Related by context. All words. (Click for frequent words.) 74 APOE4 74 APOE gene 71 ApoE4 70 apolipoprotein E 70 ApoE 70 APOE e4 66 APOE4 gene 66 ApoE4 gene 65 genetic variant 65 apolipoprotein E gene 65 APOE allele 64 ApoE gene 64 allele 64 gene variant 63 5 HTTLPR 63 CYP#C# * 62 susceptibility gene 62 gene APOE 62 ADH1B * 62 APOE ε4 61 KIF6 gene 61 e4 allele 61 alleles 61 BRCA1 mutations 61 TCF#L# 60 APOE e4 gene 60 variant alleles 60 MTHFR 60 APOC3 60 apoE4 60 neurofibromatosis type 60 MLH1 60 dysbindin 60 G allele 59 gene variants 59 #q# [001] 59 rs# [003] 59 ε4 59 rs# [002] 59 DRD2 59 CNTNAP2 59 clusterin 59 G#S mutation 59 apolipoprotein E APOE 59 CALHM1 59 BRCA1 59 noncarriers 59 MSH2 59 FTO gene 59 CDKN2A 59 polymorphisms 59 apoE 59 rs# [001] 59 sporadic ALS 59 serotonin transporter gene 59 SORL1 59 OPRM1 gene 58 mutated gene 58 GSTM1 58 elevated triglyceride levels 58 CagA 58 ApoE4 allele 58 COX2 58 HLA B# 58 IGFBP 58 CHEK2 58 C#Y 58 heterozygous 58 mutation 58 cell adhesion molecule 58 KIBRA 58 DQB1 * 58 homozygotes 58 COMT gene 58 caveolin 58 polymorphism 58 BRCA mutation 57 HTLV 57 RBP4 57 missense mutations 57 STAT4 57 FMR1 gene 57 PTPN# 57 apolipoprotein 57 Apolipoprotein E 57 rs# [004] 57 PALB2 57 genotype 57 TLR3 57 homozygous 57 gene mutation 57 5q 57 APOE genotype 57 NF1 57 genetic polymorphism 57 genetic variants 57 TGFBR1 * 6A 57 ABCB1 57 heterozygotes 57 LQTS 57 ADAM# 56 familial ALS 56 mutations 56 TCF#L# gene 56 haptoglobin 56 #p# [001] 56 PTEN mutations 56 mosaicism 56 subclinical hypothyroidism 56 CNVs 56 presenilin 56 germline mutations 56 melatonin receptor 56 MnSOD 56 microcephalin 56 gene mutations 56 KRAS mutations 56 VIPR2 56 mutated BRCA1 56 ALDH2 56 CXCL# 56 GSTP1 56 FXTAS 56 apolipoprotein E4 56 mitochondrial dysfunction 56 cystatin C 56 chemokine receptor 56 BRCA 56 genes predisposing 56 aneuploidy 56 LIS1 56 HMGA2 56 cytokine interleukin 56 #q#.# [001] 56 LRRK2 mutation 56 claudin 56 insulin resistance 56 BRCA2 mutation 55 gene variation 55 autoantibodies 55 CYP#D# 55 IGFBP 3 55 Heterozygous 55 DISC1 55 missense mutation 55 HDL2 55 homozygote 55 gene polymorphism 55 retinol binding protein 55 TMEM#B 55 Wwox 55 CAG repeats 55 inherited mutations 55 TOMM# 55 CC genotype 55 activating mutations 55 FGFR2 55 LRAT 55 homozygosity 55 shorter telomeres 55 CYP#C# [001] 55 DAT1 55 mutant gene 55 eotaxin 55 KIAA# 55 repeat allele 55 monocyte chemoattractant protein 55 Aß 55 BRCA1 mutation 55 GSTM1 gene 55 CNTNAP2 gene 55 FTLD 55 SOD1 protein 55 CDK4 55 fasting glucose levels 55 MAOA 55 genes BRCA1 55 cystatin 55 HT 2A 55 apoC III 55 susceptibility genes 55 cognitively normal 55 basal cell nevus syndrome 55 dopamine receptor gene 55 NKX2 55 genetic mutations 55 proband 55 MC1R 55 Notch1 55 #q# [002] 55 colorectal neoplasia 55 chromosome #p# [001] 55 microalbuminuria 55 IGF1 55 serotonin receptor 55 KLF4 55 FMR1 55 EGFR mutations 55 estrogen receptor alpha 55 osteopontin 54 A1 allele 54 SNPs 54 CCR3 54 klotho 54 elevated homocysteine 54 miRNA genes 54 S#A# [002] 54 Haptoglobin 54 TP# mutation 54 SOD1 54 MYH9 gene 54 SLC#A# [002] 54 TGF β 54 PKC beta 54 KIF6 54 TSP1 54 tyrosine phosphorylation 54 p# mutations 54 metabolic syndrome 54 BRCA2 mutations 54 alpha synuclein gene 54 variant allele 54 BRAF mutation 54 progressive