Related by context. All words. (Click for frequent words.) 67 LPA gene 65 alpha synuclein gene 64 TCF#L# gene 64 KIF6 gene 63 genetic variants associated 63 androgen receptor gene 63 CETP gene 63 MTHFD1L gene 63 PTPN# 63 MC4R gene 63 G allele 63 CNTNAP2 62 LRP5 62 thyrotropin 62 STAT4 62 gene APOE 62 MC1R gene 62 pathogenic mutations 62 histone modifications 62 HLA DRB1 62 SORL1 62 genes CYP#C# 62 MYH9 gene 62 BARD1 62 gene variants 62 ABCB1 62 CYP#D# gene 62 PON1 gene 61 CHI#L# 61 variant alleles 61 genetic polymorphisms 61 MYH9 61 missense mutations 61 KIAA# 61 #q# deletion 61 MDR1 61 serum BDNF 61 gene locus 61 mtDNA mutations 61 somatic mutation 61 Genetic variation 61 APOE ε4 61 apolipoprotein E gene 60 dysbindin 60 hypermethylated 60 ovarian hormones 60 GSTP1 60 ZNF# 60 chromosomal regions 60 chromosomal aberrations 60 MIF protein 60 Genetic variants 60 KRAS oncogene 60 CYP#A# gene 60 NRF2 gene 60 susceptibility gene 60 KCNH2 60 APOE allele 60 MTHFR 60 genetic polymorphism 60 ApoE gene 60 FGFR2 60 GABRA2 60 TCF#L# 60 parkinsonism 60 GBA mutations 60 DRD2 gene 60 CETP VV 60 IL#B 59 UGT#A# * 59 CYP#C# gene 59 APOE4 59 chromosome #q# [002] 59 APOE e4 59 BMPR2 59 genetic variants 59 allele frequencies 59 transthyretin 59 rs# [002] 59 SNP rs# [002] 59 CNTNAP2 gene 59 CHEK2 59 miRNA expression 59 IgA deficiency 59 HMGCR 59 microdeletions 59 RBP4 59 telomere lengths 59 genetic loci 59 transgenic mouse models 59 heterozygotes 59 familial ALS 59 Treg cell 59 DQB1 * 59 apoC III 59 HFE gene 59 sCJD 59 chromosomal rearrangement 59 gene amplification 59 rs# [003] 59 Alu elements 59 mRNA transcripts 59 inherited mutations 59 Clusterin 59 methylation patterns 59 LRRK2 gene 59 chromosome #q# [001] 59 orthologous genes 59 SMAD4 59 microcephalin 59 EBV infection 58 DEC2 58 K ras mutations 58 chromosome aberrations 58 TGFBR1 * 6A 58 CAG repeats 58 dopamine D4 receptor 58 neuroglobin 58 transgene expression 58 amyloid plaque formation 58 apolipoprotein E4 58 SLC#A# [002] 58 dopamine receptor gene 58 prion protein gene 58 virulence genes 58 CDH1 58 cyclin E 58 causal variants 58 allelic variants 58 sporadic ALS 58 Wnt#b 58 serum homocysteine 58 ENPP1 58 LIS1 58 metabolizing enzymes 58 vascular dysfunction 58 KIBRA 58 uPAR 58 DNA methylation patterns 58 APOL1 58 de novo mutations 58 TMEM#B 58 thyrotropin levels 58 chlamydial infection 58 sphingolipid 58 BDNF gene 58 CXCL5 58 spontaneous mutations 58 adiponectin levels 57 motor neuron degeneration 57 epistasis 57 ankyrin B 57 MHC molecules 57 chimpanzee genomes 57 gastric carcinogenesis 57 homozygosity 57 MAOA gene 57 genetic variations 57 genomic deletions 57 dopamine transporter 57 3'UTR 57 phenotypes 57 microdeletion 57 drug metabolizing enzymes 57 clusterin 57 dopamine transporter gene 57 enterotypes 57 polymorphisms 57 mammary cancers 57 prostate cancer CaP 57 myo inositol 57 COMT gene 57 SCN5A 57 GPR# [002] 57 neuroD2 57 penetrance 57 prion gene 57 GSTT1 57 P cadherin 57 orthologs 57 