Dermatology
Staff
| Dvorakova | Victoria | Dr | Paediatric Dermatologist |
| Irvine | Alan | Prof | Paediatric Dermatologist |
Professor Alan Irvine
PROFESSOR OF DERMATOLOGY, Clinical Medicine
PROFESSOR OF DERMATOLOGY, School Office - Medicine
Publications and Further Research Outputs
Peer-Reviewed Publications
Walsh, Carleen, Leavey, Gerard, Mc Laughlin, Marian, Paller, Amy S, Irvine, Alan D, Browne, Fiona, Mellerio, Jemima E, Bewley, Anthony, Novel mixed-method, inclusive protocol involving global key stakeholders, including carers as experts, to co-develop relevant Caregiver-Reported Outcome Domains (CRODs) in skin disease, BMJ Open, 13, (1), 2023, pe068893
Nousbeck, Janna, McAleer, Maeve A., Irvine, Alan D., Peripheral Blood Gene Expression Profile of Infants with Atopic Dermatitis, JID Innovations, 3, (2), 2023, p100165
Cathal O'Connor, Vicki Livingstone, Jonathan O'. B. Hourihane, Alan D. Irvine, Geraldine Boylan, Deirdre Murray, Parental atopy and risk of atopic dermatitis in the first two years of life in the BASELINE birth cohort study, Pediatric Dermatology, 2022
Deleuran, M, Marcoux, D, Bruin-Weller, M, Irvine, A, Baselga, E, Ahn, K, Castro, A, Bansal, A, Chao, J, Bégo-Le-Bagousse, G, Rossi, A, Dupilumab Provides Significant Clinical Benefit in a Phase 3 Trial in Adolescents with Uncontrolled Atopic Dermatitis Irrespective of Prior Systemic Immunosuppressant Use, Acta Dermato Venereologica, 101, (7), 2021, padv00504
Holm, Annegret, te Loo, Maroeska, Schultze Kool, Leo, Salminen, Päivi, Celis, Veronica, Baselga, Eulalia, Duignan, Sophie, Dvorakova, Veronika, Irvine, Alan D., Boon, Laurence M., Vikkula, Miikka, Ghaffarpour, Nader, Niemeyer, Charlotte M., Rössler, Jochen, Kapp, Friedrich G., Efficacy of Sirolimus in Patients Requiring Tracheostomy for Life-Threatening Lymphatic Malformation of the Head and Neck: A Report From the European Reference Network, Frontiers in Pediatrics, 9, 2021
Abuabara, K., Nicholls, S.G., Langan, S.M., Guttman"Yassky, E., Reynolds, N.J., Paller, A.S., Brown, S.J., , , Priority research questions in atopic dermatitis: an International Eczema Council eDelphi consensus, British Journal of Dermatology, 185, (1), 2021, p203-205
Wall, Dmitri, Alhusayen, Raed, Arents, Bernd, Apfelbacher, Christian, Balogh, Esther A., Bokhari, Laita, Bloem, Manja, Bosma, Angela L., Burton, Tim, Castelo-Soccio, Leslie, Fagan, Nicole, Feldman, Steven R., Fletcher, Godfrey, Flohr, Carsten, Freeman, Esther, French, Lars E., Griffiths, Christopher E.M., Hruza, George J., Ingram, John R., Kappelman, Michael D., Lara-Corrales, Irene, Lim, Henry W., Meah, Nekma, McMahon, Devon E., Mahil, Satveer K., McNicoll, Ian, Musters, Annelie, Naik, Haley B., Sinclair, Rodney, Smith, Catherine H., Spuls, Phyllis, Tobin, Desmond J., York, Katherine, Irvine, Alan D., Learning from disease registries during a pandemic: Moving toward an international federation of patient registries, Clinics in Dermatology, 39, (3), 2021, p467-478
Doherty AM, Colleran GC, Durcan L, Irvine AD, Barrett E, A pilot study of burnout and long covid in senior specialist doctors., Irish journal of medical science, 2021
Towell AM, Feuillie C, Vitry P, Da Costa TM, Mathelié-Guinlet M, Kezic S, Fleury OM, McAleer MA, Dufrêne YF, Irvine AD, Geoghegan JA, Staphylococcus aureus binds to the N-terminal region of corneodesmosin to adhere to the stratum corneum in atopic dermatitis, Proceedings of the National Academy of Sciences of the United States of America, 118, (1), 2021, pe2014444118
Takuya Miyano, Alan D Irvine, Reiko J Tanaka, A mathematical model to identify optimal combinations of drug targets for dupilumab poor responders in atopic dermatitis, 2021
Jennifer M. E. Boggs, Alan D. Irvine, PLACK syndrome resulting from a novel homozygous variant in CAST, Pediatric Dermatology, 2021
McCarthy, Elaine K, Murray, Deirdre M, Hourihane, Jonathan O"B, Kenny, Louise C, Irvine, Alan D, Kiely, Mairead E, Behavioral consequences at 5 y of neonatal iron deficiency in a low-risk maternal"infant cohort, The American Journal of Clinical Nutrition, 113, (4), 2021, p1032-1041
Freeman, Esther E., Chamberlin, Grace C., McMahon, Devon E., Hruza, George J., Wall, Dmitri, Meah, Nekma, Sinclair, Rodney, Balogh, Esther A., Feldman, Steven R., Lowes, Michelle A., Marzano, Angelo V., Naik, Haley B., Castelo-Soccio, Leslie, Lara-Corrales, Irene, Cordoro, Kelly M., Mahil, Satveer K., Griffiths, Christopher E.M., Smith, Catherine H., Irvine, Alan D., Spuls, Phyllis I., Flohr, Carsten, French, Lars E., Dermatology COVID-19 Registries, Dermatologic Clinics, 39, (4), 2021, p575-585
Delles, C, Dayan, C M, Dominiczak, A F, Donnelly, S C, Irvine, A D, Announcing the first AoP webinar: `Can evidence-based medicine survive in a pandemic?", QJM: An International Journal of Medicine, 114, (1), 2021, p11-12
Hotz, Alrun, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Komlosi, Katalin, Giehl, Kathrin, Bouadjar, Bakar, Bygum, Anette, Tantcheva-Poor, Iliana, Hellström Pigg, Maritta, Has, Cristina, Yang, Zhou, Irvine, Alan D., Betz, Regina C., Zambruno, Giovanna, Tadini, Gianluca, Süßmuth, Kira, Gruber, Robert, Schmuth, Matthias, Mazereeuw-Hautier, Juliette, Jonca, Natalie, Guez, Sophie, Brena, Michela, Hernandez-Martin, Angela, van den Akker, Peter, Bolling, Maria C., Hannula-Jouppi, Katariina, Zimmer, Andreas D., Alter, Svenja, Vahlquist, Anders, Fischer, Judith, Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients, Genes, 12, (1), 2021, p80
Meah, Nekma, Wall, Dmitri, York, Katherine, Bhoyrul, Bevin, Bokhari, Laita, Asz-Sigall, Daniel, Bergfeld, Wilma F., Betz, Regina C., Blume-Peytavi, Ulrike, Callender, Valerie, Chitreddy, Vijaya, Combalia, Andrea, Cotsarelis, George, Craiglow, Brittany, Donovan, Jeff, Eisman, Samantha, Farrant, Paul, Green, Jack, Grimalt, Ramon, Harries, Matthew, Hordinsky, Maria, Irvine, Alan D., Itami, Satoshi, Jolliffe, Victoria, King, Brett, Lee, Won-Soo, McMichael, Amy, Messenger, Andrew, Mirmirani, Paradi, Olsen, Elise, Orlow, Seth J., Piraccini, Bianca Maria, Rakowska, Adriana, Reygagne, Pascal, Roberts, Janet L., Rudnicka, Lidia, Shapiro, Jerry, Sharma, Pooja, Tosti, Antonella, Vogt, Annika, Wade, Martin, Yip, Leona, Zlotogorski, Abraham, Sinclair, Rodney D., The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expert opinion on diagnosis and laboratory evaluation for alopecia areata, Journal of the American Academy of Dermatology, 84, (6), 2021, p1594-1601
Bradshaw, Lucy E., Haines, Rachel H., Thomas, Kim S., Chalmers, Joanne R., Irvine, Alan D., Williams, Hywel C., Brown, Sara J., Clinical examination for hyperlinear palms to determine filaggrin genotype: A diagnostic test accuracy study, Clinical & Experimental Allergy, 51, (11), 2021, p1421-1428
Wall, Dmitri, Meah, Nekma, York, Katherine, Bhoyrul, Bevin, Bokhari, Laita, Abraham, Leonardo Spagnol, Adams, Roisín, Bergfeld, Wilma, Betz, Regina C., Blume-Peytavi, Ulrike, Callender, Valerie, Campbell, Chel, Chambers, Jen, Chen, Gang, Chitreddy, Vijaya, Cotsarelis, George, Craiglow, Brittany, Dhurat, Rachita, Dlova, Ncoza, Donovan, Jeff, Duque-Estrada, Bruna, Eisman, Samantha, Ellison, Abby, Farrant, Paul, Barberá, Juan Ferrando, Gadzhigoroeva, Aida, Grimalt, Ramon, Harries, Matthew, Hordinsky, Maria, Irvine, Alan D., Jolliffe, Victoria, Jones, Leslie, King, Brett, Lee, Won-Soo, Lortkipanidze, Nino, McMichael, Amy, Messenger, Andrew, Mirmirani, Paradi, Olsen, Elise, Orlow, Seth J., Ovcharenko, Yuliya, Piraccini, Bianca Maria, Pirmez, Rodrigo, Rakowska, Adriana, Reygagne, Pascal, Riley, Melissa, Rudnicka, Lidia, Saceda Corralo, David, Shapiro, Jerry, Sharma, Pooja, Silyuk, Tatiana, Kaiumov, Spartak, Tobin, Desmond J., Tosti, Antonella, Vañó-Galván, Sergio, Vogt, Annika, Wade, Martin, Yip, Leona, Zlotogorski, Abraham, Zhou, Cheng, Sinclair, Rodney, A Global eDelphi Exercise to Identify Core Domains and Domain Items for the Development of a Global Registry of Alopecia Areata Disease Severity and Treatment Safety (GRASS), JAMA Dermatology, 157, (4), 2021, p439
Silverberg, Jonathan I., Simpson, Eric L., Armstrong, April W., de Bruin-Weller, Marjolein S., Irvine, Alan D., Reich, Kristian, Expert Perspectives on Key Parameters that Impact Interpretation of Randomized Clinical Trials in Moderate-to-Severe Atopic Dermatitis, American Journal of Clinical Dermatology, 2021
Onoufriadis, A., Cabezas, A., Ng, J.C.F., Canales, J., Costas, M.J., Ribeiro, J.M., Rodrigues, J.R., McAleer, M.A., Castelo"Soccio, L., Simpson, M.A., Fraternali, F., Irvine, A.D., Cameselle, J.C., McGrath, J.A., Autosomal recessive hypotrichosis with loose anagen hairs associated with TKFC mutations*, British Journal of Dermatology, 184, (5), 2021, p935-943
Guttman-Yassky, Emma, Teixeira, Henrique D, Simpson, Eric L, Papp, Kim A, Pangan, Aileen L, Blauvelt, Andrew, Thaçi, Diamant, Chu, Chia-Yu, Hong, H Chih-ho, Katoh, Norito, Paller, Amy S, Calimlim, Brian, Gu, Yihua, Hu, Xiaofei, Liu, Meng, Yang, Yang, Liu, John, Tenorio, Allan R, Chu, Alvina D, Irvine, Alan D, Once-daily upadacitinib versus placebo in adolescents and adults with moderate-to-severe atopic dermatitis (Measure Up 1 and Measure Up 2): results from two replicate double-blind, randomised controlled phase 3 trials, The Lancet, 397, (10290), 2021, p2151-2168
Takuya Miyano, Alan D Irvine, Reiko J Tanaka, Model-based meta-analysis to optimise S. aureus-targeted therapies for atopic dermatitis, 2021
Fagan, Nicole, Meah, Nekma, York, Katherine, Bokhari, Laita, Fletcher, Godfrey, Chen, Gang, Tobin, Desmond J., Messenger, Andrew, Irvine, Alan D., Sinclair, Rodney, Wall, Dmitri, Shedding light on therapeutics in alopecia and their relevance to COVID-19, Clinics in Dermatology, 39, (1), 2021, p76-83
Stefanovic, Nicholas, Irvine, Alan D., Flohr, Carsten, The Role of the Environment and Exposome in Atopic Dermatitis, Current Treatment Options in Allergy, 8, (3), 2021, p222-241
Mulick, A.R., Mansfield, K.E., Silverwood, R.J., Budu"Aggrey, A., Roberts, A., Custovic, A., Pearce, N., Irvine, A.D., Smeeth, L., Abuabara, K., Langan, S.M., Four childhood atopic dermatitis subtypes identified from trajectory and severity of disease and internally validated in a large UK birth cohort, British Journal of Dermatology, 185, (3), 2021, p526-536
Xing, Chao, Kanchwala, Mohammed, Rios, Jonathan J., Hyatt, Tommy, Wang, Richard C., Tran, An, Dougherty, Irene, Tovar"Garza, Andrea, Purnadi, Christy, Kumar, Monique G., Berk, David, Shinawi, Marwan, Irvine, Alan D., Toledo"Bahena, Mirna, Agim, Nnenna G., Glass, Donald A., Biallelic variants in RNU12 cause CDAGS syndrome, Human Mutation, 42, (8), 2021, p1042-1052
Luger, T., Paller, A.S., Irvine, A.D., Sidbury, R., Eichenfield, L.F., Werfel, T., Bieber, T., Topical therapy of atopic dermatitis with a focus on pimecrolimus, Journal of the European Academy of Dermatology and Venereology, 35, (7), 2021, p1505-1518
H. Blakeway, V. Van"de"Velde, V.B. Allen, G. Kravvas, L. Palla, M.J. Page, C. Flohr, R.B. Weller, A.D. Irvine, T. McPherson, A. Roberts, H.C. Williams, N. Reynolds, S.J. Brown, L. Paternoster, S.M. Langan, What is the evidence for interactions between filaggrin null mutations and environmental exposures in the aetiology of atopic dermatitis? A systematic review, British Journal of Dermatology, 2020
Drislane, C., Irvine, A.D., The role of filaggrin in atopic dermatitis and allergic disease, Annals of Allergy, Asthma and Immunology, 124, (1), 2020, p36-43
M.A. McAleer, I. Jakasa, N. Stefanovic, W.H.I. McLean, S. Kezic, A.D. Irvine, Topical Corticosteroids Normalize both Skin and Systemic Inflammatory Markers in Infant Atopic Dermatitis, British Journal of Dermatology, 2020
Marek Haftek, Maeve A McAleer, Ivone Jakasa, WH Irwin McLean, Sanja Kezic, Alan D. Irvine, Changes in nano-mechanical properties of human epidermal cornified cells in children with atopic dermatitis, Wellcome Open Research, 5, 2020, p97
J. Nousbeck, M.A. McAleer, G. Hurault, E. Kenny, K. Harte, S. Kezic, R.J. Tanaka, A.D. Irvine, MicroRNA analysis of childhood atopic dermatitis reveals a role for miR"451a, British Journal of Dermatology, 2020
L. Cunningham, V. Dvorakova, F. Browne, A.D. Irvine, High dose Bilastine for the treatment of Bascule Syndrome, Clinical and Experimental Dermatology, 2020
