Related by context. All words. (Click for frequent words.) 77 APOE4 74 ApoE gene 74 APOE 72 APOE e4 72 ApoE 72 apolipoprotein E 71 apolipoprotein E gene 71 ApoE4 70 ApoE4 gene 69 gene APOE 68 e4 allele 68 gene variant 68 APOE allele 68 dopamine receptor gene 68 PTPN# 67 FTO gene 67 genetic variant 67 APOC3 67 MC1R 66 apolipoprotein E4 66 COMT gene 66 genes predisposing 66 apoE4 66 ABCB1 66 APOE ε4 65 rs# [002] 65 KIF6 gene 65 GSTP1 65 sporadic ALS 65 SORL1 gene 65 HLA B# 65 CNTNAP2 65 OPRM1 gene 65 MTHFR gene 65 proband 65 susceptibility gene 65 gene variation 65 rs# [001] 65 MYH9 gene 64 HDL2 64 SORL1 64 MTHFR 64 GSTM1 64 TOMM# 64 APOE genotype 64 gene mutation 64 TCF#L# 64 Apolipoprotein E 64 APOE4 gene 64 STAT4 64 BRCA1 mutations 64 apolipoprotein E APOE 64 mutated gene 64 elevated triglyceride levels 64 APOE e4 gene 64 PON1 64 HFE gene 63 ε4 63 TCF#L# gene 63 PTEN mutations 63 G allele 63 2 diabetes T2D 63 MnSOD 63 BRCA2 gene 63 BRCA2 mutations 63 allele 63 UGT#A# * 63 CCR5 delta# 63 CYP#C# gene 63 GSTT1 63 heterozygous 63 TGFBR1 * 6A 63 MSH2 63 serotonin transporter gene 63 CFH gene 63 5 HTTLPR 63 Genetic variation 63 BARD1 63 apoC III 63 SLC#A# [002] 62 rs# [004] 62 promoter polymorphism 62 DRD2 62 BRCA2 gene mutation 62 IKZF1 62 CETP gene 62 C#Y 62 mutated BRCA1 62 G#S mutation 62 insulin resistance syndrome 62 penetrance 62 genetic polymorphisms 62 gene polymorphism 62 clusterin 62 genetic variants associated 62 homozygosity 62 apoE 62 noncarriers 62 LPA gene 62 rs# [003] 62 de novo mutations 62 CC genotype 62 autosomal recessive disease 62 adiponectin levels 62 LRRK2 gene 62 CDKN2A 62 IgA deficiency 62 elevated triglycerides 62 alleles 62 missense mutations 62 inherited mutations 62 MLH1 62 klotho 62 LQTS 62 BRCA gene mutation 62 DQB1 * 62 SLC#A# [001] 62 E4 variant 62 CDH1 62 apolipoprotein 62 KIBRA 61 LRP5 61 IL#R 61 thyrotropin 61 nondemented 61 Aß 61 receptor gene 61 DRD2 gene 61 BRCA1 gene 61 5 HTT gene 61 dysbindin 61 gene variants 61 Neuregulin 1 61 ADPKD 61 Hashimoto thyroiditis 61 familial pancreatic cancer 61 gene mutations 61 HNPCC 61 BRCA mutation 61 frontotemporal dementia 61 aneuploidy 61 APOL1 61 VLDL cholesterol 61 hereditary hemochromatosis 61 #p# [001] 61 T2D 61 familial hypercholesterolemia 61 SOD2 gene 61 HLA DRB1 * 61 heterozygotes 61 autoimmune thyroid 61 subclinical hyperthyroidism 61 CALHM1 61 V Leiden 61 retinol binding protein 61 BRCA1 mutation 61 GSTM1 gene 61 CFTR gene 61 GPC5 61 FMR1 gene 61 narcolepsy cataplexy 61 Genetic variants 61 allele frequencies 61 germline mutations 61 autosomal dominant 61 SHANK3 61 #q# deletion 61 autoantibodies 60 MAOA gene 60 CETP VV 60 lipoprotein 60 COMT 60 homozygotes 60 ORMDL3 60 HMGA2 60 diabetes mellitus DM 60 shorter telomeres 60 Klinefelter syndrome 60 TMEM#B 60 MC4R gene 60 elevated homocysteine 60 SNP rs# [001] 60 variant alleles 60 BMPR2 60 genetic polymorphism 60 DRD4 60 fasting glucose levels 60 CYP#C# [002] 60 albumin excretion 60 FTLD 60 repeat allele 60 thyrotropin levels 60 genes CYP#C# 60 NF1 60 genomewide 60 folate deficiency 60 cystatin C 60 #q#.