neurodegenerative disorder 54 NNRTI resistance 54 familial hypercholesterolemia 54 MAPK pathway 54 white matter hyperintensities 54 mice lacking 54 BARD1 54 tau protein 54 GPR# [002] 54 familial pancreatic cancer 54 T1DM 54 UGT#A# * 54 oxysterols 54 ERBB2 54 prediabetes 54 DRD4 54 PDGFR 54 PON1 54 GBA mutations 54 vimentin 54 breast cancer genes BRCA1 54 SLC#A# [001] 54 gene APOE4 54 APOE e4 allele 54 pDCs 54 diabetes mellitus DM 54 BRCA2 gene 54 sCJD 54 chromosomal aberrations 54 APOL1 54 mRNA expression 54 premutation 54 elevated triglycerides 54 HDL particles 54 T2D 54 synuclein 54 5 HTT gene 54 GPC5 53 BRCA2 gene mutation 53 autosomal recessive 53 hyperinsulinemia 53 fetal hemoglobin 53 hypermethylation 53 VMAT2 53 plasminogen activator inhibitor 53 tumor suppressor gene 53 allelic variants 53 HNPCC 53 MTHFR gene 53 amnestic MCI 53 HLA B 53 TP# mutations 53 SNP rs# [001] 53 nicotinic receptor 53 receptor gene 53 impaired glucose tolerance 53 Aβ 53 microbleeds 53 glucose metabolism 53 overexpression 53 C reactive protein 53 folate deficiency 53 tumor suppressor 53 NFkB 53 BRCA gene mutation 53 subclinical atherosclerosis 53 GNAQ 53 penetrance 53 subclinical hyperthyroidism 53 ALK mutations 53 resistin 53 DRD4 gene 53 BRCA mutations 53 HLA DRB1 * 53 genetic variants associated 53 BRCA2 53 HGPS 53 G#S [002] 53 LRP5 53 SE alleles 53 nondiabetic 53 BRCA1 gene 53 LRRK2 mutations 53 germline mutation 53 HFE gene 53 haplotype 53 elevated CRP 53 STAT3 53 IDH1 53 Alzheimer disease AD 53 MetS 53 adiponectin levels 53 MYCN amplification 53 MHC molecules 53 DRD2 gene 53 JAK2 53 hyperglycaemia 53 albuminuria 53 promoter polymorphism 53 ORMDL3 53 Clusterin 53 Neuregulin 1 53 mtDNA mutations 53 Prox1 53 WT1 53 virulence genes 53 Fragile X gene 53 IL#R 53 COMT 53 diabetes mellitus T2DM 53 thyrotropin levels 53 ABCA1 53 heritable 53 genotypes 53 SHANK3 52 lipid abnormalities 52 Supplementary Table 52 lipoprotein metabolism 52 SIRT1 52 narcolepsy cataplexy 52 EoE 52 glucose intolerance 52 Abeta# 52 beta thalassemia 52 POMC neurons 52 SH#B# 52 MGUS 52 HLA DRB1 52 microRNA miR 52 T2DM 52 #p#.# [002] 52 subclinical 52 amnestic mild cognitive impairment 52 hydroxyvitamin D levels 52 haplotypes 52 FLT3 52 mGluR 52 CYP# [002] 52 SORL1 gene 52 dopamine D4 receptor 52 apolipoprotein B 52 eNOS 52 allele frequencies 52 C. pneumoniae 52 IgA deficiency 52 microdeletions 52 tumor suppressor protein 52 frontotemporal dementia 52 LRRK2 52 indels 52 DRB1 * 52 HPV# 52 TACI mutations 52 uPAR 52 leptin receptor 52 HDL C 52 gene locus 52 chromosome #q# [001] 52 lung adenocarcinoma 52 Akt 52 tHcy 52 ADPKD 52 PTEN gene 52 genetic polymorphisms 52 cardioembolic stroke 52 FOXP3 52 SCA5 52 PICALM 52 Cowden syndrome 52 breast cancer metastasis 52 BRAF mutations 52 chromosomal abnormalities 52 FGF2 52 airway hyperresponsiveness 52 MDM2 52 Lp PLA2 52 colorectal tumors 52 CFH gene 52 PCSK9 52 neuropsychiatric disorders 52 de novo mutations 52 clade B 52 HIV HCV coinfected 52 ribosomal protein 52 ACE2 52 transcription factor 52 highly heritable 52 Alzheimer disease pathology 52 OGG1 52 IL#B 52 mild cognitive impairment 52 FMRP protein 52 malignant transformation 52 epigenetic silencing 52 glycated hemoglobin levels 52 LDL receptor 52 airway hyper responsiveness 52 SMAD4 52 Bcl xL 52 