F.M. Vermeulen, L.A.A. Gerbens, J. Schmitt, M. Deleuran, A.D. Irvine, K. Logan, W. Ouwerkerk, C. Vestergaard, C. Flohr, P.I. Spuls, The European TREatment of ATopic eczema (TREAT) Registry Taskforce survey: prescribing practices in Europe for phototherapy and systemic therapy in adult patients with moderate"to"severe atopic eczema*, British Journal of Dermatology, 2020
Karina Forde, Nicoletta Resta, Carlotta Ranieri, David Rea, Olga Kubassova, Mark Hinton, Alan D Irvine, Veronika Dvorakova, Clinical Experience with the AKT1 Inhibitor Miransertib in two Children with PIK3CA-related overgrowth syndrome, 2020
Doreen Siegels, Annice Heratizadeh, Susanne Abraham, Jonas Binnmyr, Knut Brockow, Alan D. Irvine, Susanne Halken, Charlotte G Mortz, Carsten Flohr, Peter Schmid"Grendelmeier, Lauri"Ann Poel, Antonella Muraro, Stephan Weidinger, Thomas Werfel, Jochen Schmitt, Systemic treatments in the management of atopic dermatitis: A systematic review and meta"analysis, Allergy, 2020
H. Alexander, A.S. Paller, C. Traidl"Hoffmann, L.A. Beck, A. De Benedetto, S. Dhar, G. Girolomoni, A.D. Irvine, P. Spuls, J. Su, J.P. Thyssen, C. Vestergaard, T. Werfel, A. Wollenberg, M. Deleuran, C. Flohr, The role of bacterial skin infections in atopic dermatitis: expert statement and review from the International Eczema Council Skin Infection Group, British Journal of Dermatology, 2019
Nicholas Stefanovic, Carsten Flohr, Alan D. Irvine, The exposome in atopic dermatitis, Allergy, 2019
F.M. Vermeulen, L.A.A. Gerbens, A.L. Bosma, C.J. Apfelbacher, A.D. Irvine, B.W.M. Arents, S. Barbarot, M. Deleuran, L.F. Eichenfield, A. Manca, J. Schmitt, C. Vestergaard, D. Wall, S. Weidinger, M.A. Middelkamp"Hup, P.I. Spuls, C. Flohr, TRE atment of AT opic eczema ( TREAT ) Registry Taskforce: consensus on how and when to measure the core dataset for atopic eczema treatment research registries, British Journal of Dermatology, 181, (3), 2019, p492--504
Paller, A.S., Spergel, J.M., Mina-Osorio, P., Irvine, A.D., The atopic march and atopic multimorbidity: Many trajectories, many pathways, Journal of Allergy and Clinical Immunology, 143, (1), 2019, p46-55
Bosma, A.L., Spuls, P.I., Garcia-Doval, I., Naldi, L., Prieto-Merino, D., Tesch, F., Apfelbacher, C.J., Arents, B.W.M., Barbarot, S., Baselga, E., Deleuran, M., Eichenfield, L.F., Gerbens, L.A.A., Irvine, A.D., Manca, A., Mendes-Bastos, P., Middelkamp-Hup, M.A., Roberts, A., Seneschal, J., Svensson, Å., Thyssen, J.P., Torres, T., Vermeulen, F.M., Vestergaard, C., von Kobyletzki, L.B., Wall, D., Weidinger, S., Schmitt, J., Flohr, C., TREatment of ATopic eczema (TREAT) Registry Taskforce: protocol for a European safety study of dupilumab and other systemic therapies in patients with atopic eczema, British Journal of Dermatology, 2019
Harkins, C.P., Holden, M.T.G., Irvine, A.D., Antimicrobial resistance in atopic dermatitis: Need for an urgent rethink, Annals of Allergy, Asthma and Immunology, 2019
Davidson, W.F., Leung, D.Y.M., Beck, L.A., Berin, C.M., Boguniewicz, M., Busse, W.W., Chatila, T.A., Geha, R.S., Gern, J.E., Guttman-Yassky, E., Irvine, A.D., Kim, B.S., Kong, H.H., Lack, G., Nadeau, K.C., Schwaninger, J., Simpson, A., Simpson, E.L., Spergel, J.M., Togias, A., Wahn, U., Wood, R.A., Woodfolk, J.A., Ziegler, S.F., Plaut, M., Report from the National Institute of Allergy and Infectious Diseases workshop on "Atopic dermatitis and the atopic march: Mechanisms and interventions", Journal of Allergy and Clinical Immunology, 2019
E. Chasseuil, J.A. McGrath, A. Seo, X. Balguerie, N. Bodak, H. Chasseuil, M. Denis"Musquer, A. Goldenberg, R. Goussot, A.D. Irvine, N.P. Khumalo, M.C. King, S. Küry, D. Lipsker, S. Mallet, B.M. Mayosi, A. Nanda, E. Puzenat, E. Salort"Campana, R. Sidbury, A. Shimamura, S. Bézieau, S. Mercier, S. Barbarot, Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis ( POIKTMP ): a case series of 28 patients, British Journal of Dermatology, 2019
A.D. Irvine, P. Mina"Osorio, Disease trajectories in childhood atopic dermatitis: an update and practitioner's guide, British Journal of Dermatology, 2019
Leshem, Y.A., Bissonnette, R., Paul, C., Silverberg, J.I., Irvine, A.D., Paller, A.S., Cork, M.J., Guttman-Yassky, E., Optimization of placebo use in clinical trials with systemic treatments for atopic dermatitis: an International Eczema Council survey-based position statement, Journal of the European Academy of Dermatology and Venereology, 33, (5), 2019, p807-815
Revencu, N., Fastre, E., Ravoet, M., Helaers, R., Brouillard, P., Bisdorff-Bresson, A., Chung, C.W.T., Gerard, M., Dvorakova, V., Irvine, A.D., Boon, L.M., Vikkula, M., RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation, Journal of Medical Genetics, 2019
Clowry, J., Irvine, A.D., McLoughlin, R.M., Next-generation anti"Staphylococcus aureus vaccines: A potential new therapeutic option for atopic dermatitis?, Journal of Allergy and Clinical Immunology, 143, (1), 2019, p78-81
Paller, A.S., Kong, H.H., Seed, P., Naik, S., Scharschmidt, T.C., Gallo, R.L., Luger, T., Irvine, A.D., The microbiome in patients with atopic dermatitis, Journal of Allergy and Clinical Immunology, 143, (1), 2019, p26-35
Eyerich, K., Brown, S.J., Perez White, B.E., Tanaka, R.J., Bissonette, R., Dhar, S., Bieber, T., Hijnen, D.J., Guttman-Yassky, E., Irvine, A., Thyssen, J.P., Vestergaard, C., Werfel, T., Wollenberg, A., Paller, A.S., Reynolds, N.J., Human and computational models of atopic dermatitis: A review and perspectives by an expert panel of the International Eczema Council, Journal of Allergy and Clinical Immunology, 143, (1), 2019, p36-45
Hawkes, C.P., Grimberg, A., Kenny, L.C., Kiely, M., Hourihane, J.O.B., Irvine, A.D., McPhaul, M.J., Caulfield, M.P., Zemel, B.S., Murray, D.M., The relationship between IGF-I and -II concentrations and body composition at birth and over the first 2 months, Pediatric Research, 85, (5), 2019, p687-692
Ballin, N., Hotz, A., Bourrat, E., Küsel, J., Oji, V., Bouadjar, B., Brognoli, D., Hickman, G., Heinz, L., Vabres, P., Marrakchi, S., Leclerc-Mercier, S., Irvine, A., Tadini, G., Hamm, H., Has, C., Blume-Peytavi, U., Mitter, D., Reitenbach, M., Hausser, I., Zimmer, A.D., Alter, S., Fischer, J., Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4, Human Mutation, 40, (12), 2019, p2318-2333
Hawkes, C.P., Murray, D.M., Kenny, L.C., Kiely, M., O'B Hourihane, J., Irvine, A.D., Wu, Z., Argon, Y., Reitz, R.E., McPhaul, M.J., Grimberg, A., Correlation of Insulin-Like Growth Factor-I and -II Concentrations at Birth Measured by Mass Spectrometry and Growth from Birth to Two Months, Hormone Research in Paediatrics, 89, (2), 2018, p122-131
L.A.A. Gerbens, C.J. Apfelbacher, A.D. Irvine, S. Barbarot, R.J. de Booij, A.E. Boyce, M. Deleuran, L.F. Eichenfield, M.H. Hof, M.A. Middelkamp-Hup, A. Roberts, J. Schmitt, C. Vestergaard, D. Wall, S. Weidinger, P.R. Williamson, C. Flohr, P.I. Spuls, TREatment of ATopic eczema (TREAT) Registry Taskforce: an international Delphi exercise to identify a core set of domains and domain items for national atopic eczema photo- and systemic therapy registries, British Journal of Dermatology, 2018
M.A. McAleer, I. Jakasa, N. Raj, C.P.F. O'Donnell, M.E. Lane, A.V. Rawlings, R. Voegeli, W.H.I. McLean, S. Kezic, A.D. Irvine, Early-life regional and temporal variation in filaggrin-derived natural moisturizing factor, filaggrin-processing enzyme activity, corneocyte phenotypes and plasmin activity: implications for atopic dermatitis, British Journal of Dermatology, 2018
Veronika Dvorakova, David Rea, Grainne M. O'Regan, Alan D. Irvine, Generalized lymphatic anomaly successfully treated with long-term, low-dose sirolimus, Pediatric Dermatology, 2018
Hennessy, Á., Hourihane, J.O.B., Malvisi, L., Irvine, A.D., Kenny, L.C., Murray, D.M., Kiely, M.E., Antenatal vitamin D exposure and childhood eczema, food allergy, asthma and allergic rhinitis at 2 and 5 years of age in the atopic disease-specific Cork BASELINE Birth Cohort Study, Allergy: European Journal of Allergy and Clinical Immunology, 73, (11), 2018, p2182-2191
Drucker, A.M., Eyerich, K., de Bruin-Weller, M.S., Thyssen, J.P., Spuls, P.I., Irvine, A.D., Girolomoni, G., Dhar, S., Flohr, C., Murrell, D.F., Paller, A.S., Guttman-Yassky, E., Use of systemic corticosteroids for atopic dermatitis: International Eczema Council consensus statement, British Journal of Dermatology, 178, (3), 2018, p768-775
Simpson, E.L., Reynolds, N.J., Flohr, C., Paller, A.S., Silverberg, J.I., Cork, M.J., Guttman-Yassky, E., Irvine, A.D., Response to "Comment on: `When does atopic dermatitis warrant systemic therapy? Recommendations from an expert panel of the International Eczema Council"", Journal of the American Academy of Dermatology, 79, (2), 2018, pe25-e26
M.A. McAleer, I. Jakasa, G. Hurault, P. Sarvari, W.H.I. McLean, R.J. Tanaka, S. Kezic, A.D. Irvine, Systemic and stratum corneum biomarkers of severity in infant atopic dermatitis include markers of innate and T helper cell-related immunity and angiogenesis, British Journal of Dermatology, 2018
A.D. Irvine, A.P. Jones, P. Beattie, S. Baron, F. Browne, F. Ashoor, L. O'Neill, A. Rosala-Hallas, T. Sach, C. Spowart, L. Taams, C. Walker, M. Wan, N. Webb, P. Williamson, C. Flohr, A randomized controlled trial protocol assessing the effectiveness, safety and cost-effectiveness of methotrexate vs. ciclosporin in the treatment of severe atopic eczema in children: the TREatment of severe Atopic eczema Trial (TREAT), British Journal of Dermatology, 2018
McCarthy, E.K., Murray, D.M., Malvisi, L., Kenny, L.C., O'B Hourihane, J., Irvine, A.D., Kiely, M.E., Antenatal Vitamin D Status Is Not Associated with Standard Neurodevelopmental Assessments at Age 5 Years in a Well-Characterized Prospective Maternal-Infant Cohort, Journal of Nutrition, 148, (10), 2018, p1580-1586
Twelves, S., Mostafa, A., Dand, N., Burri, E., Farkas, K., Wilson, R., Cooper, H.L., Irvine, A.D., Oon, H.H., Kingo, K., Köks, S., Mrowietz, U., Puig, L., Reynolds, N., Tan, E.S.-T., Tanew, A., Torz, K., Trattner, H., Valentine, M., Wahie, S., Warren, R.B., Wright, A., Bata-Csörg", Z., Szell, M., Griffiths, C.E.M., Burden, A.D., Choon, S.-E., Smith, C.H., Barker, J.N., Navarini, A.A., Capon, F., Clinical and genetic differences between pustular psoriasis subtypes, Journal of Allergy and Clinical Immunology, 2018
Lynch, S.A., Crushell, E., Lambert, D.M., Byrne, N., Gorman, K., King, M.D., Green, A., O'Sullivan, S., Browne, F., Hughes, J., Knerr, I., Monavari, A.A., Cotter, M., McConnell, V.P.M., Kerr, B., Jones, S.A., Keenan, C., Murphy, N., Cody, D., Ennis, S., Turner, J., Irvine, A.D., Casey, J., Catalogue of inherited disorders found among the Irish Traveller population, Journal of Medical Genetics, 55, (4), 2018, p233-239
McCarthy, E.K., ní Chaoimh, C., Kenny, L.C., Hourihane, J.O.B., Irvine, A.D., Murray, D.M., Kiely, M.E., Iron status, body size, and growth in the first 2 years of life, Maternal and Child Nutrition, 14, (1), 2018
Hennessy, Á., Ní Chaoimh, C., McCarthy, E.K., Kingston, C., Irvine, A.D., Hourihane, J.O., Kenny, L.C., Murray, D.M., Kiely, M., Variation in iodine food composition data has a major impact on estimates of iodine intake in young children, European Journal of Clinical Nutrition, 72, (3), 2018, p410-419
Paller, A.S., Czarnowicki, T., Renert-Yuval, Y., Holland, K., Huynh, T., Sadlier, M., McAleer, M.A., Tran, G., Geddes, G.C., Irvine, A.D., Guttman-Yassky, E., The spectrum of manifestations in desmoplakin gene (DSP) spectrin repeat 6 domain mutations: Immunophenotyping and response to ustekinumab, Journal of the American Academy of Dermatology, 78, (3), 2018, p498-505.e2
Pigors, M., Common, J.E.A., Wong, X.F.C.C., Malik, S., Scott, C.A., Tabarra, N., Liany, H., Liu, J., Limviphuvadh, V., Maurer-Stroh, S., Tang, M.B.Y., Lench, N., Margolis, D.J., van Heel, D.A., Mein, C.A., Novak, N., Baurecht, H., Weidinger, S., McLean, W.H.I., Irvine, A.D., O'Toole, E.A., Simpson, M.A., Kelsell, D.P., Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes, Journal of Investigative Dermatology, 138, (12), 2018, p2674-2677
Gilhooley, E., Gormally, S., Irvine, A., Lynch, S.A., Collins, S., FOXN1 Duplication and Congenital Hypertrichosis, Pediatric Dermatology, 34, (2), 2017, pe77-e79