# [001] 60 homozygous 60 CYP#C# [001] 60 Fragile X gene 60 MetS 60 subclinical atherosclerosis 60 autosomal recessive 60 MAOA 60 sCJD 60 gene DRD4 60 β amyloid 60 BDNF gene 60 IGF2 60 FGFR2 60 GRK5 60 genetic variants 60 gene APOE4 60 basal cell nevus syndrome 59 Aβ 59 familial clustering 59 dopamine transporter gene 59 plasma folate 59 allelic variants 59 Oxidative stress 59 mutant gene 59 PICALM 59 Sjögren syndrome 59 synuclein 59 apolipoprotein B 59 ALDH2 59 FTO variant 59 colorectal neoplasia 59 familial ALS 59 #q# [001] 59 behavioral disinhibition 59 variant allele 59 BRCA mutations 59 mosaicism 59 metabolic abnormalities 59 isoprostane 59 p# mutation 59 fetuin 59 T1DM 59 CNTNAP2 gene 59 DAT1 59 progressive neurodegenerative disorder 59 BRCA2 mutation 59 genetic mutations 59 DRD4 gene 59 Brain derived neurotrophic 59 monozygotic twins 59 progranulin 59 missense mutation 59 serum BDNF 59 resistin 59 microalbuminuria 59 ENPP1 59 gene locus 59 CAG repeats 59 cell adhesion molecule 59 familial adenomatous polyposis 59 PON1 gene 59 HPV# 59 CYP#A# gene 59 interferon pathway 59 genes BRCA1 59 CagA 59 human leukocyte antigen 59 BCL#A 59 adiponectin concentrations 59 polygenic 59 heritable 59 amyloid peptide 59 VKORC1 59 cardioembolic stroke 59 alpha synuclein protein 59 microcephalin 59 COX2 59 filaggrin gene 59 autistic traits 59 KIAA# 59 CYP#D# 59 nicotinic receptor 59 MGUS 59 CYP#E# gene 59 metabolic syndrome 59 Cowden syndrome 59 DRB1 * 59 Abeta# 59 TT genotype 59 chromosomal aberrations 59 colorectal adenoma 59 phosphorylated tau 59 protein tyrosine phosphatase 59 T2DM 58 breast cancer genes BRCA1 58 myo inositol 58 neuropathologic 58 amino acid homocysteine 58 mutation 58 monocyte chemoattractant protein 58 genotype 58 neural tube defect 58 amnestic mild cognitive impairment 58 poorer prognosis 58 MYH9 58 HbF 58 androgen receptor gene 58 gestational diabetes mellitus 58 oxysterols 58 hydroxyvitamin D levels 58 CYP#D# gene 58 aldehyde dehydrogenase 58 recessive inheritance 58 mutant allele 58 DISC1 gene 58 neurofibrillary tangles 58 cerebral infarction 58 TP# mutation 58 RBP4 58 PALB2 58 gene polymorphisms 58 diabetes mellitus T2DM 58 IGFBP 58 haptoglobin 58 CHEK2 58 ApoE4 allele 58 arterial calcification 58 TNFAIP3 58 HLA DRB1 58 underlying pathophysiology 58 AAT deficiency 58 motor neuron degeneration 58 Wwox 58 germline mutation 58 alpha synuclein gene 58 FMRP protein 58 parkinsonism 58 R#W [002] 58 disease NAFLD 58 TYMS 58 LDL receptor 58 SE alleles 58 MEF2A 58 Vascular dementia 58 transferrin saturation 58 Low density lipoprotein 58 HGPS 58 folate intake 58 HLA genes 58 ADAMTS# 58 exfoliation glaucoma 58 1 diabetes T1D 58 fetal hemoglobin 58 MC1R gene 58 gastric carcinogenesis 58 predisposing factor 58 colorectal adenomas 58 genetic abnormality 58 amyloid ß 58 Clusterin 58 tumor suppressor protein 58 CHD7 58 neurological abnormalities 58 NAFLD 58 telomere length 58 chromosomal