Developing a comprehensive database with sensitive health information: A profile of people living with HIV in Newfoundland and Labrador, Canada

Shabnam Asghari, Sarah Boyd, John Knight, Jillian Blackmore, Oliver Hurley, Jill Allison, Laura Gilbert, Jeff Dowden, Phil Lundrigan
Published online: Feb 25, 2020

Cohort profile: The Secure Anonymised Information Linkage databank Dementia e-cohort (SAIL-DeC)

Christian Schnier, Tim Wilkinson, Ashley Akbari, Chris Orton, Kristel Sleegers, John Gallacher, Ronan A Lyons, Cathie LM Sudlow
Published online: Feb 25, 2020

Immigrant and ethnic neighbourhood concentration and reduced child developmental vulnerability

Daphne N. McRae, Nazeem Muhajarine, Magdalena Janus, Eric Duku, Marni Brownell, Barry Forer, Martin Guhn
Published online: Feb 26, 2020

Identifying young Aboriginal and Torres Strait Islander children in linked administrative data: A comparison of methods

Bridgette J McNamara, Jocelyn Jones, Carrington CJ Shepherd, Lina Gubhaju, Grace Joshy, Daniel McAullay, David B Preen, Louisa Jorm, Sandra J Eades
Published online: Mar 16, 2020

Prevalence of Down's Syndrome in England, 1998–2013

James C Doidge, PhD, Joan K Morris, PhD, Katie L Harron, PhD, Sarah Stevens, Ruth Gilbert, MD
Published online: Mar 19, 2020

Identifying incident cancer cases in dispensing claims

Benjamin Daniels, Sallie-Anne Pearson
Published online: Mar 19, 2020

Defining a study population using enhanced reporting of Aboriginality and the effects on study outcomes

Carol Anne McInerney, Siranda Torvaldsen, Jane B Ford, Jonathan M Morris, Michael Nelson, Deborah Randall
Published online: Mar 20, 2020

Is there an agreement between self-reported medical diagnosis in the CARTaGENE cohort and the Québec administrative health databases?

Yves Payette, Cristiano Soares de Moura, Catherine Boileau, Sasha Bernatsky, Nolwenn Noisel
Published online: Mar 26, 2020

The effect of number of healthcare visits on study sample selection in electronic health record data

Laura Rasmussen-Torvik, Al'ona Furmanchuk, Alexander Stoddard, Kristen Osinski, John Meurer, Nicholas Smith, Elizabeth Chrischilles, Bernard Black, Abel Kho
Published online: Apr 2, 2020

A national initiative in data science for health: an evaluation of the UK Farr Institute

Harry Hemingway, FFPH FRCP FMedSci, Ronan Lyons, Qianrui Li, Iain Buchan, John Ainsworth, Jill Pell, Andrew Morris
Published online: Apr 8, 2020

The Mortality After Release from Incarceration Consortium (MARIC): Protocol for a multi-national, individual participant data meta-analysis

Rohan Borschmann, Holly Tibble, Matthew J Spittal, David Preen, Jane Pirkis, Sarah Larney, David L Rosen, Jesse T Young, Alexander D Love, Frederick L Altice, Ingrid A Binswanger, Anne Bukten, Tony Butler, Zheng Chang, Chuan-Yu Chen, Thomas Clausen, Peer Brehm Christensen, Gabriel J Culbert, Louisa Degenhardt, Anja J.E. Dirkzwager, Kate Dolan, Seena Fazel, Colin Fischbacher, Margaret Giles, Lesley Graham, David Harding, Yen-Fang Huang, Florence Huber, Azar Karaminia, Fiona G Kouyoumdjian, Sungwoo Lim, Lars Møller, Akm Moniruzzaman, Jeffrey Morenoff, Eamonn O'Moore, Lia N Pizzicato, Daniel Pratt, Scott F Proescholdbell, Shabbar I Ranapurwala, Meghan E Shanahan, Jenny Shaw, Amanda Slaunwhite, Julian M Somers, Anne C Spaulding, Marc F Stern, Kendra M Viner, Nadia Wang, Melissa Willoughby, Bin Zhao, Stuart A Kinner
Published online: Feb 25, 2020

Parity: A key measure of confounding in data-linkage studies of outcomes after medically assisted reproduction

Georgina M Chambers, Associate Professor, Christos A Venetis, Dr, Louisa R Jorm, Professor, Claire M Vajdic, Associate Professor
Published online: Mar 16, 2020

Evaluation of the effectiveness of the Family Nurse Partnership home visiting programme in first time young mothers in Scotland: a protocol for a natural experiment

Fiona V Lugg-Widger, Michael Robling, Mandy Lau, Shantini Paranjothy, Jill Pell, Julia Sanders, James White, Rebecca Cannings-John
Published online: Mar 16, 2020

Childhood adversity, mental health and suicide (CHASE): a protocol for a longitudinal case-control linked data study

Nadine J Dougall, Jan Savinc, Margaret Maxwell, Thanos Karatzias, Rory C O'Connor, Brian Williams, Graeme Grandison, Ann John, Helen Cheyne, Claire Fyvie, Jonathan I Bisson, Carina Hibberd, Susan Abbott-Smith, Liz Nolan
Published online: Apr 2, 2020

Empowering knowledge generation through international data network: the IMeCCHI-DATANETWORK

Lucia Otero Varela, Marie-Annick Le Pogam, Amy Metcalfe, Pia Kjær Kristensen, Phil Hider, Alka Patel, Hongsoo Kim, Emanuele Carlini, Raffaele Perego, Rosa Gini
Published online: Feb 25, 2020

Data Resource: Children and Family Court Advisory and Support Service (Cafcass) public family law administrative records in England

Stuart Bedston, Rachel Pearson, Matthew A Jay, Karen Broadhurst, Ruth Gilbert, Linda Wijlaars
Published online: Mar 26, 2020

Using general practice clinical information system data for research: the case in Australia

David Youens, Rachael Moorin, Amy Harrison, Richard Varhol, Suzanne Robinson, Caroline Brooks, James Boyd
Published online: Jan 27, 2020

Unlocking the Potential of Electronic Health Records for Health Research

Seungwon Lee, Yuan Xu, Adam G D'Souza, Elliot A Martin, Chelsea Doktorchik, Zilong Zhang, Hude Quan
Published online: Jan 30, 2020