Related by context. All words. (Click for frequent words.) 79 #q# [001] 75 #q# [002] 75 #q#.# [001] 75 chromosome #q# [002] 74 #p#.# [002] 74 chromosome #q# [001] 73 #p#.# [001] 73 chromosome #p# [001] 71 chromosome #q 71 chromosome #p#.# 71 rs# [003] 70 #q#.# [002] 70 PTPN# 70 SNP rs# [001] 70 chromosome #q#.# [001] 70 #p# [003] 70 rs# [002] 68 susceptibility locus 68 TCF#L# 67 CDH1 67 susceptibility gene 67 microdeletions 66 hypermethylated 66 CDKN2A 66 rs# [004] 66 intronic 66 rs# [001] 66 heterozygosity 66 susceptibility loci 66 MYH9 gene 66 BARD1 66 chromosomal regions 66 ABCB1 65 genetic loci 65 CHEK2 65 TCF#L# gene 65 Chromosome 65 MYH9 65 GSTP1 65 sporadic ALS 64 chromosome #q#.# [002] 64 VNTR 64 missense mutations 64 haplotypes 64 ORMDL3 64 dysbindin 64 somatic mutations 64 gene locus 64 germline mutations 64 chromosome #p# [002] 64 haplotype 64 R#W [002] 64 MSH2 64 ZNF# 63 KIAA# 63 5q 63 LRP5 63 SNP rs# [002] 63 APOE e4 63 single nucleotide polymorphism 63 CNTNAP2 63 SLC#A# [001] 63 apolipoprotein E gene 63 NR#A# 63 lymph node metastases 63 KRAS oncogene 63 CC genotype 63 major histocompatibility complex 63 5 HTTLPR 63 breast cancer subtypes 63 APOL1 63 serine protease 63 functional polymorphism 63 DQB1 * 63 genetic polymorphisms 62 methylation patterns 62 GPC5 62 PIK3CA 62 DNA methylation patterns 62 colorectal carcinoma 62 #S rRNA 62 noncoding 62 karyotype 62 3'UTR 62 EGFR gene 62 PTEN gene 62 proband 62 receptor gene 62 OCA2 62 TERT 62 GSTM1 62 lymph node metastasis 62 mitochondrial DNA mtDNA 62 HLA DRB1 62 LPA gene 62 PALB2 62 apolipoprotein E 62 autism susceptibility genes 62 microdeletion 62 MLH1 62 gastric carcinoma 62 chromosomal aberrations 62 Prox1 62 MLL2 62 apoE4 62 CNVs 61 gene polymorphisms 61 splice junctions 61 KRAS mutations 61 ankyrin repeat 61 WDR# 61 promoter methylation 61 NF1 gene 61 hypermethylation 61 ribosomal DNA 61 MAPK pathway 61 COL#A# 61 entorhinal cortex 61 adenocarcinomas 61 cell adhesion molecule 61 CALHM1 61 intron 61 autosomal 61 genetic variants associated 61 proximal colon 61 TYMS 61 MTHFR 61 GNAQ 61 PICALM 61 chromosome deletion 61 HLA DQ2 61 KIF6 gene 61 FGFR2 61 aneuploidies 61 MECP2 gene 61 polymorphisms 61 BRCA1 BRCA2 61 APOE gene 61 breast cancer genes BRCA1 61 orthologs 61 ribosomal protein 61 mutated K ras 61 mitochondrial gene 61 allelic variants 61 LRRK2 gene 61 situ LCIS 61 CDH# 61 intergenic regions 61 cytokeratin 61 allele frequencies 61 IL#B 61 epigenetic modification 61 SLC#A# [002] 61 Clusterin 61 C#Y 61 BRAF V#E 61 SLC#A# gene [001] 61 genetic polymorphism 61 genomewide 61 SNPs 60 ERBB2 60 GSTT1 60 familial clustering 60 subcortical 60 breast carcinoma 60 quantitative trait loci 60 mRNA expression 60 K ras mutations 60 causal variants 60 Brodmann Area 60 MYBPC3 60 activating mutations 60 CHD7 60 ApoE4 60 IL#R 