Intrahepatic cholestasis in sickle cell disease: A review of diagnostic criteria, treatments, and case reports von Edwards, Christopher L., Scott, Sharena, Boggan, Michaela, Meek, Jordan, Alston, Kiera, Pearson, Aiden, McDougald, Alexandria, Broadnax, McKenzie, Wood, Mary, Barker, Camela S., Miller, Jessica, Whitworth, Elaine, James, Osaffo, Sollers  III, John J., Bryson, W. Jeff, Thorpe, Roland, Byrd, Goldie, Whitfield, Keith E., Sudhakar, Shiv, Parker, Debra O., Livingston, Jonathan, Shah, Nirmish, Railey, Kenyon

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Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins von Postmus, Iris, Trompet, Stella, Deshmukh, Harshal A., Barnes, Michael R., Li, Xiaohui, Warren, Helen R., Chasman, Daniel I., Zhou, Kaixin, Arsenault, Benoit J., Donnelly, Louise A., Wiggins, Kerri L., Avery, Christy L., Griffin, Paula, Feng, QiPing, Taylor, Kent D., Li, Guo, Evans, Daniel S., Smith, Albert V., de Keyser, Catherine E., Johnson, Andrew D., de Craen, Anton J. M., Buckley, Brendan M., Ford, Ian, Westendorp, Rudi G. J., Eline Slagboom, P., Sattar, Naveed, Munroe, Patricia B., Sever, Peter, Poulter, Neil, Stanton, Alice, Shields, Denis C., O’Brien, Eoin, Shaw-Hawkins, Sue, Ida Chen, Y.-D., Nickerson, Deborah A., Smith, Joshua D., Pierre Dubé, Marie, Matthijs Boekholdt, S., Kees Hovingh, G., Kastelein, John J. P., McKeigue, Paul M., Betteridge, John, Neil, Andrew, Durrington, Paul N., Doney, Alex, Carr, Fiona, Morris, Andrew, McCarthy, Mark I., Groop, Leif, Ahlqvist, Emma, Bis, Joshua C., Rice, Kenneth, Smith, Nicholas L., Lumley, Thomas, Whitsel, Eric A., Stürmer, Til, Boerwinkle, Eric, Ngwa, Julius S., O’Donnell, Christopher J., Wei, Wei-Qi, Wilke, Russell A., Liu, Ching-Ti, Sun, Fangui, Guo, Xiuqing, Heckbert, Susan R, Post, Wendy, Sotoodehnia, Nona, Arnold, Alice M., Stafford, Jeanette M., Ding, Jingzhong, Herrington, David M., Kritchevsky, Stephen B., Eiriksdottir, Gudny, Launer, Leonore J., Harris, Tamara B., Chu, Audrey Y., Giulianini, Franco, MacFadyen, Jean G., Barratt, Bryan J., Nyberg, Fredrik, Stricker, Bruno H., Uitterlinden, André G., Hofman, Albert, Rivadeneira, Fernando, Emilsson, Valur, Franco, Oscar H., Ridker, Paul M., Gudnason, Vilmundur, Liu, Yongmei, Denny, Joshua C., Ballantyne, Christie M., Adrienne Cupples, L., Psaty, Bruce M., Palmer, Colin N. A., Tardif, Jean-Claude, Colhoun, Helen M., Hitman, Graham, Krauss, Ronald M., Wouter Jukema, J, Caulfield, Mark J.

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Decarbonising our food systems: contextualising digitalisation for net zero von Pearson, Simon, Brewer, Steve, Manning, Louise, Bidaut, Luc, Onoufriou, George, Durrant, Aiden, Leontidis, Georgios, Jabbour, Charbel, Zisman, Andrea, Parr, Gerard, Frey, Jeremy, Maull, Roger

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A polygenic resilience score moderates the genetic risk for schizophrenia von Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Marie, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Stephen J.

