Incinerator von MALLARD JOHN K

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Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction von Karlsson Linnér, Richard, Mallard, Travis T., Barr, Peter B., Sanchez-Roige, Sandra, Madole, James W., Driver, Morgan N., Poore, Holly E., de Vlaming, Ronald, Grotzinger, Andrew D., Tielbeek, Jorim J., Johnson, Emma C., Liu, Mengzhen, Rosenthal, Sara Brin, Ideker, Trey, Zhou, Hang, Kember, Rachel L., Pasman, Joëlle A., Verweij, Karin J. H., Liu, Dajiang J., Vrieze, Scott, Kranzler, Henry R., Gelernter, Joel, Harris, Kathleen Mullan, Tucker-Drob, Elliot M., Waldman, Irwin D., Palmer, Abraham A., Harden, K. Paige, Koellinger, Philipp D., Dick, Danielle M.

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Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts von Mallard, Travis T, Savage, Jeanne E, Johnson, Emma C, Huang, Yuye, Edwards, Alexis C, Hottenga, Jouke J, Grotzinger, Andrew D, Gustavson, Daniel E, Jennings, Mariela V, Anokhin, Andrey, Dick, Danielle M, Edenberg, Howard J, Kramer, John R, Lai, Dongbing, Meyers, Jacquelyn L, Pandey, Ashwini K, Harden, Kathryn Paige, Nivard, Michel G, de Geus, Eco J.C, Boomsma, Dorret I, Agrawal, Arpana, Davis, Lea K, Clarke, Toni-Kim, Palmer, Abraham A, Sanchez-Roige, Sandra

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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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A distant trophoblast-specific enhancer controls HLA-G expression at the maternal–fetal interface von Ferreira, Leonardo M. R., Meissner, Torsten B., Mikkelsen, Tarjei S., Mallard, William, O’Donnell, Charles W., Tilburgs, Tamara, Gomes, Hannah A. B., Camahort, Raymond, Sherwood, Richard I., Gifford, David K., Rinn, John L., Cowan, Chad A., Strominger, Jack L.

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Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk von Barr, Peter B., Mallard, Travis T., Sanchez-Roige, Sandra, Poore, Holly E., Linnér, Richard Karlsson, Waldman, Irwin D., Palmer, Abraham A., Harden, K. Paige, Dick, Danielle M.

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A Classification Framework to Assess Ecological, Biogeochemical, and Hydrologic Synchrony and Asynchrony von Seybold, Erin C., Fork, Megan L., Braswell, Anna E., Blaszczak, Joanna R., Fuller, Matthew R., Kaiser, Kendra E., Mallard, John M., Zimmer, Margaret A.

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Mapping Pathways by Which Genetic Risk Influences Adolescent Externalizing Behavior: The Interplay Between Externalizing Polygenic Risk Scores, Parental Knowledge, and Peer Substan... von Kuo, Sally I-Chun, Salvatore, Jessica E., Barr, Peter B., Aliev, Fazil, Anokhin, Andrey, Bucholz, Kathleen K., Chan, Grace, Edenberg, Howard J., Hesselbrock, Victor, Kamarajan, Chella, Kramer, John R., Lai, Dongbing, Mallard, Travis T., Nurnberger, John I., Pandey, Gayathri, Plawecki, Martin H., Sanchez-Roige, Sandra, Waldman, Irwin, Palmer, Abraham A., Dick, Danielle M.

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Correlates of Risk for Disinhibited Behaviors in the Million Veteran Program Cohort von Barr, Peter B, Bigdeli, Tim B, Meyers, Jacquelyn L, Peterson, Roseann E, Sanchez-Roige, Sandra, Mallard, Travis T, Dick, Danielle M, Harden, K. Paige, Wilkinson, Anna, Graham, David P, Nielsen, David A, Swann, Alan C, Lipsky, Rachele K, Kosten, Thomas R, Aslan, Mihaela, Harvey, Philip D, Kimbrel, Nathan A, Beckham, Jean C

