Related by context. All words. (Click for frequent words.) 69 phenotypic variation 69 genetic loci 67 Mendelian 66 phenotypic traits 66 missense mutations 65 paralogs 65 polyploid 65 quantitative trait loci 65 introgression 65 A. thaliana 65 genetic polymorphism 65 sequence homology 64 evolutionary divergence 64 differential gene expression 64 epistasis 64 inbred strains 64 evolvability 64 heritable traits 64 transgene expression 64 metazoan 64 CNTNAP2 64 polyploidy 64 multigenic 64 etiologic 63 allele frequencies 63 methylation patterns 63 genetic heterogeneity 63 mRNA transcripts 63 QTLs 63 prodynorphin 63 MECP2 gene 63 phylogenetically 63 underlying pathophysiology 63 genotypic 63 prion strains 63 cytochrome b 63 PTPN# 63 epigenetic regulation 63 pleiotropy 63 chromosomal rearrangement 63 orthologs 63 phylogeographic 63 modifier genes 63 microcephalin 63 Alu elements 63 metabolomic profiles 62 lincRNA 62 genome rearrangements 62 Clusterin 62 histone modifications 62 homozygosity 62 phenotypic variability 62 BARD1 62 eotaxin 62 APOE genotype 62 DNA methylation patterns 62 polygenic 62 FGFs 62 epigenetic modification 62 prion gene 62 ontogenetic 62 Pseudomonas syringae 62 fungal genomes 62 spontaneous mutations 62 gene duplications 62 orthologous genes 62 coevolution 62 TCF#L# gene 62 Genetic variation 62 enterotypes 61 phenotypic differences 61 maternally inherited 61 pathogenetic 61 ortholog 61 malaria parasite genome 61 HLA DRB1 61 #S rRNA 61 virulence genes 61 splice variants 61 mtDNA mutations 61 MC1R 61 inherited mutations 61 apoE 61 protein conformation 61 STAT4 61 pathophysiological 61 aetiological 61 C. neoformans 61 phenotypic expression 61 de novo mutations 61 MC1R gene 61 ENPP1 61 Comparative genomics 61 indel 61 noncoding RNA 61 genomewide 61 amyloid cascade 61 cAMP signaling 61 MYH9 gene 61 genetic relatedness 61 P falciparum 61 endophenotypes 61 causative mutation 61 DNA demethylation 61 nucleotide substitution 61 KIAA# 61 transcriptional regulation 61 microbiomes 61 mitochondrial genomes 61 metazoans 61 bone marrow mesenchymal stem 61 microsatellite markers 61 p# activation 61 tRNA synthetases 61 tumorigenicity 60 pseudogene 60 ncRNA 60 SNP rs# [002] 60 gene locus 60 M. pneumoniae 60 clinicopathological 60 phenotypically 60 5 HTTLPR 60 nucleotide sequence 60 haplotypes 60 NNRTI resistance 60 telomere DNA 60 coexpression 60 #q#.# [001] 60 HLA genes 60 alpha synuclein gene 60 trait locus 60 previously uncharacterized 60 mitochondrial DNA mtDNA 60 epigenetic inheritance 60 L. pneumophila 60 genetic variants associated 60 TCF#L# 60 microchimerism 60 isotypes 60 TRIM5 60 phylogenetic relationships 60 CagA 60 cis regulatory 60 ORFs 60 MC4R gene 60 tyrosine phosphorylation 60 monophyletic 60 haplogroups 60 monozygotic twins 60 heterozygotes 60 mammalian genomes 60 PB1 F2 60 genetical 60 hepatoma 60 epigenetic modifications 60 gene loci 60 mutant allele 60 gametophyte 60 CHD7 60 IgA deficiency 60 nongenetic 60 KCNQ1 60 cDNAs 60 histone methylation 60 KLF4 60 mutant alleles 60 #S rDNA 60 circadian clock genes 60 intronic 59 #S rRNA gene 59 genetic modifiers 59 reproductively isolated 59 superinfection 59 CALHM1 59 genetic locus 59 pleiotropic 59 monogenic 59 eukaryote 59 SRY gene 59 LRRK2 gene 59 untranslated regions 59 chromosome #p#.