Flows for Floodplain Forests: A Successful Riparian Restoration von ROOD, STEWART B, GOURLEY, CHAD R, AMMON, ELISABETH M, HEKI, LISA G, KLOTZ, JONATHAN R, MORRISON, MICHAEL L, MOSLEY, DAN, SCOPPETTONE, G. GARY, SWANSON, SHERMAN, WAGNER, PAUL L

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Comparison of HLA allelic imputation programs von Karnes, Jason H, Shaffer, Christian M, Bastarache, Lisa, Gaudieri, Silvana, Glazer, Andrew M, Steiner, Heidi E, Mosley, Jonathan D, Mallal, Simon, Denny, Joshua C, Phillips, Elizabeth J, Roden, Dan M

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Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease von Mosley, Jonathan D, Gupta, Deepak K, Tan, Jingyi, Yao, Jie, Wells, Quinn S, Shaffer, Christian M, Kundu, Suman, Robinson-Cohen, Cassianne, Psaty, Bruce M, Rich, Stephen S, Post, Wendy S, Guo, Xiuqing, Rotter, Jerome I, Roden, Dan M, Gerszten, Robert E, Wang, Thomas J

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Benefit of Preemptive Pharmacogenetic Information on Clinical Outcome von Roden, Dan M., Driest, Sara L., Mosley, Jonathan D., Wells, Quinn S., Robinson, Jamie R., Denny, Joshua C., Peterson, Josh F.

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Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational stu... von Feng, QiPing, Wei, Wei-Qi, Chung, Cecilia P, Levinson, Rebecca T, Sundermann, Alexandra C, Mosley, Jonathan D, Bastarache, Lisa, Ferguson, Jane F, Cox, Nancy J, Roden, Dan M, Denny, Joshua C, Linton, MacRae F, Edwards, Digna R Velez, Stein, C Michael

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Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants von Karnes, JH, Bastarache, L, Shaffer, CM, Gaudieri, S, Xu, YM, Glazer, AM, Mosley, JD, Zhao, SL, Raychaudhuri, S, Mallal, S, Ye, Z, Mayer, JG, Brilliant, MH, Hebbring, SJ, Roden, DM, Phillips, EJ, Denny, JC

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Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization von Bersell, Kevin R., Yang, Tao, Mosley, Jonathan D., Glazer, Andrew M., Hale, Andrew T., Kryshtal, Dmytro O., Kim, Kyungsoo, Steimle, Jeffrey D., Brown, Jonathan D., Salem, Joe-Elie, Campbell, Courtney C., Hong, Charles C., Wells, Quinn S., Johnson, Amanda N., Short, Laura, Blair, Marcia A., Behr, Elijah R., Petropoulou, Evmorfia, Jamshidi, Yalda, Benson, Mark D., Keyes, Michelle J., Ngo, Debby, Vasan, Ramachandran S., Yang, Qiong, Gerszten, Robert E., Shaffer, Christian, Parikh, Shan, Sheng, Quanhu, Kannankeril, Prince J., Moskowitz, Ivan P., York, John D., Wang, Thomas J., Knollmann, Bjorn C., Roden, Dan M.

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Exome Sequencing Implicates an Increased Burden of Rare Potassium Channel Variants in the Risk of Drug-Induced Long QT Interval Syndrome von Weeke, Peter, MD, Mosley, Jonathan D., MD, PhD, Hanna, David, BS, Delaney, Jessica T., MD, Shaffer, Christian, BS, Wells, Quinn S., MD, Van Driest, Sara, MD, PhD, Karnes, Jason H., PharmD, PhD, Ingram, Christie, BS, Guo, Yan, PhD, Shyr, Yu, PhD, Norris, Kris, RN, Kannankeril, Prince J., MD, Ramirez, Andrea H., MD, Smith, Joshua D., BS, Mardis, Elaine R., PhD, Nickerson, Deborah, PhD, George, Alfred L., MD, Roden, Dan M., MD

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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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Phenotype risk scores identify patients with unrecognized Mendelian disease patterns von Bastarache, Lisa, Hughey, Jacob J, Hebbring, Scott, Marlo, Joy, Zhao, Wanke, Ho, Wanting T, Van Driest, Sara L, McGregor, Tracy L, Mosley, Jonathan D, Wells, Quinn S, Temple, Michael, Ramirez, Andrea H, Carroll, Robert, Osterman, Travis, Edwards, Todd, Ruderfer, Douglas, Velez Edwards, Digna R, Hamid, Rizwan, Cogan, Joy, Glazer, Andrew, Wei, Wei-Qi, Feng, QiPing, Brilliant, Murray, Zhao, Zhizhuang J, Cox, Nancy J, Roden, Dan M, Denny, Joshua C

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Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height von Shi, Mingjian, Manouchehri, Ali M, Shaffer, Christian M, Vaitinadin, Nataraja Sarma, Hellwege, Jacklyn N, Salem, Joe-Elie, Davis, Lea K, Simmons, Jill H, Roden, Dan M, Shoemaker, M Benjamin, Ferguson, Jane F, Mosley, Jonathan D

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Clinical associations with a polygenic predisposition to benign lower white blood cell counts von Mosley, Jonathan D., Shelley, John P., Dickson, Alyson L., Zanussi, Jacy, Daniel, Laura L., Zheng, Neil S., Bastarache, Lisa, Wei, Wei-Qi, Shi, Mingjian, Jarvik, Gail P., Rosenthal, Elisabeth A., Khan, Atlas, Sherafati, Alborz, Kullo, Iftikhar J., Walunas, Theresa L., Glessner, Joseph, Hakonarson, Hakon, Cox, Nancy J., Roden, Dan M., Frangakis, Stephan G., Vanderwerff, Brett, Stein, C. Michael, Van Driest, Sara L., Borinstein, Scott C., Shu, Xiao-Ou, Zawistowski, Matthew, Chung, Cecilia P., Kawai, Vivian K.

