| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.
|
Nature
|
2008
|
16.10
|
|
2
|
Lung cancer susceptibility locus at 5p15.33.
|
Nat Genet
|
2008
|
5.99
|
|
3
|
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
|
Am J Hum Genet
|
2009
|
5.62
|
|
4
|
Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA.
|
Nature
|
2003
|
5.49
|
|
5
|
Investigation of the fine structure of European populations with applications to disease association studies.
|
Eur J Hum Genet
|
2008
|
3.65
|
|
6
|
CUBN is a gene locus for albuminuria.
|
J Am Soc Nephrol
|
2011
|
2.70
|
|
7
|
Low copy number DNA template can render polymerase chain reaction error prone in a sequence-dependent manner.
|
J Mol Diagn
|
2005
|
2.66
|
|
8
|
The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study.
|
J Headache Pain
|
2006
|
2.27
|
|
9
|
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.
|
J Biol Chem
|
2002
|
2.18
|
|
10
|
The Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients.
|
Pain
|
2005
|
2.00
|
|
11
|
Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals.
|
Int J Epidemiol
|
2009
|
1.97
|
|
12
|
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
|
Hum Mol Genet
|
2012
|
1.77
|
|
13
|
Exploring joint effects of genes and the clinical efficacy of morphine for cancer pain: OPRM1 and COMT gene.
|
Pain
|
2006
|
1.72
|
|
14
|
Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.
|
Mol Pain
|
2008
|
1.41
|
|
15
|
A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity.
|
Clin Pharmacol Ther
|
2004
|
1.39
|
|
16
|
Health care providers underestimate symptom intensities of cancer patients: a multicenter European study.
|
Health Qual Life Outcomes
|
2010
|
1.34
|
|
17
|
Variation in the COMT gene: implications for pain perception and pain treatment.
|
Pharmacogenomics
|
2009
|
1.07
|
|
18
|
Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium.
|
Carcinogenesis
|
2012
|
1.05
|
|
19
|
Morphine glucuronide-to-morphine plasma ratios are unaffected by the UGT2B7 H268Y and UGT1A1*28 polymorphisms in cancer patients on chronic morphine therapy.
|
Eur J Clin Pharmacol
|
2002
|
1.04
|
|
20
|
Clinical and genetic factors associated with nausea and vomiting in cancer patients receiving opioids.
|
Eur J Cancer
|
2011
|
1.01
|
|
21
|
No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT study.
|
BMC Musculoskelet Disord
|
2006
|
0.98
|
|
22
|
High systolic blood pressure is associated with Val/Val genotype in the catechol-o-methyltransferase gene. The Nord-Trøndelag Health Study (HUNT).
|
Am J Hypertens
|
2007
|
0.98
|
|
23
|
Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.
|
PLoS Genet
|
2011
|
0.94
|
|
24
|
Genetic heterogeneity in latent autoimmune diabetes is linked to various degrees of autoimmune activity: results from the Nord-Trøndelag Health Study.
|
Diabetes
|
2009
|
0.92
|
|
25
|
Identification of possible genetic polymorphisms involved in cancer cachexia: a systematic review.
|
J Genet
|
2011
|
0.90
|
|
26
|
Genetic analysis of the murine mu opioid receptor: increased complexity of Oprm gene splicing.
|
J Mol Med (Berl)
|
2004
|
0.89
|
|
27
|
P-selectin genotype is associated with the development of cancer cachexia.
|
EMBO Mol Med
|
2012
|
0.89
|
|
28
|
Multiple Loci modulate opioid therapy response for cancer pain.
|
Clin Cancer Res
|
2011
|
0.86
|
|
29
|
Association between a 15q25 gene variant, nicotine-related habits, lung cancer and COPD among 56,307 individuals from the HUNT study in Norway.
|
Eur J Hum Genet
|
2013
|
0.85
|
|
30
|
Induction of uncoupling protein 2 mRNA in beta-cells is stimulated by oxidation of fatty acids but not by nutrient oversupply.
|
Endocrinology
|
2002
|
0.83
|
|
31
|
Depression and anxiety in relation to catechol-O-methyltransferase Val158Met genotype in the general population: the Nord-Trøndelag Health Study (HUNT).
|
BMC Psychiatry
|
2008
|
0.82
|
|
32
|
The impact of the catechol-O-methyltransferase Val158Met polymorphism on survival in the general population--the HUNT study.
|
BMC Med Genet
|
2007
|
0.81
|
|
33
|
Is there a genetic cause of appetite loss?-an explorative study in 1,853 cancer patients.
|
J Cachexia Sarcopenia Muscle
|
2012
|
0.79
|
|
34
|
Overexpression of transcription factor AP-2 stimulates the PA promoter of the human uracil-DNA glycosylase (UNG) gene through a mechanism involving derepression.
|
DNA Repair (Amst)
|
2009
|
0.78
|
|
35
|
[Genetic variation-- important for the clinical effect of opioids?].
|
Tidsskr Nor Laegeforen
|
2005
|
0.77
|
|
36
|
Prevalence of ZnT8 antibody in relation to phenotype and SLC30A8 polymorphism in adult autoimmune diabetes: results from the HUNT study, Norway.
|
Autoimmunity
|
2012
|
0.77
|
|
37
|
The N-terminally truncated µ3 and µ3-like opioid receptors are transcribed from a novel promoter upstream of exon 2 in the human OPRM1 gene.
|
PLoS One
|
2013
|
0.77
|
|
38
|
Lack of association between genetic variability and multiple pain-related outcomes in a large cohort of patients with advanced cancer: the European Pharmacogenetic Opioid Study (EPOS).
|
BMJ Support Palliat Care
|
2012
|
0.76
|
|
39
|
Transepithelial transport of morphine and mannitol in Caco-2 cells: the influence of chitosans of different molecular weights and degrees of acetylation.
|
J Pharm Pharmacol
|
2006
|
0.76
|
|
40
|
Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
|
Nat Genet
|
2017
|
0.75
|
|
41
|
COMT genotypes and use of antipsychotic medication: linking population-based prescription database to the HUNT study.
|
Pharmacoepidemiol Drug Saf
|
2008
|
0.75
|
|
42
|
Genetic findings related to pain and analgesics-why are they so inconsistent?
|
Pain
|
2016
|
0.75
|
|
43
|
Marked over expression of uncoupling protein-2 in beta cells exerts minor effects on mitochondrial metabolism.
|
Biochem Biophys Res Commun
|
2012
|
0.75
|
|
44
|
Variability in UDP-glucuronosyltransferase genes and morphine metabolism: observations from a cross-sectional multicenter study in advanced cancer patients with pain.
|
Pharmacogenet Genomics
|
2013
|
0.75
|
|
45
|
OP006. A preeclampsia genome-wide linkage scan in norwegian families.
|
Pregnancy Hypertens
|
2013
|
0.75
|
|
46
|
A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.
|
Am J Hum Genet
|
2011
|
0.75
|