1. A genome‐wide association study of recipient genotype and medium‐term kidney allograft function. (21st February 2013) Authors: O'Brien, Robert P.; Phelan, Paul J.; Conroy, Judith; O'Kelly, Patrick; Green, Andrew; Keogan, Mary; O'Neill, Derek; Jennings, Susan; Traynor, Carol; Casey, Jillian; McCormack, Mark; Conroy, Ronan; Chubb, Anthony; Ennis, Sean; Shields, Denis C.; Cavalleri, Gianpiero L.; Conlon, Peter J. Journal: Clinical transplantation Issue: Volume 27:Number 3(2013:May/Jun.) Page Start: 379 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosomal microarray in unexplained severe early onset epilepsy – A single centre cohort. (July 2015) Authors: Allen, Nicholas M.; Conroy, Judith; Shahwan, Amre; Ennis, Sean; Lynch, Bryan; Lynch, Sally A.; King, Mary D. Journal: European journal of paediatric neurology Issue: Volume 19:Number 4(2015:Jul.) Page Start: 390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cost of exome sequencing in epileptic encephalopathy: is it 'worth it'?. Issue 3 (22nd September 2017) Authors: Forman, Eva B; Gorman, Kathleen M; Conroy, Judith; Arthur, Neil; Grant, Ciara; Ennis, Sean; Allen, Nicholas M; Lynch, Sally Ann; King, Mary D Journal: Archives of disease in childhood Issue: Volume 103:Issue 3(2018) Page Start: 304 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms—A further patient. Issue 7 (3rd April 2014) Authors: Allen, Nicholas M.; Conroy, Judith; Shahwan, Amre; Ennis, Sean; Lynch, Bryan; Lynch, Sally A.; King, Mary D. Journal: American journal of medical genetics Issue: Volume 164:Issue 7(2014.) Page Start: 1863 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Inflammatory bowel disease: the role of inflammatory cytokine gene polymorphisms. Issue 3 (2004) Authors: Balding, Joanna; Livingstone, Wendy J.; Conroy, Judith; Mynett-Johnson, Lesley; Weir, Donald G.; Mahmud, Nasir; Smith, Owen P. Journal: Mediators of inflammation Issue: Volume 13:Issue 3(2004) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel SMC1A variant and epilepsy of infancy with migrating focal seizures: Expansion of the phenotype. (July 2017) Authors: Gorman, Kathleen M.; Forman, Eva; Conroy, Judith; Allen, Nicholas M.; Shahwan, Amre; Lynch, Sally A.; Ennis, Sean; King, Mary D. Journal: Epilepsia Issue: Volume 58:issue 7(2017) Page Start: 1301 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. OC48 Re-interrogation of whole exome sequencing data in developmental epileptic encephalopathies. (June 2019) Authors: Gorman, Kathleen Mary; Conroy, Judith; Forman, Eva; Lynch, Sally A; Allen, Nicholas M; Shahwan, Amre; Lynch, Brian; Ennis, Sean; King, Mary Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 3 Page Start: A20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Plasma C-Terminal Agrin Fragment as an Early Biomarker for Sarcopenia: Results From the GenoFit Study. (16th May 2021) Authors: Pratt, Jedd; De Vito, Giuseppe; Narici, Marco; Segurado, Ricardo; Pessanha, Ludmilla; Dolan, Jackie; Conroy, Judith; Boreham, Colin Editors: Le Couteur, David Journal: Journals of gerontology Issue: Volume 76:Number 12(2021) Page Start: 2090 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The variable phenotypes of KCNQ‐related epilepsy. Issue 9 (22nd July 2014) Authors: Allen, Nicholas M.; Mannion, Maria; Conroy, Judith; Lynch, Sally A.; Shahwan, Amre; Lynch, Bryan; King, Mary D. Journal: Epilepsia Issue: Volume 55:Issue 9(2014:Sep.) Page Start: e99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Towards the identification of a genetic basis for Landau‐Kleffner syndrome. Issue 6 (14th May 2014) Authors: Conroy, Judith; McGettigan, Paul A.; McCreary, Dara; Shah, Naisha; Collins, Kevin; Parry‐Fielder, Bronwyn; Moran, Margaret; Hanrahan, Donncha; Deonna, Thierry W.; Korff, Christian M.; Webb, David; Ennis, Sean; Lynch, Sally A.; King, Mary D. Journal: Epilepsia Issue: Volume 55:Issue 6(2014:Jun.) Page Start: 858 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