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(Click for frequent words.) 74 genetic variations 72 genetic variants 69 SNPs 69 genes 68 genetic makeup 68 biomarkers 67 gene variants 67 genetic 67 genetic variation 66 molecular markers 66 genomes 65 genomewide 64 genetic mutations 64 susceptibility genes 64 genome 64 genomic 63 exomes 63 single nucleotide polymorphism 63 genetic variants associated 63 haplotypes 62 microsatellite markers 62 biomarker 62 gene expression profiles 62 genetic ancestry 62 genetic determinants 62 DNA sequences 62 loci 62 mutated genes 61 genetically 61 genetic polymorphisms 61 mitochondrial DNA 61 gene expression patterns 61 gene mutations 61 CNVs 61 chromosomal regions 60 gene 60 gene sequences 60 polymorphisms 60 genotype 60 genetics 60 methylation patterns 60 mutations 60 genotyped 60 yeast genome 60 genotypes 59 maternal lineage 59 haplotype map 59 linkage disequilibrium 59 primate genomes 59 molecular biomarkers 59 quantitative trait loci 59 autism susceptibility genes 59 genetic abnormalities 59 genetic sequences 59 mtDNA 59 haplotype 59 microdeletions 58 causative genes 58 protein biomarkers 58 mitochondrial DNA mtDNA 58 geneticists 58 genetic traits 58 HLA genes 58 causative gene 58 spontaneous mutations 58 genetic variant 58 genetic loci 58 splice junctions 58 gene mutation 58 phenotypes 58 miRNAs 58 array CGH 58 genetic mutation 57 genotyping 57 gene expression 57 chromosomal abnormalities 57 susceptibility loci 57 LRRK2 gene 57 sporadic ALS 57 genetic variability 57 mammalian genomes 57 alleles 57 exome sequencing 57 causal variants 57 susceptibility gene 57 transcriptomes 57 somatic mutations 57 haplogroups 56 causative mutation 56 enterotypes 56 Single Nucleotide Polymorphisms SNPs 56 mitochondrial genome 56 allele frequencies 56 gene variant 56 genetic alterations 56 genetic predisposition 56 single nucleotide polymorphisms 56 transcriptome 56 mutation 56 differentially expressed proteins 56 genomic sequence 56 genotypic 56 methylation markers 56 genetic susceptibility 56 HapMap 56 DNA methylation patterns 56 sCJD 56 MHC genes 55 imprinted genes 55 genetic underpinnings 55 gene expression profiling 55 #S rRNA 55 genome sequences 55 phylogenetic analysis 55 genes CYP#C# 55 microRNA biomarkers 55 genetic locus 55 RNA sequences 55 aneuploidies 55 human genome 55 molecular subtypes 55 phenotype 55 modifier genes 55 BARD1 55 microarray experiments 55 microRNAs 55 positional cloning 55 MYH9 gene 55 gene locus 55 chimpanzee genomes 55 microRNA 55 VKORC1 55 Genetic testing 55 phenotypic variation 55 microRNA expression 54 genome sequence 54 Venter genome 54 chromosome #q# [001] 54 breast cancer susceptibility genes 54 fungal genomes 54 genotyping arrays 54 sequenced genome 54 mitochondrial DNA sequences 54 prognostic markers 54 #q# [001] 54 chromosomal anomalies 54 genomewide association studies 54 differentially expressed genes 54 MYH9 54 mtDNA mutations 54 hypermethylated 54 multigene 54 mutated gene 54 phylogenetic analyzes 54 genomic biomarkers 54 Hakonarson 54 gene fusions 54 #q# [002] 54 gene predisposing 