Related by context. All words. (Click for frequent words.) 71 APOE gene 70 MTHFR 70 APOE4 70 rs# [002] 69 APOE e4 69 CDH1 69 C#Y 69 ABCB1 68 MYH9 gene 68 TCF#L# gene 68 apolipoprotein E 67 Genetic variation 67 monogenic 67 Apolipoprotein E 67 ApoE gene 67 HLA DRB1 67 susceptibility gene 67 MTHFR gene 67 apolipoprotein E4 66 CYP#C# gene 66 LRP5 66 APOE ε4 66 genes predisposing 66 PTPN# 66 UGT#A# * 66 APOC3 66 SHANK3 66 #p# [003] 66 V Leiden 66 MEF2A 66 rs# [001] 66 GSTM1 66 GSTT1 66 homozygosity 65 dopamine receptor gene 65 MSH2 65 chromosome #q# [001] 65 allelic variants 65 dopamine D4 receptor 65 HFE gene 65 klotho 65 microdeletion 65 missense mutations 65 predisposing factor 65 BARD1 65 autosomal recessive 65 germline mutations 65 rs# [003] 65 inherited mutations 65 Heterozygous 65 chromosome #q# [002] 65 autosomal recessive disease 65 G allele 65 KIF6 gene 65 5 HTTLPR 65 IL#R 65 APOE genotype 65 genetic polymorphism 65 rs# [004] 65 #q# deletion 65 ADH1B * 65 progressive neurodegenerative disorder 65 APOE 65 SMAD4 65 HLA B# 65 ApoE4 65 proband 65 de novo mutations 65 CHEK2 64 promoter polymorphism 64 homozygotes 64 CNTNAP2 64 CDKN2A 64 SLC#A# [001] 64 penetrance 64 gene polymorphism 64 APOL1 64 Variant Creutzfeldt Jakob 64 genetic variant 64 K ras mutations 64 DQB1 * 64 COL#A# 64 mutated K ras 64 Genetic variants 64 CYP#C# * 64 hereditary hemochromatosis 64 mutant allele 64 G6PD deficiency 64 TT genotype 64 CYP#D# gene 64 LRAT 64 MLH1 64 Hashimoto thyroiditis 64 Vascular dementia 64 Folate deficiency 64 heterozygotes 64 gene APOE 64 variant alleles 64 gestational diabetes mellitus 64 GSTM1 gene 64 apoE4 64 autosomal dominant disorder 64 variant allele 64 gene locus 64 genetic polymorphisms 64 DRD2 64 DRB1 * 64 microdeletions 64 paraneoplastic 64 chromosome #p# [001] 64 cardioembolic stroke 64 dominantly inherited 64 TGFBR1 * 6A 64 sCJD 64 CC genotype 64 ApoE4 gene 63 Beta thalassemia 63 CYP#C# [002] 63 susceptibility alleles 63 SNP rs# [001] 63 HLA DRB1 * 63 BRCA1 BRCA2 63 regulator CFTR gene 63 breast cancer genes BRCA1 63 #p# [001] 63 LPA gene 63 ADAMTS# 63 PALB2 63 IgA deficiency 63 heterozygous 63 ADPKD 63 HLA DQ2 63 apolipoprotein E APOE 63 hereditary predisposition 63 genetic syndromes 63 elevated triglyceride levels 63 TCF#L# 63 ApoE 63 #p#.# [001] 63 homozygote 63 microcephalin 63 ORMDL3 63 lichen planus 63 autosomal dominant 63 UGT#B# 63 MC4R gene 63 apoE 63 underlying pathophysiology 63 BRIP1 63 STK# gene 63 nonischemic 63 DRD4 63 MC1R 63 CCR5 delta# 63 cause cardiac channelopathies 62 GSTP1 62 CHD7 62 COMT gene 62 TP# gene 62 Vitamin B# deficiency 62 CYP#C# [001] 62 susceptibility locus 62 CAG repeats 62 HLA DRB1 SE 62 KRAS oncogene 62 Angiotensin converting enzyme 62 CETP gene 62 methylenetetrahydrofolate reductase 62 polymorphisms 62 progranulin gene 62 HDL2 62 alleles 62 Genotypes 62 BRCA1 mutations 62 ENPP1 62 Mendelian disorders 62 germline mutation 62 #p#.