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(Click for frequent words.) 80 heterozygous 72 allele 70 homozygotes 70 alleles 69 genotype 68 heterozygotes 68 C#Y 66 polymorphism 66 homozygosity 66 genotypes 66 MTHFR 65 genotyped 65 CDKN2A 65 homozygote 65 rs# [002] 65 variant alleles 64 Homozygous 64 rs# [003] 64 mutation 64 mutated gene 64 CCR5 delta# 64 CC genotype 64 MLH1 64 rs# [004] 64 mutant allele 64 phenotype 63 rs# [001] 63 Heterozygous 63 polymorphisms 63 ABCB1 62 null mice 62 DRD2 62 autosomal recessive 62 autosomal dominant 62 variant allele 62 IL#B 62 missense mutation 62 GSTM1 62 haplotypes 62 heterozygote 62 genetic variant 62 mutant gene 62 germline mutations 61 MC1R gene 61 apolipoprotein E gene 61 CYP#C# * 61 overexpressing 61 transfected 61 FMR1 gene 61 penetrance 61 UGT#A# * 61 APOE e4 61 proband 61 apolipoprotein E 61 G allele 61 PTPN# 61 #q# [001] 60 TT genotype 60 APOE ε4 60 ApoE4 60 MYH9 gene 60 CAG repeats 60 OPRM1 gene 60 gene variant 60 A. thaliana 60 frameshift mutation 60 FMR1 60 APOE4 60 mutations 60 APOE gene 60 chromosome #q# [002] 60 orthologs 60 premutation 60 MSH2 60 ApoE gene 60 5 HTTLPR 60 wildtype 60 constitutively active 60 mosaicism 60 promoter methylation 60 diploid 59 inherited mutations 59 KRAS gene 59 missense mutations 59 mice lacking 59 sporadic ALS 59 normal karyotype 59 dopamine transporter gene 59 haplotype 59 NF1 59 GSTT1 59 EGFR gene 59 euthyroid 59 hereditary hemochromatosis 59 K#R [002] 59 autosomal 59 LRAT 59 heterozygosity 59 EGFR mutations 59 KRAS mutations 59 APOC3 59 EGFP 59 IgA deficiency 59 C#BL/#J 58 BRCA2 mutation 58 HFE gene 58 allelic variants 58 overexpress 58 gene polymorphism 58 transgene expression 58 cyclin E 58 intronic 58 mutated K ras 58 TP# mutation 58 methylenetetrahydrofolate reductase 58 CDH1 58 mutant alleles 58 activating mutation 58 BRCA1 mutation 58 HLA DQ2 58 noncarriers 58 KIF6 gene 58 HNPCC 58 constitutively 58 IKZF1 58 ApoE4 allele 58 germline mutation 58 maternally inherited 58 miR #a [001] 58 mRNA expression 58 MC1R 58 breast cancer genes BRCA1 58 familial ALS 58 recessive genes 58 BRAF V#E 58 MDM2 58 unmutated 58 activating mutations 58 GSTP1 58 CFH gene 58 receptor gene 58 IGF2 57 ZNF# 57 transgenic mice 57 SNPs 57 chromosome #q# [001] 57 APOE allele 57 myostatin gene 57 HLA DRB1 * 57 BRCA1 mutations 57 gene mutation 57 BMP2 57 basal cell nevus syndrome 57 hTERT 57 allele frequencies 57 CHD7 57 C#BL 6 mice 57 FLT3 57 phenotypes 57 TOP2A 57 K ras 57 karyotype 57 Polymorphisms 57 K ras mutations 57 spontaneous mutation 57 BRCA1 gene 57 genetic mutation 57 single nucleotide polymorphism 57 APOE 57 autosomal dominant disorder 57 ERBB2 57 MnSOD 57 c KIT 57 syngeneic 57 EGFR mutation 57 MSH6 57 HLA B 57 HepG2 cells 57 genes encoding 57 SNP rs# [001] 57 IDH2 57 protein encoded 57 Leydig cells 57 CGG repeats 57 adenoma 57 GISTs 57 breast carcinomas 57 T2DM 57 PDGFRA 57 subtype 57 seronegative 57 TMEM#B 56 #p# [003] 56 BRCA mutation 56 gene encoding 56 defective gene 56 PCa 56 K#N 56 isoenzyme 56 COMT 56 TEL AML1 56 haplogroup 56 CYP# [002] 56 IFN gamma 56 Haplogroup 56 inhibin 56 mutated BRCA1 56 DQB1 * 56 ADPKD 56 breast carcinoma 56 human leukocyte