Related by context. All words. (Click for frequent words.) 75 ApoE4 gene 75 APOE4 71 ApoE4 71 APOE e4 69 APOE allele 69 APOE e4 gene 67 Fragile X gene 67 APOE ε4 66 APOE 65 gene variant 65 variant alleles 64 gene APOE4 64 ApoE gene 64 apoE4 64 APOE gene 64 ε4 64 e4 allele 64 ApoE4 allele 63 G allele 63 CNTNAP2 62 TCF#L# gene 62 genes predisposing 62 GSTM1 62 SORL1 62 allele 61 COMT gene 61 ApoE 61 genetic variant 61 heterozygous 61 apolipoprotein E gene 61 recessive mutations 61 MC4R gene 61 FTO allele 61 C#Y 61 mutated gene 61 BRCA2 gene 60 FTO variant 60 CALHM1 60 #q# deletion 60 gene APOE 60 CYP#C# * 60 nondemented 60 FTO gene 60 KIBRA 60 DRD2 gene 60 shorter telomeres 60 alleles 60 5 HTT gene 60 CDKN2A 59 apolipoprotein E4 59 apolipoprotein E 59 narcolepsy cataplexy 59 number variations CNVs 59 BRCA1 mutations 59 proband 59 GPC5 59 G#S [002] 59 microcephalin 59 missense mutations 59 TGFBR1 * 6A 59 SMN2 gene 59 MTHFR 59 BDNF gene 59 HFE gene 59 variant allele 59 mutated genes 59 familial pancreatic cancer 58 klotho 58 CNTNAP2 gene 58 heritable genetic 58 GBA mutations 58 HLA B# 58 Genetic variants 58 Alu elements 58 TP# mutation 58 BRCA1 BRCA2 58 MC1R gene 58 APOE epsilon 4 58 KIF6 gene 58 CHEK2 58 androgen receptor gene 58 BMPR2 58 FXTAS 58 DQB1 * 58 mutated BRCA1 58 BRCA gene mutation 58 gene mutation 58 sporadic ALS 58 mutant gene 58 premutation 58 sCJD 58 BARD1 58 susceptibility gene 58 APOE genotype 58 MAOA 57 UGT#A# * 57 EGFR gene 57 STAT4 57 G#S mutation 57 noncarriers 57 GSTM1 gene 57 SE alleles 57 serotonin 2A 57 frontotemporal dementia 57 somatic mutations 57 apolipoprotein E APOE 57 miRNA genes 57 NF1 gene 57 MAOA gene 57 SHANK3 57 rs# [003] 57 APOC3 57 BRCA1 gene 57 5 HTTLPR 57 DISC1 57 CFTR gene 57 germline mutations 57 PALB2 57 inherited mutations 57 Wwox 57 CNVs 57 APOE e4 allele 57 BRCA mutation 57 progranulin gene 57 CFH gene 57 de novo mutations 57 imprinted genes 57 DAT1 57 MSH2 57 ABCB1 57 TACI mutations 57 DICER1 gene 57 mutation 57 FGFR2 57 MYH9 gene 56 mosaicism 56 KRAS oncogene 56 ABCB1 gene 56 heterozygotes 56 KIF6 gene variant 56 CYP#C# gene 56 alpha synuclein gene 56 LPA gene 56 prion gene 56 apoC III 56 ORMDL3 56 deleterious mutations 56 HGPS 56 mutant allele 56 MAPK pathway 56 dopamine transporter gene 56 TCF#L# 56 TMEM#B 56 C. pneumoniae 56 CETP VV 56 chromosomal aberrations 56 LRRK2 gene 56 SNP rs# [001] 56 autopsied brains 56 gene variants 56 homozygous 56 OPRM1 gene 56 LIS1 56 apoE 56 homozygotes 56 cognitively normal 56 chromosomal rearrangement 56 p# mutations 56 CIB1 56 A1 allele 56 PTPN# 56 nonhereditary 56 HbF 56 mutant alleles 55 BRCA1 mutation 55 HLA genes 55 mammary cancers 55 #q#.