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(Click for frequent words.) 70 mutation 69 de novo mutations 69 mosaicism 68 germline mutations 66 epigenetic silencing 66 spontaneous mutations 66 missense mutations 66 microcephalin 66 monogenic 65 mtDNA mutations 65 genetic recombination 65 Leptospira 65 genomic imprinting 65 frameshift mutation 65 Cryptococcus neoformans 65 progranulin gene 65 genetic mutation 65 mutations 65 gene rearrangements 65 phenotypic variation 65 somatic mutation 64 nucleotide substitutions 64 heterozygotes 64 pathogenic mutations 64 chromosomal instability 64 familial ALS 64 homozygosity 64 pneumococci 64 sequence homology 64 MECP2 gene 64 epigenetic alterations 64 FASPS 64 phenotypic expression 64 MLH1 64 inherited mutations 63 genetic polymorphism 63 autosomal recessive 63 recessive genes 63 epigenetic changes 63 CHD7 63 polyploidy 63 nucleotide substitution 63 chromosomal alterations 63 IgA deficiency 63 MLL gene 63 paralogs 63 TCF#L# gene 63 herpesviruses 63 HLA DRB1 63 indels 63 PTPN# 63 homozygotes 63 MSH2 63 TP# gene 63 polyploid 63 aneuploidies 63 transcriptional repression 63 chromosomal rearrangements 63 recessive trait 62 Prox1 62 chromosomal aberrations 62 Mycoplasma pneumoniae 62 S. enterica 62 SCN5A 62 Genetic variation 62 mutant alleles 62 X inactivation 62 vivax 62 Li Fraumeni syndrome 62 chromosomal mutations 62 pathogenic bacterium 62 Kufs disease 62 somatic mutations 62 allelic variants 62 monozygotic twins 62 fatty acid synthesis 62 p# activation 62 microdeletions 62 prion gene 62 autosomal dominant disorder 62 MLL2 62 transgene expression 62 T. vaginalis 62 DNA rearrangements 62 LRAT 62 inbreeding depression 62 SRY gene 62 germline mutation 62 JAK2 gene 62 virulence genes 62 chromosomal rearrangement 62 microdeletion 61 tyrosine phosphorylation 61 TP# mutation 61 maternally inherited 61 Trypanosoma brucei 61 karyotypes 61 chromosomal deletions 61 ploidy 61 VHL gene 61 outcrossing 61 recessive genetic 61 heritable variation 61 orthologs 61 CDH1 61 Trichophyton rubrum 61 deacetylation 61 epigenetic modification 61 CFTR gene 61 Epstein Barr virus EBV 61 H#Y 61 missense mutation 61 introgression 61 breast carcinomas 61 acetylation 61 Helicobacter 61 epigenetic inheritance 61 paratuberculosis 61 chromosomal anomalies 61 Phylogenetic analysis 61 S. Typhimurium 61 chromosome aberrations 61 E. histolytica 61 ADAMTS# 61 alternatively spliced 61 autosomal dominant inheritance 61 clonal expansion 61 antigenic shift 61 alleles 61 genetic loci 61 aneuploidy 61 homozygote 61 PON1 61 Leydig cell 61 epigenetic modifications 61 chromosome #q#.# [001] 61 evolutionary divergence 61 sporadic ALS 61 TP# mutations 61 N acetyltransferase 61 autosomal dominant 61 APOL1 61 selfing 61 #q#.# [001] 61 H#K#me# 60 Entamoeba histolytica 60 mesotheliomas 60 synthases 60 S. neurona 60 Kabuki syndrome 60 isoenzyme 60 MC4R gene 60 aneuploid 60 genetic abnormalities 60 amino acid substitution 60 HLA genes 60 transcriptional repressor 60 L. pneumophila 60 chromosomal translocations 60 allele frequencies 60 DNA demethylation 60 alkalosis 60 chromosome rearrangements 60 Genetic mutations 60 prodynorphin 60 replicase 60 Brugada syndrome 60 KCNQ1 60 genomic rearrangements 60 deleterious mutations 60 mitochondrial DNA mutations 60 QTLs 60 sporadic Creutzfeldt Jakob 60 Borrelia 60 histocompatibility 60 gene amplification 60 SCN1A 60 HAR1 60 budding yeast 60 meiotic recombination 60 malignant transformation 60 ZNF# 60 Aspergillus species 60 MEF2A 60 IRF6 60 CYP#B# 60 apoE4 60 gene duplications 60 breast cancer genes BRCA1 60 haematopoietic 60 P. infestans 60 FMR1 gene 60 resistant isolates 60 Rickettsia 60 blastomeres 60 MeCP2 gene 