Related by context. All words. (Click for frequent words.) 82 ApoE4 79 APOE e4 78 ApoE4 gene 77 APOE gene 75 APOE allele 75 APOE4 gene 75 APOE e4 gene 75 apolipoprotein E 74 APOE 73 ApoE gene 72 ApoE4 allele 71 APOE ε4 71 gene variant 70 apoE4 70 apolipoprotein E gene 69 Fragile X gene 69 e4 allele 69 genetic variant 69 ApoE 69 ε4 69 BRCA1 mutations 68 APOC3 68 APOE genotype 68 gene APOE 68 genes predisposing 68 susceptibility gene 68 TCF#L# 68 TGFBR1 * 6A 68 PTPN# 68 G allele 68 allele 68 FTO gene 68 TCF#L# gene 67 gene APOE4 67 sporadic ALS 67 KIBRA 67 KIF6 gene 67 SORL1 67 COMT gene 67 MYH9 gene 67 DRD2 67 PTEN gene 67 MTHFR 67 mutated gene 67 variant alleles 67 apolipoprotein E4 67 GSTM1 gene 66 HFE gene 66 HLA B# 66 MSH2 66 klotho 66 BARD1 66 CNTNAP2 66 CDKN2A 66 microcephalin 66 ABCB1 66 STAT4 66 G#S mutation 66 apoE 66 noncarriers 66 CYP#C# * 66 UGT#A# * 65 SHANK3 65 BRCA mutation 65 mtDNA mutations 65 MC4R gene 65 C#Y 65 GSTM1 65 DQB1 * 65 FMR1 gene 65 #q# deletion 65 SLC#A# [002] 65 GABRA2 65 heterozygotes 65 rs# [002] 65 apolipoprotein E APOE 65 alpha synuclein gene 65 genetic polymorphism 65 BRCA2 gene 65 CALHM1 65 5 HTT gene 65 Genetic variation 65 Wwox 65 OPRM1 gene 64 LRRK2 gene 64 apoC III 64 MLH1 64 MTHFR gene 64 TP# mutation 64 GSTT1 64 shorter telomeres 64 MIF gene 64 MAOA 64 serotonin transporter gene 64 narcolepsy cataplexy 64 5 HTTLPR 64 CYP#C# gene 64 GSTP1 64 APOE epsilon 4 64 FXTAS 64 progranulin protein 64 mutant allele 64 MnSOD 64 de novo mutations 64 CDH1 64 elevated triglyceride levels 64 polymorphism 64 mutation 64 CHEK2 64 PTEN mutations 64 rs# [003] 64 familial pancreatic cancer 64 V Leiden 64 DRD4 64 E4 variant 64 SNP rs# [001] 63 MC1R 63 G#S [002] 63 gene variation 63 LQTS 63 heterozygous 63 nondemented 63 IGF2 63 Genetic variants 63 LRP5 63 missense mutations 63 lipin 63 SORL1 gene 63 BMPR2 63 mutant gene 63 BDNF gene 63 BRCA gene mutation 63 mitochondrial dysfunction 63 ORMDL3 63 LPA gene 63 COX2 63 familial hypercholesterolemia 63 NF1 gene 63 #q#.# [001] 63 chromosomal rearrangement 63 familial adenomatous polyposis 63 CFTR gene 63 CETP gene 63 chromosomal instability 63 receptor gene 63 SE alleles 63 recessive mutations 63 HDL2 63 FTLD 63 p# mutations 63 Prox1 63 BRCA2 mutation 63 familial ALS 63 FTO variant 62 ADH1B * 62 MEF2A 62 gene mutation 62 PON1 62 homozygosity 62 MAOA gene 62 Apolipoprotein E 62 GBA mutations 62 mutated BRCA1 62 FTO allele 62 variant allele 62 alleles 62 HNPCC 62 epigenetic silencing 62 LKB1 62 BRCA2 gene mutation 62 spontaneous mutations 62 DRD2 gene 62 dopamine receptor gene 62 FGFR2 62 estrogen receptor alpha 62 CYP#C# [001] 62 TMEM#B 62 apo E 62 proband 62 SIRT6 62 inherited mutations 62 BRCA1 gene 62 Foxp3 62 clusterin 62 Alzheimer