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(Click for frequent words.) 74 SNPs 72 single nucleotide polymorphism 66 SNPs pronounced snips 63 polymorphisms 62 rs# [003] 60 CNVs 60 #q# [001] 60 nucleotide 59 rs# [002] 58 microdeletions 58 mitochondrial gene 58 haplotypes 57 #q# [002] 57 allelic 57 rs# [004] 57 chromosome #q# [001] 57 #p# [001] 57 #p#.# [001] 57 genetic variants 57 rs# [001] 57 chromosome #p# [001] 56 DNA sequences 56 genetic markers 56 chromosome #q#.# [001] 56 indels 55 genome 55 #S rRNA 55 genes CYP#C# 55 genetic variations 55 VKORC1 55 protein coding 55 haplotype 55 #p# [003] 55 PTPN# 55 alleles 55 kilobase 55 microcephalin 55 chromosomal 54 coding sequences 54 human genome 54 SNP rs# [001] 54 variant rs# 54 intergenic 54 CDH1 54 genomes 54 CDKN2A 54 LRRK2 gene 54 insertions deletions 54 ABCB1 54 CYP#C# [002] 54 chromosome #q# [002] 54 intergenic regions 54 quantitative trait loci 53 Arabidopsis genome 53 loci 53 chromosomal regions 53 human genome SNPs 53 MLH1 53 gene expression patterns 53 genetic polymorphisms 53 rs# rs# 53 #p#.# [002] 53 chromosome 53 genomic 53 gene expression 53 linkage disequilibrium 53 autosomal 53 somatic mutations 53 genetic variants associated 53 intronic 53 susceptibility gene 53 GSTP1 53 number variation CNV 53 nucleotides 53 #q#.# [002] 52 segmental duplications 52 susceptibility loci 52 PICALM 52 CYP#D# gene 52 genomewide 52 splice junctions 52 TCF#L# gene 52 exons 52 BARD1 52 KIAA# 52 gene variants 52 miRNA expression 52 sporadic ALS 52 #q#.# [001] 52 C#Y 52 transcriptome 52 insertion deletion 52 kilobases 52 genetic variation 52 methylation patterns 52 Single Nucleotide Polymorphisms SNPs 52 aneuploidies 52 gene locus 52 microarray experiments 52 genes encoding 52 genes 51 VHL gene 51 MTHFR 51 HumanHap# BeadChip 51 breast cancer genes BRCA1 51 yeast genome 51 APOL1 51 non coding RNA 51 heterozygosity 51 genotyped 51 APOE e4 51 gene 51 allele frequencies 51 UGT#A# * 51 array CGH 51 polymorphism 51 mitochondrial DNA mtDNA 51 susceptibility genes 51 encodes protein 51 MSH2 51 chromatin immunoprecipitation ChIP 51 microdeletion 51 noncoding 51 FMR1 51 gene polymorphisms 51 causative mutations 51 microRNA expression 51 genotype 51 COL#A# 51 chromosomal deletions 51 PALB2 51 mutations 51 missense mutations 51 coding genes 51 TMPRSS2 ERG 51 hypermethylated 51 gene expression profiles 51 homozygous 51 number variations CNVs 51 transcriptome sequencing 51 inherited mutations 51 nucleotide sequence 50 variant allele 50 MTHFR gene 50 IL#R 50 amino acid substitutions 50 MYH9 gene 50 PIK3CA 50 uracil 50 germline mutations 50 orthologs 50 mRNA expression 50 MC1R 50 gene encoding 50 indel 50 genetic loci 50 SLC#A# gene [001] 50 autism susceptibility genes 50 TMEM#B 50 cytogenetic 50 homozygosity 50 VNTR 50 ApoE gene 50 missense 50 #q# deletion 50 molecular markers 50 protein isoforms 50 miRNAs 50 Single Nucleotide Polymorphisms 50 SNP arrays 50 EGFR gene 50 biomarkers 50 CYP#C# [001] 50 PALB2 gene 50 CHEK2 50 microarrays 50 micro RNA 50 exon 50 heterozygosity LOH 50 intron 50 primate genomes 50 FMR1 gene 50 HOTAIR 50 Fragile X mental retardation 50 thymine 50 apolipoprotein E gene 50 genomic loci 50 NPY gene 50 comparative genomic hybridization 50 chromosomal rearrangements 50 number variants CNVs 50 chromosome #p#.