60 modifier genes 60 mutant allele 60 E. faecalis 60 LRRK2 gene 60 Candida species 60 coagulase negative staphylococci 60 congenital disorders 60 epistasis 60 LPA gene 60 neural crest 60 etiologic agent 60 subcellular compartments 60 nonhereditary 60 Inactivation 60 LMNA 60 K#R [002] 60 LIS1 60 P. patens 60 heterologous expression 60 microchimerism 60 mitochondrial mutations 60 differential gene expression 60 C#BL/#J 60 SLITRK1 60 heterozygote 60 gene MECP2 60 prion infection 59 methicillin susceptible Staphylococcus aureus 59 bacteria Pseudomonas 59 Salmonella typhi 59 MGUS 59 Xenopus laevis 59 CDKN2A 59 Spinal muscular atrophy 59 coinfection 59 trypanosome 59 Mycobacterium bovis 59 HGPS 59 Leydig cells 59 CNTNAP2 59 histone modification 59 hemagglutinin gene 59 M. pneumoniae 59 enteroviral 59 NR#A# gene 59 ADPKD 59 Fragile X gene 59 rotaviruses 59 pea aphid 59 fluoroquinolone resistance 59 protozoan parasite 59 BARD1 59 chromosomal abnormality 59 dephosphorylation 59 K#N 59 trophoblast cells 59 KRAS oncogene 59 neurona 59 polycystin 59 Dysregulation 59 gene mutations 59 genetic alteration 59 MYBPC3 59 abnormal chromosomes 59 HLA B# 59 familial pancreatic cancer 59 proteolytic cleavage 59 K ras gene 59 NF1 gene 59 polycystic kidneys 59 Bacteroides 59 sexual dimorphism 59 mRNA transcripts 59 genetic mutations 59 amino acid substitutions 59 Cryptococcus 59 A. thaliana 59 multidrug resistance 59 suppressor gene 59 recessive mutations 59 neuroligins 59 SHANK3 59 genetic alterations 59 sexually reproducing 59 SMAD4 59 mutated K ras 59 causative mutation 59 hypermethylated 59 endogenous retroviruses 59 NNRTI resistance 59 C. neoformans 59 chromosome abnormality 59 cerevisiae 59 H#K# [001] 59 CYP#C# [002] 59 C. albicans 59 N. gonorrhoeae 59 enteroviruses 59 promoter hypermethylation 59 Chromosomal 59 allele frequency 59 BRCA1 BRCA2 59 ABCB1 gene 59 TACI mutations 59 metaplasia 59 Histoplasma capsulatum 59 IGF1 59 IKZF1 59 Epstein Barr Virus EBV 59 BRCA2 gene 59 lactase persistence 59 heterozygous 59 STAT4 59 germline cells 59 β1 59 Burkholderia 59 developmental abnormalities 59 PB1 F2 59 Clusterin 59 DSBs 59 fluoroquinolone resistant 59 deleterious mutation 59 Homozygous 59 shortened telomeres 59 lymphatic vessel 59 HNPCC 59 polyomavirus 59 HMGA2 59 defensin 58 Plasmodium parasites 58 pulmonary hypoplasia 58 mutated gene 58 atherosclerotic lesion 58 medulloblastoma tumors 58 proteolysis 58 mycobacterium tuberculosis 58 chromosome translocations 58 bacterium Mycobacterium tuberculosis 58 causative genes 58 alternative splicing 58 miRNA expression 58 genomic variants 58 proband 58 PALB2 58 enterocolitis 58 telomere DNA 58 EBV infection 58 chromosomal defect 58 TACI 58 GPx 58 PCR amplified 58 Babesia 58 airway hyperresponsiveness 58 proto oncogene 58 CCR5 delta# 58 inbred strains 58 malayi 58 p# mutations 58 autosomal recessive disease 58 G6PD deficiency 58 seropositivity 58 chromosome condensation 58 clade B 58 phylogenetic analyzes 58 prion strains 58 JAK2 enzyme 58 translocations 58 enzymatic activity 58 hepatoma 58 Neisseria 58 Six3 58 genetic rearrangements 58 etiologic 58 segmental duplications 58 ectopic expression 58 chromatin modification 58 phenotypic traits 58 von Hippel Lindau 58 heterotaxy 58 autoregulation 58 chromosome #q#.