# [002] 55 genes BRCA1 55 susceptibility genes 55 ovarian hormones 55 neuropsychological impairments 55 CYP#D# gene 55 thyrotropin levels 55 PTP1B 55 KRAS mutations 55 MC1R 55 mice lacking 55 PTEN gene 55 Prox1 55 colorectal neoplasia 55 neural progenitor 55 MYH9 55 mtDNA mutations 55 defective gene 55 CDK4 55 DRD4 55 white matter hyperintensities 55 dysbindin 55 CCR5 delta# 55 TMPRSS2 ERG fusion 55 cardioembolic stroke 55 rs# [002] 55 BRCA2 gene mutation 55 elevated triglyceride levels 55 DICER1 55 FOXP2 gene 55 familial adenomatous polyposis 55 hypermethylated 55 DRD4 gene 55 mutations 55 Foxp2 55 penetrance 55 fetuin 55 GATA4 55 amyloid deposits 55 CETP gene 55 pDCs 55 neuroD2 55 familial clustering 55 CCL#L# 55 neuroligins 55 MIF protein 55 tau mutation 54 ENPP1 54 NF1 54 PTEN mutations 54 IGF1 54 genetic alteration 54 DLC1 54 GABRA2 gene 54 SOD2 gene 54 #q#.# [001] 54 missense mutation 54 hereditary predisposition 54 MEF2A 54 brain lesions 54 CAG repeats 54 MAOA L 54 HBx 54 HLA gene variant 54 mutated K ras 54 highly heritable 54 familial ALS 54 ADH1B * 54 Genetic mutations 54 APOE4 carriers 54 autosomal dominant inheritance 54 TT genotype 54 #q# [001] 54 CYP#A# gene 54 KLF# 54 chromosomal regions 54 TRIM5 54 lung adenocarcinoma 54 NPY gene 54 chronic HBV 54 BRCA2 mutations 54 TAp# 54 #q# [002] 54 serotonin transporter gene 54 Hsp# [001] 54 homozygote 54 amygdalae 54 recessive mutation 54 K ras gene 54 DRD2 54 BRAF gene 54 FMR1 54 chromosome #q# [001] 54 deleterious mutation 54 SHANK3 gene 54 MHC genes 54 MECP2 gene 54 FMR1 gene 54 E4 variant 54 SORL1 gene 54 BRCA2 mutation 54 myostatin gene 54 ACE2 gene 54 amyloid pathology 54 HSF1 54 GSTT1 54 SIRT6 54 HLA gene 54 CHD7 54 recessive trait 54 rs# [004] 54 colugos 54 BRCA2 carriers 54 NEIL1 54 amyloid beta plaques 54 M. pneumoniae 54 Pten gene 54 UGT#B# 54 ZNF# 54 genetic mutations 54 JAK mutations 54 non coding RNA 54 genetic variants 54 GPR# [002] 54 Abeta# 54 BDNF protein 54 homozygosity 54 CYP#C# [001] 54 tau pathology 54 gene mutations 54 serous ovarian cancer 53 ADAM# 53 epigenetic silencing 53 CDH1 53 klotho gene 53 JAK2 enzyme 53 pilocytic astrocytomas 53 GSTP1 53 monozygotic twin 53 repeat allele 53 basal cell nevus syndrome 53 VHL gene 53 glucose metabolism 53 KRAS gene 53 LRRK2 mutations 53 micro RNAs 53 neurofibrillary 53 Stat3 53 autosomal recessive disease 53 causative mutations 53 trisomic 53 COX2 53 breast cancer genes BRCA1 53 HER2 positive cancers 53 susceptibility alleles 53 BRIP1 53 K ras mutations 53 heritable 53 epigenetic changes 53 LRP5 53 p#INK#a 53 NNRTI resistance 53 autosomal recessive 53 gene locus 53 genetic variants associated 53 gene variation 53 mitochondrial mutations 53 telomere lengths 53 gene 53 MTHFR gene 53 mitochondrial dysfunction 53 progressive neurodegenerative disorder 53 parkin gene 53 slow metabolizers 53 CatB 53 F#del mutation 53 HLA alleles 53 FADS2 gene 53 BRAF