Related by context. All words. (Click for frequent words.) 80 chromosome #q# [001] 76 #q# [001] 75 chromosome #p# [001] 75 #p#.# [001] 75 #p# [001] 75 rs# [002] 75 rs# [004] 73 chromosome #q#.# [001] 73 #q#.# [001] 73 chromosome #q#.# [002] 73 chromosome #q 72 chromosome #p# [002] 72 #q# [002] 72 PTPN# 72 #p#.# [002] 71 chromosome #p#.# 70 functional polymorphism 70 rs# [003] 70 #q#.# [002] 70 intronic 70 TCF#L# gene 69 hypermethylated 69 genetic loci 69 MECP2 gene 69 autosomal 69 CDKN2A 69 KIAA# 69 #p# [003] 69 NR#A# 69 missense mutations 69 CNTNAP2 69 WNK1 69 TCF#L# 69 microdeletions 68 susceptibility locus 68 germline mutations 68 COL#A# 68 LPA gene 68 ABCB1 68 gene locus 68 SNP rs# [001] 68 microdeletion 67 TSC1 67 SNP rs# [002] 67 FGFR2 67 VNTR 67 promoter methylation 67 C#Y 67 GNAQ 67 polymorphisms 67 haplotypes 67 SCN5A 67 orthologs 67 #S rRNA 67 MLL2 67 MTHFR 67 ribosomal protein 67 ESR1 67 monogenic 67 MAPK pathway 67 BARD1 67 serine threonine kinase 67 UGT#B# 67 DRB1 * 67 SLITRK1 67 MSH2 67 MYH9 gene 66 HLA DRB1 66 MLH1 66 allelic variants 66 ORMDL3 66 gene MECP2 66 ZNF# 66 microcephalin 66 genetic polymorphism 66 Microarray analysis 66 cell adhesion molecule 66 dysbindin 66 SLC#A# [001] 66 susceptibility gene 66 SMAD4 66 BDNF gene 66 GSTP1 66 chromosomal aberrations 66 CDH1 66 haplotype 65 steroidogenic 65 dopamine D4 receptor 65 KIF6 gene 65 rRNA 65 somatic mutation 65 gene polymorphisms 65 cytochrome b 65 ENPP1 65 H#K#me# 65 IgA deficiency 65 noncoding 65 ribosomal DNA 65 catechol O methyltransferase 65 apolipoprotein E gene 65 synuclein 65 de novo mutations 65 Polymorphisms 65 mediated inhibition 65 SHANK3 65 VKORC1 65 chromosomal regions 65 quantitative trait loci 65 colorectal carcinoma 65 postsynaptic 65 immunoreactive 65 MC4R gene 65 polymorphism 65 CHEK2 65 ventrolateral 65 heterozygotes 65 LRP5 65 alternatively spliced 65 intergenic regions 65 somatic mutations 65 Fas ligand 65 tryptophan hydroxylase 65 inherited mutations 65 ERBB2 65 rs# rs# 65 homozygosity 65 rs# [001] 65 K ras mutations 65 frameshift mutation 65 CEACAM1 64 gene polymorphism 64 intergenic 64 E#F# 64 protein tyrosine phosphatase 64 Cathepsin B 64 Clusterin 64 Genetic variation 64 missense 64 IL#B 64 transcriptional repressor 64 CYP#D# gene 64 CYP#E# gene 64 LRP6 64 paternally inherited 64 prefrontal cortical 64 centromeric 64 subcellular localization 64 GSTT1 64 apoE4 64 MC1R 64 NF1 gene 64 TP# mutations 64 OCA2 64 indel 64 methylenetetrahydrofolate reductase 64 gene loci 64 dopamine receptor gene 64 SLC#A# [002] 64 LRAT 64 androgen receptor gene 64 sporadic ALS 64 CYP#B# 64 homeobox gene 64 HMGA2 64 Arabidopsis genome 64 transcriptional activation 64 segmental duplications 64 constitutively active 64 allelic 64 microRNA expression 64 mutant allele 