Kiely, M., O'Donovan, S.M., Kenny, L.C., Hourihane, J.O., Irvine, A.D., Murray, D.M., Vitamin D metabolite concentrations in umbilical cord blood serum and associations with clinical characteristics in a large prospective mother-infant cohort in Ireland, Journal of Steroid Biochemistry and Molecular Biology, 167, 2017, p162-168
Fleury, O.M., McAleer, M.A., Feuillie, C., Formosa-Dague, C., Sansevere, E., Bennett, D.E., Towell, A.M., McLean, W.H.I., Kezic, S., Robinson, D.A., Fallon, P.G., Foster, T.J., Dufrêne, Y.F., Irvine, A.D., Geoghegan, J.A., Clumping factor B promotes adherence of Staphylococcus aureus to corneocytes in atopic dermatitis, Infection and Immunity, 85, (6), 2017, ppii: e00994-16
Murad, A., O'Regan, G., Watson, R., McDermott, M., O'Sullivan, M., Irvine, A.D., Erythema elevatum diutinum in a healthy child, Clinical and Experimental Dermatology, 42, (4), 2017, p434-436
McCarthy, E.K., Kiely, M.E., Hannon, G., Ahearne, C., Kenny, L.C., Hourihane, J.O., Irvine, A.D., Murray, D.M., Microcytosis is associated with low cognitive outcomes in healthy 2-year-olds in a high-resource setting, British Journal of Nutrition, 118, (5), 2017, p360-367
Spuls, P.I., Gerbens, L.A.A., Apfelbacher, C.J., Wall, D., Arents, B.W.M., Barbarot, S., Roberts, A., Deleuran, M., Middelkamp-Hup, M.A., Vestergaard, C., Weidinger, S., Schmitt, J., Irvine, A.D., Flohr, C., The International TREatment of ATopic Eczema (TREAT) Registry Taskforce: An Initiative to Harmonize Data Collection across National Atopic Eczema Photo- and Systemic Therapy Registries, Journal of Investigative Dermatology, 137, (9), 2017, p2014-2016
Samuelov, L., Li, Q., Bochner, R., Najor, N.A., Albrecht, L., Malchin, N., Goldsmith, T., Grafi-Cohen, M., Vodo, D., Fainberg, G., Meilik, B., Goldberg, I., Warshauer, E., Rogers, T., Edie, S., Ishida-Yamamoto, A., Burzenski, L., Erez, N., Murray, S.A., Irvine, A.D., Shultz, L., Green, K.J., Uitto, J., Sprecher, E., Sarig, O., SVEP1 plays a crucial role in epidermal differentiation, Experimental Dermatology, 2017
Simpson, E.L., Bruin-Weller, M., Flohr, C., Ardern-Jones, M.R., Barbarot, S., Deleuran, M., Bieber, T., Vestergaard, C., Brown, S.J., Cork, M.J., Drucker, A.M., Eichenfield, L.F., Foelster-Holst, R., Guttman-Yassky, E., Nosbaum, A., Reynolds, N.J., Silverberg, J.I., Schmitt, J., Seyger, M.M.B., Spuls, P.I., Stalder, J.-F., Su, J.C., Takaoka, R., Traidl-Hoffmann, C., Thyssen, J.P., van der Schaft, J., Wollenberg, A., Irvine, A.D., Paller, A.S., When does atopic dermatitis warrant systemic therapy? Recommendations from an expert panel of the International Eczema Council, Journal of the American Academy of Dermatology, 77, (4), 2017, p623-633
Veronika Dvorakova, Grainne M. O'Regan, Alan D. Irvine, Methotrexate for Severe Childhood Atopic Dermatitis: Clinical Experience in a Tertiary Center, Pediatric Dermatology, 2017
McCarthy, E.K., Kenny, L.C., Hourihane, J.O., Irvine, A.D., Murray, D.M., Kiely, M.E., Impact of maternal, antenatal and birth-associated factors on iron stores at birth: Data from a prospective maternal-infant birth cohort, European Journal of Clinical Nutrition, 71, (6), 2017, p782-787
Kennedy, E.A., Connolly, J., Hourihane, J.O., Fallon, P.G., McLean, W.H.I., Murray, D., Jo, J.-H., Segre, J.A., Kong, H.H., Irvine, A.D., Skin microbiome before development of atopic dermatitis: Early colonization with commensal staphylococci at 2 months is associated with a lower risk of atopic dermatitis at 1 year, Journal of Allergy and Clinical Immunology, 139, (1), 2017, p166-172
Gerbens, L.A.A., Boyce, A.E., Wall, D., Barbarot, S., Booij, R.J., Deleuran, M., Middelkamp-Hup, M.A., Roberts, A., Vestergaard, C., Weidinger, S., Apfelbacher, C.J., Irvine, A.D., Schmitt, J., Williamson, P.R., Spuls, P.I., Flohr, C., TREatment of ATopic eczema (TREAT) Registry Taskforce: Protocol for an international Delphi exercise to identify a core set of domains and domain items for national atopic eczema registries, Trials, 18, (1), 2017
Storan, E.R., Irvine, A.D., Access to Genetic Diagnostics for Genodermatoses: Who Should Get Tested? Why? Who Pays?, Pediatric Dermatology, 34, (1), 2017, p105-108
Lovgren, M.-L., McAleer, M.A., Irvine, A.D., Wilson, N.J., Tavadia, S., Schwartz, M.E., Cole, C., Sandilands, A., Smith, F.J.D., Zamiri, M., Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening, British Journal of Dermatology, 176, (5), 2017, p1345-1350
Soblet, J., Kangas, J., Nätynki, M., Mendola, A., Helaers, R., Uebelhoer, M., Kaakinen, M., Cordisco, M., Dompmartin, A., Enjolras, O., Holden, S., Irvine, A.D., Kangesu, L., Léauté-Labrèze, C., Lanoel, A., Lokmic, Z., Maas, S., McAleer, M.A., Penington, A., Rieu, P., Syed, S., van der Vleuten, C., Watson, R., Fishman, S.J., Mulliken, J.B., Eklund, L., Limaye, N., Boon, L.M., Vikkula, M., Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations, Journal of Investigative Dermatology, 137, (1), 2017, p207-216
Domínguez-Hüttinger, E., Christodoulides, P., Miyauchi, K., Irvine, A.D., Okada-Hatakeyama, M., Kubo, M., Tanaka, R.J., Mathematical modeling of atopic dermatitis reveals "double-switch" mechanisms underlying 4 common disease phenotypes, Journal of Allergy and Clinical Immunology, 2016
Satveer K. Mahil, Sophie Twelves, Katalin Farkas, Niovi Setta-Kaffetzi, A. David Burden, Joanna E. Gach, Alan D. Irvine, László Képíró, Maja Mockenhaupt, Hazel H. Oon, Jason Pinner, Annamari Ranki, Marieke M.B. Seyger, Pere Soler-Palacin, Eoin R. Storan, Eugene S. Tan, Laurence Valeyrie-Allanore, Helen S. Young, Richard C. Trembath, Siew-Eng Choon, Marta Szell, Zsuzsanna Bata-Csorgo, Catherine H. Smith, Paola Di Meglio, Jonathan N. Barker, Francesca Capon, AP1S3 Mutations Cause Skin Autoinflammation by Disrupting Keratinocyte Autophagy and Up-Regulating IL-36 Production, Journal of Investigative Dermatology, 136, (11), 2016, p2251--2259
Bieber, T., Akdis, C., Lauener, R., Traidl-Hoffmann, C., Schmid-Grendelmeier, P., Schäppi, G., Allam, J.-P., Apfelbacher, C., Augustin, M., Beck, L., Biedermann, T., Braun-Fahrländer, C., Chew, F.T., Clavel, T., Crameri, R., Darsow, U., Deleuran, M., Dittlein, D., Duchna, H.-W., Eichenfeld, L., Eyerich, K., Frei, R., Gelmetti, C., Gieler, U., Gilles, S., Glatz, M., Grando, K., Green, J., Gutermuth, J., Guttman-Yassky, E., Hanifin, J., Hijnen, D., Hoetzenecker, W., Irvine, A., Kalweit, A., Katoh, N., Knol, E., Koren, H., Möhrenschlager, M., Münch, D., Novak, N., O'Mahony, L., Paller, A.S., Rhyner, C., Roduit, C., Schiesser, K., Schröder, J., Simon, D., Simon, H.-U., Sokolowska, M., Spuls, P., Stalder, J.-F., Straub, D., Szalai, Z., Taieb, A., Takaoka, R., Todd, G., Todorova, A., Vestergaard, C., Werfel, T., Wollenberg, A., Ring, J., Global Allergy Forum and 3rd Davos Declaration 2015: Atopic dermatitis/Eczema: Challenges and opportunities toward precision medicine, Allergy: European Journal of Allergy and Clinical Immunology, 71, (5), 2016, p588-592
Eichenfield, L.F., Friedlander, S.F., Simpson, E.L., Irvine, A.D., Assessing the New and Emerging Treatments for Atopic Dermatitis, Seminars in cutaneous medicine and surgery, 35, (5), 2016, pS92-S96
Jessica Strid, W.H. Irwin McLean, Alan D. Irvine, Too Much, Too Little or Just Enough: A Goldilocks Effect for IL-13 and Skin Barrier Regulation?, Journal of Investigative Dermatology, 136, (3), 2016, p561--564
Schmitt J, Schwarz K, Baurecht H, Hotze M, Fölster-Holst R, Rodríguez E, Lee YA, Franke A, Degenhardt F, Lieb W, Gieger C, Kabesch M, Nöthen MM, Irvine AD, McLean WH, Deckert S, Stephan V, Schwarz P, Aringer M, Novak N, Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetes., 2016
Kelleher MM, Dunn-Galvin A, Gray C, Murray DM, Kiely M, Kenny L, McLean WH, Irvine AD, Hourihane JO, Skin barrier impairment at birth predicts food allergy at 2 years of age., The Journal of allergy and clinical immunology, 2016
Chaoimh, C., Murray, D.M., Kenny, L.C., Irvine, A.D., O'Hourihane, J.B., Kiely, M., Cord blood leptin and gains in body weight and fat mass during infancy, European Journal of Endocrinology, 175, (5), 2016, p403-410
Mccarthy, E.K., ní Chaoimh, C., O'B Hourihane, J., Kenny, L.C., Irvine, A.D., Murray, D.M., Kiely, M., Iron intakes and status of 2-year-old children in the Cork BASELINE Birth Cohort Study, Maternal and Child Nutrition, 2016
Irvine, A.D., Eichenfield, L.F., Friedlander, S.F., Simpson, E.L., Review of Critical Issues in the Pathogenesis of Atopic Dermatitis, Seminars in cutaneous medicine and surgery, 35, (5), 2016, pS89-S91
Hawkes, C.P., Zemel, B.S., Kiely, M., Irvine, A.D., Kenny, L.C., O'B Hourihane, J., Murray, D.M., Body composition within the first 3 months: Optimized correction for length and correlation with BMI at 2 Years, Hormone Research in Paediatrics, 86, (3), 2016, p178-187
O'Donovan SM, O'B Hourihane J, Murray DM, Kenny LC, Khashan AS, Chaoimh CN, Irvine AD, Kiely M, Neonatal adiposity increases the risk of atopic dermatitis during the first year of life., The Journal of allergy and clinical immunology, 137, (1), 2016, p108-17
Simpson, E.L., Irvine, A.D., Eichenfield, L.F., Friedlander, S.F., Update on Epidemiology, Diagnosis, and Disease Course of Atopic Dermatitis, Seminars in cutaneous medicine and surgery, 35, (5), 2016, pS84-S88
Dvorakova V, Watson RM, Terron-Kwiatkowski A, Andrew N, Irvine AD, Congenital reticular ichthyosiform erythroderma., Clinical and experimental dermatology, 2016
Janna Nousbeck, Alan D. Irvine, Atopic Dermatitis According to GARP: New Mechanistic Insights in Disease Pathogenesis, Journal of Investigative Dermatology, 136, (12), 2016, p2340--2341
Ní Chaoimh, C., McCarthy, E.K., Hourihane, J.O., Kenny, L.C., Irvine, A.D., Murray, D.M., Kiely, M.E., Low vitamin D deficiency in Irish toddlers despite northerly latitude and a high prevalence of inadequate intakes, European Journal of Nutrition, 2016, p1-12
Friedlander, S.F., Simpson, E.L., Irvine, A.D., Eichenfield, L.F., The Changing Paradigm of Atopic Dermatitis Therapy, Seminars in cutaneous medicine and surgery, 35, (5), 2016, pS97-S99
McAleer MA, Pohler E, Smith FJ, Wilson NJ, Cole C, MacGowan S, Koetsier JL, Godsel LM, Harmon RM, Gruber R, Crumrine D, Elias PM, McDermott M, Butler K, Broderick A, Sarig O, Sprecher E, Green KJ, McLean WH, Irvine AD, Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin., The Journal of allergy and clinical immunology, 2015
Baurecht H, Hotze M, Brand S, Büning C, Cormican P, Corvin A, Ellinghaus D, Ellinghaus E, Esparza-Gordillo J, Fölster-Holst R, Franke A, Gieger C, Hubner N, Illig T, Irvine AD, Kabesch M, Lee YA, Lieb W, Marenholz I, McLean WH, Morris DW, Mrowietz U, Nair R, Nöthen MM, Novak N, O'Regan GM, Schreiber S, Smith C, Strauch K, Stuart PE, Trembath R, Tsoi LC, Weichenthal M, Barker J, Elder JT, Weidinger S, Cordell HJ, Brown SJ, Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms., American journal of human genetics, 96, (1), 2015, p104-20
O"Donovan, S.M., Murray, D.M., Hourihane, J.O., Kenny, L.C., Irvine, A.D., Kiely, M., Adherence with early infant feeding and complementary feeding guidelines in the Cork BASELINE Birth Cohort Study, Public Health Nutrition, 2015
Chen, Y.-C., Auer-Grumbach, M., Matsukawa, S., Zitzelsberger, M., Themistocleous, A.C., Strom, T.M., Samara, C., Moore, A.W., Cho, L.T.-Y., Young, G.T., Weiss, C., Schabhüttl, M., Stucka, R., Schmid, A.B., Parman, Y., Graul-Neumann, L., Heinritz, W., Passarge, E., Watson, R.M., Hertz, J.M., Moog, U., Baumgartner, M., Valente, E.M., Pereira, D., Restrepo, C.M., Katona, I., Dusl, M., Stendel, C., Wieland, T., Stafford, F., Reimann, F., Von Au, K., Finke, C., Willems, P.J., Nahorski, M.S., Shaikh, S.S., Carvalho, O.P., Nicholas, A.K., Karbani, G., McAleer, M.A., Cilio, M.R., McHugh, J.C., Murphy, S.M., Irvine, A.D., Jensen, U.B., Windhager, R., Weis, J., Bergmann, C., Rautenstrauss, B., Baets, J., De Jonghe, P., Reilly, M.M., Kropatsch, R., Kurth, I., Chrast, R., Michiue, T., Bennett, D.L.H., Woods, C.G., Senderek, J., Erratum: Transcriptional regulator PRDM12 is essential for human pain perception (Nature Genetics (2015) 47 (803-808)), Nature Genetics, 47, (8), 2015