IGF1 57 mitochondrial proteins 57 familial clustering 57 chromosomal translocations 57 klotho 57 ABCB1 gene 57 phenotypic variation 57 MLL2 57 IgG antibody 57 GABRA2 gene 57 vimentin 57 HLA B# 57 genetic variant 57 GLUT1 57 C#Y 57 MECP2 gene 57 GSTM1 57 NF1 gene 57 lobular breast cancer 57 salivary amylase 57 prion infection 57 CYP#A# [002] 57 HER2 expression 57 mitochondrial gene 57 quantitative trait loci 57 sequence homology 57 miRNA genes 57 monogenic 57 urate levels 57 metabolic syndrome MetS 57 monozygotic twins 57 BCL#A 57 germline mutations 57 HbF 57 humanin 57 plasma lipid 57 prodynorphin 57 splice variants 57 DISC1 gene 57 genes encoding 57 CALHM1 57 RUNX3 57 synaptic proteins 57 STK# gene 57 APOE genotype 57 5 HTTLPR 57 mitochondrial DNA mtDNA 57 enterovirus infection 57 gene polymorphisms 57 GRK5 57 PTEN mutations 57 allelic 57 β amyloid 57 serotonin transporter gene 57 haplotypes 57 lactase persistence 57 subclinical hyperthyroidism 57 transcriptional profiles 57 SCD1 57 CHD7 57 molecular abnormalities 57 EAAT2 56 MC4R 56 E4 variant 56 transgenic rats 56 CFTR gene 56 Darapladib 56 NR#A# gene 56 ADH1B * 56 microRNA expression 56 Wwox 56 colorectal neoplasia 56 parkin gene 56 Fragile X gene 56 synuclein 56 beta1 integrin 56 rs# [001] 56 SNCA 56 receptor gamma 56 splice junctions 56 Jhdm2a 56 NNRTI resistance 56 #p# [003] 56 Cortisol levels 56 neuroimaging studies 56 endogenous opioid 56 receptor gene 56 QTLs 56 clade B 56 CDK4 56 palladin 56 Sonic Hedgehog 56 segmental duplications 56 Upregulation 56 gastric carcinoma 56 A1 allele 56 metabolizing enzyme 56 nAChR 56 PrPSc 56 SHANK3 56 folate deficiency 56 SMN2 gene 56 missense mutation 56 differential gene expression 56 chromosome #p#.# 56 IGF2 56 ORMDL3 56 DRD2 56 UCRs 56 APOE gene 56 promoter methylation 56 fluoroquinolone resistance 56 MEF2A 56 cardioembolic stroke 56 mutant allele 56 DRD4 56 colorectal adenoma 56 major histocompatibility complex 56 plasma kallikrein 56 gene rearrangements 56 phenotypic traits 56 genes predisposing 56 #p#.# [001] 56 klotho gene 56 gene variant 56 genomic variants 56 CHRNA5 56 #q#.# [002] 56 KLF4 56 FOXP2 gene 56 CD#c 56 gene encoding 56 autoantibody 56 nanomolar 56 serotonin transporter 56 CEACAM1 56 MLH1 56 adrenal cortex 56 SIRT1 gene 56 Epidemiological studies 56 apoE 56 CD# expression [001] 56 APOC3 56 circadian genes 56 BDNF protein 56 MSMB 56 haplotype 56 polycystic ovary syndrome PCOS 56 chromosome #p# [001] 56 mitochondrial mutations 56 HIV HCV coinfected 56 #q# [002] 56 Multiple logistic regression 56 p# mutations 56 NR#A# 56 narcolepsy cataplexy 56 H#K#me# 56 miR #b [002] 56 serum retinol 56 HER2 overexpression 56 resistin 56 colorectal adenomas 56 glycosylated 56 linkage disequilibrium 56 FSHR 56 thyroid hormone levels 56 TCF4 56 globin genes 56 generalized vitiligo 56 CagA 56 sortilin 56 proband 56 RNA sequences 56 HNPCC 56 allelic variation 56 intronic 56 metabolic disturbances 56 #p# [001] 56 histone methylation 55 