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Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration

PloS one, 2008-12, Vol.3 (12), p.e3833-e3833

2008

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Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein

Journal of Immunology, 2007-03, Vol.178 (6), p.3831-3836

2007

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The IL-8 , VEGF , and CFH Polymorphisms and Bevacizumab in Age-related Macular Degeneration

Ophthalmology (Rochester, Minn.), 2014-04, Vol.121 (4), p.973-974.e2

2014

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Vascular Endothelial Growth Factor Gene Variation and the Response to Photodynamic Therapy in Age-Related Macular Degeneration

Ophthalmology (Rochester, Minn.), 2010, Vol.117 (1), p.103-108

2010

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Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration

Retina (Philadelphia, Pa.), 2013-10, Vol.33 (9), p.1815

2013

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Complement factor H Y402H polymorphism and characteristics of exudative age‐related macular degeneration lesions

Acta ophthalmologica (Oxford, England), 2008-06, Vol.86 (4), p.390-394

2008

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A founder mutation in CERKL is a major cause of retinal dystrophy in Finland

Acta ophthalmologica (Oxford, England), 2018-03, Vol.96 (2), p.183-191

2018

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Military supply, everyday demand, and reindeer: Zooarchaeology of Nazi German Second World War military presence in Finnish Lapland, Northernmost Europe

International journal of osteoarchaeology, 2022-01, Vol.32 (1), p.3-17

2022

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Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

Acta ophthalmologica (Oxford, England), 2023-03, Vol.101 (2), p.215-221

2023

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Burnt bones by Europe's largest lake: Zooarchaeology of the Stone Age and Early Metal period hunter-gatherers at Lake Ladoga, NW Russia

Journal of archaeological science, reports, 2017-02, Vol.11, p.131-146

2017

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Leucocyte telomere length in age‐related macular degeneration

Acta ophthalmologica (Oxford, England), 2013-08, Vol.91 (5), p.453-456

2013

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Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish population

Neuroscience letters, 2012-04, Vol.513 (2), p.233-237

2012

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Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration

Human molecular genetics, 2016-12, Vol.25 (23), p.5276-5285

2016

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Genetic findings in over 600 individuals with inherited retinal disorders in Finland

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

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A military camp in the middle of nowhere: mobilities, dislocation and the archaeology of a Second World War German military base in Finnish Lapland

Journal of conflict archaeology, 2017-01, Vol.12 (1), p.3-28

2017

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The genetic variant rs4073 A→T of the Interleukin‐8 promoter region is associated with the earlier onset of exudative age‐related macular degeneration

Acta ophthalmologica (Oxford, England), 2015-12, Vol.93 (8), p.726-733

2015

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Lack of Complement Inhibitors in the Outer Intracranial Artery Aneurysm Wall Associates with Complement Terminal Pathway Activation

The American journal of pathology, 2010-12, Vol.177 (6), p.3224-3232

2010

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The genetic variant rs4073 A arrow right T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration

Acta ophthalmologica (Oxford, England), 2015-12, Vol.93 (8), p.726-733

2015

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Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: Characterization, ethnic distribution and evolutionary implications

Annals of medicine (Helsinki), 2006, Vol.38 (8), p.592-604

2006

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A Novel Mutation W388X Underlying Properdin Deficiency in a Finnish Family

Scandinavian journal of immunology, 2012-04, Vol.75 (4), p.445-448

2012

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The effect of complement factor H Y402H polymorphism on the outcome of photodynamic therapy in age-related macular degeneration

European journal of ophthalmology, 2007-11, Vol.17 (6), p.943-949

2007

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Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population

Molecular vision, 2006-07, Vol.12, p.796-801

2006

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Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration

Molecular vision, 2009-04, Vol.15, p.762-770

2009

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Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein1

The Journal of immunology (1950), 2007-03, Vol.178 (6), p.3831-3836

2007

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Pathogenesis of age-related macular degeneration: Disrupted binding of complement factor H to C-reactive protein

Molecular immunology, 2007, Vol.44 (1), p.202-202

2007

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Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration

Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein

The IL-8 , VEGF , and CFH Polymorphisms and Bevacizumab in Age-related Macular Degeneration

Vascular Endothelial Growth Factor Gene Variation and the Response to Photodynamic Therapy in Age-Related Macular Degeneration

Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration

Complement factor H Y402H polymorphism and characteristics of exudative age‐related macular degeneration lesions

A founder mutation in CERKL is a major cause of retinal dystrophy in Finland

Military supply, everyday demand, and reindeer: Zooarchaeology of Nazi German Second World War military presence in Finnish Lapland, Northernmost Europe

Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

Burnt bones by Europe's largest lake: Zooarchaeology of the Stone Age and Early Metal period hunter-gatherers at Lake Ladoga, NW Russia

Leucocyte telomere length in age‐related macular degeneration

Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish population

Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration

Genetic findings in over 600 individuals with inherited retinal disorders in Finland

A military camp in the middle of nowhere: mobilities, dislocation and the archaeology of a Second World War German military base in Finnish Lapland

The genetic variant rs4073 A→T of the Interleukin‐8 promoter region is associated with the earlier onset of exudative age‐related macular degeneration

Lack of Complement Inhibitors in the Outer Intracranial Artery Aneurysm Wall Associates with Complement Terminal Pathway Activation

The genetic variant rs4073 A arrow right T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: Characterization, ethnic distribution and evolutionary implications

A Novel Mutation W388X Underlying Properdin Deficiency in a Finnish Family

The effect of complement factor H Y402H polymorphism on the outcome of photodynamic therapy in age-related macular degeneration

Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population

Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration

Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein1

Pathogenesis of age-related macular degeneration: Disrupted binding of complement factor H to C-reactive protein

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