Related by context. All words. (Click for frequent words.) 79 #p# [001] 79 chromosome #q# [001] 77 #q#.# [001] 76 #p#.# [001] 76 #p#.# [002] 76 chromosome #q# [002] 75 #q# [002] 75 rs# [003] 74 chromosome #q 74 #q#.# [002] 74 rs# [004] 73 rs# [002] 73 chromosome #p# [001] 73 chromosome #q#.# [001] 71 #p# [003] 70 rs# [001] 70 PTPN# 70 polymorphisms 70 SNP rs# [001] 70 chromosomal regions 70 CDKN2A 69 missense mutations 69 CDH1 69 chromosome #q#.# [002] 69 susceptibility gene 69 chromosome #p#.# 69 ABCB1 69 haplotype 68 IL#R 68 hypermethylation 68 GSTP1 68 haplotypes 68 intronic 68 functional polymorphism 67 microdeletions 67 5 HTTLPR 67 MLH1 67 dysbindin 67 sporadic ALS 67 chromosome #p# [002] 67 TCF#L# 67 susceptibility locus 67 loci 67 proband 67 germline mutations 67 alleles 66 C#Y 66 DQB1 * 66 gene polymorphisms 66 MECP2 gene 66 apolipoprotein E 66 genetic loci 66 APOL1 66 KIAA# 66 MYH9 gene 66 NR#A# 66 microdeletion 66 MTHFR 66 CNVs 65 TCF#L# gene 65 homozygosity 65 gene polymorphism 65 GSTM1 65 Clusterin 65 FGFR2 65 heterozygosity 65 ankyrin repeat 65 DRD2 65 BRAF V#E 65 single nucleotide polymorphism 65 inherited mutations 65 polymorphism 65 genetic polymorphisms 65 rs# rs# 65 hypermethylated 65 MLL2 65 SNPs 65 orthologs 65 genetic variants associated 65 susceptibility loci 65 CHEK2 65 genetic polymorphism 65 MSH2 65 KIF6 gene 64 cell adhesion molecule 64 linkage disequilibrium 64 ZNF# 64 PRNP 64 caveolin 64 susceptibility genes 64 proto oncogene 64 EGFR gene 64 BARD1 64 autism susceptibility genes 64 genes encoding 64 familial pancreatic cancer 64 neuroligins 64 tryptophan hydroxylase 64 MAPK pathway 64 SNP rs# [002] 64 5q 64 IKZF1 64 miRNA genes 64 APOE e4 64 gene MECP2 64 gene variants 64 TSC1 64 serine protease 64 TMEM#B 64 VNTR 64 heterozygotes 63 microcephalin 63 allele frequencies 63 CNTNAP2 63 intron 63 LRP5 63 K ras mutations 63 allelic variants 63 COL#A# 63 Chromosome 63 astrocytomas 63 clusterin 63 CYP#B# 63 mRNA expression 63 CDH# 63 FMR1 63 APOA5 63 promoter methylation 63 CCR5 delta# 63 JAK2 mutation 63 SMAD4 63 PALB2 63 SLC#A# [002] 63 LIS1 63 UGT#A# * 63 intergenic 63 VIPR2 63 NF1 gene 63 allelic 63 HLA DR 63 GNAQ 63 VEGF receptor 63 GPC5 63 ADPKD 63 indels 63 variant rs# 63 genomic rearrangement 63 H#K#me# 63 methylenetetrahydrofolate reductase 62 LRRK2 gene 62 missense mutation 62 microRNA expression 62 SLITRK1 62 CHD7 62 ORMDL3 62 hepatic lipase 62 LPA gene 62 CC genotype 62 ribosomal protein 62 UGT#B# 62 major histocompatibility complex 62 monozygotic twins 62 chromosomal rearrangements 62 synuclein 62 PICALM 62 #S rRNA 62 Genotypes 62 periventricular 62 gastric carcinogenesis 62 CYP#C# [002] 62 heterozygous 62 Polymorphisms 62 chromosomal aberrations 62 NF1 62 genomic deletions 62 