Related by context. All words. (Click for frequent words.) 74 APOE gene 73 APOE4 70 APOE e4 69 apolipoprotein E 69 MYH9 gene 68 CFH gene 68 susceptibility gene 68 Genetic variants 67 CNTNAP2 67 APOE ε4 67 apolipoprotein E gene 67 STAT4 67 MTHFR gene 67 gene APOE 67 ApoE4 gene 66 APOE genotype 66 TOMM# 66 ApoE4 66 UGT#A# * 66 MTHFR 66 nondemented 66 ABCB1 66 ApoE 66 proband 65 TCF#L# gene 65 de novo mutations 65 CHEK2 65 CYP#C# gene 65 dopamine receptor gene 65 APOC3 65 homozygosity 65 variant allele 65 genes predisposing 65 GSTP1 65 COMT gene 65 DRD2 gene 65 apoE4 65 neuropathologic 65 HFE gene 65 sporadic ALS 65 G allele 65 APOE allele 64 APOE4 gene 64 SHANK3 64 Wwox 64 APOE 64 DRD2 64 LPA gene 64 BDNF gene 64 APOE e4 gene 64 gene locus 64 #q# deletion 64 human leukocyte antigen 64 BARD1 64 MECP2 gene 64 5 HTT gene 64 mosaicism 64 V Leiden 64 C#Y 64 KIBRA 64 apoE 64 IL#R 63 variant alleles 63 germline mutation 63 GBA mutations 63 CCR5 delta# 63 familial clustering 63 sCJD 63 BRCA1 BRCA2 63 MC1R 63 apolipoprotein E4 63 clade B 63 GPC5 63 autosomal recessive disease 63 autosomal recessive 63 COX2 63 apolipoprotein E APOE 63 human leukocyte antigen HLA 63 PTPN# 63 COL#A# 63 CHD7 63 insulin resistance syndrome 63 GSTM1 gene 63 PON1 gene 63 #q#.# [001] 63 5 HTTLPR 63 microcephalin 63 motor neuron degeneration 63 CFTR gene 63 susceptibility alleles 63 serotonin transporter gene 63 ApoE4 allele 62 CALHM1 62 HLA DRB1 62 familial adenomatous polyposis 62 UGT#B# 62 MC4R gene 62 Hashimoto thyroiditis 62 parkin gene 62 MSH2 62 inherited mutations 62 mutated K ras 62 familial ALS 62 vWD 62 FTLD 62 CDH1 62 CYP#A# gene 62 MIF gene 62 Fragile X gene 62 K ras mutations 62 CETP gene 62 neuroligins 62 mild cognitive impairments 62 LRP5 62 KRAS oncogene 62 Genetic variation 62 SNP rs# [001] 62 heterozygous 62 TGFBR1 * 6A 62 CYP#D# gene 62 Leukemias 62 C#Y mutation 62 astrocytomas 62 CYP#C# [002] 62 ERK signaling 62 SLC#A# [002] 62 ADPKD 62 SCN5A 62 MYH9 62 mutant allele 62 Lipodystrophy 62 #q# [001] 62 familial pancreatic cancer 62 missense mutations 62 FGFR2 62 homozygote 61 SORL1 61 allele frequencies 61 PTEN gene 61 rs# [001] 61 hereditary predisposition 61 androgen receptor gene 61 chromosomal rearrangement 61 obesity insulin resistance 61 MLH1 61 penetrance 61 CCL#L# 61 PTEN mutations 61 thyrotropin levels 61 allelic variants 61 CDKN2A 61 narcolepsy cataplexy 61 CC genotype 61 genetic variants associated 61 e4 allele 61 G#S mutation 61 G6PD deficiency 61 KIF6 gene 61 genetic loci 61 gastric carcinogenesis 61 c KIT 61 familial hypercholesterolemia 61 transgene expression 61 GABRA2 61 germline mutations 61 LRRK2 mutations 61 #p# [003] 61 klotho 61 VKORC1 61 MEF2A 61 PALB2 61 clefting 61 p# mutations 61 CYP#C# [001] 61 chromosomal regions 61 SORL1 gene 61 HNPCC 61 rs# [004] 61 LRAT 61 DQB1 * 61 C#T [002] 61 ADAM# 61 ADH1B * 61 NF1 61 E4 variant 61 alpha synuclein protein 61 Epstein Barr virus EBV 61 gene APOE4 61 Leydig cell 61 coinfection 61 acquired immunodeficiency syndrome 61 autopsied brains 61 HBeAg negative 61 microdeletion 61 ATG#L# 61 gene MECP2 60 PDGFR 60 Alzheimer pathology 60 KIAA# 60 progranulin gene 60 APOE epsilon 4 60 HLA B# 60 thyrotropin 60 seropositivity 60 #q#.