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List of works by Mikko Seppänen

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Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease

scientific article
The evolution of cellular deficiency in GATA2 mutation

scientific article published on 17 December 2013
Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

scientific article
TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk

scientific article
Dermatologic Features of ADA2 Deficiency in Cutaneous Polyarteritis Nodosa

scientific article published in July 2015
Mannose-binding lectin 2 gene polymorphism in recurrent herpes simplex virus 2 infection

scientific article published on 4 February 2009
Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes

scientific article published on 20 January 2017
Complement C4 deficiency and HLA homozygosity in patients with frequent intraoral herpes simplex virus type 1 infections

scientific article published on 26 September 2001
Serum complement C3/C4 ratio, a novel marker for recurrent cardiovascular events

scientific article
Immunoglobulins and complement factor C4 in adult rhinosinusitis

scientific article published on 01 August 2006
Rhinovirus/enterovirus RNA in tonsillar tissue of children with tonsillar disease

scientific article published on 8 November 2005
Subtly impaired humoral immunity predisposes to frequently recurring genital herpes simplex virus type 2 infection and herpetic neuralgia

scientific article published on 24 July 2006
Proinflammatory HLA-DRB1*01-haplotype predisposes to ST-elevation myocardial infarction

scientific article published on 20 January 2012
Human MHC region harbors both susceptibility and protective haplotypes for coronary artery disease

scientific article published on 01 January 2007
HLA-DRB1 allele frequencies and C4 copy number variation in Finnish sarcoidosis patients and associations with disease prognosis

scientific article published on 23 October 2011
Major histocompatibility complex class II and BTNL2 associations in sarcoidosis

scientific article published in August 2013
Changes in brain function and morphology in patients with recurring herpes simplex virus infections and chronic pain

scientific article published on 15 May 2009
Copy number analysis of complement C4A, C4B and C4A silencing mutation by real-time quantitative polymerase chain reaction

scientific article
ADA2 deficiency: clonal lymphoproliferation in a subset of patients

scientific article published on 29 January 2018
Terminal deletion of 11q with significant late-onset combined immune deficiency

scientific article
Recurrent lymphocytic meningitis positive for herpes simplex virus type 2.

scientific article published on July 2009
Occurrence of human bocaviruses and parvovirus 4 in solid tissues

scientific article published in August 2012
Is there a need to redefine the diagnostic criteria for common variable immunodeficiency?

scientific article published on 10 December 2013
C4A deficiency in children and adolescents with recurrent respiratory infections

scientific article published on 26 February 2012
Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland

scientific article published on 28 September 2017
Inhibition of rubella virus replication by the broad-spectrum drug nitazoxanide in cell culture and in a patient with a primary immune deficiency

scientific article published on 30 September 2017
Complement and C4 Null Alleles in Severe Chronic Adult Periodontitis

scientific article published on 01 February 2007
Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

scientific article published on 04 May 2016
Widespread unilateral pain associated with herpes simplex virus infections

scientific article published on 15 April 2008
HLA-DRB1*01 allele and low plasma immunoglobulin G1 concentration may predispose to herpes-associated recurrent lymphocytic meningitis

scientific article
Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

scientific article published on 19 March 2019
Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia

scientific article published on 8 March 2017
SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations

scientific article published on 19 April 2017
Complement C4 deficiency--a plausible risk factor for non-tuberculous mycobacteria (NTM) infection in apparently immunocompetent patients

scientific article
X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world

scientific article published on 22 March 2019
Myiasis during adventure sports race

scientific article published in January 2004
Diversity of extended HLA-DRB1 haplotypes in the Finnish population

scientific article
Binding of complement regulators factor H and C4b binding protein to group A streptococcal strains isolated from tonsillar tissue and blood

scientific article published on 16 April 2008
Genetic variation in schlafen genes in a patient with a recapitulation of the murine Elektra phenotype

article
Lymphotoxin alpha LTA+496C allele is a risk factor for periodontitis in patients with coronary artery disease

scientific article
A High Prevalence of Gastrointestinal Manifestations in Common Variable Immunodeficiency

scientific article published on 01 April 2019
Peripheral hypertrophic subepithelial corneal degeneration: characterization, treatment and association with human leucocyte antigen genes

scientific article published on 7 February 2013
Emerging Infections and Pertinent Infections Related to Travel for Patients with Primary Immunodeficiencies.

scientific article published on 7 August 2017
Echovirus type 4 as a probable cause of meningitis associated with bilateral optic neuritis: a case report

scientific article published in March 2004
Haploinsufficiency of A20 impairs protein-protein interactome and leads into caspase-8-dependent enhancement of NLRP3 inflammasome activation

scientific article published on 17 October 2018
Primary immunodeficiency associated with chromosomal aberration - an ESID survey

scientific article published on 02 August 2016
Association of Chlamydia pneumoniae infection with HLA-B*35 in patients with coronary artery disease

scientific article
Novel DSP Spectrin 6 Region Variant Causes Neonatal Erythroderma, Failure to Thrive, Severe Herpes Simplex Infections and Brain Lesions

scientific article published on 01 July 2019
Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease

scientific article published on 27 June 2019
Immunoglobulin G treatment of secondary immunodeficiencies in the era of novel therapies

scientific article published on December 1, 2014

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