Related by context. All words. (Click for frequent words.) 83 rs# [002] 80 rs# [004] 75 #q# [001] 75 rs# [001] 74 SNP rs# [001] 74 chromosome #q# [001] 73 polymorphisms 72 DRD2 71 PTPN# 71 #p# [001] 70 chromosome #q# [002] 70 ABCB1 70 polymorphism 70 mRNA expression 70 5 HTTLPR 69 C#Y 69 GSTP1 69 SNP rs# [002] 69 haplotype 69 chromosome #p# [001] 68 single nucleotide polymorphism 68 #q# [002] 68 SNPs 68 haplotypes 68 heterozygotes 68 CDKN2A 68 GSTM1 68 IL#B 68 #p#.# [002] 67 MTHFR 67 gene polymorphisms 67 #p# [003] 67 homozygotes 67 TCF#L# 67 MLH1 67 TT genotype 66 MetS 66 gene polymorphism 66 G allele 66 variant rs# 66 homozygosity 66 apolipoprotein E 66 SLC#A# [002] 66 CC genotype 66 loci 66 intronic 66 alleles 65 allele 65 functional polymorphism 65 ESR1 65 heterozygous 65 HLA DRB1 65 proband 65 apolipoprotein E gene 65 variant alleles 65 allele frequencies 65 catechol O methyltransferase 65 ZNF# 65 dopamine transporter gene 65 DQB1 * 65 PCa 64 promoter methylation 64 VKORC1 64 HLA DRB1 SE 64 UGT#A# * 64 BRAF V#E 64 APOC3 64 homozygous 64 APOE e4 64 chromosome #p# [002] 64 IL#R 64 SLC#A# [001] 64 genetic polymorphisms 64 DRD2 gene 64 #q#.# [001] 64 allelic variants 64 tHcy 64 hypermethylation 64 heterozygosity 64 COL#A# 64 susceptibility locus 64 rs# rs# 64 lymph node metastasis 64 APOE4 64 chromosome #q 64 HLA DRB1 * 64 microdeletions 63 FGFR2 63 GSTT1 63 TRAF1 C5 63 ERBB2 63 hypermethylated 63 chromosomal regions 63 CYP#A# [002] 63 germline mutations 63 IKZF1 63 MYH9 gene 63 HDL2 63 RASSF1A 63 #q#.# [002] 63 KIF6 gene 63 apolipoprotein E APOE 63 LPA gene 63 SE alleles 63 BARD1 63 adenoma 63 TCF#L# gene 63 ribosomal protein 63 APOE ε4 63 CagA 63 clusterin 63 confidence interval #.#-#.# 63 fasting insulin 63 c KIT 63 MSH2 63 DRD4 63 susceptibility gene 63 ADRB2 63 #p#.# [001] 63 genetic variant 62 serotonin transporter gene 62 cagA 62 monozygotic twins 62 adenocarcinomas 62 caveolin 62 chromosome #p#.# 62 missense mutation 62 immunoreactivity 62 CHEK2 62 abdominal adiposity 62 prostate cancer CaP 62 GABRA2 62 gene variants 62 missense mutations 62 T2D 62 genotyped 62 nondiabetic 62 PON1 62 dysbindin 62 univariate analysis 62 APOE gene 62 K ras mutations 62 methylenetetrahydrofolate reductase 62 colorectal adenoma 62 MnSOD 62 gene locus 62 promoter polymorphism 62 genetic polymorphism 62 rheumatoid factor 62 single nucleotide polymorphisms 62 fasting glucose levels 62 ALDH2 62 NAT2 62 sporadic ALS 62 noncarriers 62 serum leptin 62 atypical hyperplasia 61 Polymorphisms 61 Ki# 61 variant allele 61 VNTR 61 CYP#C# [002] 61 genotype 61 colorectal neoplasia 61 intergenic 61 HOMA IR 61 apolipoprotein E4 61 plasma adiponectin 61 WNK1 61 HMGA1 61 allelic 61 KRAS mutations 61 activating mutations 61 chromosome #q#.# [001] 61 susceptibility loci 61 highest tertile 61 CDH1 61 cystatin C 61 linkage disequilibrium 61 PTEN mutations 61 receptor gene 61 dopamine receptor gene 61 SMAD4 61 genetic loci 61 RRM1 61 EGFR gene 61 microdeletion 61 multivariate Cox 61 APOL1 61 DRB1 * 61 apolipoprotein B 61 A1 allele 61 thyrotropin levels 61 cell adhesion molecule 61 miRNA expression 61 subclinical atherosclerosis 61 advanced adenomas 61 advanced adenoma 61 Apolipoprotein E 61 CNVs 61 Clusterin 61 serum concentrations 61 alanine aminotransferase ALT 61 HLA DR 61 APOE allele 61 gene APOE 61 hypomethylation 61 adiponectin concentrations 