antigen 56 microdeletions 56 hepatocellular carcinomas 56 TTR gene 56 Cowden syndrome 56 autosomal recessive disease 56 SHANK3 56 serum concentrations 56 recessive gene 56 FGFR2 56 unmethylated 56 Leydig cell 56 p# mutation 56 R#W [002] 56 homolog 56 mRNA transcripts 56 ApoE4 gene 56 seropositivity 56 KRAS wild 56 periventricular 56 missense 56 CagA 56 HLA DR4 immune 56 Jhdm2a 56 dopamine receptor gene 56 hepatic lipase 56 SLC#A# [002] 56 nondiabetic 56 APOE4 gene 56 downregulated 56 beta thalassemia 56 X chromosome 56 phenotypically 56 ERCC1 56 HLA B# 56 genes predisposing 56 CYP#C# [002] 56 constitutively expressed 56 ApoE 56 #q# [002] 56 genotypic 56 VNTR 56 paternally inherited 56 coinfected 56 leukemic cell 56 differentially expressed 56 PAX5 56 SMN1 56 loci 56 NNRTI resistance 56 SLC#A# [001] 56 MHC genes 56 BRCA2 gene 56 overexpressed 56 COL#A# 56 HLA DR 55 FLT3 ITD 55 autosomes 55 TYMS 55 HNSCC 55 GABRA2 55 recessive mutation 55 gene 55 transgenic mice expressing 55 FXTAS 55 SMN2 gene 55 C#T [001] 55 xenograft tumors 55 inactivating mutations 55 Neuregulin 1 55 CD8 + 55 ploidy 55 tyrosine phosphorylation 55 valine 55 transgene 55 kDa protein 55 probands 55 overexpression 55 HGPIN 55 deficient mice 55 estrogen receptor ER 55 APOE e4 gene 55 CYP#B# 55 ADH1B * 55 mtDNA 55 inherited maternally 55 selfing 55 functional polymorphism 55 hypermethylated 55 STAT1 55 V Leiden 55 CD#c 55 MECP2 gene 55 immunoreactivity 55 BARD1 55 microsatellite instability 55 GBM tumors 55 poorer prognosis 55 HBsAg 55 HCV infected 55 At#g# 55 APOE epsilon 4 55 transduced 55 nonsense mutation 55 BRCA2 carriers 55 K ras gene 55 apoC III 55 immunofluorescence staining 55 FLT3 mutations 55 decarboxylase 55 apolipoprotein E4 55 NPM1 mutations 55 Genotypes 55 MHC molecules 55 Fragile X gene 55 gene mutations 55 DRD4 55 UGT#B# 55 CFTR gene 55 Klinefelter syndrome 55 apoE 55 TP# mutations 55 BRCA1 BRCA2 55 JAK2 V#F 55 dinucleotide 55 T#I [002] 55 dizygotic 55 nonischemic 55 haplogroups 55 DICER1 gene 55 BRCA2 mutations 55 RRM1 55 GSTM1 gene 55 MLL gene 55 MetS 55 heritable traits 55 PDGFR 55 prion gene 55 microdeletion 55 S#A# [002] 55 progranulin gene 55 gene expression patterns 55 promoter polymorphism 55 HBeAg 55 upregulated 55 aldehyde dehydrogenase 55 Asymptomatic 55 familial pancreatic cancer 55 cell adhesion molecule 55 sequence homology 55 atypical hyperplasia 55 LQTS 55 adenocarcinomas 55 TRAF1 C5 55 F#del mutation 55 estrogen receptor negative 55 COMT gene 55 exomes 55 vimentin 54 Wwox 54 apolipoprotein 54 uniparental 54 pancreatic adenocarcinoma 54 PTEN mutations 54 V#F mutation 54 homologue 54 XLHED 54 PON1 54 genetic variability 54 RASSF1A 54 BRAF mutation 54 CYP#C# gene 54 mutant p# 54 ε4 54 mediated apoptosis 54 CNVs 54 BRCA1 mutation carriers 54 familial hypercholesterolemia 54 BRCA mutations 54 allelic 54 #q#.# [002] 54 haptoglobin 54 HBeAg positive 54 PALB2 54 D. melanogaster 54 5q 54 succinate dehydrogenase 54 mtDNA mutations 54 heritable 54 glutamic acid decarboxylase 54 receptor blocker 54 invasive ductal 54 thymocytes 54 indels 54 ESR1 54 KLF4 54 androgen receptor AR 54 activin 54 CpG 54 aneuploidies 54 immunodeficient 54 interferon IFN 54 induced apoptosis 54 Foxp3 54 WT1 54 V#E 54 orthologous 54 #q#.