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Influence from genetic variability on opioid use for cancer pain: A European genetic association study of 2294 cancer pain patients

Pain (Amsterdam), 2011-05, Vol.152 (5), p.1139-1145

2011

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Time dynamics of autoantibodies are coupled to phenotypes and add to the heterogeneity of autoimmune diabetes in adults: the HUNT study, Norway

Diabetologia, 2012-05, Vol.55 (5), p.1310-1318

2012

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The causal role of smoking on the risk of headache. A Mendelian randomization analysis in the HUNT study

European journal of neurology, 2018-09, Vol.25 (9), p.1148-e102

2018

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The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study

Psychological medicine, 2013-04, Vol.43 (4), p.711-719

2013

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Genetic variability and clinical efficacy of morphine

Acta anaesthesiologica Scandinavica, 2005-08, Vol.49 (7), p.902-908

2005

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The 118 A > G polymorphism in the human µ-opioid receptor gene may increase morphine requirements in patients with pain caused by malignant disease

Acta anaesthesiologica Scandinavica, 2004-11, Vol.48 (10), p.1232-1239

2004

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The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT Study

Osteoarthritis and cartilage, 2017-06, Vol.25 (6), p.817-823

2017

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The rare Arg181Cys mutation in the μ opioid receptor can abolish opioid responses

Acta anaesthesiologica Scandinavica, 2016-09, Vol.60 (8), p.1084-1091

2016

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Nociceptive stimuli responses at different levels of general anaesthesia and genetic variability

Acta anaesthesiologica Scandinavica, 2013-01, Vol.57 (1), p.89-99

2013

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Variable response to opioid treatment: any genetic predictors within sight?

Palliative medicine, 2008-06, Vol.22 (4), p.310-327

2008

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A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)

Molecular human reproduction, 2011-07, Vol.17 (7), p.439-446

2011

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The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis. a mendelian randomization analysis of the nord-trØndelag health study

Osteoarthritis and cartilage, 2017-04, Vol.25, p.S181-S182

2017

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MON-PP096: Changes in Plasma Levels of Omega-3 Pufas in Response to Supplementation with Omega-3 Pufa-Enriched Oral Nutritional Supplements in Advanced Cancer Patients

Clinical nutrition (Edinburgh, Scotland), 2015-09, Vol.34, p.S163-S163

2015

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Is there a genetic cause for cancer cachexia? - a clinical validation study in 1797 patients

British journal of cancer, 2011-10, Vol.105 (8), p.1244-1251

2011

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Genetic clustering of European cancer patients indicates that opioid-mediated pain relief is independent of ancestry

The pharmacogenomics journal, 2012-10, Vol.12 (5), p.412-416

2012

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Nuclear and mitochondrial uracil-DNA glycosylases are generated by alternative splicing and transcription from different positions in the UNG gene

Nucleic acids research, 1997-02, Vol.25 (4), p.750-755

1997

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The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study

Journal of headache and pain, 2006-04, Vol.7 (2), p.70-74

2006

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Variation in the COMT gene: implications for pain perception and pain treatment

Pharmacogenomics, 2009-04, Vol.10 (4), p.669-684

2009

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Regulation of expression of nuclear and mitochondrial forms of human uracil-DNA glycosylase

Nucleic acids research, 1998-03, Vol.26 (6), p.1449-1457

1998

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The Val158Met polymorphism of the human catechol -O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients

Pain (Amsterdam), 2005-07, Vol.116 (1), p.73-78

2005

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Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids

European journal of cancer (1990), 2011-07, Vol.47 (11), p.1682-1691

2011

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Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA

Nature (London), 2003-02, Vol.421 (6925), p.859-863

2003

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A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity

Clinical pharmacology and therapeutics, 2004-03, Vol.75 (3), p.223-233

2004

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hUNG2 Is the Major Repair Enzyme for Removal of Uracil from U:A Matches, U:G Mismatches, and U in Single-stranded DNA, with hSMUG1 as a Broad Specificity Backup

The Journal of biological chemistry, 2002-10, Vol.277 (42), p.39926-39936

2002

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Base excision repair of DNA in mammalian cells

FEBS Letters, 2000-06, Vol.476 (1), p.73-77

2000

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Influence from genetic variability on opioid use for cancer pain: A European genetic association study of 2294 cancer pain patients

Time dynamics of autoantibodies are coupled to phenotypes and add to the heterogeneity of autoimmune diabetes in adults: the HUNT study, Norway

The causal role of smoking on the risk of headache. A Mendelian randomization analysis in the HUNT study

The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study

Genetic variability and clinical efficacy of morphine

The 118 A > G polymorphism in the human µ-opioid receptor gene may increase morphine requirements in patients with pain caused by malignant disease

The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT Study

The rare Arg181Cys mutation in the μ opioid receptor can abolish opioid responses

Nociceptive stimuli responses at different levels of general anaesthesia and genetic variability

Variable response to opioid treatment: any genetic predictors within sight?

A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)

The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis. a mendelian randomization analysis of the nord-trØndelag health study

MON-PP096: Changes in Plasma Levels of Omega-3 Pufas in Response to Supplementation with Omega-3 Pufa-Enriched Oral Nutritional Supplements in Advanced Cancer Patients

Is there a genetic cause for cancer cachexia? - a clinical validation study in 1797 patients

Genetic clustering of European cancer patients indicates that opioid-mediated pain relief is independent of ancestry

Nuclear and mitochondrial uracil-DNA glycosylases are generated by alternative splicing and transcription from different positions in the UNG gene

The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study

Variation in the COMT gene: implications for pain perception and pain treatment

Regulation of expression of nuclear and mitochondrial forms of human uracil-DNA glycosylase

The Val158Met polymorphism of the human catechol -O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients

Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids

Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA

A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity

hUNG2 Is the Major Repair Enzyme for Removal of Uracil from U:A Matches, U:G Mismatches, and U in Single-stranded DNA, with hSMUG1 as a Broad Specificity Backup

Base excision repair of DNA in mammalian cells

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