Related by context. All words. (Click for frequent words.) 73 APOE e4 71 APOE4 69 Genetic variants 69 APOE allele 69 APOE e4 gene 68 ε4 68 subclinical hyperthyroidism 68 UGT#A# * 68 ApoE4 68 APOE genotype 68 ApoE4 gene 68 penetrance 68 narcolepsy cataplexy 67 PTEN mutations 67 inherited mutations 67 GBA mutations 67 ApoE gene 67 thyrotropin levels 67 GABRA2 67 DQB1 * 67 ABCB1 67 TT genotype 67 shorter telomere length 67 APOE4 gene 67 familial pancreatic cancer 66 basal cell nevus syndrome 66 TGFBR1 * 6A 66 MMSE scores 66 apolipoprotein E gene 66 5 HTTLPR 66 shorter telomeres 66 PTPN# 66 NNRTI resistance 66 alexithymia 66 apolipoprotein E 66 dopamine receptor gene 66 MGUS 66 variant alleles 66 nonalcoholic steatohepatitis NASH 66 de novo mutations 66 GSTM1 gene 66 APOE gene 65 apolipoprotein E4 65 hereditary predisposition 65 familial clustering 65 CNTNAP2 65 epigenetic changes 65 parous women 65 COMT gene 65 folate deficiency 65 parkinsonism 65 GSTM1 65 SHANK3 65 GABRA2 gene 65 missense mutations 65 GSTT1 65 #q# deletion 65 CYP#C# [001] 65 thiopurine 65 sCJD 65 genes predisposing 65 SE alleles 65 atypical neuroleptics 65 mutated K ras 65 nonmelanoma skin cancers 65 atypical hyperplasia 65 Genetic predisposition 64 EBV infection 64 TCF#L# gene 64 heterozygotes 64 CYP#A# gene 64 elevated triglyceride levels 64 KIBRA 64 TCF#L# 64 osteosarcomas 64 KCNH2 64 apoE4 64 untreated celiac disease 64 CP CPPS 64 ovarian hormones 64 APOE epsilon 4 64 apoC III 64 DRD2 64 nonhereditary 64 nondemented 64 BMPR2 64 T1DM 64 Leydig cell 64 albumin excretion 64 IL#R 64 telomere lengths 64 MSH2 64 KIF6 gene 64 APOC3 64 CYP#D# 64 ADPKD 64 HbF 64 neurodevelopmental outcome 64 BRCA1 mutations 64 klotho 64 multivariate adjustment 64 dopamine transporter gene 64 brain lesions 63 DRD2 gene 63 MLH1 63 CETP VV 63 adrenal function 63 chromosomal instability 63 germline mutations 63 STAT4 63 SNP rs# [002] 63 coronary calcification 63 G allele 63 gene APOE 63 mitochondrial mutations 63 CC genotype 63 subclinical atherosclerosis 63 gene APOE4 63 colorectal neoplasia 63 neuropsychological impairments 63 rs# [002] 63 heritable variation 63 hypermethylated 63 TRAF1 C5 63 monozygotic twins 63 PTEN gene 63 comorbid depression 63 familial ALS 63 CDKN2A 63 SLC#A# [002] 63 homozygosity 63 affective psychosis 63 nondepressed 63 euthymic patients 63 BRCA mutation 63 chlamydial infection 63 airway hyper responsiveness 63 monozygotic twin 63 MetS 63 #q#.# deletion syndrome 63 heterozygous 63 noncarriers 63 HLA B# 63 KRAS mutations 63 amenorrhoea 63 HNPCC 63 seropositivity 63 HER2 overexpression 63 5 HTT gene 63 neuritic 63 MYH9 gene 63 allele frequencies 63 mutant worms 63 corticosterone levels 63 rs# [003] 63 proband 63 G6PD deficiency 63 APOE e4 allele 63 SNP rs# [001] 63 arterial thickening 63 colorectal adenoma 63 Hashimoto thyroiditis 63 bronchopulmonary dysplasia 63 postnatally 63 neurocognitive function 63 LQTS 63 genetic polymorphism 63 extrapyramidal symptoms 63 HIV HCV coinfected 63 HLA DRB1 62 juvenile idiopathic arthritis JIA 62 homozygotes 62 TMEM#B 62 folate metabolism 62 CHRNA5 gene 62 hippocampal function 62 familial aggregation 62 Genetic variation 62 hematopoietic cancers 