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(Click for frequent words.) 74 alleles 74 haplotypes 70 allele 70 polymorphisms 69 chromosome #q# [001] 69 #q# [001] 69 rs# [003] 68 SNPs 68 genetic variant 68 loci 68 single nucleotide polymorphism 67 linkage disequilibrium 67 polymorphism 67 genotype 67 rs# [004] 66 heterozygous 66 mutation 66 rs# [002] 66 chromosome #q# [002] 65 #q# [002] 65 phenotype 65 genotypes 65 subtype 65 orthologs 65 mtDNA 65 haplogroups 65 chromosome #p# [001] 64 gene variants 64 homozygosity 64 intron 64 CNVs 64 gene 64 #p# [001] 64 SNP rs# [001] 63 genetic variants 63 C#Y 63 genotyped 63 mutations 63 chromosome 63 nucleotide sequence 63 PTPN# 63 germline mutations 63 chromosome #q 63 Haplotype 63 haplogroup 63 microsatellite markers 63 genetic variation 62 mutated gene 62 VNTR 62 gene variant 62 autosomal 62 chromosomal regions 62 allele frequencies 62 GSTP1 62 heterozygosity 62 PALB2 61 genomewide 61 proband 61 gene mutations 61 clades 61 gene encoding 61 mutant allele 61 MYH9 gene 61 ZNF# 61 microdeletions 61 IL#B 61 intergenic 61 heterozygotes 61 missense mutations 60 allelic 60 DRD2 60 mitochondrial genome 60 GSTM1 60 gene mutation 60 susceptibility gene 60 apolipoprotein E gene 60 gene locus 60 BARD1 60 homozygote 60 allelic variants 60 HLA B# 60 APOE e4 60 MLH1 60 #S rRNA 60 MTHFR 60 #q#.# [001] 60 G allele 60 kilobase 60 rs# [001] 60 nucleotide 60 ABCB1 60 homologs 60 penetrance 60 5 HTTLPR 59 quantitative trait loci 59 genotypic 59 chromosomal 59 MTHFR gene 59 #p#.# [001] 59 genes encoding 59 epitope 59 homozygotes 59 major histocompatibility complex 59 exon 59 #q#.# [002] 59 homozygous 59 LPA gene 59 HLA DRB1 59 susceptibility genes 59 receptor gene 59 CDKN2A 59 Alu elements 59 genes 59 genome 59 KIAA# 59 epistasis 59 MECP2 gene 59 chromosome #q#.# [001] 59 SNP rs# [002] 59 chromosome #q#.# [002] 59 APOC3 59 genetic markers 59 coding sequences 59 clusterin 59 mitochondrial gene 59 karyotype 59 promoter methylation 59 intronic 58 genetic polymorphisms 58 KIF6 gene 58 indel 58 subtypes 58 variant allele 58 sporadic ALS 58 #p# [003] 58 ERBB2 58 CAG repeats 58 VKORC1 58 IgA deficiency 58 ORFs 58 mitochondrial DNA mtDNA 58 apoE4 58 MSH2 58 TCF#L# gene 58 alternatively spliced 58 mRNA transcripts 58 CHEK2 58 phenotypes 58 rRNA 58 mutant gene 58 transcriptome 58 amino acid substitutions 58 #p#.# [002] 58 methylated DNA 58 miRNAs 58 EGFR gene 58 APOE gene 58 ESR1 58 amino acid substitution 58 indels 58 NF1 gene 57 missense mutation 57 COL#A# 57 CNTNAP2 57 At#g# 57 genetic loci 57 DRD2 gene 57 FGFR2 57 paternally inherited 57 tumor suppressor gene 57 cDNA 57 STAT4 57 subfamily 57 noncoding 57 cytochrome b 57 mRNA expression 57 uPAR 57 Haplogroup 57 breast cancer genes BRCA1 57 APOL1 57 autosomal dominant 57 centromere 57 ribosomal protein 57 genes predisposing 57 deleterious mutation 57 dysbindin 57 QTLs 57 genetic variations 57 BDNF gene 57 cM 57 LRRK2 gene 57 hypermethylation 57 amino acid residues 57 OPRM1 gene 57 PICALM 57 allele frequency 57 genomes 57 variant alleles 57 phylogenetic analysis 57 A. thaliana 57 causal variants 57 protein fragment 57 DNA sequences 57 TCF#L# 57 gene polymorphisms 57 phenotypic variation 56 Phylogenetic analysis 56 PCa 56 operon 56 paralogs 56 maternally inherited 56 isoform 56 SLC#A# [001] 56 human leukocyte antigen 56 SLC#A# [002] 56 gene expression patterns 56 centromeres 56 dopamine transporter gene 56 monogenic 56 TP# gene 56 MC1R gene 56 subfamilies 56 synuclein 56 codons 56 chromosome #p#.