Výsledky vyhledávání - Walton Nephi

Creating a Home for Genomic Data in the Electronic Health Record Autor Walton, Nephi, Johnson, Darren, Heale, Bret, Person, Thomas, Williams, Marc

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

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Legal Challenges in Precision Medicine: What Duties Arising From Genetic and Genomic Testing Does a Physician Owe to Patients? Autor McGrath, Scott P., Peabody, Arthur E., Walton, Derek, Walton, Nephi

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Are providers prepared for genomic medicine: interpretation of Direct-to-Consumer genetic testing (DTC-GT) results and genetic self-efficacy by medical professionals Autor McGrath, Scott P., Walton, Nephi, Williams, Marc S., Kim, Katherine K., Bastola, Kiran

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

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Modeling the variations in pediatric respiratory syncytial virus seasonal epidemics Autor Leecaster, Molly, Gesteland, Per, Greene, Tom, Walton, Nephi, Gundlapalli, Adi, Rolfs, Robert, Byington, Carrie, Samore, Matthew

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Future directions for high-throughput splicing assays in precision medicine Autor 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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Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants Autor Dexter, Paul, Ong, Henry, Elsey, Amanda, Bell, Gillian, Walton, Nephi, Chung, Wendy, Rasmussen, Luke, Hicks, Kevin, Owusu-obeng, Aniwaa, Scott, Stuart, Ellis, Steve, Peterson, Josh

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Infobuttons for Genomic Medicine: Requirements and Barriers Autor Rasmussen, Luke V., Connolly, John J., Del Fiol, Guilherme, Freimuth, Robert R., Pet, Douglas B., Peterson, Josh F., Shirts, Brian H., Starren, Justin B., Williams, Marc S., Walton, Nephi, Taylor, Casey Overby

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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis Autor 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... Autor 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 Autor 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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Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis Autor Sadler, Brooke, Haller, Gabe, Antunes, Lilian, Bledsoe, Xavier, Morcuende, Jose A., Giampietro, Philip, Raggio, Cathleen, Hadley-Miller, Nancy, Kidane, Yared, Wise, Carol A., Amarillo, Ina, Walton, Nephi, Seeley, Mark, Johnson, Darren, Jenkins, Conner, Jenkins, Troy, Oetjens, Matthew, Tong, R. Spencer, Druley, Todd E., Dobbs, Matthew B., Gurnett, Christina A.

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Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions Autor Yu, Jingzhi, Pacheco, Jennifer A., Ghosh, Anika S., Luo, Yuan, Weng, Chunhua, Shang, Ning, Benoit, Barbara, Carrell, David S., Carroll, Robert J., Dikilitas, Ozan, Freimuth, Robert R., Gainer, Vivian S., Hakonarson, Hakon, Hripcsak, George, Kullo, Iftikhar J., Mentch, Frank, Murphy, Shawn N., Peissig, Peggy L., Ramirez, Andrea H., Walton, Nephi, Wei, Wei-Qi, Rasmussen, Luke V.

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POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 Autor Elodie Sanchez, Béryl Laplace-Builhé, Frédéric Tran Mau‐Them, Eric Richard, Alice Goldenberg, Tomi L. Toler, Thomas Guignard, Vincent Gâtinois, Marie Vincent, Catherine Blanchet, Anne Boland, Marie Thérèse Bihoreau, Jean‐François Deleuze, Robert Olaso, Walton Nephi, Hermann‐Josef Lüdecke, Joanne Verheij, Florence Moreau-Lenoir, Françoise Denoyelle, Jean‐Baptiste Rivière, Jean Laplanche, Marcia Willing, Guillaume Captier, Florence Apparailly, Dagmar Wieczorek, Corinne Collet, Farida Djouad, David Geneviève

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Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hyp... Autor 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 Autor 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 Autor 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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A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources Autor Wiley, Ken, Findley, Laura, Goldrich, Madison, Rakhra-Burris, Tejinder K, Stevens, Ana, Williams, Pamela, Bult, Carol J, Chisholm, Rex, Deverka, Patricia, Ginsburg, Geoffrey S, Green, Eric D, Jarvik, Gail, Mensah, George A, Ramos, Erin, Relling, Mary V, Roden, Dan M, Rowley, Robb, Alterovitz, Gil, Aronson, Samuel, Bastarache, Lisa, Cimino, James J, Crowgey, Erin L, Del Fiol, Guilherme, Freimuth, Robert R, Hoffman, Mark A, Jeff, Janina, Johnson, Kevin, Kawamoto, Kensaku, Madhavan, Subha, Mendonca, Eneida A, Ohno-Machado, Lucila, Pratap, Siddharth, Taylor, Casey Overby, Ritchie, Marylyn D, Walton, Nephi, Weng, Chunhua, Zayas-Cabán, Teresa, Manolio, Teri A, Williams, Marc S

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