Genetic diversity fuels gene discovery for tobacco and alcohol use by Wang, Xingyan, Jang, Seon-Kyeong, Jiang, Yu, Khunsriraksakul, Chachrit, Addison, Clifton, Aliev, Fazil, Arnett, Donna K., Ashley-Koch, Allison E., Barr, R. Graham, Bielak, Lawrence F., Benjamin, Emelia J., Bis, Joshua C., Bjornsdottir, Gyda, Blangero, John, Chavan, Sameer, Chen, Yii-Der Ida, Chen, Zhengming, Cheng, Iona, Choquet, Hélène, Cole, John W., Cucca, Francesco, Dick, Danielle M., Fernandes Silva, Lilian, Fiorillo, Edoardo, Garrett, Melanie E., Glahn, David C., Gordon, Scott D., Gu, Dongfeng, Gudbjartsson, Daniel F., Hall, Michael E., Haller, Toomas, Harris, Kathleen Mullan, He, Jiang, Hewitt, John K., Hickie, Ian, Hidalgo, Bertha, Hokanson, John E., Hottenga, JoukeJan, Hwu, Chii-Min, Jee, Yon Ho, Joo, Yoonjung Y., Kamatani, Yoichiro, Kaplan, Robert C., Kelly, Tanika N., Kraft, Peter, Krauter, Kenneth, Laakso, Markku, Lasky-Su, Jessica, Li, Liming, Lloyd-Jones, Donald M., Mägi, Reedik, Manichaikul, Ani, Mathur, Ravi, Matoba, Nana, McArdle, Patrick F., Metspalu, Andres, Moll, Matthew, Montasser, May E., Nielsen, Jonas B., Oelsner, Elizabeth C., Orrù, Valeria, Palmer, Nicholette D., Park, S. Lani, Peters, Ulrike, Peters, Annette, Polderman, Tinca J. C., Rafaels, Nicholas, Reiner, Alex P., Roan, Carol, Rotter, Jerome I., Runarsdottir, Valgerdur, Saccone, Nancy L., Shadyab, Aladdin H., Shringarpure, Suyash S., Sicinski, Kamil, Smith, Jennifer A., Smith, Nicholas L., Sotoodehnia, Nona, Stallings, Michael C., Stefansson, Hreinn, Syed, Moin, Tal-Singer, Ruth, Telen, Marilyn J., Tiwari, Hemant, Wall, Tamara L., White, Wendy B., Whitfield, John B., Wiggins, Kerri L., Willemsen, Gonneke, Willer, Cristen J., Xu, Huichun, Yanek, Lisa R., Young, Kendra A., Yu, Bing, Zhao, Wei, Zöllner, Sebastian, Bierut, Laura J., Gagliano Taliun, Sarah A., Munafò, Marcus R., Liu, Dajiang J.

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project by Ceyhan-Birsoy, Ozge, Murry, Jaclyn B., Machini, Kalotina, Lebo, Matthew S., Yu, Timothy W., Fayer, Shawn, Genetti, Casie A., Schwartz, Talia S., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Rehm, Heidi L., Beggs, Alan H., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Guiterrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W.

Common genetic variants influence human subcortical brain structures by Hibar, Derrek P., Desrivières, Sylvane, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Bernard, Manon, Chen, Qiang, Giddaluru, Sudheer, Janowitz, Deborah, Lee, Phil H., Ramasamy, Adaikalavan, Risacher, Shannon L., Rose, Emma J., Salami, Alireza, Schmaal, Lianne, Schork, Andrew J., Strike, Lachlan T., Walters, Raymond K., Winkler, Anderson M., Zwiers, Marcel P., Athanasiu, Lavinia, Hakobjan, Marina M. H., Hartberg, Cecilie B., Heister, Angelien J. G. A. M., Hoehn, David, Kasperaviciute, Dalia, Makkinje, Remco R. R., Reese McKay, D., Shen, Li, Walton, Esther, Ames, David, Corvin, Aiden, Curran, Joanne E., Dillman, Allissa, Erk, Susanne, Foroud, Tatiana M., Guelfi, Sebastian, Hegenscheid, Katrin, Hernandez, Dena G., Heslenfeld, Dirk J., Hottenga, Jouke-Jan, Jenkinson, Mark, Kanai, Ryota, Kent, Jack W., McMahon, Katie L., Meisenzahl, Eva, Mohnke, Sebastian, Mühleisen, Thomas W., Nalls, Michael A., Nichols, Thomas E., Potkin, Steven G., Reppermund, Simone, Rujescu, Dan, Schnell, Knut, Thalamuthu, Anbupalam, Turner, Jessica A., van 't Ent, Dennis, Wassink, Thomas H., Westman, Eric, Ashbrook, David G., Lu, Lu, Williams, Robert W., Buckner, Randy L., Calhoun, Vince D., Cavalleri, Gianpiero L., Dale, Anders M., Espeseth, Thomas, Hoffmann, Wolfgang, Le Hellard, Stephanie, Meyer-Lindenberg, Andreas, Müller-Myhsok, Bertram, Nyberg, Lars, Penninx, Brenda W. J. H., van Bokhoven, Hans, van Haren, Neeltje E. M., Völzke, Henry, Weiner, Michael W., White, Tonya, Agartz, Ingrid, Blangero, John, Boomsma, Dorret I., Fernández, Guillén, Fisher, Simon E., Francks, Clyde, Grabe, Hans J., Hashimoto, Ryota, Hulshoff Pol, Hilleke E., Jönsson, Erik G., McIntosh, Andrew M., Singleton, Andrew, Schmidt, Reinhold, Satizabal, Claudia L., Ebling, Maritza, Nyquist, Paul, Vinke, Louis N., Xue, Luting, Mazoyer, Bernard, Martin, Nicholas G., Wright, Margaret J., Schumann, Gunter