54 causative mutations 54 genetic biomarkers 54 EGFR mutations 54 MC1R gene 54 malaria parasite genome 54 germline mutations 54 epigenomes 54 micro RNA 54 genetic defects 54 epigenetic markers 54 Neanderthal genes 54 maternally inherited 54 HLA DRB1 54 Arabidopsis genome 54 HLAs 54 phenotypic 54 pathogenic mutations 54 autosomal 53 genomic variation 53 mutant genes 53 orthologs 53 cDNA libraries 53 genomic alterations 53 #S rRNA gene 53 trait locus 53 bacterial genomes 53 transcriptome sequencing 53 genomic loci 53 coding exons 53 LQTS 53 cytogenetic 53 genetic aberrations 53 gene loci 53 RNA seq 53 amino acid sequences 53 Y STR 53 Dr. Victor Velculescu 53 PALB2 53 molecular abnormalities 53 Sanger sequencing 53 chromosomal alterations 53 subpopulations 53 familial pancreatic cancer 53 sequenced genomes 53 chromosome #p# [001] 53 Genetics Consortium 53 microRNA molecules 53 Geneticists 53 histone modifications 53 chromosome rearrangements 53 heritable traits 53 susceptibility locus 53 allelic variation 53 metabolomic profiling 53 genomewide association study 53 miRNA 53 paternal lineages 53 HNPCC 53 International HapMap Project 53 microbiomes 53 microarray 53 Human SNP Array 53 Y chromosomal 53 chromosome #p#.# 53 SNP arrays 53 Drosophila genome 53 molecular profiling 53 maize genome 53 pyrosequencing 53 BRCA mutation 53 TGFBR1 * 6A 53 genetic makeups 53 genomic proteomic 52 landraces 52 CYP#D# gene 52 genomic sequencing 52 epigenetic changes 52 serum biomarkers 52 HLA typing 52 chromosome #q#.# [001] 52 genetic trait 52 mitochondrial gene 52 cDNA microarray 52 chromosome #q# [002] 52 TCF#L# gene 52 proteomes 52 metabolome 52 body louse genome 52 methylated DNA 52 Velculescu 52 chromosomal 52 mitochondrial genomes 52 microbial genomes 52 coding sequences 52 molecular biomarker 52 endophenotypes 52 diagnostic biomarker 52 HLA alleles 52 splice variants 52 GSTP1 52 diploid genome 52 miRNA genes 52 highly heritable 52 indels 52 KRAS mutation 52 genome sequenced 52 missense mutations 52 gene amplification 52 IgA deficiency 52 miRNA expression 52 UTRs 52 exome 52 HLA markers 52 NPY gene 52 genetic lineages 52 chromosomal anomaly 52 pharmacogenetic 52 cardiac channelopathies 52 TOMM# 52 HLA molecules 52 mutant allele 52 Neanderthal genome 52 CDH1 52 PITX2 52 Genetic variants 52 microarray analysis 52 APOE genotype 52 nucleotide sequence 52 methylated genes 52 ZNF# 52 tumor biopsies 52 non coding RNA 52 morphological characteristics 52 proband 52 heritable 52 druggable targets 52 epigenetic mechanisms 52 eTag assays 52 cDNAs 52 aCGH 52 QTLs 51 comparative genomic hybridization CGH 51 APOE e4 51 chromosome #q 51 FDG PET scans 51 inherited mutations 51 prognostic marker 51 platypus genome 51 genomic markers 51 chromosome 51 BRCA mutations 51 paternal ancestry 51 breast cancer genes BRCA1 51 subtypes 51 HLA DQ 51 dbSNP 51 biologic pathways 51 human leukocyte antigen 51 Arabidopsis genes 51 BRCA2 mutation 51 Neanderthal fossils 51 Mitochondrial DNA 51 diagnostic biomarkers 51 K ras mutations 51 proteome 51 bioinformatic analysis 51 oligonucleotide arrays 51 