62 CagA 62 fluoroquinolone resistance 62 p# activation 62 autistic traits 62 dizygotic twins 62 MTHFR 62 rheumatoid factor 62 adiponectin levels 62 assortative mating 62 CIN3 62 LRRK2 mutations 62 atopic 62 poorer prognosis 62 CVD mortality 62 androgenic hormones 62 endoxifen 62 behavioral disinhibition 62 AAT deficiency 62 autonomic dysfunction 62 multivariate analyzes 62 CCR5 delta# 62 C#Y 62 autoimmune thyroid 62 hydroxyvitamin D concentrations 62 mtDNA mutations 62 genes BRCA1 62 CALHM1 62 ABCB1 gene 62 prostate carcinogenesis 62 serum BDNF 62 chromosomal rearrangement 62 subclinical 62 ApoE4 allele 62 onset diabetes mellitus 62 FGF2 62 TEAEs 62 carotid IMT 62 DRD4 62 chromosomal aberrations 62 GLUT1 62 mosaicism 62 genetic polymorphisms 62 elevated homocysteine 62 hydroxyvitamin D levels 62 serous ovarian cancer 62 epigenetic alterations 62 spontaneous mutations 62 H pylori 62 gestational diabetes mellitus 62 p# mutations 62 p# mutation 62 comorbid disorders 62 HNSCC 62 causal variants 62 diabetes mellitus DM 62 estrogen receptor ER 62 CFH gene 62 affective psychoses 62 depressive symptomatology 62 deleterious mutations 62 serum lipid levels 62 neurological abnormalities 62 epigenetic silencing 62 MHC genes 62 testicular germ cell 62 dysglycemia 62 BDNF gene 62 seminomas 62 habitual snoring 62 mammary cancers 62 BRCA1 mutation carriers 62 obstructive coronary artery 62 MC1R gene 62 unmeasured factors 62 insulin resistance syndrome 62 APOE 62 hyper IgE syndrome 62 estrogen receptor negative 62 estrone 62 CYP#D# gene 61 #q# deletion syndrome 61 BRCA mutations 61 SCN1A 61 MC4R gene 61 dopamine D2 receptor 61 Relapsing remitting MS 61 Wwox 61 neurocognitive impairment 61 CAG repeats 61 ataxias 61 infarcts 61 Chronic pancreatitis 61 atopy 61 #q#.# [001] 61 CYP#C# gene 61 BRCA2 carriers 61 BRCA2 mutations 61 prostate cancer CaP 61 NPY expression 61 leukaemias 61 androgen receptor gene 61 BARD1 61 schizophreniform disorder 61 missense mutation 61 Treg cell 61 metabolic disturbances 61 neurodevelopmental impairment 61 white matter hyperintensities 61 genetic loci 61 PON1 61 T2DM 61 aortic atherosclerosis 61 methylation patterns 61 serotonin transporter gene 61 pre eclamptic 61 dopamine D4 receptor 61 chorioamnionitis 61 thyrotropin 61 Fragile X gene 61 C. pneumoniae 61 olfactory dysfunction 61 mutant allele 61 mitochondrial disorders 61 transgenic rats 61 comorbid anxiety 61 dysbindin 61 monogenic 61 K ras mutations 61 familial adenomatous polyposis 61 neuropsychological deficits 61 IgA deficiency 61 psychiatric comorbidity 61 overt hypothyroidism 61 susceptibility gene 61 APOL1 61 chromosomal alterations 61 plasma lipid 61 airway responsiveness 61 MC1R 61 SHBG levels 61 proliferative diabetic retinopathy 61 cognitively normal 61 mutated BRCA1 61 enterovirus infection 61 polycystic ovary syndrome PCOS 61 DFMO 61 CHD7 61 testosterone secretion 61 HIV uninfected 61 #p#.