Quinn, N., Macmahon, J., Irvine, A.D., Lowry, C., Sweet syndrome revealing Systemic Lupus Erythematosus, Irish Medical Journal, 108, (2), 2015
Kelleher M, Dunn-Galvin A, Hourihane JO, Murray D, Campbell LE, McLean WH, Irvine AD, Skin barrier dysfunction measured by transepidermal water loss at 2 days and 2 months predates and predicts atopic dermatitis at 1 year., The Journal of allergy and clinical immunology, 135, (4), 2015, p930-5.e1
Berki DM, Liu L, Choon SE, Burden AD, Griffiths CE, Navarini AA, Tan ES, Irvine AD, Ranki A, Ogo T, Petrof G, Mahil SK, Duckworth M, Allen MH, Vito P, Trembath RC, McGrath J, Smith CH, Capon F, Barker JN, Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris., The Journal of investigative dermatology, 135, (12), 2015, p2964-70
Mercier S, Küry S, Salort-Campana E, Magot A, Agbim U, Besnard T, Bodak N, Bou-Hanna C, Bréhéret F, Brunelle P, Caillon F, Chabrol B, Cormier-Daire V, David A, Eymard B, Faivre L, Figarella-Branger D, Fleurence E, Ganapathi M, Gherardi R, Goldenberg A, Hamel A, Igual J, Irvine AD, Israël-Biet D, Kannengiesser C, Laboisse C, Le Caignec C, Mahé JY, Mallet S, MacGowan S, McAleer MA, McLean I, Méni C, Munnich A, Mussini JM, Nagy PL, Odel J, O'Regan GM, Péréon Y, Perrier J, Piard J, Puzenat E, Sampson JB, Smith F, Soufir N, Tanji K, Thauvin C, Ulane C, Watson RM, Khumalo NP, Mayosi BM, Barbarot S, Bézieau S, Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations., Orphanet journal of rare diseases, 10, 2015, p135
Saunders SP, Moran T, Floudas A, Wurlod F, Kaszlikowska A, Salimi M, Quinn EM, Oliphant CJ, Núñez G, McManus R, Hams E, Irvine AD, McKenzie AN, Ogg GS, Fallon PG, Spontaneous atopic dermatitis is mediated by innate immunity, with the secondary lung inflammation of the atopic march requiring adaptive immunity., The Journal of allergy and clinical immunology, 2015
Wedgeworth E, Glover M, Irvine AD, Neri I, Baselga Torres E, Clayton TH, Beattie PE, Bjerre JV, Burrows NP, Foelster-Holst R, Hedelund L, Hernandez-Martin A, Audrain H, Bhate K, Brown SJ, Baryschpolec S, Darne S, Durack A, Dvorakova V, Gach J, Goldstraw N, Goodyear H, Grabcyznska S, Greenblatt D, Halpern J, Hearn RM, Hoey S, Hughes B, Jayaraj R, Johansson EK, Lam M, Leech S, O'Regan GM, Morrison D, Porter W, Ramesh R, Schill T, Shaw L, Taylor AE, Taylor R, Thomson J, Tiffin P, Tsakok M, Janmohamed SR, Laguda B, McPherson T, Oranje A, Patrizi A, Ravenscroft J, Shahidullah H, Soloman L, Svensson A, Wahlgren CF, Hoeger PH, Flohr C, Propranolol in the treatment of infantile haemangiomas: Lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce Survey., The British journal of dermatology, 2015
Hussain, S., Berki, D.M., Choon, S.-E., Burden, A.D., Allen, M.H., Arostegui, J.I., Chaves, A., Duckworth, M., Irvine, A.D., Mockenhaupt, M., Navarini, A.A., Seyger, M.M.B., Soler-Palacin, P., Prins, C., Valeyrie-Allanore, L., Vicente, M.A., Trembath, R.C., Smith, C.H., Barker, J.N., Capon, F., IL36RN mutations define a severe autoinflammatory phenotype of generalized pustular psoriasis: To the editor, Journal of Allergy and Clinical Immunology, 135, (4), 2015, p1067-1070.e9
Hussain Safia, Berki Dorottya M., Choon Siew-Eng, Burden A. David, Allen Michael H., Arostegui Juan I., Chaves Antonio, Duckworth Michael, Irvine Alan D., Mockenhaupt Maja, Navarini Alexander A., Seyger Marieke M.B., Soler-Palacin Pere, Prins Christa, Valeyrie-Allanore Laurence, Vicente M. Asuncion, Trembath Richard C., Smith Catherine H., Barker Jonathan N., Capon Francesca, IL36RN mutations define a severe autoinflammatory phenotype of generalized pustular psoriasis , Journal of Allergy and Clinical Immunology , 135 , (4 ), 2015, p1067 - 1070.e9
Oosthuizen L, Mc Aleer MA, Watson RM, O"Regan GM, Byrne A, Crispino-O"Connell G, Irvine AD, Nottingham Eczema Severity Scoring tool can identify children at high risk of food allergy to cow"s milk, egg and peanut., 2015
O'Rafferty, C., O'Regan, G.M., Irvine, A.D., Smith, O.P., Kasabach-Merritt syndrome, kaposiform haemangioendothelioma and platelet blockade, British Journal of Haematology, 2015
Purcell, C., Cant, A., Irvine, A.D., DOCK8 primary immunodeficiency syndrome, The Lancet, 2015
Riethmuller C, McAleer MA, Koppes SA, Abdayem R, Franz J, Haftek M, Campbell LE, MacCallum SF, McLean WH, Irvine AD, Kezic S, Filaggrin breakdown products determine corneocyte conformation in patients with atopic dermatitis., The Journal of allergy and clinical immunology, 2015
Connor S, O'Brien M, Irvine A, O'Marcaigh A, Smith O, C3-C4 shingles post haematopoietic stem-cell transplantation., 2015
O'Donovan SM, Murray DM, Hourihane JO, Kenny LC, Irvine AD, Kiely M, Cohort profile: The Cork BASELINE Birth Cohort Study: Babies after SCOPE: Evaluating the Longitudinal Impact on Neurological and Nutritional Endpoints., 2015
Chen YC, Auer-Grumbach M, Matsukawa S, Zitzelsberger M, Themistocleous AC, Strom TM, Samara C, Moore AW, Cho LT, Young GT, Weiss C, Schabhüttl M, Stucka R, Schmid AB, Parman Y, Graul-Neumann L, Heinritz W, Passarge E, Watson RM, Hertz JM, Moog U, Baumgartner M, Valente EM, Pereira D, Restrepo CM, Katona I, Dusl M, Stendel C, Wieland T, Stafford F, Reimann F, von Au K, Finke C, Willems PJ, Nahorski MS, Shaikh SS, Carvalho OP, Nicholas AK, Karbani G, McAleer MA, Cilio MR, McHugh JC, Murphy SM, Irvine AD, Jensen UB, Windhager R, Weis J, Bergmann C, Rautenstrauss B, Baets J, De Jonghe P, Reilly MM, Kropatsch R, Kurth I, Chrast R, Michiue T, Bennett DL, Woods CG, Senderek J, Transcriptional regulator PRDM12 is essential for human pain perception., Nature genetics, 47, (7), 2015, p803-8
Paternoster L, Standl M, Waage J, Baurecht H, Hotze M, Strachan DP, Curtin JA, Bønnelykke K, Tian C, Takahashi A, Esparza-Gordillo J, Alves AC, Thyssen JP, den Dekker HT, Ferreira MA, Altmaier E, Sleiman PM, Xiao FL, Gonzalez JR, Marenholz I, Kalb B, Pino-Yanes M, Xu CJ, Carstensen L, Groen-Blokhuis MM, Venturini C, Pennell CE, Barton SJ, Levin AM, Curjuric I, Bustamante M, Kreiner-Møller E, Lockett GA, Bacelis J, Bunyavanich S, Myers RA, Matanovic A, Kumar A, Tung JY, Hirota T, Kubo M, McArdle WL, Henderson AJ, Kemp JP, Zheng J, Smith GD, Rüschendorf F, Bauerfeind A, Lee-Kirsch MA, Arnold A, Homuth G, Schmidt CO, Mangold E, Cichon S, Keil T, Rodríguez E, Peters A, Franke A, Lieb W, Novak N, Fölster-Holst R, Horikoshi M, Pekkanen J, Sebert S, Husemoen LL, Grarup N, de Jongste JC, Rivadeneira F, Hofman A, Jaddoe VW, Pasmans SG, Elbert NJ, Uitterlinden AG, Marks GB, Thompson PJ, Matheson MC, Robertson CF, Ried JS, Li J, Zuo XB, Zheng XD, Yin XY, Sun LD, McAleer MA, O'Regan GM, Fahy CM, Campbell L, Macek M, Kurek M, Hu D, Eng C, Postma DS, Feenstra B, Geller F, Hottenga JJ, Middeldorp CM, Hysi P, Bataille V, Spector T, Tiesler CM, Thiering E, Pahukasahasram B, Yang JJ, Imboden M, Huntsman S, Vilor-Tejedor N, Relton CL, Myhre R, Nystad W, Custovic A, Weiss ST, Meyers DA, Söderhäll C, Melén E, Ober C, Raby BA, Simpson A, Jacobsson B, Holloway JW, Bisgaard H, Sunyer J, Probst-Hensch NM, Williams LK, Godfrey KM, Wang CA, Boomsma DI, Melbye M, Koppelman GH, Jarvis D, McLean WH, Irvine AD, Zhang XJ, Hakonarson H, Gieger C, Burchard EG, Martin NG, Duijts L, Linneberg A, Jarvelin MR, Nöthen MM, Lau S, Hübner N, Lee YA, Tamari M, Hinds DA, Glass D, Brown SJ, Heinrich J, Evans DM, Weidinger S, Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis., Nature genetics, 47, (12), 2015, p1449-56
Higgins, E., Al Shehri, T., McAleer, M.A., Conlon, N., Feighery, C., Lilic, D., Irvine, A.D., Use of ruxolitinib to successfully treat chronic mucocutaneous candidiasis caused by gain-of-function signal transducer and activator of transcription 1 (STAT1) mutation, Journal of Allergy and Clinical Immunology, 135, (2), 2015, p551-553
O"Donovan SM, Murray DM, Hourihane JO, Kenny LC, Irvine AD, Kiely M, No association between food allergens in the complementary feeding diet and eczema during the first 12-months in the Cork BASELINE Birth Cohort., 2015
O'Rafferty, C., O'Regan, G.M., Irvine, A.D., Smith, O.P., Recent advances in the pathobiology and management of Kasabach-Merritt phenomenon, British Journal of Haematology, 2015
Kiely C, Devaney D, Fischer J, Lenane P, Irvine AD, Ichthyosis prematurity syndrome: a case report and review of known mutations., Pediatric dermatology, 31, (4), 2014, p517-8
Foley C, Moran B, McMenamin M, McDermott R, Ormond P, Irvine AD, Spontaneous regression of cutaneous metastases of squamous cell carcinoma., QJM : monthly journal of the Association of Physicians, 107, (1), 2014, p61-3
Cole C, Kroboth K, Schurch NJ, Sandilands A, Sherstnev A, O'Regan GM, Watson RM, Irwin McLean WH, Barton GJ, Irvine AD, Brown SJ, Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis., The Journal of allergy and clinical immunology, 134, (1), 2014, p82-91
Thawer-Esmail F, Jakasa I, Todd G, Wen Y, Brown SJ, Kroboth K, Campbell LE, O'Regan GM, McLean WH, Irvine AD, Kezic S, Sandilands A, South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin., The Journal of allergy and clinical immunology, 133, (1), 2014, p280-282.e2
Irvine AD, Crossing barriers; restoring barriers? Filaggrin protein replacement takes a bow., The Journal of investigative dermatology, 134, (2), 2014, p313-4
Courtney DG, Atkinson SD, Allen EH, Moore JE, Walsh CP, Pedrioli DM, MacEwen CJ, Pellegrini G, Maurizi E, Serafini C, Fantacci M, Liao H, Irvine AD, McLean WH, Moore CB, siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy., Investigative ophthalmology & visual science, 55, (5), 2014, p3352-60
Kelleher M, Dunn AG, Irvine A, Smith H, Hourihane OJ, O08 - Increased early life Transepidermal Water Loss (TEWL) values can predate atopic dermatitis in asymptomatic infants: results from the BASELINE study., 2014
Irvine AD, Commentary: Methotrexate and ciclosporin in the treatment of severe eczema in children., The British journal of dermatology, 170, (3), 2014, p499-500
Nason GJ, Baker JF, Seoighe D, Irvine AD, McDermott M, Orr D, Capra M, Kelly PM, Congenital-infantile fibrosarcoma of the foot--avoidance of amputation., Irish medical journal, 107, (5), 2014, p148-9
Hughes, R., McAleer, M., Watson, R., Collins, S., Irvine, A., White, M., Rapidly involuting congenital hemangioma with pustules: Two cases, Pediatric Dermatology, 31, (3), 2014, p398-400
Gallagher, A., Hourihane, J.O.B., Kenny, L.C., Irvine, A.D., Khashan, A.S., A longitudinal study of skin barrier function in pregnancy and the postnatal period, Obstetric Medicine, 7, (4), 2014, p156-159
Courtney, D.G., Atkinson, S.D., Allen, E.H.A., Moore, J.E., Walsh, C.P., Pedrioli, D.M.L., MacEwen, C.J., Pellegrini, G., Maurizi, E., Serafini, C., Fantacci, M., Liao, H., Irvine, A.D., McIrwin Lean, W.H., Tara Moore, C.B., SiRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy, Investigative Ophthalmology and Visual Science, 55, (5), 2014, p3352-3360
Salinas, C.F., Irvine, A.D., Itin, P.H., Di Giovanna, J.J., Schneider, H., Clarke, A.J., McGovern, L.S., Fete, M., Second international conference on a classification of ectodermal dysplasias: Development of a multiaxis model, American Journal of Medical Genetics, Part A, 164, (10), 2014, p2482-2489
Langan SM, Irvine AD, Childhood eczema and the importance of the physical environment., The Journal of investigative dermatology, 133, (7), 2013, p1706-9
Weidinger S, Willis-Owen SA, Kamatani Y, Baurecht H, Morar N, Liang L, Edser P, Street T, Rodriguez E, O'Regan GM, Beattie P, Fölster-Holst R, Franke A, Novak N, Fahy CM, Winge MC, Kabesch M, Illig T, Heath S, Söderhäll C, Melén E, Pershagen G, Kere J, Bradley M, Lieden A, Nordenskjold M, Harper JI, McLean WH, Brown SJ, Cookson WO, Lathrop GM, Irvine AD, Moffatt MF, A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis., Human molecular genetics, 22, (23), 2013, p4841-56
Fahy CM, Fortune A, Quinn F, McMenamin ME, Browne PV, Langabeer S, McCarron S, Hayden P, Marren P, Ni Chonghaile M, Irvine AD, Vandenberghe E, Barnes L, Development of mycosis fungoides after bone marrow transplantation for chronic myeloid leukaemia; transmission from allogeneic donor., The British journal of dermatology, 2013