disorders 58 GBA mutations 58 chromosomal alterations 58 postmenopausal breast cancer 58 habitual snoring 58 mtDNA mutations 58 polymorphism 58 insulin resistance 58 elevated LDL 58 amnestic MCI 58 haplotype 58 euthymic patients 58 chromosome #p# [001] 58 metabolizing enzyme 58 shorter telomere length 58 synaptic function 58 protein kinase C 58 c KIT 58 adenoma 58 serotonin transporter 58 endogenous estrogen 58 #p# [003] 58 CNVs 58 ApoB 58 dopamine D4 receptor 58 plasma lipid 58 5q 58 TACI mutations 58 chromosome #q# [002] 58 TRAF1 C5 58 ADH1B * 58 #q#.# deletion syndrome 58 NKX2 58 COL#A# 58 affective psychoses 58 Haptoglobin 57 S#A# [002] 57 HLA molecules 57 mitochondrial dysfunction 57 Klotho gene 57 cardiolipin 57 leptin receptor 57 defective gene 57 C reactive protein 57 elevated CRP 57 esophageal squamous cell carcinoma 57 Genetic predisposition 57 TCF4 57 DNA methylation patterns 57 lowers homocysteine 57 impaired glucose metabolism 57 G6PD deficiency 57 autonomic dysfunction 57 fasting insulin 57 plasminogen activator inhibitor 57 subclinical hypothyroidism 57 placental malaria 57 Homocysteine 57 lipid abnormalities 57 hippocampal volume 57 protein encoded 57 APOE e4 allele 57 genetic mutation 57 aneuploidies 57 corticosterone levels 57 deleterious mutation 57 epigenetic changes 57 APOA5 57 prostate cancer CaP 57 apolipoproteins 57 isoenzyme 57 tau protein 57 follicle stimulating hormone FSH 57 SCN1A 57 hereditary predisposition 57 EBV infection 57 valine 57 troponin T 57 white matter hyperintensities 57 mitochondrial mutations 57 RIP1 57 Lewy bodies 57 Cockayne syndrome 57 SRBD 57 impaired fasting glucose 57 UGT#B# 57 SHBG 57 hypovitaminosis D 57 prostate carcinogenesis 57 testicular germ cell 57 Leydig cell 57 nonalcoholic fatty liver 57 coinfection 57 cyclin E 57 serum IGF 57 gallstone disease 57 PTEN gene 57 abnormal hemoglobin 57 hormone therapy estrogen 57 GABRA2 gene 57 serotonin receptor 57 obesity insulin resistance 57 CYP#B# 57 thiopurine 57 paraneoplastic 57 Angiotensin converting enzyme 57 tHcy 57 dopamine transporter 57 HLA DRB1 SE 57 ribosomal protein 57 osteopontin 57 p# mutations 57 ACE2 gene 57 CYP# [002] 57 Rh factor 57 glucose intolerance 57 BRCA2 57 MODY 57 mRNA expression 57 FXTAS 57 microdeletion 57 GABRA2 57 HPA axis 57 breast cancer metastasis 57 onset Alzheimer disease 57 airway hyperresponsiveness 57 Genetic mutation 57 autoantibody 57 PCa 57 advanced adenoma 57 ERK signaling 57 genetic susceptibility 57 FGF2 57 MYCN amplification 57 isoenzymes 57 BRAF V#E 57 MECP2 gene 57 alpha1 57 Insulin resistance 57 cTnT 57 seropositivity 57 HGPIN 57 muscular dystrophies 57 haemochromatosis 57 encodes protein 57 vWF 57 protein tau 57 FGFR2 gene 57 serum retinol 57 telomere dysfunction 57 homozygote 57 neuropsychiatric disorders 57 prefrontal cortical 57 polymorphisms 57 serum cholesterol 57 PDE#A 57 recessive mutations 57 ependymomas 57 gestational diabetes mellitus GDM 57 ADAM# 57 SMN2 gene 57 genetic syndromes 57 cholesteryl ester