Genetic determinants of daytime napping and effects on cardiometabolic health von Dashti, Hassan S., Daghlas, Iyas, Lane, Jacqueline M., Huang, Yunru, Udler, Miriam S., Wang, Heming, Ollila, Hanna M., Jones, Samuel E., Kim, Jaegil, Wood, Andrew R., Weedon, Michael N., Aslibekyan, Stella, Garaulet, Marta, Saxena, Richa

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Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci von Dudding, Tom, Haworth, Simon, Lind, Penelope A., Sathirapongsasuti, J. Fah, Tung, Joyce Y., Mitchell, Ruth, Colodro-Conde, Lucía, Medland, Sarah E., Gordon, Scott, Elsworth, Benjamin, Paternoster, Lavinia, Franks, Paul W., Thomas, Steven J., Martin, Nicholas G., Timpson, Nicholas J.

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Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct von Ferreira, Manuel A.R., Mathur, Riddhima, Vonk, Judith M., Szwajda, Agnieszka, Brumpton, Ben, Granell, Raquel, Brew, Bronwyn K., Ullemar, Vilhelmina, Lu, Yi, Jiang, Yunxuan, Magnusson, Patrik K.E., Karlsson, Robert, Hinds, David A., Paternoster, Lavinia, Koppelman, Gerard H., Almqvist, Catarina

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Genetic predisposition to mosaic Y chromosome loss in blood von Thompson, Deborah J., Genovese, Giulio, Halvardson, Jonatan, Ulirsch, Jacob C., Wright, Daniel J., Terao, Chikashi, Davidsson, Olafur B., Day, Felix R., Sulem, Patrick, Jiang, Yunxuan, Danielsson, Marcus, Davies, Hanna, Dennis, Joe, Dunlop, Malcolm G., Easton, Douglas F., Fisher, Victoria A., Zink, Florian, Houlston, Richard S., Ingelsson, Martin, Kar, Siddhartha, Kerrison, Nicola D., Kinnersley, Ben, Kristjansson, Ragnar P., Law, Philip J., Li, Rong, Loveday, Chey, Mattisson, Jonas, McCarroll, Steven A., Murakami, Yoshinori, Murray, Anna, Olszewski, Pawel, Rychlicka-Buniowska, Edyta, Scott, Robert A., Thorsteinsdottir, Unnur, Tomlinson, Ian, Moghadam, Behrooz Torabi, Turnbull, Clare, Wareham, Nicholas J., Gudbjartsson, Daniel F., Kamatani, Yoichiro, Hoffmann, Eva R., Jackson, Steve P., Stefansson, Kari, Auton, Adam, Ong, Ken K., Machiela, Mitchell J., Loh, Po-Ru, Dumanski, Jan P., Chanock, Stephen J., Forsberg, Lars A., Perry, John R. B.

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Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population von Nakka, Priyanka, Pattillo Smith, Samuel, O’Donnell-Luria, Anne H., McManus, Kimberly F., Agee, Michelle, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Lin, Keng-Han, McCreight, Jennifer C., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McIntyre, Matthew H., Noblin, Elizabeth S., Northover, Carrie A.M., Pitts, Steven J., Poznik, G. David, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y., Vacic, Vladimir, Wang, Xin, Mountain, Joanna L., Ramachandran, Sohini, Sathirapongsasuti, J. Fah

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An ensemble penalized regression method for multi-ancestry polygenic risk prediction von Zhang, Jingning, Zhan, Jianan, Jin, Jin, Ma, Cheng, Zhao, Ruzhang, O’Connell, Jared, Jiang, Yunxuan, Koelsch, Bertram L., Zhang, Haoyu, Chatterjee, Nilanjan

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Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure von Arvanitis, Marios, Tampakakis, Emmanouil, Zhang, Yanxiao, Wang, Wei, Auton, Adam, Dutta, Diptavo, Glavaris, Stephanie, Keramati, Ali, Chatterjee, Nilanjan, Chi, Neil C., Ren, Bing, Post, Wendy S., Battle, Alexis

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Characterizing mood disorders in the AFFECT study: a large, longitudinal, and phenotypically rich genetic cohort in the US von Dalby, Maria, Vitezic, Morana, Plath, Niels, Hammer-Helmich, Lene, Jiang, Yunxuan, Tian, Chao, Dhamija, Devika, Wilson, Catherine H., Hinds, David, Sullivan, Patrick F., Buckholtz, Joshua W., Smoller, Jordan W.