mutations 53 #p# [001] 53 SMN1 gene 53 nondiabetic 53 monogenic 53 MLH1 53 pathogenic mutations 53 neuroblastomas 53 gene BRCA2 53 predisposing factor 53 Li Fraumeni 53 IgA deficiency 53 V Leiden 53 microdeletions 53 SCN1A 53 IGF2 53 poorer prognosis 53 MYCN amplification 53 rs# [001] 53 MLL2 53 palladin 53 chromosomal translocations 53 CC genotype 53 HER2 gene 53 neurological abnormalities 53 corticosterone levels 53 squamous cell lung cancer 53 SLC#A# [002] 53 genes 53 G#D mutation 53 MIF gene 53 genomic imprinting 53 chromosomal rearrangements 53 lipin 53 haplotype 53 colorectal tumor 53 APOE4 variant 53 atypical neuroleptics 53 inherited predisposition 53 neuroblastoma tumors 53 ERK signaling 53 LKB1 53 EGFR mutations 53 ERK2 53 mutant worms 53 carotid plaques 53 phthalate syndrome 53 BRCA2 mutation carriers 53 2D 4D ratio 53 FGF2 53 cypin 53 synuclein 52 ß amyloid 52 activating mutations 52 progranulin mutations 52 KCNQ1 52 CYP#E# gene 52 S#A# [002] 52 GNAQ 52 genetic loci 52 mutant genes 52 tau protein 52 MnSOD 52 HLA DRB1 SE 52 CYP#D# 52 spontaneous mutations 52 ultraconserved elements 52 p# gene 52 LQTS 52 histone modification 52 polymorphisms 52 clade B 52 p# mutation 52 TP# mutations 52 transthyretin 52 R#W [002] 52 parkinsonism 52 probands 52 habitual snoring 52 NKT cells 52 RKIP 52 SCN5A 52 insoluble plaques 52 mitochondrial DNA mtDNA 52 osteopontin 52 number variants CNVs 52 leptin deficiency 52 fetal hemoglobin 52 PDGFR 52 Pten 52 GBM tumors 52 HLA DQ2 52 clusterin 52 Klotho gene 52 D2 receptors 52 adiponectin levels 52 neuroglobin 52 dysbindin gene 52 atypical hyperplasia 52 FLT3 52 granzyme B 52 morphogen 52 HMGCR 52 K ras mutation 52 mammary stem cells 52 tarenflurbil 52 circadian clock genes 52 PPARγ 52 cerebral infarction 52 MMSE scores 52 allelic variants 52 Hashimoto thyroiditis 52 Ets2 52 EBV infection 52 cAMP signaling 52 tumor suppressor protein 52 receptor gene 52 SCA5 52 alpha synuclein protein 52 Alzheimer disease pathology 52 HNPCC 52 faulty BRCA2 gene 52 asymptomatic carriers 52 mitochondrial proteins 52 PON1 52 BRAF mutation 52 MDR1 52 TLR3 52 Entamoeba 52 OGG1 52 CTVT 52 breast cancer gene mutation 52 cerebellar 52 dopamine D4 receptor 52 ALK gene 52 PKD1 52 Aß 52 gene loci 52 SERT gene 52 BCL#A 52 TP# gene 52 KIAA# 52 beta catenin protein 52 gut microbes 52 fronto temporal dementia 52 Heterozygous 52 monolinguals 52 SIDS infants 52 progranulin 52 holoprosencephaly 52 salivary gland tumors 52 KIF6 52 dizygotic twins 52 CREB protein 52 C1q 52 HbF levels 52 ERBB2 52 humanin 52 toxoplasma 52 albumin excretion 52 Treg cell 52 atherosclerotic lesions 52 shorter telomere length 52 MLL gene 52 Foxp3 52 fasting glucose levels 52 nicotine receptor 51 indels 51 CagA 51 frontotemporal dementia FTD 51 mammary tumors 51 