transfer 57 rheumatoid factor 57 APOE epsilon 4 57 alternatively spliced 57 grade cervical intraepithelial 56 BRCA1 BRCA2 56 Meckel Gruber 56 Lafora disease 56 nonischemic 56 CYP#C# * 56 Niemann Pick disease 56 susceptibility genes 56 atopy 56 neuroblastomas 56 hepatic steatosis 56 Tay Sachs disease 56 TSP1 56 familial aggregation 56 LDLs 56 pathogenic mutations 56 metabolizing enzymes 56 apo B 56 neuropsychiatric disorder 56 Fas ligand 56 elevated LDL cholesterol 56 atherogenic dyslipidemia 56 oxidized LDL 56 hippocampal atrophy 56 MMSE score 56 HLA DQ2 56 telomere lengths 56 adrenal cortex 56 DHEAS 56 C. pneumoniae 56 APOE4 variant 56 central adiposity 56 atypical hyperplasia 56 serum PTH 56 neuroD2 56 monogenic 56 YKL 56 BRCA1 56 Aß# 56 eotaxin 56 hsCRP 56 chromosomal rearrangement 56 systemic amyloidosis 56 Lp PLA 2 56 neurodegenerative disorder 56 Socioeconomic status 56 BRAF gene 56 CHRNA5 gene 56 hypothalamic pituitary adrenal axis 56 HER2 overexpression 56 HLA B 56 idiopathic PAH 56 HMGA1 56 VLDL 56 RASSF1A 56 congenital adrenal hyperplasia CAH 56 nondiabetic 56 HDL C 56 atherosclerosis 56 lung adenocarcinoma 56 major histocompatibility complex 56 low density lipoproteins 56 NPY gene 56 neurodevelopmental impairment 56 WNK1 56 nonalcoholic steatohepatitis NASH 56 antiphospholipid antibodies 56 angiotensin converting enzyme 56 human leukocyte antigen HLA 56 clade B 56 density lipoprotein 56 microsatellite instability 56 VLDL C 56 C#Y mutation 56 cognitively normal 56 #q# deletion syndrome 56 HbF levels 56 eNOS 56 MHC genes 56 Becker muscular dystrophy 56 prion protein PrP 56 C#T [002] 56 genetic defect 56 estrogen metabolism 56 microbleeds 56 thyroid hormone levels 56 methylenetetrahydrofolate reductase 56 hyperinsulinemia 56 transthyretin 56 dopamine signaling 56 homocysteine concentrations 56 urate 56 density lipoprotein cholesterol 56 dopamine D2 receptors 56 chlamydial infection 56 brain derived neurotrophic 56 SGPT 56 genetic predisposition 56 multivariable analysis 56 SMAD4 56 thyroglobulin 56 Wiskott Aldrich syndrome 56 ABCB1 gene 56 autosomal dominant disorder 56 serum folate 56 #p#.# [002] 56 FMR1 56 neuroblastoma tumors 56 chromosomal abnormalities 56 triglyceride concentrations 56 alpha synuclein 56 hyperglycaemia 56 chromosome #q# [001] 56 neuroligins 56 chromosome abnormality 56 ectodermal dysplasia 56 systemic lupus erythematosus SLE 56 pre eclamptic 56 chemokine receptor 56 adrenal function 56 spontaneous mutations 56 phenotypic variation 56 ERBB2 56 SIDS infants 56 overt hypothyroidism 56 glycated hemoglobin levels 56 Epstein Barr virus EBV 56 SCN5A 56 myelodysplasia 56 susceptibility alleles 56 LIS1 56 karyotype 56 MDM2 56 BRIP1 56 genetic variation 56 heterozygote 56 KRAS mutations 56 CIN2 + 56 amino acid methionine 56 microdeletions 56 PDGFR 56 Li Fraumeni syndrome 56 COMT enzyme 56 amyloid beta plaques 56 nonfasting triglyceride levels 56 prothrombotic 56 prognostic factor 56 beta amyloid peptides 56 Myocardial infarction 56 