# 59 ribosomal RNA rRNA 59 Phylogenetic 59 Haptoglobin 59 nucleosome positioning 59 phylogenies 59 somatic mutations 59 Genotypic 59 allelic 59 sRNA 59 Htt 59 gambiae 59 aneuploid cells 59 CYP#C# gene 59 eusociality 59 frameshift mutation 59 nitrogenase 59 genomic variation 59 genomic alterations 59 prion protein gene 59 Treg cell 59 linkage disequilibrium 59 NOD mouse 59 evolutionary lineages 59 observable traits 59 mitochondrial proteins 59 #q#.# [002] 59 paratuberculosis 59 bacterial symbiont 59 outbred 59 sexually dimorphic 59 karyotype 59 indels 59 rRNA 59 selfing 59 proteoglycan 59 PRNP 59 genetic lineages 59 phenotype 59 molecular determinants 59 genetic variability 59 bacterial genomes 59 chronicity 59 insulin signaling pathway 59 familial clustering 59 Borrelia 59 miRNA expression 59 genomic imprinting 59 proband 59 KRAS oncogene 59 E. histolytica 59 QTL mapping 59 IL#R 59 lactase persistence 59 pleiotropic effects 59 3'UTR 59 positional cloning 59 microRNA molecules 59 artifactual 59 phylogenetics 59 SMAD4 59 BCL#A 59 phylogenetic analyzes 59 intergenic 59 DLC1 59 T. brucei 59 clades 59 SLC#A# [002] 59 PrPSc 59 lactose tolerance 59 Chlamydia pneumoniae 59 extramedullary 59 #S rRNA genes 59 orthologous 59 alexithymia 59 inbreeding depression 58 PON1 58 epigenetic mechanisms 58 primate genomes 58 uPAR 58 serovar 58 HAR1 58 fluoroquinolone resistance 58 recessive mutation 58 ADRB2 58 LRP5 58 D. melanogaster 58 splice junctions 58 H#K#me# 58 morphological characteristics 58 transcriptomes 58 microdeletion 58 thiopurine 58 underlying molecular mechanisms 58 hypermethylated 58 Karayiorgou 58 quasispecies 58 Phytophthora species 58 5 methylcytosine 58 Prevotella 58 clefting 58 functional polymorphism 58 EBV infection 58 autosomal 58 SSc 58 nucleotide substitutions 58 plant Arabidopsis 58 ZEBOV 58 MYH9 58 histone H4 58 steroidogenic 58 Candida species 58 Trichophyton rubrum 58 transgenic mouse models 58 ABCB1 gene 58 synteny 58 evolutionarily conserved 58 morphologic 58 LPA gene 58 maternally transmitted 58 body louse genome 58 missense mutation 58 UGT#A# * 58 FOXP2 gene 58 PrPC 58 silico prediction 58 phenotypic characteristics 58 endosymbiosis 58 operons 58 chromosomal aberrations 58 intestinal microflora 58 β1 58 genotypes 58 Bt toxins 58 cytopathic 58 isoenzymes 58 inferential statistics 58 PCR RFLP 58 Mycobacterium smegmatis 58 genetic determinants 58 chromosomal translocations 58 IGF1 58 Cyclin E 58 K ras mutations 58 neutralizing antibody 58 H#K# [001] 58 histone demethylase 58 proteomes 58 loci 58 Leydig cells 58 mitochondrial gene 58 TP# gene 58 TOMM# 58 eukaryotic cell 58 gene polymorphisms 58 VNTR 58 spontaneous mutation 58 amphioxus 58 morphological traits 58 homochirality 58 posttranslational modifications 58 #p#.