Samuelov L, Sarig O, Harmon RM, Rapaport D, Ishida-Yamamoto A, Isakov O, Koetsier JL, Gat A, Goldberg I, Bergman R, Spiegel R, Eytan O, Geller S, Peleg S, Shomron N, Goh CS, Wilson NJ, Smith FJ, Pohler E, Simpson MA, McLean WH, Irvine AD, Horowitz M, McGrath JA, Green KJ, Sprecher E, Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting., Nature genetics, 45, (10), 2013, p1244-8
McAleer MA, Irvine AD, The multifunctional role of filaggrin in allergic skin disease., The Journal of allergy and clinical immunology, 131, (2), 2013, p280-91
McLean WH, Irvine AD, Old King Coal - molecular mechanisms underlying an ancient treatment for atopic eczema., The Journal of clinical investigation, 2013, p1-3
Kelleher MM, O'Carroll M, Gallagher A, Murray DM, Dunn Galvin A, Irvine AD, Hourihane JO, Newborn transepidermal water loss values: a reference dataset., Pediatric dermatology, 30, (6), 2013, p712-6
Asai, Yuka Greenwood, Celia Hull, Peter R. Alizadehfar, Reza Ben-Shoshan, Moshe Brown, Sara J. Campbell, Linda Michel, Deborah L. Bussières, Johanne Rousseau, François Fujiwara, T. Mary Morgan, Kenneth Irvine, Alan D. McLean, W.H. Irwin Clarke, Ann , Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status , Journal of Allergy and Clinical Immunology , 132 , (1 ), 2013, p239 - 242.e7
Conte MI, Pescatore A, Paciolla M, Esposito E, Miano MG, Lioi MB, McAleer MA, Giardino G, Pignata C, Irvine AD, Scheuerle AE, Royer G, Hadj-Rabia S, Bodemer C, Bonnefont JP, Munnich A, Smahi A, Steffann J, Fusco F, Ursini MV, Insight into IKBKG/NEMO Locus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease., Human mutation, 2013
Baclig, A.C., Bakker Schut, T.C., O'Regan, G.M., Irvine, A.D., McLean, W.H.I., Puppels, G.J., Caspers, P.J., Possibilities for human skin characterization based on strongly reduced Raman spectroscopic information, Journal of Raman Spectroscopy, 44, (3), 2013, p340-345
Foley CC, McMenamin M, Gordon KD, Irvine AD, An unusual case of genital swelling., Clinical and experimental dermatology, 38, (8), 2013, p946-8
Higgins E, Capra M, Schwartz ME, Smith FJD, McLean WHI, Irvine AD, Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma , British Journal of Dermatology , 169 , (6 ), 2013, p1357 - 1360
Wall D, McMenamin M, O'Mahony D, Irvine AD, Kaposi sarcoma in an patient with atopic dermatitis treated with ciclosporin., BMJ case reports, 2013, 2013
Revencu N, Boon LM, Mendola A, Cordisco MR, Dubois J, Clapuyt P, Hammer F, Amor DJ, Irvine AD, Baselga E, Dompmartin A, Syed S, Martin-Santiago A, Ades L, Collins F, Smith J, Sandaradura S, Barrio VR, Burrows PE, Blei F, Cozzolino M, Brunetti-Pierri N, Vicente A, Abramowicz M, Désir J, Vilain C, Chung WK, Wilson A, Gardiner CA, Dwight Y, Lord DJ, Fishman L, Cytrynbaum C, Chamlin S, Ghali F, Gilaberte Y, Joss S, Boente Mdel C, Léauté-Labrèze C, Delrue MA, Bayliss S, Martorell L, González-Enseñat MA, Mazereeuw-Hautier J, O'Donnell B, Bessis D, Pyeritz RE, Salhi A, Tan OT, Wargon O, Mulliken JB, Vikkula M, RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation., Human mutation, 34, (12), 2013, p1632-41
Ellinghaus D, Baurecht H, Esparza-Gordillo J, Rodríguez E, Matanovic A, Marenholz I, Hübner N, Schaarschmidt H, Novak N, Michel S, Maintz L, Werfel T, Meyer-Hoffert U, Hotze M, Prokisch H, Heim K, Herder C, Hirota T, Tamari M, Kubo M, Takahashi A, Nakamura Y, Tsoi LC, Stuart P, Elder JT, Sun L, Zuo X, Yang S, Zhang X, Hoffmann P, Nöthen MM, Fölster-Holst R, Winkelmann J, Illig T, Boehm BO, Duerr RH, Büning C, Brand S, Glas J, McAleer MA, Fahy CM, Kabesch M, Brown S, McLean WH, Irvine AD, Schreiber S, Lee YA, Franke A, Weidinger S, High-density genotyping study identifies four new susceptibility loci for atopic dermatitis., Nature genetics, 45, (7), 2013, p808-12
Flohr C, Irvine AD, Systemic therapies for severe atopic dermatitis in children and adults., The Journal of allergy and clinical immunology, 132, (3), 2013, p774-774.e6
Saunders, S.P., Goh, C.S.M., Brown, S.J., Palmer, C.N.A., Porter, R.M., Cole, C., Campbell, L.E., Gierlinski, M., Barton, G.J., Schneider, G., Balmain, A., Prescott, A.R., Weidinger, S., Baurecht, H., Kabesch, M., Gieger, C., Lee, Y.-A., Tavendale, R., Mukhopadhyay, S., Turner, S.W., Madhok, V.B., Sullivan, F.M., Relton, C., Burn, J., Meggitt, S., Smith, C.H., Allen, M.A., Barker, J.N.W.N., Reynolds, N.J., Cordell, H.J., Irvine, A.D., McLean, W.H.I., Sandilands, A., Fallon, P.G., Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects, Journal of Allergy and Clinical Immunology, 132, (5), 2013, p1121-1129
Kezic S, O'Regan GM, Lutter R, Jakasa I, Koster ES, Saunders S, Caspers P, Kemperman PM, Puppels GJ, Sandilands A, Chen H, Campbell LE, Kroboth K, Watson R, Fallon PG, McLean WH, Irvine AD, Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency., The Journal of allergy and clinical immunology, 129, (4), 2012, p1031-9.e1
Sandilands Aileen, Brown Sara J, Goh Christabelle S, Pohler Elizabeth, Wilson Neil J, Campbell Linda E, Miyamoto Kenichi, Kubo Akiharu, Irvine Alan D, Thawer-Esmail Fatema, Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin , The Journal of investigative dermatology , 132 , (5 ), 2012, p1507 -
Krawczyk J, McDermott M, Irvine AD, O'Marcaigh A, Storey L, Smith O, Skin involvement in Down syndrome transient abnormal myelopoiesis., British journal of haematology, 157, (3), 2012, p280
Knight J, Spain SL, Capon F, Hayday A, Nestle FO, Clop A, Wellcome Trust Case Control Consortium, Genetic Analysis of Psoriasis Consortium§, I-chip for Psoriasis Consortium, Barker JN. Weale ME, Trembath RC, Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis, Human Molecular Genetics, 21, (23), 2012, p5185 - 5192
Brown SJ, Kroboth K, Sandilands A, Campbell LE, Pohler E, Kezic S, Cordell HJ, McLean WH, Irvine AD, Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect., The Journal of investigative dermatology, 132, (1), 2012, p98-104
Crushell E, O'Leary D, Irvine AD, O'Shea A, Mayne PD, Reardon W, Methylenetetrahydrofolate reductase (MTHFR) deficiency presenting as a rash., American journal of medical genetics. Part A, 158A, (9), 2012, p2254-7
Hackett BC, Phelan E, Ryan A, Kenny L, Murphy M, Irvine AD, Watson RM, Use of Systemic Corticosteroids in Management of a Large Congenital Haemangioma of the Scalp., Pediatric dermatology, 2012
McAleer MA, Flohr C, Irvine AD, Management of difficult and severe eczema in childhood., BMJ (Clinical research ed.), 345, 2012, pe4770
Pohler E, Mamai O, Hirst J, Zamiri M, Horn H, Nomura T, Irvine AD, Moran B, Wilson NJ, Smith FJ, Goh CS, Sandilands A, Cole C, Barton GJ, Evans AT, Shimizu H, Akiyama M, Suehiro M, Konohana I, Shboul M, Teissier S, Boussofara L, Denguezli M, Saad A, Gribaa M, Dopping-Hepenstal PJ, McGrath JA, Brown SJ, Goudie DR, Reversade B, Munro CS, McLean WH, Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma., Nature genetics, 44, (11), 2012, p1272-6
Irvine AD, Double trouble: homozygous dominant mutations and hair loss in pachyonychia congenita., The Journal of investigative dermatology, 132, (7), 2012, p1757-9
Porokeratoses in, editor(s)Goldsmith LA, Katz SI, Gilchrest BA, Paller A, Leffell DJ , Fitzpatrick's Dermatology in General Medicine , New York , McGraw Hill, 2012, ppxxx - xxx, [O'Regan GM, Irvine AD]
Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li Y, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, Schalkwijk J, Ståhle M, Burden AD, Smith CH, Cork MJ, Estivill X, Bowcock AM, Krueger GG, Weger W, Worthington J, Tazi-Ahnini R, Nestle FO, Hayday A, Hoffmann P, Winkelmann J, Wijmenga C, Langford C, Edkins S, Andrews R, Blackburn H, Strange A, Band G, Pearson RD, Vukcevic D, Spencer CC, Deloukas P, Mrowietz U, Schreiber S, Weidinger S, Koks S, Kingo K, Esko T, Metspalu A, Lim HW, Voorhees JJ, Weichenthal M, Wichmann HE, Chandran V, Rosen CF, Rahman P, Gladman DD, Griffiths CE, Reis A, Kere J, Nair RP, Franke A, Barker JN, Abecasis GR, Elder JT, Trembath RC, Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity., Nature genetics, 44, (12), 2012, p1341-1348
McLean WH, Irvine AD, Heritable filaggrin disorders: the paradigm of atopic dermatitis., The Journal of investigative dermatology, 132, (E1), 2012, pE20-1
Weidinger, S., Irvine, A.D., Genetics of Atopic Dermatitis, Harper's Textbook of Pediatric Dermatology: Third Edition, 1, 2011, p1-17
Scurr I, Wilson L, Lees M, Robertson S, Kirk E, Turner A, Morton J, Kidd A, Shashi V, Stanley C, Berry M, Irvine AD, Goudie D, Turner C, Brewer C, Smithson S, Cantú syndrome: report of nine new cases and expansion of the clinical phenotype., American journal of medical genetics. Part A, 155A, (3), 2011, p508-18
Bracken J, Robinson I, Snow A, Watson R, Irvine AD, Rea D, Phelan E, PHACE syndrome: MRI of intracerebral vascular anomalies and clinical findings in a series of 12 patients., Pediatric radiology, 41, (9), 2011, p1129-38
Atopic Dermatitis: Genetics in, editor(s)Irvine AD, Hoeger PH, Yan A , Textbook of Pediatric Dermatology , London , Blackwell-Wiley, 2011, pp1 - 23, [Weidinger S, Irvine AD ]
Clericuzio C, Harutyunyan K, Jin W, Erickson RP, Irvine AD, McLean WH, Wen Y, Bagatell R, Griffin TA, Shwayder TA, Plon SE, Wang LL, Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia., American journal of medical genetics. Part A, 155A, (2), 2011, p337-42
Ricciardo B, Irvine A, McDermott M, Ryan J, Collins S, A case of congenital solitary Langerhans cell histiocytoma., The Australasian journal of dermatology, 52, (2), 2011, pe1-3
Ectodermal Dysplasias in, editor(s)Irvine AD, Hoeger PH, Yan A , Textbook of Pediatric Dermatology, London, Blackwell‐Wiley, 2011, pp1 - 127, [Asai Y, Irvine AD ]
Liao H, Irvine AD, Macewen CJ, Weed KH, Porter L, Corden LD, Gibson AB, Moore JE, Smith FJ, McLean WH, Moore CB, Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy., PloS one, 6, (12, e28582), 2011
Chen H, Common JE, Haines RL, Balakrishnan A, Brown SJ, Goh CS, Cordell HJ, Sandilands A, Campbell LE, Kroboth K, Irvine AD, Goh DL, Tang MB, van Bever HP, Giam YC, McLean WH, Lane EB, Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations., The British journal of dermatology, 165, (1), 2011, p106-14
Keohane, C., Bacon, C.L., Moran, B., Irvine, A.D., Smith, O.P., Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome induced by cidofovir, Pediatric Transplantation, 15, (1), 2011
Miajlovic H, Fallon PG, Irvine AD, Foster TJ., Effect of filaggrin breakdown products on growth of and protein expression by Staphylococcus aureus, Journal of Allergy and Clinical Immunology, 126, (6), 2011, p1184-1190
Kezic S, O'Regan GM, Yau N, Sandilands A, Chen H, Campbell LE, Kroboth K, Watson R, Rowland M, McLean WH, Irvine AD, Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity., Allergy, 66, (7), 2011, p934-40
Fleming P, Fitzgerald K, Watson R, Irvine A. , Response to "dental caries as a side effect of infantile hemangioma treatment with propanolol solution", Pediatric Dermatology, 28, 2011, p602 - 602
Brown SJ, Asai Y, Cordell HJ, Campbell LE, Zhao Y, Liao H, Northstone K, Henderson J, Alizadehfar R, Ben-Shoshan M, Morgan K, Roberts G, Masthoff LJ, Pasmans SG, van den Akker PC, Wijmenga C, Hourihane JO, Palmer CN, Lack G, Clarke A, Hull PR, Irvine AD, McLean WH, Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy., The Journal of allergy and clinical immunology, 127, (3), 2011, p661-7
Irvine AD, McLean WH, Leung DY, Filaggrin mutations associated with skin and allergic diseases., The New England journal of medicine, 365, (14), 2011, p1315-27
Pediatric Dermatology in, editor(s)Irvine AD, Hoeger PH, Yan A , Harper's Textbook of Pediatric Dermatology , London, Blackwell-Wiley, 2011, pp2816 - [Weidinger S, Irvine AD]
Hawkes CP, Hourihane JO, Kenny LC, Irvine AD, Kiely M, Murray DM, Gender- and gestational age-specific body fat percentage at birth., Pediatrics, 128, (3), 2011, pe645-51
Irvine, A.D., Hoeger, P.H., Yan, A.C., Harper's Textbook of Pediatric Dermatology: Third Edition, Harper's Textbook of Pediatric Dermatology: Third Edition, 1-2, 2011
Moriarty B, Bourke JF, Fitzgibbon J, Irvine AD, An unusual rash in a neonate. X-linked dominant ichthyosis (XLDI)., Clinical and experimental dermatology, 35, (3), 2010, pe62-4