# deletion syndrome 60 number variations CNVs 60 gene deletions 60 LQTS 60 non coding RNA 60 T1DM 60 diabetes mellitus DM 60 causative genes 60 TCF#L# 60 mutated BRCA1 60 genetic polymorphism 60 hereditary hemochromatosis 60 basal cell nevus syndrome 60 OPRM1 gene 60 Genetic mutation 60 genes CYP#C# 60 essential thrombocythemia 60 predisposing factor 60 squamous cell lung cancer 60 Li Fraumeni syndrome 60 HLA DRB1 * 60 FLT3 60 transgenic mouse models 60 MAPK pathway 60 gene polymorphism 60 CNTNAP2 gene 60 CAG repeats 60 HIV HCV coinfected 60 euthymic patients 60 XLHED 60 TMEM#B 60 ABCB1 gene 60 susceptibility loci 60 IgA deficiency 60 MTHFD1L gene 60 mitochondrial disorders 60 neuroD2 60 arterial calcification 60 HLA B 60 rs# [002] 60 DNA methylation patterns 60 phenotypic expression 60 M. pneumoniae 60 monozygotic twin 60 NPY gene 60 dysbindin 60 BRCA2 gene 60 Prox1 60 homozygous 60 ORMDL3 60 HER2 overexpression 60 telomere shortening 60 ADAMTS# 60 rs# [003] 60 PON1 60 mitochondrial mutations 60 aneuploidies 60 chromosome abnormality 60 Relapsing remitting MS 60 mtDNA mutations 60 testicular germ cell 60 autosomal dominant inheritance 60 SMN2 gene 60 NF1 gene 60 Haptoglobin 60 LRRK2 gene 60 gastric carcinoma 59 neurocognitive impairment 59 monogenic 59 Genetic predisposition 59 #p# [001] 59 HMGCR 59 exfoliation glaucoma 59 ENPP1 59 heterozygotes 59 CDK4 59 Wernicke Korsakoff syndrome 59 ALDH2 59 chemokine receptor 59 HLA DQ2 59 etiologic 59 Squamous 59 nonalcoholic steatohepatitis NASH 59 protein isoforms 59 TACI mutations 59 GSTM1 59 T2DM 59 frontotemporal dementia 59 progressive neurodegenerative disorder 59 G#D mutation 59 Kufs disease 59 Vascular dementia 59 MC1R gene 59 G#S [002] 59 KLF4 59 APOL1 59 hereditary deafness 59 Nonalcoholic fatty liver 59 paternally inherited 59 gene amplification 59 protein tyrosine phosphatase 59 ataxias 59 diabetic kidney 59 chromosome #q# [002] 59 Klinefelter syndrome 59 atypical parkinsonism 59 elevated triglyceride levels 59 STAT3 signaling 59 nongenetic 59 PDE#A 59 multigenic 59 #q#.# [002] 59 BRCA2 gene mutation 59 microdeletions 59 CYP#D# 59 C. pneumoniae 59 MAOA gene 59 CHRNA5 gene 59 osteosarcomas 59 GSTT1 59 CYP#C# * 59 Rh factor 59 telomere lengths 59 Sjögren syndrome 59 maternally inherited 59 gastrointestinal stromal tumors GISTs 59 MIF protein 59 beta amyloid peptides 59 chlamydial infection 59 C. trachomatis 59 Cognitive impairment 59 alleles 59 UGT#A# 59 metabolic abnormalities 59 hepatocellular carcinomas 59 GABRA2 gene 59 5q 59 BRCA gene mutation 59 FMRP protein 59 DLX5 59 PIGF 59 Hp2 2 59 amyloid plaque formation 59 aetiological 59 C1q 59 paraneoplastic 59 idiopathic PAH 59 enteroviruses 59 prostate carcinogenesis 59 synuclein 59 recessive trait 59 isoenzymes 59 IGFBP 59 methylation patterns 59 DGAT1 59 hepatitis B infection 59 