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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome von Aung, Tin, Ozaki, Mineo, Li, Zheng, Uebe, Steffen, Harder, Jeffrey M, Chan, Anita S Y, Lee, Mei Chin, Burdon, Kathryn P, Pakravan, Mohammad, Wang, Ya Xing, Williams, Susan, Huang, Lulin, Foo, Jia Nee, Kumar, Rajesh S, Ueno, Morio, Manabe, Shin-ichi, Hayashi, Ken, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Yoshida, Akitoshi, Yanagi, Masahide, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Yamashiro, Kenji, Gotoh, Norimoto, Osman, Essam A, Al-Obeidan, Saleh A, Al-Jasim, Leyla, Shahwan, Sami Al, Leo, Paul, Yetkin, Yaz, Oğuz, Çilingir, Kanavi, Mozhgan Rezaei, Yazdani, Shahin, Akopov, Evgeny L, Howell, Gareth R, Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N, Wong, Tien Yin, Liu, Yutao, Challa, Pratap, Hewitt, Alex W, Mitchell, Paul, Ziskind, Ari, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Guadarrama-Vallejo, Dalia, Perera, Shamira A, Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Schloetzer-Schrehardt, Ursula, Herms, Stefan, Nöthen, Markus M, Weisschuh, Nicole, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A, Lischinsky, Ignacio, Crowston, Jonathan G, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Founti, Panayiota, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Rhee, Douglas J, May-Bolchakova, Inna, Heegaard, Steffen, Alward, Wallace L M, Jonas, Jost B, Xu, Liang, Chowbay, Balram, Schaeffeler, Elke, Lerner, Fabian, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Inatani, Masaru, Tashiro, Kei, Reis, André, Edward, Deepak P, Pasquale, Louis R, Wiggs, Janey L, Yoshimura, Nagahisa, Ritch, Robert, Khor, Chiea-Chuen

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Common genetic determinants of intraocular pressure and primary open-angle glaucoma von van Koolwijk, Leonieke M E, Ramdas, Wishal D, Ikram, M Kamran, Jansonius, Nomdo M, Pasutto, Francesca, Hysi, Pirro G, Macgregor, Stuart, Janssen, Sarah F, Hewitt, Alex W, Viswanathan, Ananth C, ten Brink, Jacoline B, Hosseini, S Mohsen, Amin, Najaf, Despriet, Dominiek D G, Willemse-Assink, Jacqueline J M, Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S, Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y, Gramer, Eugen, Welge-Lüssen, Ulrich, Montgomery, Grant W, Carbonaro, Francis, Young, Terri L, Bellenguez, Céline, McGuffin, Peter, Foster, Paul J, Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y, Czudowska, Monika A, Hofman, Albert, Uitterlinden, Andre G, Wolfs, Roger C W, de Jong, Paulus T V M, Oostra, Ben A, Paterson, Andrew D, Mackey, David A, Bergen, Arthur A B, Reis, André, Hammond, Christopher J, Vingerling, Johannes R, Lemij, Hans G, Klaver, Caroline C W, van Duijn, Cornelia M

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Ischemic stroke is associated with the ABO locus: The EuroCLOT study von Williams, Frances M. K., Carter, Angela M., Hysi, Pirro G., Surdulescu, Gabriela, Hodgkiss, Dylan, Soranzo, Nicole, Traylor, Matthew, Bevan, Steve, Dichgans, Martin, Rothwell, Peter M. W., Sudlow, Cathie, Farrall, Martin, Silander, Kaisa, Kaunisto, Mari, Wagner, Peter, Saarela, Olli, Kuulasmaa, Kari, Virtamo, Jarmo, Salomaa, Veikko, Amouyel, Philippe, Arveiler, Dominique, Ferrieres, Jean, Wiklund, Per-Gunnar, Arfan Ikram, M., Hofman, Albert, Boncoraglio, Giorgio B., Parati, Eugenio A., Helgadottir, Anna, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Thorleifsson, Gudmar, Stefansson, Kari, Seshadri, Sudha, DeStefano, Anita, Gschwendtner, Andreas, Psaty, Bruce, Longstreth, Will, Mitchell, Braxton D., Cheng, Yu-Ching, Clarke, Robert, Ferrario, Marco, Bis, Joshua C., Levi, Christopher, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Fornage, Myriam, Sharma, Pankaj, Furie, Karen L., Rosand, Jonathan, Nalls, Mike, Meschia, James, Mosely, Thomas H., Evans, Alun, Palotie, Aarno, Markus, Hugh S., Grant, Peter J., Spector, Tim D.