alpha synuclein 52 interleukin 52 TIMP 1 52 isoform 52 K ras mutations 52 spinocerebellar ataxia 52 HLA DRB1 SE 52 insulin resistance syndrome 52 amyloid beta plaques 52 autosomal dominant 52 fetuin 52 presymptomatic 52 autoantibody 52 HLA DR 52 major histocompatibility complex 52 β amyloid 52 estrogen receptor 52 mutant allele 52 TNFAIP3 52 proto oncogene 52 EBV infection 52 CCR5 delta# 52 LPA gene 52 matrix metalloproteinase 52 PTP1B 52 hedgehog signaling 52 thymosin 52 obesity insulin resistance 51 MECP2 gene 51 PPARγ 51 HDL cholesterol 51 CFTR gene 51 urocortin 51 Fragile X 51 MEK1 51 NF2 51 #q#.# [002] 51 impaired fasting glucose 51 human leukocyte antigen 51 poorer prognosis 51 dopamine transporter 51 CYP#E# gene 51 Src 51 NR#A# 51 histone deacetylases 51 intron 51 amyloid deposition 51 HMGA2 gene 51 MIF gene 51 TIMP 51 LRRK2 gene 51 SHBG 51 MMSE scores 51 mitochondrial mutations 51 prognostic factor 51 Argonaute 51 adiponectin 51 p# mutation 51 LKB1 51 IGF2 51 Lewy bodies 51 APOE epsilon 4 51 adenoma 51 chromosomal rearrangement 51 tarenflurbil 51 HLA genes 51 CDH1 51 NAFLD 51 micro RNAs 51 Li Fraumeni 51 Notch signaling 51 anaplastic lymphoma kinase 51 homolog 51 amyloid cascade 51 promoter methylation 51 synaptic function 51 insulin receptors 51 CYP#E# 51 susceptibility loci 51 gene polymorphisms 51 Apolipoprotein 51 estrogen receptor ER 51 gene encoding 51 endothelial dysfunction 51 BMP2 51 onset Alzheimer disease 51 CETP gene 51 neuroblastoma tumors 51 palladin 51 K#R [002] 51 DICER1 51 IKZF1 51 medulloblastomas 51 BRAF V#E 51 Pten 51 TGF beta 51 protein kinase C 51 rheumatoid factor 51 mutated genes 51 loci 51 Pin1 51 beta amyloid plaques 51 phenotype 51 inherited predisposition 51 amyloid 51 cardiac hypertrophy 51 metabolic abnormalities 51 hippocampal atrophy 51 microvascular complications 51 TNFα 51 insulin secretion 51 PIK3CA 51 LRP6 51 TOP2A 51 atherogenic dyslipidemia 51 activin 51 hypocretin 51 MUC1 51 downregulated 51 isoprostane 51 NRG1 51 IL 1beta 51 autosomal recessive disease 51 histone modification 51 TSC1 51 adrenergic receptors 51 T1D 51 postmenopausal breast cancer 51 airway remodeling 51 sortilin 51 defensin 51 BCL#A 51 K#N 51 Insulin resistance 51 HOTAIR 51 MEF2A 51 thrombospondin 51 fronto temporal dementia 51 systemic lupus erythematosus SLE 51 KRAS gene 51 oncogenic 51 #p# [003] 51 TLR4 51 Kupffer cells 51 BRIP1 51 familial clustering 51 central adiposity 51 chromosomal translocations 51 alpha synuclein protein 51 TT genotype 51 serum BDNF 51 IDH1 mutation 51 calcium homeostasis 51 epigenetic changes 51 aneuploidies 51 GSTT1 51 colorectal carcinoma 51 #q# deletion 51 epigenetic regulation 51 SGK1 51 hyperphosphorylated tau 51 IL6 51 human herpesvirus 51 ApoB 51 BRAF V#E mutation 51 FCGR3A 51 PI3K pathway 51 insulin sensitizers 51 hsCRP 51 MYH9 51 MC4R gene 51 BMPR2 51 cystic fibrosis transmembrane conductance 50 HCV genotype 50 cAMP signaling 50 Hashimoto thyroiditis 50 neuroligins 50 KLF# 50 advanced adenoma 50 CaM kinase II 50 phosphorylated tau 50 NF1 gene 50 KIF6 gene variant 50 defective gene 50 thyrotropin 50 Genetic variants 50 sarcosine 50 NRTI resistance 50 dysregulation 50 chromosome #p#.