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CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice von Sanchez-Roige, Sandra, Jennings, Mariela V., Thorpe, Hayley H. A., Mallari, Jazlene E., van der Werf, Lieke C., Bianchi, Sevim B., Huang, Yuye, Lee, Calvin, Mallard, Travis T., Barnes, Samuel A., Wu, Jin Yi, Barkley-Levenson, Amanda M., Boussaty, Ely C., Snethlage, Cedric E., Schafer, Danielle, Babic, Zeljana, Winters, Boyer D., Watters, Katherine E., Biederer, Thomas, Mackillop, James, Stephens, David N., Elson, Sarah L., Fontanillas, Pierre, Khokhar, Jibran Y., Young, Jared W., Palmer, Abraham A.

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Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease von Smolensky, Luba, Amondikar, Ninad, Crawford, Karen, Neu, Scott, Kopil, Catherine M., Daeschler, Margaret, Riley, Lindsey, Brown, Ethan, Toga, Arthur W., Tanner, Caroline

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Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero von Warrington, Nicole M, Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G, Jiang, Yunxuan, Auton, Adam, Boer, Cindy G, Mangino, Massimo, Wang, Carol A, Kemp, John P, McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, M Arfan, Montgomery, Grant W, Felix, Janine F, Wright, Margaret J, Mackey, David A, Jaddoe, Vincent W, Martin, Nicholas G, Tung, Joyce Y, Davey Smith, George, Pennell, Craig E, Spector, Tim D, van Meurs, Joyce, Rivadeneira, Fernando, Medland, Sarah E, Evans, David M

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Dissecting Vancomycin-Intermediate Resistance in Staphylococcus aureus Using Genome-Wide Association von Alam, Md Tauqeer, Petit, Robert A., Crispell, Emily K., Thornton, Timothy A., Conneely, Karen N., Jiang, Yunxuan, Satola, Sarah W., Read, Timothy D.

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A Permutation Procedure to Correct for Confounders in Case-Control Studies, Including Tests of Rare Variation von Epstein, Michael P., Duncan, Richard, Jiang, Yunxuan, Conneely, Karen N., Allen, Andrew S., Satten, Glen A.

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Inhibitions inflammatory response in clicks alleviates LPS induced myocardial injury by total polysaccharides of Pinus massoniana Lamb. pollen von Wang, Cheng, Shang, Hongqi, Zhang, Shuyu, Wang, Xiangkun, Shen, Mingyue, Li, Ning, Liu, Defeng, Jiang, Yunxuan, Wei, Kai, Zhu, Ruiliang

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Enhancing immunotherapy efficacy against MHC-I deficient triple-negative breast cancer using LCL161-loaded macrophage membrane-decorated nanoparticles von Zhang, Wen, Zhai, Yihui, Cai, Ying, Gong, Xiang, Jiang, Yunxuan, Rong, Rong, Zheng, Chao, Zhu, Binyu, Zhu, Helen He, Wang, Hao, Li, Yaping, Zhang, Pengcheng

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FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression von Puan, Kia Joo, San Luis, Boris, Yusof, Nurhashikin, Kumar, Dilip, Andiappan, Anand Kumar, Lee, Wendy, Cajic, Samanta, Vuckovic, Dragana, Chan, Jing De, Döllner, Tobias, Hou, Han Wei, Jiang, Yunxuan, Tian, Chao, Rapp, Erdmann, Poidinger, Michael, Wang, De Yun, Soranzo, Nicole, Lee, Bernett, Rötzschke, Olaf

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Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank von Meng, Weihua, Adams, Mark J., Palmer, Colin N. A., Shi, Jingchunzi, Auton, Adam, Ryan, Kathleen A., Jordan, Joanne M., Mitchell, Braxton D., Jackson, Rebecca D., Yau, Michelle S., McIntosh, Andrew M., Smith, Blair H.

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Genome-Wide Association Study Identifies Loci Associated with Sensitive Skin von Farage, Miranda A., Jiang, Yunxuan, Tiesman, Jay P., Fontanillas, Pierre, Osborne, Rosemarie

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A population-specific reference panel for improved genotype imputation in African Americans von O’Connell, Jared, Yun, Taedong, Moreno, Meghan, Li, Helen, Litterman, Nadia, Kolesnikov, Alexey, Noblin, Elizabeth, Chang, Pi-Chuan, Shastri, Anjali, Dorfman, Elizabeth H., Shringarpure, Suyash, Auton, Adam, Carroll, Andrew, McLean, Cory Y.

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Assessing the Impact of Population Stratification on Association Studies of Rare Variation von Jiang, Yunxuan, Epstein, Michael P., Conneely, Karen N.

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