MetS 51 distantly related species 51 susceptibility loci 51 amyloid plaque formation 51 dopamine D2 receptors 51 enterovirus infection 51 STK# gene 51 microdeletion 51 Jhdm2a 51 virulence genes 51 familial adenomatous polyposis FAP 51 protein alpha synuclein 51 TOMM# 51 Brd4 51 CaM kinase II 51 vitamin D receptors 51 MHC molecules 51 osteosarcomas 51 chromosome #p# [001] 51 FTLD 51 pneumococci 51 Leydig cell 51 epigenetically 51 Akt1 51 chromosomal alterations 51 genetic polymorphism 51 dopamine receptor gene 51 DNA methylation patterns 51 monozygotic twins 51 neuronal dysfunction 51 serotonin receptor 51 nicotinic receptor 51 recessive inheritance 51 CLL cells 51 leukaemias 51 mitochondrial disorders 51 orthologs 51 ADPKD 51 abnormal chromosome 51 glutamate signaling 51 autistic traits 51 polymorphism 51 vasopressin receptors 51 TB bacterium 51 KCNH2 51 hair follicle stem cells 51 Notch1 51 SOD1 protein 51 Parkinsonian 51 chromosome translocations 51 genotypes 51 DEC2 51 β amyloid 51 SNP rs# [002] 51 epigenetic modification 51 BRCA2 51 XMRV infection 51 CHRNA5 gene 51 malignant transformation 51 heterozygosity 51 recessive gene 51 progranulin protein 51 Lyn kinase 51 BRCA1 51 gene DRD4 51 NRTI resistance 51 microbleeds 51 subclinical hyperthyroidism 51 HOTAIR 51 hippocampal atrophy 51 Colon polyps 51 Sonic Hedgehog 51 fewer dopamine receptors 51 tau protein tangles 51 multiprotein complex 51 BRAC2 51 suppressor gene 51 microRNA expression 51 tumor suppressor gene 51 SIRT1 51 major histocompatibility complex 51 SMAD4 51 CD8 cells 51 activity MAOA 51 genetic mutation 51 Glioblastoma Multiforme GBM 51 neurofibrillary tangles 51 genetically inherited 51 prostate carcinogenesis 51 NOMID 51 germline mutation 51 EZH2 51 MiRNAs 51 hippocampal volume 51 recessive genes 51 male hormone androgen 51 BRCA gene mutations 51 Androgen receptor 51 transmembrane receptor 51 autoantibodies 51 hematopoetic stem cells 51 TH# cells 51 CD8 + 51 IL#R 51 normal karyotype 51 Dpp 51 Runx1 51 postoperative delirium 51 WT1 51 ependymomas 51 cyclophilin D 51 serotonin transporter 51 5q 51 metabolic abnormalities 51 GBV C 51 epigenetic mechanisms 51 #p#.# [001] 51 orthologous genes 51 leukemic stem cells 51 Genetic predisposition 51 HLA molecules 51 autosomes 51 KLF4 51 estrogen receptors 51 chromosome #q# [002] 51 LRRK2 51 HLA B 51 giant danio 51 untreated sleep apnea 51 chromosomal deletions 51 RUNX3 51 GABRA2 51 LRAT 51 GAB2 51 chromosomal instability 51 gene p# 51 F#del 51 NFKBIA 51 HIV HCV coinfected 51 Nrf2 51 NR#A# gene 51 BRCA mutations 51 promoter hypermethylation 51 IDH1 mutation 51 evolutionarily conserved 51 IKKa 51 Mendelian disorders 51 CCR5 mutation 51 ataxias 51 NFkB 51 Aß# 51 GLUT1 51 transgenic mouse models 50 GG genotype 50 prefrontal regions 50 eotaxin 