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Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals von Zhou, Hang, Kember, Rachel L., Deak, Joseph D., Xu, Heng, Toikumo, Sylvanus, Yuan, Kai, Lind, Penelope A., Farajzadeh, Leila, Wang, Lu, Hatoum, Alexander S., Johnson, Jessica, Lee, Hyunjoon, Mallard, Travis T., Xu, Jiayi, Johnston, Keira J. A., Johnson, Emma C., Nielsen, Trine Tollerup, Galimberti, Marco, Dao, Cecilia, Levey, Daniel F., Overstreet, Cassie, Byrne, Enda M., Gillespie, Nathan A., Gordon, Scott, Hickie, Ian B., Whitfield, John B., Xu, Ke, Zhao, Hongyu, Huckins, Laura M., Davis, Lea K., Sanchez-Roige, Sandra, Madden, Pamela A. F., Heath, Andrew C., Medland, Sarah E., Martin, Nicholas G., Ge, Tian, Smoller, Jordan W., Hougaard, David M., Børglum, Anders D., Demontis, Ditte, Krystal, John H., Gaziano, J. Michael, Edenberg, Howard J., Agrawal, Arpana, Justice, Amy C., Stein, Murray B., Kranzler, Henry R., Gelernter, Joel

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macroH2A2 antagonizes epigenetic programs of stemness in glioblastoma von Nikolic, Ana, Maule, Francesca, Bobyn, Anna, Ellestad, Katrina, Paik, Seungil, Marhon, Sajid A., Mehdipour, Parinaz, Lun, Xueqing, Chen, Huey-Miin, Mallard, Claire, Hay, Alexander J., Johnston, Michael J., Gafuik, Christopher J., Zemp, Franz J., Shen, Yaoqing, Ninkovic, Nicoletta, Osz, Katalin, Labit, Elodie, Berger, N. Daniel, Brownsey, Duncan K., Kelly, John J., Biernaskie, Jeff, Dirks, Peter B., Derksen, Darren J., Jones, Steven J. M., Senger, Donna L., Chan, Jennifer A., Mahoney, Douglas J., De Carvalho, Daniel D., Gallo, Marco

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Audiovestibular adverse events following COVID-19 vaccinations von Shetty, Aishwarya N., Morgan, Hannah J., Phuong, Linny K., Mallard, John, Vlasenko, Diana, Pearce, Christopher, Crawford, Nigel W., Buttery, Jim P., Clothier, Hazel J.

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Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis von Tielbeek, Jorim J., Uffelmann, Emil, Williams, Benjamin S., Colodro-Conde, Lucía, Gagnon, Éloi, Mallard, Travis T., Levitt, Brandt E., Jansen, Philip R., Johansson, Ada, Sallis, Hannah M., Pistis, Giorgio, Saunders, Gretchen R. B., Allegrini, Andrea G., Rimfeld, Kaili, Konte, Bettina, Klein, Marieke, Hartmann, Annette M., Salvatore, Jessica E., Nolte, Ilja M., Demontis, Ditte, Malmberg, Anni L. K., Burt, S. Alexandra, Savage, Jeanne E., Sugden, Karen, Poulton, Richie, Harris, Kathleen Mullan, Vrieze, Scott, McGue, Matt, Iacono, William G., Mota, Nina Roth, Mill, Jonathan, Viana, Joana F., Mitchell, Brittany L., Morosoli, Jose J., Andlauer, Till F. M., Ouellet-Morin, Isabelle, Tremblay, Richard E., Côté, Sylvana M., Gouin, Jean-Philippe, Brendgen, Mara R., Dionne, Ginette, Vitaro, Frank, Lupton, Michelle K., Martin, Nicholas G., Castelao, Enrique, Räikkönen, Katri, Eriksson, Johan G., Lahti, Jari, Hartman, Catharina A., Oldehinkel, Albertine J., Snieder, Harold, Liu, Hexuan, Preisig, Martin, Whipp, Alyce, Vuoksimaa, Eero, Lu, Yi, Jern, Patrick, Rujescu, Dan, Giegling, Ina, Palviainen, Teemu, Kaprio, Jaakko, Harden, Kathryn Paige, Munafò, Marcus R., Morneau-Vaillancourt, Geneviève, Plomin, Robert, Viding, Essi, Boutwell, Brian B., Aliev, Fazil, Dick, Danielle M., Popma, Arne, Faraone, Stephen V., Børglum, Anders D., Medland, Sarah E., Franke, Barbara, Boivin, Michel, Pingault, Jean-Baptiste, Glennon, Jeffrey C., Barnes, J. C., Fisher, Simon E., Moffitt, Terrie E., Caspi, Avshalom, Polderman, Tinca J. C., Posthuma, Danielle