maternally inherited 62 gene locus 62 R#W [002] 62 deacetylation 62 protein encoded 62 autosomal dominant disorder 62 cagA 62 SHANK3 62 orthologous 62 catechol O methyltransferase 62 APOC3 62 E#F# 62 splice junctions 62 MYH9 62 histone acetylation 62 ERBB2 62 methylation patterns 62 HLA DRB1 62 ApoE gene 62 TP# mutations 62 gastric carcinoma 62 SLC#A# [001] 62 causal variants 62 intergenic regions 62 SCN5A 62 CALHM1 61 non coding RNA 61 SNCA 61 DRD2 gene 61 breast carcinomas 61 TTR gene 61 mitogen activated protein kinase 61 tyrosine kinases 61 TYMS 61 oncogenic proteins 61 CpG 61 Upregulation 61 HLA DRB1 * 61 homozygotes 61 fibrillin 1 61 NFKBIA 61 WT1 61 INF2 61 de novo mutations 61 tumor suppressor gene 61 cadherin 61 monogenic 61 IgA deficiency 61 potent inhibition 61 airway hyperresponsiveness 61 SH#B# 61 Janus kinase 61 carcinoembryonic antigen 61 allele 61 CYP# [002] 61 ApoE 61 essential thrombocythemia 61 endophenotypes 61 presenilin 61 L#R 61 genetic variant 61 PDGFR 61 lymph node metastases 61 gene encoding 61 COX2 61 Li Fraumeni syndrome 61 breast cancer genes BRCA1 61 splice variants 61 miRNAs miR 61 syngeneic 61 probands 61 noncoding RNAs 61 quantitative trait loci 61 myeloproliferative neoplasms 61 MDM2 61 ERK signaling 61 apolipoprotein E gene 61 receptor tyrosine kinase 61 HNPCC 61 lymph node metastasis 61 autosomal 61 TRAF1 C5 61 KRAS mutations 61 CagA 61 alpha synuclein gene 61 TERT 61 microglial 61 apolipoprotein E APOE 61 CYP#A# [002] 61 CYP#D# 61 catenin 61 BRCA1 BRCA2 61 somatic mutations 61 LDL receptor 61 lymphoid 61 vimentin 61 apolipoprotein E4 61 adenocarcinomas 61 TOP2A 61 CD#b 61 V#F mutation 61 HPV# 61 FMR1 gene 61 familial ALS 61 homozygous 61 apoE4 61 Dysregulation 61 BDNF gene 61 colorectal carcinoma 61 KLF4 60 OCA2 60 microsatellite instability 60 Genetic variants 60 penetrance 60 S#A# [002] 60 transmembrane protein 60 neurofibromatosis type 60 EGFR mutations 60 autosomal dominant 60 promoter polymorphism 60 bcl 2 60 adenoma 60 human leukocyte antigen 60 STAT4 60 gene loci 60 KCNQ1 60 PTEN gene 60 FLT3 60 KRAS oncogene 60 sCJD 60 variant allele 60 CpG island 60 activating mutations 60 aneuploidies 60 CNTNAP2 gene 60 Wwox 60 PIK3CA 60 genotyped 60 proapoptotic 60 Prox1 60 glutamatergic neurons 60 metalloprotease 60 mosaicism 60 COMT 60 PTEN mutations 60 LRAT 60 homologues 60 methyltransferase 60 JAK2 enzyme 60 cM 60 cyclin dependent kinase 60 c KIT 60 testicular germ cell 60 VKORC1 60 ABCB1 gene 60 G allele 60 apoE 60 sequence homology 60 IL#B 60 haplogroups 60 cytochrome b 60 calcium calmodulin dependent 60 PDGFRA 60 PON1 60 LRP6 60 cyclin E 60 mutations 60 WDR# 60 progressive neurodegenerative disorder 60 CEACAM1 60 variant alleles 60 Leukemias 60 Apolipoprotein E 60 HMGA1 60 