Mendel’s laws, Mendelian randomization and causal inference in observational data: substantive and nomenclatural issues by Davey Smith, George, Holmes, Michael V., Davies, Neil M., Ebrahim, Shah

Characterizing the Causal Pathway for Genetic Variants Associated with Neurological Phenotypes Using Human Brain-Derived Proteome Data by Kibinge, Nelson K., Relton, Caroline L., Gaunt, Tom R., Richardson, Tom G.

The mutational constraint spectrum quantified from variation in 141,456 humans by Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

Common genetic variation drives molecular heterogeneity in human iPSCs by Kilpinen, Helena, Goncalves, Angela, Leha, Andreas, Afzal, Vackar, Alasoo, Kaur, Ashford, Sofie, Bala, Sendu, Bensaddek, Dalila, Casale, Francesco Paolo, Culley, Oliver J., Danecek, Petr, Faulconbridge, Adam, Harrison, Peter W., Kathuria, Annie, McCarthy, Davis, McCarthy, Shane A., Meleckyte, Ruta, Memari, Yasin, Moens, Nathalie, Soares, Filipa, Mann, Alice, Streeter, Ian, Agu, Chukwuma A., Alderton, Alex, Nelson, Rachel, Harper, Sarah, Patel, Minal, White, Alistair, Patel, Sharad R., Clarke, Laura, Halai, Reena, Kirton, Christopher M., Kolb-Kokocinski, Anja, Beales, Philip, Birney, Ewan, Danovi, Davide, Lamond, Angus I., Ouwehand, Willem H., Vallier, Ludovic, Watt, Fiona M., Durbin, Richard, Stegle, Oliver, Gaffney, Daniel J.

The evolution of mendelian randomization for investigating drug effects by Gill, Dipender, Burgess, Stephen

A global reference for human genetic variation by Abecasis, Gonçalo R., Durbin, Richard M., Mardis, Elaine R., Marth, Gabor T., Nickerson, Deborah A., Wang, Jun, Muzny, Donna, Wang, Jun, Li, Yingrui, Wang, Guangbiao, Wu, Honglong, Wu, Renhua, Zhang, Wenwei, Zhao, Jiao, Zhao, Meiru, Gupta, Namrata, Gharani, Neda, Clarke, Laura, Kelman, Gavin, Smith, Richard E., Bentley, David R., Grocock, Russell, Humphray, Sean, James, Terena, Belaia, Zinaida, Cook, Charles, Hefferon, Timothy, Kimelman, Mikhail, Slotta, Douglas, Keane, Thomas M., Kolb-Kokocinski, Anja, Davies, Christopher J., Auton, Adam, Coin, Lachlan J. M., Zhang, Fan, Alkan, Can, Kahveci, Fatma, Garrison, Erik P., Daly, Mark J., Bhatia, Gaurav, del Angel, Guillermo, McCarroll, Steven A., Rodriguez-Flores, Juan L., Fritz, Markus H., Beal, Kathryn, Sabeti, Pardis C., Bauer, Markus, Ye, Kai, Gravel, Simon, Chew, Emily, DeGorter, Marianne K., Lee, Charles, Cerveira, Eliza, Romanovitch, Mallory, Christoforides, Alexis, Gujral, Madhusudan, Haussler, David, James Kent, W., Blackwell, Tom, Lyons, Robert, Awadalla, Philip, Quitadamo, Andrew, Marchini, Jonathan L., Mathieson, Iain, Fu, Yunxin, Witherspoon, David, Browning, Sharon R., Jostins, Luke, Walter, Klaudia, Chen, Jieming, Zhang, Jing, Shakir, Khalid, Degenhardt, Jeremiah, Hall, Ira, Chen, Tenghui, Nelson, Bradley J., Challis, Danny, Lu, James, Habegger, Lukas, Dunham, Ian, Narechania, Apurva, Beiswanger, Christine, Durbin, Richard M., Kerasidou, Angeliki, Mathias, Rasika, Royal, Charmaine D., Wang, Yuhong, Yang, Ling, Bodmer, Walter, Peltonen, Leena, Dutil, Julie, LaRocque, Regina, Tariyal, Ridhi, Jallow, Muminatou, Corrah, Tumani, Kooner, Jaspal, Dunstan, Sarah J., Thuy Hang, Nguyen, Schieffelin, John, Saleheen, Danish