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Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes von Toikumo, Sylvanus, Jennings, Mariela V., Pham, Benjamin K., Lee, Hyunjoon, Mallard, Travis T., Bianchi, Sevim B., Meredith, John J., Vilar-Ribó, Laura, Xu, Heng, Hatoum, Alexander S., Johnson, Emma C., Pazdernik, Vanessa K., Jinwala, Zeal, Pakala, Shreya R., Leger, Brittany S., Niarchou, Maria, Ehinmowo, Michael, Jenkins, Greg D., Batzler, Anthony, Pendegraft, Richard, Palmer, Abraham A., Zhou, Hang, Biernacka, Joanna M., Coombes, Brandon J., Gelernter, Joel, Xu, Ke, Hancock, Dana B., Cox, Nancy J., Smoller, Jordan W., Davis, Lea K., Justice, Amy C., Kranzler, Henry R., Kember, Rachel L., Sanchez-Roige, Sandra

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F76. GENOME-WIDE ASSOCIATION STUDY OF DELAY DISCOUNTING IN 134,935 23 AND ME PARTICIPANTS von Cupertino, Renata, Fontanillas, Pierre, Bianchi, Sevim B., Meredith, John J., Pakala, Shreya, Jennings, Mariela V., Mallard, Travis T., Niarchou, Maria, Elson, Sarah L., Gustavson, Daniel E., Davis, Lea K., Palmer, Abraham, Sanchez-Roige, Sandra

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Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits von Choudhuri, Avik, Trompouki, Eirini, Abraham, Brian J., Colli, Leandro M., Kock, Kian Hong, Mallard, William, Yang, Min-Lee, Vinjamur, Divya S., Ghamari, Alireza, Sporrij, Audrey, Hoi, Karen, Hummel, Barbara, Boatman, Sonja, Chan, Victoria, Tseng, Sierra, Nandakumar, Satish K., Yang, Song, Lichtig, Asher, Superdock, Michael, Grimes, Seraj N., Bowman, Teresa V., Zhou, Yi, Takahashi, Shinichiro, Joehanes, Roby, Cantor, Alan B., Bauer, Daniel E., Ganesh, Santhi K., Rinn, John, Albert, Paul S., Bulyk, Martha L., Chanock, Stephen J., Young, Richard A., Zon, Leonard I.

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Defective insulin receptor signaling in hPSCs skews pluripotency and negatively perturbs neural differentiation von Teo, Adrian Kee Keong, Nguyen, Linh, Gupta, Manoj K., Lau, Hwee Hui, Loo, Larry Sai Weng, Jackson, Nicholas, Lim, Chang Siang, Mallard, William, Gritsenko, Marina A., Rinn, John L., Smith, Richard D., Qian, Wei-Jun, Kulkarni, Rohit N.

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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., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., van der Zee, Matthijs D., Cheesman, Rosa Catherine Gillespie, 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, Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth Claire, 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 Minor, 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., Koellinger, Philipp D., Benjamin, Daniel J., Turley, Patrick, 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, Kaprio, Jaakko, Medland, Sarah E., Walters, Robin G., Evans, David M., Smith, George Davey, Hayward, Caroline, Hemani, Gibran, Davies, Neil Martin, 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, Næss, Øyvind Erik, Davey Smith, George, Brumpton, Ben Michael

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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., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., van der Zee, Matthijs D., Cheesman, Rosa Catherine Gillespie, 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, Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth Claire, 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 Minor, 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., Koellinger, Philipp D., Benjamin, Daniel J., Turley, Patrick, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G., Oskarsson, Sven, Justice, Anne E., Millwood, Iona Y., Hveem, Kristian, Willer, Cristen J., Åsvold, Bjørn Olav, Kaprio, Jaakko, Medland, Sarah E., Walters, Robin G., Evans, David M., Smith, George Davey, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil Martin, 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, Næss, Øyvind Erik, Davey Smith, George, Brumpton, Ben Michael

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Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits von Choudhuri, Avik, Trompouki, Eirini, Abraham, Brian J, Colli, Leandro M, Kock, Kian Hong, Mallard, William, Yang, Min-Lee, Vinjamur, Divya S, Ghamari, Alireza, Sporrij, Audrey, Hoi, Karen, Hummel, Barbara, Boatman, Sonja, Chan, Victoria, Tseng, Sierra, Nandakumar, Satish K, Yang, Song, Lichtig, Asher, Superdock, Michael, Grimes, Seraj N, Bowman, Teresa V, Zhou, Yi, Takahashi, Shinichiro, Joehanes, Roby, Cantor, Alan, Bauer, Daniel, Ganesh, Santhi K, Rinn, John, Albert, Paul S, Bulyk, Martha, Chanock, Stephen J, Young, Richard, Zon, Leonard

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