Cohort Profile: The Danish Venous Thromboembolism Cohort – A Linkage Between Danish National Health Surveys and Health Registers by Horváth-Puhó E, Pedersen L, Martiny SK, Amdisen L, Viuff JH, Ekholm O, Sørensen HT

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An international comparison of longitudinal health data collected on long COVID in nine high income countries: a qualitative data analysis by Josephine Exley, Edmund Stubbs, Raphael Wittenberg, Nicholas Mays

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Traversable Ledger for Responsible Data Sharing and Access Control in Health Research by Sunanda Bose, Dusica Marijan

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Community‐engaged efforts to increase retention of Black American online registry participants by Miriam T. Ashford, Anna Aaronson, Danqi Zhu, Xinyue Deng, Sandhya Kannan, Catherine Conti, Roxanne Alaniz, Jennefer Sorce, Carole Cypress, Derek Flenniken, Monica Camacho, Juliet Fockler, Diana Truran, R. Scott Mackin, Carl Hill, Michael W. Weiner, Desiree Byrd, Robert W. Turner II, Heining Cham, Monica Rivera Mindt, Rachel L. Nosheny

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Subjective cognitive decline predicts longitudinal neuropsychological test performance in an unsupervised online setting in the Brain Health Registry by Jae Myeong Kang, Manchumad Manjavong, Chengshi Jin, Adam Diaz, Miriam T. Ashford, Joseph Eichenbaum, Emily Thorp, Elizabeth Wragg, Kenton H. Zavitz, Francesca Cormack, Anna Aaronson, R. Scott Mackin, Rachana Tank, Bernard Landavazo, Erika Cavallone, Diana Truran, Sarah Tomaszewski Farias, Michael W. Weiner, Rachel L. Nosheny

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