# 50 methylation 50 genetic determinants 50 UTRs 50 methylenetetrahydrofolate reductase 50 Alu elements 50 functional polymorphism 50 ChIP Seq 49 SLC#A# [001] 49 chromosome #q 49 coding exons 49 miRNA genes 49 Arabidopsis genes 49 heterozygous 49 receptor gene 49 aCGH 49 lung adenocarcinoma 49 CHD7 49 microarray 49 TSC1 49 chromosome #p# [002] 49 comparative genomic hybridization CGH 49 causative mutation 49 CpG island 49 MYH9 49 WDR# 49 biomarker 49 DNA rearrangements 49 histone modifications 49 eukaryotic genomes 49 codons 49 homeobox gene 49 alternatively spliced 49 LPA gene 49 3' UTR 49 Single Nucleotide Polymorphism 49 SNP rs# [002] 49 microRNAs miRNAs 49 mutational analysis 49 genotyping 49 genetic 49 dopamine transporter gene 49 karyotype 49 paternally inherited 49 SNP Array #.# 49 matrix metalloproteinase 49 amino acid 49 NF1 gene 49 cardiac channelopathies 49 mRNA transcripts 49 tumor suppressor gene 49 platypus genome 49 KCNQ1 49 genomic rearrangements 49 K ras mutations 49 MLL2 49 MSH6 49 human leukocyte antigens 49 mammalian genomes 49 mtDNA 49 frontotemporal dementia 49 NF1 49 gene deletions 49 FOXP2 49 FGFR3 48 susceptibility locus 48 multigene 48 CC genotype 48 protein coding RNAs 48 deCODE AF TM 48 APOE gene 48 phenotype 48 microsatellite markers 48 monogenic 48 alternative splicing 48 human leukocyte antigen 48 chimpanzee genomes 48 IL#B 48 causal variants 48 allele 48 chromatin structure 48 BRCA1 BRCA2 48 gene mutations 48 mutated genes 48 nucleotide sequences 48 genetic variant 48 cytosine 48 apolipoprotein E4 48 differentially expressed genes 48 epigenomes 48 FGFR2 48 International HapMap Project 48 exome 48 Haptoglobin 48 miR #b [002] 48 CFTR cystic fibrosis transmembrane 48 ChIP seq 48 HLA DR4 immune 48 CFTR gene 48 Apolipoprotein E 48 valine 48 positional cloning 48 imprinted genes 48 androgen receptor gene 48 DNA methylation 48 nondiabetic 48 chromosomal aberrations 48 mammalian genome 48 gene fusions 48 ORMDL3 48 microarray analysis 48 noncoding RNAs 48 uncharacterized genes 48 GPC5 48 UGT#B# 48 ependymomas 48 TCF#L# 48 transcriptional regulation 48 neuroligins 48 pseudogenes 48 RNA sequences 48 IKZF1 48 KIF6 gene 48 microRNA molecules 48 gene sequences 48 bisulfite sequencing 48 genetic mutations 48 PITX2 48 stranded nucleic acids 48 PRNP 48 Haplotype 48 gene expression assays 48 Caenorhabditis elegans 48 chromosomal abnormalities 48 gene variant 48 apolipoprotein E APOE 48 chromatin immunoprecipitation 48 generalized vitiligo 48 whole genome genotyping 48 DQB1 * 48 Cytogenetic 48 TYMS 47 exomes 47 histone H4 47 GNAQ 47 5 hydroxymethylcytosine 47 tumor suppressor genes 47 narcolepsy cataplexy 47 nucleotide variations 47 5 HTTLPR 47 TMPRSS2 ERG fusion 47 CpG islands 47 mitogen activated protein kinase 47 SNP genotyping 47 untranslated regions 47 monozygotic twins 47 telomere length 47 WTCCC 47 HG PIN 47 heritable traits 47 HFE gene 47 major histocompatibility complex 47 HER2 gene 47 Clusterin 47 guanine G 47 rRNA 47 QTLs 47 RRM1 47 vitamin D receptor 47 ribonucleic acid RNA 47 recombination hotspots 47 genomic DNA 47 Sanger sequencing 47 orthologous 47 RNA molecules 47 splice variants 47 genes BRCA1 47 mitochondrial genome 47 phenotypes 47 promoter methylation 47 Transcription factors 47 CDH# 47 Wwox 47 PCa 47 Bardet Biedl syndrome 47 familial ALS 47 SMAD4 47 breast cancer susceptibility genes 47 genotypes 47 LRP5 47 CNTNAP2 47 telomeric 47 myelofibrosis polycythemia vera 47 situ hybridization FISH 47 MLL gene 47 MDM2 47 CYP#D# 47 PON1 47 regulator CFTR gene 47 TP# gene 47 dbSNP 47 glycoproteins 47 conserved sequences 47 homologs 47 c KIT 47 haplotype map 47 DRD2 gene 47 molecular biomarker 47 CpG 47 BRAF V#E 47 perilipin 47 chromosomal anomalies 47 K#N 47 breast carcinomas 47 chromosomes 47 phenotypic variation 47 BDNF gene 47 proteins 47 adenine 47 V#F mutation 47 de novo mutations 47 chromosome #q#.