Zobrazeno 1 - 10
of 11
pro vyhledávání: '"David A. Kreda"'
Autor:
Shawn Rynearson, Michael Baudis, Eric Moyer, Kirill Tsukanov, Malachi Griffith, Tristan Nelson, Sarah E. Hunt, Kevin Riehle, Reece K. Hart, Daniel L Cameron, Robert R. Freimuth, Ronak Y. Patel, Melissa S. Cline, Gil Alterovitz, Obi L. Griffith, Heidi L. Rehm, Lawrence J. Babb, Alex H. Wagner, David A. Kreda, Melissa A. Konopko, Jennifer M. Lee, Helen Schuilenburg, Andrew D. Yates, Matthew H. Brush, Stephanie Li, Peter N. Robinson, Javier Lopez, Brian Walsh
Publikováno v:
Cell genomics. 1(2)
Summary Maximizing the personal, public, research, and clinical value of genomic information will require the reliable exchange of genetic variation data. We report here the Variation Representation Specification (VRS, pronounced “verse”), an ext
Autor:
William J. Gordon, Joshua C. Mandel, Kenneth D. Mandl, Isaac S. Kohane, Daniel J. Gottlieb, David A. Kreda
Publikováno v:
J Am Med Inform Assoc
The 21st Century Cures Act, passed in 2016, and the Final Rules it called for create a roadmap for enabling patient access to their electronic health information. The set of data to be made available, as determined by the Office of the National Coord
Autor:
David A. Kreda, Powell Zhang, Anvita Gupta, Xiangyin Chen, Hantian Li, Huanqin Dai, Lixin Zhang, Gil Alterovitz, Insung Na
Publikováno v:
Synthetic and Systems Biotechnology
Synthetic and Systems Biotechnology, Vol 6, Iss 4, Pp 429-436 (2021)
Synthetic and Systems Biotechnology, Vol 6, Iss 4, Pp 429-436 (2021)
Tuberculosis drug resistance continues to threaten global health but the underline molecular mechanisms are not clear. Ethambutol (EMB), one of the well-known first - line drugs in tuberculosis treatment is, unfortunately, not free from drug resistan
Autor:
Heidi L. Rehm, Malachi Griffith, Obi L. Griffith, Reece K. Hart, Helen Schuilenburg, Eric Moyer, Peter N. Robinson, Brian Walsh, Kirill Tsukanov, Ronak Y. Patel, David A. Kreda, Gil Alterovitz, Jennifer Lee, Alex H. Wagner, Sarah E. Hunt, Michael Baudis, Melissa S. Cline, Melissa Konopko, Lawrence J. Babb, Matthew H. Brush, Shawn Rynearson, Andrew D. Yates, Javier Lopez, Daniel L Cameron, Robert R. Freimuth, Tristan Nelson, Kevin Riehle
Maximizing the personal, public, research, and clinical value of genomic information will require that clinicians, researchers, and testing laboratories exchange genetic variation data reliably. Developed by a partnership among national information r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7d218cb33d84039746ad3b91beb551e
https://doi.org/10.1101/2021.01.15.426843
https://doi.org/10.1101/2021.01.15.426843
Publikováno v:
American Society of Clinical Oncology Educational Book. :450-459
In the information age, we expect data systems to make us more effective and efficient—not to make our lives more difficult! In this article, we discuss how we are using data systems, such as electronic health records (EHRs), to improve care delive
Publikováno v:
Journal of the American Medical Informatics Association : JAMIA
Objective In early 2010, Harvard Medical School and Boston Children’s Hospital began an interoperability project with the distinctive goal of developing a platform to enable medical applications to be written once and run unmodified across differen
Autor:
David A. Kreda, Peijin Zhang, Gil Alterovitz, Yishen Chen, Mollie Ullman-Cullere, Jeremy L. Warner, Isaac S. Kohane
Publikováno v:
Journal of the American Medical Informatics Association. 22:1173-1178
Background Supporting clinical decision support for personalized medicine will require linking genome and phenome variants to a patient’s electronic health record (EHR), at times on a vast scale. Clinico-genomic data standards will be needed to uni
Autor:
Kenneth D. Mandl, Heming Yao, Jeremy L. Warner, Matthew J. Rioth, Isaac S. Kohane, Daniel Carbone, Ross Oreto, Shilin Zhu, David A. Kreda, Joshua C. Mandel, Lucy L. Wang, Gil Alterovitz
Publikováno v:
Journal of the American Medical Informatics Association : JAMIA. 23(4)
Background Precision cancer medicine (PCM) will require ready access to genomic data within the clinical workflow and tools to assist clinical interpretation and enable decisions. Since most electronic health record (EHR) systems do not yet provide s
Our aim was to uncover unrecognized phenomic relationships using force-based network visualization methods, based on observed electronic medical record data. A primary phenotype was defined from actual patient profiles in the Multiparameter Intellige
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e57dc9f4887ed43b52f41768b84a2a8
https://europepmc.org/articles/PMC6080728/
https://europepmc.org/articles/PMC6080728/
Autor:
John D. D'Amore, David A. Kreda, Rachel B. Ramoni, Kenneth D. Mandl, Liora Alschuler, Robert H. Dolin, Ashley Swain, Sumesh Sundareswaran, Joshua C. Mandel, George Augustine Koromia, Isaac S. Kohane
Publikováno v:
Journal of the American Medical Informatics Association : JAMIA
Background and objective Upgrades to electronic health record (EHR) systems scheduled to be introduced in the USA in 2014 will advance document interoperability between care providers. Specifically, the second stage of the federal incentive program f