# 56 exons 56 CC genotype 56 microdeletion 56 NNRTI resistance 56 genetic variants associated 56 Multivariate analysis 56 CYP#D# gene 56 methylation 56 alpha synuclein gene 56 histone modifications 56 JAK2 mutation 56 leucine zipper 56 segmental duplications 56 miRNA expression 56 functional polymorphism 56 ApoE4 56 substrate specificity 56 DRB1 * 56 RUNX3 56 phylogenetic analyzes 56 genomic DNA 56 amino acid sequence 56 somatic mutations 56 ribosomal DNA 56 heterozygote 56 virulence genes 56 CYP#E# gene 56 genetic mutation 56 X chromosome 56 ApoE gene 56 IKZF1 56 LIS1 56 dinucleotide 56 neutralizing antibody 56 NPY gene 56 familial pancreatic cancer 56 variant rs# 56 APOE4 56 methylation patterns 56 gene sequences 56 KLF4 56 rDNA 56 hypermethylated 56 multivariate Cox 56 PON1 56 autosomal recessive 56 pseudogenes 56 gene polymorphism 56 isoforms 56 syngeneic 56 C. neoformans 56 valine 56 HLA B 56 subcellular localization 55 constitutively active 55 hnRNP 55 cyclin E 55 APOE allele 55 CDK4 55 HLA DQ2 55 FMR1 gene 55 apolipoprotein E 55 HCMV 55 CDH1 55 MAPK pathway 55 PCR RFLP 55 CCL#L# 55 FMR1 55 familial ALS 55 TT genotype 55 apoE 55 ADRB2 55 autoantibody 55 BRCA2 mutation 55 CNTNAP2 gene 55 RNA sequences 55 UGT#A# * 55 microcephalin 55 orthologous 55 gene expression 55 CpG 55 mutant alleles 55 H#K# [002] 55 germline mutation 55 phenotypically 55 K ras mutations 55 Chromosome 55 HNPCC 55 S. cerevisiae 55 genetic polymorphism 55 heritable 55 nucleotide sequences 55 HFE gene 55 multigenic 55 activating mutation 55 sCJD 55 breast carcinomas 55 miRNA genes 55 colorectal neoplasia 55 viral genome 55 ALK mutations 55 PTEN gene 55 HLA genes 55 Genotype 55 single nucleotide polymorphisms 55 mRNA 55 DNA methylation 55 clade B 55 AMACR 55 chromosomal rearrangements 55 CFH gene 55 TMEM#B 55 P. falciparum 55 c KIT 55 defensin 55 protein encoded 55 SARS CoV 55 SMAD4 55 codon 55 gene loci 55 microRNA expression 55 D. melanogaster 55 centromeric 55 genetic 55 3'UTR 55 linkage disequilibrium LD 55 amplicons 55 chromosomal aberrations 55 cytokeratin 55 Mitochondrial DNA 55 microRNA miR 55 HPV# 55 inbred strains 55 MnSOD 55 beta globin 55 transgene 55 prognostic factor 55 prognostic marker 55 caveolin 55 autism susceptibility genes 55 EBNA1 55 monozygotic twins 55 micro RNA 55 ALDH2 55 PAX5 55 chromosomal alterations 55 hepatocellular carcinomas 55 MLL2 55 RRM1 55 mRNAs 55 PTEN mutations 55 SHANK3 55 enzymatic activity 55 immunohistochemical staining 55 K#N 54 GAPDH 54 gene expression profiles 54 hereditary hemochromatosis 54 differentially expressed genes 54 mutated genes 54 RASSF1A 54 distinct subtypes 54 germline 54 Supplementary Fig 54 TRAF1 C5 54 T2D 54 E#F# 54 susceptibility loci 54 contigs 54 HLA molecules 54 monophyletic 54 gene amplification 54 serotype 54 imprinted genes 54 EGFR mutations 54 telomere lengths 54 DISC1 54 HLA DR 54 genomic deletions 54 Homozygous 54 BAC clones 54 TOMM# 54 amino