# [002] 47 MIF protein 47 TERT 47 IRF6 gene 47 IGF2 47 heterozygotes 47 archaeal 47 Decoding genome 47 #S rDNA 47 clusterin 47 HMGA2 47 nucleic acid sequence 47 DRD2 47 virulence genes 47 somatic mutation 47 guanine 47 epigenetic 47 subcellular localization 47 methylated DNA 47 HNPCC 47 ADAM# 47 HLA DRB1 47 thymine T 47 phenotypic 47 breast cancer subtypes 47 paralogs 46 ZNF# 46 genetic polymorphism 46 massively parallel sequencing 46 lysine residues 46 PTEN gene 46 Venter genome 46 Chromosome 46 essential thrombocythemia 46 hypermethylation 46 tumor suppressor protein 46 pyrosequencing 46 oligonucleotide probes 46 M. genitalium 46 BRCA2 46 A. thaliana 46 aldehyde dehydrogenase 46 Whole Genome 46 non coding RNAs 46 serine threonine kinase 46 epigenetic markers 46 adenoma 46 vimentin 46 AAT deficiency 46 molecular biomarkers 46 sequence homology 46 STAT4 46 gene amplification 46 alpha synuclein gene 46 cell adhesion molecule 46 HLA DRB1 SE 46 immunohistochemical 46 genomic variants 46 maize genome 46 pathogenic mutations 46 ribosomal RNA rRNA 46 NFKBIA 46 qRT PCR 46 metabolomic 46 KRAS mutation 46 fibrillin 1 46 #S rRNA gene 46 WAGR syndrome 46 microRNA 46 Genetic variants 46 HLA DR2 46 ChIP chip 46 KRAS oncogene 46 ADPKD 46 Mutational 46 recessive mutations 46 tyrosine kinases 46 P. patens 46 SMN1 46 CALHM1 46 APOA5 46 tRNA synthetase 46 lincRNAs 46 mosaicism 46 subfamily 46 subfamilies 46 COMT 46 PDE#A 46 missense mutation 46 genetic makeup 46 protein biomarkers 46 gene expression microarrays 46 voxel 46 maternally inherited 46 macaque genome 46 voxels 46 methyltransferase 46 KRAS mutations 46 ZFN TM 46 BAC clones 46 TCF4 46 c myc 46 lipoprotein associated phospholipase 46 Lewy bodies 46 reverse vaccinology 46 dopamine receptor gene 46 3'UTR 46 RNA transcripts 46 clinicopathological 46 catechol O methyltransferase 46 isoforms 46 parkin gene 46 megabases 46 linkage disequilibrium LD 46 CFH gene 46 polynucleotide 46 differential gene expression 46 codon 46 FASPS 46 Human SNP Array 46 UGT#A# 46 molecular subtypes 46 glutamic acid decarboxylase 46 neurexin 46 microRNAs 46 RNA splicing 46 differentially expressed proteins 46 colorectal carcinoma 46 autosomal dominant 46 NSCLC tumors 46 OCA2 46 genomic variation 46 TOMM# 46 carboxyl terminal 46 SCN5A 46 ribosomal DNA 46 quantitative PCR 46 SPINK1 46 ALK mutations 46 V#E 46 succinate dehydrogenase 46 C#T [002] 46 bacterial genomes 46 evolutionary conserved 46 deuterostomes 46 MECP2 gene 46 CYP#A# gene 46 APOE ε4 46 organism genome 46 phenotypic differences 46 BeadChips 46 frameshift mutation 46 SNCA 46 methylated 46 genome rearrangements 46 DNA methylation patterns 46 small RNAs encoded 46 medulloblastomas 46 LRAT 46 forkhead 46 chromosomal translocations 46 H#K#me# 46 cadherin 46 immunoblotting 46 KRAS gene 46 c Myb 46 nucleotide bases 46 BRCA1 46 S. pombe 46 chimp genomes 46 SORL1 45 genetic locus 45 APOC3 45 MECP2 45 tyrosine kinase receptor 45 genotypic 45 DARPP 45 MC1R gene 45 progressive neurodegenerative disorder 45 gene APOE 45 NR#A# 45 