syndromic 59 susceptibility genes 59 GPR# [002] 59 Li Fraumeni 59 susceptibility locus 59 LKB1 59 hypermethylated 59 CYP#E# gene 59 Apolipoprotein E 59 circadian genes 59 BRIP1 59 neuropsychiatric disorder 59 presymptomatic 58 autosomal 58 gene rearrangements 58 promoter hypermethylation 58 chromosome #q# [001] 58 CYP#B# 58 beta globin gene 58 SRY gene 58 TT genotype 58 tumor suppressor protein 58 lipodystrophy syndrome 58 polymorphism 58 deleterious mutation 58 neurofibrillary tangles 58 type2 diabetes 58 missense mutation 58 R#W [002] 58 DISC1 gene 58 Angiotensin converting enzyme 58 Klotho gene 58 modifier genes 58 DNA demethylation 58 Neuregulin 1 58 neuritic 58 Aromatase 58 enteroviral infection 58 somatic mutations 58 genomic rearrangement 58 interferon pathway 58 epigenetic modification 58 HMMR 58 allelic 58 generalized vitiligo 58 single nucleotide polymorphism 58 gene variant 58 WDR# 58 NRTI resistance 58 genetic variant 58 #p#.# [002] 58 transgenic mouse model 58 NNRTI resistance 58 SMAD4 58 smoldering myeloma 58 allele 58 congenital deficiency 58 cyclophilin D 58 IGF1 58 Alu elements 58 Cowden syndrome 58 LIS1 58 HLA genes 58 Parkinsonian Syndromes 58 #p#.# [001] 58 homozygotes 58 monozygotic twins 58 HGPS 58 metaplasia 58 Foxp2 58 dopamine transporter gene 58 muscular dystrophy cystic fibrosis 58 CagA 58 cardiac channelopathies 58 TEL AML1 58 JAK2 enzyme 58 underlying pathophysiology 58 IGF2 58 amnestic MCI 58 genetic polymorphisms 58 childhood leukaemias 58 leukaemias 58 murine leukemia virus 58 systemic amyloidosis 58 Alzheimer Disease AD 58 abdominal adiposity 58 alpha synuclein gene 58 K#N 58 STK# gene 58 DRD4 58 nonmelanoma skin cancers 58 p# activation 58 IPAH 58 Hutchinson Gilford progeria 58 β amyloid 58 transgenic rats 58 myeloid 58 spontaneous mutations 58 maternally transmitted 58 chromosome #q#.# [001] 58 autosomal dominant 58 KCNH2 58 BMPR2 58 PDGFRA 58 malignant lymphoma 58 BRAF V#E 58 genomewide 58 prion gene 58 NEIL1 58 autosomal dominant disorder 58 TCF4 58 chromosome #p#.# 58 immunopathology 58 epigenetically 58 monoclonal gammopathy 58 BRAF gene 58 tyrosine phosphorylation 58 FXTAS 58 myeloproliferative neoplasms 58 apoC III 58 IGFBP2 58 subclinical atherosclerosis 58 SCN1A 58 alternatively spliced 58 Homozygous 58 cell adhesion molecule 58 HSV1 58 C#BL/#J 58 cyclin E 58 genomic alterations 58 histological subtype 58 comorbid disorders 58 haptoglobin 58 gene DRD4 58 TP# gene 58 capsular polysaccharide 58 Brain derived neurotrophic 58 prodynorphin 58 #q# deletion syndrome 58 1 diabetes T1D 58 nonhereditary 58 NF2 58 diagnostic biomarker 58 lymphocyte activation 58 lupus anticoagulant 58 multifactorial disease 58 hepatoma 58 heterozygote 58 Chlamydia pneumoniae 58 Fas ligand 58 NR#A# 58 MHC genes 58 tumor histology 58 brain lesions 58 Prolactin 58 fetuin 58 senile plaques 58 F#del mutation 58 chromosomal translocations 58 aberrant methylation 58 HbF 58 basal cell carcinoma BCC 58 FGFs 58 Nf1 58 Dystrophin 58 humanin 58 heritable genetic 57 neuronal