biological pathways 51 Genetic 51 cardiac progenitor cells 51 Neandertal DNA 51 amino acid sequence 51 nomogram 51 homozygosity 51 genomic sequences 51 organism genome 51 KRAS mutations 51 chromosomes 51 validate biomarkers 51 HLA DQ2 51 virulence genes 51 Li Fraumeni 51 protein biomarker 51 monozygotic twins 51 prion infection 51 heritability 51 Getzenberg 51 GeneChip 51 DNA methylation biomarker 51 quantitative RT PCR 51 methylation 51 peptide sequences 51 serum protein biomarkers 51 BAC clones 51 epigenetic marks 51 CHEK2 51 #S rDNA 51 miRNA biomarkers 51 molecular underpinnings 51 prion protein gene 51 BRCA1 mutations 51 genetic sequencing 51 chromosomal DNA 51 DNA methylation 51 genomically 51 chimp genome 51 ALK mutations 51 genes predisposing 51 chromosome translocations 51 Multiple logistic regression 51 mRNA transcripts 51 fetal aneuploidy 51 predictive biomarker 51 VNTR 51 BRCA1 gene 51 microcephalin 51 previously undescribed 51 Genomes Project 51 chromosomal disorders 50 transcriptional profiling 50 Affymetrix microarray technology 50 epitopes 50 CpG islands 50 GBA mutations 50 mammalian genome 50 HumanHap# BeadChip 50 kilobase 50 #p#.# [001] 50 DNA 50 STK# gene 50 pharmacogenetic test 50 miRNA sequences 50 MSH2 50 genomic profiling 50 mtDNA sequences 50 predictive biomarkers 50 genome rearrangements 50 ChIP Seq 50 bisulfite sequencing 50 DeCode 50 ChIP chip 50 Illumina genotyping 50 rs# [002] 50 microdeletion 50 genes BRCA1 50 5 hydroxymethylcytosine 50 BRCA genes 50 clefting 50 microbial genome 50 NSCLC tumors 50 pilocytic astrocytomas 50 generalized vitiligo 50 glycan 50 dizygotic twins 50 APOL1 50 rs# [001] 50 inbred strains 50 promoter hypermethylation 50 distinct subtypes 50 exons 50 chromosome aberrations 50 lincRNAs 50 homologs 50 genetic abnormality 50 antibodies 50 miRview ™ squamous 50 pharmacogenetic testing 50 biospecimens 50 MIF protein 50 metabolomic 50 hypermethylation 50 FGFR2 gene 50 PTEN mutations 50 familial ALS 50 telomere lengths 50 Genotyping 50 biomarker assay 50 CFTR gene mutations 50 sequence homology 50 gene polymorphisms 50 CGG repeats 50 serum samples 50 lactase persistence 50 DNA methylation biomarkers 50 orthologous genes 50 plant Arabidopsis 50 phenotypic traits 50 transcriptional profiles 50 BRAF mutation 50 human leukocyte antigens 50 P. falciparum 50 RNA Seq 50 proteomic 50 noncoding RNAs 50 genetic relatedness 50 gene expression assays 50 epistasis 50 SELDI TOF 50 SNP genotyping 50 lineages 50 SLC#A# [002] 50 transcriptomic 50 defective gene 50 ancestries 50 polymorphism 50 ELISpot 50 bovine genome 50 metabolomics 50 Ashkenazi Jewish 50 MLH1 50 Logistic regression 50 IDH1 50 whole exome sequencing 50 Alleles 50 biomarker identification 50 tissue samples 49 chimpanzee genome 49 proteins 49 uncharacterized genes 49 deCODE BreastCancer TM 49 proteomic analysis 49 allelic 49 PALB2 gene 49 miRview ™ mets 49 genetic fingerprinting 49 computational methods 49 Whole Genome 49 obstructive coronary artery 49 Corus CAD 49 CCL#L# 49 ancestry 49 telomere length 49 #q#.