The Impact of Inherited Retinal Diseases in the Republic of Ireland (ROI) and the United Kingdom (UK) from a Cost-of-Illness Perspective by Galvin, Orla, Chi, Gloria, Brady, Laura, Hippert, Claire, Del Valle Rubido, Marta, Daly, Avril, Michaelides, Michel

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Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in Ireland by Somanadhan, Suja, Nicholson, Emma, Dorris, Emma, Brinkley, Aoife, Kennan, Avril, Treacy, Eileen, Atif, Awan, Ennis, Sean, McGrath, Vicky, Mitchell, Derick, O’Sullivan, Grace, Power, Julie, Lawlor, Anne, Harkin, Paul, Lynch, Sally Ann, Watt, Philip, Daly, Avril, Donnelly, Susie, Kroll, Thilo

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Genetic Testing Experiences of People Living with Inherited Retinal Degenerations: Results of a Global Survey by Paudel, Nabin, Daly, Avril, Waters, Fiona, Stratieva, Petia

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The Landscape of Genomic Services for Inherited Retinal Degenerations by Paudel, Nabin, Stratieva, Petia, Moran, Ellen Margaret, Daly, Avril

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Retinal layer segmentation in multiple sclerosis: a systematic review and meta-analysis by Petzold, Axel, Balcer, Laura J, Calabresi, Peter A, Costello, Fiona, Frohman, Teresa C, Frohman, Elliot M, Martinez-Lapiscina, Elena H, Green, Ari J, Kardon, Randy, Outteryck, Olivier, Paul, Friedemann, Schippling, Sven, Vermersch, Patrik, Villoslada, Pablo, Balk, Lisanne J, Aktas, Orhan, Albrecht, Philipp, Ashworth, Jane, Asgari, Nasrin, Balcer, Laura, Balk, Lisanne, Black, Graeme, Boehringer, Daniel, Behbehani, Raed, Benson, Leslie, Bermel, Robert, Bernard, Jacqueline, Brandt, Alexander, Burton, Jodie, Calabresi, Peter, Calkwood, Jonathan, Cordano, Christian, Costello, Fiona, Courtney, Ardith, Cruz-Herranz, Andrés, Diem, Ricarda, Daly, Avril, Dollfus, Helene, Fasser, Christina, Finke, Carsten, Frederiksen, Jette, Frohman, Elliot, Frohman, Teresa, Garcia-Martin, Elenaw, Suárez, Inés González, Pihl-Jensen, Gorm, Graves, Jennifer, Green, Ari, Havla, Joachim, Hemmer, Bernhard, Huang, Su-Chun, Imitola, Jaime, Jiang, Hong, Keegan, David, Kildebeck, Eric, Klistorner, Alexander, Knier, Benjamin, Kolbe, Scott, Korn, Thomas, LeRoy, Bart, Leocani, Letizia, Leroux, Dorothee, Levin, Netta, Liskova, Petra, Lorenz, Birgit, Preiningerova, Jana Lizrova, Martínez-Lapiscina, Elena Hernández, Mikolajczak, Janine, Montalban, Xavier, Morrow, Mark, Nolan, Rachel, Oberwahrenbrock, Timm, Oertel, Frederike Cosima, Oreja-Guevara, Celia, Osborne, Benjamin, Outteryck, Olivier, Papadopoulou, Athina, Paul, Friedemann, Petzold, Axel, Ringelstein, Marius, Saidha, Shiv, Sanchez-Dalmau, Bernardo, Sastre-Garriga, Jaume, Schippling, Sven, Shin, Robert, Shuey, Neil, Soelberg, Kerstin, Toosy, Ahmed, Torres, Rubén, Vidal-Jordana, Angela, Villoslada, Pablo, Waldman, Amy, White, Owen, Yeh, Ann, Wong, Sui, Zimmermann, Hanna

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Therapies for Inherited Retinal Dystrophies: What is Enough? by Leroy, Bart P., Daly, Avril, Héon, Elise, Sahel, José-Alain, Dollfus, Hélène

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Correction: Save our Sight (SOS): a collective call-to-action for enhanced retinal care across health systems in high income countries by Loewenstein, Anat, Berger, Alan, Daly, Avril, Creuzot-Garcher, Catherine, Gale, Richard, Ricci, Federico, Zarranz-Ventura, Javier, Guymer, Robyn