60 allelic 60 homozygosity 60 cis regulatory 60 ADRB2 60 atypical hyperplasia 60 non coding RNA 60 apolipoprotein E4 60 indel 60 human leukocyte antigen 60 nucleotide sequence 60 gene amplification 60 susceptibility genes 60 MC1R 60 caveolin 60 aggrecan 60 adenoma 60 Li Fraumeni 60 evolutionarily conserved 60 APOC3 60 TOP2A gene 60 SMAD4 60 proto oncogene 60 cyclin E 60 IKZF1 60 segmental duplications 60 p# mutation 60 deleterious mutation 60 APOE4 60 PCa 60 causative mutations 60 surgically resected 60 periventricular 60 INF2 60 CYP#D# gene 60 gene polymorphism 60 IRF6 60 methyltransferase 60 LRP6 60 UGT#B# 60 genetic variant 60 gene variants 60 WNK1 60 basal forebrain 60 IgA deficiency 60 intergenic 60 Her2 gene 60 FGFR2 gene 60 linkage disequilibrium 60 distant metastasis 59 ERK signaling 59 ApoE gene 59 cagA 59 microRNA expression 59 clinicopathologic 59 clinicopathological 59 TMEM#B 59 etiologic 59 chemokine receptor 59 sequence homology 59 number variation CNV 59 cardioembolic stroke 59 Wwox 59 ALK gene 59 urothelial 59 activating mutation 59 CYP#A# [002] 59 subcellular localization 59 p# mutations 59 apolipoprotein E APOE 59 genetic locus 59 FMR1 59 TMPRSS2 ERG fusion 59 cyclin dependent kinase 59 inactivating mutations 59 Genetic variants 59 cytochrome b 59 monogenic 59 dentate gyrus 59 eIF 4E 59 succinate dehydrogenase 59 PITX2 59 MEF2A 59 H#K#me# 59 CpG islands 59 NFKBIA 59 paraganglioma 59 p# biomarker 59 microRNA molecules 59 KLF4 59 morphologic 59 tryptophan hydroxylase 59 palladin 59 node metastases 59 TP# gene 59 microsatellite instability 59 DRB1 * 59 hamartomas 59 inherited mutations 59 MTHFR gene 59 dopamine transporter gene 59 TT genotype 59 PTEN mutations 59 prostate cancer CaP 59 ADPKD 59 Microarray analysis 59 chromosomal 59 HOTAIR 59 variant rs# 59 rs# rs# 59 advanced adenoma 59 matrix metalloproteinase 59 clade B 59 autoantibody 59 lymphovascular invasion 59 NAT2 59 EGFR mutations 59 HLA B# 59 OGG1 59 PNET 59 Dysregulation 59 prognostic significance 59 SHANK3 59 STK# gene 59 DRD2 59 supratentorial 59 nicotinic receptor 59 microbleeds 59 differentially methylated 59 MIF protein 59 UGT#A# * 59 TRAF1 59 microglial 59 HER2 expression 59 TOP2A 59 immunohistochemical 59 hyperhomocysteinemia 59 somatic mutation 59 de novo mutations 59 LDL receptor 59 gastric carcinogenesis 59 CCR5 delta# 59 SCN5A 59 papillary renal cell carcinoma 59 chromosomal rearrangement 59 histologic 59 variant allele 59 NAFLD 59 chromosome 59 subventricular zone 59 ALK mutations 59 susceptibility alleles 59 FGFR3 58 TGFBR1 * 6A 58 synuclein 58 microcephalin 58 NPM1 gene 58 gene loci 58 genomic rearrangement 58 diagnostic biomarker 58 SORL1 58 STAT4 58 histopathologic 58 TIMP 1 58 genomic alterations 58 Chromosomal 58 causative genes 58 RNase L 58 VKORC1 58 monoclonal gammopathy 58 