64 KRAS oncogene 64 chemokine receptor 64 serine protease 64 NFKBIA 64 Upregulation 64 R#W [002] 64 adenocarcinomas 64 caveolin 64 miRNA expression 64 CNTNAP2 gene 64 allele frequencies 64 immunoblotting 64 CHD7 63 evolutionary conserved 63 chromosomal rearrangement 63 progranulin gene 63 BRCA1 BRCA2 63 histone acetylation 63 proband 63 cis regulatory 63 CpG island 63 mutated K ras 63 periventricular 63 TOP2A gene 63 carboxyl terminal 63 CCR5 delta# 63 C#T [002] 63 hepatoma 63 acetylcholine receptor 63 hepatic lipase 63 anterior pituitary 63 mRNA transcripts 63 JAK2 enzyme 63 gastrointestinal stromal tumors GISTs 63 FMR1 gene 63 heterozygosity 63 DQB1 * 63 HLA DQ2 63 constitutively expressed 63 receptor gene 63 carboxy terminal 63 prodynorphin 63 5 HTTLPR 63 hypermethylation 63 CHI#L# 63 major histocompatibility complex 63 p# mutation 63 thyrotropin 63 cyclin dependent kinase inhibitor 63 CREBBP 63 ERK signaling 63 amino terminal 63 missense mutation 63 lysine residues 63 apolipoprotein E4 63 gastric carcinoma 63 MYBPC3 63 hypoperfusion 63 histone methylation 63 genes encoding 63 ADPKD 63 succinate dehydrogenase 63 FGFR3 63 IKZF1 63 loci 63 ORFs 63 dinucleotide 63 epigenetic modification 63 RRM1 63 HFE gene 63 phenotype 63 cytoplasmic domain 63 CYP#C# [002] 63 NKX#.# 63 MC1R gene 63 methylation patterns 63 cytokeratin 63 indels 63 vitamin D receptor 63 causal variants 63 mitochondrial gene 63 proline rich 63 DRD2 gene 63 GSTM1 63 3'UTR 63 ERalpha 63 mitogen activated protein kinase 63 SOCS3 63 KLF4 63 gene rearrangements 63 Genetic variants 63 coding exons 63 CDH# 63 RASSF1A 63 HLA DRB1 * 63 polyadenylation 63 ALK gene 63 SSc 63 genes CYP#C# 63 adipogenic 63 splice junctions 63 hypothalamic pituitary 63 SNPs 63 ADAMTS# 63 Single Nucleotide Polymorphism 63 At#g# 62 single nucleotide polymorphism 62 microglial 62 transmembrane protein 62 Jhdm2a 62 posterior cingulate 62 mRNA expression 62 hyperplastic 62 BRAF V#E 62 APOL1 62 Dysregulation 62 apoE 62 PKC isoforms 62 TIMP 1 62 deacetylation 62 TMEM#B 62 transmembrane receptor 62 hydroxylase 62 SNCA 62 mitochondrial DNA mtDNA 62 IL#R 62 intron 62 DNA methyltransferase 62 evolutionarily conserved 62 c KIT 62 orthologous 62 CYP #D# 62 phosphorylates 62 PON1 gene 62 PTHrP 62 hypomethylation 62 microsatellite instability 62 variant rs# 62 subventricular zone 62 receptor tyrosine kinase 62 metalloprotease 62 entorhinal cortex 62 HepG2 cells 62 FKBP# 62 autism susceptibility genes 62 maternally inherited 62 PALB2 62 genes differentially expressed 62 ABCB1 gene 62 Ki# 62 p# mutations 62 nucleotide sequence 62 fig. S4 62 protein phosphorylation 62 apolipoprotein E APOE 62 ankyrin repeat 62 causative mutations 62 papillary renal cell carcinoma 62 KCNQ1 62 FGF signaling 62 GPC5 62 proteolytic cleavage 