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Save our Sight (SOS): a collective call-to-action for enhanced retinal care across health systems in high income countries by Loewenstein, Anat, Berger, Alan, Daly, Avril, Creuzot-Garcher, Catherine, Gale, Richard, Ricci, Federico, Zarranz-Ventura, Javier, Guymer, Robyn

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The Landscape of Genomic Services for Inherited Retinal Degenerations (IRDs) Across Europe by Paudel, Nabin, Daly, Avril, Moran, Ellen Margaret, Stratieva, Petia

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The Impact of Inherited Retinal Diseases in the United States of America (US) and Canada from a Cost-of-Illness Perspective by Gong, Jennifer, Cheung, Simone, Fasso-Opie, Alivia, Galvin, Orla, Moniz, Larissa S, Earle, Doug, Durham, Todd, Menzo, Jason, Li, Nan, Duffy, Stephanie, Dolgin, Jill, Shearman, Mark S, Fiorani, Chiara, Banhazi, Judit, Daly, Avril

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The Impact of Inherited Retinal Diseases in the Republic of Ireland from a Cost-of-Illness Perspective by Galvin, Orla, Chi, Gloria, Brady, Laura, Hippert, Claire, Rubido, Marta Del Valle, Daly, Avril, Michaelides, Michel

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The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement by Black, Graeme C, Sergouniotis, Panagiotis, Sodi, Andrea, Leroy, Bart P, Van Cauwenbergh, Caroline, Liskova, Petra, Grønskov, Karen, Klett, Artur, Kohl, Susanne, Taurina, Gita, Sukys, Marius, Haer-Wigman, Lonneke, Nowomiejska, Katarzyna, Marques, João Pedro, Leroux, Dorothée, Cremers, Frans P M, De Baere, Elfride, Dollfus, Hélène

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The Impact of Inherited Retinal Diseases in the United States of America by Fiorani, Chiara, Banhazi, Judit, Dolgin, Jill, Menzo, Jason, Fasso-Opie, Alivia, Galvin, Orla, Durham, Todd, Gong, Jennifer, Li, Nan, Cheung, Simone, Earle, Doug, Duffy, Stephanie, Moniz, Larissa S, Daly, Avril, Shearman, Mark S

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Artificial intelligence extension of the OSCAR‐IB criteria by Albrecht, Philipp, Balcer, Laura, Brandt, Alexander U., Calabresi, Peter A., Green, Ari, Sander, Josemir W., Paul, Friedemann, Villoslada, Pablo, Aktas, Orhan, Antel, Jack, Asgari, Nasrin, Audo, Isabelle, Avasarala, Jagannadha, Avril, Daly, Bagnato, Francesca R, Banwell, Brenda, Bar‐Or, Amit, Manterola, Arnaldo Belzunce, Bernard, Jacqueline, Bremond‐Gignac, Dominique, Britze, Josefine, Calkwood, Jonathan, Carroll, William, Cohen, Jeffrey, Comi, Giancarlo, Cordano, Christian, Costa, Silvana, Courtney, Ardith, Cruz‐Herranz, Anes, Crabb, David, Delott, Lindsey, Dollfuss, Helene, Fasser, Christina, Finke, Carsten, Fischer, Dominik, Fonseca, Pedro, Frederiksen, Jette L, Frohman, Elliot, Frohman, Teresa, Fujihara, Kazuo, Cuellar, Iñigo Gabilondo, Garcia‐Martin, Elena, Giovannoni, Gavin, Suárez, Inés González, Jensen, Gorm Pihl, Hartung, Hans‐Peter, Havla, Joachim, Huang, Su‐Chun, Jasinskas, Vytautas, Kafieh, Rahele, Kappos, Ludwig, Keegan, David, Kildebeck, Eric, Knier, Benjamin, Kolbe, Scott, Korn, Thomas, Lagrèze, Wolf, Leocani, Letizia, Preiningerova, Jana Lizrova, May, Eugene, Miller, David, Montalban, Xavier, Morrow, Mark, Mowry, Ellen, Murta, Joaquim, Nolan, Rachel, Oertel, Frederike Cosima, Oreja‐Guevara, Celia, Orssaud, Christophe, Osborne, Benjamin, Paiva, Catarina, Patsopoulos, Nikos, Preiningerova, Jana Lizrova, Pontikos, Nikolas, Prince, Jerry, Rodriguez de Antonio, Luis, Sahel, Jose‐Alain, Sastre‐Garriga, Jaume, Schippling, Sven, Shuey, Neil, Specovius, Svenja, Suppiej, Agnese, Torres, Rubén, Touitou, Valérie, Trauzettel‐Klosinski, Susanne, van der Walt, Anneke, Vidal‐Jordana, Angela, Waldman, Amy T, Waters, Christian, Wheeler, Russell, White, Owen, Wilhelm, Helmut, Winges, Kimberly M, Wiehe, Lenja, Wisnewski, Thomas, Würfel, Jens, You, Yuyi, Yu, Zhaoxia, Žemaitien≐, Reda, Zimmermann, Hanna