50 leptin receptor 50 FTO gene variant 50 frequently benign tumor 50 protein encoded 50 p# protein 50 T#I [002] 50 genetic polymorphisms 50 relapsed ALL 50 parahippocampal gyrus 50 C. trachomatis 50 infarcts 50 hippocampi 50 estrogen receptor alpha 50 cyclin E 50 nestin 50 Skp2 50 Glioblastoma multiforme GBM 50 exfoliation glaucoma 50 HMGA2 50 Kufs disease 50 APOL1 50 herpesviruses 50 unmeasured factors 50 molecularly defined 50 telomeres shorten 50 IDH1 50 Vascular dementia 50 chromosomal disorders 50 type2 diabetes 50 bilinguals 50 tumor suppressor p# 50 enteroviral infection 50 gastric carcinogenesis 50 genomic alterations 50 noninfected 50 IRF5 50 dopamine D2 receptor 50 Ras pathway 50 NF kB pathway 50 colon tumors 50 heterozygote 50 BRCA2 gene mutations 50 genital tract infections 50 autonomic dysfunction 50 IL#B 50 oxidized phospholipids 50 NF kB signaling 50 asymptomatic PAD 50 neurones 50 motor neuron degeneration 50 PPARg 50 nondepressed 50 prostate cancer CaP 50 poor metabolizers 50 FOXP2 50 paternally inherited 50 BRCA gene 50 nonalcoholic steatohepatitis NASH 50 presymptomatic 50 3kg heavier 50 tumorigenicity 50 CHI#L# 50 UCP2 50 medulloblastomas 50 Aβ 50 nucleoli 50 telomere length 50 maternally inherited 50 oncoproteins 50 tau gene 50 SGS# 50 genotoxic stress 50 adiponectin 50 KCNE2 50 PI3K signaling 50 hematopoietic cancers 50 genes CYP#C# 50 miRNAs 50 TNFAIP3 50 familial hypercholesterolemia 50 D2 receptor 50 chromosomal defects 50 K#N 50 MMP# 50 leptin deficient 50 aneuploidy 50 PARP inhibition 50 X chromosome genes 50 untreated celiac disease 50 LRRK2 mutation 50 genes encoding 50 #q# deletion syndrome 50 NR2B subunit 50 globin genes 50 TGF beta pathway 50 XLHED 50 PGCs 50 MeCP2 gene 50 WAGR syndrome 50 mutated protein 50 protein isoforms 50 aneuploidies 50 ATG#L# 50 MTHFD1L gene 50 DLX5 50 CHD5 50 histone modifications 50 E#F# 50 p# deficient 50 Li Fraumeni syndrome 50 juvenile idiopathic arthritis JIA 50 glycosylated 50 dopamine signaling 50 genetic abnormality 50 sexually dimorphic 50 neuritic 50 amnestic mild cognitive impairment 50 pCR 50 elevated triglycerides 50 primary cilia 50 ERBB4 50 overactivated 50 APOA5 50 Rb gene 50 commonly mutated genes 50 CYP#D# genotype 50 Hepatitis B virus 50 lentiviruses 50 phenotypic variability 50 BRCA2 breast cancer 50 epigenetic alterations 50 hedgehog signaling 50 Uterine cancer 50 hippocampal neurons 50 prion infection 50 microRNA molecules 50 microfilariae 50 CYP#B# 50 T1DM 50 RASSF1A 50 NKX#.