61 UGT#B# 61 microcephalin 61 colorectal adenomas 61 AMACR 61 univariate analyzes 61 LRP5 61 gene variant 61 phenotype 60 LV ejection fraction 60 nitrotyrosine 60 frameshift mutation 60 CYP#A# gene 60 serum triglycerides 60 genetic variants 60 ORMDL3 60 TP# mutations 60 COMT gene 60 apoE4 60 Raf MEK ERK 60 alanine aminotransferase 60 microsatellite instability 60 IL 1ß 60 microalbuminuria 60 multivariate adjustment 60 BDNF gene 60 HLA B# 60 parkinsonism 60 induced apoptosis 60 CNTNAP2 60 cytokeratin 60 BMP2 60 plasma folate 60 intron 60 CFH gene 60 % CI #.#-#.# [006] 60 serotonin transporter 60 gene encoding 60 carotid IMT 60 COMT 60 esophageal squamous cell carcinoma 60 CCR5 delta# 60 NAFLD 60 susceptibility genes 60 CYP#D# 60 HFE gene 60 MGUS 60 ADH1B 60 familial clustering 60 dopamine D4 receptor 60 MSMB 60 thyrotropin 60 ApoE gene 60 elevated triglyceride levels 60 isoprostane 60 LDLR 60 Genetic variants 60 PIK3CA 60 gallstone disease 60 cyclin E 60 hyperinsulinemia 60 colorectal carcinoma 60 constitutively active 60 CaP 60 major histocompatibility complex 60 albuminuria 60 KIAA# 60 orthologs 60 catenin 60 ERalpha 60 missense 59 confidence interval CI 59 airway hyperresponsiveness 59 apoC III 59 APOE 59 isoenzyme 59 causal variants 59 chromosome #q#.# [002] 59 genes CYP#C# 59 MAOA 59 ApoE4 59 C#T [002] 59 COX2 59 5q 59 MECP2 gene 59 mitogen activated protein kinase 59 R#W [002] 59 phenotypes 59 genes encoding 59 TOP2A gene 59 estrone 59 normotensive 59 serum selenium 59 breast cancer genes BRCA1 59 rCBF 59 PALB2 59 carcinoembryonic antigen 59 inhibin B 59 striatal 59 Heterozygous 59 telomere lengths 59 TYMS 59 APOE e4 allele 59 LDL receptor 59 GPC5 59 plasma lipids 59 vimentin 59 TNFalpha 59 overexpression 59 hepatic lipase 59 prognostic factor 59 genetic variants associated 59 adipogenic 59 estrogen receptor ER 59 lowest tertile 59 Genetic variation 59 methylation patterns 59 malondialdehyde 59 Aß 59 cardiovascular mortality 59 GLUT1 59 HepG2 cells 59 immunostaining 59 hyperhomocysteinemia 59 allele frequency 59 Multivariate analysis 59 inherited mutations 59 HNPCC 59 prefrontal cortical 59 penetrance 59 OPRM1 gene 59 tertile 59 BCL2 59 H#K#me# 59 testicular germ cell 59 SNCA 59 central adiposity 59 μmol L 59 NPY gene 59 CD#b 59 Univariate analysis 59 SHBG 59 GLI1 59 BRCA1 BRCA2 59 fasting plasma 59 valine 59 methylation 59 tertiles 59 pg ml 59 orthologous 59 PICALM 59 P = .# 59 creatinine ratio 59 AML MDS 59 apolipoproteins 59 CYP#C# [001] 59 CYP#E# 59 EphB4 59 MAPK pathway 59 IL6 59 atopy 59 CYP# [002] 59 P cadherin 59 CVD mortality 59 obstructive coronary artery 59 intima media thickness 59 extrapyramidal symptoms 59 CYP#C# * 59 genotypes 59 TIMP 1 59 subcellular localization 59 differentially expressed genes 59 narcolepsy cataplexy 59 STAT4 59 TMEM#B 58 β 58 subclinical hyperthyroidism 58 familial pancreatic cancer 58 gastric carcinogenesis 58 MDM2 58 KLF4 58 NNRTI resistance 58 upregulated 58 T2DM 58 CHD7 58 Dysregulation 58 5 HT1A 58 proto oncogene 58 probands 58 downregulated 58 autoantibodies 58 adiposity 58 multivariable adjusted 58 e4 allele 58 coronary calcification 58 TOP2A 58 APOA5 58 eNOS 58 ADAM# 58 indels 58 transferrin saturation 58 lung adenocarcinoma 58 NMIBC 58 homozygote 58 invasive carcinomas 58 hydroxylase 58 CAG repeats 58 c MYC 58 cTnT 58 HER2 expression 58 univariate 58 CYP#A# [001] 