pathology 62 EBV infection 62 penetrance 62 APOA5 62 germline mutations 62 chromosomal aberrations 62 missense mutation 62 genomic imprinting 62 dysbindin 62 ALDH2 62 rs# [001] 62 APOE e4 allele 62 elevated homocysteine 62 homozygote 62 CFH gene 62 heritable genetic 62 amyloid ß 62 CAG repeats 62 FGF2 62 GPC5 62 IL#R 61 germline mutation 61 cognitively normal 61 Aß 61 homozygotes 61 rs# [004] 61 mice lacking 61 tumor suppressor protein 61 TT genotype 61 mitochondrial mutations 61 subclinical 61 fetuin 61 hypermethylated 61 progranulin 61 osteopontin 61 hyperinsulinemia 61 HMGA2 61 NNRTI resistance 61 CYP#A# gene 61 p#INK#a 61 Heterozygous 61 basal cell nevus syndrome 61 Alu elements 61 progranulin gene 61 humanin 61 gene locus 61 LRAT 61 neuroD2 61 NPC1 61 somatic mutations 61 LIS1 61 haptoglobin 61 HLA DRB1 * 61 genetic polymorphisms 61 LRP6 61 subclinical hyperthyroidism 61 CNVs 61 C. pneumoniae 61 CNTNAP2 gene 61 gene variants 61 MYH9 61 telomere length 61 TLR3 61 type2 diabetes 61 mutations 61 mutated K ras 61 fasting glucose levels 61 β amyloid 61 insulin resistance syndrome 61 K ras mutations 61 susceptibility genes 61 CC genotype 61 APOL1 61 subclinical atherosclerosis 61 MIF protein 61 ADAM# 61 SOD2 gene 61 APOE4 variant 61 CHD7 61 DAT1 61 autosomal recessive disease 61 MHC molecules 61 KLF4 61 KRAS oncogene 61 MECP2 gene 61 FMR1 61 HOTAIR 61 LDL receptor 61 RUNX3 61 CagA 61 prothrombotic 61 parkin gene 61 TOMM# 61 parkinsonism 60 LRRK2 mutations 60 androgen receptor gene 60 leptin receptor 60 genetic variants 60 GPR# [002] 60 resistin 60 Leydig cell 60 thyrotropin 60 BRCA mutations 60 CYP#D# gene 60 PALB2 60 BRCA1 BRCA2 60 folate deficiency 60 gene polymorphism 60 genetic variants associated 60 KRAS mutations 60 FMRP protein 60 transgenic mouse models 60 heterozygote 60 autosomal recessive 60 oxysterols 60 MC1R gene 60 CCR5 delta# 60 IDH1 60 SLC#A# [001] 60 ZNF# 60 premutation 60 DNA methylation patterns 60 2 diabetes T2D 60 Hashimoto thyroiditis 60 ApoB 60 BRCA1 mutation 60 HLA B 60 CYP#D# 60 alpha1 60 polymorphisms 60 BRAF gene 60 BRCA2 carriers 60 CXCL# 60 amyloid pathology 60 sCJD 60 IgA deficiency 60 NF1 60 progressive neurodegenerative disorder 60 CCL#L# 60 shorter telomere length 60 synaptic function 60 homozygous 60 ERK2 60 SH#B# 60 MLL2 60 epigenetic modification 60 transthyretin 60 UCP2 60 ENPP1 60 prostate cancer CaP 60 Genetic predisposition 60 dopamine D4 receptor 60 adiponectin levels 60 mosaicism 60 colorectal neoplasia 60 BRCA2 mutations 60 #p# [001] 60 HBx 60 IGFBP2 60 VKORC1 60 familial clustering 60 poorer prognosis 60 p# activation 60 miRNA genes 60 CETP VV 60 HLA genes 60 elevated CRP 60 hepatitis B infection 60 PON1 gene 60 KIF6 gene variant 60 aldehyde dehydrogenase 60 