Search Results - "Borglund, Erin M"

Impact of a Collective Intelligence Tailored Messaging System on Smoking Cessation: The Perspect Randomized Experiment by Sadasivam, Rajani Shankar, Borglund, Erin M, Adams, Roy, Marlin, Benjamin M, Houston, Thomas K

“…Outside health care, content tailoring is driven algorithmically using machine learning compared to the rule-based approach used in current implementations of…”
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Reporting of clinical trial safety results in ClinicalTrials.gov for FDA-approved drugs: A cross-sectional analysis by Chen, Krista Y, Borglund, Erin M, Postema, Emma Charlotte, Dunn, Adam G, Bourgeois, Florence T

“…Background Adverse events identified during clinical trials can be important early indicators of drug safety, but complete and timely data on safety results…”
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Correction: The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system by Mandl, Kenneth D., Glauser, Tracy, Krantz, Ian D., Avillach, Paul, Bartels, Anna, Beggs, Alan H., Biswas, Sawona, Bourgeois, Florence T., Corsmo, Jeremy, Dauber, Andrew, Devkota, Batsal, Fleisher, Gary R., Heath, Allison P., Helbig, Ingo, Hirschhorn, Joel N., Kilbourn, Judson, Kong, Sek Won, Kornetsky, Susan, Majzoub, Joseph A., Marsolo, Keith, Martin, Lisa J., Nix, Jeremy, Schwarzhoff, Amy, Stedman, Jason, Strauss, Arnold, Sund, Kristen L., Taylor, Deanne M., White, Peter S., Marsh, Eric, Grimberg, Adda, Hawkes, Colin

“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
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Development of the Precision Link Biobank at Boston Children's Hospital: Challenges and Opportunities by Bourgeois, Florence T, Avillach, Paul, Kong, Sek Won, Heinz, Michelle M, Tran, Tram A, Chakrabarty, Ramkrishna, Bickel, Jonathan, Sliz, Piotr, Borglund, Erin M, Kornetsky, Susan, Mandl, Kenneth D

“…Increasingly, biobanks are being developed to support organized collections of biological specimens and associated clinical information on broadly consented,…”
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The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system by Mandl, Kenneth D., Glauser, Tracy, Krantz, Ian D., Avillach, Paul, Bartels, Anna, Beggs, Alan H., Biswas, Sawona, Bourgeois, Florence T., Corsmo, Jeremy, Dauber, Andrew, Devkota, Batsal, Fleisher, Gary R., Heath, Allison P., Helbig, Ingo, Hirschhorn, Joel N., Kilbourn, Judson, Kong, Sek Won, Kornetsky, Susan, Majzoub, Joseph A., Marsolo, Keith, Martin, Lisa J., Nix, Jeremy, Schwarzhoff, Amy, Stedman, Jason, Strauss, Arnold, Sund, Kristen L., Taylor, Deanne M., White, Peter S., Marsh, Eric, Grimberg, Adda, Hawkes, Colin

“…Purpose Clinicians and researchers must contextualize a patient’s genetic variants against population-based references with detailed phenotyping. We sought to…”
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The Genomics Research and Innovation Network: creating aninteroperable, federated, genomics learning system by Mandl, Kenneth D, Glauser, Tracy, Krantz, Ian D, Avillach, Paul, Bartels, Anna, Beggs, Alan H, Biswas Sawona, Bourgeois, Florence T, Corsmo Jeremy, Dauber, Andrew, Devkota Batsal, Fleisher, Gary R, Heath, Allison P, Helbig Ingo, Hirschhorn, Joel N, Kilbourn Judson, Kong Sek Won, Kornetsky, Susan, Majzoub, Joseph A, Marsolo Keith, Martin, Lisa J, Nix, Jeremy, Schwarzhoff Amy, Stedman, Jason, Strauss, Arnold, Sund, Kristen L, Taylor, Deanne M, White, Peter S, Marsh, Eric, Grimberg Adda, Hawkes, Colin, Barkman Darlene, Borglund, Erin M, Chakrabarty Ramkrishna, Chandel Alka, Degala Anil Kumar, DeSain, Thomas, Dexheimer, Philip, Divekar Parth, Ellis, Alyssa, Furgason, Mike, Geehan, Christopher, Guidetti, Andrew Joseph, Gutierrez, Alba, Hallinan, Barbara, Harper, Becca, Jalali Niloofar, Khanna Jaspreet, Kirby, Christopher, Korodi Gabor, Kouril Michal, Kratchman, Amy, Kumar Ranjay, Labilloy Guillaume, Lee, In-Hee, Bria, Morgan, Morgan, James, Muglia, Louis J, Nikitin Aleksandr, Pistone, Mike, Poduri, Anna, Rupert, Andrew, Safier, Kristen, Sliz Piotr, Stevenson Gelvina, Geme Joseph St III, Thaker Vidhu, Temporal Simone, Velayutham Prakash, Wijesooriya Julie, Wolf, Bryan, Wooten, Andrew, Yen, Alan, Zhang, Yu

“…PurposeClinicians and researchers must contextualize a patient’s genetic variants against population-based references with detailed phenotyping. We sought to…”
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