# [001] 49 molecular pathways 49 NF1 gene 49 biochemical markers 49 phylogenetic trees 49 salivary proteins 49 heterozygosity 49 abnormalities 49 Neanderthal DNA 49 LPA gene 49 comparative genomic hybridization 49 SNP Array #.# 49 odorant receptors 49 mitochondrial DNA sequence 49 FTLD 49 paternally inherited 49 Alu elements 49 differential gene expression 49 LRRK2 mutation 49 HER2 gene 49 colorectal neoplasia 49 probands 49 microsatellite instability 49 Meckel Gruber 49 tiling arrays 49 epigenetic modification 49 YKL 49 Genetics 49 LRRK2 mutations 49 protein isoforms 49 genes BRCA 49 MAPCs 49 C#Y 49 mRNA molecules 49 alpha synuclein gene 49 homozygous 49 microsatellite loci 49 nucleotide sequences 49 genomics 49 lactose tolerance 49 gene variation 49 cytosine methylation 49 Genetic variations 49 immunohistochemical 49 de novo mutations 49 situ hybridization 49 Victor Velculescu 49 splice variant 49 microRNA miRNA 49 thrombophilia 49 tumor subtypes 49 Resource Exchange AGRE 49 PCR assay 49 EGFR mutation status 49 perfusion CT 49 breast cancer subtypes 49 haplotyping 49 NEDD9 49 narcolepsy cataplexy 49 genotyping assay 49 S. maltophilia 49 microRNA sequences 49 PTEN gene 49 #p# [001] 49 miRNA expression patterns 49 DNA methylation markers 49 ribosomal RNA rRNA 49 medulloblastomas 49 IGF2 49 conserved sequences 49 breast cancer gene mutations 49 metazoan 49 genetic alteration 49 Her2/neu 49 dopamine transporter gene 49 PARP inhibition 49 micro RNAs 49 HHMI investigator 49 chromosome abnormalities 49 CNTNAP2 49 metabolomic profiles 49 woolly mammoth genome 49 phenotyping 49 Fragile X gene 49 morphological traits 49 mutant gene 49 JAK2 mutation 49 zebra finch genome 49 breast cancer metastasis 49 identifying genetic markers 49 VeraCode 49 FGFR2 49 breast carcinomas 49 HPV genotypes 49 tandem mass spectrometry 49 genetic rearrangements 49 telomere DNA 49 logistic regression analysis 49 STK# [002] 49 intergenic 49 mitochondrial mutations 49 CRISPR Cas 49 multiplex ligation dependent 49 metagenomes 49 synteny 49 protein kinases 49 bioluminescent imaging 49 FMR1 gene 49 HNSCC 49 Yamanaka recipe 49 KIAA# 49 Neandertal 49 whole genome sequencing 49 ortholog 49 deleterious mutation 49 allele 49 whole genome genotyping 49 Stuttering tends 49 BeadChip 49 epigenome 49 genetic syndromes 49 Pericak Vance 49 mosaicism 49 BRCA2 gene mutations 49 OncotypeDX 49 immunochemical 48 PIK3CA 48 quantitative gene expression 48 maternal lineages 48 SNP rs# [001] 48 viral genomes 48 evolutionary lineage 48 homozygote 48 kilobases 48 IL#B 48 X chromosome genes 48 phenotypic differences 48 PCA3 gene 48 TP# mutation 48 RT PCR assay 48 glycan microarray 48 IDH1 mutation 48 primordial germ cells 48 MC1R 48 researchers 48 Li Fraumeni syndrome 48 NNRTI resistance 48 ApoE gene 48 gene sequencing 48 longitudinal studies 48 NPM1 48 coding genes 48 hereditary breast cancer 48 susceptibility alleles 48 evolutionary relatedness 48 SORL1 gene 48 genomic deletions 48 miRNA profiling 48 Y chromosome 48 fetal chromosomal abnormalities 48 Brachypodium 48 INF2 48 human microbiome 48 histone modification 48 traits 48 rs# [003] 48 genetically