MeCP2 gene 60 H#K# [002] 60 YKL 60 QTLs 60 entorhinal cortex 60 matrix metalloproteinase 60 noncoding 60 inducible nitric oxide synthase 60 phosphatidylinositol 3 60 mitochondrial DNA mtDNA 60 transgenic mouse model 60 single nucleotide polymorphisms 60 TGFBR1 * 6A 60 genes predisposing 60 miRNA expression 60 androgen receptor AR 60 Cyclin D1 60 narcolepsy cataplexy 60 chromosome deletion 60 RRM1 60 melatonin receptor 60 GPR# [002] 60 homeobox gene 60 mitochondrial gene 60 phosphorylates 60 lysine residues 60 DRB1 * 60 serine threonine kinase 60 evolutionarily conserved 60 posterior cingulate 60 3'UTR 60 uPAR 60 selective antagonists 60 receptor gene 60 inactivating mutations 60 ADAM# 60 succinate dehydrogenase 60 hypomethylation 59 genetic variants 59 ALK mutations 59 G#S mutation 59 BMPR2 59 APOE 59 p# mutations 59 B7 H3 59 IDH1 59 basal forebrain 59 cytokeratin 59 BMP2 59 breast cancer subtypes 59 Lp PLA 2 59 ataxias 59 paternally inherited 59 #q# deletion 59 ETV1 59 heterozygote 59 autosomal recessive 59 IPAH 59 upregulates 59 nicotinic receptor 59 gene APOE 59 PDE#A 59 HLA DQ2 59 methylation 59 node metastases 59 TMPRSS2 ERG 59 normal karyotype 59 subcellular localization 59 distant metastasis 59 hypoperfusion 59 AMACR 59 phenotype 59 circadian genes 59 LDLR 59 germline mutation 59 genes differentially expressed 59 ALK gene 59 MTHFR gene 59 DNA methylation patterns 59 APOE gene 59 Plasmodium vivax 59 thyrotropin levels 59 colorectal adenomas 59 Fibroblast Growth Factor Receptor 59 breast carcinoma 59 familial aggregation 59 pRb 59 heritable 59 immunoreactive 59 IL8 59 Supplementary Table 59 Chromosomal 59 mutated genes 59 KLF# 59 medulloblastomas 59 HOTAIR 59 ADAMTS# 59 immunoreactivity 59 motor neuron degeneration 59 carboxyl terminal 59 Smad3 59 IDH1 mutation 59 Alu elements 59 NAFLD 59 generalized vitiligo 59 micro RNA 59 NAT2 59 HER2 receptor 59 seropositivity 59 mRNA transcripts 59 advanced adenoma 59 encodes protein 59 myeloproliferative 59 PAX5 59 paralogs 59 A. thaliana 59 JAK2 59 forkhead 59 CDK4 59 adipogenic 59 Rap1 59 MSH6 59 At#g# 59 microsatellite markers 59 clade B 59 chromosomal rearrangement 59 microRNA molecules 59 DNA methyltransferase 59 D#N 59 SOX9 59 VHL gene 59 atypical hyperplasia 59 Leydig cells 59 pheochromocytoma 59 hamartomas 59 CCR9 59 aldehyde dehydrogenase 59 mesotheliomas 59 exon 59 miR #a [001] 59 3' UTR 59 cyclin D1 59 p# mutation 59 AML MDS 59 protein kinases 59 HFE gene 59 promoter hypermethylation 59 microRNA miR 59 MELAS 59 BRCA1 mutations 59 TNFalpha 59 postsynaptic 59 Wnt signaling pathway 59 G6PD 59 situ LCIS 59 monocytic 59 CYP#D# gene 59 Bcl XL 59 methylated DNA 59 mutated BRCA1 59 Li Fraumeni 59 chromosome rearrangements 59 β amyloid 59 G#S [002] 59 DAT1 59 