Development of next generation sequencing panel for UMOD and association with kidney disease

por Bailie, Caitlin, Kilner, Jill, Maxwell, Alexander P., McKnight, Amy Jayne
Publicado 2017

Evaluating the impact of COVID-19 on rare disease support groups

por McMullan, Julie, Crowe, Ashleen L., Bailie, Caitlin, McKnight, Amy Jayne
Publicado 2021

A scoping review and proposed workflow for multi-omic rare disease research

por Kerr, Katie, McAneney, Helen, Smyth, Laura J., Bailie, Caitlin, McKee, Shane, McKnight, Amy Jayne
Publicado 2020

Improvements needed to support people living and working with a rare disease in Northern Ireland: current rare disease support perceived as inadequate

por McMullan, Julie, Crowe, Ashleen L., Bailie, Caitlin, Moore, Kerry, McMullan, Lauren S., Shamandi, Nahid, McAneney, Helen, McKnight, Amy Jayne
Publicado 2020

A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland

por Kerr, Katie, McKenna, Caoimhe, Heggarty, Shirley, Bailie, Caitlin, McMullan, Julie, Crowe, Ashleen, Kilner, Jill, Donnelly, Michael, Boyle, Saralynne, Rea, Gillian, Flanagan, Cheryl, McKee, Shane, McKnight, Amy Jayne
Publicado 2022