Clinical use of current polygenic risk scores may exacerbate health disparities von Martin, Alicia R., Kanai, Masahiro, Kamatani, Yoichiro, Okada, Yukinori, Neale, Benjamin M., Daly, Mark J.

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Genetic architectures of psychiatric disorders: the emerging picture and its implications von Sullivan, Patrick F., Daly, Mark J., O'Donovan, Michael

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Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations von Martin, Alicia R., Gignoux, Christopher R., Walters, Raymond K., Wojcik, Genevieve L., Neale, Benjamin M., Gravel, Simon, Daly, Mark J., Bustamante, Carlos D., Kenny, Eimear E.

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The ExAC browser: displaying reference data information from over 60 000 exomes von Karczewski, Konrad J, Weisburd, Ben, Thomas, Brett, Solomonson, Matthew, Ruderfer, Douglas M, Kavanagh, David, Hamamsy, Tymor, Lek, Monkol, Samocha, Kaitlin E, Cummings, Beryl B, Birnbaum, Daniel, Daly, Mark J, MacArthur, Daniel G

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Genetic Mapping in Human Disease von Altshuler, David, Daly, Mark J, Lander, Eric S

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Predicting Polygenic Risk of Psychiatric Disorders von Martin, Alicia R., Daly, Mark J., Robinson, Elise B., Hyman, Steven E., Neale, Benjamin M.

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Genetics of 35 blood and urine biomarkers in the UK Biobank von Sinnott-Armstrong, Nasa, Tanigawa, Yosuke, Amar, David, Mars, Nina, Benner, Christian, Aguirre, Matthew, Venkataraman, Guhan Ram, Wainberg, Michael, Ollila, Hanna M., Kiiskinen, Tuomo, Havulinna, Aki S., Pirruccello, James P., Qian, Junyang, Shcherbina, Anna, Rodriguez, Fatima, Assimes, Themistocles L., Agarwala, Vineeta, Tibshirani, Robert, Hastie, Trevor, Ripatti, Samuli, Pritchard, Jonathan K., Daly, Mark J., Rivas, Manuel A.

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Schizophrenia risk from complex variation of complement component 4 von Sekar, Aswin, Bialas, Allison R., de Rivera, Heather, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa, Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A.

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Partitioning heritability by functional annotation using genome-wide association summary statistics von Finucane, Hilary K, Bulik-Sullivan, Brendan, Gusev, Alexander, Trynka, Gosia, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle, Ripke, Stephan, Day, Felix R, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R B, Okada, Yukinori, Raychaudhuri, Soumya, Daly, Mark J, Patterson, Nick, Neale, Benjamin M, Price, Alkes L

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Variant TREM2 as Risk Factor for Alzheimer's Disease von Neumann, Harald, Daly, Mark J

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Searching for missing heritability: Designing rare variant association studies von Zuk, Or, Schaffner, Stephen F, Samocha, Kaitlin, Do, Ron, Hechter, Eliana, Kathiresan, Sekar, Daly, Mark J, Neale, Benjamin M, Sunyaev, Shamil R, Lander, Eric S

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Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power von Atkinson, Elizabeth G., Maihofer, Adam X., Kanai, Masahiro, Martin, Alicia R., Karczewski, Konrad J., Santoro, Marcos L., Ulirsch, Jacob C., Kamatani, Yoichiro, Okada, Yukinori, Finucane, Hilary K., Koenen, Karestan C., Nievergelt, Caroline M., Daly, Mark J., Neale, Benjamin M.

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Abundant contribution of short tandem repeats to gene expression variation in humans von Gymrek, Melissa, Willems, Thomas, Guilmatre, Audrey, Zeng, Haoyang, Markus, Barak, Georgiev, Stoyan, Daly, Mark J, Price, Alkes L, Pritchard, Jonathan K, Sharp, Andrew J, Erlich, Yaniv

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Genome-wide association studies for common diseases and complex traits von Hirschhorn, Joel N, Daly, Mark J

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RICOPILI: Rapid Imputation for COnsortias PIpeLIne von Lam, Max, Awasthi, Swapnil, Watson, Hunna J, Goldstein, Jackie, Panagiotaropoulou, Georgia, Trubetskoy, Vassily, Karlsson, Robert, Frei, Oleksander, Fan, Chun-Chieh, De Witte, Ward, Mota, Nina R, Mullins, Niamh, Brügger, Kim, Lee, S Hong, Wray, Naomi R, Skarabis, Nora, Huang, Hailiang, Neale, Benjamin, Daly, Mark J, Mattheisen, Manuel, Walters, Raymond, Ripke, Stephan

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A framework for variation discovery and genotyping using next-generation DNA sequencing data von DePristo, Mark A, Banks, Eric, Poplin, Ryan, Garimella, Kiran V, Maguire, Jared R, Hartl, Christopher, Philippakis, Anthony A, del Angel, Guillermo, Rivas, Manuel A, Hanna, Matt, McKenna, Aaron, Fennell, Tim J, Kernytsky, Andrew M, Sivachenko, Andrey Y, Cibulskis, Kristian, Gabriel, Stacey B, Altshuler, David, Daly, Mark J

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Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies von Sohail, Mashaal, Maier, Robert M, Ganna, Andrea, Bloemendal, Alex, Martin, Alicia R, Turchin, Michael C, Chiang, Charleston Wk, Hirschhorn, Joel, Daly, Mark J, Patterson, Nick, Neale, Benjamin, Mathieson, Iain, Reich, David, Sunyaev, Shamil R

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Genetic and epigenetic fine mapping of causal autoimmune disease variants von Farh, Kyle Kai-How, Marson, Alexander, Zhu, Jiang, Kleinewietfeld, Markus, Housley, William J., Beik, Samantha, Shoresh, Noam, Whitton, Holly, Ryan, Russell J. H., Shishkin, Alexander A., Hatan, Meital, Carrasco-Alfonso, Marlene J., Mayer, Dita, Luckey, C. John, Patsopoulos, Nikolaos A., De Jager, Philip L., Kuchroo, Vijay K., Epstein, Charles B., Daly, Mark J., Hafler, David A., Bernstein, Bradley E.

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Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples von Kosmicki, Jack A, Samocha, Kaitlin E, Howrigan, Daniel P, Sanders, Stephan J, Slowikowski, Kamil, Lek, Monkol, Karczewski, Konrad J, Cutler, David J, Devlin, Bernie, Roeder, Kathryn, Buxbaum, Joseph D, Neale, Benjamin M, MacArthur, Daniel G, Wall, Dennis P, Robinson, Elise B, Daly, Mark J

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants von Pe'er, Itsik, Yelensky, Roman, Altshuler, David, Daly, Mark J.

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