# [002] 62 coinfection 62 MC1R gene 62 insulin resistance syndrome 62 WNK1 62 spinocerebellar ataxia type 62 catechol O methyltransferase 62 ABCB1 gene 62 mutated BRCA1 62 Genetic predisposition 62 Polymorphisms 62 von Hippel Lindau 62 Lipodystrophy 62 SLC#A# [002] 62 Chlamydia pneumoniae 62 PON1 gene 62 APOE allele 62 nonhereditary 62 Alleles 62 mosaicism 62 BRCA2 gene 62 BCL#A 62 deleterious mutation 62 thrombophilia 62 #q#.# [001] 62 c KIT 62 BRAF V#E 62 type2 diabetes 62 hypermethylated 62 APOA5 62 microsatellite instability 62 GPC5 62 MLL gene 62 polymorphism 61 missense mutation 61 Irritable bowel syndrome 61 noncarriers 61 CDK4 61 chromosomal rearrangement 61 phenotypic expression 61 CETP VV 61 CFTR gene 61 C#T [002] 61 Trichomonas vaginalis 61 leiomyomas 61 homozygous 61 gene DRD4 61 VKORC1 61 mutation 61 autoimmune thyroid 61 HIV HCV coinfected 61 C. pneumoniae 61 R#W [002] 61 ZNF# 61 familial ALS 61 GRK5 61 SCN1A 61 genetic loci 61 SORL1 61 TEL AML1 61 FGFR2 61 GABRA2 61 DRD2 gene 61 chronic myeloid 61 genes CYP#C# 61 subclinical hyperthyroidism 61 BMPR2 61 Cystic fibrosis CF 61 neuritic 61 gene polymorphisms 61 SOD2 gene 61 Genetic mutation 61 metaplasia 61 APOE4 gene 61 clade B 61 colorectal carcinoma 61 PON1 61 KIAA# 61 Kufs disease 61 TMEM#B 61 Fas ligand 61 chromosomal anomalies 61 STAT4 61 CFH gene 61 Li Fraumeni syndrome 61 TP# mutations 61 Upregulation 61 Lipoprotein 61 OPRM1 gene 61 #q# [001] 61 homocystinuria 61 gene MECP2 61 leptin deficiency 61 NF1 gene 61 CALHM1 61 SNPs pronounced snips 61 autosomal recessive disorder 61 apoC III 61 familial adenomatous polyposis FAP 61 Genetic mutations 61 ε4 61 allele 61 gastric carcinogenesis 61 p# mutation 61 obesity insulin resistance 61 gastric adenocarcinoma 61 missense 61 KRAS mutations 61 recessive inheritance 61 enteroviral 61 Homozygous 61 ALK gene 61 Fatty liver 61 COX2 61 latent celiac disease 61 familial hypercholesterolemia 61 IL#B 61 Sjögren syndrome 61 chromosome #q#.# [002] 61 #q#.# [002] 61 anaplastic lymphoma kinase 61 NPY gene 61 human herpesvirus 61 metabolizing enzyme 61 retinol binding protein 61 serotonin transporter gene 61 idiopathic PAH 61 TP# mutation 61 thyrotropin 61 colorectal adenoma 61 hepatocellular carcinomas 60 microvascular disease 60 cardiolipin 60 Single Nucleotide Polymorphisms 60 androgen receptor gene 60 hepatoma 60 K#N 60 KCNH2 60 repeat allele 60 nephronophthisis 60 airway hyperresponsiveness 60 thyrotropin levels 60 plasminogen activator inhibitor 60 parkinsonism 60 e4 allele 60 chromosomal disorders 60 Polycystic ovary syndrome PCOS 60 CYP#A# gene 60 familial pancreatic cancer 60 haplotype 60 receptor gene 60 cholesteryl ester transfer 60 VHL gene 60 autosomal 60 CagA 60 allele frequencies 60 amino acid substitution 60 MMP# 60 Subclinical 60 hyperhomocysteinemia 60 Arrhythmogenic Right Ventricular Cardiomyopathy 60 KLF4 60 Chronic pancreatitis 60 aminotransferase 60 BRCA2 mutation 60 diabetic kidney 60 MECP2 gene 60 Irritable bowel syndrome IBS 60 nonalcoholic steatohepatitis NASH 60 nonmelanoma skin cancers 60 BRCA2 breast cancer 60 ERBB2 60 neuroblastoma tumors 60 functional polymorphism 60 Hypertrophic cardiomyopathy 60 BRCA2 carriers 60 genetic variants associated 60 chromosome #p#.