58 TEAEs 58 inflammatory markers 58 lactate dehydrogenase LDH 58 hereditary hemochromatosis 58 BRCA1 mutations 58 multivariate analyzes 58 MMP# 58 left ventricular hypertrophy 58 MC4R gene 58 ADPKD 58 clinicopathological 58 CEACAM1 58 HNSCC 58 ENPP1 58 carotid intima media 58 3' UTR 58 apoE 58 Lp PLA 2 58 microRNA expression 58 nonfatal MI 58 CA1 58 TSC1 58 visceral adiposity 58 heterozygote 58 breast carcinoma 58 hydroxyvitamin D levels 58 RhoA 58 NR#A# 58 elevated ALT 58 ERK signaling 58 PDGFR 58 nonfasting triglycerides 58 IFN γ 58 microbleeds 58 adiponectin 58 gene expression patterns 58 nonobese 58 MDR1 58 myeloperoxidase 58 MYH9 58 cadherin 58 Lp PLA2 58 monogenic 58 serum ALT 58 LRAT 58 MTHFR gene 58 receptor subtypes 58 Wwox 58 serum albumin 58 % CI #.#-#.# [002] 58 IL#B gene 58 caveolin 1 58 amino terminal 58 diastolic hypertension 58 Leydig cell 58 Hashimoto thyroiditis 58 isoform 58 amino acid substitutions 58 cerebral infarction 58 C#BL/#J 58 serum BDNF 58 CYP#B# 58 collagenous colitis 58 TNFAIP3 58 inverse association 58 prostate carcinoma 58 nonalcoholic steatohepatitis NASH 58 MLL2 58 transgenic mice expressing 58 nondemented 58 PRNP 58 substrate specificity 58 repeat allele 58 serum PTH 58 hormone receptor negative 58 BRAF mutations 58 neoplasm 58 BRCA2 mutation 58 differentially expressed 58 elevated triglycerides 58 impaired glucose metabolism 57 apolipoprotein 57 alkaline phosphatase 57 ERCC1 57 coronary artery calcification 57 troponin T 57 hypothalamic pituitary adrenal axis 57 D#N 57 TTR gene 57 androgen receptor gene 57 biochemical recurrence 57 fractional anisotropy 57 DNA methylation patterns 57 oncogenic 57 EAAT2 57 immunohistochemical 57 homolog 57 left ventricular systolic 57 Mutational 57 chromosomal rearrangement 57 haplogroups 57 Haplotype 57 null mice 57 quantitative trait loci 57 CYP#D# gene 57 EGFR mutations 57 BRCA2 carriers 57 matrix metalloproteinase 57 receptor kinase 57 catechol O methyltransferase COMT 57 impaired fasting glucose 57 LV dysfunction 57 kDa protein 57 IL 1beta 57 subclinical hypothyroidism 57 cognitively normal 57 tumor suppressor protein 57 multivariable analysis 57 estrogen receptor negative 57 microglial 57 triacylglycerol 57 SSc 57 GSTM1 gene 57 mutant allele 57 synuclein 57 mutated K ras 57 cryptorchidism 57 transactivation 57 K#R [002] 57 PON1 gene 57 BMPR2 57 chromosomal aberrations 57 protein encoded 57 protein tyrosine phosphatase 57 situ LCIS 57 aldehyde dehydrogenase 57 LPS induced 57 airway responsiveness 57 HLA DQ2 57 IGFBP 57 femoral neck BMD 57 mutated BRCA1 57 affective psychosis 57 depressive symptomatology 57 APOE4 gene 57 TMPRSS2 ERG fusion 57 lymphovascular invasion 57 autosomes 57 histopathological 57 plasminogen activator inhibitor 57 genes predisposing 57 LRRK2 gene 57 angiotensin converting enzyme 57 breast carcinomas 57 IL 1β 57 inducible nitric oxide synthase 57 soluble CD# ligand 57 MIF protein 57 homologue 57 Alu elements 57 TIMP 57 FasL 57 osteocalcin 57 paternally inherited 57 cTnI 57 FTO gene 57 phospho 57 confidence intervals CIs 57 kDa 57 transcriptional activation 57 intact parathyroid hormone 57 SCN5A 57 serum cotinine levels 57 neoplasias 57 V#F mutation 57 Serum concentrations 57 Overexpression 57 gene loci 57 Cx# [001] 57 E selectin 57 superior temporal gyrus 57 Upregulation 57 glomerular 57 logistic regression analysis 