Linda Ferrante

  • Researcher; PhD
  • +47 230 13 117

Publications not in PubMed:

Ferrante L: Spiller arvelige variasjoner noen rolle for livstruende ubalanse i immunsystemet? Oss foreldre imellom 2006

Ferrante L: Kan en feil regulering i cytokin-nettverket medvirke til krybbedød? Oss foreldre imellom 2008.

Ferrante L: Interleukiner og krybbedød. Oss foreldre imellom 2009. 

Ferrante L: Hva kan genene avsløre om krybbedød?  Oss foreldre imellom 2013

Ferrante L: Kan genenes kommunikasjonsmønster bidra til en bedre forståelse av predisponerende genetiske faktorer ved krybbedød? Oss foreldre imellom 2015

Publications indexed in PubMed:

 

Publications 2023

Ferrante L, Opdal SH, Byard RW (2023)
Understanding the immune profile of sudden infant death syndrome - proteomic perspectives
Acta Paediatr, 113 (2), 249-255
DOI 10.1111/apa.16988, PubMed 37792385

Rognum TO, Opdal SH, Vege, Stray-Pedersen A, Ferrante L, Bøylestad L (2023)
Krybbedød
In Lærebok i rettsmedisin, Gyldendal Norsk Forlag AS, Oslo
PublikaID 502, ISBN 9788205584167

Skogvold HB, Wilson SRH, Rønning PO, Ferrante L, Opdal SH, Rognum TO, Rootwelt H, Elgstøen KBP (2023)
A global metabolomics minefield: Confounding effects of preanalytical factors when studying rare disorders
Anal Sci Adv, 4 (7-8), 255-266
DOI 10.1002/ansa.202300010, PubMed 38716308

Publications 2021

Opdal SH, Ferrante L, Rognum TO, Stray-Pedersen A (2021)
Aquaporin-1 and aquaporin-9 gene variations in sudden infant death syndrome
Int J Legal Med, 135 (3), 719-725
DOI 10.1007/s00414-020-02493-9, PubMed 33462668

Publications 2020

Ferrante L, Opdal SH, Nygård S, Vege Å, Rognum TO (2020)
Gene expression profile in cases of infectious death in infancy
Pediatr Res, 89 (3), 483-487
DOI 10.1038/s41390-020-0896-4, PubMed 32299088

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

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 2009

Ferrante L, Opdal SH, Vege A, Rognum T (2009)
Cytokine gene polymorphisms and sudden infant death syndrome
Acta Paediatr, 99 (3), 384-8
DOI 10.1111/j.1651-2227.2009.01611.x, PubMed 19958302

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

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