dysfunction 57 GRK5 57 FGFR2 gene 57 antiphospholipid antibodies 57 microRNA expression 57 spongiform encephalopathies 57 breast cancer subtypes 57 micro RNA 57 pathological hallmark 57 transcriptional repressor 57 methylenetetrahydrofolate reductase 57 #ß 57 gene BRCA2 57 haplotypes 57 epigenetic inheritance 57 mito 57 polygenic 57 MnSOD 57 atypical hemolytic uremic syndrome 57 MELAS 57 autistic traits 57 number variants CNVs 57 chromosomal anomalies 57 FTO gene 57 Peutz Jeghers syndrome 57 chromosomal aberrations 57 CYP#D# genotype 57 lung adenocarcinoma 57 distinct subtypes 57 oncogenic transformation 57 SCD1 57 progranulin mutations 57 H#K#me# 57 SNP rs# [002] 57 immunoregulation 57 micro RNAs 57 autonomic dysfunction 57 number variation CNV 57 ZNF# 57 EGFR gene 57 NR#A# gene 57 FMR1 57 hyper IgE syndrome 57 NKX2 57 chromosomal disorders 57 CCR3 57 amyloid beta plaques 57 GH deficiency 57 transcriptional regulation 57 Treg cell 57 Helicobacter 57 parkinsonism 57 heterotaxy 57 oxysterols 57 synaptic function 57 microscopic colitis 57 thiopurine 57 behavioral disinhibition 57 2 diabetes T2D 57 N. gonorrhoeae 57 COMT 57 MGUS 57 idiopathic myelofibrosis 57 carotid plaques 57 homozygous FH 57 recessive genetic 57 DAT1 57 proliferative retinopathy 57 FMR1 gene 57 neuropsychiatric diseases 57 MLL gene 57 childhood leukemias 57 nonnucleoside reverse transcriptase inhibitors 57 HPV# 57 lymphocytic 57 von Willebrand disease 57 ALK mutations 57 receptor gene 57 gene polymorphisms 57 androgen deficiency 57 thrombophilia 57 holoprosencephaly 57 metastatic gastric 57 impaired glucose metabolism 57 Fibroblast growth 57 relapsed ALL 57 mitochondrial DNA mtDNA 57 BCL#A 57 neurodevelopmental disorder 57 HMGA2 57 recessive inheritance 57 virus HBV 57 elevated triglycerides 57 Single Nucleotide Polymorphisms SNPs 57 Waldenstrom macroglobulinemia 57 E selectin 57 HIVAN 57 Papillary 57 T2D 57 p# mutation 57 autoinflammatory 57 monozygotic 57 pDCs 57 parietal cortices 57 EBV infection 57 noncarriers 57 Aß 57 serine protease 57 virulence genes 57 Hemophilia B 57 BRAF protein 57 TP# mutation 57 gene variation 57 genes BRCA1 57 chromosome #p# [001] 57 Thyroid hormone 57 IL#B 57 #beta HSD1 57 transmembrane receptor 57 SSc 57 hypogonadotropic hypogonadism 57 recessive mutations 57 dopamine D4 receptor 57 Severe Primary IGFD 57 causative mutations 57 demyelinating 57 unfavorable prognostic 57 epigenetic changes 57 alpha2 57 microsatellite instability 57 MetS 57 glycogen metabolism 57 haplogroups 57 cardioembolic stroke 57 ovarian hormones 57 colorectal adenoma 57 cell adhesion molecules 57 neurologic disorder 57 prefrontal cortical 57 IDH1 mutation 57 nicotinic receptor 57 IKZF1 57 IDH mutations 57 Sezary syndrome 57 promoter polymorphism 57 ribosomal protein 57 untreated celiac disease 57 Niemann Pick disease 57 mutated gene 57 gestational diabetes mellitus 57 Chronic lymphocytic leukemia 57 neurosensory 57 AAT deficiency 57 PICALM 57 suppressor gene 57 alpha1 antitrypsin deficiency 57 FADS2 57 Cyclin D1 57 chromosome #q#.