# [001] 54 BRCA2 54 CHEK2 54 BRCA2 gene mutation 54 isoform 54 Bos taurus 54 CYP#C# [001] 54 TIMP 1 54 homozygous FH 54 C#BL 6 54 homologs 54 constitutively activated 54 parkin gene 54 Nf2 54 differentially expressed genes 54 aneuploidy 54 Clusterin 54 MEFs 54 CD4 + CD# 54 lysine residues 54 CD3 + 54 intron 54 UGT#A# 54 thymic 54 familial adenomatous polyposis 54 #p#.# [002] 54 synthases 54 monogenic 54 V#F 54 haploid 54 mammary tumors 54 subcellular localization 54 splice variants 54 catechol O methyltransferase 54 Overexpression 54 chromosome #p# [001] 54 androgen receptor gene 54 MAOA gene 54 HbF 54 GLUT1 54 HMGA2 54 VKORC1 54 transfected cells 54 BRCA gene mutation 54 primordial germ cells 54 aneuploid 54 transferase 54 PGCs 54 genetic polymorphism 54 methylation patterns 54 BRAF V#E mutation 54 autoantibody 54 BRIP1 54 adipogenic 54 cells transfected 54 pDC 54 TACI mutations 54 circadian genes 54 immunocompetent 54 isoforms 54 microcephalin 54 #q#.# deletion syndrome 54 survivin 54 BRCA1 54 apoE4 54 AAT deficiency 54 G#D 54 #p# [001] 54 globin genes 54 miRNA genes 54 normotensive 54 HLA DR2 54 KIT mutations 54 CYP#D# 54 db db mice 54 atopic 54 serotonin transporter gene 54 hepatoma 54 MeCP2 gene 54 transmembrane protein 54 BRCA2 breast cancer 54 gene MECP2 54 SNP rs# [002] 53 mitochondrial DNA mtDNA 53 adenylate cyclase 53 lymphoid cells 53 transiently transfected 53 CpG island 53 BMPR2 53 monozygotic 53 ChR2 53 PBMCs 53 PRNP 53 colorectal carcinoma 53 HCV genotype 53 chromosomal abnormalities 53 spontaneous mutations 53 haematopoietic 53 susceptibility gene 53 mutated KRAS 53 caveolin 1 53 overexpressing cells 53 HLA genes 53 GPx 53 ovules 53 causative gene 53 inbred strains 53 Supplemental Figure 53 III EGFRvIII 53 prion protein gene 53 prion protein PrP 53 immunoreactive 53 germline 53 ALDH2 53 peripheral blood mononuclear 53 histological subtype 53 herpesviruses 53 genetic abnormality 53 gonadotropins 53 Nf1 53 Haptoglobin 53 GNAQ 53 HPV# 53 apolipoprotein E APOE 53 PTEN gene 53 latently infected 53 colorectal neoplasia 53 pathogenic mutations 53 HIV uninfected 53 type KRAS 53 chromosomal rearrangement 53 CD# CD# 53 cognitively normal 53 CIN2 + 53 Li Fraumeni syndrome 53 isogenic 53 prostate cancer CaP 53 RPE# 53 DRB1 * 53 dizygotic twins 53 neuroD2 53 eNOS 53 synuclein 53 insertion deletion 53 IGFBP 53 MTHFR gene 53 Abl 53 caveolin 53 DRB1 53 epigenetic silencing 53 virulence genes 53 Ser# 53 alternatively spliced 53 DAT1 53 autosomal recessive disorder 53 EGFRvIII 53 androgen independent 53 germline cells 53 lymph node metastasis 53 tetraploid 53 Hashimoto thyroiditis 53 cysteines 53 defensin 53 ortholog 53 CYP#A# [002] 53 ribosomal proteins 53 TOMM# 53 prognostic factor 53 BDNF gene 53 seropositive 53 RCAN1 53 TSC1 53 basal forebrain 53 IL#R 53 lacZ 53 endostatin 53 prostate adenocarcinoma 53 isoprostane 53 suppressor gene 53 HLA molecules 53 #q# deletion 53 poor metabolizers 53 TCF#L# 53 μg ml 53 LNCaP cells 53 LRRK2 gene 53 colon carcinoma 53 cell carcinomas 53 ovariectomized 53 neoplasm 53 MIF gene 53 B. fragilis 53 prostate carcinoma 53 monocytic 53 gastric carcinoma 