Merja Helminen - Concepedia

Author

Merja Helminen

Tampere University Hospital

Also Known As

M E Helminen, M HELMINEN, M Helminen, M. E. Helminen, M. Helminen, MERJA HELMINEN, Merja Helminen, Merja E. Helminen

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Tampere University Hospital Tampere University Seinäjoki University of Applied Sciences University of Turku

About

Merja Helminen is an author at Tampere University Hospital specializing in medicine, immunology, and autoimmunity.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	17	1.2K
2	Health Sciences	2	2	132
3	Education	1	1	114
4	Engineering	1	1	51
5	Social Sciences	1	1	121

Merja Helminen

Publications

Citations

H-Index

Page 1

	Year	Citations
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections Kerry Dobbs, Cecilia Domínguez Conde, Shen‐Ying Zhang, New England Journal of Medicine Lymphocyte DevelopmentAdaptive Immune SystemImmunodeficienciesCellular ImmunologyImmunology	2015	194
Increased Plasma Levels of Pro‐ and Anti‐inflammatory Cytokines in Patients with Febrile Seizures Miia Virta, Mikko Hurme, Merja Helminen Epilepsia	2002	188
Polymorphism of the Interleukin‐10 Gene Is Associated with Susceptibility to Epstein‐Barr Virus Infection Merja Helminen, Nina Lahdenpohja, Mikko Hurme The Journal of Infectious Diseases	1999	146
Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases René Martin Linka, Sarah L. Risse, K. Bienemann, Leukemia Primary ImmunodeficiencyImmunologyEbv-associated Lymphoproliferative DiseasesPathologyAutoimmunity	2012	132
Reactive Oxygen Species Deficiency Induces Autoimmunity with Type 1 Interferon Signature Tiina Kelkka, Deborah Kienhöfer, Markus Hoffmann, Antioxidants and Redox Signaling	2014	127
Increased frequency of interleukin-1β (−511) allele 2 in febrile seizures Miia Virta, Mikko Hurme, Merja Helminen Pediatric Neurology Molecular NeuroscienceMedicineFebrile SeizuresNeurologyNeuroscience	2002	121
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, Journal of Allergy and Clinical Immunology Autoimmune DiseaseGenetic DisorderMedicineGeneticsImmunologic Phenotype	2020	120
Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes Meri Kaustio, Emma Haapaniemi, Helka Göös, Journal of Allergy and Clinical Immunology Genome InstabilityImmunogeneticsGeneticsImmunologyNfkb1 Lead	2017	118
Susceptibility to Primary Epstein‐Barr Virus Infection Is Associated with Interleukin‐10 Gene Promoter Polymorphism Merja Helminen, Sanna Kilpinen, Miia Virta, The Journal of Infectious Diseases	2001	114
Preschool asthma after bronchiolitis in infancy Petri Koponen, Merja Helminen, Marita Paassilta, European Respiratory Journal AsthmaViral DiagnosticsRespiratory ComplicationsPediatric Lung DiseaseEducation	2011	114

Page 1