Randomised double-blind controlled trial of non-invasive preimplantation genetic testing for aneuploidy in in vitro fertilisation: a protocol paperHiu Yee Heidi Cheng, Judy F C Chow, Kevin K W Lam, Shui Fan Lai, William Shu Biu Yeung, Ernest H Y Ng
27 July 2023
Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocolSophie E Bouffler, Ling Lee, Fiona Lynch, Melissa Martyn, Elly Lynch, Ivan Macciocca, Lisette Curnow, Giulia McCorkell, Sebastian Lunke, Belinda Chong, Justine E Marum, Martin Delatycki, Lilian Downie, Ilias Goranitis, Danya F VearsSee the full list of authors
2 June 2023
Protocol for a comprehensive prospective cohort study of trio-based whole-genome sequencing for underlying cancer predisposition in paediatric and adolescent patients newly diagnosed with cancer: the PREDICT studyNoemi Auxiliadora Fuentes Bolanos, Bhavna Padhye, Macabe Daley, Jacqueline Hunter, Kate Hetherington, Meera Warby, Eliza Courtney, Judy Kirk, Sarah Josephi-Taylor, Yuyan Chen, Frank Alvaro, Kristine Barlow-Stewart, Marie Wong-Erasmus, Paulette Barahona, Pamela AjuyahSee the full list of authors
30 May 2023
Implementation of a culturally competent APOL1 genetic testing programme into living donor evaluation: A two-site, non-randomised, pre–post trial designJustin D Smith, Akansha Agrawal, Catherine Wicklund, Debra Duquette, John Friedewald, Luke V Rasmussen, Jessica Gacki-Smith, S. Darius Tandon, Lutfiyya N Muhammad, Clyde W Yancy, Siyuan Dong, Matthew Cooper, Alexander Gilbert, Aneesha Shetty, Elisa J Gordon
15 May 2023
Genetic and genomic nursing competency among nurses in tertiary general hospitals and cancer hospitals in mainland China: a nationwide surveyXiaomin Zhao, Xuying LI, Yi Liu, Kathleen Calzone, Juan Xu, Xueling Xiao, Honghong Wang
30 December 2022
Epidemiology, aetiology, interventions and genomics in children with arthrogryposis multiplex congenita: protocol for a multisite registryNoémi Dahan-Oliel, Harold van Bosse, Vasiliki Betty Darsaklis, Frank Rauch, Tanya Bedard, Ghalib Bardai, Michelle James, Ellen Raney, Krister Freese, Lauren Hyer, Haluk Altiok, Jonathan Pellett, Philip Giampietro, Judith Hall, Reggie Charles Hamdy
28 October 2022
Positioning whole exome sequencing in the diagnostic pathway for rare disease to optimise utility: a protocol for an observational cohort study and an economic evaluationRobin Z Hayeems, Francois Bernier, Kym M Boycott, Taila Hartley, Christine Michaels-Igbokwe, Deborah A Marshall
10 October 2022
Implementation of genetic screening test to reduce the incidence of dapsone hypersensitivity syndrome among patients with leprosy in Papua, Indonesia: a study protocolHana Krismawati, Astri Ferdiana, Astrid Irwanto, Teky Budiawan, Clara Imaniar, Tri Wahyuni, Pushpendra Singh, Liesbeth Mieras, Arry Pongtiku
11 May 2022
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service deliverySalma Shickh, Daena Hirjikaka, Marc Clausen, Rita Kodida, Chloe Mighton, Emma Reble, Jordan Sam, Seema Panchal, Melyssa Aronson, Tracy Graham, Susan Randall Armel, Emily Glogowski, Christine Elser, Andrea Eisen, June C CarrollSee the full list of authors
29 April 2022
Assessing the cost-effectiveness of precision medicine: protocol for a systematic review and meta-analysisWenjia Chen, Thunyarat Anothaisintawee, Dimple Butani, Yi Wang, Yaroslava Zemlyanska, Chong Boon Nigel Wong, Suchin Virabhak, M A Hrishikesh, Yot Teerawattananon
5 April 2022