neuroligins 58 gene MECP2 58 colorectal adenomas 58 mucinous 58 transcriptional coactivator 58 demyelinating 58 adipogenic 58 HFE gene 58 CagA 58 monozygotic twins 58 Brain derived neurotrophic 58 subgenual cingulate 58 uPAR 58 catechol O methyltransferase 58 CpG 58 MMP# 58 neoplasm 58 sCJD 58 astrocytomas 58 nodal metastases 58 polymorphism 58 centromeric 58 COMT gene 58 extracellular domains 58 membrane proximal 58 atherothrombosis 58 HG PIN 58 hematological relapse 58 cadherin 58 Arabidopsis genome 58 c KIT 58 tumor suppressor gene 58 immunohistochemical analysis 58 CYP#C# [002] 58 FGFR1 58 PARP inhibition 58 methylenetetrahydrofolate reductase 58 prognostic marker 58 chromosomal deletions 58 Single Nucleotide Polymorphisms SNPs 58 histologic subtype 58 hepatocellular carcinomas 58 ApoE 58 FMR1 gene 58 serine threonine kinase 58 ERalpha 58 APOA5 58 colorectal adenoma 58 CHI#L# 58 ABCB1 gene 58 prostate carcinoma 58 KRAS mutation 58 Lp PLA 2 58 micrometastasis 58 multivariate Cox 58 CYP#B# 58 DNA rearrangements 58 unmethylated 58 HLA DRB1 * 58 Li Fraumeni syndrome 58 penetrance 58 hepatic lipase 58 mRNA transcripts 58 immunohistochemical staining 58 fig. S4 58 prognostic factor 58 ESR1 58 #q# deletion 58 paternally inherited 58 VEGF receptor 58 Sonic Hedgehog 58 TP# mutations 58 carboxyl terminal 58 melatonin receptor 58 Plasmodium vivax 58 exon 58 methylated DNA 58 Alu elements 58 hepatoma 58 paraneoplastic 58 CpG island 58 CYP#E# gene 58 FLT3 58 PON1 58 HGPIN 58 miRNA genes 58 glycogen synthase kinase 58 immunoreactivity 58 loci 58 periaqueductal gray 58 hyperplastic 58 ependymomas 58 upregulates 58 anogenital 58 Immunohistochemical analysis 58 Brugada syndrome 58 GATA4 58 SOX9 58 CFTR cystic fibrosis transmembrane 58 histone modifications 58 ADAM# 58 anterior temporal 58 heterozygotes 58 amino terminal 58 histopathological 58 carotid plaque 58 TIMP 58 carcinoembryonic antigen 58 TRAF1 C5 57 micrometastases 57 fibrillin 1 57 kilobase 57 XLHED 57 LRAT 57 nucleotide sequences 57 colorectal neoplasms 57 nodal metastasis 57 indels 57 inferior frontal 57 Janus kinase 57 calcium calmodulin dependent 57 rRNA 57 receptor tyrosine kinase 57 cisplatin resistant 57 SLITRK1 57 C#T [002] 57 clefting 57 Haplotype 57 perivascular 57 endophenotypes 57 DRD2 gene 57 TET2 57 isotype 57 Recurrence Score 57 hormone receptor negative 57 immunoreactive 57 Estrogen Receptor 57 K ras mutation 57 CIN2 + 57 PCR RFLP 57 kinase domain 57 breast carcinomas 57 arcuate nucleus 57 Haptoglobin 57 apoE 57 KCNQ1 57 phenotypic variation 57 CREBBP 57 aberrant methylation 57 genome rearrangements 57 BRAF V#E mutation 57 catenin 57 liver metastasis 57 sarcomatoid 57 posterior cingulate 57 genetic determinants 57 mtDNA 57 splice variants 57 RASSF1A 57 Smad3 57 CYP#D# 57 mosaicism 57 Histologic 57 IDH1 57 