indels 55 oxysterols 55 neuritic 55 ApoE4 gene 55 UCP2 55 PTHrP 55 PPAR γ 55 molecular determinants 55 inherited maternally 55 methylation markers 55 inhibin B 55 genomewide 55 hereditary hemochromatosis 55 protein encoded 55 VKORC1 55 body fatness 55 K ras gene 55 periodontal bacteria 55 TMPRSS2 ERG fusion 55 metabolic parameters 55 serum leptin 55 progranulin gene 55 PER2 55 PON1 55 protein tyrosine phosphatase 55 MSH2 55 causative mutations 55 androgen excess 55 Foxp2 55 #q# [001] 55 tryptase 55 deCODE BreastCancer TM 55 promoter hypermethylation 55 circadian clock genes 55 albumin excretion 55 genes BRCA1 55 Brd4 55 micronuclei 55 ApoE4 55 nondemented 55 cellular prion protein 55 HPV# 55 S#A# [002] 55 trans palmitoleate 55 neuropathologic 55 cortical excitability 55 metabolic abnormalities 55 serum PTH 55 peptide antigens 55 salivary cortisol 55 Leydig cell 55 HLA genes 55 HER2 neu 55 lung epithelium 55 adiponectin concentrations 55 colorectal carcinogenesis 55 fetal chromosomal 55 transgenic mouse model 55 catechol O methyltransferase 55 HbF levels 55 hyperinsulinemia 55 dysbindin gene 55 serotonin synthesis 55 protein alpha synuclein 55 CCR5 delta# 55 short hairpin RNAs 55 mammary cells 55 OGG1 55 cerebellar 55 haplogroups 55 PDE#A 55 FXTAS 55 neutralizing antibody responses 55 OPRM1 gene 55 apolipoprotein E APOE 55 PCA3 gene 55 genetic aberrations 55 Mechanistic studies 55 genomic alterations 55 C. neoformans 55 TGF ß1 55 diagnostic biomarker 55 MAP kinases 55 intracellular bacteria 55 estrogen metabolism 55 metabolic dysfunction 55 alternatively spliced 55 carotid atherosclerosis 55 familial pancreatic cancer 55 proteins encoded 55 autosomal dominant inheritance 55 CVD mortality 55 FGFR2 gene 55 ependymomas 55 prefrontal cortical 55 glucocorticoid receptors 55 breast cancer metastasis 55 gene APOE4 55 #q#.# [001] 55 sarcosine 55 DRD4 gene 55 SNP rs# [001] 55 genetic susceptibility 55 CYP# [002] 55 single nucleotide polymorphism 55 microglial 55 pituitary hormone 55 eosinophil count 55 elevated CRP 55 FTLD 55 CCL#L# 55 vitamin D receptors 55 RRM1 55 GAB2 55 plasma folate 55 Genetic predisposition 55 β1 55 HMGA1 55 XLHED 55 SLC#A# [001] 55 FGFR1 55 susceptibility loci 55 clefting 55 Peptide YY 55 genetic heterogeneity 55 ERBB2 55 alleles 55 M. pneumoniae 55 arterial thickening 55 visceral adiposity 55 IL#R 55 cystatin C 55 IgG4 55 abnormal prions 55 subclinical disease 55 CNVs 55 primate genomes 55 thyroid dysfunction 55 Lp PLA2 55 gene expression 55 Hashimoto thyroiditis 55 BRAF protein 55 tumorigenicity 55 gallstone disease 55 noncoding RNAs 55 corticosterone levels 55 inbred strains 55 ε4 55 nucleotide variations 55 GPC5 55 evolutionary conserved 55 viral genomes 54 respiratory viral infections 54 hypermethylation 54 #p#.