Global variation in sequencing impedes SARS- CoV-2 surveillance von Crawford, Dana C., Williams, Scott M.

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PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations von Denny, Joshua C., Ritchie, Marylyn D., Basford, Melissa A., Pulley, Jill M., Bastarache, Lisa, Brown-Gentry, Kristin, Wang, Deede, Masys, Dan R., Roden, Dan M., Crawford, Dana C.

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Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study von Carlson, Christopher S, Matise, Tara C, North, Kari E, Haiman, Christopher A, Fesinmeyer, Megan D, Buyske, Steven, Schumacher, Fredrick R, Peters, Ulrike, Franceschini, Nora, Ritchie, Marylyn D, Duggan, David J, Spencer, Kylee L, Dumitrescu, Logan, Eaton, Charles B, Thomas, Fridtjof, Young, Alicia, Carty, Cara, Heiss, Gerardo, Le Marchand, Loic, Crawford, Dana C, Hindorff, Lucia A, Kooperberg, Charles L

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Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data von Denny, Joshua C, Bastarache, Lisa, Ritchie, Marylyn D, Carroll, Robert J, Zink, Raquel, Mosley, Jonathan D, Field, Julie R, Pulley, Jill M, Ramirez, Andrea H, Bowton, Erica, Basford, Melissa A, Carrell, David S, Peissig, Peggy L, Kho, Abel N, Pacheco, Jennifer A, Rasmussen, Luke V, Crosslin, David R, Crane, Paul K, Pathak, Jyotishman, Bielinski, Suzette J, Pendergrass, Sarah A, Xu, Hua, Hindorff, Lucia A, Li, Rongling, Manolio, Teri A, Chute, Christopher G, Chisholm, Rex L, Larson, Eric B, Jarvik, Gail P, Brilliant, Murray H, McCarty, Catherine A, Kullo, Iftikhar J, Haines, Jonathan L, Crawford, Dana C, Masys, Daniel R, Roden, Dan M

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Replication of European hypertension associations in a case-control study of 9,534 African Americans von Kaur, Harpreet, Crawford, Dana C., Liang, Jingjing, Benchek, Penelope, Zhu, Xiaofeng, Kallianpur, Asha R., Bush, William S.

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Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record von Ritchie, Marylyn D., Denny, Joshua C., Crawford, Dana C., Ramirez, Andrea H., Weiner, Justin B., Pulley, Jill M., Basford, Melissa A., Brown-Gentry, Kristin, Balser, Jeffrey R., Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.

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Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groups von Limdi, Nita A., Wadelius, Mia, Cavallari, Larisa, Eriksson, Niclas, Crawford, Dana C., Lee, Ming-Ta M., Chen, Chien-Hsiun, Motsinger-Reif, Alison, Sagreiya, Hersh, Liu, Nianjun, Wu, Alan H.B., Gage, Brian F., Jorgensen, Andrea, Pirmohamed, Munir, Shin, Jae-Gook, Suarez-Kurtz, Guilherme, Kimmel, Stephen E., Johnson, Julie A., Klein, Teri E., Wagner, Michael J.

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Definition and clinical importance of haplotypes von Crawford, Dana C, Nickerson, Deborah A

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Editorial: Translating clinical genomics and health informatics into precision oncology von Yang, Hsih-Te, Crawford, Dana C., Abazeed, Mohamed E.

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Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies von Denny, Joshua C., Crawford, Dana C., Ritchie, Marylyn D., Bielinski, Suzette J., Basford, Melissa A., Bradford, Yuki, Chai, High Seng, Bastarache, Lisa, Zuvich, Rebecca, Peissig, Peggy, Carrell, David, Ramirez, Andrea H., Pathak, Jyotishman, Wilke, Russell A., Rasmussen, Luke, Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Weston, Noah, Matsumoto, Martha, Kopp, Peter A., Newton, Katherine M., Jarvik, Gail P., Li, Rongling, Manolio, Teri A., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Larson, Eric B., McCarty, Catherine A., Masys, Daniel R., Roden, Dan M., de Andrade, Mariza

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Assessment of multi-population polygenic risk scores for lipid traits in African Americans von Drouet, Domenica E, Liu, Shiying, Crawford, Dana C

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Unravelling the human genome–phenome relationship using phenome-wide association studies von Bush, William S., Oetjens, Matthew T., Crawford, Dana C.