# 60 MYBPC3 60 dopamine transporter gene 60 narcolepsy cataplexy 60 serum BDNF 60 gallstone disease 60 Asymptomatic 60 myelofibrosis polycythemia vera 60 ataxias 60 chromosomal alterations 60 Nonalcoholic fatty liver 60 collagenous colitis 60 JAK mutations 60 Hutchinson Gilford progeria 60 hypovitaminosis D 60 eotaxin 60 BRCA1 mutation 60 Mycoplasma pneumoniae 60 cell adhesion molecule 60 Fragile X gene 60 VLDL cholesterol 60 2 diabetes T2D 60 Epstein Barr virus EBV 60 #q# [002] 60 Haptoglobin 60 motor neuron degeneration 60 inherited neurological disorder 60 CYP#D# 60 parkin gene 60 apo B 60 HER2 overexpression 60 Glucocorticoids 60 indels 60 human leukocyte antigen 60 BRCA2 gene mutation 60 monoclonal gammopathy 60 C#Y mutation 60 promoter methylation 60 induce orthostatic hypotension 60 Helicobacter pylori infection 60 impaired glucose metabolism 60 leiomyoma 60 Brugada Syndrome 60 gastric carcinoma 60 UGT#A# 60 hydrops 60 single nucleotide polymorphism 60 ribosomal protein 60 sporadic ALS 60 BDNF gene 60 null mice 60 chromosomal aberrations 60 del 5q 60 DNA methylation patterns 60 Autoimmune hepatitis 60 normal karyotype 60 genotype 60 Endometrial cancer 59 PTEN mutations 59 liver metastasis 59 dysbindin 59 TPMT 59 caveolin 59 Squamous 59 Cryptococcus neoformans 59 Bacterial vaginosis 59 basal cell carcinoma BCC 59 LIS1 59 neuropsychiatric disorder 59 seropositivity 59 MLL2 59 synuclein 59 Papillary 59 antiphospholipid antibodies 59 5 HTT gene 59 genes BRCA1 59 modifier genes 59 PIGF 59 NNRTI resistance 59 allelic 59 mutated gene 59 CD#c 59 H. influenzae 59 causative mutations 59 Heavy menstrual bleeding 59 postoperative delirium 59 Trichophyton rubrum 59 prolonged QT interval 59 diabetes dyslipidemia 59 herpesviruses 59 Hurthle cell 59 Klotho gene 59 PTEN gene 59 familial clustering 59 invasive ductal 59 ApoE4 allele 59 transfusion syndrome 59 lupus anticoagulant 59 gene variant 59 obliterans 59 cyclin E 59 serous ovarian cancer 59 familial adenomatous polyposis 59 fructose intolerance 59 BRCA2 mutations 59 testicular tumors 59 SHANK3 gene 59 constitutively expressed 59 folate deficiency 59 human metapneumovirus 59 Treponema 59 phenothiazines 59 F#del 59 APOE e4 allele 59 fetal chromosomal 59 oesophageal adenocarcinoma 59 mtDNA mutations 59 aneuploidies 59 maternally inherited 59 Dilated cardiomyopathy 59 causative gene 59 gene BRCA2 59 abdominal adiposity 59 unmutated 59 HMGA2 59 Apolipoprotein 59 susceptibility loci 59 neoplasm 59 GISTs 59 Brugada syndrome 59 Polymorphism 59 IPAH 59 E selectin 59 ALDH2 59 SE alleles 59 prodynorphin 59 Premature Aging 59 deletion 5q 59 eosinophil count 59 Li Fraumeni 59 TSC1 59 Leukemias 59 1 diabetes T1D 59 antiphospholipid syndrome 59 MDR1 59 Entamoeba 59 klotho gene 59 recessive mutations 59 M. pneumoniae 59 arterial calcification 59 BMP2 59 infarcts 59 chromosomal defects 59 recessive trait 59 teratogens 59 Gastric cancer 59 Subtype 59 NR#A# 59 glutamic acid decarboxylase 59 heterozygote 59 Creutzfeldt Jacob 59 