# [002] 54 pressure natriuresis 54 brain lesions 54 coding sequences 54 SORL1 gene 54 neurological abnormalities 54 Brugada syndrome 54 chromosomal alterations 54 chlamydial 54 glutamate signaling 54 genetic susceptibilities 54 colorectal tumor 54 DHEAS 54 meiotic recombination 54 transmembrane receptor 54 picomolar 54 gene expression patterns 54 p# activation 54 ribosomal RNA rRNA 54 allergic airway inflammation 54 SE alleles 54 cisplatin resistant 54 variant rs# 54 metabolomic profiles 54 heritable 54 IgE antibody 54 white matter hyperintensities 54 endogenous estrogen 54 mRNA expression 54 gene variation 54 microsatellite instability 54 H#Y 54 genetic determinants 54 cAMP signaling 54 SOX3 gene 54 ESR1 54 neuronal dysfunction 54 leptin receptor 54 LRRK2 mutation 54 A. thaliana 54 perilipin 54 GPI anchored 54 epigenetic modification 54 Sjögren syndrome 54 receptor subtypes 54 DNA demethylation 54 fasting glucose levels 54 CYP#C# [002] 54 synovial cells 54 MTHFR gene 54 C. pneumoniae 54 chromosomal anomalies 54 homozygotes 54 PB1 F2 54 MHC genes 54 ERK2 54 bivariate analyzes 54 intergenic 54 gene loci 54 autosomal 54 subcellular localization 54 serum biomarkers 54 Epidemiologic studies 54 Klotho gene 54 Microarray analysis 54 nucleotide sequence 54 phenotypic 54 cytopathic 54 multivariate logistic regression 54 calcium excretion 54 uncharacterized genes 54 mRNA molecules 54 progranulin 54 basal cell nevus syndrome 54 central adiposity 54 LRAT 54 fetal hemoglobin 54 hypogonadotropic hypogonadism 54 leukaemias 54 genomewide association studies 54 GnRH neurons 54 genotype phenotype 54 epigenetic alterations 54 GABA receptor 54 non coding RNA 54 KLF# 54 hormone secretion 54 genetic variation 54 Cochrane Systematic Review 54 #ß HSD1 54 T1DM 54 transgenic mice expressing 54 serum antibodies 54 differentially expressed genes 54 genotyping arrays 54 APOE4 gene 54 5 HTT gene 54 KCNQ1 54 cytochrome b 54 X chromosome inactivation 54 IFN γ 54 BRCA1 BRCA2 54 repeat allele 54 siRNA knockdown 54 Chlamydia trachomatis infection 54 cardiac troponin T 54 lentiviruses 54 somatic mutations 54 serum estradiol 54 MetS 54 mice lacking 54 nucleotide substitutions 54 ADRB2 54 Plasmodium falciparum malaria 54 HepG2 cells 54 TT genotype 54 Candida species 54 rs# [004] 54 COL#A# 54 NPC1 54 miR #a [001] 54 prostate carcinogenesis 54 FMR1 gene 54 posttranslational modifications 54 HLA DRB1 SE 54 serum uric acid 54 neuroblastoma tumors 54 recessive trait 54 BRAF V#E 54 paralogs 54 microRNA miR 54 monoamine 54 hepatic enzyme 54 SLITRK1 54 Genetic variations 54 periodontal pathogens 54 chlamydial infections 54 mutated K ras 54 perilipin gene 54 HLA alleles 54 tumor suppressor protein 54 SERT gene 54 c KIT 54 picornavirus 54 K#N 54 protein isoforms 54 TEL AML1 54 selenium supplementation 54 CYP#C# * 54 #q#.