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A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program von Verma, Anurag, Tsao, Noah L, Thomann, Lauren O, Ho, Yuk-Lam, Iyengar, Sudha K, Luoh, Shiuh-Wen, Carr, Rotonya, Crawford, Dana C, Efird, Jimmy T, Huffman, Jennifer E, Hung, Adriana, Ivey, Kerry L, Levin, Michael G, Lynch, Julie, Natarajan, Pradeep, Pyarajan, Saiju, Bick, Alexander G, Costa, Lauren, Genovese, Giulio, Hauger, Richard, Madduri, Ravi, Pathak, Gita A, Polimanti, Renato, Voight, Benjamin, Vujkovic, Marijana, Zekavat, Seyedeh Maryam, Zhao, Hongyu, Ritchie, Marylyn D, Chang, Kyong-Mi, Cho, Kelly, Casas, Juan P, Tsao, Philip S, Gaziano, J Michael, O'Donnell, Christopher, Damrauer, Scott M, Liao, Katherine P

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Maturation and application of phenome-wide association studies von Liu, Shiying, Crawford, Dana C.

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Using electronic health records for clinical pharmacology research: Challenges and considerations von Jafari, Eissa, Blackman, Marisa H., Karnes, Jason H., Van Driest, Sara L., Crawford, Dana C., Choi, Leena, McDonough, Caitrin W.

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Editorial: The Importance of Diversity in Precision Medicine Research von Cooke Bailey, Jessica N., Bush, William S., Crawford, Dana C.

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Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection von Ferar, Kathleen, Hall, Taryn O., Crawford, Dana C., Rowley, Robb, Satterfield, Benjamin A., Li, Rongling, Gragert, Loren, Karlson, Elizabeth W., de Andrade, Mariza, Kullo, Iftikhar J., McCarty, Catherine A., Kho, Abel, Hayes, M. Geoffrey, Ritchie, Marylyn D., Crane, Paul K., Mirel, Daniel B., Carlson, Christopher, Connolly, John J., Hakonarson, Hakon, Crenshaw, Andrew T., Carrell, David, Luo, Yuan, Dikilitas, Ozan, Denny, Joshua C., Jarvik, Gail P., Crosslin, David R.

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Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection von Ferar, Kathleen, Hall, Taryn O., Crawford, Dana C., Rowley, Robb, Satterfield, Benjamin A., Li, Rongling, Gragert, Loren, Karlson, Elizabeth W., de Andrade, Mariza, Kullo, Iftikhar J., McCarty, Catherine A., Kho, Abel, Hayes, M. Geoffrey, Ritchie, Marylyn D., Crane, Paul K., Mirel, Daniel B., Carlson, Christopher, Connolly, John J., Hakonarson, Hakon, Crenshaw, Andrew T., Carrell, David, Luo, Yuan, Dikilitas, Ozan, Denny, Joshua C., Jarvik, Gail P., Crosslin, David R.

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Detection of pleiotropy through a Phenome-wide association study (PheWAS) of epidemiologic data as part of the Environmental Architecture for Genes Linked to Environment (EAGLE) st... von Hall, Molly A, Verma, Anurag, Brown-Gentry, Kristin D, Goodloe, Robert, Boston, Jonathan, Wilson, Sarah, McClellan, Bob, Sutcliffe, Cara, Dilks, Holly H, Gillani, Nila B, Jin, Hailing, Mayo, Ping, Allen, Melissa, Schnetz-Boutaud, Nathalie, Crawford, Dana C, Ritchie, Marylyn D, Pendergrass, Sarah A

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Imputation and quality control steps for combining multiple genome-wide datasets von Verma, Shefali S, de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P, Kottyan, Leah C, Burt, Amber, Bradford, Yuki, Armstrong, Gretta D, Derr, Kimberly, Crawford, Dana C, Haines, Jonathan L, Li, Rongling, Crosslin, David, Ritchie, Marylyn D

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