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Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis von Holliday, Elizabeth G, Smith, Albert V, Cornes, Belinda K, Buitendijk, Gabriëlle H S, Jensen, Richard A, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N, Boerwinkle, Eric, Cheng, Ching Yu, van Duijn, Cornelia M, Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W, Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E K, Launer, Lenore, Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M, Rochtchina, Elena, Rotter, Jerome I, Scott, Rodney J, Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, André G, Viswanathan, Ananth, Xie, Sophia, Vingerling, Johannes R, Klaver, Caroline C W, Tai, E Shyong, Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y, Attia, John, Wang, Jie Jin

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Common variant at 16p11.2 conferring risk of psychosis von Steinberg, S, de Jong, S, Pietiläinen, O P H, Lin, K, Papiol, S, Huttenlocher, J, Sigurdsson, E, Giegling, I, Breuer, R, Fraser, G, Walker, N, Melle, I, Djurovic, S, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Olsen, L, Ingason, A, Pirinen, M, Strengman, E, Hougaard, D M, Ørntoft, T, Didriksen, M, Abramova, L, Kaleda, V, Arrojo, M, Arango, C, Etain, B, Bellivier, F, Méary, A, Schürhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rossner, M, Christiansen, C, Kiemeney, L A, Franke, B, Veldink, J, Curran, S, Bolton, P, Poot, M, Rehnstrom, K, Freitag, C M, Magnusson, P, Saemundsen, E, Martsenkovsky, I, Bikshaieva, I, Martsenkovska, I, Vashchenko, O, Raleva, M, Paketchieva, K, Pejovic Milovancevic, M, Naneishvili, N, Mikeladze, N, Vincent, J B, Farmer, A, Mitchell, P B, Wright, A, Schofield, P R, Fullerton, J M, Montgomery, G W, Rubino, I A, Kenis, G, Bitter, I, Terenius, L, Jönsson, E G, Bakker, S, van Os, J, Jablensky, A, Powell, J, Murray, R, Corvin, A, Gill, M, Morris, D, O'Neill, F A, Kendler, K, Riley, B, Craddock, N, O'Donovan, M C, Thorsteinsdottir, U, Ehrenreich, H, Carracedo, A, Golimbet, V, Børglum, A D, Mortensen, P B, Werge, T, Ophoff, R A, Rietschel, M, Cichon, S, Ruggeri, M, Tosato, S, Palotie, A, St Clair, D, Rujescu, D, Collier, D A, Stefansson, K

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The correlation between reading and mathematics ability at age twelve has a substantial genetic component von Davis, Oliver S. P., Band, Gavin, Pirinen, Matti, Haworth, Claire M. A., Meaburn, Emma L., Kovas, Yulia, Harlaar, Nicole, Docherty, Sophia J., Hanscombe, Ken B., Trzaskowski, Maciej, Curtis, Charles J. C., Strange, Amy, Freeman, Colin, Bellenguez, Céline, Su, Zhan, Pearson, Richard, Vukcevic, Damjan, Langford, Cordelia, Deloukas, Panos, Hunt, Sarah, Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Edkins, Sarah, Bumpstead, Suzannah J., Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz A. Z., Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Barroso, Ines, Peltonen, Leena, Dale, Philip S., Petrill, Stephen A., Schalkwyk, Leonard S., Craig, Ian W., Lewis, Cathryn M., Price, Thomas S., Donnelly, Peter, Plomin, Robert, Spencer, Chris C. A.

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 von Rees, Elliott, Walters, James T R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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A robust clustering algorithm for identifying problematic samples in genome-wide association studies von Bellenguez, Céline, Strange, Amy, Freeman, Colin, Donnelly, Peter, Spencer, Chris C.A.