terminal 54 subunit 54 mosaicism 54 CYP#D# 54 bacterial genomes 54 IL#R 54 ortholog 54 mtDNA mutations 54 methylated 54 missense 54 protein tyrosine phosphatase 54 PCR amplified 54 BRAF mutation 54 H#K#me# 54 glycoproteins 54 transmembrane receptor 54 MMP# 54 exome 54 chromosomal rearrangement 54 repeat allele 54 TP# mutation 54 genome rearrangements 54 microsatellite instability 54 SLC#A# gene [001] 54 UTRs 54 chromosomal DNA 54 GTPase 54 transfected 54 lipoprotein 54 synteny 54 activating mutations 54 lung adenocarcinoma 54 ApoE 54 myostatin gene 54 GSTT1 54 TERT 54 CagA 54 MYBPC3 54 DLC1 54 unmethylated 54 chromosomes 54 intergenic regions 54 adenoma 54 R#W [002] 54 genetic determinants 54 MLL gene 54 sequence homology 54 CYP#C# [002] 54 CYP# [002] 54 CYP#C# [001] 54 CFTR gene 54 somatic mutation 54 cDNA libraries 54 homolog 54 VHL gene 54 globin 54 overexpression 54 phosphorylated 54 proto oncogene 54 epigenetic modification 54 HTLV 54 HMGA2 54 frameshift mutation 54 DNMT1 54 TGFBR1 * 6A 54 SMN2 gene 54 CEACAM1 54 YKL 54 heterodimers 54 PRNP 54 evolutionarily conserved 54 COMT gene 54 APOE ε4 54 MetS 54 homology 54 Foxp3 54 MIF protein 54 PKD1 54 logistic regression analysis 54 retrotransposon 54 p# mutation 54 splice junctions 53 methylenetetrahydrofolate reductase 53 perilipin 53 catechol O methyltransferase 53 yeast genome 53 cystatin C 53 mitochondrial genomes 53 coding genes 53 genetic mutations 53 susceptibility locus 53 non coding RNA 53 amplicon 53 HLA DRB1 * 53 miRNAs miR 53 conserved sequences 53 hepatoma 53 vimentin 53 univariate 53 fusion protein 53 ribosomal proteins 53 unmutated 53 UGT#A# 53 HLA DRB1 SE 53 tRNA synthetase 53 probands 53 coexpression 53 heritability 53 splice variants 53 PrP 53 serotonin transporter 53 CpG islands 53 transgene expression 53 centrosome 53 globin genes 53 translocations 53 p# mutations 53 C#BL/#J 53 causative genes 53 homologous genes 53 nucleotide substitutions 53 TMPRSS2 ERG fusion 53 PITX2 53 telomere length 53 DQB1 * 53 fig. S1 53 immunohistochemical 53 ankyrin repeat 53 quantitative RT PCR 53 dopamine receptor 53 cagA 53 Genetic variation 53 CHD7 53 kilobases 53 genomic sequences 53 chromosome #p# [002] 53 amino acid sequences 53 endogenous retroviruses 53 K#R [002] 53 cytosolic 53 MYH9 53 multivariable analysis 53 BRAF V#E 53 nucleotide substitution 53 MDM2 53 endogenous retrovirus 53 WT1 53 Saccharomyces cerevisiae 53 #S rRNA gene 53 Rap1 53 dopamine receptor gene 53 exomes 53 genes CYP#C# 53 hierarchical clustering 53 Li Fraumeni syndrome 53 chemokine receptor 53 Plasmodium falciparum 53 rs# rs# 53 NAT2 53 C#T [002] 53 Genotypes 53 allelic variation 53 karyotypes 53 APOE 53 Apolipoprotein E 53 transcriptional repressor 53 BMAL1 53 sequenced genomes 53 immunoreactivity 53 methyltransferase 53 isoleucine 53 HLA DQ 53 activin 53 ADPKD 53 D#N 53 apolipoproteins 53 N Myc 53 histone modification 53 PB1 F2 53 glycosylated 53 breast cancer subtypes 53 airway hyperresponsiveness 53 COMT 53 FTLD 53 causative mutations 53 mutated K ras 53 homologues 53 trypanosome 53 susceptibility alleles 53 FLT3 53 PIK3CA 53 histone 53 BRCA1 gene 53 Cyclin D1 53 prostate cancer CaP 53 BRCA2 53 clade 53 E3 ubiquitin ligase 53 IGF2 53 APOE4 gene 