62 FMR1 62 β1 62 IRAK1 62 allergic airway inflammation 62 BRAF protein 62 nitrotyrosine 62 HMGCR 62 carcinoembryonic antigen 62 amino acid substitutions 62 microvessel density 62 MEF2A 62 lymphoblastoid cell lines 62 LDL receptor 62 cagA 62 neurite outgrowth 62 IgG1 62 membrane proximal 62 cyclin E 62 FSHR 62 isotype 62 HIF 1α 62 germline mutation 62 PAX5 62 TMPRSS2 ERG fusion 62 miRNA genes 62 D#N 62 PICALM 62 STAT1 62 neuroligins 62 alpha synuclein gene 62 oxytocin receptor 62 CALHM1 62 NAT2 62 androgen receptor AR 62 dopamine transporter gene 62 DNA methylation patterns 62 MLL gene 62 Leydig cells 62 5 HT1A 62 μ opioid receptor 62 ubiquitinated 62 GLUT1 62 glomerular 62 MMP# 62 erythroid 62 lymphangiogenesis 62 renal cysts 62 SLC#A# gene [001] 62 tRNA synthetase 62 pDC 62 Polymorphism 62 exocrine 62 downregulation 62 CYP#A# [002] 62 glucose transporter 62 proapoptotic 62 splice variants 62 airway hyperresponsiveness 62 downstream effectors 62 gastric carcinogenesis 62 PRNP 62 heterozygous 61 ALK mutations 61 linkage disequilibrium 61 aneuploidies 61 TrkB 61 TTR gene 61 isoenzyme 61 TP# gene 61 aminotransferase 61 DRD2 61 beta globin 61 promoter hypermethylation 61 susceptibility loci 61 beta globin gene 61 serine threonine 61 transmembrane domain 61 genetic polymorphisms 61 NPM1 gene 61 Oncogenic 61 CFTR cystic fibrosis transmembrane 61 phospholipase A2 61 mosaicism 61 overactivation 61 nucleoli 61 condensin 61 nicotinic receptor 61 phosphatidylinositol 3 61 LRRK2 gene 61 Rap1 61 cyclin dependent kinase 61 immunohistochemical 61 Apolipoprotein E 61 ERK1 2 61 virulence genes 61 CpG 61 ETV1 61 histone modifications 61 unmethylated 61 Single Nucleotide Polymorphisms SNPs 61 apolipoprotein E 61 noradrenergic 61 clefting 61 transcriptional repression 61 null mice 61 TT genotype 61 basal forebrain 61 granulosa cell 61 chromatin structure 61 uPAR 61 PCR RFLP 61 eNOS 61 nAChRs 61 NS5B 61 paralogs 61 5q 61 APOC3 61 Cyclin D1 61 encodes protein 61 PTEN gene 61 BMP2 61 chromosomal alterations 61 urothelial 61 aldehyde dehydrogenase 61 transgenic mice expressing 61 proto oncogene 61 metabolizing enzyme 61 tumorigenicity 61 subgenual cingulate 61 aberrant methylation 61 RNA binding 61 eIF4E 61 IDH1 gene 61 ALDH2 61 CD# expression [001] 61 coexpression 61 epigenetic modifications 61 receptor gamma 61 autosomal recessive 61 3' UTR 61 TIMP 61 Histone 61 NR2B subunit 61 Epstein Barr Virus EBV 61 EBNA1 61 differential gene expression 61 variant allele 61 APOA5 61 inactivating mutations 61 WDR# 61 JAK STAT 61 VHL gene 61 CYP#C# gene 61 microglial activation 61 p# alpha [002] 61 gene APOE 61 tyrosine phosphorylation 61 protein phosphatase 61 CDK4 61 presynaptic 61 OCA2 gene 61 Supplementary Table 61 CYP#A# gene 61 clade B 61 MAOA gene 61 IDH1 mutation 