Siri Hauge Opdal
- Senior research fellow; PhD, Dr. philos
Publications 2023
Brain water content in sudden unexpected infant death
Forensic Sci Med Pathol, 19 (4), 507-516
DOI 10.1007/s12024-023-00584-8, PubMed 36735187
Understanding the immune profile of sudden infant death syndrome - proteomic perspectives
Acta Paediatr, 113 (2), 249-255
DOI 10.1111/apa.16988, PubMed 37792385
Krybbedød
In Lærebok i rettsmedisin, Gyldendal Norsk Forlag AS, Oslo
PublikaID 502, ISBN 9788205584167
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
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, PubMed 33945852
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
CaMKII is activated in opioid induced conditioned place preference, but αCaMKII Thr286 autophosphorylation is not necessary for its establishment
Behav Brain Res, 390, 112676
DOI 10.1016/j.bbr.2020.112676, PubMed 32407818
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
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 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, PubMed 30877967
Publications 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 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, PubMed 28520217
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, PubMed 26959483
Estimation of time since death by vitreous humor hypoxanthine, potassium, and ambient temperature
Forensic Sci Int, 262, 160-5
DOI 10.1016/j.forsciint.2016.03.001, PubMed 26994446
Publications 2015
Sudden infant death syndrome and the genetics of inflammation
Front Immunol, 6, 63
DOI 10.3389/fimmu.2015.00063, PubMed 25750641
Publications 2014
Mitochondrial DNA and sudden infant death syndrome
Acta Paediatr, 103 (7), 685-6
DOI 10.1111/apa.12667, PubMed 24903445
Publications 2013
Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome
Acta Paediatr, 103 (4), 393-7
DOI 10.1111/apa.12526, PubMed 24286237
Publications 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 2011
The brain-derived neutrophic factor val66met polymorphism and sudden unexpected infant death
Acta Paediatr, 100 (1), 86-9
DOI 10.1111/j.1651-2227.2010.01960.x, PubMed 20653606
Publications 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
Gene variants predisposing to SIDS: current knowledge
Forensic Sci Med Pathol, 7 (1), 26-36
DOI 10.1007/s12024-010-9182-9, PubMed 20623341
Aquaporin-4 gene variation and sudden infant death syndrome
Pediatr Res, 68 (1), 48-51
DOI 10.1203/PDR.0b013e3181df4e7c, PubMed 20351659
Publications 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
TNF-alpha promoter polymorphisms in sudden infant death
Hum Immunol, 69 (6), 368-73
DOI 10.1016/j.humimm.2008.04.006, PubMed 18571009
Serotonin transporter gene variation in sudden infant death syndrome
Acta Paediatr, 97 (7), 861-5
DOI 10.1111/j.1651-2227.2008.00813.x, PubMed 18477062
Surfactant protein A and D gene polymorphisms and protein expression in victims of sudden infant death
Acta Paediatr, 98 (1), 62-8
DOI 10.1111/j.1651-2227.2008.01090.x, PubMed 18983439
Publications 2007
A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome
Acta Paediatr, 96 (2), 206-10
DOI 10.1111/j.1651-2227.2007.00022.x, PubMed 17429906
The IL6 -174G/C polymorphism and sudden infant death syndrome
Hum Immunol, 68 (6), 541-3
DOI 10.1016/j.humimm.2007.02.008, PubMed 17509454
Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome
Acta Paediatr, 96 (2), 211-4
DOI 10.1111/j.1651-2227.2007.00085.x, PubMed 17429907
Publications 2006
Sudden infant death syndrome (SIDS)--standardised investigations and classification: recommendations
Forensic Sci Int, 165 (2-3), 129-43
DOI 10.1016/j.forsciint.2006.05.028, PubMed 16806765
Publications 2004
IL-10 gene polymorphisms in infectious disease and SIDS
FEMS Immunol Med Microbiol, 42 (1), 48-52
DOI 10.1016/j.femsim.2004.06.006, PubMed 15325397
New insight into sudden infant-death syndrome
Lancet, 364 (9437), 825-6
DOI 10.1016/S0140-6736(04)16998-5, PubMed 15351175
The sudden infant death syndrome gene: does it exist?
Pediatrics, 114 (4), e506-12
DOI 10.1542/peds.2004-0683, PubMed 15466077
Publications 2003
IL-10 gene polymorphisms are associated with infectious cause of sudden infant death
Hum Immunol, 64 (12), 1183-9
DOI 10.1016/j.humimm.2003.08.359, PubMed 14630401
Publications 2002
Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?
Acta Paediatr, 91 (10), 1060-4
DOI 10.1080/080352502760311557, PubMed 12434891
Possible role of mtDNA mutations in sudden infant death
Pediatr Neurol, 27 (1), 23-9
DOI 10.1016/s0887-8994(02)00384-3, PubMed 12160969
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 1999
Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome
Acta Paediatr, 88 (9), 957-60
DOI 10.1080/08035259950168441, PubMed 10519336
The complement component C4 in sudden infant death
Eur J Pediatr, 158 (3), 210-2
DOI 10.1007/s004310051051, PubMed 10094440
Publications 1998
Objective measurements of nicotine exposure in victims of sudden infant death syndrome and in other unexpected child deaths
J Pediatr, 133 (2), 232-6
DOI 10.1016/s0022-3476(98)70225-2, PubMed 9709711
Hypoxanthine levels in vitreous humor: a study of influencing factors in sudden infant death syndrome
Pediatr Res, 44 (2), 192-6
DOI 10.1203/00006450-199808000-00009, PubMed 9702913
Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome
Acta Paediatr, 87 (10), 1039-44
DOI 10.1080/080352598750031347, PubMed 9825969
SIDS--changes in the epidemiological pattern in eastern Norway 1984-1996
Forensic Sci Int, 93 (2-3), 155-66
DOI 10.1016/s0379-0738(98)00048-6, PubMed 9717266
Publications 1995
Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?
Eur J Pediatr, 154 (2), 166-7
DOI 10.1007/BF01991929, PubMed 7720752
Publications 1994
Genteknologiske og immunologiske studier hos barn som døri krybbedød
[S.H. Opdal], Oslo, 87 bl.
BIBSYS 940119250
Is partial deletion of the complement C4 genes associated with sudden infant death?
Eur J Pediatr, 153 (4), 287-90
DOI 10.1007/BF01954522, PubMed 8194566
Vitreous humor hypoxanthine levels in SIDS and infectious death
Acta Paediatr, 83 (6), 634-9
DOI 10.1111/j.1651-2227.1994.tb13096.x, PubMed 7919762