# 50 amyloid beta plaque 50 seasonal influenza viruses 50 genotyped 50 astrocyte 50 NKX2 50 excitatory neurotransmitter glutamate 50 modifier genes 50 hippocampal volumes 50 amyloids 50 apo E 50 impaired cognition 50 subclinical hypothyroidism 50 serum BDNF 50 atypical parkinsonism 50 DISC1 gene 50 p# activation 50 orangutan genome 50 phenotypic variation 50 c KIT 50 CD#c 50 cognitively intact 50 PDGFRA 50 genetic trait 50 distinct subtypes 50 FGFR2 gene 50 dominantly inherited 50 genetic makeups 50 HMGA2 gene 50 JAK STAT signaling 50 SIRT3 50 microsatellite instability 50 NPC1 50 genomic rearrangement 50 alpha synuclein 50 CXCL5 50 methylation patterns 50 immunocompetent 50 thyroid hormone levels 50 #p#.# [002] 50 polyglutamine diseases 50 T. vaginalis 50 PIK3CA 50 huntingtin gene 50 vmPFC 50 adenoma 50 mitochondrial gene 50 maternally transmitted 50 #q#.# deletion syndrome 49 clefting 49 recessive genetic 49 Genetic variation 49 SPINK1 49 genomewide association studies 49 Hh 49 epistasis 49 neurodegenerative disorder 49 hippocampal function 49 cisplatin resistant 49 BDNF 49 TrkB 49 allele frequencies 49 MDM2 49 mitochondrial metabolism 49 Lafora disease 49 de ath 49 C EBP alpha 49 HMPV 49 AML MDS 49 Mitochondrial dysfunction 49 basal forebrain 49 CXCL# 49 C#Y mutation 49 K#R [002] 49 cytopathic 49 PHLPP 49 elevated cortisol 49 TSP1 49 homozygous FH 49 sex hormone estrogen 49 mGluR 49 Immune responses 49 genomic deletions 49 beta1 integrin 49 Leydig cells 49 NR#A# 49 transgene expression 49 mutant flies 49 prodynorphin 49 heritable diseases 49 EBNA1 49 fascin 49 NF kB 49 Kv#.# channels 49 alpha thalassemia 49 amnestic MCI 49 S#K# 49 pyruvate kinase 49 L1s 49 prefrontal cortical 49 FGFs 49 IKZF1 49 comorbid anxiety 49 genetic predisposition 49 PI3K 49 dentate gyrus 49 TYMS 49 radiosensitive 49 excitatory synapses 49 BRAF V#E 49 gastric carcinoma 49 carotid plaque 49 X chromosome 49 genomic variants 49 NPM1 mutations 49 3'UTR 49 molecular abnormalities 49 hepatoma 49 hormone therapy estrogen 49 nonmelanoma skin cancers 49 histone H4 49 phenotypic expression 49 SOD1 gene 49 ERK activation 49 entorhinal cortex 49 tyrosine phosphorylation 49 Notch signaling 49 TEL AML1 49 sphingolipid 49 mutant mouse 49 pathological hallmark 49 histone deacetylases 49 FOXO 49 Smad3 49 MEF2D 49 genetic variation 49 SIRT1 gene 49 chromosome #q#.# [001] 49 N Myc 49 mild cognitive 49 Wnt signaling 49 inherited gene mutation 49 SRY gene 49 S. maltophilia 49 neuropathologic 49 H5 viruses 49 nongenetic 49 Multivariate analyzes 49 proteins encoded 49 beta thalassemia 49 HLA DRB1 * 49 abdominally obese 49 dopamine receptor 49 Apobec3 49 dopamine receptors 49 abnormal proteins 49 obstructive coronary artery 49 airway responsiveness 49 hyper IgE syndrome 49 neurosensory 49 mirror neuron 49 breast epithelial cells 49 Her2 gene 49 somatic mutation 49 cystatin C 49 leptin receptors 49 oxysterols 49 SLC#A# gene [001] 49 Stat5 49 NFAT 49 ALK mutations 49 caveolin 49 colorectal tumors 49 EGFR mutation 49 behavioral disinhibition 49 BRAF protein 49 fractional anisotropy