# [002] 57 chlamydial 57 mitochondrial gene 57 simian immunodeficiency virus 57 metabolic abnormality 57 genomic variants 57 HLA DRB1 SE 57 Ets2 57 miRNA genes 57 neoplasias 57 colorectal tumor 57 indels 57 affective psychosis 57 Leydig cells 57 nonalcoholic steatohepatitis 57 Opportunistic infections 57 BRCA1 mutations 57 adult neurogenesis 57 lipid abnormalities 57 incomplete penetrance 57 HLA DR 57 systemic lupus erythematosus 57 replicon 57 metabolic syndrome MetS 57 Abeta# 57 prostate cancer CaP 57 WAGR syndrome 57 A1 allele 57 NPC1 57 Heterozygous 57 FGF2 57 pancreatic endocrine 57 isoenzyme 57 placental malaria 57 myo inositol 57 Mild cognitive impairment 57 von Willebrand 57 atypical neuroleptics 57 familial aggregation 56 cholinergic tone 56 IDDM 56 DRB1 * 56 tumor subtype 56 KRAS mutations 56 ependymomas 56 Janus kinase 56 chromatin structure 56 adipogenic 56 tau protein tangles 56 spinocerebellar ataxia 56 Clusterin 56 synaptogenesis 56 APOE e4 allele 56 phosphorylated tau 56 haematopoietic 56 neonatal lupus 56 VIPR2 56 gestational diabetes mellitus GDM 56 Lafora disease 56 human leukocyte antigens 56 serum BDNF 56 mitochondrial dysfunction 56 histocompatibility 56 TrkB 56 IRF6 56 mGluR 56 MYCN amplification 56 TGF β1 56 SNPs pronounced snips 56 grade cervical intraepithelial 56 SLITRK1 56 acute myelogenous leukemia AML 56 klotho gene 56 immunodeficiencies 56 testicular tumors 56 LHON 56 MLL2 56 Neurodegenerative diseases 56 SNCA 56 Entamoeba 56 BRCA1 gene 56 recessive mutation 56 imatinib resistance 56 HMGA2 gene 56 BRAF V#E mutation 56 SOD2 gene 56 Acetylcholine 56 synthetic analogues 56 regulates gene expression 56 ribosomal proteins 56 amyloid pathology 56 ANCA associated 56 PPAR γ 56 Genetic susceptibility 56 activin 56 acute myeloid 56 Polymorphisms 56 orthologs 56 COX enzymes 56 androgen excess 56 Upregulation 56 ductal breast cancer 56 miRNA expression 56 epigenetic alterations 56 PARP inhibition 56 esophageal squamous cell carcinoma 56 fronto temporal dementia 56 triiodothyronine 56 KCNE2 56 neuropsychological impairments 56 abnormal lipid 56 LMNA 56 SE alleles 56 Gestational 56 DHFR 56 Single Nucleotide Polymorphisms 56 TGF ß 56 caveolin 56 cognitively normal 56 onset diabetes mellitus 56 HER2 neu 56 γ secretase 56 small molecule activators 56 multisystem disease 56 Genetic mutations 56 EoE 56 cystatin 56 juvenile idiopathic arthritis JIA 56 TMPRSS2 ERG fusion 56 MHC molecules 56 amnestic 56 ß1 56 annexin 56 AMACR 56 choroidal neovascularization 56 cytopathic 56 DICER1 gene 56 clade C 56 Acute myeloid leukemia 56 muscarinic receptors 56 atypical hyperplasia 56 elevated serum ALT 56 hormone therapy estrogen 56 CYP# [002] 56 atherothrombosis 56 oesophageal adenocarcinoma 56 DRD4 gene 56 lipoprotein metabolism 56 Phenylketonuria PKU 56 cranial irradiation 56 beta thalassemia 56 K#R [002] 56 inherited predisposition 56 tumorigenicity 56 SHANK3 gene 56 APOE4 variant 56 chronic myeloid 56 osteocalcin protein 56 neurocognitive