hypogonadotropic hypogonadism 59 C. trachomatis 59 chitinase 59 Haplotype 59 CCR3 59 Rh factor 59 TRAF1 C5 59 Neurofibromatosis type 59 Pulmonary hypertension 59 EGFR gene 59 CNTNAP2 gene 59 GNAQ 59 lung adenocarcinoma 59 mucinous 59 Gene Mutation 59 Sporadic CJD 59 arrhythmogenic right 59 Leydig cell 59 MGUS 59 Gestational 59 Cognitive impairment 59 GBA mutations 59 cytopathic 59 bexarotene 59 abnormal glucose metabolism 59 alveolar epithelial cells 59 SLC#A# gene [001] 59 airway hyperreactivity 59 cardiomyopathies 59 LPS induced 59 Inactivation 59 DICER1 gene 59 HLA B 59 Estrogen Receptor 59 CYP#A# CYP#D# 59 ERK signaling 59 chromosome #p# [002] 59 AAT deficiency 59 HMGCR 59 prostate cancer CaP 59 breast carcinomas 59 mitochondrial mutations 59 gene amplification 59 Aortic stenosis 59 familial dysautonomia 59 amyloid cascade 59 JAK2 enzyme 59 LV dysfunction 59 HNPCC 59 GLUT1 59 cerebral infarction 59 bronchoalveolar 59 Nf1 59 CSF biomarkers 59 alpha synuclein gene 59 LRRK2 gene 59 plasma lipid 59 epigenetic modification 59 protein tyrosine phosphatase 59 haplotypes 59 urethritis 59 susceptibility genes 59 alternatively spliced 59 cryptogenic 59 Amino acid 59 vWD 59 Nilotinib 59 SNPs 59 hamartomas 59 tryptase 59 endometrial cancers 58 amyloid deposition 58 myopathies 58 SCN5A 58 FMR1 58 recessive mutation 58 apo E 58 SORL1 gene 58 Genotype 58 #q#.# deletion syndrome 58 replicase 58 gene loci 58 fetal malformations 58 heterozygosity 58 congenital adrenal hyperplasia CAH 58 Hyperthyroidism 58 neurological abnormalities 58 Jhdm2a 58 KCNQ1 58 apolipoprotein B 58 neurological manifestations 58 chromosomal anomaly 58 TOMM# 58 C#BL/#J 58 monozygotic twins 58 paternally inherited 58 G#S mutation 58 Low density lipoprotein 58 basal cell nevus syndrome 58 gene variation 58 K ras gene 58 chronic eosinophilic leukemia 58 diabetes mellitus DM 58 apolipoproteins 58 FTLD 58 muscular dystrophies 58 III EGFRvIII 58 CFTR cystic fibrosis transmembrane 58 Hp2 2 58 ADAM# 58 NRTI resistance 58 T2D 58 IDH2 58 hormone therapy estrogen 58 paraganglioma 58 cystic fibrosis Duchenne muscular 58 transgenic mice expressing 58 airway hyper responsiveness 58 FASPS 58 ovarian dysfunction 58 HMMR 58 gastrointestinal stromal tumors GISTs 58 hypokalemia hypomagnesemia 58 isoenzyme 58 ANCA associated 58 Eur J Endocrinol 58 Von Willebrand disease 58 IDDM 58 frameshift mutation 58 Urinary tract 58 pancreatic endocrine 58 advanced adenoma 58 chorioamnionitis 58 PAOD 58 pathophysiologic 58 supratentorial 58 polyp recurrence 58 bronchogenic carcinoma 58 Wwox 58 amnestic 58 atrophic gastritis 58 gastric carcinomas 58 tyrosine phosphorylation 58 monozygotic twin 58 variant rs# 58 CYP #A# 58 Janus kinase 58 hypereosinophilic syndrome 58 leptin receptor 58 glucose transporter 58 cytogenetic abnormalities 58 human leukocyte antigen HLA 58 prostate abnormalities 58 hyperparathyroidism 58 multivariate Cox 58 angiotensin receptor blockers ARBs 58 genetic locus 58 Erythropoietic therapies may 58 aldehyde dehydrogenase 58 silent myocardial ischemia 58 adnexal mass 58 P. falciparum malaria 58 Alanine 58 inverse agonist 58 BRAF gene 58 neoplasias 58 Myocardial infarction 58 familial aggregation 58 CYP#B# 58 galactosemia 58 multi infarct dementia 58 MIF protein 58 Systemic lupus erythematosus SLE 58 Sezary syndrome 58 APOE epsilon 4 58 carotid plaques 58 chromosome #q#.