Siri Hauge Opdal
- Senior research fellow; PhD, Dr. philos
Publications 2023
Krybbedød
In Lærebok i rettsmedisin, Gyldendal Norsk Forlag AS, Oslo
PublikaID 502, ISBN 9788205584167
Publications 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
Gene expression profile in cases of infectious death in infancy
Pediatr. Res., 89 (3), 483-487
DOI 10.1038/s41390-020-0896-4
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
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
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
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
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
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
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
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
Sudden infant death syndrome and the genetics of inflammation
Front. Immunol., 6, 63
DOI 10.3389/fimmu.2015.00063
Publications 2014
Mitochondrial DNA and sudden infant death syndrome
Acta Paediatr., 103 (7), 685-686
DOI 10.1111/apa.12667
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
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
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
Gene variants predisposing to SIDS: current knowledge
Forensic Sci. Med. Pathol., 7 (1), 26-36
DOI 10.1007/s12024-010-9182-9
Publications 2010
Cytokine gene polymorphisms and sudden infant death syndrome
Acta Paediatr., 99 (3), 384-388
DOI 10.1111/j.1651-2227.2009.01611.x
IL-1 gene cluster polymorphisms and sudden infant death syndrome
Hum. Immunol., 71 (4), 402-406
DOI 10.1016/j.humimm.2010.01.011
Aquaporin-4 Gene Variation and Sudden Infant Death Syndrome
Pediatr. Res., 68 (1), 48-51
DOI 10.1203/PDR.0b013e3181df4e7c
Publications 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
TNF-alpha promoter polymorphisms in sudden infant death
Hum. Immunol., 69 (6), 368-373
DOI 10.1016/j.humimm.2008.04.006
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
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
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
The IL6-174G/C polymorphism and sudden infant death syndrome
Hum. Immunol., 68 (6), 541-543
DOI 10.1016/j.humimm.2007.02.008
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
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
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
Genteknologiske og immunologiske studier hos barn som døri krybbedød
[S.H. Opdal], Oslo, 87 bl.
BIBSYS 940119250