TNFAIP3 59 TET2 59 chemokine receptor 59 MLL gene 59 chromosome 58 Meckel Gruber 58 glutamic acid decarboxylase 58 HBeAg negative 58 dopamine D4 receptor 58 dopamine D2 58 homologs 58 mutant allele 58 catechol O methyltransferase COMT 58 WNK1 58 OPRM1 gene 58 TOP2A gene 58 prefrontal cortical 58 IL 1beta 58 renal fibrosis 58 tyrosine kinase receptor 58 Arabidopsis genome 58 HbF 58 mtDNA 58 indel 58 miRNAs 58 striatal 58 chromosomal deletions 58 phospholipase A2 58 perilipin 58 Immunohistochemical analysis 58 Brain derived neurotrophic 58 dizygotic twins 58 ependymomas 58 resistin 58 protein isoforms 58 somatic mutation 58 dopamine transporter gene 58 alanine aminotransferase 58 TACI 58 extramedullary 58 genome rearrangements 58 causative mutations 58 HLA DRB1 SE 58 spontaneous mutations 58 transcriptional regulation 58 MAP kinase 58 hepatocellular carcinomas 58 Rb gene 58 neurodevelopmental disorder 58 IRF6 58 JAK2 gene 58 hydroxylase 58 COMT gene 58 phenotypic variation 58 mtDNA mutations 58 BRAF mutations 58 regulator CFTR gene 58 histone modifications 58 EAAT2 58 MGUS 58 familial clustering 58 HLA B# 58 supratentorial 58 IDH1 gene 58 pDC 58 BRCA2 mutations 58 FGFR3 58 #q#.# deletion syndrome 58 subgenual cingulate 58 hyperinsulinemia 58 segmental duplications 58 CpG islands 58 immunohistochemical staining 58 distinct subtypes 58 RNase L 58 Raf MEK ERK 58 miR #a [002] 58 cyclin dependent kinase inhibitor 58 OPRM1 58 TNF α 58 karyotypes 58 CFH gene 58 ubiquitinated 58 SPINK1 58 serum leptin 58 mutation 58 splenocytes 58 Histone 58 RUNX3 58 phylogenetic analyzes 58 TIMP 58 FTLD 58 gene mutations 58 paraneoplastic 58 DEAR1 58 upregulated 58 ectopic expression 58 oxytocin receptor 58 eotaxin 58 CYP#A# gene 58 IGFBP 58 KCNE2 58 Fas ligand 58 Rb#/p# 58 nephronophthisis 58 TIMP 1 58 genomewide 58 miRs 58 5q chromosome 58 MTDH 58 metachronous 58 ortholog 58 C#T [002] 58 kDa protein 58 alpha synuclein protein 58 Epidermal Growth Factor Receptor 58 TAp# 58 Sjögren syndrome 58 constitutively active 58 SGPT 58 MDR1 58 etiologic 58 adhesion molecule 58 BRCA1 mutation carriers 58 miR #b [002] 58 lymphangiogenesis 58 IL #R 58 MC1R 58 virulence genes 58 Cathepsin B 58 amyloid deposition 58 glycogen synthase kinase 58 haematopoietic 58 mediated inhibition 58 PKD1 58 APOE4 58 PARP inhibition 58 HER2 expression 58 transmembrane receptor 58 prothrombotic 58 thioredoxin 58 homolog 58 IRAK1 58 IDH2 58 neoplastic 58 histone deacetylases 58 T#M 58 estrogen receptor alpha 58 IL 1ß 58 Polymorphism 58 urothelial 58 rRNA 58 APOE allele 58 dorsolateral prefrontal 58 TMPRSS2 ERG fusion 58 HepG2 cells 58 TT genotype 58 ALDH2 58 substrate specificity 58 TRAIL induced apoptosis 58 ribosomal DNA 58 Trichophyton rubrum 58 cause cardiac channelopathies 