Fiona Moghaddas
Fiona Moghaddas
The Walter and Eliza Hall Institute of Medical Research, The Royal Melbourne Hospital
Verified email at wehi.edu.au
Title
Cited by
Cited by
Year
Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation
SL Masters, V Lagou, I Jéru, PJ Baker, L Van Eyck, DA Parry, D Lawless, ...
Science translational medicine 8 (332), 332ra45-332ra45, 2016
1902016
A novel Pyrin-Associated Autoinflammation with Neutrophilic Dermatosis mutation further defines 14-3-3 binding of pyrin and distinction to Familial Mediterranean Fever
F Moghaddas, R Llamas, D De Nardo, H Martinez-Banaclocha, ...
Annals of the rheumatic diseases 76 (12), 2085-2094, 2017
812017
A mutation outside the dimerization domain causing atypical STING-associated vasculopathy with onset in infancy
RG Saldanha, KR Balka, S Davidson, BK Wainstein, M Wong, ...
Frontiers in immunology 9, 1535, 2018
372018
Monogenic autoinflammatory diseases: cytokinopathies
F Moghaddas, SL Masters
Cytokine 74 (2), 237-246, 2015
322015
Autoinflammatory mutation in NLRC4 reveals a leucine-rich repeat (LRR)–LRR oligomerization interface
F Moghaddas, P Zeng, Y Zhang, H Schützle, S Brenner, SR Hofmann, ...
Journal of Allergy and Clinical Immunology 142 (6), 1956-1967. e6, 2018
312018
Posttranslational modification as a critical determinant of cytoplasmic innate immune recognition
PJ Baker, D De Nardo, F Moghaddas, LS Tran, A Bachem, T Nguyen, ...
Physiological reviews 97 (3), 1165-1209, 2017
312017
The classification, genetic diagnosis and modelling of monogenic autoinflammatory disorders
F Moghaddas, SL Masters
Clinical Science 132 (17), 1901-1924, 2018
172018
Need for intensive care in patients admitted for asthma: red flags from the social history
F Moghaddas, C Smith, D Pilcher, R O'Hehir, M Hew, E Dabscheck
Respirology 21 (7), 1251-1254, 2016
92016
Novel genes and mechanisms in monogenic autoinflammatory disorders
FE Moghaddas
2018
Autoantibodies directed to centromere protein F in a patient with BRCA1 gene mutation
F Moghaddas, F Joshua, R Taylor, MJ Fritzler, BH Toh
BMC research notes 9 (1), 1-4, 2016
2016
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