# [001] 58 gene rearrangements 58 globin genes 58 HMGA2 58 Arabidopsis genome 58 vasopressin receptor 58 phenotypic plasticity 58 TMPRSS2 ERG fusion 58 ZNF# 58 genetic polymorphisms 58 WNK1 58 mRNA decay 58 chromosome #q#.# [001] 58 IGFBP 58 molecular phylogenetic 58 beta globin gene 58 phylogenetic trees 58 intracellular bacteria 58 germline mutations 58 telomere lengths 58 DARPP 58 SHANK3 58 SCN1A 58 allelic variants 58 Phenotypic 58 CYP#D# gene 58 metabolite concentrations 58 differentially regulated 58 sCJD 58 sequenced genomes 58 salivary proteins 58 #q# deletion 58 Genetic variants 58 epigenetic alterations 58 ADAMTS# 58 autosomal dominant disorder 58 dysbindin 58 plasma kallikrein 58 amino acid substitutions 58 intestinal microbiota 58 protein acetylation 58 chromosomal imbalance 57 outcrossing 57 sexual dimorphism 57 5 hydroxymethylcytosine 57 S. neurona 57 metabolic abnormalities 57 NR#A# 57 polyploids 57 cytosine methylation 57 behavioral disinhibition 57 differentially expressed genes 57 neuropsychiatric diseases 57 neuroanatomical 57 NPM1 gene 57 histone acetylation 57 chromosomal regions 57 diploid genome 57 PCR amplified 57 synuclein 57 mRNA molecules 57 familial aggregation 57 ontogeny 57 Yamanaka recipe 57 HLA alleles 57 chromatin structure 57 vivax 57 catechol O methyltransferase 57 SCD1 57 homologues 57 cellular prion protein 57 VHL gene 57 Jhdm2a 57 CCL#L# 57 Hashimoto thyroiditis 57 Klotho gene 57 serum biomarkers 57 S. cerevisiae 57 DEC2 57 sphingolipid 57 hammerhead ribozyme 57 miRNA genes 57 BDNF gene 57 ADH1B * 57 airway hyperresponsiveness 57 mammalian evolution 57 lactase gene 57 epigenetic changes 57 neuroligins 57 motor neuron degeneration 57 HLA DQ2 57 N. gonorrhoeae 57 MLL2 57 psychobiological 57 imprinted genes 57 NF1 gene 57 gut microbiota 57 aneuploid 57 CDH1 57 Leydig cell 57 APOE ε4 57 chromosome aberrations 57 C. albicans 57 constitutively expressed 57 ChIP seq 57 maize genome 57 alternative splicing 57 bilaterians 57 R#W [002] 57 univariate 57 phenotypes 57 morphogenetic 57 coding sequences 57 prehuman 57 microRNA expression 57 prostate carcinogenesis 57 symbiont 57 operon 57 codon usage 57 HMGCR 57 chimp genomes 57 antigenic epitopes 57 GABRA2 57 LIS1 57 odorant receptor 57 receptor gene 57 Skeletal muscle 57 germline cells 57 Prox1 57 JAK STAT 57 recessive trait 57 N glycan 57 plastids 57 genetically encoded 57 heterosis 57 causative genes 57 subcellular localization 57 alternatively spliced 57 epigenetically 57 binding affinities 57 transitivity 57 immunomodulation 57 thale cress Arabidopsis thaliana 57 mitochondrial mutations 57 evolutionary lineage 57 Foxp2 57 COMT gene 57 Y chromosomal 57 Lamarckian 57 Cryptococcus neoformans 57 chromosome #q# [002] 57 genetic ancestry 57 laterality 57 P cadherin 57 androgen receptor gene 57 HFE gene 57 C#Y 57 chitinase 57 genetic recombination 57 androgen signaling 57 pathophysiological mechanisms 57 tumor subtypes 57 hypogonadotropic hypogonadism 57 