recessive trait 56 atherothrombotic disease 56 GNAQ 56 Heritability 56 estrogen receptor ER 56 Lipodystrophy 56 Kufs disease 56 EZH2 56 TSC1 56 fractional anisotropy 56 somatic mutations 56 TP# gene 56 ZNF# 56 causative genes 56 FASPS 56 WT1 55 palladin 55 haplogroup 55 BRCA2 carriers 55 hereditary nonpolyposis colorectal cancer 55 HNSCC 55 polycystic ovary syndrome PCOS 55 premutation 55 dysbindin gene 55 Polycystic ovary syndrome PCOS 55 beta carotene supplementation 55 SOD1 protein 55 KCNE2 55 Chlamydia pneumoniae 55 Prehypertension 55 genetic abnormalities 55 mGluR 55 DRB1 55 Adiponectin 55 genetic variations 55 2D 4D ratio 55 WDR# 55 BMI z 55 hippocampal function 55 neuropeptide Y NPY 55 gene BRCA2 55 dizygotic twins 55 gonadotropins 55 A1 allele 55 epigenetic modification 55 UCP2 55 ABCA1 55 adiponectin 55 suppressor gene 55 Prolactin 55 obstructive coronary artery 55 inflammatory markers 55 inherited predisposition 55 chromosomal instability 55 SOD1 gene 55 phenotype 55 NF1 gene 55 cardiac channelopathies 55 untreated celiac disease 55 CXCL5 55 HDL cholesterol 55 beta thalassemia 55 neuritic 55 MMSE scores 55 elevated fasting glucose 55 lupus anticoagulant 55 mutations 55 subclinical 55 dysglycemia 55 generalized epilepsy 55 nonhereditary 55 Polycystic kidney disease 55 recessive gene 55 BRAF mutation 55 carotid IMT 55 amyloid protein 55 Wernicke Korsakoff syndrome 55 gamma tocopherol 55 indels 55 BRCA1 gene mutation 55 mammographic density 55 coronary artery calcification 55 hepatocellular carcinomas 55 factor BDNF 55 juvenile idiopathic arthritis JIA 55 cryptogenic 55 EGFR gene 55 mice lacking 55 Cognitive impairment 55 AAT Deficiency 55 atherogenic 55 IL#B 55 LRRK2 mutations 55 bowel polyps 55 myeloproliferative neoplasms 55 cranial irradiation 55 androgen deficiency 55 reticulocytes 55 pneumococci 55 angiotensin receptor blockers ARBs 55 macrovascular disease 55 metabolic syndrome MetS 55 HIV HCV coinfected 55 Coronary artery calcification 55 serum urate levels 55 onset diabetes mellitus 55 dysregulation 55 persistent pulmonary hypertension 55 lymphocytic 55 Apert syndrome 55 ataxias 55 ptau 55 FLT3 55 cholinergic tone 55 Hp2 2 55 K#N 55 STK# gene 55 cardiac troponin T 55 genetic loci 55 Apolipoprotein 55 estrogen receptor negative 55 Glucocorticoids 55 regulated kinase ERK 55 body fatness 55 HMGA2 gene 55 cortisol secretion 55 protein tyrosine phosphatase 1B 55 eosinophil count 55 syntaxin 55 CYP #D# 55 extrapyramidal symptoms 55 tibolone 55 hepatic lipase 55 antioxidant enzyme 55 CDK4 55 HTLV 55 CVD mortality 55 colorectal carcinoma 55 recurrent wheezing 55 neurodevelopmental disorder 55 atherosclerotic lesion 55 mutated K ras 55 CYP#D# genotype 55 ATG#L# 55 hydroxyvitamin D 55 gastric adenocarcinoma 55 interleukin IL -6 55 p#INK#a 55 paraoxonase 55 progranulin protein 55 astrocytomas 55 PPAR γ 55 serum calcium 55 C1q 55 von Willebrand factor 55 EoE 55 endocannabinoid signaling 55 urate levels 55 mild cognitive impairments 55 Genetic variations 