# [002] 61 azoospermia 61 allergic sensitization 61 progressive neurodegenerative disorder 61 hippocampal atrophy 61 dopamine signaling 61 selenium deficiency 61 androgen deficiency 61 LPA gene 61 e4 allele 61 #OHD levels 61 herpesviruses 61 CHD mortality 61 chromosomal anomalies 61 serum vitamin D 61 elevated CRP 61 2 diabetes T2D 61 apoE 61 C1q 61 gene variant 61 BRCA2 mutation 61 TP# mutation 61 M. pneumoniae 61 Leydig cells 61 NPY gene 61 Zinc deficiency 61 ALDH2 61 thyroid dysfunction 61 beta carotene supplementation 61 fasting glucose levels 61 MAOA 61 prefrontal regions 61 genetic variant 60 antenatal depression 60 Severe Primary IGFD 60 TP# mutations 60 aldehyde dehydrogenase 60 CNTNAP2 gene 60 neurofibrillary 60 hormone therapy estrogen 60 microdeletions 60 hypercholesterolaemia 60 fetal malformations 60 amnestic MCI 60 Sjögren syndrome 60 ZNF# 60 psychiatric morbidity 60 SGPT 60 DAT1 60 HBeAg negative 60 slow metabolizers 60 atopic disorders 60 LRAT 60 homozygous 60 invasive ductal 60 T2D 60 arterial calcification 60 rs# [001] 60 typical antipsychotics 60 SSc 60 MnSOD 60 TMPRSS2 ERG fusion 60 microcephalin 60 recurrent VTE 60 epistasis 60 testicular tumors 60 Cognitive impairment 60 biochemical abnormalities 60 immunodeficient 60 NAT2 60 cytopathic 60 Leukemias 60 type2 diabetes 60 motor neuron degeneration 60 carotid plaques 60 inbred strains 60 neuroblastomas 60 autosomal dominant inheritance 60 ApoE 60 immunized mice 60 receptor inhibitor 60 BRAF V#E mutation 60 gene deletions 60 premenstrual syndrome PMS 60 KRAS oncogene 60 LV dysfunction 60 lupus anticoagulant 60 fasting insulin 60 2D 4D ratio 60 gallstone disease 60 IGFBP 60 serum folate 60 nondiabetic 60 BRCA1 mutation 60 COX2 60 BRCA gene mutation 60 genetic variants associated 60 hepatoma 60 serum estradiol 60 amyloid plaque formation 60 genital ulcer disease 60 genital HPV infections 60 SIDS infants 60 LRRK2 gene 60 hypercoagulable 60 UGT#B# 60 eosinophil count 60 urate levels 60 monozygotic 60 colorectal adenomas 60 Rh factor 60 bile acid metabolism 60 genomic variants 60 GBM tumors 60 tHcy 60 airway hyperresponsiveness 60 homozygote 60 behavioral abnormalities 60 sporadic ALS 60 polycystic ovarian syndrome PCOS 60 metabolic syndrome MetS 60 MMSE score 60 HbF levels 60 prothrombotic 60 TACI mutations 60 colorectal carcinogenesis 60 impaired glucose metabolism 60 PCa 60 Vascular dementia 60 BRCA2 gene mutation 60 haematopoietic 60 β blockers 60 autosomal dominant disorder 60 poor metabolizers 60 hepatitis B infection 60 K#R [002] 60 alleles 60 Wernicke Korsakoff syndrome 60 advanced adenoma 60 cystatin C 60 preeclamptic 60 thyroid hormone levels 60 elevated serum creatinine 60 sleeve lobectomy 60 bexarotene 60 T. vaginalis 60 Angiotensin converting enzyme 60 FMRP protein 60 IKZF1 60 nonischemic 60 CETP gene 60 MECP2 gene 60 predisposing factor 60 MTHFR gene 60 psychiatric comorbidities 60 LRP5 60 nucleoside analogues 60 EoE 60 NOMID 60 Kufs disease 60 hormone receptor negative 60 etiological factors 60 humanin 60 autosomal recessive 60 BRIP1 60 unipolar depression 60 DHEAS 60 hypovitaminosis D 60 coinfection 60 XMRV infection 60 serum selenium 60 CYP#D# genotype 60 vascular dysfunction 60 ORMDL3 60 ENPP1 60 SORL1 60 GSTP1 60 GPC5 60 schizotypal traits 60 Mood disorders 60 intravenous bisphosphonates 60 gene variants 60 obstructive coronary 60 aneuploidy 60 serum PTH 60 transgene expression 60 premenopause 60 Prox1 59 FXTAS 59 Subgroup analyzes 59 