61 dopamine D2 61 upregulates 61 ADH1B * 61 surgically resected 61 CYP# [002] 61 homolog 61 basolateral 61 genes predisposing 61 KCNH2 61 prostate cancer CaP 61 inactive X chromosome 61 astrocytic 61 immunodominant 61 autosomal dominant disorder 61 matrix metalloproteinase 61 untranslated regions 61 protein encoded 61 isoenzymes 61 Cytogenetic 61 plastid 61 TET2 61 circadian genes 61 human leukocyte antigen 61 susceptibility genes 61 endophenotypes 61 AMACR 61 synthetase 61 transcriptionally 61 Western blotting 61 cAMP signaling 61 Phosphorylation 61 pathogenic mutations 61 cytopathic 61 metabolizing enzymes 61 haematopoietic 61 Cx# [001] 61 thrombospondin 61 Prox1 61 genomewide 61 alleles 61 STAT4 61 Brugada syndrome 61 esterase 61 lyase 61 transmembrane 61 osteoblastic 61 MYH9 61 phosphoprotein 61 Genotypes 61 sequence homology 61 meiotic recombination 61 CHRNA5 61 cytogenetic abnormalities 60 Single Nucleotide Polymorphisms 60 MTHFR gene 60 TRAF1 60 P cadherin 60 Y chromosomal 60 deacetylase 60 CYP#E# 60 DISC1 60 LIS1 60 tropomyosin 60 clinicopathologic 60 histone deacetylation 60 radial glia 60 mucinous 60 penetrance 60 Protein Kinase C 60 heterozygote 60 PKD1 60 G allele 60 cerebral cortical 60 CAG repeats 60 Haplotype 60 kilobase 60 PTP1B 60 FGFs 60 Plasmodium vivax 60 karyotype 60 regulator CFTR gene 60 p# MAPK 60 CD#b 60 Macrophage 60 exon intron 60 X inactivation 60 EGFR gene 60 LKB1 60 raphe 60 ncRNA 60 progressive neurodegenerative disorder 60 monozygotic twins 60 genomic deletions 60 perivascular 60 H#K# [002] 60 cystic fibrosis transmembrane conductance 60 1beta 60 CDK5 60 osteoprotegerin 60 MDR1 60 hypogonadotropic hypogonadism 60 globin genes 60 embryonal carcinoma 60 susceptibility alleles 60 ADRB2 60 BRAF gene 60 IRS1 60 CpG islands 60 PDE#A 60 EF Tu 60 superior temporal gyrus 60 DNMT1 60 transferase 60 amyloidogenic 60 EGFR protein 60 non coding RNA 60 myeloid 60 thyroid carcinoma 60 neuronal dysfunction 60 homodimer 60 pancreatic endocrine 60 catalytic subunit 60 LMNA 60 immunocytochemistry 60 Monocyte 60 myelofibrosis polycythemia vera 60 beta1 integrin 60 HER2 expression 60 5 HT1A receptor 60 retinoic acid receptor 60 heterochromatic 60 4E BP1 60 H#K# [001] 60 OPRM1 60 immunoreactivity 60 autosomal dominant 60 number variation CNV 60 protein tyrosine phosphatase 1B 60 drug metabolizing enzyme 60 hepatocellular carcinomas 60 CNVs 60 PON1 60 pheochromocytomas 60 tau gene 60 Runx1 60 neoplastic transformation 60 pRb 60 alpha synuclein protein 60 VIPR2 60 hypervariable 60 Amino acid 60 breast cancer subtypes 60 Supplemental Figure 60 alpha subunit 60 glutamatergic neurons 60 SCN1A 60 Tasigna prolongs 60 microRNA molecules 60 BCL2 60 autosomes 60 SPINK1 60 activating mutations 60 dimeric 60 ectopic expression 60 breast