Siri Hauge Opdal

  • Senior research fellow; PhD, Dr. philos
 

Publications 2023

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

Publications 2021

Eidahl JML, Stray-Pedersen A, Rognum TO, Opdal SH (2021)
Aquaporin 4 expression in the hippocampus in sudden infant death syndrome and sudden unexplained death in childhood
J. Chem. Neuroanat., 115, 101962
DOI 10.1016/j.jchemneu.2021.101962

Ferrante L, Opdal SH, Nygard S, Vege A, Rognum TO (2021)
Gene expression profile in cases of infectious death in infancy
Pediatr. Res., 89 (3), 483-487
DOI 10.1038/s41390-020-0896-4

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

Publications 2020

Andersen JM, Opdal SH, Muller CP, Boix F (2020)
CaMKII is activated in opioid induced conditioned place preference, but alpha CaMKII Thr286 autophosphorylation is not necessary for its establishment
Behav. Brain Res., 390, 112676
DOI 10.1016/j.bbr.2020.112676

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

Publications 2019

Bjornvall CD, Opdal SH, Rognum TO, Ferrante L (2019)
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

Eidahl JML, Opdal SH, Rognum TO, Stray-Pedersen A (2019)
Postmortem evaluation of brain edema: An attempt with measurements of water content and brain-weight-to-inner-skull-circumference ratio
J. Forensic Leg. Med., 64, 1-6
DOI 10.1016/j.jflm.2019.03.003

Publications 2017

Opdal SH, Vege A, Stray-Pedersen A, Rognum TO (2017)
The gene encoding the inwardly rectifying potassium channel Kir4.1 may be involved in sudden infant death syndrome
Acta Paediatr., 106 (9), 1474-1480
DOI 10.1111/apa.13928

Publications 2016

Ferrante L, Rognum TO, Vege A, Nygard 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

Rognum TO, Holmen S, Musse MA, Dahlberg PS, Stray-Pedersen A, Saugstad OD, Opdal SH (2016)
Estimation of time since death by vitreous humor hypoxanthine, potassium, and ambient temperature
Forensic Sci.Int., 262, 160-165
DOI 10.1016/j.forsciint.2016.03.001

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

Publications 2014

Opdal SH (2014)
Mitochondrial DNA and sudden infant death syndrome
Acta Paediatr., 103 (7), 685-686
DOI 10.1111/apa.12667

Opdal SH, Vege A, Rognum TO (2014)
Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome
Acta Paediatr., 103 (4), 393-397
DOI 10.1111/apa.12526

Publications 2013

Ferrante L, Opdal SH, Vege A, Rognum TO (2013)
Is there any correlation between HLA-DR expression in laryngeal mucosa and interleukin gene variation in sudden infant death syndrome?
Acta Paediatr., 102 (3), 308-313
DOI 10.1111/apa.12107

Publications 2011

Opdal SH, Melien O, Hynnekleiv T, Rognum TO (2011)
The brain-derived neutrophic factor val66met polymorphism and sudden unexpected infant death
Acta Paediatr., 100 (1), 86-89
DOI 10.1111/j.1651-2227.2010.01960.x

Opdal SH, Rognum TO (2011)
Gene variants predisposing to SIDS: current knowledge
Forensic Sci. Med. Pathol., 7 (1), 26-36
DOI 10.1007/s12024-010-9182-9

Publications 2010

Ferrante L, Opdal SH, Vege A, Rognum TO (2010)
Cytokine gene polymorphisms and sudden infant death syndrome
Acta Paediatr., 99 (3), 384-388
DOI 10.1111/j.1651-2227.2009.01611.x

Ferrante L, Opdal SH, Vege A, Rognum TO (2010)
IL-1 gene cluster polymorphisms and sudden infant death syndrome
Hum. Immunol., 71 (4), 402-406
DOI 10.1016/j.humimm.2010.01.011

Opdal SH, Vege A, Stray-Pedersen A, Rognum TO (2010)
Aquaporin-4 Gene Variation and Sudden Infant Death Syndrome
Pediatr. Res., 68 (1), 48-51
DOI 10.1203/PDR.0b013e3181df4e7c

Publications 2009

Stray-Pedersen A, Vege A, Opdal SH, Moberg S, Rognum TO (2009)
Surfactant protein A and D gene polymorphisms and protein expression in victims of sudden infant death
Acta Paediatr., 98 (1), 62-68
DOI 10.1111/j.1651-2227.2008.01090.x

Publications 2008

Ferrante L, Opdal SH, Vege A, Rognum TO (2008)
TNF-alpha promoter polymorphisms in sudden infant death
Hum. Immunol., 69 (6), 368-373
DOI 10.1016/j.humimm.2008.04.006

Opdal SH, Vege A, Rognum TO (2008)
Serotonin transporter gene variation in sudden infant death syndrome
Acta Paediatr., 97 (7), 861-865
DOI 10.1111/j.1651-2227.2008.00813.x

Publications 2007

Arnestad M, Opdal SH, Vege A, Rognum TO (2007)
A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome
Acta Paediatr., 96 (2), 206-210
DOI 10.1111/j.1651-2227.2007.00022.x

Bajanowski T, Vege A, Byard RW, Krous HF, Arnestad M, Bachs L, Banner J, Blair PS, Borthne A, Dettmeyer R, Fleming P, Gaustad P, Gregersen M, Grogaard J, Holter E, Isaksen CV, Jorgensen JV, de Lange C, Madea B, Moore I, Morland J, Opdal SH, Rasten-Almqvisti P, Schlaud M, Sidebotham P et al. (2007)
Sudden infant death syndrome (SIDS) - Standardised investigations and classification: Recommendations
Forensic Sci.Int., 165 (2-3), 129-143
DOI 10.1016/j.forsciint.2006.05.028

Opdal SH, Rognum TO (2007)
The IL6-174G/C polymorphism and sudden infant death syndrome
Hum. Immunol., 68 (6), 541-543
DOI 10.1016/j.humimm.2007.02.008

Opdal SH, Vege A, Arnestad M, Musse MA, Rognum TO (2007)
Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome
Acta Paediatr., 96 (2), 211-214
DOI 10.1111/j.1651-2227.2007.00085.x

Publications 2006

Opdal SH, Melien O, Rootwelt H, Vege A, Arnestad M, Rognum TO (2006)
The G protein beta 3 subunit 825C allele is associated with sudden infant death due to infection
Acta Paediatr., 95 (9), 1129-1132
DOI 10.1080/08035250600580529

Publications 2001

Opdal SH (2001)
Molecular biological and biochemical studies of sudden infant death syndrome
Department Group of Laboratory Medicine, Institute of Forensic Medicine, Rikshospitalet, University of Oslo, Oslo, 1 b. (flere pag.)
BIBSYS 012056960, ISBN 82-7633-115-7

Publications 1994

Opdal SH (1994)
Genteknologiske og immunologiske studier hos barn som døri krybbedød
[S.H. Opdal], Oslo, 87 bl.
BIBSYS 940119250