# [001] 58 maternally transmitted 58 Oxidative stress 58 CYP#A# [002] 58 steroidogenic 58 Parkinsonian 58 FLT3 58 gestational diabetes mellitus GDM 58 C1q 58 SCA5 58 Angiotensin receptor blockers 58 ERBB4 58 transferrin saturation 58 MYH9 58 5q 58 cystatin C 58 esophageal squamous cell carcinoma 58 Polymorphic Ventricular Tachycardia CPVT 58 Non Alcoholic Steatohepatitis 58 CYP#E# gene 58 Opportunistic infections 58 Creutzfeld Jakob disease 58 T#I [002] 58 Chronic lymphocytic leukemia 58 abnormal vaginal bleeding 58 MELAS 58 Cockayne syndrome 58 TMPRSS2 ERG fusion 58 activating mutations 58 COMT enzyme 58 aberrant methylation 58 IKZF1 58 sonographic appearance 58 pyelonephritis 58 spontaneous mutation 58 NAT2 58 multisystem disease 58 FGFR2 gene 58 pre eclamptic 58 somatic mutations 58 Single Nucleotide Polymorphism 58 thyroglobulin 58 C Reactive Protein 58 ventricular myocardium 58 E#F# 58 number variations CNVs 58 hepatic lipase 58 Epstein Barr Virus EBV 58 HBeAg negative 58 Metastases 58 monozygotic 58 disease NAFLD 58 hamartoma 58 BRCA1 gene 58 NOTCH1 58 obstructive coronary artery 58 Nedd4 58 endocannabinoid signaling 58 inherited predisposition 58 HLA genes 58 transgenic mouse models 58 Thiazolidinediones 58 histologic subtype 58 homolog 58 gene APOE4 58 bowel polyps 58 eNOS 58 FGFs 58 syngeneic 58 isoenzymes 58 Angiotensin II 58 LVNC 58 obstructive coronary 58 HGPS 58 alpha1 58 granulomatous 58 HepG2 cells 58 MHC molecules 58 APOE e4 gene 58 Diabetic neuropathy 58 extramedullary 58 subclinical atherosclerosis 58 lactose malabsorption 58 metabolizing enzymes 58 breast endometrial 58 ATG#L# 58 thromboembolism 58 presymptomatic 58 genetically inherited 58 FMR1 gene 58 glycosylated 58 macroalbuminuria 58 GATA4 58 Leukotriene 58 miRNAs miR 58 gastrointestinal GI bleeding 58 severe congenital neutropenia 58 genomic deletions 58 extrapyramidal symptoms 58 heterotaxy 58 invasive lobular 58 renal tubular 58 G#S [002] 58 primary aldosteronism 58 HbF 58 Parkinsonian Syndromes 58 SGPT 58 deCODE BreastCancer 58 estrogen receptor ER 58 Autoantibodies 58 Mg Uk 58 promoter hypermethylation 58 chromosome abnormality 58 diagnostic biomarker 58 protein encoded 58 Heritability 58 gene deletions 58 haematopoietic 58 beta adrenergic receptor 58 rheumatoid factor 58 KCNE2 58 intronic 58 cagA 58 inherited maternally 58 virulence genes 58 dyskeratosis congenita 58 Diverticulosis 58 exfoliation glaucoma 58 orthologs 58 NPC1 58 apolipoprotein 58 HMGA1 58 Estrogen receptor 58 BRAF V#E mutation 58 TIMP 1 58 subependymal giant cell 58 mutant huntingtin protein 58 idiopathic myelofibrosis 58 histological subtype 58 Aneuploidy 58 Single Nucleotide Polymorphisms SNPs 58 hyperplastic 58 atypical hyperplasia 58 Systemic lupus erythematosus 