea, LeBlanc, Heidi, Lewis, Laura R, Litton, Michelle M, Martin, Katie S, Martin, Shadai, Martinelli, Sarah, Mazzeo, John, Merrill, Scott C, Neff, Roni, Nguyen, Esther, Ohri-Vachaspati, Punam, Orbe, Abigail, Otten, Jennifer J, Parmer, Sondra, Pemberton, Salome, Qusair, Zain Al Abdeen, Rivkina, Victoria, Robinson, Joelle, Rose, Chelsea M, Sadeghzadeh, Saloumeh, Sivaramakrishnan, Brinda, Arroyo, Mariana Torres, Voorhees, McKenna, Yerxa, Kathryn

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Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium von Wan, Xuesi, Perry, James, Zhang, Haichen, Jin, Feng, Ryan, Kathleen A, Van Hout, Cristopher, Reid, Jeffrey, Overton, John, Baras, Aris, Han, Zhe, Streeten, Elizabeth, Li, Yanbing, Mitchell, Braxton D, Shuldiner, Alan R, Fu, Mao

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Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank von Wang, Louise, Desai, Heena, Verma, Shefali S., Le, Anh, Hausler, Ryan, Verma, Anurag, Judy, Renae, Doucette, Abigail, Gabriel, Peter E., Abecasis, Goncalo, Bai, Xiaodong, Balasubramanian, Suganthi, Baras, Aris, Blumenfeld, Andrew, Boutkov, Boris, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Jones, Marcus B., Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Lotta, Luca A., Mansfield, Adam J., Maxwell, Evan K., Mighty, Jason, Mitnaul, Lyndon J., Nafde, Mrunali, O’Keeffe, Sean, Orelus, Max, Overton, John D., Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Reid, Jeffrey G., Salerno, William, Staples, Jeffrey C., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Manoochehri, Kia, Pradhan, Manasi, Schleicher, Thomas D., Padilla, Maria Sotiropoulos, Ulloa, Ricardo H., Widom, Louis, Wolf, Sarah E., Nathanson, Katherine L., Damrauer, Scott M., Mowery, Danielle L., Ritchie, Marylyn D., Kember, Rachel L., Maxwell, Kara N.

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Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies von Cavazos, Taylor B, Kachuri, Linda, Graff, Rebecca E, Nierenberg, Jovia L, Thai, Khanh K, Alexeeff, Stacey, Van Den Eeden, Stephen, Corley, Douglas A, Kushi, Lawrence H, Hoffmann, Thomas J, Ziv, Elad, Habel, Laurel A, Jorgenson, Eric, Sakoda, Lori C, Witte, John S

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