53 fig. S2 53 phylogenetic 53 cyclin 53 mutational 53 KRAS mutations 53 archaeal 53 hypervariable 53 cytoplasmic tail 53 subpopulations 53 transmembrane protein 53 tumor suppressor protein 53 qRT PCR 53 matrix metalloproteinase 53 genomic sequence 53 lymph node metastasis 53 MAOA 53 Arabidopsis genome 53 CYP#B# 53 coding exons 53 transposable elements 53 deacetylation 53 autoantibodies 53 prion protein gene 53 mitochondrial 53 gene APOE 53 Wwox 53 microRNA molecules 53 SCN5A 52 catenin 52 glycosyltransferase 52 synthase 52 LRAT 52 Plasmodium vivax 52 protein isoforms 52 array CGH 52 lymphoblastoid cell lines 52 thymine 52 phylogenetically 52 homologous 52 E cadherin 52 proteolytic cleavage 52 IGF1 52 subpopulation 52 short hairpin RNA 52 transcriptional profiles 52 lysine residues 52 MAOA gene 52 DLX5 52 viral RNA 52 colorectal carcinoma 52 GenBank accession 52 gene variation 52 nucleotide variations 52 lineages 52 ε4 52 biomarker 52 transgenic mouse model 52 cytosine 52 Clusterin 52 LRP5 52 miR #a [001] 52 nucleolar 52 membrane proximal 52 maize genome 52 apolipoprotein E4 52 heterodimer 52 palladin 52 G#S mutation 52 segmental duplication 52 kinase domain 52 amyloidogenic 52 acetylation 52 Genotypic 52 SMN1 52 #q# deletion 52 gp# [002] 52 immunoblotting 52 ApoE4 gene 52 organism genome 52 NRTI resistance 52 Supplementary Table 52 Plasmodium 52 autosomes 52 Polymorphism 52 noncoding RNAs 52 adiponectin concentrations 52 TP# mutations 52 leptin receptor 52 lactase persistence 52 isotypes 52 monocyte 52 extracellular domain 52 mammalian genomes 52 Notch1 52 monozygotic 52 spontaneous mutations 52 BRCA1 mutations 52 promoter hypermethylation 52 heterochromatin 52 FTO gene 52 seropositivity 52 distinct lineages 52 TRIM5 52 independent prognostic marker 52 SRY gene 52 homologue 52 Fig. 1C 52 gastric carcinogenesis 52 tumor suppressor genes 52 LRRK2 mutation 52 miR #a [002] 52 esophageal squamous cell carcinoma 52 serologic 52 BRCA2 mutations 52 binding affinity 52 SORL1 52 Argonaute 52 IL#B gene 52 transcriptional activation 52 Polymorphisms 52 BRCA1 52 micro RNAs 52 scavenger receptor 52 genetic locus 52 tumor suppressor 52 tetramers 52 ORMDL3 52 ERK signaling 52 hydroxylase 52 TACI mutations 52 carboxy terminal 52 spontaneous mutation 52 NAFLD 52 RNA binding 52 cohesin 52 hTERT 52 esterase 52 incomplete penetrance 52 C#BL 6 52 aldehyde dehydrogenase 52 genetic sequences 52 encodes protein 52 serovar 52 histologic subtype 52 CCR5 delta# 52 polyadenylation 52 CYP #D# 52 meiotic recombination 52 IRAK1 52 Sanger sequencing 52 subclinical 52 transcriptomes 52 agouti gene 52 FOXP2 52 immunostaining 52 genomic variation 52 GABRA2 52 BRCA2 gene 52 DAT1 52 superfamily 52 hydrolase 52 cytopathic 52 BCR ABL 52 polygenic 52 Activating mutations 52 transcription factor 52 Y chromosomal 52 VEGF receptor 52 demethylase 52 DR4 52 piRNAs 52 dimerization 52 heritable traits 52 5 hydroxymethylcytosine 52 c Myb 52 receptor CD# 52 MC1R 52 polypeptide 52 promoter polymorphism 52 BCL#A 52 virus subtype 52 coronavirus 52 MyoD 52 HER2 receptor 52 serogroup 52 C#Y mutation 52 isotype 52 herpesviruses 52 HDAC 52 T. gondii 52 homodimers 52 transmembrane 52 outbred 52 serine threonine kinase 52 P. reichenowi 