genomic variants 57 prognostic indicators 57 post translational modifications 57 thyrotropin 57 FGFR2 57 CPEB 57 cybrid 57 sympatric speciation 57 Prochlorococcus 57 #beta HSD1 57 homologies 57 RCAN1 57 animal phyla 57 H. habilis 57 dysbindin gene 57 pseudogenes 57 ABCB1 57 proteolytic activity 57 heritable variation 57 organogenesis 57 RUNX3 57 KCNH2 57 transcriptional repressor 57 spore formation 57 mRNA sequences 57 conserved sequences 57 H#Y 57 RNA polymerases 57 glabrata 57 unmeasured confounders 57 MAPK pathway 57 Kufs disease 57 phylogenetic 57 segmental duplications 57 prognostic markers 57 klotho 57 autism susceptibility genes 57 NKT cell 57 mutant huntingtin protein 57 E#F# 57 morphologically 57 EoE 57 peroxisome 57 hybridizations 57 incomplete penetrance 57 COX2 57 Plasmodium vivax 57 chromosome rearrangements 57 proline rich 57 RNA ribonucleic acid 57 p# MAPK 57 convergent validity 57 somatic mutation 57 highly heritable 57 beta1 integrin 57 miR #a [001] 57 deacetylation 57 Apobec3 57 gene deletions 57 morphological similarities 57 AVPR1A 57 Rickettsia 57 posttranslational modification 57 Ehrlichia 57 Trypanosoma brucei 57 prognostic significance 57 histocompatibility 57 ataxias 57 Genetic variations 57 HLA DRB1 * 57 Genetic predisposition 57 fig. S1 57 causal variants 56 S. maltophilia 56 childhood leukemias 56 transcriptomic 56 immunodominant 56 X chromosome inactivation 56 defensins 56 recombination hotspots 56 evolutionary relatedness 56 NEIL1 56 ultraconserved 56 Arabidopsis genes 56 colorectal carcinogenesis 56 causative mutations 56 IgG1 56 myocardial dysfunction 56 p#/CBP 56 dermatophytes 56 developmental abnormalities 56 distinct subtypes 56 artiodactyls 56 amyloid peptide 56 neurodevelopmental outcome 56 spatio temporal 56 serine protease 56 CCR7 56 HGPS 56 clade B 56 hitherto unrecognized 56 intracellular signal transduction 56 jawed vertebrates 56 assortative mating 56 amyloid deposition 56 outer membrane proteins 56 S. pombe 56 multicellularity 56 P. vivax 56 herpesviruses 56 paternally inherited 56 neuropathologic 56 vertebrate genomes 56 broadly neutralizing 56 Deinococcus 56 Mycoplasma pneumoniae 56 monocots 56 microRNAs miRNAs 56 intergenic regions 56 synthases 56 cynomolgus macaques 56 A. ramidus 56 coinfection 56 lymphoid tumors 56 ramidus 56 vertebrate evolution 56 immunological responses 56 CD1d 56 noncoding RNAs 56 eicosanoid 56 phenotypic 56 viral genomes 56 TRAF1 C5 56 V#F mutation 56 GPx 56 microRNA miR 56 ligand receptor 56 S. sanguinis 56 miRNAs miR 56 mRNA degradation 56 Eg5 56 coding exons 56 N Myc 56 terrestrial vertebrates 56 linear pharmacokinetics 56 cerevisiae 56 evolutionarily distant 56 rDNA 56 mitochondrial defects 56 MAOA gene 56 autosomal recessive 56 commensal bacteria 56 Bonferroni correction 56 deleterious mutations 56 susceptibility loci 56 plectasin 56 phylogenetic analysis 56 neutralizing antibody responses 56 pea aphid 56 Macaca mulatta 56 mtDNA sequence 56 PALB2 56 noncoding DNA 56 bile acid metabolism 56 