| 1 | -- | 0 | Lucila Ohno-Machado. Sharing data for the public good and protecting individual privacy: informatics solutions to combine different goals |
| 2 | -- | 6 | Bradley A. Malin, Khaled El Emam, Christine M. O'Keefe. Biomedical data privacy: problems, perspectives, and recent advances |
| 7 | -- | 15 | Kelly Caine, Rima Hanania. Patients want granular privacy control over health information in electronic medical records |
| 16 | -- | 24 | Maja van der Velden, Khaled El Emam. know": a qualitative study of teenage patients, privacy, and social media |
| 25 | -- | 28 | Caitlin Pencarrick Hertzman, Nancy Meagher, Kimberlyn M. McGrail. Privacy by Design at Population Data BC: a case study describing the technical, administrative, and physical controls for privacy-sensitive secondary use of personal information for research in the public interest |
| 29 | -- | 34 | Deven McGraw. Building public trust in uses of Health Insurance Portability and Accountability Act de-identified data |
| 35 | -- | 37 | Carolyn Petersen, Paul DeMuro, Kenneth W. Goodman, Bonnie Kaplan. IMS Health: issues and opportunities for informaticians |
| 38 | -- | 43 | Patricia Kosseim, Daryl Pullman, Astrid Perrot-Daley, Kathy Hodgkinson, Catherine Street, Proton Rahman. Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador |
| 44 | -- | 51 | Juhee Kwon, M. Eric Johnson. Security practices and regulatory compliance in the healthcare industry |
| 52 | -- | 60 | Daniel Fabbri, Kristen LeFevre. Explaining accesses to electronic medical records using diagnosis information |
| 61 | -- | 68 | Ryen White, Eric Horvitz. From web search to healthcare utilization: privacy-sensitive studies from mobile data |
| 69 | -- | 76 | Christopher A. Cassa, Rachel A. Miller, Kenneth D. Mandl. A novel, privacy-preserving cryptographic approach for sharing sequencing data |
| 77 | -- | 83 | Óscar Ferrández, Brett R. South, Shuying Shen, F. Jeffrey Friedlin, Matthew H. Samore, Stéphane M. Meystre. BoB, a best-of-breed automated text de-identification system for VHA clinical documents |
| 84 | -- | 94 | Louise Deléger, Katalin Molnár, Guergana Savova, Fei Xia, Todd Lingren, Qi Li, Keith Marsolo, Anil G. Jegga, Megan Kaiser, Laura Stoutenborough, Imre Solti. Large-scale evaluation of automated clinical note de-identification and its impact on information extraction |
| 95 | -- | 101 | Ravi V. Atreya, Joshua C. Smith, Allison B. McCoy, Bradley Malin, Randolph A. Miller. Reducing patient re-identification risk for laboratory results within research datasets |
| 102 | -- | 108 | Cynthia Dwork, Rebecca Pottenger. Toward practicing privacy |
| 109 | -- | 116 | James J. Gardner, Li Xiong, Yonghui Xiao, Jingjing Gao, Andrew R. Post, Xiaoqian Jiang, Lucila Ohno-Machado. SHARE: system design and case studies for statistical health information release |
| 117 | -- | 121 | George Hripcsak, David J. Albers. Next-generation phenotyping of electronic health records |
| 122 | -- | 124 | Keith Marsolo. Informatics and operations - let's get integrated |
| 125 | -- | 127 | Daniela M. Witten, Robert Tibshirani. Scientific research in the age of omics: the good, the bad, and the sloppy |
| 128 | -- | 133 | Toni R. Farley, Jeff Kiefer, Preston Lee, Daniel Von Hoff, Jeffrey M. Trent, Charles J. Colbourn, Spyro Mousses. The BioIntelligence Framework: a new computational platform for biomedical knowledge computing |
| 134 | -- | 140 | Caitlin M. Cusack, George Hripcsak, Meryl Bloomrosen, S. Trent Rosenbloom, Charlotte A. Weaver, Adam Wright, David K. Vawdrey, Jim Walker, Lena Mamykina. The future state of clinical data capture and documentation: a report from AMIA's 2011 Policy Meeting |
| 141 | -- | 143 | Kenneth W. Goodman, Samantha Adams, Eta S. Berner, Peter J. Embi, Robert C. Hsiung, John F. Hurdle, Dixie A. Jones, Christoph U. Lehmann, Sarah Maulden, Carolyn Petersen, Enrique Terrazas, Peter Winkelstein. AMIA's Code of Professional and Ethical Conduct |
| 144 | -- | 151 | Nicole Gray Weiskopf, Chunhua Weng. Methods and dimensions of electronic health record data quality assessment: enabling reuse for clinical research |
| 152 | -- | 156 | Jessica S. Ancker, Michael Silver, Melissa C. Miller, Rainu Kaushal. Consumer experience with and attitudes toward health information technology: a nationwide survey |
| 157 | -- | 163 | Yaorong Ge, David K. Ahn, Bhagyashree Unde, H. Donald Gage, J. Jeffrey Carr. Patient-controlled sharing of medical imaging data across unaffiliated healthcare organizations |
| 164 | -- | 171 | John F. Hurdle, Stephen C. Haroldsen, Andrew Hammer, Cindy Spigle, Alison M. Fraser, Geraldine P. Mineau, Samir J. Courdy. Identifying clinical/translational research cohorts: ascertainment via querying an integrated multi-source database |
| 172 | -- | 179 | Marc D. Natter, Justin Quan, David M. Ortiz, Athos Bousvaros, Norman T. Ilowite, Christi J. Inman, Keith Marsolo, Andrew J. McMurry, Christy Sandborg, Laura E. Schanberg, Carol A. Wallace, Robert W. Warren, Griffin M. Weber, Kenneth D. Mandl. An i2b2-based, generalizable, open source, self-scaling chronic disease registry |
| 180 | -- | 183 | David Cumin, Vanessa Newton-Wade, Michael J. Harrison, Alan F. Merry. Two open access, high-quality datasets from anesthetic records |
| 184 | -- | 192 | Paul Avillach, Preciosa M. Coloma, Rosa Gini, Martijn J. Schuemie, Fleur Mougin, Jean-Charles Dufour, Giampiero Mazzaglia, Carlo Giaquinto, Carla Fornari, Ron Herings, Mariam Molokhia, Lars Pedersen, Annie Fourrier-Réglat, Marius Fieschi, Miriam C. J. M. Sturkenboom, Johan van der Lei, Antoine Pariente, Gianluca Trifirò. Harmonization process for the identification of medical events in eight European healthcare databases: the experience from the EU-ADR project |
| 193 | -- | 198 | Stephen G. Jones, Steven Coulter, William Conner. Using administrative medical claims data to supplement state disease registry systems for reporting zoonotic infections |
| 199 | -- | 207 | Kensaku Kawamoto, Tonya Hongsermeier, Adam Wright, Janet Lewis, Douglas S. Bell, Blackford Middleton. Key principles for a national clinical decision support knowledge sharing framework: synthesis of insights from leading subject matter experts |
| 208 | -- | 210 | Kevin M. Fickenscher. President's column: An AMIA update - new directions and new opportunities |