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Seza Ozen
Seza Ozen
Verified email at hacettepe.edu.tr
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Cited by
Cited by
Year
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
M Choi, UI Scholl, W Ji, T Liu, IR Tikhonova, P Zumbo, A Nayir, ...
Proceedings of the National Academy of Sciences 106 (45), 19096-19101, 2009
18232009
EULAR/PRINTO/PRES criteria for Henoch–Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II …
S Ozen, A Pistorio, SM Iusan, A Bakkaloglu, T Herlin, R Brik, ...
Annals of the rheumatic diseases 69 (5), 798-806, 2010
15792010
EULAR/PReS endorsed consensus criteria for the classification of childhood vasculitides
S Ozen, N Ruperto, MJ Dillon, A Bagga, K Barron, JC Davin, T Kawasaki, ...
Annals of the rheumatic diseases 65 (7), 936-941, 2006
11522006
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study
M Tunca, H Ozdogan, O Kasapcopur, F Yalcinkaya, E Tutar, R Topaloglu, ...
Medicine (Baltimore) 84 (1), 1-11, 2005
10022005
2016 classification criteria for macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a European League Against Rheumatism/American College of …
A Ravelli, F Minoia, S Davì, AC Horne, F Bovis, A Pistorio, M Aricò, ...
Arthritis & rheumatology 68 (3), 566-576, 2016
8442016
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness
FE Karet, KE Finberg, RD Nelson, A Nayir, H Mocan, SA Sanjad, ...
Nature genetics 21 (1), 84-90, 1999
8121999
Two randomized trials of canakinumab in systemic juvenile idiopathic arthritis
N Ruperto, HI Brunner, P Quartier, T Constantin, N Wulffraat, G Horneff, ...
New England Journal of Medicine 367 (25), 2396-2406, 2012
7922012
Early-onset stroke and vasculopathy associated with mutations in ADA2
Q Zhou, D Yang, AK Ombrello, AV Zavialov, C Toro, AV Zavialov, ...
New England Journal of Medicine 370 (10), 911-920, 2014
7902014
A new set of criteria for the diagnosis of familial Mediterranean fever in childhood
F Yalçınkaya, S Özen, ZB Özçakar, N Aktay, N Çakar, A Düzova, ...
Rheumatology 48 (4), 395-398, 2009
5872009
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
Q Zhou, H Wang, DM Schwartz, M Stoffels, YH Park, Y Zhang, D Yang, ...
Nature genetics 48 (1), 67-73, 2016
5472016
EULAR recommendations for the management of familial Mediterranean fever
S Ozen, E Demirkaya, B Erer, A Livneh, E Ben-Chetrit, G Giancane, ...
Annals of the rheumatic diseases 75 (4), 644-651, 2016
5432016
Mutation frequency of familial Mediterranean fever and evidence for a high carrier rate in the Turkish population
E Yilmaz, S Ozen, B Balcı, A Duzova, R Topaloglu, N Besbas, U Saatci, ...
European journal of human genetics 9 (7), 553-555, 2001
5242001
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing
AN Smith, J Skaug, KA Choate, A Nayir, A Bakkaloglu, S Ozen, SA Hulton, ...
Nature genetics 26 (1), 71-75, 2000
5202000
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations
HJ Lachmann, B Şengül, TU Yavuzşen, DR Booth, SE Booth, A Bybee, ...
Rheumatology 45 (6), 746-750, 2006
5172006
Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review
N Ter Haar, H Lachmann, S Özen, P Woo, Y Uziel, C Modesto, ...
Annals of the rheumatic diseases 72 (5), 678-685, 2013
4682013
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies
GAM Sanchez, A Reinhardt, S Ramsey, H Wittkowski, PJ Hashkes, ...
The Journal of clinical investigation 128 (7), 3041-3052, 2018
4492018
Canakinumab for the treatment of autoinflammatory recurrent fever syndromes
F De Benedetti, M Gattorno, J Anton, E Ben-Chetrit, J Frenkel, ...
New England Journal of Medicine 378 (20), 1908-1919, 2018
4372018
Clinical features, treatment, and outcome of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a multinational, multicenter study of 362 patients
F Minoia, S Davì, AC Horne, E Demirkaya, F Bovis, C Li, K Lehmberg, ...
Arthritis & rheumatology 66 (11), 3160-3169, 2014
4312014
Textbook of pediatric rheumatology
RE Petty, RM Laxer, CB Lindsley, L Wedderburn, RC Fuhlbrigge, ...
Elsevier Health Sciences, 2020
4192020
Type I interferonopathies: a novel set of inborn errors of immunity
YJ Crow
Annals of the New York Academy of Sciences 1238 (1), 91-98, 2011
4042011
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