55 Nf1 55 cholesterol metabolism 55 probands 55 vWD 55 SOD1 55 KCNH2 55 null mice 55 multivariate Cox 55 neuroglobin 55 Homozygous 55 herpes simplex virus 55 folate metabolism 55 microRNA miR 55 Single Nucleotide Polymorphisms 55 SLC#A# gene [001] 55 PB1 F2 55 Chronic ITP 55 myotonic dystrophy 55 #ß 55 BMI percentile 55 p# protein 55 superoxide dismutase 55 Heterozygous 55 Heredity 55 thrombophilia 55 thyroid stimulating hormone TSH 55 albuminuria 55 density lipoproteins HDL 55 LRP6 55 NAT2 55 c reactive protein 55 E selectin 55 von Willebrand 55 ALK mutations 55 androgen receptor AR 55 MLL2 55 amino acid valine 55 CCR3 55 late onset hypogonadism 55 arachidonic acid AA 55 familial dysautonomia 55 JAK2 enzyme 55 aminotransferase 55 alpha carotene 55 hepatoma 55 von Willebrand disease 55 SHANK3 gene 55 serous ovarian cancer 55 ADDLs 55 inherited genetic mutations 55 lipoprotein levels 55 heterozygosity 55 Angelman syndrome 55 CCL#L# 55 SIRT6 55 K ras mutations 55 Eur J Endocrinol 55 IGFBP 3 55 DICER1 gene 55 SGK1 55 aminotransferase levels 55 Rh incompatibility 55 holoprosencephaly 55 familial hypercholesterolaemia 55 psychiatric comorbidity 55 parkin gene 55 linoleic acids 55 AUDs 55 caveolin 55 catechol O methyltransferase 55 amyloid deposition 55 postoperative delirium 54 neuropathological 54 GPx 54 activating mutations 54 SOX3 gene 54 miRNA genes 54 HOMA IR 54 IL#B gene 54 cognitive decline 54 fructose intolerance 54 neoplasm 54 allelic 54 beta amyloid peptide 54 IGF1 54 NNRTI resistance 54 pyruvate kinase 54 poor metabolizers 54 regulates gene expression 54 vitamin B# deficiency 54 systemic inflammation 54 invasive ductal 54 sitosterol 54 MCAD deficiency 54 hemochromatosis 54 abnormal lipids 54 fronto temporal dementia 54 lipid concentrations 54 GISTs 54 fraternal twin pairs 54 transcriptional repressor 54 LRAT 54 modifier genes 54 varicella zoster virus 54 transgene expression 54 neuronal dysfunction 54 enterolactone 54 globin 54 phospholipase A2 54 syndrome FXTAS 54 SCA5 54 BRCA gene 54 MHC molecules 54 kidney allograft 54 Alzheimer Disease AD 54 neovascular 54 endothelial dysfunction 54 polyp recurrence 54 uric acid levels 54 hormone adiponectin 54 low density lipoprotein 54 thrombospondin 54 intestinal polyps 54 sortilin 54 prefrontal regions 54 hyperinsulinism 54 latent celiac disease 54 regulator CFTR gene 54 lobular breast cancer 54 TIMP 1 54 Neuroticism 54 albumin excretion rate 54 depressive symptomatology 54 chromosomal regions 54 prostate cancer PCa 54 CaM kinase II 54 glucocorticoid 54 Insulin sensitivity 54 SNPs 54 ovarian hormones 54 hydroxylase 54 TEL AML1 54 Dpp 54 virulence genes 54 tau mutation 54 galactosemia 54 modifiable risk 54 schizophreniform disorder 54 Major depressive disorder 54 sodium glucose cotransporter 54 PTP1B 54 vascular dementia 54 trans palmitoleic acid 54 T1D 54 remnant lipoproteins 54 serum selenium 54 Glioblastoma multiforme GBM 54 human metapneumovirus 54 lipid levels 54 cognitive impairment 54 inherited maternally