58 immunohistochemical 58 HLA loci 58 ErbB3 58 constitutively expressed 58 hyperplastic 58 genotypes 58 surgically resected 58 Alleles 58 parkinsonism 58 transcriptional repressor 58 cytokine interleukin 58 pancreatic prostate 58 transcriptional activation 58 protein tyrosine phosphatase 58 Ki# 58 null mice 58 tRNA synthetase 58 epigenetic modification 58 chromosomal translocations 58 ß catenin 58 SORL1 58 IGF1 58 kaempferol 58 FUS1 58 pathogenic mutations 58 gene variant 58 microbleeds 58 P2X 58 karyotype 58 clefting 57 inactive X chromosome 57 ERK1 57 NOD2 57 EGFR HER2 57 wildtype 57 extracellular domain 57 paraganglioma 57 PB1 F2 57 Cx# [001] 57 PCa 57 neuroblastoma tumors 57 pulvinar 57 TGF β 57 causative genes 57 muscarinic receptors 57 CXCL# 57 EGFR mutant 57 neuropathological 57 neuroblastomas 57 DNMT1 57 renal cell carcinomas 57 FOXP3 57 Wnt beta catenin 57 monozygotic 57 Arrhythmogenic Right Ventricular Cardiomyopathy 57 leptin receptor 57 receptor kinase 57 polygenic 57 serotonin transporter 57 lymphovascular invasion 57 genes BRCA1 57 coding exons 57 ERBB4 57 serotonin receptor 57 SLC#A# gene [002] 57 papillary renal cell carcinoma 57 nucleotide sequence 57 IL #p# 57 differentially expressed genes 57 proline rich 57 ENPP1 57 TrkB 57 Kupffer cells 57 chromosomal anomalies 57 HT 2A 57 meiotic recombination 57 chromosomal 57 immunoblotting 57 CCR2 57 HMGA2 57 activating mutation 57 downregulation 57 Dpp 57 PAR1 57 Hashimoto thyroiditis 57 PNET 57 genomic instability 57 prostate cancer CaP 57 centrosome 57 dentate gyrus 57 pharmacodynamic biomarkers 57 aggrecan 57 tumor suppressor genes 57 ESR1 57 PITX2 57 caveolae 57 IGFBP2 57 ERalpha 57 hypothalamic pituitary 57 SNPs pronounced snips 57 genetic variations 57 LRRK2 mutations 57 CHI#L# 57 mutated K ras 57 amino terminal 57 beta1 integrin 57 E selectin 57 clinicopathologic 57 DISC1 57 colorectal neoplasia 57 nonsense mutations 57 TACI mutations 57 deleterious mutation 57 cystic fibrosis transmembrane conductance 57 HGPIN 57 ER alpha 57 AT1R 57 HLA B 57 isoenzyme 57 pheochromocytomas 57 LRRK2 mutation 57 T2D 57 transactivation 57 primary biliary cirrhosis 57 repeat allele 57 anaplastic lymphoma kinase 57 hepatocellular carcinoma HCC 57 kinase pathway 57 downstream effector 57 subcortical 57 HLA DR4 immune 57 palladin 57 polyadenylation 57 MEF2A 57 proteoglycan 57 nitrotyrosine 57 ERK2 57 Activating mutations 57 hereditary predisposition 57 CREBBP 57 iNOS 57 Six3 57 IKK beta 57 SLC#A# gene [001] 57 metaplasia 57 phenotypes 57 papillary RCC 57 Angiotensin converting enzyme 57 dorsal root ganglia 57 ORFs 57 MMP9 57 BRAF protein 57 globin genes 57 Brodmann Area 57 NFkB 57 glutathione S transferase 57 autosomal recessive disease 57 RASSF1A 57 diabetes