O'Regan GM, Kemperman PMJH, Sandilands A, Chen H, Campbell LE, Kroboth K, Watson R, Rowland M, Puppels GJ, McLean WHI, Caspers PJ Irvine AD, Raman Profiles of the Stratum Corneum Define Three FLG Genotype-determined Atopic Dermatitis Endophenotypes , Journal of Allergy and Clinical Immunology, 126, 2010, p574-580
O'Regan GM, Irvine AD, The role of filaggrin in the atopic diathesis., Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 40, (7), 2010, p965-72
O'Regan GM, Campbell LE, Cordell HJ, Irvine AD, McLean WH, Brown SJ, Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutations., The Journal of allergy and clinical immunology, 125, (1), 2010, p170-4.e1-2
O'Regan GM, Kemperman PM, Sandilands A, Chen H, Campbell LE, Kroboth K, Watson R, Rowland M, Puppels GJ, McLean WH, Caspers PJ, Irvine AD, Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes., The Journal of allergy and clinical immunology, 126, (3), 2010, p574-80.e1
Moriarty, B., Bourke, J.F., Fitzgibbon, J., Irvine, A.D., An unusual rash in a neonate, Clinical and Experimental Dermatology, 35, (3), 2010
Genetics and Genodermatoses in, editor(s)Burns T, Breathnach S, Cox N, Griffiths C , Rook's Textbook of Dermatology, Chichester , Wiley Blackwell, 2010, pp1 - 15.97, [Mellerio JE and Irvine AD]
Bergboer JG, Zeeuwen PL, Irvine AD, Weidinger S, Giardina E, Novelli G, Heijer MD, Rodriguez E, Illig T, Riveira-Munoz E, Campbell LE, Tyson J, Dannhauser EN, O'Regan GM, Galli E, Klopp N, Koppelman GH, Novak N, Estivill X, McLean WH, Postma DS, Armour JA, Schalkwijk J, Deletion of Late Cornified Envelope 3B and 3C Genes Is Not Associated with Atopic Dermatitis, Journal of Investigative Dermatology, 130, 2010, p2057-2061
Ichthyosis Vulgaris in, editor(s)Schnacher L and Hansen R , Pediatric Dermatology, London, Mosby, 2010, pp578 - 580, [Irvine AD ]
Strange A, Capon F, Spencer CC, Knight J, Weale ME, Allen MH, Barton A, Band G, Bellenguez C, Bergboer JG, Blackwell JM, Bramon E, Bumpstead SJ, Casas JP, Cork MJ, Corvin A, Deloukas P, Dilthey A, Duncanson A, Edkins S, Estivill X, Fitzgerald O, Freeman C, Giardina E, Gray E, Hofer A, Hüffmeier U, Hunt SE, Irvine AD, Jankowski J, Kirby B, Langford C, Lascorz J, Leman J, Leslie S, Mallbris L, Markus HS, Mathew CG, McLean WH, McManus R, Mössner R, Moutsianas L, Naluai AT, Nestle FO, Novelli G, Onoufriadis A, Palmer CN, Perricone C, Pirinen M, Plomin R, Potter SC, Pujol RM, Rautanen A, Riveira-Munoz E, Ryan AW, Salmhofer W, Samuelsson L, Sawcer SJ, Schalkwijk J, Smith CH, Ståhle M, Su Z, Tazi-Ahnini R, Traupe H, Viswanathan AC, Warren RB, Weger W, Wolk K, Wood N, Worthington J, Young HS, Zeeuwen PL, Hayday A, Burden AD, Griffiths CE, Kere J, Reis A, McVean G, Evans DM, Brown MA, Barker JN, Peltonen L, Donnelly P, Trembath RC, A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1., Nature genetics, 42, (11), 2010, p985-990
Other Syndromes associated with Ichthyosis in, editor(s)Schnacher L and Hansen R , Pediatric Dermatology , London, Mosby, 2010, pp612 - 614, [Irvine AD]
Bergboer JG, Zeeuwen PL, Irvine AD, Weidinger S, Giardina E, Novelli G, Den Heijer M, Rodriguez E, Illig T, Riveira-Munoz E, Campbell LE, Tyson J, Dannhauser EN, O'Regan GM, Galli E, Klopp N, Koppelman GH, Novak N, Estivill X, McLean WH, Postma DS, Armour JA, Schalkwijk J, Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis., The Journal of investigative dermatology, 130, (8), 2010, p2057-61
Hackett BC, Fitzgerald D, Watson RM, Hol F.A, Irvine AD, Genotype-Phenotype Correlations with TGM1: Clustering of Mutations in the Bathing Suit Ichthyosis and Self Healing Collodion Baby Variants of Lamellar Ichthyosis, British Journal of Dermatology, 162, (2), 2010, p448-451
O'Regan GM, Campbell LE, Cordell HJ, Irvine AD, McLean WHI, Brown SJ, Chromosome 11q13.5 variant associated with childhood eczema; an effect supplementary to filaggrin mutations, Journal of Allergy and Clinical Immunology, 125, 2010, p170-174
Peeling Skin Syndrome in, editor(s)Schnacher L and Hansen R , Pediatric Dermatology, London, Mosby, 2010, pp1 - 23, [Irvine AD]
Fallon, PG, Sasaki, T, Sandilands, A, Campbell, LE, Saunders, SP, Mangan, NE, Callanan, JJ, Kawasaki, H, Shiohama, A, Kubo, A, Sundberg, JP, Presland, RB, Fleckman, P, Shimizu, N, Kudoh, J, Irvine, AD, Amagai, M, McLean, WH, A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming., Nature Genetics, 41, (5), 2009, p602 - 608
Irvine AD, Towards a unified classification of the ectodermal dysplasias: opportunities outweigh challenges., American journal of medical genetics. Part A, 149A, (9), 2009, p1970-2
Irvine, AD., Towards a unified classification of the ectodermal dysplasias: Opportunities outweigh challenges. , American Journal Of Medical Genetics Part A, 149A, (9), 2009, p1970-1972
Sun M, Li N, Dong W, Chen Z, Liu Q, Xu Y, He G, Shi Y, Li X, Hao J, Luo Y, Shang D, Lv D, Ma F, Zhang D, Hua R, Lu C, Wen Y, Cao L, Irvine AD, McLean WH, Dong Q, Wang MR, Yu J, He L, Lo WH, Zhang X, Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia., American journal of human genetics, 84, (6), 2009, p807-13
Wen, Y., Liu, Y., Xu, Y., Zhao, Y., Hua, R., Wang, K., Sun, M., Li, Y., Yang, S., Zhang, X.-J., Kruse, R., Cichon, S., Betz, R.C., Nöthen, M.M., Van Steensel, M.A.M., Van Geel, M., Steijlen, P.M., Hohl, D., Huber, M., Dunnill, G.S., Kennedy, C., Messenger, A., Munro, C.S., Terrinoni, A., Hovnanian, A., Bodemer, C., De Prost, Y., Paller, A.S., Irvine, A.D., Sinclair, R., Green, J., Shang, D., Liu, Q., Luo, Y., Jiang, L., Chen, H.-D., Lo, W.H.-Y., McLean, W.H.I., He, C.-D., Zheng, X., Erratum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis (Nature Genetics (2009) 41 (228-233)), Nature Genetics, 41, (6), 2009
Rodriguez S, Hall AJ, Granell R, McLean WH, Irvine AD, Palmer CN, Smith GD, Henderson J, Day IN, Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort, PLoS ONE, 4, (6), 2009, pe5784
Sun M, Li N, Dong W, Chen Z, LiuQ, XuY, He G, Shi Y, Li X, Hao J, Luo Y, Shang D, Lv D, Ma F, Zhang D, Hua R, Lu C, Wen Y, Cao L, Irvine AD, McLean WHI, Dong Q, Wang M-R, Yu J, He L, Lo WHY, Zhang X, Copy number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia, American Journal of Human Genetics, 84, (6), 2009, p807-813.
Rodríguez E, Baurecht H, Herberich E, Wagenpfeil S, Brown SJ, Cordell HJ, Irvine AD, Weidinger S, Meta analysis of filaggrin polymorphisms in eczema and asthma: robust risk factors in atopic disease, Journal of Allergy and Clinical Immunology, 123, (6), 2009, p1361-1370.e7
Wen, Y, Liu, Y, Xu, Y, Zhao, Y, Hua, R, Wang, K, Sun, M, Li, Y, Yang, S, Zhang, XJ, Kruse, R, Cichon, S, Betz, RC, Nöthen, MM, van Steensel, MA, van Geel, M, Steijlen, PM, Hohl, D, Huber, M, Dunnill, GS, Kennedy, C, Messenger, A, Munro, CS, Terrinoni, A, Hovnanian, A, Bodemer, C, de Prost, Y, Paller, AS, Irvine, AD, Sinclair, R, Green, J, Shang, D, Liu, Q, Luo, Y, Jiang, L, Chen, HD, Lo, WH, McLean, WH, He, CD, Zhang, X, Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis., Nature genetics, 41, (2), 2009, p228 - 233
O'Regan, G.M., Irvine, A.D., Yao, N., O'Marcaigh, A., Sheridan-Pereira, M., Phelan, E., McDermott, M.B., (...), Watson, R., Mediastinal and neck kaposiform hemangioendothelioma , Pediatric Dermatology, 26, (3), 2009, p331-337
O'Regan GM, Irvine AD, Yao N, O'Marcaigh A, Sheridan-Pereira M, Phelan E, McDermott MB, Twomey A, Russell J, Watson R, Mediastinal and neck kaposiform hemangioendothelioma: report of three cases., Pediatric dermatology, 26, (3), 2009, p331-7
Sandilands, A, Sutherland, C, Irvine, AD, McLean, WH, Filaggrin in the frontline: role in skin barrier function and disease., Journal of Cell Science, 122, (Pt 9), 2009, p1285-1294
Genetics in, editor(s)Beiber T, Leung D , Atopic Dermatitis, London, Informa Healthcare, 2009, [Weidinger S, Rodriguez E, Irvine AD]
Henderson, J, Northstone, K, Lee, SP, Liao, H, Zhao, Y, Pembrey, M, Mukhopadhyay, S, Smith, GD, Palmer, CN, McLean, WH, Irvine, AD, The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study., The Journal of allergy and clinical immunology, 121, (4), 2008, p872-877
Weidinger, S, Baurecht, H, Wagenpfeil, S, Henderson, J, Novak, N, Sandilands, A, Chen, H, Rodriguez, E, O'Regan, GM, Watson, R, Liao, H, Zhao, Y, Barker, JN, Allen, M, Reynolds, N, Meggitt, S, Northstone, K, Smith, GD, Strobl, C, Stahl, C, Kneib, T, Klopp, N, Bieber, T, Behrendt, H, Palmer, CN, Wichmann, HE, Ring, J, Illig, T, McLean, WH, Irvine, AD, Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk., The Journal of allergy and clinical immunology, 122, (3), 2008, p560-568.e4
Genomics of the Epidermis and Appendages, Skin Pigmentation, And Skin Cancer in, editor(s)Kumar D, Weatherall D , Genomics and Clinical Medicine, New York , Oxford University Press, 2008, pp507-529 , [Healy E, Irvine AD, Lear JT, Munro CS]
O'Regan, GM, Sandilands, A, McLean, WH, Irvine, AD, Filaggrin in atopic dermatitis., The Journal of Allergy and Clinical Immunology, 122, (4), 2008, p689-693
Cusack, C, Fitzgerald, D, Clayton, TM, Irvine, AD, Successful treatment of florid cutaneous warts with intravenous cidofovir in an 11-year-old girl., Pediatric Dermatology, 25, (3), 2008, p387-389
Brown, SJ, Irvine, AD, Atopic eczema and the filaggrin story., Seminars in cutaneous medicine and surgery, 27, (2), 2008, p128-137
McLean, W.H.I., Palmer, C.N.A., Henderson, J., Kabesch, M., Weidinger, S., Irvine, A.D., Filaggrin variants confer susceptibility to asthma , Journal of Allergy and Clinical Immunology, 121, (5), 2008, p1294-1295
Grainne M. O'Regan, Aileen Sandilands, WH Irwin McLean and Alan D. Irvine , Current Perspectives Series: Filaggrin in Atopic Dermatitis, Journal of Allergy and Clinical Immunology, 122, (4), 2008, p689-693
O'Regan, GM, Irvine, AD, The role of filaggrin loss-of-function mutations in atopic dermatitis., Current opinion in allergy and clinical immunology, 8, (5), 2008
Weidinger, S, O'Sullivan, M, Illig, T, Baurecht, H, Depner, M, Rodriguez, E, Ruether, A, Klopp, N, Vogelberg, C, Weiland, SK, McLean, WH, von Mutius, E, Irvine, AD, Kabesch, M, Filaggrin mutations, atopic eczema, hay fever, and asthma in children., The Journal of allergy and clinical immunology, 121, (5), 2008, p1203-1209.e1
Field S, Irvine AD, Kirby B., The treatment of viral warts with topical cidofovir 1%: our experience of seven paediatric patients., British Journal of Dermatology, 160, (1), 2008, p223-224
Kezic S, Kemperman PMJH, Koster E, de Jongh C, Thio BH, Campbell LE, Irvine AD, McLean WHI, Puppels GJ, Caspers PJ, Loss-of-function mutations in the filaggrin gene lead to reduced levels of natural moisturizing factor in the stratum corneum, Journal of Investigative Dermatology, 128, (8), 2008, p2117-2119
Cox, D, O' Regan, G, Collins, S, Byrne, A, Irvine, A, Watson, R, Juvenile localised scleroderma: a retrospective review of response to systemic treatment., Irish Journal of Medical Science, 177, (4), 2008, p343-346
Irvine AD, Fleshing out filaggrin phenotypes, Journal of Investigative Dermatology, 127, (3), 2007, p504 - 507
Disorders of cornification in, Esterly N, Eichenfield L, Frieden I , Neonatal Dermatology, Philadelphia, Elsevier, 2007, pp285-310 , [Irvine AD, Paller AS ]
Porokeratoses in, Wolff K, Katz S, Goldsmith L, Gilchrest B , Paller A, Leffell D , Fitzpatrick's Dermatology in General Medicine, New York , McGraw Hill, 2007, [O'Regan GM, Irvine AD]
Irvine AD, Fleshing out filaggrin phenotypes., The Journal of investigative dermatology, 127, (3), 2007, p504-7
O'Regan, GM, Zurada, J, Martinez-Mir, A, Christiano, AM, Irvine, AD, A recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families., The British Journal of Dermatology, 156, (4), 2007, p744-747
Liao, H., Sayers, J.M., Wilson, N.J., Irvine, A.D., Mellerio, J.E., Baselga, E., Bayliss, S.J., (...), Smith, F.J.D., A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita , Journal of Dermatological Science, 48, (3), 2007, p199-205
Dermatology in, editor(s)Strobel S, Smith P, El Habbal MH, Spitz, L, , The Great Ormond Street Colour Handbook of Paediatric Medicine and Surgery, London, Manson Publishing, 2007, pp131-159 , [Irvine AD, Lomas D, Atherton DJ, Harper JI ]
McLean, WH, Irvine, AD, Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues., The Ulster Medical Journal, 76, (2), 2007, p72-82