carcinogenesis 60 Rb#/p# 60 anaplastic lymphoma kinase ALK 60 tyrosine kinase receptor 60 neuronal nitric oxide synthase 60 homozygous 60 #q# deletion 60 CC genotype 60 previously uncharacterized 60 Aß 60 EAAT2 60 MAP kinase 60 Lyn kinase 60 segmental duplication 60 breast cancer genes BRCA1 60 transcriptional regulation 60 mRNA encoding 60 Immunohistochemical staining 60 Corynebacterium 60 microsatellite markers 60 circadian clock genes 60 IFRD1 60 extracellular signal 60 PrPSc 60 TERT 60 nicotine receptor 60 GTPase 60 TGF ß 60 transactivation 60 genome rearrangements 60 V#F mutation 60 miRNAs miR 60 FasL 60 ß catenin 60 peroxisomal 60 Lp PLA 2 60 soluble CD# ligand 60 gastric cardia 60 CFTR gene 60 homologues 60 CHD5 60 downstream effector 60 syngeneic 60 unmethylated DNA 60 metaplasia 60 ortholog 60 hypothalamic pituitary adrenal axis 60 posttranslational modifications 60 colonic mucosa 60 PPARg 60 PDGFR 60 K#N 60 C1q 60 GlcNAc 60 inducible nitric oxide synthase 60 colocalization 60 etiologic 60 NSCLC tumors 60 motor neuron degeneration 60 lymphoid 60 serum leptin 60 familial ALS 60 breast carcinoma 60 histologic subtype 60 trophoblast 60 cytosolic 60 5 hydroxytryptamine 60 adenylate cyclase 60 PI3K AKT 60 isoform 60 TRAF1 C5 60 gene encoding 60 miR #a [001] 60 TYMS 60 haplogroups 60 FGFR1 60 iNOS 60 Immunohistochemical analysis 60 resistin 60 caveolin 1 60 extramedullary 60 receptor kinase 59 RUNX3 59 chromatin modification 59 IGF1 59 PARP inhibition 59 lipoxygenase 59 hydrolase 59 IGF2 59 inverse agonist 59 β amyloid 59 NOTCH1 59 monocytic 59 familial clustering 59 TNFalpha 59 NPY gene 59 TOP2A 59 immunohistochemical staining 59 variant alleles 59 c Myb 59 vimentin 59 HDAC3 59 renal fibrosis 59 DRD4 59 Genetic variations 59 CFH gene 59 polygenic 59 cerebellar 59 Leukemias 59 SOD2 59 IL #p# 59 Single nucleotide polymorphisms 59 CD#c 59 BCL#A 59 homologs 59 VEGF receptor 59 impaired glucose metabolism 59 endothelial activation 59 G6PD 59 aggrecan 59 OGG1 59 Fig. 1C 59 HER2 neu 59 MAP#K# 59 IKK beta 59 Aromatase 59 amyloid ß 59 epigenetic alterations 59 HLA DRB1 SE 59 nephronophthisis 59 parkin gene 59 PNET 59 cysteines 59 FGFR2 gene 59 vacuolar 59 nonsense mutations 59 Sp1 59 FGFR4 59 kinase domain 59 multivariate Cox 59 Sonic Hedgehog 59 methylated DNA 59 Histologic 59 trinucleotide 59 NOD2 59 inferior frontal 59 NAc 59 Treg cell 59 NR2B 59 IL8 59 GABAA receptor 59 T#M 59 Foxp3 59 transcriptional profiles 59 epigenetically 59 methyltransferase 59 glycolipid 59 N Myc 59 CYP#A# CYP#D# 59 ectodermal 59 Dpp 59 CagA 59 phylogenetic analyzes 59 DRB1 59 codon 59 hamartomas 59 RAS RAF MEK 59 pseudogene 59 fig. S2 59 Kir#.