neurologic complications 59 GBV C 59 Hurthle cell 59 primary ovarian insufficiency 59 BRAF mutation 59 non aspirin NSAIDs 59 Nicotine dependence 59 HLA DRB1 * 59 hepatocellular carcinomas 59 sFlt 1 59 amyloid deposition 59 cerebral microbleeds 59 nongenetic 59 dopamine D2 receptors 59 unmeasured confounders 59 Colon polyps 59 HDL2 59 serum parathyroid hormone 59 abdominal adiposity 59 HER2 expression 59 androgen excess 59 synaptic function 59 CD#c 59 prodynorphin 59 alpha thalassemia 59 Multivariate analyzes 59 vivax 59 JAK2 mutation 59 SMAD4 59 lupus scleroderma 59 metabolic abnormalities 59 ERBB2 59 glucocorticoid receptors 59 pathophysiological mechanisms 59 AGILECT R 59 underlying pathophysiology 59 latent celiac disease 59 gene polymorphisms 59 astrocytomas 59 prolonged QT interval 59 elevated serum ALT 59 antioxidant supplementation 59 probands 59 familial hypercholesterolemia 59 angiotensin receptor blockers ARBs 59 paraneoplastic 59 histocompatibility 59 differential gene expression 59 transaminase elevations 59 somatoform disorders 59 lung adenocarcinoma 59 troponin T 59 disease NAFLD 59 apolipoprotein E APOE 59 NMDA receptor antagonists 59 subclinical hypothyroidism 59 allelic variants 59 dizygotic 59 pathogenic mutations 59 Li Fraumeni syndrome 59 hyperinsulinemia 59 PDGFR 59 bronchopulmonary dysplasia BPD 59 Moderate drinkers 59 TYMS 59 β amyloid 59 MAOA gene 59 Clusterin 59 C. trachomatis 59 univariate analyzes 59 hypochondriasis 59 amnestic mild cognitive impairment 59 carotid atherosclerosis 59 alpha synuclein gene 59 hypertensives 59 psychosocial functioning 59 maternally inherited 59 plasma folate 59 serum urate levels 59 serum creatinine levels 59 VEGF expression 59 phthalate syndrome 59 BRCA2 gene 59 testosterone supplementation 59 flavopiridol 59 advanced adenomas 59 cagA 59 neurosensory 59 TP# gene 59 postoperative delirium 59 variant allele 59 CYP #A# 59 BRAF V#E 59 hypogonadotropic hypogonadism 59 KLF4 59 male hormone androgen 59 intelligence quotient IQ 59 generalized epilepsy 59 AML MDS 59 hyperhomocysteinemia 59 TPMT 59 adiponectin concentrations 59 DRB1 * 59 recurrent miscarriages 59 LDL cholesterol concentrations 59 CDH1 59 neoplasias 59 cranial irradiation 59 deletion 5q 59 elevated triglycerides 59 elevated ALT 59 ductal breast cancer 59 indinavir 59 toxoplasma 59 inducible nitric oxide synthase 59 neurocognitive deficits 59 HER2 neu 59 SORL1 gene 59 non affective psychosis 59 neurodevelopmental outcomes 59 G6PD 59 internalizing disorders 59 bivariate analyzes 59 clinically detectable 59 SRBD 59 esophageal squamous cell carcinoma 59 GPx 59 inherit predisposition 59 endogenous estrogen 59 thrombophilia 59 polyp recurrence 59 EGFR mutations 59 PARP inhibition 59 BCR ABL mutations 59 Heavy menstrual bleeding 59 ethosuximide 59 rs# [004] 59 histological subtype 59 psychotic illnesses 59 potassium sparing diuretics 59 socioeconomic status SES 59 alpha2 59 tumor histology 59 CYP#B# 59 PON1 gene 59 chromosome #q# [001] 59 IL#B 59 MTHFD1L gene 59 Apolipoprotein E 59 G#S mutation 59 lipid abnormalities 59 Haptoglobin 59 androgen depletion 59 initiating HAART 59 hamartomas 59 atrophic gastritis 59 HLA DRB1 SE 59 leptin deficiency 