TP# gene 60 nonalcoholic steatohepatitis NASH 60 chromosome #p# [001] 60 serotonin transporter 60 APOE4 carriers 60 ovarian hormones 60 BRAF mutation 60 NOD2 60 nonalcoholic fatty liver 60 repeat allele 60 tau protein 60 hereditary predisposition 60 arterial calcification 60 DICER1 gene 60 HGPS 60 CYP#C# [002] 60 recessive trait 60 Abeta# 60 Clusterin 60 MGUS 60 epigenetic inheritance 59 insulin resistance 59 T1DM 59 epigenetic changes 59 NPY gene 59 thyrotropin levels 59 GATA4 59 autoantibodies 59 elevated triglycerides 59 dopamine transporter 59 CCR3 59 MAOA L 59 Treg cell 59 euthymic patients 59 cardiolipin 59 motor neuron degeneration 59 melatonin receptor 59 A1 allele 59 granzyme B 59 autoantibody 59 aneuploidy 59 CIB1 59 Aβ 59 eotaxin 59 autistic traits 59 RBP4 59 phenotype 59 dopamine transporter gene 59 gastric carcinogenesis 59 chromosome #q# [001] 59 SCD1 59 KRAS gene 59 dysbindin gene 59 Li Fraumeni 59 BRCA2 mutation carriers 59 inherited predisposition 59 malignant transformation 59 Irs2 59 neurological abnormalities 59 UGT#B# 59 p# mutation 59 tyrosine phosphorylation 59 telomere lengths 59 TEL AML1 59 LDLR 59 amnestic mild cognitive impairment 59 alpha synuclein protein 59 synuclein 59 circadian clock genes 59 breast cancer genes BRCA1 59 DRD4 gene 59 KIAA# 59 SCN1A 59 PDGFR 59 CYP#E# gene 59 glucose metabolism 59 eNOS 59 ankyrin B 59 unmeasured factors 59 CRTC3 59 Jhdm2a 59 HbF 59 EphA2 59 TSP1 59 transgenic mouse model 59 Haptoglobin 59 genetic mutations 59 cyclin E 59 Brd4 59 allele frequencies 59 serum BDNF 59 MAPK pathway 59 silent myocardial ischemia 59 sortilin 59 collagen VI 59 ABCA1 59 OGG1 59 virulence genes 59 brain derived neurotrophic 59 WNK1 59 BRAF V#E 59 gene mutations 59 Aß# 59 TACI mutations 59 TRAF1 C5 59 DISC1 59 deleterious mutation 59 HMGCR 59 subclinical hypothyroidism 59 Notch1 59 HLA DRB1 59 pDCs 59 KCNH2 59 genomewide 59 HLA molecules 59 K#N 59 adipogenic 59 neurofibrillary 59 SMN2 gene 59 hereditary hemochromatosis 59 genotype 59 CaM kinase II 59 protein tyrosine phosphatase 59 coronary calcification 59 leukaemias 59 Notch signaling 59 HER2 overexpression 59 PPARγ 59 neurofibrillary tangles 59 IGF1 59 BRAF mutations 59 #q# deletion syndrome 59 Kufs disease 59 PTP1B 59 pRb 59 protein tau 59 DISC1 gene 59 KLF# 59 white matter hyperintensities 59 glucocorticoid receptors 59 microdeletion 59 insulin receptors 59 gene p# 59 mitochondrial metabolism 59 Brain derived neurotrophic 58 hypermethylation 58 FOXP2 gene 58 amyloid peptide 58 TGF ß 58 obesity insulin resistance 58 HLA DRB1 SE 58 M. pneumoniae 58 genetic predisposition 58 Parkinsonian 58 palladin 58 Entamoeba 58 dentate gyrus 58 hippocampal function 58 KCNE2 58 amyloid beta plaques 58 genes BRCA1 58 nestin 