52 Immunohistochemical analysis 52 HepG2 cells 51 UGT#B# 51 RFLP 51 upregulated 51 dopamine transporter 51 CYP#E# 51 EGFRvIII 51 X inactivation 51 adenocarcinomas 51 tetramer 51 lentiviruses 51 aberrant methylation 51 constitutively 51 multivariate logistic regression 51 DNA methylation patterns 51 G#S [002] 51 apolipoprotein 51 uncharacterized genes 51 untranslated regions 51 thyrotropin 51 beta globin gene 51 PON1 gene 51 kinases 51 estrogen receptor 51 IGFBP 51 cytidine 51 mitochondrial DNA 51 KLF# 51 CXCL5 51 oncogenic 51 GPx 51 pRb 51 cystatin 51 microglial 51 M. genitalium 51 prion gene 51 beta1 integrin 51 glutathione S transferase 51 seroprevalence 51 nucleic acid sequence 51 prion protein 51 COX2 51 EGFP 51 Epstein Barr virus EBV 51 glycoprotein 51 genotyping 51 non coding RNAs 51 survivin 51 molecular subtypes 51 CHIKV 51 transmembrane domain 51 DRD4 51 cyclin D1 51 histone deacetylases 51 progranulin gene 51 TLR3 51 diploid 51 gene APOE4 51 multivariate analyzes 51 genomic 51 genetic lineages 51 downregulation 51 ALK gene 51 Anopheles gambiae 51 GPC5 51 ADAM# 51 univariate analysis 51 retrovirus 51 IgG antibody 51 trimer 51 ERCC1 51 cadherin 51 GSTM1 gene 51 site directed mutagenesis 51 operons 51 PCR assay 51 transactivation 51 recessive mutation 51 syntaxin 51 gene MECP2 51 #S rDNA 51 coinfection 51 HLA alleles 51 histone H4 51 TAp# 51 postsynaptic 51 ApoB 51 H#D 51 SNPs pronounced snips 51 haplotype map 51 vitamin D receptor 51 osteopontin 51 number variations CNVs 51 neuroblastoma cells 51 lipoprotein associated phospholipase 51 miR #b [002] 51 transcriptome sequencing 51 bcl 2 51 mammary stem cells 51 serous ovarian cancer 51 inhibin 51 S. Typhimurium 51 histone protein 51 eotaxin 51 differential gene expression 51 mutant protein 51 cyclin dependent kinase 51 serine protease 51 provirus 51 prion infection 51 serotonin transporter gene 51 CRISPR 51 introns 51 cysteines 51 causative mutation 51 coactivator 51 mammalian genome 51 H#Y 51 KRAS mutation 51 IKK beta 51 number variation CNV 51 MC4R gene 51 transposon 51 guanine 51 mutational analysis 51 PFGE 51 C. trachomatis 51 cis regulatory 51 TSC1 51 Cre recombinase 51 deletion mutant 51 genetic susceptibility 51 PrPSc 51 CGG repeats 51 molecular markers 51 de novo mutations 51 Li Fraumeni 51 OCA2 51 dimers 51 maternal lineage 51 D#G 51 antibody titer 51 haploid 51 BMP2 51 genes BRCA1 51 ChIP seq 51 genotyping arrays 51 cytogenetic 51 CYP#A# [002] 51 PGCs 51 Y chromosome 51 T2DM 51 thymidine 51 Apolipoprotein 51 phenotypic 51 DGGE 51 ADH1B * 51 HMGA1 51 S#A# [002] 51 histone acetylation 51 genetic alterations 51 Single Nucleotide Polymorphism 51 Single Nucleotide Polymorphisms SNPs 51 PTP1B 51 parkin gene 51 RAR beta 51 antigenic 51 HbF 51 eukaryotic 51 genetic alteration 51 ncRNAs 51 WNK1 51 clinicopathological 51 genetic relatedness 51 genetic abnormality 51 MSH6 51 QTL mapping 51 splice variant 51 Mendelian 51 transcriptional regulation 51 IL# [001] 51 bivalent 51 ciliated 51 oxytocin receptor 51 primate genomes 51 tertile 51 parkinsonism 51 EZH2 51 SE alleles 51 superinfection 51 genetic variability 51 ultraconserved elements 51 thyroglobulin 51 micrometastases 51 genetic heterogeneity 51 EGFR mutation