J. Curtin's Profile

Role	Title	Level	Year	L/R
🐜	Association between physical activity and risk of bleeding in children with hemophilia. 8 auth. C. Broderick, R. Herbert, J. Latimer, C. Barnes, J. Curtin, E. Mathieu, ... P. Monagle, S. Brown	6	2012	6 🐜
🐜	Cost‐utility analysis of Canadian tailored prophylaxis, primary prophylaxis and on‐demand therapy in young children with severe haemophilia A 7 auth. N. Risebrough, P. Oh, P. Oh, V. Blanchette, J. Curtin, J. Hitzler, ... B. Feldman	6	2008	6 🐜
🐜	A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias 28 auth. N. Roy, Edward A. Wilson, S. Henderson, Katherine Wray, C. Babbs, S. Okoli, W. Atoyebi, A. Mixon, M. Cahill, P. Carey, J. Cullis, J. Curtin, H. Dreau, D. Ferguson, B. Gibson, ... G. Hall, J. Mason, Mary Morgan, M. Proven, A. Qureshi, Joaquin Sanchez Garcia, N. Sirachainan, J. Teo, U. Tedgård, D. Higgs, D. Roberts, I. Roberts, A. Schuh	6	2016	6 🐜
🐜	Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia. 27 auth. K. Boztug, P. Rosenberg, M. Dorda, S. Banka, T. Moulton, J. Curtin, N. Rezaei, John S. Corns, J. Innis, Z. Avcı, H. C. Tran, I. Pellier, P. Pierani, R. Fruge, N. Parvaneh, ... S. Mamishi, R. Mody, P. Darbyshire, J. Motwani, J. Murray, G. Buchanan, W. Newman, B. Alter, L. Boxer, J. Donadieu, K. Welte, C. Klein	6	2012	6 🐜
🐜	Heterozygous loss of platelet glycoprotein (GP) Ib-V-IX variably affects platelet function in velocardiofacial syndrome (VCFS) patients 7 auth. H. Liang, M. Morel-Kopp, J. Curtin, Meredith Wilson, J. Hewson, Walter Chen, ... C. Ward	5	2007	5 🐜
🐜	Long-Acting Recombinant Fusion Protein Linking Coagulation Factor IX with Albumin (rIX-FP) in Children 12 auth. G. Kenet, H. Chambost, C. Male, T. Lambert, S. Halimeh, T. Chernova, ... M. Mancuso, J. Curtin, Christine Voigt, Yanyan Li, Iris Jacobs, E. Santagostino	5	2016	5 🐜
🐜	Treatment of an infant with X‐linked severe combined immunodeficiency (SCID‐X1) by gene therapy in Australia 18 auth. S. L. Ginn, J. Curtin, C. Smyth, M. Latham, S. Cunningham, M. Zheng, Linda Hobson, P. B. Rowe, I. Alexander, B. Kramer, ... M. Wong, A. Kakakios, G. McCowage, D. Watson, S. Alexander, A. Fischer, M. Cavazzana‐Calvo, S. Hacein-Bey-Abina	5	2005	5 🐜
🐜	Allogeneic bone marrow transplantation: cure for familial Mediterranean fever. 8 auth. J. Milledge, P. Shaw, A. Mansour, S. Williamson, B. Bennetts, T. Roscioli, ... J. Curtin, J. Christodoulou	5	2002	5 🐜
🐜	ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder 46 auth. Lloyd Williams, Asif Javed, Asif Javed, Amin Sabri, Denise J. Morgan, C. Huff, C. Huff, J. Grigg, J. Grigg, Xiu Ting Heng, A. Khng, I. Hollink, M. Morrison, Leah A. Owen, K. Anderson, ... Krista I Kinard, Rebecca Greenlees, Danica Novacic, H. Sen, W. Zein, G. Rodgers, A. Vitale, N. Haider, A. Hillmer, P. Ng, Shankaracharya, Anson Cheng, Linda Zheng, M. Gillies, M. V. Slegtenhorst, P. V. Hagen, T. Missotten, G. L. Farley, M. Polo, J. Malatack, J. Curtin, F. Martin, S. Arbuckle, S. Alexander, M. Chircop, S. Davila, K. Digre, R. Jamieson, R. Jamieson, R. Jamieson, M. DeAngelis	5	2019	5 🐜