Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nephi Walton"'
Autor:
Jennifer A. Pacheco, Luke V. Rasmussen, Ken Wiley, Thomas Nate Person, David J. Cronkite, Sunghwan Sohn, Shawn Murphy, Justin H. Gundelach, Vivian Gainer, Victor M. Castro, Cong Liu, Frank Mentch, Todd Lingren, Agnes S. Sundaresan, Garrett Eickelberg, Valerie Willis, Al’ona Furmanchuk, Roshan Patel, David S. Carrell, Yu Deng, Nephi Walton, Benjamin A. Satterfield, Iftikhar J. Kullo, Ozan Dikilitas, Joshua C. Smith, Josh F. Peterson, Ning Shang, Krzysztof Kiryluk, Yizhao Ni, Yikuan Li, Girish N. Nadkarni, Elisabeth A. Rosenthal, Theresa L. Walunas, Marc S. Williams, Elizabeth W. Karlson, Jodell E. Linder, Yuan Luo, Chunhua Weng, WeiQi Wei
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract The electronic Medical Records and Genomics (eMERGE) Network assessed the feasibility of deploying portable phenotype rule-based algorithms with natural language processing (NLP) components added to improve performance of existing algorithms
Externí odkaz:
https://doaj.org/article/9c81a942e0f84bc7870a1d35de1a798a
Autor:
Nykole Sutherland, Wendy Kohlmann, Karen Curtin, Debra Ma, Therese Berry, Kelly Stantuci, Alison Fraser, Lisa Pappas, Taylor Jump, Nephi Walton, Nicola Camp
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100059- (2023)
Externí odkaz:
https://doaj.org/article/5a7d3a10c1c0438eb6681f70cf31d247
Autor:
Stacey Knight, Nephi Walton, Jeffrey Anderson, Michael Cutler, Melanie Emmerson, Virginia Hebl, Viet Le, John Carlquist, Heidi May, Shelby Moench, Kirk Knowlton
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100243- (2023)
Externí odkaz:
https://doaj.org/article/f75e65f7dfa444619fe4f03a70cf45d3
Autor:
Nephi Walton, Jeffrey Anderson, Melanie Emmerson, Kirk Knowlton, Jared Evans, Bryce Christensen, Stacey Knight
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100372- (2023)
Externí odkaz:
https://doaj.org/article/e1a36316aff94bd08c48ff7739f04a8e
Autor:
Jingzhi Yu, Jennifer A. Pacheco, Anika S. Ghosh, Yuan Luo, Chunhua Weng, Ning Shang, Barbara Benoit, David S. Carrell, Robert J. Carroll, Ozan Dikilitas, Robert R. Freimuth, Vivian S. Gainer, Hakon Hakonarson, George Hripcsak, Iftikhar J. Kullo, Frank Mentch, Shawn N. Murphy, Peggy L. Peissig, Andrea H. Ramirez, Nephi Walton, Wei-Qi Wei, Luke V. Rasmussen
Publikováno v:
BMC Medical Informatics and Decision Making, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Introduction Currently, one of the commonly used methods for disseminating electronic health record (EHR)-based phenotype algorithms is providing a narrative description of the algorithm logic, often accompanied by flowcharts. A challenge wi
Externí odkaz:
https://doaj.org/article/8ee69ddf0a344c46bc959566a833582c
Publikováno v:
BMC Health Services Research, Vol 19, Iss 1, Pp 1-12 (2019)
Abstract Background Precision medicine is set to deliver a rich new data set of genomic information. However, the number of certified specialists in the United States is small, with only 4244 genetic counselors and 1302 clinical geneticists. We condu
Externí odkaz:
https://doaj.org/article/d8eb0f160ec04e9a9d9919dfffb9c26b
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Precision medicine is increasingly incorporated into clinical practice via three primary data conduits: environmental, lifestyle, and genetic data. In this manuscript we take a closer look at the genetic tier of precision medicine. The volume and var
Externí odkaz:
https://doaj.org/article/bc9a066196c3459da4f74fdf982de9a5
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