58 NR#A# 58 GABRA2 gene 58 CHRNA5 gene 58 myo inositol 58 predisposing factor 58 allelic variants 58 estrogen metabolism 58 nonhereditary 58 genes CYP#C# 58 COMT 58 Smad7 58 FANCD2 58 activin 58 MC4R 58 Akt 58 Stat5 58 BRCA1 58 VLDL cholesterol 58 PECAM 1 58 BCL#A 58 caveolin 58 neuroligins 58 IGFBP 3 58 TrkB 58 disease NAFLD 58 BRIP1 58 fetal hemoglobin 58 genetic mutation 58 SIRT3 58 chromosomal regions 58 SGK1 58 SCN5A 58 Apobec3 58 S#A# [002] 58 inherit predisposition 58 TNFAIP3 58 protein kinase C 58 major histocompatibility complex 58 ERK signaling 58 prion gene 58 diabetes mellitus T2DM 58 mitochondrial proteins 58 chromosomal translocations 58 fronto temporal dementia 58 telomere shortening 58 Hsp# [001] 58 PB1 F2 58 microglial 58 ERBB2 58 aneuploidies 58 maternally inherited 58 presymptomatic 58 cardioembolic stroke 58 JAK2 enzyme 58 genomic instability 58 immunized mice 58 ENaC 58 progerin 58 TP# mutations 58 neuroglobin 58 SHANK3 gene 58 #beta HSD1 58 phosphorylated tau 58 deleterious mutations 58 CD8 + 58 breast cancer gene mutation 58 microdeletions 58 5q 58 monogenic 58 frontotemporal dementia 58 XMRV infection 58 metabolic abnormalities 58 TCF4 58 amnestic MCI 58 S#K# 58 cAMP signaling 58 endocannabinoid signaling 58 IKZF1 58 mGluR5 antagonist 58 FoxO1 58 pathogenic mutations 58 EZH2 58 phenotypic variation 58 ATG#L# 58 FOXP3 58 TAp# 58 Leydig cells 58 colorectal adenomas 58 brain lesions 58 #q# [001] 58 CD4 + CD# 58 metabolic syndrome MetS 58 mutated genes 58 BRCA2 58 interferon gamma 58 prodynorphin 58 clade B 58 Smad3 58 serum cholesterol 58 mutant alleles 58 G6PD 58 postoperative delirium 58 NAT2 58 cystatin C 58 CYP#A# [002] 58 hypovitaminosis D 58 plasma lipid 58 PI3K pathway 58 amyloid beta plaque 58 glucose intolerance 58 ß amyloid 58 GAB2 58 Neuregulin 1 58 FASPS 58 LRRK2 mutation 58 prostate carcinogenesis 58 FGF# 58 Telomere length 58 autonomic dysfunction 58 SIRT1 58 CDK4 58 transgene expression 58 apolipoprotein 58 SIRT1 gene 58 DNMT1 58 MDR1 58 estrogen receptor negative 58 plasma folate 58 antioxidant enzyme 58 huntingtin gene 58 ADPKD 58 hepatic steatosis 58 Cognitive impairment 58 POMC neurons 58 IKKa 58 angiotensin converting enzyme 58 serotonin 2A 58 HSV1 58 ABCB1 gene 58 telomere dysfunction 58 neuroblastoma tumors 58 TYMS 58 genetic variation 58 PTEN protein 58 underlying pathophysiology 58 GNAQ 58 Ets2 58 systemic inflammation 58 EGFR gene 58 Chronic pancreatitis 58 ataxias 58 Ras pathway 57 #q# [002] 57 FGFR2 gene 57 JAK2 mutation 57 non coding RNA 57 seropositivity 57 TGF β 57 #p#.