Patient-Generated Collections for Organizing Electronic Health Record Data to Elevate Personal Meaning, Improve Actionability, and Support Patient-Health Care Provider Communicatio... von Nakikj, Drashko, Kreda, David, Luthria, Karan, Gehlenborg, Nils

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Alerts and Collections for Automating Patients’ Sensemaking and Organizing of Their Electronic Health Record Data for Reflection, Planning, and Clinical Visits: Qualitative Researc... von Nakikj, Drashko, Kreda, David, Gehlenborg, Nils

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New Ways for Patients to Make Sense of Their Electronic Health Record Data Using the Discovery Web Application: Think-Aloud Evaluation Study von Nakikj, Drashko, Kreda, David, Gehlenborg, Nils

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Effective Communication of Personalized Risks and Patient Preferences During Surgical Informed Consent Using Data Visualization: Qualitative Semistructured Interview Study With Pat... von Gisladottir, Undina, Nakikj, Drashko, Jhunjhunwala, Rashi, Panton, Jasmine, Brat, Gabriel, Gehlenborg, Nils

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DisVis: Visualizing Discussion Threads in Online Health Communities von Nakikj, Drashko, Mamykina, Lena

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How surgeons use risk calculators and non-clinical factors for informed consent and shared decision making: A qualitative study von Panton, Jasmine, Beaulieu-Jones, Brendin R., Marwaha, Jayson S., Woods, Alison P., Nakikj, Drashko, Gehlenborg, Nils, Brat, Gabriel A.

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