COX2 57 molecular abnormalities 57 TSC1 57 MC1R gene 57 IRAK1 57 5q chromosome 57 pheochromocytomas 57 ADH1B * 57 TP# mutation 57 HMGA1 57 alpha synuclein gene 57 cytogenetic 57 Polymorphisms 57 KCNE2 57 BDNF gene 57 exons 57 HMGA2 57 chromosomal instability 57 mtDNA mutations 57 familial pancreatic cancer 57 MGUS 57 S#A# [002] 57 prefrontal cortical 57 postsynaptic 57 gastric adenocarcinoma 57 lymphangiogenesis 57 radial glia 57 promoter hypermethylation 57 aminotransferase 57 UTRs 57 DLC1 57 gene APOE 57 histologically 57 klotho 57 vimentin 57 TMPRSS2 ERG 57 metachronous 57 Immunohistochemical staining 57 LDLR 57 chromosomal alterations 57 trinucleotide 57 downstream effector 57 E#F# 57 Cowden syndrome 57 nucleolar 57 forkhead 57 extramedullary 57 striatal 57 multivariable analysis 57 single nucleotide polymorphisms 57 mutant allele 57 thyroglobulin 57 clusterin 57 miRNA expression 57 SNCA 57 gene encoding 57 HER2 overexpression 57 FGFs 57 caveolae 57 Upregulation 57 genes differentially expressed 57 epithelial tumors 57 nephronophthisis 57 RNA splicing 57 HER2 neu 57 haematopoietic 57 T2 weighted images 57 Six3 57 Eg5 57 DEAR1 57 basal ganglia 57 FCGR3A 57 PDGFR 57 homeobox gene 57 UGT#A# 57 F FDG PET 57 AMACR 57 IGF2 57 narcolepsy cataplexy 57 TOMM# 57 RRM1 57 ALDH2 57 EphA2 57 maize genome 57 C. pneumoniae 57 substantia nigra 57 ENPP1 57 urothelial carcinoma 57 adiponectin concentrations 57 transmembrane protein 57 CFTR gene 57 ADAMTS# 57 lysine residues 57 metalloprotease 57 Rb#/p# 57 autosomal dominant disorder 56 hypometabolism 56 centrosome 56 PI3K AKT 56 retrotransposon 56 primary visual cortex 56 YKL 56 IL#B gene 56 Hutchinson Gilford progeria 56 transcriptional regulation 56 CHD5 56 T1a 56 β amyloid 56 WT1 56 hypomethylation 56 DNA methyltransferase 56 #q 56 adnexal mass 56 p tau 56 Methylation 56 ortholog 56 PRNP 56 progranulin gene 56 homozygotes 56 familial aggregation 56 G6PD 56 progesterone receptor PR 56 carboxy terminal 56 distant metastases 56 Subgroup analysis 56 molecular subtypes 56 annexin 56 glucose transporter 56 hyperplastic polyps 56 Multivariate analysis 56 phenotypic expression 56 VHL gene 56 BRAF mutations 56 APOE 56 Cyclin D1 56 telomeric 56 PDGFR alpha 56 progressive neurodegenerative disorder 56 beta globin 56 midbrain 56 lymph node involvement 56 orthologous 56 guanine nucleotide exchange 56 Genotype 56 essential thrombocythemia 56 hypercoagulable 56 variant alleles 56 SH#B# 56 Apolipoprotein E 56 DRD4 56 LIS1 56 MC4R gene 56 microRNA miR 56 genotyped 56 lobular carcinoma 56 chromosomal translocations 56 genomic deletions 56 polyglutamine 56 p# MAPK 56 transcriptional repressor 56 endometrioid 56 HNPCC 56 abnormal prion protein 56 substrate specificity 56 FANCD2 56 tumor suppressor protein 56 heterochromatic 56 ductal adenocarcinoma 56 