Genetic and transcriptional evolution alters cancer cell line drug response by Ben-David, Uri, Siranosian, Benjamin, Ha, Gavin, Tang, Helen, Oren, Yaara, Hinohara, Kunihiko, Strathdee, Craig A., Dempster, Joshua, Lyons, Nicholas J., Burns, Robert, Nag, Anwesha, Kugener, Guillaume, Cimini, Beth, Tsvetkov, Peter, Maruvka, Yosef E., O’Rourke, Ryan, Garrity, Anthony, Tubelli, Andrew A., Bandopadhayay, Pratiti, Tsherniak, Aviad, Vazquez, Francisca, Wong, Bang, Birger, Chet, Ghandi, Mahmoud, Thorner, Aaron R., Bittker, Joshua A., Meyerson, Matthew, Getz, Gad, Beroukhim, Rameen, Golub, Todd R.

The use of Mendelian randomisation to identify causal cancer risk factors: promise and limitations by Gala, Harvinder, Tomlinson, Ian

Rare and low-frequency coding variants alter human adult height by Wood, Andrew R., Kjaer, Troels R., Lu, Yingchang, Thorleifsson, Gudmar, Turcot, Valérie, Young, Kristin L., Rivas, Manuel A., Abecasis, Goncalo, Aben, Katja K., Allin, Kristine H., Blüher, Matthias, Bots, Michiel L., Brilliant, Murray H., Carey, David J., Chambers, John C., Chasman, Daniel I., Chen, Yii-Der Ida, Chu, Audrey Y., Collins, Francis S., Cook, James P., de Groot, Mark C. H., de Mutsert, Renée, Ebeling, Tapani, Evangelou, Evangelos, Feng, Shuang, Ford, Ian, Fornage, Myriam, Gandin, Ilaria, Gordon, Scott D., Gustafsson, Stefan, Hattersley, Andrew T., Heid, Iris M., Helgeland, Øyvind, Hewitt, Alex W., Hovingh, G. Kees, Hoyng, Carel B., Huang, Paul L., Hveem, Kristian, Ikram, M. Arfan, Jansson, Jan-Håkan, Jarvik, Gail P., Jiang, Xuejuan, Jukema, J. Wouter, Kitajima, Hidetoshi, Kluivers, Kirsten B., Kontto, Jukka, Kooner, Jaspal S., Kriebel, Jennifer, Kuusisto, Johanna, Langenberg, Claudia, Lee, I-Te, Li, Huaixing, Lin, Honghuang, Lophatananon, Artitaya, Lyytikäinen, Leo-Pekka, Madden, Pamela A. F., Männistö, Satu, Mazul, Angela L., Metspalu, Andres, Mook-Kanamori, Dennis O., Morgan, Anna, Morris, Andrew P., Müller-Nurasyid, Martina, Nalls, Mike A., Nielsen, Sune F., Njølstad, Pål R., Palmer, Colin N. A., Pasterkamp, Gerard, Pedersen, Oluf, Perola, Markus, Perry, James A., Person, Thomas N., Salomaa, Veikko, Samani, Nilesh J., Sandow, Kevin, Schmidt, Marjanka K., Segura-Lepe, Marcelo P., Sim, Xueling, Small, Kerrin S., Southam, Lorraine, Steinthorsdottir, Valgerdur, Stumvoll, Michael, Tansey, Katherine E., Tardif, Jean-Claude, Taylor, Kent D., Thompson, Deborah J., Tyrer, Jonathan P., Uitterlinden, André G., van Schoor, Natasja M., Vozzi, Diego, Wang, Shuai, Wang, Yiqin, Wilson, James G., Young, Robin, Willer, Cristen J., Liu, Dajiang J., North, Kari E., Kutalik, Zoltán, Loos, Ruth J. F., Deloukas, Panos

Analysis of protein-coding genetic variation in 60,706 humans by Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.