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MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls von Cosgrove, D, Harold, D, Mothersill, O, Anney, R, Hill, M J, Bray, N J, Blokland, G, Petryshen, T, Richards, A, Mantripragada, K, Owen, M, O'Donovan, M C, Gill, M, Corvin, A, Morris, D W, Donohoe, G

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The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis von Robinson, P C, Leo, P J, Pointon, J J, Harris, J, Cremin, K, Bradbury, L A, Stebbings, S, Harrison, A A, Evans, D M, Duncan, E L, Wordsworth, B P, Brown, M A

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17q25 Locus Is Associated With White Matter Hyperintensity Volume in Ischemic Stroke, But Not With Lacunar Stroke Status von ADIB-SAMII, Poneh, ROST, Natalia, GSCHWENDTNER, Andreas, MALIK, Rainer, RICHIE, Alexa, GAMBLE, Dale, SEGAL, Helen, PARATI, Eugenio A, CIUSANI, Emilio, HOLLIDAY, Elizabeth G, MAGUIRE, Jane, WARDLAW, Joanna, TRAYLOR, Matthew, WORRALL, Bradford, BIS, Joshua, WIGGINS, Kerri L, LONGSTRETH, Will, KITTNER, Steve J, CHENG, Yu-Ching, MOSLEY, Thomas, FALCONE, Guido J, FURIE, Karen L, LEIVA-SALINAS, Carlos, DEVAN, William, LAU, Benison C, MUHAMMED SALEEM KHAN, SHARMA, Pankaj, FORNAGE, Myriam, MITCHELL, Braxton D, PSATY, Bruce M, SUDLOW, Cathie, LEVI, Christopher, BONCORAGLIO, Giorgio B, ROTHWELL, Peter M, BIFFI, Alessandro, MESCHIA, James, DICHGANS, Martin, ROSAND, Jonathan, MARKUS, Hugh S, LANFRANCONI, Silvia, FITZPATRICK, Kaitlin, BEVAN, Steve, KANAKIS, Allison, VALANT, Valerie

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Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases von Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart

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Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus von Strange, Amy, Bellenguez, Céline, Sim, Xueling, Luben, Robert, Hysi, Pirro G., Ramdas, Wishal D., van Koolwijk, Leonieke M.E., Freeman, Colin, Pirinen, Matti, Su, Zhan, Band, Gavin, Pearson, Richard, Vukcevic, Damjan, Langford, Cordelia, Deloukas, Panos, Hunt, Sarah, Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Edkins, Sarah, Bumpstead, Suzannah J., Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz A.Z., Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N.A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Wood, Nicholas W., Barroso, Ines, Peltonen, Leena, Healey, Paul, McGuffin, Peter, Topouzis, Fotis, Klaver, Caroline C.W., van Duijn, Cornelia M., Mackey, David A., Young, Terri L., Hammond, Christopher J., Khaw, Kay-Tee, Wareham, Nick, Wang, Jie Jin, Wong, Tien Y., Foster, Paul J., Mitchell, Paul, Spencer, Chris C.A., Donnelly, Peter, Viswanathan, Ananth C.

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4:45 PM COMMON AND RARE RISK VARIANTS IMPLICATE PAK SIGNALING IN THE MOLECULAR ETIOLOGY OF SCHIZOPHRENIA von Corvin, Aiden, Morris, Derek, Pearson, Richard, Cormican, Paul, Kenny, Elaine, O'Neill, Francis, Trust, Wellcome, Kendler, Kenneth, Gill, Michael, Riley, Brien, Spencer, Chris

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Genome-Wide Association Study of Receptive Language Ability of 12-Year-Olds von Harlaar, Nicole, Meaburn, Emma L, Hayiou-Thomas, Marianna E, Davis, Oliver S. P, Docherty, Sophia, Hanscombe, Ken B, Haworth, Claire M. A, Price, Thomas S, Trzaskowski, Maciej, Dale, Philip S, Plomin, Robert

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A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility von Damotte, V, Guillot-Noel, L, Patsopoulos, N A, Madireddy, L, El Behi, M, De Jager, P L, Baranzini, S E, Cournu-Rebeix, I, Fontaine, B

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