O'Connell S, O'Regan GM, Bolger T, Hoffman HM, Cant A, Irvine AD, Watson R, Response to Il-1-Receptor Antagonist in a child with Familial Cold Autoinflammatory Syndrome, Pediatric Dermatology, 24, (1), 2007, p85 - 89
Zhao, Y, Terron-Kwiatkowski, A, Liao, H, Lee, SP, Allen, MH, Hull, PR, Campbell, LE, Trembath, RC, Capon, F, Griffiths, CE, Burden, D, McManus, R, Hughes, R, Kirby, B, Rogers, SF, Fitzgerald, O, Kane, D, Barker, JN, Palmer, CN, Irvine, AD, McLean, WH, Filaggrin null alleles are not associated with psoriasis., The Journal of investigative dermatology, 127, (8), 2007, p1878-1882
O'Regan, GM, Watson, R, Orr, D, O'Donovan, D, Russell, J, Phelan, E, Ryan, M, Brosnahan, O, Irvine, A, Management of vascular birthmarks: review of a multidisciplinary clinic., Irish Medical Journal, 100, (4), 2007
Baurecht, H, Irvine, AD, Novak, N, Illig, T, Bühler, B, Ring, J, Wagenpfeil, S, Weidinger, S, Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data., The Journal of allergy and clinical immunology, 120, (6), 2007, p1406-1412
Clayton, T.H., Barry, J., Fitzgerald, D., Watson, R., Irvine, A.D., Clarithromycin suspension-associated toxic epidermal necrolysis in a 2-year-old girl [5] , Clinical and Experimental Dermatology , 32, (6), 2007, p755-756
Sandilands, A, Smith, FJ, Irvine, AD, McLean, WH, Filaggrin's fuller figure: a glimpse into the genetic architecture of atopic dermatitis., The Journal of Investigative Dermatology, 127, (6), 2007, p1282-1284
Sandilands A, Terron-Kwiatkowski A, Hull PR, O'Regan GM, Clayton TH, Watson RM, Carrick T, Evans AT, Liao H, Zhao Y, Campbell LE, Schmuth M, Gruber R, Janecke AR, Elias PM, van Steensel MAM, Nagtzaam I, van Geel M, Steijlen PM, Munro CS, Bradley DG, Palmer CNA, Smith FJD, McLean WHI, Irvine AD, Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema , Nature Genetics, 39, (5), 2007, p650 - 654
Weidinger S, Illig T, Baurecht H, Irvine AD, Rodriguez E, Diaz-Lacava A, Klopp N, Wagenpfeil S, Zhao Y, Liao H, Lee SP, Palmer CNA, Jenneck C, Maintz L, Hagemann T, Behrendt H, Ring J, Nothen MM, McLean WHI, Novak N, Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations, Journal of Allergy and Clinical Immunology, 118, (1), 2006, p214 - 219
Sandilands A, O'Regan GM, Smith FJD, McLean WHI, Irvine AD, Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis, Journal of Investigative Dermatology, 126, 2006, p1770 - 1775
Smith FJD, Irvine AD, Terron-Kwiatkowski A, Sandilands A, Campbell LE, Zhao Y, Liao L, Evans AT, Goudie DR, Lewis-Jones S, Arseculeratne G, Munro CS, Sergeant A, O'Regan G, Bale SJ, Compton JG, DiGiovanna JJ, Presland RB, Fleckman P, Irwin McLean WHI, Loss-of-function mutations in the filaggrin gene cause ichthyosis vulgaris, Nature Genetics, 38, (3), 2006, p337 - 342
Collins SM, Dominguez M, Ilmarinen T, C Costigan C, Irvine AD, Dermatological manifestations of autoimmune polyendocrinopathy - candidiasis - ectodermal dystrophy (APECED) syndrome, British Journal of Dermatology, 154, (6), 2006, p1088 - 1093
Palmer CNA, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, Goudie DR, Sandilands A, Campbell LE, Smith FJD, O'Regan GM, Watson RM, Cecil JE, Bale SJ, Compton JG, DiGiovanna JJ, Fleckman P, Lewis-Jones S, Arseculeratne G, Sergeant A, Munro CS, El Houate B, McElreavey K, Halkjaer LB, Bisgaard H, Mukhopadhyay S, McLean WHI, Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis, Nature Genetics, 38, (4), 2006, p441 - 446
O'Regan GM, Canny G, Irvine AD, Peeling paint' dermatitis as a presenting sign of cystic fibrosis, Journal of Cystic Fibrosis, 5, (4), 2006, p257 - 259
Madasseri A, McDermott MB, Irvine AD, Lipoatrophic panniculitis of the ankles, Clinical and Experimental Dermatology, 31, (2), 2006, p303 - 530
Genetics of Hidradenitis Suppurativa in, editor(s)Jemec GBE, Revuz J and Leyden JJ , Hirdadenitis Suppurativa, Berlin & Heidelberg , Springer, 2006, pp70-85 , [von der Werth J, Wood P, Irvine AD, McLean WHI ]
O'Regan, G.M., Canny, G., Irvine, A.D., 'Peeling paint' dermatitis as a presenting sign of cystic fibrosis, Journal of Cystic Fibrosis, 5, (4), 2006, p257-259
Irvine AD and McLean WHI, Breaking the (un) sound barrier: filaggrin is a major gene for atopic dermatitis, Journal of Investigative Dermatology, 126, (6), 2006, p1200 - 1202
Irvine AD, McLean WH, Breaking the (un)sound barrier: filaggrin is a major gene for atopic dermatitis., The Journal of investigative dermatology, 126, (6), 2006, p1200-2
Dominguez M, Crushell E, Ilmarinen T, McGovern E, Collins S, Chang B, Fleming P, Irvine AD, Brosnahan D, Ulmanen I, Murphy N, Costigan C, Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) in the Irish Population, Journal of Pediatric Endocrinology and Metabolism, 19, (11), 2006, p1343 - 1352
Smith, F.J.D., Irvine, A.D., Terron-Kwiatkowski, A., Sandilands, A., Campbell, L.E., Zhao, Y., Liao, H., Evans, A.T., Goudie, D.R., Lewis-Jones, S., Arseculeratne, G., Munro, C.S., Sergeant, A., O'Regan, G., Bale, S.J., Compton, J.G., Digiovanna, J.J., Presland, R.B., Fleckman, P., McLean, W.H.I., Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris, Nature Genetics, 38, (3), 2006, p337-342
O'Regan, G.M., Irvine, A.D., Disorders due to mutations in keratin genes , Giornale Italiano di Dermatologia e Venereologia, 140, (6), 2005, p667-676
Tobin AM, Cotter M, Irvine AD, Kirby B, Successful treatment of a refractory verruca in a child with acute lymphoblastic leukaemia with topical cidofovir, British Journal of Dermatology, 152, (2), 2005, p386 - 388
Irvine AD, Inherited defects in keratins, Clinics in Dermatology, 23, (1), 2005, p6-14
Ectodermal dysplasias in, editor(s)Harper JI, Oranje OP, Prose N , Pediatric Dermatology , Oxford , Blackwell Scientific, 2005, pp1412-1466 , [Irvine AD]
Terron-Kwiatkowski A, Terrinoni A, Didona B, Melino G, Atherton D, Irvine AD, Mclean WHI, Atypical Epidermolytic Palmoplantar Keratoderma Presentation Associated With A Mutation In The Keratin 1 Gene, British Journal of Dermatology, 150, (6), 2004, p1096 - 1103
Veugelers M, Wilkes D, Burton K, McDermott D, Song Y, Vaughan CJ, La Perle K, Goldstein G, Kligfield P, O'Hagan A, Bennett K, Meyer BJ, Legius E, Kartunnen M, Lavyne M, Neau J-P, Richter G, Kirali K, Stapleton K, Morelli P, Norio R, Takanashi Y, Farnsworth A, Bamforth J-S, Eitelberger F, Manfroi W, Ko GTC, Powers J, Mochizuki Y, Imai T, Driscoll DA, Goldmuntz E, Edelberg J, Eccles D, Irvine AD, McKnight GS, Basson CT, Comparative PRKAR1 a Genotype-Phenotype Analyses in Humans with Carney complex and prkar1 a Haploinsufficient Mice, Proceedings of The National Academy of Sciences, 101, (39), 2004, p14222 - 14227
Veugelers, M., Wilkes, D., Burton, K., McDermott, D.A., Song, Y., Goldstein, M.M., La Perle, K., (...), Basson, C.T., Erratum: Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice (Proceedings of the National Academy of Sciences of the United States of America (September 28, 2004) 101:39 (14222-14227)), 2004, - 15546
McLean, W.H.I., Irvine, A.D., Hamill, K.J., Whittock, N.V., Coleman-Campbell, C.M., Mellerio, J.E., Ashton, G.S., (...), McGrath, J.A., Erratum: An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome, 2004, - 2395-2409
McLean, W.H.I., Irvine, A.D., Hamill, K.J., Whittock, N.V., Coleman-Campbell, C.M., Mellerio, J.E., Ashton, G.S., Dopping-Hepenstal, P.J.H., Eady, R.A.J., Jamil, T., Phillips, R.J., Ghulam Shabbir, S., Haroon, T.S., Khurshid, K., Moore, J.E., Page, B., Darling, J., Atherton, D.J., van Steensel, M.A.M., Munro, C.S., Smith, F.J.D., McGrath, J.A., Erratum: An unusual N-terminal deletion of the laminin "3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome (Human Molecular Genetics (2003) vol. 12 (2395-2409)), Human Molecular Genetics, 13, (3), 2004
O'Hagan, AH, Irvine AD, Sands A, O'Donaghue D, Casey F, Bingham EA, Miliary Neonatal Hemangiomatosis with Fulminant Heart Failure and Cardiac Septal Hypertrophy in Two Infants, Pediatric Dermatology, 21, (4), 2004, p469 - 472
McLean WH, Irvine AD, Hamill KJ, Whittock NV, Coleman-Campbell CM, Mellerio JE, Ashton GS, Dopping-Hepenstal PJ, Eady RA, Jamil T, Phillips R, Shabbir SG, Haroon TS, Khurshid K, Moore JE, Page B, Darling J, Atherton DJ, Van Steensel MA, Munro CS, Smith FJ, McGrath JA, Phillips RJ, An unusual N-terminal deletion of the laminin alpha3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome., Human molecular genetics, 12, (18), 2003, p2395-409
Skin: Hereditary Disorders in, Cooper DN , Nature Encyclopaedia of the Human Genome, London., John Wiley and Sons Ltd, 2003, pp314-325 , [Corden LD, McLean WHI and Irvine AD]
McLean WHI, Irvine AD, Hamill KJ, Whittock NV, Coleman CM, Mellerio JE, Ashton GS, Dopping-Hepenstal PJH, Eady RAJ, Jamil T, Phillips RJ, Shabbir SG, Haroon TS, Khurshid K, Moore JE, Page B, Darling J, Atherton DJ, Munro CS, Smith FJD, McGrath JA, An unusual N-terminal deletion of the laminin α3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndrome, Human Molecular Genetics, 12, (18), 2003, p2395 - 2409
Wang LL, Gannavarapu A, Clericuzio CL, Erickson RP, Irvine AD, Plon SE, Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients, American Journal of Medical Genetics A, 118, (3), 2003, p299 - 301
Epithelial corneal dystrophies. in, editor(s)Wang M, Flatten N , Cornea: Dystrophies and Degenerations: A Molecular Genetics Approach, San Francisco, Oxford University Press Inc, 2003, pp19-45 , [Irvine AD, Wang M, McLean WHI ]
Hair Loss: Genetics. in, editor(s)Cooper DN , Nature Encyclopaedia of the Human Genome, London , John Wiley and Sons Ltd, 2003, pp153-159 , [Irvine AD]
Paller AS, Irvine AD, Russi DC, Raised limb bands developing in infancy, British Journal of Dermatology, 149, (2), 2003, p436 - 437
McMullen EA, McCarron P, Irvine AD, Dolan OM, Allen GE, Association between long-term acitretin therapy and osteoporosis: no evidence of increased risk, Clinical and Experimental Dermatology, 28, (3), 2003, p307 - 309
Irvine AD and McLean WHI, The Molecular Genetics of The Genodermatoses: Progress To Date And Future Directions, British Journal of Dermatology, 148, (1), 2003, p1-13
Irvine, A.D., McLean, W.H.I., The molecular genetics of the genodermatoses: Progress to date and future directions, British Journal of Dermatology, 148, (1), 2003, p1-13
Terron-Kwiatkowski A, Paller AS, Compton J, Atherton DJ, McLean WHI, Irvine AD, Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1, Journal of Investigative Dermatology, 119, (4), 2002, p966 - 971
Irvine, A.D., Paller, A.S., Molecular genetics of the inherited disorders of cornification: an update., Advances in dermatology, 18, 2002, p111-149
Irvine AD, Sun P, Kos L, Wang X, Paller AS, A colorimetric bead-binding assay for detection of intermolecular interactions, Experimental Dermatology, 11, (5), 2002, p465 - 471
Irvine AD, Paller AS, The Molecular Genetics of the Inherited Disorders of Keratinization: An update, Advances in Dermatology, 18, 2002, p111-49
Bitoun E, Chavanas S, Irvine AD, Lonie L, Bodemer C, Paradisi M, Hamel-Teillac D, Ansai S, Mitsuhashi Y, Taïeb A, de Prost Y, Zambruno G, Harper JI, Hovnanian A, Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families., The Journal of investigative dermatology, 118, (2), 2002, p352-61
Terron-Kwiatkowski A, Paller AS, Compton J, Atherton DJ, McLean WH, Irvine AD, Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1., The Journal of investigative dermatology, 119, (4), 2002, p966-71
Irvine AD, Coleman CM,. Moore JE, Swensson O, Morgan SJ, McCarthy JH, Smith FJD, Black GCM, McLean WHI, A novel mutation in KRT12 associated with Meesmann's Epithelial Corneal Dystrophy, British Journal of Ophthalmology, 86, (7), 2002, p729 - 732
Bitoun E, Chavanas S, Irvine AD, Lonie L, Bodemer C, Paradisi M, Hamel-Teillac, Ansai S, Mitsuhashi Y, Taïeb A, de Prost Y, Zambruna G, Harper JI, Hovnanian A, Netherton Syndrome: Disease expression and Spectrum of SPINK5 Mutations in 21 families, Journal of Investigative Dermatology, 118, (2), 2002, p352 - 361
Hay-Wells syndrome. in, editor(s)Gruson ES , NORD Guide to Rare Disorders, Philadelphia , Lippincott, Williams & Wilkins, 2002, pp116-117 , [Irvine AD, McGrath JA]
Irvine AD, Paller AS, Inherited disorders of Keratinization, Current Problems in Dermatology, 14, (3), 2002, p71-116