# [001] 57 epigenetic mechanisms 57 WDR# 57 cranial irradiation 57 neuropathologic 57 CYP #A# 57 Helicobacter 57 IL#B 57 SNP rs# [002] 57 microsatellite instability 57 retinol binding protein 57 amyloid deposits 57 mutant worms 57 Oxidative stress 57 atypical hyperplasia 57 impaired cognition 57 mutated protein 57 HIV HCV coinfected 57 BDNF protein 57 Hp2 2 57 lung adenocarcinoma 57 C EBP alpha 57 mild cognitive impairments 57 RIP1 57 RAS blockers 57 urate levels 57 neuronal dysfunction 57 amyloid deposition 57 Dpp 57 factor BDNF 57 Epstein Barr virus EBV 57 PARP inhibition 57 NR#A# gene 57 uPAR 57 c Abl 57 gestational diabetes mellitus 57 gene DRD4 57 chromosome #q# [002] 57 CHD5 57 astrocyte 57 Akt1 57 CXCL5 57 IGFBP 57 neuroinflammation 57 CatB 57 dopamine D2 receptors 57 tarenflurbil 57 serotonin receptor 57 chromosomal alterations 57 abnormal glucose metabolism 57 susceptibility loci 57 N Myc 57 nonmelanoma skin cancers 57 NFkB 57 FADS2 57 beta amyloid peptides 57 TRIM5 57 vitamin D receptors 57 TTR gene 57 nicotinic receptor 57 epigenetic alterations 57 MetS 57 adiponectin 57 genetic loci 57 mutant protein 57 estrogen receptor 57 T1D 57 glutamic acid decarboxylase 57 amyloid plaque formation 57 TNFa 57 cell adhesion molecule 57 GPx 57 Cyclin D1 57 number variations CNVs 57 gene rearrangements 57 Fas ligand 57 DLC1 57 chromosome #p#.# 57 airway hyperresponsiveness 57 atherosclerotic lesions 57 CYP# [002] 57 HMGA2 gene 57 DEC2 57 synaptogenesis 57 coinfection 57 Klinefelter syndrome 57 Lyn kinase 57 fatty acid synthase 57 inflammasome 57 serum antibodies 57 EGFR mutations 57 γ secretase 57 thiopurine 57 amyloid protein 57 hematopoietic cancers 57 neuropathological 57 PICALM 57 susceptibility locus 57 SMAD4 57 microglial activation 57 human leukocyte antigen 57 RASSF1A 57 amyloid cascade 57 Nf1 57 suppressor gene 57 MYCN amplification 57 defective gene 57 HSF1 57 inactive X chromosome 57 tau tangles 57 folate intake 57 follistatin 57 ADRB2 57 dyskeratosis congenita 57 catechol O methyltransferase 57 p# gene 57 gene amplification 57 PKCi 57 GRK5 57 BRCA2 breast cancer 57 NOD mice 57 susceptibility alleles 57 abnormal proteins 57 serum selenium 57 V#F mutation 57 #ß 57 Wnt#b 57 promoter methylation 57 Amyloid plaques 57 MeCP2 gene 57 fasting insulin 57 transferrin saturation 57 CYP#E# 57 TSC1 57 antiphospholipid antibodies 57 lipoprotein metabolism 57 anaplastic lymphoma kinase 57 albumin excretion 57 Lafora disease 57 NKX#.# 57 NKX2 57 DLX5 57 extrapyramidal symptoms 57 HDL C 57 protein SIRT1 57 IFN γ 57 Wernicke Korsakoff syndrome 57 chemokine receptor 57 colorectal adenoma 57 cagA 57 periodontal infection 57 SMN1 gene 57 TMPRSS2 ERG fusion 57 Apolipoprotein E4 57 morphogen 57 Alzheimer's linked 57 postmenopausal breast cancer 57 molecular abnormalities 57 protein p# 57 T2D 57 chitinase 57 recessive mutation 57 apolipoprotein B 57 tHcy 57 dietary folate 57 microglial cells 57 mRNA transcripts 57 endogenous estrogen 57 NAFLD 57 prefrontal regions 57 tau protein tangles 57 R#W [002] 57 p# protein 57 Skp2 57 PPAR γ 57 CGG repeats 57 vitamin B# deficiency 57 modifier genes 57 #q#.