identical 48 genes differentially expressed 48 SCN5A 48 metabolomic profile 48 chromosomal aberrations 48 BRCA2 gene mutation 48 DNA rearrangements 48 epigenomic 48 PTPN# 48 molecular pathway 48 KIF6 gene variant 48 Human Leukocyte Antigen 48 microsatellites 48 IKZF1 48 human genome sequence 48 Phylomer ® 48 prion strains 48 chromosomal translocations 48 BRCA2 gene 48 genomic variants 48 CISH 48 reverse vaccinology 48 homologous genes 48 clusterin 48 Y chromosomes 48 interactome 48 HG PIN 48 haptoglobin 48 CpG methylation 48 PICALM 48 NAFLD 48 conditional logistic regression 48 HapMap Project 48 karyotype 48 p# mutations 48 pharmacogenetics 48 serologic 48 DNA microarrays 48 genetic imprinting 48 Pääbo 48 multiplex PCR 48 PRNP 48 SNPs pronounced snips 48 miRNA expression profiles 48 patient subpopulations 48 genetic diversity 48 intergenic regions 48 subtype 48 oligonucleotide probes 48 phenotypic characteristics 48 lentiviruses 48 tissue microarrays 48 A. thaliana 48 recessive trait 48 segmental duplications 48 biochemical pathways 48 ependymomas 48 Mendelian 48 odorant receptor 48 admixed populations 48 Neanderthal genome sequence 48 epidemiological studies 48 Mammostrat 48 chromosomal rearrangement 48 diagnose Alzheimer disease 48 pseudogenes 48 aberrant methylation 48 chimp genomes 48 KCNQ1 48 miRNA molecules 48 CC genotype 48 Single Nucleotide Polymorphisms 48 MTHFR 48 G#S mutation 48 Apobec3 48 nongenetic 48 epigenetically 48 cytochrome b 48 lymphoblastoid cell lines 48 HAR1 48 STAT4 48 #q# deletion 48 etiologic 48 chromatin immunoprecipitation ChIP 48 Linear regression 48 Clusterin 48 genomes sequenced 48 vitro assay 48 Polychronakos 48 Septin9 48 PD2i ® 48 QTL mapping 48 paralogs 48 Wwox 48 PGRN 48 BRCA1 48 prognostic indicators 48 microRNA genes 48 APOE4 48 DeCode Genetics 48 transcriptomics 48 genetic heterogeneity 48 Haptoglobin 48 EBVs 48 qRT PCR 48 proteomic technologies 48 primate species 48 Manfred Kayser 48 Sjögren syndrome 48 recessive mutations 48 epigenetic 48 RNA transcripts 48 DNA sequencing 48 jawed vertebrates 48 Illumina Genome Analyzer 48 bacterial symbiont 48 genetic fingerprint 48 achromatopsia 48 comparative genomic 48 rhesus macaque 48 nucleotide substitutions 48 CYP#C# [001] 48 genetic defect 48 IgE antibody 48 PGDH 48 GBM tumors 48 CYP#E# gene 48 Abecasis 48 basal cell nevus syndrome 48 Comparative genomics 48 secreted proteins 48 K ras 48 epiblast stem cells 48 T2D 48 Tischfield 48 common ancestor 48 X chromosome 48 DeCODE 48 Array CGH 48 paternal lineage 48 DNA microarray 48 CSF biomarkers 48 Microarray 48 drosophila 48 genomic rearrangement 48 genomic biomarker 48 prognostic biomarkers 48 genomic rearrangements 47 multiplexed assays 47 quantitative proteomics 47 genes encoding 47 Affymetrix arrays 47 Bos taurus 47 #q#.