dyslipidemia 57 clinicopathological 57 glial 57 Aß 57 homodimers 57 susceptibility alleles 57 heterotaxy 57 glucose transporter 57 monocyte chemoattractant protein 57 GSTT1 57 circadian clock genes 57 Phosphorylation 57 alanine aminotransferase ALT 57 PIGF 57 5 HT1A 57 paragangliomas 57 basal cell nevus syndrome 57 CISH 57 FGFs 57 ERK1 2 57 autoantibodies 57 myeloproliferative diseases 57 CYP #D# 57 advanced adenomas 57 CD8 + 57 proximal colon 57 P cadherin 57 thyrotropin 57 c MYC 57 NKX2 57 regulated kinase ERK 57 prostate carcinoma 57 overexpression 57 elevated ALT 57 BRAF mutation 57 receptor subtype 57 cis regulatory 57 TNFR1 57 dinucleotide 57 MMP# 57 beta amyloid peptides 57 APOE ε4 57 epigenetic silencing 57 neuronal dysfunction 57 aplastic anemia AA 57 myo inositol 57 serum BDNF 57 FGFR1 57 KCNH2 57 eNOS 57 RhoA 57 BRCA2 mutation carriers 57 5 hydroxytryptamine 57 Lyn kinase 57 Cowden syndrome 57 DLC1 57 TRAF1 57 Overexpression 57 enolase 57 gallstone disease 57 ribosomal proteins 57 somatostatin 57 dizygotic 57 genetic locus 57 HER2 HER3 57 AVPR1A 57 lung adenocarcinomas 57 #q 57 serotonin 2A 57 anaplastic lymphoma kinase ALK 57 NKX#.# 57 subclinical atherosclerosis 57 microglial activation 57 histologic subtype 57 Brugada syndrome 57 genomic loci 57 CD# + [001] 57 autosomal dominant inheritance 57 parkin gene 57 hyperhomocysteinemia 57 serotonin transporter gene 57 neoplasm 57 Cytogenetic 57 superior temporal gyrus 57 unmethylated 57 SMN1 57 dorsal root ganglion 57 CYP#E# gene 57 tau protein 57 nondemented 57 TP# gene 57 chromosomal instability 57 MC4R gene 57 chronic eosinophilic leukemia 57 granule cells 57 cerebellar 57 downregulated 57 APOE e4 allele 57 OGG1 57 progranulin gene 57 lymphoblastoid cell lines 57 Foxp3 57 membrane proximal 57 neuropsychiatric diseases 57 Abl 57 annexin 57 HGPS 57 FHIT 57 NKG2D 57 abdominal adiposity 57 non syndromic 56 BCL2 56 hormone receptor negative 56 histone H3 56 BCL#A 56 myeloproliferative disorders 56 idiopathic PAH 56 herpesviruses 56 cytochrome P 56 SSc 56 folate metabolism 56 NPM1 gene 56 MnSOD 56 Bardet Biedl syndrome 56 centromeric 56 operon 56 ultraconserved elements 56 diagnostic biomarker 56 IL 1β 56 cholesteryl ester transfer 56 nonhereditary 56 CDX2 56 isoforms 56 BRAF V#E mutation 56 genotype 56 Karayiorgou 56 CYP#E# 56 tumor suppressor protein 56 gene rearrangements 56 TEAEs 56 ErbB2 positive 56 decarboxylase 56 LMNA 56 CXCL5 56 sphingolipid 56 caveolin 1 56 CD# CD# 56 NPM1 56 HLA DR4 56 tyrosine phosphorylation 56 colonic mucosa 56 fronto temporal dementia 56 oncogenic 56 p# p# 56 airway remodeling 56 aneuploidy 56 HG PIN 56 hereditary hemochromatosis 56 isoenzymes 56 transmembrane 56 T#I [002] 56 pulmonary metastases 56 homodimer 56 Neuregulin 1