histone modification 56 MRSA isolates 56 previously undescribed 56 downregulated 56 clonal expansion 56 serum leptin 56 HbF 56 meiotic recombination 56 tumor suppressor protein 56 major histocompatibility complex 56 genotype phenotype 56 ALK mutations 56 prokaryotic 56 symbioses 56 Chlamydomonas 56 Mycobacterium bovis 56 DQB1 * 56 N acetyltransferase 56 mammalian proteins 56 Genetic mutations 56 neuronal plasticity 56 multi celled organisms 56 cDNA libraries 56 parasitaemia 56 ipRGCs 56 methylated DNA 56 Supplementary Table 56 GABAB receptors 56 urinary calculi 56 downregulation 56 multivariable Cox 56 MHC molecules 56 underexpressed 56 C1q 56 placental mammal 56 C. jejuni 56 lymphoblastoid cell lines 56 Hsp# [001] 56 TIMP 1 56 glycosylated 56 coagulopathy 56 homologous genes 56 DNA polymerases 56 intraspecific 56 epistatic 56 CD#c 56 serum antibodies 56 aetiology 56 genomically 56 ribosomal protein 56 folate metabolism 56 S. enterica 56 pathogenic mechanisms 56 heritable trait 56 amyloidogenic 56 parasitoid wasp 56 breast cancer subtypes 56 CRISPR Cas 56 zebrafish genome 56 transgenic mosquitoes 56 eusocial 56 lentiviruses 56 epigenetic markers 56 CHEK2 56 FUS1 56 cyclin E 56 ncRNAs 56 methyltransferase 56 FGF2 56 plant Arabidopsis thaliana 56 inhibitory receptor 56 T. vaginalis 56 Th2 immune 56 budding yeast 56 chordates 56 RNA silencing 56 Segmental duplications 56 epigenetic silencing 56 Arabidopsis thaliana 56 proteolysis 56 oncogenic transformation 56 prokaryotes 56 bacterial virulence 56 mammalian species 56 Gene Ontology 56 olfactory receptor 56 hamartomas 56 evolutionary origins 56 simian immunodeficiency virus 56 Alternative splicing 56 Xenopus laevis 56 FOXP2 56 genus Plasmodium 56 STK# gene 56 lung epithelium 56 activin 56 ORMDL3 56 ESR1 56 noncoding 56 P. falciparum 56 HLA molecules 56 coding genes 56 FLT3 56 protein tyrosine phosphatase 56 gene expression patterns 56 HepG2 cells 56 taxon 56 fatty acid biosynthesis 56 plasma lipid 56 prion infection 56 perilipin 56 recessive genetic 56 non coding RNA 56 laforin 56 Wnts 56 spermidine 56 penetrance 56 cathepsin B 56 myopathies 56 X. laevis 56 multivariate Cox 56 stochasticity 56 receptor ligand 56 herpes virus infection 56 habilis 56 SLC#A# [001] 56 axon guidance 56 bronchopulmonary dysplasia BPD 56 chromosome translocations 56 physiological adaptations 56 NPY gene 56 protein coding RNAs 56 observable characteristics 56 chromosomal anomalies 56 HMGA1 56 sporadic ALS 55 prokaryote 55 miRs 55 axonal degeneration 55 Contagious yawning 55 chromosome #q#.# [002] 55 A. gambiae 55 genes predisposing 55 TLE3 55 proteomic analysis 55 alleles 55 Paranthropus robustus 55 T. gondii 55 dopamine transporter gene 55 fission yeast 55 Marambaud 55 lipoprotein metabolism 55 subfamily 55 genetic aberrations 55 genetic variation 55 chromosome #p# [001] 55 serum PTH 55 inherited maternally 55 Multiple logistic regression 55 familial predisposition 55 #p#.