檢索結果 - Walton, Nephi A

The Complex Genetic Basis of Congenital Heart Defects 由 Akhirome, Ehiole, Walton, Nephi A., Nogee, Julie M., Jay, Patrick Y.

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Predicting the start week of respiratory syncytial virus outbreaks using real time weather variables 由 Walton, Nephi A, Poynton, Mollie R, Gesteland, Per H, Maloney, Chris, Staes, Catherine, Facelli, Julio C

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Future directions for high-throughput splicing assays in precision medicine 由 Rhine, Christy L., Neil, Christopher, Glidden, David T., Cygan, Kamil J., Fredericks, Alger M., Wang, Jing, Walton, Nephi A., Fairbrother, William G.

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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis 由 Kulchak Rahm, Alanna, Walton, Nephi A, Feldman, Lynn K, Jenkins, Conner, Jenkins, Troy, Person, Thomas N, Peterson, Joeseph, Reynolds, Jonathon C, Robinson, Peter N, Woltz, Makenzie A, Williams, Marc S, Segal, Michael M

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Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Networ... 由 Williams, Marc S., Taylor, Casey Overby, Walton, Nephi A., Goehringer, Scott R., Aronson, Samuel, Freimuth, Robert R., Rasmussen, Luke V., Hall, Eric S., Prows, Cynthia A., Chung, Wendy K., Fedotov, Alexander, Nestor, Jordan, Weng, Chunhua, Rowley, Robb K., Wiesner, Georgia L., Jarvik, Gail P., Del Fiol, Guilherme

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Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System 由 Taylor, Casey Overby, Lemke, Klaus W., Richards, Thomas M., Roe, Kenneth D., He, Ting, Arruda-Olson, Adelaide, Carrell, David, Denny, Joshua C., Hripcsak, George, Kiryluk, Krzysztof, Kullo, Iftikhar, Larson, Eric B., Peissig, Peggy, Walton, Nephi A., Wei-Qi, Wei, Ye, Zi, Chute, Christopher G., Weiner, Jonathan P.

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Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hyp... 由 Campbell-Salome, Gemme, Jones, Laney K., Masnick, Max F., Walton, Nephi A., Ahmed, Catherine D., Buchanan, Adam H., Brangan, Andrew, Esplin, Edward D., Kann, David G., Ladd, Ilene G., Kelly, Melissa A., Kindt, Iris, Kirchner, H. Lester, McGowan, Mary P., McMinn, Megan N., Morales, Ana, Myers, Kelly D., Oetjens, Matthew T., Rahm, Alanna Kulchak, Schmidlen, Tara J., Sheldon, Amanda, Simmons, Emilie, Snir, Moran, Strande, Natasha T., Walters, Nicole L., Wilemon, Katherine, Williams, Marc S., Gidding, Samuel S., Sturm, Amy C.

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Semantic integration of clinical laboratory tests from electronic health records for deep phenotyping and biomarker discovery 由 Zhang, Xingmin Aaron, Yates, Amy, Vasilevsky, Nicole, Gourdine, J. P., Callahan, Tiffany J., Carmody, Leigh C., Danis, Daniel, Joachimiak, Marcin P., Ravanmehr, Vida, Pfaff, Emily R., Champion, James, Robasky, Kimberly, Xu, Hao, Fecho, Karamarie, Walton, Nephi A., Zhu, Richard L., Ramsdill, Justin, Mungall, Christopher J., Köhler, Sebastian, Haendel, Melissa A., McDonald, Clement J., Vreeman, Daniel J., Peden, David B., Bennett, Tellen D., Feinstein, James A., Martin, Blake, Stefanski, Adrianne L., Hunter, Lawrence E., Chute, Christopher G., Robinson, Peter N.

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Association of Genetic Risk for Obesity with Postoperative Complications Using Mendelian Randomization 由 Robinson, Jamie R., Carroll, Robert J., Bastarache, Lisa, Chen, Qingxia, Mou, Zongyang, Wei, Wei-Qi, Connolly, John J., Mentch, Frank, Sleiman, Patrick, Crane, Paul K., Hebbring, Scott J., Stanaway, Ian B., Crosslin, David R., Gordon, Adam S., Rosenthal, Elisabeth A., Carrell, David, Hayes, M. Geoffrey, Wei, Wei, Petukhova, Lynn, Namjou, Bahram, Zhang, Ge, Safarova, Maya S., Walton, Nephi A., Still, Christopher, Bottinger, Erwin P., Loos, Ruth J. F., Murphy, Shawn N., Jackson, Gretchen P., Kullo, Iftikhar J., Hakonarson, Hakon, Jarvik, Gail P., Larson, Eric B., Weng, Chunhua, Roden, Dan M., Denny, Joshua C.

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