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Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify the top 15 research priorities for rare diseases by Somanadhan, Suja, Nicholson, Emma, Dorris, Emma, Brinkley, Aoife, Kennan, Avril, Treacy, Eileen, Atif, Awan, Ennis, Sean, McGrath, Vicky, Mitchell, Derick, O’Sullivan, Grace, Power, Julie, Lawlor, Anne, Harkin, Paul, Lynch, Sally Ann, Watt, Philip, Daly, Avril, Donnelly, Susie, Kroll, Thilo

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Designing Rare Disease Care Pathways in the Republic of Ireland – A Co-operative Model by Ward, A J, Murphy, Daniel, Marron, Rita, McGrath, V, Bolz-Johnson, M, Cullen, Walter, Daly, Avril, Hardiman, Orla, Lawlor, A, Lynch, Sally Ann, MacLachlan, Mac, McBrien, Jackie, O'Byrne, James, Turner, Jacqueline, O'Connell, Susan, Treacy, Eileen P

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Fit for purpose? A cross-sectional study to evaluate the acceptability and usability of HeadUp, a novel neck support collar for neurological neck weakness by Sproson, Lise, Lanfranchi, Vitaveska, Collins, Alexis, Chhetri, Suresh K., Daly, Niamh, Ennis, Michelle, Glennon, Lucie, Gorrie, George, Jay, Emily, Marsden, Rachael, McCarthy, Avril D., Pryde, Liz, Roberts, Rhys, Rutherford, Anna, Ryan, Jessica, Stot, Gill, Tindale, Wendy B., Shaw, Pamela J., McDermott, Christopher J.

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Risk and protective genetic variants in suicidal behaviour: association with SLC1A2, SLC1A3, 5-HTR1B &NTRK2 polymorphisms by Murphy, Therese M, Ryan, Maria, Foster, Tom, Kelly, Chris, McClelland, Roy, O'Grady, John, Corcoran, Eleanor, Brady, John, Reilly, Michael, Jeffers, Anne, Brown, Katherine, Maher, Anne, Bannan, Noreen, Casement, Alison, Lynch, Dermot, Bolger, Sharon, Tewari, Prerna, Buckley, Avril, Quinlivan, Leah, Daly, Leslie, Kelleher, Cecily, Malone, Kevin M

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Validation of 28 and 15 item versions of the SCORE family assessment questionnaire with adult mental health service users by O'Hanrahan, Kevin, Daly White, Megan, Carr, Alan, Cahill, Paul, Keenleyside, Mairi, Fitzhenry, Mark, Harte, Elizabeth, Hayes, Jennifer, Noonan, Hester, O'Shea, Helen, McCullagh, Avril, McGuinness, Shaun, Rodgers, Catherine, Whelan, Neal, Sheppard, Noel, Browne, Stephen

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Child maltreatment and adult psychopathology in an Irish context by Fitzhenry, Mark, Harte, Elizabeth, Carr, Alan, Keenleyside, Mairi, O’Hanrahan, Kevin, White, Megan Daly, Hayes, Jennifer, Cahill, Paul, Noonan, Hester, O'Shea, Helen, McCullagh, Avril, McGuinness, Shaun, Rodgers, Catherine, Whelan, Neal, Sheppard, Noel, Browne, Stephen

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