ENPP1 45 COMT gene 45 homologues 45 mutation 45 transcriptomes 45 activating mutations 45 noncoding DNA 45 VeraCode 45 ADRB2 45 K ras 45 IDH1 45 microbial genomes 45 SETDB1 45 euchromatin 45 primary biliary cirrhosis 45 Microarrays 45 transposable elements 45 yeast Saccharomyces cerevisiae 45 muscular dystrophies 45 PARP inhibition 45 ribonucleic acids 45 ORFs 45 LQTS 45 circadian genes 45 multiplex ligation dependent 45 HLA loci 45 FTLD 45 FLT3 45 synuclein 45 biochemical markers 45 TOP2A 45 metabolites 45 GSTM1 45 kinases 45 Meckel Gruber 45 TRAF1 C5 45 TP# mutation 45 segmental duplication 45 epigenetic modification 45 colorectal adenomas 45 mRNA molecules 45 cDNAs 45 DNA methyltransferases 45 MSMB 45 receptor subunits 45 amino terminal 45 miRNA molecules 45 Mycoplasma genitalium 45 regulate gene expression 45 ortholog 45 deCODE BreastCancer TM 45 aggrecan 45 protein kinases 45 gene duplications 45 MC4R gene 45 phylogenetic analyzes 45 karyotyping 45 SLC#A# [002] 45 CGG repeats 45 epigenetic alterations 45 transmembrane proteins 45 atypical hyperplasia 45 situ hybridization 45 CYP# [002] 45 cDNA microarray 45 cysteines 45 rRNA genes 45 transfected 45 miRview ™ squamous 45 chromatin 45 dopamine D4 receptor 45 viral genome 45 Single Nucleotide Polymorphism SNP 45 ubiquitinated 45 lung adenocarcinomas 45 gene loci 45 transcription factors 45 reaction RT PCR 45 operons 45 exon intron 45 contigs 45 human microbiome 45 rDNA 45 BRCA mutations 45 SMN2 45 #S ribosomal RNA 45 STK# gene 45 miRNA profiling 45 IRS1 45 genotyping arrays 45 DICER1 gene 45 aberrant methylation 45 ChIP 45 cardiac troponin T 45 serous ovarian cancer 45 immunofluorescence 45 CYP#A# CYP#D# 45 sequenced genomes 45 MicroRNA 45 IDH1 gene 45 aneuploidy 45 SLITRK1 45 FGFR1 45 SOD1 gene 45 microsatellite instability 45 mRNAs 45 multigenic 45 familial clustering 45 HLA DRB1 * 45 gene mutation 45 F#del mutation 45 Chromosomes 45 LIS1 45 prion protein gene 45 neurofibromatosis type 45 proband 45 neoplastic 45 MiRNAs 45 ERCC1 45 evolutionarily conserved 45 protein conformation 45 ALK gene 45 gene variation 45 ssDNA 45 chromosome aberrations 45 NF2 45 BRCA1 gene 45 unmethylated 45 5q 45 enterotypes 45 palladin 45 assay detects 45 epithelial tumors 45 T2D 45 inactivating mutations 45 drug metabolizing enzymes 45 lipoprotein 45 small RNAs 45 NFkB 45 molecular abnormalities 45 HPV# 45 genomewide association studies 45 microarray datasets 45 gene rearrangements 45 chromosomal alterations 45 IKAROS alterations 45 H#K# [002] 45 FXTAS 45 CCR5 delta# 45 Li Fraumeni syndrome 45 Yamanaka recipe 45 APOE4 45 p# p# 45 genomic deletions 45 epigenome 45 PCR RFLP 45 oligonucleotide ligation 45 protein 45 white matter hyperintensities 45 glycan 45 antisense oligonucleotides 45 genes predisposing 45 HAR1 44 shRNAs 44 hierarchical clustering 44 Transcriptome 44 HapMap 44 cytokeratin 44 amplicon 44 mutated gene 44 Cathepsin B 44 defensin 44 cDNA 44 DLX5 44 avidin 44 proto oncogene 44 comparative genomics 44 JAK2 enzyme 44 Phenotype 44 clefting 44 HMMR 44 CagA 44 differentially expressed 44 BMP2 44 SOD1 44 myostatin gene 44 malignant nodules 44 cnidarians 44 Histone 44 WT1 44 differentially regulated 44 cis regulatory 44 radial glia 44 TTR gene 44 MAPK pathway 44 NAT2 44 ABCB1 gene 44 causative genes 44 HLA genes 44 dopamine transporter 44 abnormal p# 44 activating mutation 44 Chromosomal 44 amino acid substitution 44 genomewide