# 59 TLE3 59 somatostatin 59 TMPRSS2 ERG 59 Alu elements 59 acinar 59 paraganglioma 59 ApoE gene 59 siRNAs targeting 59 prostate carcinoma 59 E3 ubiquitin ligase 59 number variations CNVs 59 histone H3 59 glycogen synthase kinase 59 huntingtin gene 59 SORL1 59 PCR amplified 59 HIF 1alpha 59 autosomal recessive disease 59 serotonin receptor 59 Chromosome 59 paragangliomas 59 cytoplasmic tail 59 catenin 59 clusterin 59 chromosomal deletions 59 PGC 1α 59 melanocyte 59 kDa protein 59 amyloid peptide 59 promoter polymorphism 59 myeloperoxidase 59 distal colon 59 RNA polymerases 59 lysophosphatidic acid 59 chromosomal instability 59 leucine zipper 59 mutant alleles 59 UGT#A# * 59 pheochromocytoma 59 chromosomal rearrangements 59 Her2 gene 59 bronchoalveolar lavage fluid 59 #HT#A 59 muscarinic receptor 59 KRAS mutations 59 coding genes 59 retinoid X 59 Foxp2 59 endogenous ligands 59 proviral DNA 59 inhibin B 59 GH IGF 59 amyloid deposition 59 DICER1 gene 59 pleiotropic 59 PI3K Akt 59 endometrioid 59 genetic variants associated 59 Serum concentrations 59 cyclic AMP cAMP 59 CYP#D# 59 sCJD 59 breast carcinomas 59 Chromosomal 59 NFkB 59 telomerase reverse transcriptase 59 S#A# [002] 59 linkage disequilibrium LD 59 APOE e4 59 autocrine 59 secretory pathway 59 klotho 59 LPS induced 59 NKG2D 59 BMAL1 59 superoxide dismutase 59 diagnostic biomarker 59 hyperhomocysteinemia 59 cyclooxygenase COX 59 mitotic progression 59 MeCP2 gene 59 c myc 59 DNA demethylation 59 activin 59 MIF protein 59 amino acid substitution 59 Igf2 59 multiplex ligation dependent 59 recessive mutation 59 gene amplification 59 squamous cell lung cancer 59 enkephalin 59 DNA hypermethylation 59 forkhead 59 fibrillin 1 59 MnSOD 59 isotypes 59 gp# protein [002] 59 nucleolar 59 replicon 59 eotaxin 59 PDZ domain 59 Epidermal Growth Factor Receptor 59 annexin 59 potent inhibition 59 autosomal recessive disorder 59 Htt 59 C. pneumoniae 59 homozygotes 59 c Src 59 abnormal p# 59 HBx 59 Cyclin E 59 FUS1 59 PTEN mutations 59 mediated apoptosis 59 fruitfly Drosophila 59 CETP VV 59 micro RNA 59 lymph node metastasis 59 HLA DR 59 KLF# 59 MTDH 59 anaplastic lymphoma kinase 59 axon guidance 59 morphogen 59 HNSCC 59 proteoglycan 59 Brain derived neurotrophic 59 homodimers 59 SCD1 59 lung epithelium 59 DLC1 59 pancreatic prostate 59 chromatin immunoprecipitation ChIP 59 thymocyte 59 CCL#L# 59 phospholipase 59 synaptogenesis 59 caveolae 59 HER2 HER2 59 GABA receptor 59 ultrastructural 59 COOH terminal 59 JNK1 59 transcriptional silencing 59 HGPIN 59 polypeptide 59 HOTAIR 59 distinct subtypes 59 cutaneous lesions 59 hypothalamic 59 uniparental 59 drug metabolizing enzymes 59 eosinophil count 59 RNase L 59 folate metabolism 59 gastric adenocarcinoma 59 metabolite concentrations 59 nucleotide variations 59 Mycoplasma pneumoniae 59 proximal colon 59 histopathologic 59 M1 muscarinic 59 guanine nucleotide exchange 59 leiomyomas