# [002] 55 Froguel 55 plasma lipoprotein 55 Plasmodium falciparum 55 organophosphorus compounds 55 proteins encoded 55 neural underpinnings 55 SCA5 55 airway remodeling 55 Morphological 55 Corynebacterium 55 Dictyostelium 55 Telomere length 55 WAGR syndrome 55 transcriptome sequencing 55 Gram stain 55 PON1 gene 55 insertional mutagenesis 55 morphometrics 55 Th2 responses 55 Phylogenetic analysis 55 immunoregulatory 55 antigenicity 55 CHI#L# 55 GLUT1 55 hermaphroditism 55 microRNA genes 55 IgG4 55 CCR5 delta# 55 brucei 55 Fas ligand 55 antitumor efficacy 55 Wwox 55 potent inhibitors 55 neural crest 55 Castorocauda 55 membrane permeability 55 COMMD1 55 dopamine D4 receptor 55 Neuregulin 1 55 normal prion protein 55 susceptibility locus 55 molecular phylogeny 55 RNA sequences 55 BVDV 55 electrophysiologic 55 amino acid sequence 55 protein tyrosine phosphatases 55 HMPV 55 Multivariate analysis 55 karyotypes 55 ectopic expression 55 ultrastructural 55 cone photoreceptors 55 Hh pathway 55 condensin 55 adipogenic 55 physicochemical properties 55 SLITRK1 55 molecular underpinnings 55 tRNA synthetase 55 comparative genomic 55 susceptibility gene 55 haploid 55 oxysterols 55 Xenopus 55 meta analytic 55 hematopoietic cancers 55 beta lactamases 55 endocannabinoid signaling 55 mitochondrial genome 55 haplotype map 55 annexin 55 IKK2 55 DEAR1 55 JNK1 55 genomic loci 55 transcriptomics 55 polynucleotide 55 interferon γ 55 ribonucleic acids 55 mitochondrial metabolism 55 primate lineage 55 malarial parasites 55 ant genomes 55 Sgk1 55 polymorphisms 55 Bayesian inference 55 Fc receptor 55 endogenous retroviruses 55 mycobacterial 55 archaeal 55 constitutively active 55 clonally 55 CYP#C# [002] 55 replicon 55 secretory pathway 55 IRS1 55 FMRP protein 55 splice variant 55 fibrotic disease 55 bioengineered mice 55 pharmacodynamic biomarkers 55 enzymatic pathways 55 distinct lineages 55 metalloprotease 55 developmental neurotoxicity 55 evolutionary conserved 55 Hfq 55 microglial 55 assortative 55 stathmin 55 Plasmodium species 55 GSTT1 55 neurexins 55 MT1 MMP 55 BMAL1 55 #q#.# deletion syndrome 55 rifamycins 55 mucosal immune 55 Mendelian genetics 55 residual confounding 55 pathophysiologic 55 rs# [002] 55 teleost fish 55 Kaplan Meier curve 55 chromosomal DNA 55 hippocampal neurons 55 serologic 55 moderately heritable 55 microarray experiments 55 H. sapiens 55 unmeasured factors 55 glycolytic 55 progranulin gene 55 MEF2A 55 phthalate syndrome 55 hematopoietic cells 55 2D 4D ratio 55 neuropsychiatric disorder 55 chromosomal anomaly 55 GSTM1 gene 55 small RNAs encoded 55 fully sequenced genomes 55 chromosome #q 55 M. leprae 55 CYP#E# 55 genetic alteration 55 soluble proteins 55 earliest hominid 55 transcriptional activation 55 granulosa cell 55 siRNA knockdown 55 filoviruses 55 haematopoietic 55 Caenorhabditis 55 neuroinflammation 55 histone deacetylases 55 Leishmania parasites 55 predisposing factors 55 Heterodontosaurus 55 periodontal tissues 55 chromosome #q# [001] 55 heterologous expression 55 RRM1 55 IntroductionThe 55 immunological 55 Pol IV 55 deuterostomes