O'Hagan AH, Irvine AD, Brennan T, Walsh MY, Bingham EA, Fibrous histiocytoma in a nine week old male infant, European Journal of Pediatric Dermatology, 11, (1), 2001, p13 - 18
Moore JE, Dua HS, Page AB, Irvine AD, Archer DB, Ocular surface reconstruction in LOGIC syndrome by amniotic membrane transplantation, Cornea, 20, (1), 2001, p753 - 756
Irvine AD, Christiano AM, Hair on a gene string: recent advances in understanding the molecular genetics of hair loss, Clinical and Experimental Dermatology, 26, (1), 2001, p59-714
McGrath JA, Duijf PH, Doetsch V, Irvine AD, de Waal R, Vanmolkot KR, Wessagowit V, Kelly A, Atherton DJ, Griffiths WA, Orlow SJ, van Haeringen A, Ausems MG, Yang A, McKeon F, Bamshad MA, Brunner HG, Hamel BC, van Bokhoven H, Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63., Human molecular genetics, 10, (3), 2001, p221-9
McGrath JA, Duijf P, Doetsch V, Irvine AD, de Waal R, Vanmolkot K, Wessagowit VA, Kelly K, Atherton DJ, Griffiths WAD, Orlow SJ, van Haeringen A, Ausems M, Yang A, McKeon F, Bamshad MA, Brunner HG, Hamel BCJ, van Bokhoven H, Hay-Wells syndrome is caused by missense mutations in the SAM domain of p63, Human Molecular Genetics, 10, (3), 2001, p221 - 229
Irvine AD, Rugg EL, Lane EB, Hoare S, Peret C, Hughes AE, Heagerty AH, Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation, British Journal of Dermatology, 144, (1), 2001, p40 - 46
Chavanas S, Bodemer C, Rochat A, Hamel-Teillac D, Ali M, Irvine AD, Bonafé J-L, Taïeb A, Barrandon Y, Harper JI, de Prost, Y, Hovnanian A, Mutations in SPINK5 encoding a novel serine protease inhibitor cause Netherton Syndrome, Nature Genetics, 25, (2), 2000, p141 - 142
Irvine AD, Smith FJD, Shum KW, Williams HC, McLean WHI, A novel mutation in the 2B domain of keratin 2e causing Ichthyosis Bullosa of Siemens, Clinical and Experimental Dermatology, 25, (8), 2000, p648 - 652
Korge BP, Hamm H, Jury CS, Traupe H, Irvine AD, Healy E, Birch-MacHin M, Rees JL, Messenger AG, Holmes SC, Parry DA, Munro CS, Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype., The Journal of investigative dermatology, 113, (4), 1999, p607-12
Irvine AD and McLean WHI, Human keratin diseases: the increasing spectrum of disease and the subtlety of genotype-phenotype correlation, British Journal of Dermatology, 140, (5), 1999, p815-828
Korge BP, Hamm H, Jury CS, Traupe H, Irvine AD, Healey E, Birch-Machin, M, Rees JL, Messenger AG, Holmes SC, Parry DAD, Munro CS, Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype, Journal of Investigative Dermatology, 113, (4), 1999, p607 - 612
Smith FJD, McKenna KE, Irvine AD, Bingham EA, Coleman CM, Uitto J, McLean WHI, A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1, Experimental Dermatology, 8, (2), 1999, p109 - 111
Ahmad W, Irvine AD, Lam H, Buckley C, Bingham EA, Panteleyev AA, Ahmad A, McGrath JA, Christiano AM, A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers, American Journal of Human Genetics, 63, (4), 1998, p984 - 991
Covello SP, Irvine AD, McKenna KE, Munro CS, Nevin NC, Smith FJD, Uitto J, McLean WHI, Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland, Journal of Investigative Dermatology, 111, 1998, p1207 - 1209
Sais, G., Vidaller, A., Jucgla, A., Gallardo, F., Peyri, J., Irvine, A.D., Bruce, I.N., Antineutrophil cytoplasmic antibodies in leukocytoclastic vasculitis [1] (multiple letters), Archives of Dermatology, 134, (2), 1998, p239-240
O'Hagan A, Irvine AD, Allen GE, Mefenamic acid induced pseudoporphyria, British Journal of Dermatology, 139, (6), 1998, p1131 - 1132
O'Hagan A, Irvine AD, Walsh M, Allen GE, Pyodermatitis-pyostomatitis vegetans: evidence of an entirely mucocutaneous variant, British Journal of Dermatology, 138, (3), 1998, p552 - 555
Casey M, Mah C, Merliss AD, Kirschner LS, Taymans SE, Denio AE, Korf B, Irvine AD, Hughes A, Carney JA, Stratakis CA, Basson CT, Identification of a novel genetic locus for familial cardiac myxomas and Carney complex., Circulation, 98, (23), 1998, p2560-6
Ahmad W, Irvine AD, Lam H, Buckley C, Bingham EA, Panteleyev AA, Ahmad M, McGrath JA, Christiano AM, A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers., American journal of human genetics, 63, (4), 1998, p984-91
Casey M, Mah C, Merliss AD, Kirschner LS, Taymans SE, Denio AE, Korf B, Irvine AD, Hughes AE, Carney JA, Stratakis CA, Basson CT, Identification of a novel genetic locus for familial cardiac myxoma and Carney complex, Circulation, 98, (23), 1998, p2560 - 2566
Irvine AD, Armstrong DKB, Bingham EA, Hadden DR, Nevin NC, Hughes AE, Evidence for a second genetic locus in Carney complex, British Journal of Dermatology, 138, 1998, p572 - 576
O'Hagan, A.H., Irvine, A.D., Allen, G.E., Walsh, M., Pseudoporphyria induced by mefenamic acid [16], British Journal of Dermatology, 139, (6), 1998, p1131-1132
Irvine AD, Bruce IN, Walsh MY, Bingham EA, Antineutrophil cytoplasmic antibodies in leukocytoclastic vasculitis, Archives of Dermatology, 134, (2), 1998, p239 - 240
Irvine AD, Bruce IN, Walsh MY, Bingham EA, Microscopic polyangiitis. Delineation of a cutaneous-limited variant associated with antimyeloperoxidase autoantibody., Archives of Dermatology, 133, (4), 1997, p474 - 477
Armstrong DKB, Irvine AD, Handley JM, Walsh MY, Hadden DR, Bingham EA, Carney complex: report of a new kindred with predominantly cutaneous manifestations, British Journal of Dermatology, 136, (4), 1997, p578 - 582
Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJD, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WHI., Mutations in cornea-specific keratins K3 or K12 cause Meesmann's corneal dystrophy, Nature Genetics, 16, 1997, p184 - 187
Irvine AD, McKenna KE, Bingham A, Nevin NC, Hughes AE, A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-Meara., The Journal of investigative dermatology, 109, (6), 1997, p815-6
Loughrey MB, Irvine AD, Girdwood RWA, McMillan CM, Cutaneous larva migrans: the case for routine oral treatment, British Journal of Dermatology, 137, (1), 1997, p155 - 158
Irvine AD, McKenna KE, Bingham EA, Nevin NC, Hughes AE, A novel mutation in the helix termination peptide of keratin 5 causing Epidermolysis bullosa simplex Dowling-Meara, Journal of Investigative Dermatology, 109, 1997, p815 - 816
Irvine AD, McKenna KE, Jenkinson H, Hughes AE, A mutation in the V1 Domain of keratin 5 causes Epidermolysis Bullosa Simplex with Mottled Pigmentation, Journal of Investigative Dermatology, 108, (5), 1997, p809 - 810
Irvine AD, Bruce IN, Walsh M, Burrows D, Handley J, Dermatological presentation of ANCA associated disease: a report of two contrasting cases and review of the literature, British Journal of Dermatology, 134, (5), 1996, p924 - 928
Irvine AD, Stewart FJ, Bingham EA, Nevin NC, Boston VE, Focal dermal hypoplasia (Goltz Syndrome) associated with intestinal malrotation and mediastinal dextroposition., American Journal of Medical Genetics, 62, (3), 1996, p213-215
Irvine AD, Stewart FJ, Bingham EA, Nevin NC, Boston VE, Focal dermal hypoplasia (Goltz Syndrome) associated with intestinal malrotation and mediastinal dextroposition, American Journal of Medical Genetics, 62, (3), 1996, p213 - 215
Irvine AD, Sweeney LE, Corbett JR, Lymphangioma circumscriptum associated with paravesical cystic retroperitoneal lymphangioma, British Journal of Dermatology, 134, (6), 1996, p1135 - 1137
Irvine, A.D., Bruce, I.N., Walsh, M., Burrows, D., Handley, J., Dermatological presentation of disease associated with antineutrophil cytoplasmic antibodies: A report of two contrasting cases and a review of the literature, British Journal of Dermatology, 134, (5), 1996, p924-928
Irvine AD, Dolan OM, Hadden DR, Stewart FJ, Bingham EA, Nevin NC, An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis., Journal of medical genetics, 33, (11), 1996, p972-4
Irvine AD, Dolan OM, Hadden DR, Stewart FJ, Bingham EA, Nevin NC, An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis, Journal of Medical Genetics, 33, (11), 1996, p972 - 974
Irvine AD, Kenny B, Walsh MY, Burrows D, Primary cutaneous adenoid cystic carcinoma, Clinical and Experimental Dermatology, 21, 1996, p249 - 250
Armstrong DKB, Irvine A, Walsh MY, Mayne EE, Burrows D, Multiple dermatofibromas in a patient with HIV infection, Clinical and Experimental Dermatology, 20, (6), 1995, p474 - 476
Dolan OM, Burrows D, Irvine A, Walsh M, The value of a baseline liver biopsy prior to methotrexate therapy, British Journal of Dermatology, 131, (6), 1994, p891 - 894
Sakas, D.E., O"Connor, G., Singh, J., Dias, L., Eljamel, M.S., Mathew, B., Clements, B., Irvine, A., Gray, W.J., Byrnes, D.P., Bailey, I.C., Pathirana, N., Refsum, S., Bell, K.E., McKinstry, C.S., Callaghan, N., Crowley, M., Goggin, T., MacDermott, N., O"Driscoll, K.J., Neary, D., Pearson, N.A., Snowden, J.S., Brown, S., Vaughan, M., McMackin, D., Phillips, J., Burke, T., Murphy, S., Staunton, H., Cristea, R.L., Hourihane, M., Farrell, M.A., Morrison, P.J., Nevin, N.C., Collins, A.D., Gibson, M., Behan, W.M.H., Simpson, K.S., Cavanagh, H.M., Gow, J.W., Gillespie, J.S., Behan, P.O., Sklar, R.M., Brown, R.H., Gillian, A.M., O"Mahony, D., Breen, K.C., Hutchinson, J., Burke, T., Hutchinson, M., Droogan, A.G., Crockard, A.D., Hawkins, S.A., McNeill, T.A., Gutowski, N.J., Chirico, S., Pinkham, J.M., Smith, C., Akanu, D., Kaur, H., Strange, R.C., Halliwell, B., Murphy, R.P., Rogers, L., Weick, J., Estes, M., Elrington, G.M., Morris, C.S., Reffin, J.P., Tregear, S.J., Ripley, L.J., Rees, J.E., Irvine, A.D., O"Brien, D.P., Dias, P.S., Herity, N., Hawkins, S., McMenamin, J.B., Mirakhur, M., Allen, I.V., Bresnihan, B., Fitzsimmons, M., Sawhney, B., Patterson, V., Bailey, I.C., Byrnes, D., Watt, M., Lee, K.-C., Redmond, J.M.T., McKenna, M.J., Feingold, M., Ahmad, B.K., Watt, M., Cunningham, R.T., Winder, J., Lawson, J.A., Johnston, C.F., Buchanan, K.D., Dean, G., Elian, M., Gray, W.P., Ryder, D.Q., Buckley, T.F., Breathnach, K., Ooi, A., Farrell, M., Doherty, C., Hayes, F.J., Redmond, J.J.T., McKenna, M.M., Redmond, J.M.T., Farrell, M., Watt, M., Gibson, J.M., Patterson, V.H., Redmond, J.M.T., McKenna, M.J., Feingold, M., Ahmad, B.K., Moran, M., Burke, M., King, M.D., Moran, M., Burke, M., Hardiman, O., Reid, V., Dowd, J.O., Murphy, R., Rashad, E., Toland, J., Phillips, J.P., Staunton, H., Shu-Ming, P., Coughlin, A., Phillips, J.P., McCoy, D.M., Qureshi, A., Black, M.A., Grace, P.A., Bouchier-Hayes, D., Dwyer, R., Irish neurological association: Proceedings of 28th annual meeting, beaumont hospital, Dublin, 15th-16th may, 1992, Irish Journal of Medical Science, 162, (11), 1993, p474-484
Research Expertise
Recognition
Representations
Grant Reviewer: The Wellcome Trust, Medical Research Council (UK), The Italian National Telethon, DEBRA International, British Skin Foundation
Reviewer: The Journal of Investigative Dermatology, The British Journal of Dermatology, Experimental Dermatology, European Journal of Human Genetics, Clinical and Experimental Dermatology, Journal of Allergy And Clinical Immunology, Allergy
Editorial Board: Journal of Lymphoedema
Editorial Board Member: Faculty of 1000 Medicine (F1000), Paediatric Dermatology Section
Editorial Board Member: Pediatric Dermatology
Awards and Honours
Fellowship (FRCP) Royal College of Physicians of London
Paul Gerson Unna Prize
Prix de La Foundation La Roche-Posay
Fulbright Scholarship
Geoffrey Dowling Fellowship, British Association of Dermatologists
Canadian Dermatology Association Prize, Best paper presented at the British Association of Dermatologists Annual Meeting
Young Investigator Fellowship, British Society for Investigative Dermatology
Memberships
Association of Physicians of Great Britain & Ireland - Member
Royal College of Physicians of London - Fellow
The Royal College of Physicians of Ireland - Fellow
American Academy of Dermatology International - Fellow
Society for Pediatric Dermatology - Member
British Association of Dermatologists - Ordinary Member
Irish Association of Dermatologists - Member
Irish Society of Human Genetics - Member
British Society for Pediatric Dermatology - Member
Royal Academy of Medicine in Ireland - Member
European Society for Dermatological Research - Member
Society for Investigative Dermatology - Member
British Society for Investigative Dermatology - Member
The Dowling Club - Member