Sanna Seitsonen
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View article: Natural history and biomarkers of retinal dystrophy caused by the biallelic <i>TULP1</i> variant c.148delG
Natural history and biomarkers of retinal dystrophy caused by the biallelic <i>TULP1</i> variant c.148delG Open
Purpose To report clinical features and potential disease markers of inherited retinal dystrophy (IRD) caused by the biallelic c.148delG variant in the tubby‐like protein 1 ( TULP1 ) gene. Methods A retrospective observational study of 16 …
View article: Military supply, everyday demand, and reindeer: Zooarchaeology of Nazi German Second World War military presence in Finnish Lapland, Northernmost Europe
Military supply, everyday demand, and reindeer: Zooarchaeology of Nazi German Second World War military presence in Finnish Lapland, Northernmost Europe Open
During the Second World War, in 1941–1944, Nazi German troops held the frontal responsibility of the Arctic front in Finnish Lapland. In this paper, we present the first zooarchaeological study of the wartime faunal remains from German mil…
View article: Susacin oireyhtymä: silmänpohjan, sisäkorvan ja aivojen pienten valtimoiden tulehdussairaus
Susacin oireyhtymä: silmänpohjan, sisäkorvan ja aivojen pienten valtimoiden tulehdussairaus Open
View article: Interleukin-8 production by cells in peripheral blood is associated with age-related macular degeneration lesion activity during anti-VEGF treatment and with variants of the interleukin-8 gene
Interleukin-8 production by cells in peripheral blood is associated with age-related macular degeneration lesion activity during anti-VEGF treatment and with variants of the interleukin-8 gene Open
View article: A founder mutation in <i><scp>CERKL</scp></i> is a major cause of retinal dystrophy in Finland
A founder mutation in <i><span>CERKL</span></i> is a major cause of retinal dystrophy in Finland Open
Purpose To study the genetic aetiology of retinal dystrophies ( RD ) in Finnish patients. Methods A targeted next‐generation sequencing (NGS) panel of 105 retinal dystrophy genes was used in a cohort of 55 RD patients. Results The overall …
View article: A military camp in the middle of nowhere: mobilities, dislocation and the archaeology of a Second World War German military base in Finnish Lapland
A military camp in the middle of nowhere: mobilities, dislocation and the archaeology of a Second World War German military base in Finnish Lapland Open
This article discusses military mobilities and encampment, and associated themes such as dislocation and displacement of people, through the case of a Second World War German military camp in Finnish Lapland. The article describes the camp…
View article: Protective coding variants in<i>CFH</i>and<i>PELI3</i>and a variant near<i>CTRB1</i>are associated with age-related macular degeneration<sup>†</sup>
Protective coding variants in<i>CFH</i>and<i>PELI3</i>and a variant near<i>CTRB1</i>are associated with age-related macular degeneration<sup>†</sup> Open
Although numerous common age-related macular degeneration (AMD) alleles have been discovered using genome-wide association studies, substantial disease heritability remains unexplained. We sought to identify additional common and rare vari…
View article: Protective coding variants in<i>CFH</i>and<i>PELI3</i>and a variant near<i>CTRB1</i>are associated with age-related macular degeneration
Protective coding variants in<i>CFH</i>and<i>PELI3</i>and a variant near<i>CTRB1</i>are associated with age-related macular degeneration Open
Although >20 common frequency age-related macular degeneration (AMD) alleles have been discovered with genome-wide association studies, substantial disease heritability remains unexplained. In this study we sought to identify additional va…
View article: The genetic variant rs4073 A→T of the <i>Interleukin‐8</i> promoter region is associated with the earlier onset of exudative age‐related macular degeneration
The genetic variant rs4073 A→T of the <i>Interleukin‐8</i> promoter region is associated with the earlier onset of exudative age‐related macular degeneration Open
Purpose To study the association of the single nucleotide polymorphism ( SNP ) rs4073 in the interleukin‐8 ( IL ‐8) promoter region with the diagnosis and age of onset of exudative age‐related macular degeneration ( AMD ) in association wi…