# deletion syndrome 54 MIF gene 54 prostate ovarian 54 FTO gene 54 murine leukemia virus 54 atypical hyperplasia 54 essential thrombocythemia 54 GNAQ 54 TTR gene 54 tic severity 54 molecular mechanisms underlying 54 adenovirus vector 54 cortisol concentrations 54 methylated DNA 54 triglyceride concentrations 54 FOXP2 54 adiponectin 54 microRNA molecules 54 V#F mutation 54 EGFR gene 54 Univariate analysis 54 nongenetic 54 pathogenic mechanisms 54 granule cells 54 airway responsiveness 54 ascertainment bias 54 oligomerization 54 MC1R 54 biochemical marker 54 pDCs 54 human leukocyte antigen 54 genomic variation 54 fascin 54 trophoblast cells 54 Genetic mutations 54 chromosome rearrangements 54 medulloblastomas 54 troponin T 54 viral titers 54 HLA DQ2 54 epigenetic inheritance 54 urinary BPA 54 germline mutation 54 prion strains 54 neuroligins 54 hepatic steatosis 54 insertions deletions 54 ALDH2 54 Insulin sensitivity 54 antisense inhibition 54 RNA transcripts 54 overactivation 54 B7 H3 54 HMGA2 54 FGF2 54 colorectal tumors 53 eotaxin 53 Foxp3 53 FTO variant 53 alexithymia 53 genital abnormalities 53 homozygote 53 myeloperoxidase 53 neutralizing antibody 53 PALB2 53 tyrosine phosphorylation 53 functional polymorphism 53 microbiomes 53 exfoliation glaucoma 53 underlying pathophysiology 53 etiologic 53 pathophysiological mechanisms 53 gene expression profiles 53 BRCA1 mutations 53 hepatoma 53 costimulatory 53 serum concentrations 53 TOMM# 53 ncRNAs 53 BRCA2 gene 53 quasispecies 53 epigenetic markers 53 variant allele 53 Boston DbTechNo Results 53 endothelial activation 53 neuroanatomical 53 cagA 53 PCR amplified 53 CHRNA5 gene 53 genotypic 53 previously undescribed 53 endometrial cancers 53 nucleotide substitution 53 vitamin B# deficiency 53 acetylcholine receptor 53 APOE e4 allele 53 regulates gene expression 53 YKL 53 multiple logistic regression 53 susceptibility genes 53 autistic traits 53 chromosome #q 53 osteoprotegerin 53 Cognitive impairment 53 MAPK pathway 53 proteomes 53 calcium homeostasis 53 abnormal glucose tolerance 53 G6PD deficiency 53 IgG1 53 PPARg 53 tau mutation 53 bile acid metabolism 53 oncogenic transformation 53 mosaicism 53 periodontal infections 53 estrogen receptor ER 53 cardioprotective effects 53 X chromosome genes 53 chromosomal anomaly 53 mutated genes 53 genetic mutations 53 ApoB 53 coinfection 53 SHANK3 gene 53 JAK mutations 53 probiotic supplementation 53 inflammatory biomarkers 53 vasopressin receptor 53 autoantigens 53 CYP#E# gene 53 paternal lineages 53 Hcrt 53 XMRV infection 53 p#INK#a 53 T2D 53 adiponectin hormone 53 neuroinflammation 53 Chlamydia pneumoniae 53 familial aggregation 53 superantigens 53 molecular markers 53 subclinical atherosclerosis 53 fluoroquinolone resistant 53 phenotypic differences 53 neurofibrillary 53 previously uncharacterized 53 Subgroup analysis 53 aneuploid cells 53 CCR3 53 paricalcitol 53 IDH1 53 SNP arrays 53 apoE4 53 micro RNAs 53 MnSOD 53 isoenzymes 53 p# mutation 53 COX2 53 enkephalin 53 chromatin structure 53 IGFBP 53 DICER1 gene 53 synaptogenesis 53 Immunohistochemical analysis 53 MMP# 53 hippocampal neurons 53 folate concentrations 53 Plasmodium infection 53 metabolite concentrations 53 NRTI resistance 53 anterior pituitary 53 alpha synuclein protein 53 eIF4E 53 TAp# 53 aneuploidy 53 chromosome translocations 