57 HGPIN 57 papillary renal cell carcinoma 57 logistic regression model 57 p# activation 57 SORL1 57 isoforms 57 serine protease 57 familial aggregation 57 Jhdm2a 57 Foxp3 57 subtype 57 plasma leptin 57 apo B 57 folate deficiency 57 alpha subunit 57 thyroid peroxidase 57 progesterone receptor negative 57 autonomic dysfunction 57 mucinous 57 hormone binding globulin 57 PDGFR alpha 57 KRAS oncogene 57 carotid plaque 57 IPAH 57 SHANK3 57 atherosclerotic lesions 57 CpG 57 serous ovarian cancer 57 IgG antibody 57 epithelial tumors 57 ß catenin 57 steroidogenic 57 BRCA2 mutation carriers 57 distal colon cancer 57 fibrillin 1 57 comorbidity 57 neuritic 57 periventricular 57 autoantibody 57 lysine residues 57 lipid abnormalities 57 JAK2 mutation 57 endocannabinoid signaling 57 nmol L 57 hTERT 56 syngeneic 56 immunoreactive 56 phosphorylates 56 dopamine transporter 56 HBx 56 DNMT1 56 chromosomal instability 56 lipoxygenase 56 dopamine D2 receptor 56 Bcl XL 56 DAT1 56 ApoB 56 Leydig cells 56 tryptase 56 neuroligins 56 oxytocin receptor 56 ECG abnormalities 56 TNF α 56 MAPT 56 ApoE 56 somatic mutations 56 Genotypes 56 QTLs 56 apo AI 56 NKG2D 56 GNAQ 56 nicotinic receptor 56 metabolizing enzyme 56 glutathione S transferase 56 GlcNAc 56 circadian clock genes 56 thyroglobulin 56 atopic 56 haplogroup 56 FMR1 56 FDG uptake 56 Hcy 56 Rap1 56 MIF gene 56 serum cholesterol 56 prognostic significance 56 TCF4 56 osteoblast 56 astrocytomas 56 E#F# 56 nonfasting triglyceride levels 56 distant metastasis 56 serum GGT 56 hypothalamic pituitary 56 decarboxylase 56 #q# deletion 56 constitutively expressed 56 unmethylated 56 hepatic steatosis 56 C Reactive Protein 56 proapoptotic 56 K + ATPase 56 kaempferol 56 advanced neoplasia 56 upregulates 56 dinucleotide 56 mineral density 56 fig. S1 56 lactate dehydrogenase 56 fasting glucose 56 IDDM 56 mutations 56 lignan intake 56 ERa 56 diabetes mellitus DM 56 FMR1 gene 56 modifiable lifestyle 56 indel 56 deacetylation 56 HPA axis 56 multivariate analysis 56 1beta 56 hepatocellular carcinomas 56 ubiquitinated 56 pg mL 56 CpG island 56 infarcts 56 CREBBP 56 OCA2 56 NKX#.# 56 tyrosine kinases 56 cytosine 56 beta carotene supplementation 56 tyrosine phosphorylation 56 CD8 + 56 lyase 56 p# p# 56 Hazard Ratio HR 56 poorer prognosis 56 microvessel density 56 chromosomal alterations 56 density lipoprotein cholesterol 56 Microarray analysis 56 telomere length 56 genetic variations 56 heritable 56 circadian genes 56 forkhead 56 serum testosterone 56 -#.# ± [002] 56 serum ferritin 56 ipsilateral 56 alcohol dehydrogenase 56 serum CRP 56 aminotransferases 56 eosinophil count 56 SGPT 56 VLDL cholesterol 56 survivin 56 ER alpha 56 transmembrane 56 FGFR3 56 invasive lobular 56 carotid plaques 56 2 diabetes T2D 56 adipokines 56 PBMCs 56 serum uric acid 56 miRNA genes 56 IgA deficiency 56 carotid atherosclerosis 56 invasive ductal 56 elevated CRP 56 hip BMD 56 CYP#E# gene 56 seropositivity 56 cardiac troponin T 56 VCAM 1 56 methylated 56 urinary excretion 56 metabolic abnormalities 56 histone deacetylases 56 basal cell nevus syndrome 56 Alanine 56 N acetylaspartate 56 BMI ≥ 56 highest quintile 56 histological subtype 56 immunoblotting 56 hyperparathyroidism 56 CHRNA5 56 Cathepsin B 56 paralogs 56 cytogenetic abnormalities 56 RUNX3 56 alpha synuclein gene 56 TNF blocker therapy 56 LRRK2 mutation 56 astrocytic 56 