dysfunction 56 Related Dementia 56 segmental duplications 56 hypercoagulable 56 dominantly inherited 56 hypothalamic pituitary adrenal axis 56 telomere dysfunction 56 hypereosinophilic syndrome 56 cypin 56 CYP #D# 56 interferon IFN 56 aneuploidy 56 CaM kinase II 56 dyslipidaemia 56 phenotypic variation 56 aminotransferase 56 abnormal hemoglobin 56 CDK inhibitor 56 pathogenetic 56 Interferon Beta 56 HLA DR4 56 mutated BRCA 56 TAp# 56 Socioeconomic status 56 neuroblastomas 56 SLC#A# [001] 56 myostatin gene 56 retinoid X 56 IgG1 56 Polycystic ovary syndrome PCOS 56 ERBB2 56 BRAF mutation 56 aMCI precursor 56 immunocompetent 56 calcium calmodulin dependent 56 ORFs 56 ABO blood 56 cryptogenic 56 genetic determinants 56 gastric adenocarcinoma 56 NSCLC tumors 56 MODY 56 hematopoietic cancers 56 Psoriatic arthritis 56 chromosomal alterations 56 Diabetic neuropathy 56 airway hyperresponsiveness 56 plasminogen activator inhibitor 56 sortilin 56 telomere length 56 gonadotropins 56 hepatic steatosis 56 ALK gene 56 arterial hypertension 56 myeloproliferative diseases 56 highly heritable 56 Alzheimer disease vascular dementia 56 comorbid anxiety 56 Beta thalassemia 56 gene variants 56 glycosylated 56 PIK3CA 56 multivariate logistic regression 56 haplotype 56 shorter telomeres 56 pyridostigmine 56 HMGA1 56 neurofibrillary 56 diabetes mellitus T2DM 56 cytogenetic abnormalities 56 variant rs# 56 albumin excretion 56 NFkB 56 TNFAIP3 56 protein tau 56 lysosomal storage disease 56 Vpu 56 mitochondrial function 56 Dysregulation 56 inhibin 56 virus XMRV 56 Estrogen Receptor 56 polymorphisms 56 TYMS 56 muscular dystrophies 56 HepG2 cells 56 IDH2 56 SOD1 gene 56 trastuzumab Herceptin ® 56 nondiabetic 56 HGPIN 56 tau pathology 56 WT1 56 KCNQ1 56 amyloidogenic 56 p#INK#a 56 herpes zoster shingles 56 CHI#L# 56 uPA 56 granzyme B 56 GCase 56 airway remodeling 56 HLA gene 56 mRNA transcripts 56 liver metastasis 56 Amino acid 56 Brugada Syndrome 56 PsA 56 DNA methyltransferases 56 differential gene expression 56 cyclin dependent kinase inhibitor 56 bioengineered mice 56 RhuDex ™ 56 lysosomal storage diseases 56 PB1 F2 56 spontaneous mutation 56 amnestic mild cognitive impairment 56 inherited neurological disorder 56 hyperinsulinemia 56 atherosclerotic vascular disease 56 Brd4 56 null mice 56 orchitis 56 cervical intraepithelial neoplasia 56 assortative mating 56 epigenetic regulation 56 polyarticular 56 murine models 56 proto oncogene 56 Hurthle cell 56 angiotensin converting enzyme 56 chromosome #q 56 myeloproliferative 56 Vitamin B# deficiency 56 functional polymorphism 56 folate metabolism 56 Chronic pancreatitis 56 abnormal prion protein 56 congenital adrenal hyperplasia CAH 56 autism spectrum disorders ASDs 56 NOMID 56 nephronophthisis 56 pituitary hormone 56 Parkinsonian 56 serum PTH 56 Huntingtons disease 56 epithelial tissues 56 elevated CRP 56 Nedd4 56 nonmetastatic 56 SIRT1 gene 56 beta amyloid plaques 55 neovascular 55 pancreatic ductal adenocarcinoma 55 major histocompatibility complex 55 IKK beta