53 H#K#me# 53 asymptomatic carriers 53 recessive mutations 53 CDK4 53 gene amplification 53 pDCs 53 atherosclerotic lesions 53 AGTR1 53 chromosomal anomalies 53 fetuin 53 intergenic 53 hypomethylation 53 perilipin 53 glycosylated 53 inducible 53 polyploid 53 NFkB 53 ADRB2 53 diabetes mellitus DM 53 P. patens 53 MDA MB 53 receptor kinase 53 HLA DRB1 SE 53 paralogs 53 HDL2 53 hydroxylase 53 cyclin dependent kinase inhibitor 53 gene variation 53 TGF β1 53 2n = 53 outbred 53 gene locus 53 cDNAs 53 Alu elements 53 rs# rs# 53 VHL gene 53 NF1 gene 53 ribosomal protein 53 SOD1 gene 53 coding sequences 53 alkaline phosphatase ALP 52 mCRC patients 52 1α 52 gene expression profiles 52 thyrotropin 52 cagA 52 T2D 52 telomere lengths 52 abnormal chromosome 52 myeloid 52 amplicons 52 Supplementary Fig 52 ectopic expression 52 methylated 52 CISH 52 1 diabetes T1D 52 Squamous 52 genetic alteration 52 transactivation 52 epigenetically 52 non mutated KRAS 52 DLC1 52 clonally 52 DRD2 gene 52 #p#.# [001] 52 STAT4 52 catechol O methyltransferase COMT 52 TMPRSS2 ERG 52 Upregulation 52 H#D 52 beta subunit 52 de novo mutations 52 endogenous retrovirus 52 lobular 52 basal cell carcinoma BCC 52 G6PD 52 aged ≥ 52 Immunohistochemical analysis 52 autoantibodies 52 chromosomal abnormality 52 recessive trait 52 KRAS oncogene 52 SLC#A# gene [002] 52 MDR1 52 HLA DR4 52 differentially regulated 52 clusterin 52 chromosome abnormality 52 SSc 52 tumorigenicity 52 thrombospondin 52 alpha synuclein gene 52 colocalization 52 5 HTT gene 52 LDL receptor 52 chromosomal alterations 52 erythrocytes 52 phenotypic variation 52 independent prognostic marker 52 transcriptional repressor 52 JAK2 mutation 52 leukemia CLL 52 amino acid substitution 52 phosphorylate 52 major histocompatibility complex 52 mutant worms 52 gestational diabetes mellitus 52 melanocyte 52 CLL cells 52 IGF1 52 advanced adenoma 52 p# deficient 52 WNK1 52 ADAMTS# 52 ovarian carcinoma 52 neovascular 52 downregulation 52 embryonal carcinoma 52 aggrecan 52 HER2/neu 52 CCR7 52 HLA DRB1 52 interleukin IL -# 52 PTHrP 52 elevated triglyceride levels 52 ErbB2 positive 52 YKL 52 Th1 52 cytokeratin 52 MAOA 52 erythroid 52 JAK2 52 pg ml 52 lymphoblasts 52 Hh 52 X chromosomes 52 del 5q 52 miRNAs miR 52 BRAF protein 52 SCN5A 52 C#T [002] 52 GPC3 52 monocyte chemotactic protein 52 metaplasia 52 phosphorylated 52 enzymatic activity 52 tyrosine kinase receptor 52 E selectin 52 P2X 52 TMPRSS2 ERG fusion 52 NAT2 52 infantile onset 52 deletion 5q 52 Fas ligand 52 APOL1 52 coexpression 52 hypercholesterolemic 52 TCF#L# gene 52 sCJD 52 DRD4 gene 52 cystic fibrosis transmembrane conductance 52 presenilin 52 matrix metalloproteinase 52 HER2 neu 52 Alleles 52 SMN1 gene 52 Aß 52 monozygotic twins 52 gastric adenocarcinoma 52 chromosome #q 52 alpha2 52 EAAT2 52 FasL 52 C. albicans 52 leukemia AML 52 GlcNAc 52 ubiquitinated 52 CYP#D# genotype 52 JAK2 gene 52 BCR ABL 52 immunostaining 52 alpha1 52 isoenzymes 52 homologous 52 IFN γ 52 pCR 52 Runx1 52 susceptibility genes 52 microsatellite markers 52 pseudogenes 52 antibody titers 52 homodimers 52 Single Nucleotide Polymorphisms 52 alkaline phosphatase 52 CCR5 mutation 52 HLA loci 52 cytochrome 52 colorectal tumor 52 knockout mice 52 PsA 52 MC4R gene 52 Pharmacokinetics PK 52 histologically 52 nondemented 52 carcinoembryonic antigen 52 OCA2 52 immunized mice 52 serine 52 adrenal cortex 52 subclinical 52 Apolipoprotein 52 genetic mutations 52 liver metastasis 52 ERK1 2 52 genes BRCA1 52 HMGA1 52 T1D 52 Dpp 52 gastric carcinomas 52 Igf2 52 CHRNA5 gene 52 lymphocytic 52 LPA gene 52 neuroblastoma tumors 52 miRNA expression 52 chromosome #q#.