association study 44 dimers 44 eukaryotic 44 GABRA2 44 spontaneous mutations 44 ARID1A 44 heterochromatin 44 CETP VV 44 CREBBP 44 genetic abnormalities 44 transgenic mouse models 44 synthetases 44 R#W [002] 44 amplicons 44 CYP#E# 44 epigenomics 44 prodynorphin 44 synthases 44 chimp genome 44 TOP2A gene 44 cM 44 variant alleles 44 heterozygote 44 allelic variants 44 RNA seq 44 Wnt#b 44 adenocarcinomas 44 pilocytic astrocytomas 44 immunocytochemistry 44 ERBB2 44 encode proteins 44 TT genotype 44 dysbindin 44 HAAH 44 luminal cells 44 heritable 44 GSTT1 44 cyclin E 44 spontaneous mutation 44 immunohistochemical staining 44 Autism Genome Project 44 salivary proteins 44 PCA3 gene 44 NAFLD 44 amino acid sequence 44 DNA methyltransferase 44 amino acid residue 44 situ hybridisation 44 fraternal twin pairs 44 kaempferol 44 Alleles 44 tests miRview TM 44 multiprotein complex 44 LMNA gene 44 p# gene 44 mammalian organisms 44 CFTR gene mutations 44 Cryptococcus 44 array comparative genomic 44 hamartomas 44 BRCA2 gene 44 meiotic recombination 44 Arabidopsis thaliana 44 Prevotella 44 fruitfly Drosophila 44 CYP#B# 44 mutated K ras 44 causative gene 44 Sjögren syndrome 44 Fragile X gene 44 centrosome 44 TMEM 44 MRSA isolates 44 RNAs 44 kDa protein 44 genomic sequences 44 chemokine receptor 44 catenin 44 von Hippel Lindau 44 apolipoprotein E 44 EGFR mutations 44 cognitively normal 44 myeloproliferative neoplasms 44 phosphoprotein 44 OGG1 44 pyrimidine 44 APOE e4 gene 44 tetramer 44 BMAL1 44 nucleotide substitutions 44 hexamer 44 Brd4 44 promoter hypermethylation 44 ultraconserved elements 44 MicroRNAs 44 inflammatory markers 44 haplotyping 44 serine protease 44 genetic biomarkers 44 Typhi 44 autosomal dominant disorder 44 histone modification 44 cytochrome P#s 44 substrate specificity 44 TP# mutations 44 syngeneic 44 HLA DQ2 44 poor metabolizers 44 superfamily 44 kinase domain 44 gene polymorphism 44 subtype 44 ß lactamase 44 polymorphic 44 endophenotypes 44 genes differentially expressed 44 Genetic variations 44 marbled lungfish 44 penetrance 44 subtypes 44 TPMT 44 HER2 expression 44 transcriptomic 44 colorectal cancer CRC 44 operon 44 2 diabetes T2D 44 p# biomarker 44 periodontal pathogens 44 Jhdm2a 44 BRIP1 44 ataxias 44 oligonucleotide arrays 44 G#D 44 circulating endothelial cells 44 TaqMan 44 heterochromatic 44 BRCA1 mutation carriers 44 cyclin dependent kinase 44 TLE3 44 COX2 44 FLT3 ITD 44 ApoE 44 X chromosome 44 clade B 44 LRRK2 mutation 44 transgenic mice expressing 44 studies GWAS 44 beta globin gene 44 IGFBP2 44 hypomethylation 44 alpha synuclein protein 44 FUS1 44 immunodominant 44 BRCA1 mutations 44 constitutively expressed 44 MTHFD1L gene 44 transgenic mice 44 BRAF mutations 44 HMGA1 44 bile acid metabolism 44 centromeric 44 homolog 44 Drosha 44 RASSF1A 44 IGFBP 44 HER2 receptor 44 WNK1 43 E#F# 43 serum BDNF 43 tiny roundworm 43 MetS 43 Rad# 43 microsatellite loci 43 ncRNA 43 bacterial genome 43 PTEN mutations 43 genetic syndromes 43 FTO gene 43 cystic fibrosis transmembrane conductance 43 retrotransposons 43 proteomes 43 IRAK1 43 ALCLS 43 BeadChip 43 proline 43 KRAS BRAF 43 Resequencing 43 miRNA 43 multiplex PCR 43 microRNA miRNA 43 advanced adenomas 43 huntingtin 43 hepatocellular carcinomas 43 microarray gene expression 43 amphioxus 43 inbred strains 43 Polymorphisms 43 mRNA sequences 43 IDH1 mutation 43 Infinium assay 43 5 methylcytosine 43 haematopoietic