Publications 2020

Ferrante L, Opdal SH, Nygaard V (2020)
No association to sudden infant death syndrome detected by targeted amplicon sequencing of 24 genes
Acta Paediatr, 109 (12), 2636-2640
DOI 10.1111/apa.15295, PubMed 32271962

Ferrante L, Opdal SH, Nygård S, Vege Å, Rognum TO (2020)
Gene expression profile in cases of infectious death in infancy
Pediatr Res
DOI 10.1038/s41390-020-0896-4, PubMed 32299088

Publications 2018

Bjørnvall CD, Opdal SH, Rognum TO, Ferrante L (2018)
Polymorphisms in the myeloid differentiation primary response 88 pathway do not explain low expression levels in sudden infant death syndrome
Acta Paediatr, 108 (7), 1262-1266
DOI 10.1111/apa.14696, PubMed 30550627

Publications 2016

Ferrante L, Rognum TO, Vege Å, Nygård S, Opdal SH (2016)
Altered gene expression and possible immunodeficiency in cases of sudden infant death syndrome
Pediatr Res, 80 (1), 77-84
DOI 10.1038/pr.2016.45, PubMed 26959483

Publications 2015

Ferrante L, Opdal SH (2015)
Sudden infant death syndrome and the genetics of inflammation
Front Immunol, 6, 63
DOI 10.3389/fimmu.2015.00063, PubMed 25750641

Publications 2012

Ferrante L, Opdal SH, Vege A, Rognum TO (2012)
Is there any correlation between HLA-DR expression in laryngeal mucosa and interleukin gene variation in sudden infant death syndrome?
Acta Paediatr, 102 (3), 308-13
DOI 10.1111/apa.12107, PubMed 23186119

Publications 2010

Ferrante L, Opdal SH, Vege A, Rognum TO (2010)
IL-1 gene cluster polymorphisms and sudden infant death syndrome
Hum Immunol, 71 (4), 402-6
DOI 10.1016/j.humimm.2010.01.011, PubMed 20080142

Publications 2008

Ferrante L, Opdal SH, Vege A, Rognum TO (2008)
TNF-alpha promoter polymorphisms in sudden infant death
Hum Immunol, 69 (6), 368-73
DOI 10.1016/j.humimm.2008.04.006, PubMed 18571009