# [001] 52 proto oncogene 52 iNOS 52 mutant mice 52 nmol L 52 cytochrome b 52 castrate resistant 52 incomplete penetrance 52 LIS1 52 trisomy 52 GenBank accession 52 stably transfected 52 linkage disequilibrium 52 steatohepatitis 52 cyclin 52 L#R 52 hepatocyte 52 gene variants 52 gambiae 52 aromatase 52 Fig. 1C 52 QTLs 52 chimeric 52 MLL2 52 seroconverted 51 subependymal giant cell 51 replicon 51 Her2/neu 51 Immunohistochemical staining 51 transgenes 51 EoE 51 myeloproliferative neoplasms 51 parkinsonism 51 BCG vaccinated 51 beta globin 51 BRAF mutations 51 fig. S1 51 5alpha reductase 51 RAR beta 51 nonsense mutations 51 multivariate Cox 51 Drosophila melanogaster 51 splenocytes 51 brucei 51 operable breast cancer 51 simian immunodeficiency virus 51 CD4 + CD8 + 51 Wistar rats 51 Meckel Gruber 51 cystatin 51 xeroderma pigmentosum 51 DU# [002] 51 hemagglutinin H 51 ApoB 51 HBV genotype 51 astrocytomas 51 ENPP1 51 TACI 51 murine 51 heterodimers 51 rhesus 51 cytopathic 51 immunoblotting 51 regulator CFTR gene 51 Lymphocyte 51 adiponectin concentrations 51 nonalcoholic steatohepatitis NASH 51 rDNA 51 gene polymorphisms 51 subfamily 51 lung adenocarcinoma 51 SOD2 gene 51 acute myelogenous leukemia AML 51 tissue transglutaminase 51 situ LCIS 51 Single Nucleotide Polymorphism 51 thyroid carcinoma 51 EP4 51 chromosome #p# [002] 51 rheumatoid factor 51 tumor histology 51 malignant lymphoma 51 APOA5 51 tumor specific antigen 51 Bacteroides 51 VSV G 51 mucinous 51 mesotheliomas 51 C1q 51 FDG uptake 51 catenin 51 TIMP 51 chromosomal aberrations 51 1beta 51 HER2 receptor 51 differential gene expression 51 HLA gene variant 51 hippocampal neurons 51 genetic variation 51 procollagen 51 #S rRNA 51 CD# + [001] 51 mouse testes 51 allele frequency 51 karyotypes 51 gametophyte 51 4E BP1 51 transgenic mouse models 51 troponin T 51 methylation 51 decitabine 51 CXCL# 51 HIV HCV coinfected 51 severe congenital neutropenia 51 M#V 51 protein tyrosine phosphatase 51 TLR3 51 HLA gene 51 KCNQ1 51 hyperplastic 51 Karayiorgou 51 quantitative trait loci 51 IgA antibodies 51 Fibroblasts 51 budding yeast 51 hypermethylation 51 Hp2 2 51 transcriptionally 51 BCL#A 51 mutated genes 51 essential thrombocythemia 51 fusion protein 51 chromosome abnormalities 51 syntaxin 51 IgG1 51 thyroglobulin 51 Cx# [001] 51 abnormal chromosomes 51 papillary renal cell carcinoma 51 SOD1 protein 51 PC# cells 51 NFKBIA 51 SPINK1 51 Cyclin E 51 dopamine D4 receptor 51 HER-2/neu 51 Philadelphia Chromosome Positive 51 cholesteryl ester transfer 51 esterase 51 Estrogen receptor 51 Notch1 51 mitochondrial genomes 51 Pdx1 51 nitrotyrosine 51 granulocyte 51 phosphorothioate 51 X inactivation 51 p# mutations 51 T1DM 51 BRCA2 mutation carriers 51 ENaC 51 TrkB