# deletion syndrome 47 LIS1 47 IKAROS alterations 47 HIV tropism 47 Shendure 47 Septin 9 47 autosomal dominant inheritance 47 MECP2 gene 47 methylation profiling 47 toxicogenomic 47 warfarin dosing 47 inheritable diseases 47 cnidarians 47 HSPCs 47 CDKN2A 47 massively parallel sequencing 47 immunohistochemistry IHC 47 Froguel 47 heterozygous 47 MGUS 47 NGAL 47 aneuploidy 47 microbiota 47 VHL gene 47 CFTR gene 47 genetic disorders 47 ultraconserved elements 47 lung adenocarcinoma 47 serological 47 Biomarker 47 FCGR3A 47 genome sequencing 47 ESTs 47 macaque genome 47 chimerism 47 KRAS oncogene 47 DRD2 gene 47 clades 47 CHD7 47 phenotypic expression 47 molecular determinants 47 behavioral traits 47 comparative genomics 47 mechanistic pathways 47 PCR RFLP 47 DARPP 47 artificial chromosomes 47 TACI mutations 47 ncRNA 47 distantly related species 47 mitochondrial disorders 47 promoter methylation 47 Aravinda Chakravarti 47 Haplotype 47 faecal samples 47 vitamin D receptors 47 subclinical atherosclerosis 47 stratifying patients 47 Affymetrix GeneChip 47 exfoliation glaucoma 47 SMN2 47 pre malignant lesions 47 Epidemiologic studies 47 autopsied brains 47 Dr. Pasinetti 47 honeybee genome 47 EGFR mutation 47 Genetic variation 47 5 hmC 47 body fatness 47 introgression 47 IL#R 47 tissue biopsies 47 Sequencing 47 M. genitalium 47 broadly neutralizing antibodies 47 genome annotation 47 prognostic 47 epitope 47 molecular geneticists 47 BeadArray 47 biochemical signaling pathway 47 Genotypic 47 underlying molecular mechanisms 47 Affymetrix SNP Array 47 penetrance 47 shotgun sequencing 47 blastomeres 47 mammographic density 47 contigs 47 gene deletions 47 APOE e4 gene 47 Kufs disease 47 Wolbachia infection 47 MammaPrint R 47 phylogenetic relationships 47 transcriptome profiling 47 MetaChip 47 CpG island 47 RRM1 47 abnormal methylation 47 gut microbes 47 EBV infection 47 bioinformatic 47 chromosome #q#.# [002] 47 myostatin gene 47 PCR amplified 47 RT qPCR 47 PrPSc 47 MSMB 47 Nano Biochip 47 genetically diverse 47 deCODE AF TM 47 mutational analysis 47 chromatin immunoprecipitation 47 gene rearrangements 47 cynomolgus macaques 47 chromosomally normal 47 Affibody ® molecules 47 Leptospira 47 chloroplast DNA 47 LRAT 47 homology 47 HLA loci 47 cDNA library 47 Genes 47 genetic polymorphism 47 multivariate logistic regression 47 PHLPP 47 MicroRNA 47 recessive traits 47 GFP gene 47 polyploid 47 SRY gene 47 phenotypically 47 oxysterols 47 elevated CRP 47 mutated K ras 47 pharmacogenetic tests 47 plasma kallikrein 47 advanced neoplasia 47 mRNAs 47 colorectal cancer CRC 47 monogenic 47 retrospective cohort 47 DNA deoxyribonucleic acid 47 BeadChips 47 connectome 47 prion disease 47 cDNA 47 Chromosome 47 neuronal circuitry 47 KRAS BRAF 47 chromosome #p# [002] 47 SLITRK1 47 sea urchin genome 47 BioMAP ® 47 biological underpinnings 47 zebrafish genome 47 Western blot 47 BRCA gene 47 microarrays 47 sarcosine 47 FTO gene 47 quantitative PCR qPCR 47 placental mammals 47 genome mapping 47 neural circuitry 47 familial clustering 47 morphological 47 causative agent 47 SORL1 47 metagenomic 47 Sequencing Systems 47 pathogenic mechanisms 47 mtDNA sequence 47 kinases 47 herpesviruses 47 heterozygotes 47 abnormal cytology 47 microRNAs miRNAs 47 FLT3 47 malignant nodules 47 developmental plasticity 47 chromatin proteins 47 noninvasive imaging 47 epigenetic alterations 47 HER2 expression 47 K RAS