neuroblastoma tumors 56 γ secretase 56 HPV# 56 protein tyrosine phosphatase 56 cTnT 56 neoplasias 56 IDH1 mutation 56 gallstone disease 56 G#D 56 androgen receptor gene 56 cytogenetic abnormalities 56 FTLD 56 transmembrane receptor 56 histone H4 56 CD#b 56 CYP#A# gene 56 medial prefrontal cortex mPFC 56 p# p# 56 IGFBP 56 soluble CD# ligand 56 infarcts 56 myeloproliferative neoplasms 56 histone acetylation 56 dorsolateral prefrontal 56 genes CYP#C# 56 prognostic biomarker 56 Sjögren syndrome 56 HER2 gene 56 SSc 56 homodimers 56 heterozygosity LOH 56 cardiac troponin T 56 MLL gene 56 cTnI 56 neurexin 56 tRNA synthetase 56 isoenzyme 56 HNSCC 56 gene APOE4 56 BRCA1 mutations 56 advanced adenomas 56 meiotic recombination 56 alleles 56 Supplementary Table 56 T#I [002] 56 ccRCC 56 thyroid carcinoma 56 methylated 56 coding genes 56 MeCP2 gene 56 nonalcoholic steatohepatitis 56 IPAH 56 neuritic 56 Cytogenetic 56 beta defensin 56 nasopharyngeal carcinoma 56 extracellular domain 56 hypoperfusion 56 FDG uptake 56 #q#.# deletion syndrome 56 P cadherin 56 PB1 F2 56 MAP#K# 56 alternatively spliced 56 Leydig cells 56 ORFs 56 3' UTR 56 motor neuron degeneration 56 OCA2 gene 56 mutational analysis 56 G allele 56 neuregulin 56 gene rearrangements 56 phosphorylates 56 GISTs 56 V#F mutation 56 genes predisposing 56 metaplasia 56 IgG1 56 paralogs 56 NSCLC tumors 56 cyclin dependent kinase inhibitor 56 MMP9 56 Glioma 56 ectopic expression 56 Polymorphism 56 Karayiorgou 56 CA1 56 prodynorphin 56 parkin gene 56 esophageal squamous cell carcinoma 56 polygenic 56 virulence genes 56 intestinal metaplasia 56 cytosine methylation 56 #F FDG PET 56 Lymphocytic 56 CFH gene 56 prothrombotic 56 colorectal neoplasia 56 proapoptotic 56 SVZ 56 mRNA encoding 56 medial prefrontal 56 phospholipase A2 56 von Hippel Lindau 56 heterozygote 56 cAMP signaling 56 plasma lipid 56 number variations CNVs 56 previously undescribed 56 Hashimoto thyroiditis 56 L#R 56 esophageal carcinoma 56 ventrolateral 56 thyroid peroxidase 56 NKX2 56 thrombospondin 56 obstructive coronary artery 56 APOE genotype 56 atherosclerotic lesions 56 ribosomal RNA rRNA 56 Y chromosomal 56 atherothrombotic disease 56 Genetic variation 56 neuropathologic 56 serous ovarian cancer 56 CYP#E# 56 transthyretin amyloidosis 56 JAK2 mutation 56 Figure 2C 56 circadian genes 56 inhibin B 56 MECP2 56 Cathepsin B 56 NPY gene 55 N Myc 55 IRS1 55 PDGFRA 55 VIPR2 55 B7 H3 55 hepatic steatosis 55 bladder carcinoma 55 myeloproliferative diseases 55 Mutational 55 sulcal 55 Ki# 55 CNTNAP2 gene 55 vitamin D receptor 55 amyloid deposition 55 generalized vitiligo 55 Aß 55 regulated kinase ERK 55 thyrotropin levels 55 DLX5 55 FOXO3a 55 epigenetic regulation 55 JAK2 55 glutamic acid decarboxylase 55 TTR gene 55 parahippocampal gyrus 55 lung adenocarcinoma 55 polyadenylation 