The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States von Bryc, Katarzyna, Durand, Eric Y., Macpherson, J. Michael, Reich, David, Mountain, Joanna L.

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Disease risk scores for skin cancers von Fontanillas, Pierre, Alipanahi, Babak, Furlotte, Nicholas A., Johnson, Michaela, Wilson, Catherine H., Pitts, Steven J., Gentleman, Robert, Auton, Adam

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A High-Coverage Genome Sequence from an Archaic Denisovan Individual von Meyer, Matthias, Kircher, Martin, Gansauge, Marie-Theres, Li, Heng, Racimo, Fernando, Mallick, Swapan, Schraiber, Joshua G., Jay, Flora, Prüfer, Kay, de Filippo, Cesare, Sudmant, Peter H., Alkan, Can, Fu, Qiaomei, Do, Ron, Rohland, Nadin, Tandon, Arti, Siebauer, Michael, Green, Richard E., Bryc, Katarzyna, Briggs, Adrian W., Stenzel, Udo, Dabney, Jesse, Shendure, Jay, Kitzman, Jacob, Hammer, Michael F., Shunkov, Michael V., Derevianko, Anatoli P., Patterson, Nick, Andrés, Aida M., Eichler, Evan E., Slatkin, Montgomery, Reich, David, Kelso, Janet, Pääbo, Svante

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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 patterns of population structure and admixture among Hispanic/Latino populations von Bryc, Katarzyna, Velez, Christopher, Karafet, Tatiana, Moreno-Estrada, Andres, Reynolds, Andy, Auton, Adam, Hammer, Michael, Bustamante, Carlos D, Ostrer, Harry

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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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Serum copeptin as a predictor of risk of hyponatremia after transurethral prostatectomy von Bryc-Walczak, Katarzyna, Bryc, Władysław, Nowicki, Michał

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Genome-wide patterns of population structure and admixture in West Africans and African Americans von Bryc, Katarzyna, Auton, Adam, Nelson, Matthew R, Oksenberg, Jorge R, Hauser, Stephen L, Williams, Scott, Froment, Alain, Bodo, Jean-Marie, Wambebe, Charles, Tishkoff, Sarah A, Bustamante, Carlos D

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Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets von Márquez-Luna, Carla, Gazal, Steven, Loh, Po-Ru, Kim, Samuel S., Furlotte, Nicholas, Auton, Adam, Price, Alkes L.

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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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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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Genome-wide association studies of antidepressant class response and treatment-resistant depression von Li, Qingqin S., Tian, Chao, Hinds, David

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Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry von Sanchez-Roige, Sandra, Fontanillas, Pierre, Jennings, Mariela V., Bianchi, Sevim B., Huang, Yuye, Hatoum, Alexander S., Sealock, Julia, Davis, Lea K., Elson, Sarah L., Palmer, Abraham A.

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Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality von Adewuyi, Emmanuel O., Mehta, Divya, Sapkota, Yadav, Auta, Asa, Yoshihara, Kosuke, Nyegaard, Mette, Griffiths, Lyn R., Montgomery, Grant W., Chasman, Daniel I., Nyholt, Dale R.

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A novel approach to estimating heterozygosity from low-coverage genome sequence von Bryc, Katarzyna, Patterson, Nick, Reich, David

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On identifying the optimal number of population clusters via the deviance information criterion von Gao, Hong, Bryc, Katarzyna, Bustamante, Carlos D

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Resource profile and user guide of the Polygenic Index Repository von Becker, Joel, Burik, Casper A. P., Goldman, Grant, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Belsky, Daniel W., Karlsson Linnér, Richard, Ahlskog, Rafael, Kleinman, Aaron, Hinds, David A., Caspi, Avshalom, Corcoran, David L., Moffitt, Terrie E., Poulton, Richie, Sugden, Karen, Williams, Benjamin S., Harris, Kathleen Mullan, Steptoe, Andrew, Ajnakina, Olesya, Milani, Lili, Esko, Tõnu, Iacono, William G., McGue, Matt, Magnusson, Patrik K. E., Mallard, Travis T., Harden, K. Paige, Tucker-Drob, Elliot M., Herd, Pamela, Freese, Jeremy, Young, Alexander, Beauchamp, Jonathan P., Koellinger, Philipp D., Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Meyer, Michelle N., Laibson, David, Cesarini, David, Benjamin, Daniel J., Turley, Patrick, Okbay, Aysu

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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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Global distribution of genomic diversity underscores rich complex history of continental human populations von Auton, Adam, Bryc, Katarzyna, Boyko, Adam R, Lohmueller, Kirk E, Novembre, John, Reynolds, Andy, Indap, Amit, Wright, Mark H, Degenhardt, Jeremiah D, Gutenkunst, Ryan N, King, Karen S, Nelson, Matthew R, Bustamante, Carlos D

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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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