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Heart failure clinical care analysis uncovers risk reduction opportunities for preserved ejection fraction subtype von Levinson, Rebecca T., Vaitinidin, Nataraja Sarma, Farber-Eger, Eric, Roden, Dan M., Lasko, Thomas A., Wells, Quinn S., Mosley, Jonathan D.

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Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations von Lennon, Niall J., Kottyan, Leah C., Kachulis, Christopher, Abul-Husn, Noura S., Arias, Josh, Belbin, Gillian, Below, Jennifer E., Berndt, Sonja I., Chung, Wendy K., Cimino, James J., Clayton, Ellen Wright, Connolly, John J., Crosslin, David R., Dikilitas, Ozan, Velez Edwards, Digna R., Feng, QiPing, Fisher, Marissa, Freimuth, Robert R., Ge, Tian, Glessner, Joseph T., Gordon, Adam S., Patterson, Candace, Hakonarson, Hakon, Harden, Maegan, Harr, Margaret, Hirschhorn, Joel N., Hoggart, Clive, Hsu, Li, Irvin, Marguerite R., Jarvik, Gail P., Karlson, Elizabeth W., Khan, Atlas, Khera, Amit, Kiryluk, Krzysztof, Kullo, Iftikhar, Larkin, Katie, Limdi, Nita, Linder, Jodell E., Loos, Ruth J. F., Luo, Yuan, Malolepsza, Edyta, Manolio, Teri A., Martin, Lisa J., McCarthy, Li, McNally, Elizabeth M., Meigs, James B., Mersha, Tesfaye B., Mosley, Jonathan D., Musick, Anjene, Namjou, Bahram, Pai, Nihal, Pesce, Lorenzo L., Peters, Ulrike, Peterson, Josh F., Prows, Cynthia A., Puckelwartz, Megan J., Rehm, Heidi L., Roden, Dan M., Rosenthal, Elisabeth A., Rowley, Robb, Sawicki, Konrad Teodor, Schaid, Daniel J., Smit, Roelof A. J., Smith, Johanna L., Smoller, Jordan W., Thomas, Minta, Tiwari, Hemant, Toledo, Diana M., Vaitinadin, Nataraja Sarma, Veenstra, David, Walunas, Theresa L., Wang, Zhe, Wei, Wei-Qi, Weng, Chunhua, Wiesner, Georgia L., Yin, Xianyong, Kenny, Eimear E.

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LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins von Wei, Wei-Qi, Li, Xiaohui, Feng, Qiping, Kubo, Michiaki, Kullo, Iftikhar J, Peissig, Peggy L, Karlson, Elizabeth W, Jarvik, Gail P, Lee, Ming Ta Michael, Shang, Ning, Larson, Eric A, Edwards, Todd, Shaffer, Christian M, Mosley, Jonathan D, Maeda, Shiro, Horikoshi, Momoko, Ritchie, Marylyn, Williams, Marc S, Larson, Eric B, Crosslin, David R, Bland, Sarah T, Pacheco, Jennifer A, Rasmussen-Torvik, Laura J, Cronkite, David, Hripcsak, George, Cox, Nancy J, Wilke, Russell A, Stein, C Michael, Rotter, Jerome I, Momozawa, Yukihide, Roden, Dan M, Krauss, Ronald M, Denny, Joshua C

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Screening for Acute I Kr Block Is Insufficient to Detect Torsades de Pointes Liability: Role of Late Sodium Current von Yang, Tao, Chun, Young Wook, Stroud, Dina M., Mosley, Jonathan D., Knollmann, Bjorn C., Hong, Charles, Roden, Dan M.

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Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations von Mosley, Jonathan D, Van Driest, Sara L, Weeke, Peter E, Delaney, Jessica T, Wells, Quinn S, Bastarache, Lisa, Roden, Dan M, Denny, Josh C

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Association of white matter microstructural integrity with cognition and dementia von Power, Melinda C., Su, Dan, Wu, Aozhou, Reid, Robert I., Jack, Clifford R., Knopman, David S., Coresh, Joe, Huang, Juebin, Kantarci, Kejal, Sharrett, A. Richey, Gottesman, Rebecca G., Griswold, Mike E., Mosley, Thomas H.

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Opportunities and Challenges in Cardiovascular Pharmacogenomics: From Discovery to Implementation von Roden, Dan M, Van Driest, Sara L, Wells, Quinn S, Mosley, Jonathan D, Denny, Joshua C, Peterson, Josh F

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Genome‐Wide Approach to Measure Variant‐Based Heritability of Drug Outcome Phenotypes von Muhammad, Ayesha, Aka, Ida T., Birdwell, Kelly A., Gordon, Adam S., Roden, Dan M., Wei, Wei‐Qi, Mosley, Jonathan D., Van Driest, Sara L.

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