53 assortative mating 53 RNA polymerase II 53 systemic inflammation 53 causative mutation 53 abnormally elevated 53 gene duplications 53 haplotype map 53 DRB1 * 53 galanin 53 Drosophila genome 53 morphologic 53 phthalate exposure 53 Notch1 53 parietal cortices 53 downregulation 53 EGFR expression 53 plasma selenium 53 Androgen receptor 53 retinol binding protein 53 susceptibility locus 53 polymorphism 53 progressive neurodegenerative disorder 53 gene mutations 53 FGFs 53 myocardial infarctions MIs 53 activated microglia 53 recessive mutation 53 internalizing disorders 53 neuropeptide Y 53 intestinal microflora 53 MECP2 53 amyloid deposition 53 JAK2 mutation 53 pathophysiological effects 53 SNPs 53 heterozygosity 53 broadly neutralizing 53 plastids 53 chromosomal rearrangements 53 orofacial clefts 53 mutant mouse 53 carotid plaques 53 viral proteins 53 serum lipid levels 53 trans palmitoleic acid 53 biochemical abnormalities 53 nematode C. elegans 53 cytidine 53 lactate dehydrogenase 53 giant danio 53 CFH gene 53 mammographic density 53 coding exons 53 NSCLC tumors 53 L1s 53 L. pneumophila 53 adipokines 53 TRAF1 C5 53 genetic locus 53 extrapyramidal symptoms 53 tau protein tangles 53 evolutionarily conserved 53 number variations CNVs 53 isotype 53 pathogenetic 53 metalloprotease 53 GBM tumors 53 E. faecalis 53 loci 53 CC genotype 53 behavioral disinhibition 53 FASPS 53 coding genes 53 transcriptional silencing 53 allostatic load 53 CYP#E# 53 miRNAs miR 53 Kufs disease 53 IUGR 53 CREB protein 53 cortical thinning 53 bacterial virulence 53 enteroviruses 53 metabolic abnormality 53 distinct subtypes 53 apolipoprotein E 53 allele frequency 53 murine models 53 NFKBIA 53 connexin 53 Arabidopsis genes 53 Entamoeba histolytica 53 toxoplasma 53 herpes viruses 53 cis regulatory 53 Prox1 53 heritable variation 53 SETDB1 53 hereditary predisposition 53 allergic sensitization 53 C. trachomatis 53 S. maltophilia 53 Neuregulin 1 53 proteolytic cleavage 53 methylenetetrahydrofolate reductase 53 prothrombotic 53 Mycoplasma pneumoniae 53 IKZF1 53 gene deletions 53 cytochrome c oxidase 53 8 OHdG 53 CHD mortality 53 sexual dimorphism 53 TMPRSS2 ERG 53 SOD2 gene 53 mutant alleles 53 aneuploid 53 invasive lobular 53 vitamin D inadequacy 53 ataxias 53 Inappropriate activation 53 tHcy 53 p# MAPK 53 Dpp 53 ankyrin repeat 53 #S rRNA 53 γ secretase 53 HMPV 53 FCGR3A 53 P. falciparum malaria 53 epithelial tumors 53 TSP1 53 leptin hormone 53 imprinted genes 53 FLT3 53 raphe 53 neurocognitive impairment 53 ADAMTS# 53 airway hyperresponsiveness 53 striated muscle 53 dietary nitrate 53 inflammatory markers 53 apolipoprotein A1 53 CISH 53 histone modification 53 dietary folate 53 lupus anticoagulant 52 human genome SNPs 52 mutation 52 triacylglycerol 52 developmental abnormalities 52 selective antagonists 52 malondialdehyde 52 aberrant methylation 52 PRNP 52 C#T [002] 52 Entamoeba 52 androgen deficiency 52 intestinal microbiota 52 neuropsychiatric diseases