59 dietary calcium intake 59 heterotaxy 59 hyperprolactinemia 59 undiagnosed celiac disease 59 tarenflurbil 59 glial tumors 59 multivariable analysis 59 neutrophil counts 59 depressive symptoms 59 intestinal polyps 59 chloride secretion 59 phenotypic variation 59 lichen planus 59 recurrent miscarriage 59 neuropsychiatric symptoms 59 pilocytic astrocytomas 59 medulloblastoma tumors 59 unhealthier lifestyles 59 gastrointestinal stromal tumors GISTs 59 fetuin 59 SNCA 59 immunodeficiencies 59 neurofibromas 59 Male infertility 59 colorectal tumors 59 allele 59 attain statistical significance 59 HSV1 59 glitazones 59 promoter methylation 59 bronchoalveolar 59 somatostatin 59 HPV# 59 Prostatitis 59 idiopathic PAH 59 albumin excretion rate 59 Vitamin B# deficiency 59 extrapyramidal symptoms EPS 59 venlafaxine XR 59 impaired insulin secretion 59 muscle dysmorphia 59 FASPS 59 endotoxin exposure 59 metabolic abnormality 59 selenium supplementation 59 myo inositol 59 microdeletion 59 hypokalemia hypomagnesemia 59 neuroligins 59 postmenopausal hormones 59 impair fertility 59 FGFR2 59 homocysteine concentrations 59 malignant neoplasm 59 SGS# 59 heterozygote 59 5q 59 Chlamydia pneumoniae 59 mitochondrial dysfunction 59 JAK2 enzyme 59 parkinsonian 59 serum homocysteine 59 heterozygosity 59 Mendelian disorders 59 transgenic mouse models 59 ADAM# 59 NF1 59 steatohepatitis 59 Apolipoprotein E4 59 estrogen receptor alpha 59 asymptomatic PAD 59 atherosclerotic lesions 59 metabolizer 59 inhibitory neurotransmitters 59 squamous cell lung cancer 59 oligodendrogliomas 58 AChE inhibitors 58 Neuroticism 58 BRCA1 BRCA2 58 T1D 58 germline mutation 58 Subgroup analysis 58 E selectin 58 polygenic 58 synovial cells 58 genital tract infections 58 maternally transmitted 58 ADH1B * 58 unmutated 58 gene polymorphism 58 macrovascular disease 58 hereditary hemochromatosis 58 coronary artery aneurysms 58 comorbid illnesses 58 alanine aminotransferase ALT 58 abdominally obese 58 dyslipidaemia 58 endocannabinoid signaling 58 clefting 58 GISTs 58 COMT enzyme 58 KIF6 carriers 58 HER2 positive cancers 58 neuronal dysfunction 58 Longitudinal studies 58 cybrid 58 DISC1 gene 58 postmenopausal hormone therapy 58 Alzheimer disease vascular dementia 58 HIVAN 58 lobular carcinoma 58 serum concentrations 58 aneuploidies 58 pCR 58 monoclonal gammopathy 58 mice lacking 58 Candida species 58 EAAT2 58 herpes infection 58 chlamydial infections 58 gastric carcinoma 58 urine cytology 58 recessive genetic 58 myeloproliferative neoplasms 58 chitinase 58 microglial 58 CDK4 58 neurobehavioural 58 autoimmune thyroiditis 58 BCL#A 58 pancreatic adenocarcinoma 58 recurrent UTI 58 progranulin gene 58 Heritability 58 clade B 58 BCG vaccinated 58 allostatic load 58 phenotypic expression 58 elevated LDL cholesterol 58 sulphonylureas 58 immunocompetent 58 Uterine cancer 58 N. gonorrhoeae 58 fronto temporal dementia 58 microchimerism 58 S. aureus isolates 58 S#A# [002] 58 gene locus 58 NRTI resistance 58 recurrent wheezing 58 excitatory synapses 58 chromosomal anomaly 58 CYP#C# * 58 fluoxetine Prozac 58 frontotemporal dementia 58 diabetic kidney 58 gene BRCA2 58 loop diuretics 58 deleterious mutation 58 aetiological 