Fine-mapping inflammatory bowel disease loci to single-variant resolution by Huang, Hailiang, Fang, Ming, Jostins, Luke, Umićević Mirkov, Maša, Boucher, Gabrielle, Anderson, Carl A., Andersen, Vibeke, Cleynen, Isabelle, Cortes, Adrian, Crins, François, D’Amato, Mauro, Deffontaine, Valérie, Dmitrieva, Julia, Docampo, Elisa, Elansary, Mahmoud, Farh, Kyle Kai-How, Franke, Andre, Gori, Ann-Stephan, Goyette, Philippe, Halfvarson, Jonas, Haritunians, Talin, Knight, Jo, Lawrance, Ian C., Lees, Charlie W., Louis, Edouard, Mariman, Rob, Meuwissen, Theo, Mni, Myriam, Momozawa, Yukihide, Parkes, Miles, Spain, Sarah L., Théâtre, Emilie, Trynka, Gosia, Satsangi, Jack, van Sommeren, Suzanne, Vermeire, Severine, Xavier, Ramnik J., Weersma, Rinse K., Duerr, Richard H., Mathew, Christopher G., Rioux, John D., McGovern, Dermot P. B., Cho, Judy H., Georges, Michel, Daly, Mark J., Barrett, Jeffrey C.

The landscape of somatic copy-number alteration across human cancers by Beroukhim, Rameen, Mermel, Craig H., Porter, Dale, Wei, Guo, Raychaudhuri, Soumya, Donovan, Jerry, Barretina, Jordi, Boehm, Jesse S., Dobson, Jennifer, Urashima, Mitsuyoshi, Mc Henry, Kevin T., Pinchback, Reid M., Ligon, Azra H., Cho, Yoon-Jae, Haery, Leila, Greulich, Heidi, Reich, Michael, Winckler, Wendy, Lawrence, Michael S., Weir, Barbara A., Tanaka, Kumiko E., Chiang, Derek Y., Bass, Adam J., Loo, Alice, Hoffman, Carter, Prensner, John, Liefeld, Ted, Gao, Qing, Yecies, Derek, Signoretti, Sabina, Maher, Elizabeth, Kaye, Frederic J., Sasaki, Hidefumi, Tepper, Joel E., Fletcher, Jonathan A., Tabernero, Josep, Baselga, José, Tsao, Ming-Sound, Demichelis, Francesca, Rubin, Mark A., Janne, Pasi A., Daly, Mark J., Nucera, Carmelo, Levine, Ross L., Ebert, Benjamin L., Gabriel, Stacey, Rustgi, Anil K., Antonescu, Cristina R., Ladanyi, Marc, Letai, Anthony, Garraway, Levi A., Loda, Massimo, Beer, David G., True, Lawrence D., Okamoto, Aikou, Pomeroy, Scott L., Singer, Samuel, Golub, Todd R., Lander, Eric S., Getz, Gad, Sellers, William R., Meyerson, Matthew

Mendelian randomization analysis identified genes pleiotropically associated with the risk and prognosis of COVID-19 by Liu, Di, Yang, Jingyun, Feng, Bowen, Lu, Wenjin, Zhao, Chuntao, Li, Lizhuo