# [002] 57 impaired glucose metabolism 57 #q#.# deletion syndrome 57 BMP2 57 Chlamydia pneumoniae 57 fibrous tangles 56 DGAT1 56 c KIT 56 IRF5 56 coronary artery calcium 56 FCGR3A 56 glucocorticoid receptor 56 interferon pathway 56 MECP2 56 osteocalcin 56 phenotypes 56 Insulin resistance 56 SMN2 56 null mice 56 transcriptional repressor 56 methylation patterns 56 FGFs 56 PlGF 56 squamous cell lung cancer 56 corticosterone levels 56 BRAC2 56 pyruvate kinase 56 alpha synuclein 56 Alzheimer disease pathology 56 nonischemic 56 selenium supplementation 56 adenylate cyclase 56 K#R [002] 56 KCNQ1 56 histone deacetylases 56 enzymatic activity 56 affective psychoses 56 sphingolipid 56 hepatic lipase 56 T2DM 56 DICER1 56 GLUT1 56 MMP# 56 heritable 56 Dr. Bezprozvanny 56 Mild cognitive impairment 56 histone modification 56 neuritic 56 LRRK2 56 nNOS 56 GRK2 56 carotid plaque 56 oesophageal adenocarcinoma 56 SIDS infants 56 causative gene 56 trans palmitoleic acid 56 airway remodeling 56 NF2 56 proto oncogene 56 retinoid X 56 nitric oxide synthase 56 cardioprotective effects 56 CYP#B# 56 antibody mediated 56 amyloids 56 diabetic kidney 56 abdominal adiposity 56 carotid atherosclerosis 56 Genetic mutation 56 lactose malabsorption 56 conserved sequences 56 BRCA gene 56 HLA gene 56 Lp PLA2 56 autosomal dominant 56 hormone adiponectin 56 airway responsiveness 56 fatty acid metabolism 56 TIMP 1 56 G6PD deficiency 56 abnormal prion protein 56 highly heritable 56 transmembrane receptor 56 lipoprotein 56 leptin signaling 56 pathological hallmark 56 mRNA expression 56 dopamine signaling 56 HER2 expression 56 neurotransmitter GABA 56 Vascular dementia 56 chromosome abnormality 56 diabetes mellitus DM 56 reticulocytes 56 macrovascular disease 56 ADDLs 56 evolutionarily conserved 56 chromosomal disorders 56 protein alpha synuclein 56 Rap1 56 SOD1 gene 56 multifactorial disease 56 elevated fasting glucose 56 Her2/neu 56 immunopathology 56 serum leptin 56 NR2B 56 adrenal cortex 56 arginase 56 Mendelian disorders 56 amyloid β 56 MDM2 56 FUS1 56 paternally inherited 56 TLR4 56 nondiabetic 56 DUX4 56 mitochondrial toxicity 56 beta thalassemia 56 DRB1 * 56 cofilin 56 TFH cells 56 Pten 56 herpesviruses 56 estrogen receptor ER 56 p# MAPK 56 genotoxic stress 56 epigenetic markers 56 prion infection 56 Bcl xL 56 neuronal plasticity 56 Lewy bodies 56 RANKL 56 PDE#A 56 p tau 56 ribosomal proteins 56 HER2 neu 56 CSF biomarkers 56 HOMA IR 56 TNFalpha 56 activating mutations 56 synapse formation 56 cyclophilin D 56 NOMID 56 E1A 56 3'UTR