Search Results - Walton, Nephi A
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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis by 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
Published 2021Text -
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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... by 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
Published 2019Text -
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Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System by 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.
Published 2019Text -
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Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hyp... by 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.
Published 2021Text -
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Semantic integration of clinical laboratory tests from electronic health records for deep phenotyping and biomarker discovery by 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.
Published 2019Text -
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Association of Genetic Risk for Obesity with Postoperative Complications Using Mendelian Randomization by 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.
Published 2020Text