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues by D’Antonio, Matteo, Chwialkowska, Karolina, Tenesa, Albert, D’Mellow, Kenton, Aprile von Hohenstaufen, Kathrin, Eltoukhy, Madonna M., Yassen, Amr M., Moahmed, Hanteera S., Tobin, Martin D., Guyatt, Anna L., Hollox, Edward J., Sharififard, Bahareh, Abdollahi, Hamed, Puthanakit, Thanyawee, Suchartlikitwong, Pintip, Sodsai, Pimpayao, Alaamery, Manal, Aljawini, Nora, Albesher, Nour, Alahmadey, Ziab Z., Suliman, Bandar A., Al-Afghani, Hani, Massadeh, Salam, Muiño, Elena, Coto, Eliecer, Albaiceta, Guillermo M., Dietl, Beatriz, Martí-Fàbregas, Joan, Villalonga, Joan Montaner, Menéndez-Valladares, Paloma, Glessner, Joseph R., Forgetta, Vincenzo, Ghosh, Biswarup, Guiot, Julien, Guntz, Julien, Beguin, Yves, Claassen, Sabine, Malaise, Olivier, Daya, Michelle, Chavan, Sameer, Laisk, Triin, Alavere, Helene, Metsalu, Kristjan, Peterson, Pärt, Cortés, Beatriz, Torrents, David, Fallerini, Chiara, Doddato, Gabriella, Bruttini, Mirella, Pinto, Anna Maria, Bruno, Raffaele, Picchiotti, Nicola, Mantovani, Stefania, Bargagli, Elena, D’Alessandro, Miriana, Franchi, Federico, Cantarini, Luca, Tacconi, Danilo, Desanctis, Elena, Antinori, Andrea, Vergori, Alessandra, Baratti, Stefano, Menatti, Elisabetta, Trotta, Tullio, Martinelli, Enrico, Bachetti, Tiziana, Ceri, Stefano, Parati, Gianfranco, Ravaglia, Sabrina, Catena, Emanuele, Pessina, Gloria, Tumbarello, Mario, Guarnaccia, Alessandra, Boughton, Andrew P., Annis, Aubrey, Carey, Dave J., Gass, Matthew C., Abecasis, Goncalo R., Butterworth, Adam S., Nivard, Michel (M.G.), de geus, Eco (E.J.C.), Verma, Anurag, Ritchie, Marylyn D., Verma, Shefali S., Lucas, Anastasia, Karczewski, Konrad J., Walters, Raymond K., Palmer, Duncan S., Sarma, Gopal, Crook, Derrick W., Koelling, Nils, Moutsianas, Loukas, Rhodes, Daniel, Ball, Catherine A., Baltzell, Asher Haug, Gaddis, Michael, Noto, Keith, Tang, Lara, Nadkarni, Girish N., Choi, Sam

The UK10K project identifies rare variants in health and disease by Min, Josine L., Hendricks, Audrey E., Danecek, Petr, Floyd, James, Barroso, Inês, Hurles, Matthew E., Zeggini, Eleftheria, Bala, Senduran, Clapham, Peter, Cox, Tony, Huang, Liren, Joyce, Chris, Keane, Thomas, Muddyman, Dawn, Quail, Michael A., Stalker, Jim, Zhang, Pingbo, Clement, Gail, Davey Smith, George, Dunham, Ian, Evans, David M., Hubbard, Tim, Jamshidi, Yalda, Karczewski, Konrad J., Kemp, John P., MacArthur, Daniel G., Mangino, Massimo, Metrustry, Sarah, Paternoster, Lavinia, Quaye, Lydia, Ring, Susan, Ritchie, Graham R. S., Shihab, Hashem A., Small, Kerrin S., Soranzo, Nicole, St Pourcain, Beate, Surdulescu, Gabriela, Tachmazidou, Ioanna, Tobin, Martin D., Valdes, Ana M., Visscher, Peter M., Yang, Jian, Zheng, Hou-Feng, Anney, Richard, Craddock, Nick, Gallagher, Louise, Holmans, Peter, Lee, Irene, Lönnqvist, Jouko, McGuffin, Peter, McIntosh, Andrew M., McKechanie, Andrew G., McQuillin, Andrew, Morris, James, Palotie, Aarno, Pietilainen, Olli, Skuse, David, St Clair, David, Suvisaari, Jaana, Walters, James T. R., Barroso, Inês, Bochukova, Elena, Bounds, Rebecca, Farooqi, I. Sadaf, Smith, Blair H., Antony, Dinu, Beales, Phil, Calissano, Mattia, Carss, Keren, Reghan Foley, A., Grozeva, Detelina, Hurles, Matthew E., Onoufriadis, Alexandros, Parker, Victoria, Lucy Raymond, F., Savage, David B., Semple, Robert K., Williamson, Kathleen A., Whyte, Tamieka, Bobrow, Martin, Griffin, Heather, Kaye, Jane, Charlton, Ruth, Lopes, Luis R., Migone, Nicola, Payne, Stewart J., Scott, Richard H., Taylor, Rohan, Vandersteen, Anthony M., Owen, Michael J., Palotie, Aarno, Amuzu, Antoinette, Pablo Casas, Juan, Dedoussis, George, Isaacs, Aaron, Kleber, Marcus E., Kooner, Jaspal S., Luan, Jian'an, März, Winfried, Varbo, Anette

Mendelian randomization identifies blood metabolites previously linked to midlife cognition as causal candidates in Alzheimer’s disease by Lord, Jodie, Jermy, Bradley, Green, Rebecca, Wong, Andrew, Xu, Jin, Legido-Quigley, Cristina, Dobson, Richard, Richards, Marcus, Proitsi, Petroula

Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders by Sullivan, Patrick F., Geschwind, Daniel H.