58 intensive statin therapy 58 affective psychoses 57 endometrial hyperplasia 57 untreated celiac disease 57 atherogenic 57 Cathepsin B 57 Homocysteine 57 Carcinoid tumors 57 A1 allele 57 Clusterin 57 endostatin 57 neovascular 57 hyperinsulinism 57 TGF ß 57 KIBRA 57 E. faecalis 57 premenstrual syndrome PMS 57 filaggrin gene 57 activin 57 gene variants 57 COMT 57 Endothelial dysfunction 57 malignant neoplasm 57 hemoglobinopathies 57 karyotype 57 cyclin dependent kinase inhibitor 57 SOD1 gene 57 etiologic agent 57 lipoprotein metabolism 57 prognostic marker 57 etiologic 57 gastric cardia 57 HMGA2 gene 57 leukoencephalopathy 57 recessive genetic 57 Alzheimer Disease AD 57 OCA2 57 TNFAIP3 57 Major depressive disorder 57 Prostatitis 57 de ath 57 RCAN1 57 Lymphocytic 57 erythrocytes 57 Hemophilia B 57 unmeasured confounders 57 cytochrome b 57 PB1 F2 57 HLA molecules 57 Proteinuria 57 epigenetic changes 57 CHRNA5 gene 57 GAB2 57 homozygous familial hypercholesterolemia 57 Treg cell 57 PUFA intake 57 Gastritis 57 testicular germ cell 57 abnormal hemoglobin 57 mutant gene 57 myo inositol 57 TACI mutations 57 Bucindolol 57 5 HT1A receptor 57 pathogenic mutations 57 isotypes 57 mRNA transcripts 57 untreated hypothyroidism 57 MIF gene 57 ASCUS 57 neurofibrillary 57 Plasmodium vivax 57 TOP2A gene 57 elevated CRP 57 protein tyrosine phosphatase 1B 57 incomplete penetrance 57 diabetes mellitus T2DM 57 lacunar 57 overactive thyroid gland 57 inherited genetic mutations 57 anemias 57 HER2 positivity 57 nicotinic receptor 57 Acute myeloid leukemia 57 melatonin receptor 57 calcium oxalate stones 57 Bullous 57 microbleeds 57 genomewide 57 thiopurine 57 hypercholesterolemia 57 LRRK2 mutations 57 serine threonine kinase 57 hereditary deafness 57 Entamoeba histolytica 57 MTHFD1L gene 57 proliferator activated receptor 57 JAK2 mutation 57 Cytogenetic 57 nondemented 57 brain lesions 57 virus XMRV 57 breast cancer subtypes 57 immunoreactivity 57 fronto temporal dementia 57 alpha2 57 p# MAPK 57 chromosomal regions 57 inhibin 57 prognostic factor 57 polygenic 57 pheochromocytoma 57 Klinefelter syndrome 57 spontaneous mutations 57 mitochondrial DNA mtDNA 57 chromosomal deletions 57 Hypoglycaemia 57 cTnT 57 potent inducer 57 tumor suppressor protein 57 neuroD2 57 constitutively active 57 HER2 neu 57 atopic asthma 57 lymphocytic 57 MnSOD 57 adipogenic 57 recurrent acute pancreatitis 57 PDE#A 57 huntingtin gene 57 #:#-# [029] 57 urothelial carcinoma 57 tyrosine kinase receptor 57 MSMB 57 Niemann Pick disease 57 gene mutations 57 endogenous estrogen 57 transcriptional repressor 57 atherothrombosis 57 mice lacking 57 abnormal lipids 57 Familial hypercholesterolemia 57 haemochromatosis 57 adrenal cortex 57 subtype 57 CYP#E# 57 K#R [002] 57 CFTR gene mutations 57 multivariable adjusted 57 PCNSL 57 Smad3 57 Darapladib 57 cardiac troponin T 57 nongenetic 57 clefting 57 sequence homology 57 histone deacetylases 57 carotid atherosclerosis 57 SMN2 gene 57 Ischaemic heart 57 Supplementary Table 57 Selective Inhibitor 57 H pylori 57 KRAS mutation