Understanding the reasons for declining to participate in cancer genetics and genomic studies in the USA: a scoping review protocolJoel Sanchez Mendez, Jessica Sanchez, Chenya Zhao, Vernon Shane Pankratz, Andrew L Sussman, Ursa Brown-Glaberman, Stephanie Cargill, Shiraz I Mishra, Mariana C Stern
30 April 2025
European Registry of Hereditary Pancreatic Diseases (EUROPAC): protocol for primary and secondary screening in individuals with inherited pancreatic disease syndromes for pancreatic ductal adenocarcinoma and complications of other pancreatic diseasesAnnabelle Boughey, Phil Hopley, Ioannis Sarantitis, Paul Thomas, Beata Gubacsi, Kayleigh Jevons, Emma Crowe, Eleri Hughes, Isobel Quinn, Liam Royle, Richard J Jackson, William Greenhalf, Chris Halloran
3 April 2025
Diagnostic yield of cystic fibrosis from a South Australian monocentric cohort: a retrospective studyJasmina Markulić, Maria Fuller
23 January 2025
Relationship between vaginal and gut microbiome and pregnancy outcomes in eastern Ethiopia: a protocol for a longitudinal maternal-infant cohort study (the EthiOMICS study)Fitsum Weldegebreal, Desalegn Admassu Ayana, Tara Wilfong, Merga Dheresa, Tesfaye Assebe Yadeta, Akewok Sime Negesa, Yohannes Mulugeta Demmu, Tewodros Tesfa, Tegbaru Nibrat Alemu, Tadesse Gure Eticha, Abraham Geremew, Kedir Teji Roba, Alemseged Abdissa, Nega Assefa, Abel Abera NegashSee the full list of authors
6 January 2025
A phase II double-blind multicentre, placebo-controlled trial to assess the efficacy and safety of alpelisib (BYL719) in paediatric and adult patients with Megalencephaly-CApillary malformation Polymicrogyria syndrome (MCAP): the SESAM study protocolMaxime Luu, Pierre Vabres, Aurélie Espitalier, Agnès Maurer, Aurore Garde, Caroline Racine, Maud Carpentier, Adélaide Rega, Romaric Loffroy, Nawale Hadouiri, Nathalie Boddaert, Aurore Curie, Laurent Guibaud, Mouna Chebbi, Julie CharlignySee the full list of authors
20 December 2024
Who has the responsibility to inform relatives at risk of hereditary cancer? A population-based survey in SwedenKalle Grill, Amicia Phillips, Barbro Numan Hellquist, Anna Rosén
27 November 2024
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocolKirsten M Farncombe, Lauren K Hughes, Elif Tuzlali, Mohammad Reza Akbari, Irene L Andrulis, Melyssa Aronson, Kathleen Bell, Michelle D Brazas, Melissa Cable-Cibula, Brandon Chan, Melanie Courtot, Harriet Feilotter, Jamie Harland, Katie Lark, Jordan Lerner-EllisSee the full list of authors
24 November 2024
Scoping review of enablers and challenges of implementing pharmacogenomics testing in the primary care settingsChun-Wai Mai, Sathvik B Sridhar, Mohammed Salim Karattuthodi, Perishithaa M Ganesan, Javedh Shareef, E Lyn Lee, Keivan Armani
5 November 2024
Experiences across a genetic screening and testing programme pathway: a qualitative study of mammogram patient perspectivesClaire Devine, Kate R Emery, Kimberly K Childers, Sandra Brown, Ora Gordon, Sarah E Roth
23 October 2024
Perceptions of genomic newborn screening: a cross-sectional survey conducted with UK medical studentsLydia Seed, Anna Scott, Amanda Pichini, Michelle Peter, Shereen Tadros, Cristine Sortica da Costa, Melissa Hill
24 September 2024