Seza Özen - Concepedia

Author

Seza Özen

Also Known As

E Cortis, Ebru Cengel Kultur, Elizabeth D. Mellins, Eurofever and Eurotraps Projects, F Shahram, Faysal Gok, Hagen, E. C., Irama Maldonado, J Kuemmerle-Deschner, Montealegre Sanchez, Gina A.

685

Publications

30.3K

Citations

H-Index

175

Concepts

All Affiliations

Hacettepe University Istituto Giannina Gaslini University College London University Medical Center Utrecht Istanbul University

SÖ

About

Seza Özen is an author at Hacettepe University specializing in medicine, pathology, and autoimmune disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	72	5.7K
2	Public Health	11	12	801
3	Health Sciences	4	4	218
4	Arts	1	1	11
5	Education	1	1	88

Seza Özen

208

Publications

22.1K

Citations

H-Index

Page 1

	Year	Citations
EULAR/PRINTO/PRES criteria for Henoch–Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria Seza Özen, Angela Pistorio, S. M. Iusan, Annals of the Rheumatic Diseases	2010	1.4K
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing Murim Choi, Ute I. Scholl, Weizhen Ji, Proceedings of the National Academy of Sciences	2009	1.3K
Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 Qing Zhou, Dan Yang, Amanda K. Ombrello, New England Journal of Medicine	2014	871
EULAR/PReS endorsed consensus criteria for the classification of childhood vasculitides Seza Özen Annals of the Rheumatic Diseases	2005	831
2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative Angelo Ravelli, Francesca Minoia, Sergio Davì, Arthritis & Rheumatology	2015	742
Two Randomized Trials of Canakinumab in Systemic Juvenile Idiopathic Arthritis Nicolino Ruperto, Hermine I. Brunner, Pierre Quartier, New England Journal of Medicine	2012	689
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness Fiona E. Karet, Karin E. Finberg, Raoul D. Nelson, Nature Genetics Renal FunctionMolecular PhysiologyBiochemistrySodium HomeostasisPhysiology	1999	681
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease Qing Zhou, Hongying Wang, Daniella M. Schwartz, Nature Genetics InflammationRheumatologyA20 Haploinsufficiency CauseAutoimmune DiseaseAutoantibody Production	2015	601
EULAR recommendations for the management of familial Mediterranean fever Seza Özen, Erkan Demirkaya, Burak Erer, Annals of the Rheumatic Diseases	2016	578
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies Gina A. Montealegre Sanchez, Adam Reinhardt, Suzanne Ramsey, Journal of Clinical Investigation	2018	496

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