cardioembolic stroke 56 ERK1 2 56 hypothalamic 56 gestational diabetes mellitus 56 albumin excretion 56 EpCAM expression 56 MC1R 56 sulcal 56 ANOVA 56 ß = 56 predisposing factor 56 inversely associated 56 somatic mutation 56 subtypes 56 nmol 56 p#Kip# 56 HLA DR4 immune 56 BRAF mutation 56 TMPRSS2 ERG 56 euthymic patients 56 germline mutation 56 diastolic BP 56 CYP #D# 56 RNA binding 56 C reactive protein 56 Brain derived neurotrophic 56 acetylcholine receptor 56 receptor gamma 56 nondiabetic patients 56 cM 56 K#N 56 lymph node metastases 56 CXCL# 56 p# mutation 56 lymphoid 56 etiologic 56 inactivating mutations 56 proinflammatory cytokine 56 elevated serum creatinine 56 hypogonadotropic hypogonadism 56 alkaline phosphatase ALP 56 aberrant methylation 56 PDE#A 56 chromosomal 56 hypogonadal 55 melatonin receptor 55 white matter hyperintensities 55 iNOS 55 proteinuria 55 WT1 55 Helicobacter pylori infection 55 LDL particle 55 TSP1 55 5 hydroxytryptamine 55 HER2 overexpression 55 albumin excretion rate 55 eIF4E 55 mammographic density 55 nondrinkers 55 hyperintense lesions 55 eotaxin 55 c myc 55 ectopic expression 55 HOTAIR 55 BMI z 55 aggrecan 55 ε4 55 BRCA2 mutations 55 H#K# [002] 55 erythroid 55 BMAL1 55 macroalbuminuria 55 metaplasia 55 Insulin sensitivity 55 nucleotide sequence 55 MMP2 55 immunohistochemical staining 55 Angiotensin converting enzyme 55 esterase 55 activating mutation 55 mesotheliomas 55 myo inositol 55 histologic subtype 55 virulence genes 55 ankyrin repeat 55 paraneoplastic 55 serine threonine kinase 55 lobular carcinoma 55 mU liter 55 pro inflammatory cytokine 55 multivariate adjusted 55 cyclin dependent kinase 55 HBeAg negative 55 3'UTR 55 ALK gene 55 PI3K pathway 55 gastric adenocarcinoma 55 SPINK1 55 SOX9 55 HMGA2 55 urinary albumin 55 tumor histology 55 ADH1B * 55 SOD2 gene 55 kinase domain 55 histologically 55 Recurrence Score 55 pulvinar 55 CHD mortality 55 serum IGF 55 genotypic 55 renal fibrosis 55 acyltransferase 55 HBeAg 55 overexpressed 55 regulator CFTR gene 55 plasma lipid 55 urothelial carcinoma 55 HPV# 55 receptor tyrosine kinase 55 myocardial infarction MI 55 p# mutations 55 dimeric 55 MMSE score 55 BRCA1 mutation carriers 55 encodes protein 55 arachidonic acid AA 55 serum retinol 55 benign breast 55 inverse agonist 55 pRb 55 UGT#A# 55 thyroid carcinoma 55 causative mutations 55 apoA 55 gene mutations 55 nicotine receptor 55 homologs 55 thrombospondin 55 alternatively spliced 55 K ras 55 posterior cingulate 55 cystatin 55 mosaicism 55 alexithymia 55 pDC 55 tic severity 55 antiphospholipid antibodies 55 KCNQ1 55 monozygotic 55 antinuclear antibodies 55 2D 4D ratio 55 CYP#C# gene 55 epithelia 55 OGG1 55 hepatic enzymes 55 beta1 integrin 55 PITX2 55 hsCRP 55 KIT mutations 55 cerebellar 55 PAX5 55 chromosomal deletions 55 SHBG levels 55 downstream effector 55 GPx 55 AT1R 55 somatostatin 55 GATA4 55 myopathies 55 pheochromocytoma 55 sequence homology 55 glucose insulin 55 serum folate 55 cytopathic 55 genes differentially expressed 55 multivariate logistic regression 55 uM 55 gastric carcinoma 55 genomewide 55 #S rRNA 55 basal forebrain 55 hyperintensity 55 troponins 55 potent inhibition 55 preoperative PSA 55 APOE e4 gene 55 hippocampal volume 55 airway hyper responsiveness 55 lipoprotein 55 HRCT 55 fasting serum 55 inactive X chromosome 55 alpha1 55 monocytic 55 FLT3 55 nucleotide