58 irregular menstrual cycles 58 neuroblastoma tumors 58 obesity insulin resistance 58 cardio metabolic 58 metastatic prostate 58 functional polymorphism 58 impaired cognition 58 PDE#A 58 Cryptococcus neoformans 58 ADAMTS# 58 aneuploid cells 58 serotonin synthesis 58 bowel polyps 58 nonseminoma 58 NAFLD 58 neuropathologic 58 androgen deprivation 58 elevated LDH 58 SOD2 gene 58 Anxiety disorders 58 VHL gene 58 Helicobacter pylori infection 58 transferrin saturation 58 micronuclei 58 baseline HbA1c 58 MMP# 58 imatinib resistance 58 inherited predisposition 58 Suicidal ideation 58 intracranial hemorrhage ICH 58 neurocognitive functioning 58 oxysterols 58 cerebral infarction 58 phytoestrogen intake 58 GH deficiency 58 metabolite concentrations 58 intracellular signal transduction 58 consanguineous marriages 58 spermidine 58 de ath 58 epigenetic modification 58 BMI z 58 mRNA expression 58 cyclin E 58 nonnucleoside reverse transcriptase inhibitors 58 histologic subtype 58 atopic eczema 58 clomipramine 58 anovulatory infertility 58 M. genitalium 58 hyperoxia 58 hematologic toxicity 58 Mild cognitive impairment 58 cyclophilin D 58 hepatic fibrosis 58 hypermethylation 58 aneuploid 58 IGFBP 3 58 lymphocytic 58 HFE gene 58 HepG2 cells 58 giant danio 58 immunopathology 58 antiandrogens 58 mu opioid 58 TNF blocker therapy 58 Thal Dex 58 hereditary deafness 58 heritable genetic 58 tricyclics 58 oesophageal adenocarcinoma 58 aminotransferases 58 EGFR expression 58 histologic subtypes 58 amisulpride 58 HRQOL 58 cryptogenic 58 circadian genes 58 lymphatic cancers 58 neoplastic 58 BDNF protein 58 BRCA gene mutations 58 liver metastasis 58 pneumococci 58 V Leiden 58 MEF2A 58 VCFS 58 mutant huntingtin protein 58 cellularity 58 imipramine 58 cisplatin resistant 58 MHC molecules 58 lactose malabsorption 58 phylloquinone 58 dysbindin gene 58 CMV infection 58 genetic alteration 58 M. leprae 58 elevated cortisol 58 serum triglycerides 58 Hp2 2 58 FKBP# 58 Brugada syndrome 58 MYH9 58 perfusion abnormalities 58 OPRM1 58 atherothrombotic disease 58 bioavailable testosterone 58 ERK signaling 58 modifier genes 58 lobular involution 58 dopaminergic therapy 58 outbred 58 HMGA2 58 CXCL5 58 karyotypes 58 endometrial carcinoma 58 glycosylated 58 precancerous tumors 58 promoter polymorphism 58 dysthymic disorder 58 insulin sensitizing drug 58 congenital malformations 58 genetic syndromes 58 FUS1 58 probiotic supplementation 58 spontaneous mutation 58 repeat allele 58 placental malaria 58 shortened telomeres 58 neovascular 58 BRCA2 gene mutations 58 nonexposed 58 obstructive lung 58 FUS protein 58 persistent pulmonary hypertension 58 haptoglobin 58 TEL AML1 58 telomere shortening 58 OSAHS 58 familial predisposition 58 torsade de pointes 58 primary aldosteronism 58 Chlamydia infection 58 cardioembolic stroke 58 ß amyloid 58 orchitis 58 anovulation 58 chromosome #p# [001] 58 gestational diabetes mellitus GDM 58 lipid lowering medications 58 LVNC 58 cardiomyopathies 58 Folate deficiency 58 Peutz Jeghers syndrome 58 PIGF 58 FLT3 mutations 58 hypertrophic cardiomyopathy HCM 58 vascular cognitive impairment 58 plasma homocysteine levels 58 VaD 58 idiopathic myelofibrosis 58 FMR1 gene