# 50 genes encoding 50 phosphorylate 50 enzymatic activity 50 isoforms 50 evolutionarily conserved 50 myelination 50 papillary RCC 50 TNFalpha 50 genetic variations 50 coding genes 50 familial adenomatous polyposis 50 dopamine transporter gene 50 EZH2 50 prognostic marker 50 microsatellite instability 50 protein tyrosine phosphatase 50 IFN gamma 50 gene 50 FTO variant 50 amyloid peptide 50 GISTs 50 EGFR gene 50 BDNF gene 50 recessive mutations 50 transcriptional repressor 50 immunoreactivity 50 abdominal adiposity 50 Aß# 50 serum folate 50 dopamine receptor 50 neurological abnormalities 50 Six3 50 Posiphen 50 SOD1 gene 50 p# activation 50 telomere dysfunction 50 exfoliation glaucoma 50 methylenetetrahydrofolate reductase 50 JAK2 mutation 50 genetic variation 50 CETP VV 50 WNK1 50 genomic imprinting 50 peroxisome proliferator activated 50 nondemented 50 CYP#A# gene 50 SNP rs# [002] 50 RIP1 50 PPARg 50 APOE4 variant 50 urate levels 50 CYP#C# [002] 50 atherosclerosis 50 miRNAs 50 amyloid pathology 50 TGF ß 50 Genetic variation 50 thioredoxin 50 mitochondrial function 50 Foxp3 50 colorectal polyps 50 PP2A 50 elevated LDL 50 chromosomal regions 50 adiponectin concentrations 50 mutant protein 50 cardiolipin 50 hippocampal volume 50 parkin gene 50 HbF 50 E4 variant 50 interferon pathway 50 catechol O methyltransferase 50 susceptibility locus 50 Hp2 2 50 FGFR1 50 Alu elements 50 PDE#A 50 herpes simplex virus 50 CIB1 50 postoperative delirium 50 TCF4 50 Alzheimers disease 50 perilipin 50 RASSF1A 50 cognitive impairment 50 causative gene 50 Genotype 50 interleukin IL -6 50 IRF6 gene 50 neurofibrillary tangles 50 BRCA2 breast cancer 50 sodium glucose cotransporter 50 miR #a [001] 50 neuroblastomas 50 albumin excretion 50 lipid metabolism 50 Treg cell 50 somatic mutations 50 Kufs disease 50 thiopurine 50 Glucose Metabolism 50 protein encoded 50 progranulin 50 serum IGF 50 ZNF# 50 Fragile X syndrome 50 IL# [001] 50 overexpress 50 2 diabetes T2D 50 autoantigens 50 p# MAPK 50 urate 50 isoenzymes 50 telomere shortening 50 RANKL 50 MLL2 50 Alzheimer Disease AD 50 cardioprotective effects 50 PTEN protein 50 CaMKII 50 AAT deficiency 50 gestational diabetes mellitus 50 metabolic disturbances 50 aldosterone 50 Homozygous 50 mGluR2 NAM 50 infarcts 50 Nf1 50 lipoprotein 50 ERCC1 50 MODY 50 transgenic mouse model 50 amino acid substitutions 50 factor BDNF 50 leukaemias 50 noncoding RNAs 50 functional polymorphism 50 transmembrane receptor 50 adrenal function 50 E selectin 50 parkinsonism 50 genetic mutation 50 spontaneous mutations 50 hydroxyvitamin D 50 donepezil 50 neuroimaging studies 50 poor metabolizers 50 telomere length 50 UCP2 50 folate intake 50 N Myc 50 transgenic mouse models 49 mitogen activated protein kinase 49 microvascular disease 49 pRb 49 HNSCC 49 motor neuron degeneration 49 chromosomal instability 49 proteinuria 49 MELAS 49 glucocorticoid receptor 49 prefrontal cortical 49 Wnt signaling 49 H. pylori 49 TRAF1 C5 49 FOXP2 49 multivariable analysis 49 calcineurin 49 NOMID 49 essential thrombocythemia 49 HGPIN 49 TZDs 49 tau mutation 49 ENPP1 49 ADAMTS# 49 methylation patterns 49 VHL gene 49 MIF protein 49 atherosclerotic lesions 49 euthymic patients 49 CFTR 49 ADDLs 49 amyloid β 49 prostate carcinogenesis 49 CCR7 49 chromosome #q# [002] 49 p# protein 49 Chromosome 49 SLITRK1 49 BRAF gene 49 uric acid levels 49 cyclin D1 49 cognitive dysfunction 49 GPx 49 