55 IL6 55 perilipin 55 maternally inherited 55 causative mutation 55 nonhereditary 55 distinct subtypes 55 methylation 55 BRAF protein 55 aneuploidy 55 mitogen activated protein kinase 55 At#g# 55 deacetylation 55 T2D 55 prostate carcinogenesis 55 HLA DQ 55 HOX genes 55 TAp# 55 missense mutation 55 BRCA mutation carriers 55 HER2 receptor 55 EAAT2 55 C1q 55 colorectal tumor 55 K ras 55 pT2 55 gastric cardia 55 haplogroups 55 coding exons 55 mammographic density 55 visceral adiposity 55 SCN1A 55 chemoresistant 55 breast cancer metastasis 55 CAG repeats 55 lymphoid 55 ectodermal 55 HbF 55 nonalcoholic steatohepatitis NASH 55 superior temporal gyrus 55 KLF# 55 ependymoma 55 nonischemic 55 TLE3 55 gastrointestinal stromal tumors GISTs 55 genes encoding 55 Wnt signaling pathway 55 Fas ligand 55 peroxisomal 55 Supplemental Figure 55 transgenic mouse model 55 Rap1 55 dinucleotide 55 germline mutation 55 myopathies 55 neoplastic transformation 55 LKB1 55 Raf MEK ERK 55 miR #a [002] 55 CYP #D# 55 NKX#.# 55 centromere 55 nonmetastatic 55 inducible nitric oxide synthase 55 PKD1 55 splenocytes 55 amnestic MCI 55 genomic instability 55 microsatellite markers 55 downregulation 55 antigen binding 55 LMNA 55 papillary RCC 55 nucleoli 55 gene fusions 55 T1DM 55 DNA methylation 55 Notch receptor 55 CYP#C# gene 55 TrkB 55 chromosomal rearrangements 55 Trichophyton rubrum 55 Leukemias 55 JAK2 gene 55 pancreatic adenocarcinoma 55 TMEM 55 miRNAs miR 55 phenotype 55 microarray experiments 55 eotaxin 55 Lymph node 55 ventral pallidum 55 amyloid deposits 55 JAK2 enzyme 55 nicotine receptor 55 missense 55 coding sequences 55 melanocyte 55 renal cell carcinomas 55 HLA B 55 CISH 55 myelofibrosis polycythemia vera 55 repeat allele 55 PTHrP 55 ERCC1 55 occipital 55 Aβ 55 TCF4 55 phylogenetic analyzes 55 protein encoded 55 EZH2 55 #S rDNA 55 amyloid peptide 55 resistin 55 protein p# 55 primary cilium 55 insertions deletions 55 plasma kallikrein 55 alpha synuclein protein 55 florbetaben 55 BMP2 55 atypia 55 estrogen receptor ER 55 tumorigenicity 55 promoter polymorphism 55 transmembrane domain 55 Human Leukocyte Antigen 55 uncharacterized genes 55 MTDH 55 testicular germ cell 55 monocyte chemoattractant protein 55 morphogen 55 predictive biomarker 55 5 hydroxytryptamine 55 mediated inhibition 55 chromosomal mutations 55 lateral orbitofrontal cortex 55 lymphoblastoid cell lines 55 DICER1 gene 55 LRRK2 mutation 55 invasive ductal 55 airway hyperresponsiveness 55 squamous cell lung cancer 55 PIGF 55 AT1R 55 immunostaining 55 dopamine D4 receptor 55 SNP arrays 55 mesotheliomas 55 renal fibrosis 55 Histopathologic 55 pilocytic astrocytomas 55 breast cancer susceptibility genes 55 HBx 55 untranslated regions 55 cholangiocarcinoma 55 karyotypes 55 proline rich 55 transmembrane 55 beta1 integrin 55 A. thaliana