microglial activation 49 hs CRP 49 DNA methylation patterns 49 NPY gene 49 SIRT6 49 diabetes mellitus 49 NRTIs 49 Brain derived neurotrophic 49 PCa 49 androgen receptor gene 49 genetic susceptibility 49 YKL 49 Dysregulation 49 deleterious mutation 49 neovascular 49 estrogen receptor negative 49 genomewide 49 PDGFRA 49 GATA4 49 phosphorylated 49 bile acid metabolism 49 PB1 F2 49 neoplastic 49 COL#A# 49 cyclooxygenase 49 paraneoplastic 49 beta catenin 49 angiotensin converting enzyme 49 Smad3 49 macroalbuminuria 49 homozygous familial hypercholesterolemia 49 NKT cells 49 MAOA gene 49 nicotinic receptors 49 cagA 49 tumor suppressor genes 49 advanced adenomas 49 E cadherin 49 hypovitaminosis D 49 hereditary hemochromatosis 49 amyloid deposits 49 neuropeptide Y 49 microdeletion 49 casein kinase 49 LDLs 49 HER2 overexpression 49 VEGF 49 tau tangles 49 macrovascular disease 49 chromosomal alterations 49 osteocalcin 49 ultraconserved elements 49 monoclonal gammopathy 49 MC4R 49 neurodevelopmental disorders 49 CHD7 49 normal karyotype 49 miRNAs miR 49 clade C 49 HDACs 49 polyploidy 49 receptor subtype 49 carotid plaque 49 enteroviral infection 49 arterial calcification 49 single nucleotide polymorphism 49 regulator CFTR gene 49 MDR1 49 adenomas 49 Sjögren syndrome 49 Vpu 49 downregulation 49 KCNE2 49 CIN2 + 49 lipid levels 49 genes 49 miR# 49 PTHrP 49 HER2/neu 49 plasma leptin 49 CD4 + CD# 49 imprinted genes 49 DHEAS 49 RUNX3 49 KCNH2 49 PPAR gamma 49 prolactin 49 myotonic dystrophy 49 miR 49 apoA 49 VKORC1 49 venous thrombosis 49 affective psychoses 49 TP# gene 49 genetic loci 49 lymph node metastases 49 plasma folate 49 HDAC2 49 linkage disequilibrium 49 humanin 49 behavioral disinhibition 49 fasting glucose 49 Vascular dementia 49 mammographic density 49 suppressor gene 49 MAO B 49 Wnt signaling pathway 49 microglial 49 depressive symptoms 49 FANCD2 49 E#F# 49 gene loci 49 D2 receptors 49 prefrontal regions 49 neurodegenerative disorder 49 oxidized LDL 49 modifiable risk 49 Cdk5 49 brain shrinkage 49 EGFR mutation 49 CatB 49 CYP#C# gene 49 INF2 49 karyotype 49 overt hypothyroidism 49 PrP 49 #p#.# [001] 49 upregulated 49 JAK mutations 49 receptor molecule 49 neurodegeneration 49 tumorigenesis 49 hypercholesterolemia 49 NGAL 49 metalloprotease 49 FASPS 49 esophageal squamous cell carcinoma 49 JAK2 enzyme 49 mRNA decay 49 preeclampsia 49 IGFBP2 49 genetic alteration 49 AAT Deficiency 49 neuropathologic 49 IL 1ß 49 Angelman syndrome 49 endothelin 49 colorectal adenomas 49 BACE1 49 baseline HbA1c 49 Alzheimer pathology 49 TNFa 49 circulating IGF 49 CCL#L# 49 autosomal dominant disorder 49 BRCA1 mutation carriers 49 follistatin 49 hypermethylated 49 FGFs 49 autoimmune thyroid 49 CGG repeats 49 Aldosterone 49 epigenetic modification 49 commonly mutated genes 48 MLL gene 48 monozygotic twins 48 serotonin transporter 48 IDH2 48 insulin resistant 48 galectin 3 48 Niemann Pick disease 48 protein tau 48 glucocorticoids 48 catenin 48 extrapyramidal symptoms 48 non affective psychosis 48 mutant alleles 48 Lp PLA 2 48 carotid plaques 48 lysosomal 48 apolipoproteins 48 ß1 48 TH# cells 48 genomic deletions 48 DEC2 48 fatty liver disease 48 transgene expression 48 hypothalamic pituitary adrenal axis 48 chromosome abnormality 48 ependymomas 48 drusen 48 telomere lengths