# [002] 58 Ehrlichia 58 Vesivirus 58 isotypes 58 CEACAM1 58 DNA methylation patterns 58 Amino acid 58 S aureus 58 parasite Trypanosoma cruzi 58 S. cerevisiae 58 spontaneous remission 58 epigenetically 58 V#F mutation 58 X chromosome inactivation 58 unmutated 58 NR#A# 58 pleiotropic effects 58 outer membrane proteins 58 vesicular stomatitis virus 58 endosymbiosis 58 Genetic mutation 58 functional polymorphism 58 misregulation 58 gene deletions 58 mRNA decay 58 downregulation 58 KCNH2 58 fungal genomes 58 apolipoprotein E gene 58 medulloblastomas 58 kinase gene 58 dominantly inherited 58 dysgenesis 58 intracellular bacteria 58 PARP inhibition 58 UGT#B# 58 staphylococci 58 recessive mutation 58 allelic variation 58 Hashimoto thyroiditis 58 M. bovis 58 CpG island 58 histone methylation 58 C. perfringens 58 LRP5 58 chorioamnionitis 58 cybrid 58 obligate intracellular 58 SMN1 58 GPC5 58 ABCB1 58 pyelonephritis 58 epigenetic mechanisms 58 synaptogenesis 58 mycobacterium 58 Arabidopsis genome 58 BRAF V#E 58 SOX3 gene 58 Chlamydia psittaci 58 rifamycins 58 vacuolar 58 Brugada Syndrome 58 genotypic 58 huntingtin gene 58 cytochrome b 58 oncogenic transformation 58 Mendelian 58 asymptomatically 58 beta thalassemia 58 Corynebacterium 58 phthalate syndrome 58 APOE ε4 58 TMEM#B 58 undiagnosed celiac disease 58 sCJD 58 bronchoalveolar 58 maternally transmitted 58 genotoxic stress 58 phenotypic differences 58 NKX#.# 58 WNK1 58 TEL AML1 58 dyskeratosis congenita 58 overexpressing 58 immunodeficiency 58 acrosome reaction 58 dedifferentiation 58 transcriptional regulation 58 chromosomal imbalance 58 dizygotic 58 HBV genotype 58 CPEB 58 Polymorphisms 58 inherited genetic mutations 58 histone acetylation 58 posttranslational modifications 58 FGFR2 58 Apc 58 mammary gland tumors 58 RUNX3 58 #q# deletion 58 asymptomatic carriers 58 Chlamydia trachomatis 58 holoprosencephaly 58 multigenic 57 Dpp 57 Neisseria meningitidis 57 tubercle bacillus 57 ALK gene 57 chlamydial 57 chromosome #q# [002] 57 Dystrophin 57 genus Plasmodium 57 hyper IgE syndrome 57 Plasmodium vivax 57 neuronal dysfunction 57 herpes viruses 57 metazoan 57 KCNE2 57 FGFR3 57 FGFs 57 Folic acid deficiency 57 colocalization 57 gene expression patterns 57 Xenopus 57 #q#.# [002] 57 coexpression 57 BRAF protein 57 generalized vitiligo 57 KLF4 57 PrPSc 57 mitochondrial gene 57 lung adenocarcinomas 57 HFE gene 57 prion protein gene 57 neurofibromas 57 gene mutation 57 Anaplasma 57 monozygotic 57 murine leukemia virus 57 mutant huntingtin protein 57 isoenzymes 57 protein tyrosine phosphatase 57 transfusion syndrome 57 genetic imprinting 57 methyltransferase 57 atypical scrapie 57 TOP2A gene 57 quantitative trait loci 57 S. typhimurium 57 neuritic 57 Cathepsin B 57 BRAF gene 57 methylation patterns 57 Streptococcus agalactiae 57 CHEK2 57 Beta thalassemia 57 GNAQ 57 lymphocytic 57 autosomal 57 TIR1 57 genomic instability 57 JAK2 mutation 57 clefting 57 Yersinia enterocolitica 57 evolvability 57 serovar 57 microglial 57 inherited maternally 57 CYP #D# 57 Plasmodium infection 57 epigenetic markers 57 overactivation 57 collagen VI 57 granulosa cell 57 MMP# 57 gene polymorphisms 57 klotho 57 thymidine kinase 57 Bardet Biedl syndrome 57 thale cress 57 IL#R 57 Citrobacter 57 susceptibility gene 57 bacteraemia 57 autosomes 57 M. genitalium 57 cytopathic 57 monozygotic twin 57 GIST tumors 57 motor neuron degeneration 57 A. fumigatus 57 olfactory receptor 57 nonvascular 57 homozygous 57 asexual reproduction 57 Salmonella enterica 57 Chlamydia pneumoniae 57 MTHFR 57 Trypanosoma cruzi 57 mutational 57 Moraxella bovis 57 ERK signaling 57 phylogenetically 57 Upregulation 57 nodulation 57 M. capricolum 57 causal variants 57 HepG2 cells 57 epidermidis 57 apolipoprotein E4 57 pyloric stenosis 57 mammary tumors 57 beta globin 57 multigene 57 Trichomonas vaginalis 57 penetrance 57 p# mutation 57 operons 57 lysine residues 57 adenylate cyclase 57 #p#.# [002] 57 ductal lobular 57 causative pathogens 57 missense 57 Immunohistochemical analysis 57 childhood leukemias 57 Borrelia burgdorferi 57 paraganglioma 57 CYP#D# gene 57 Treg cell 57 SSc 57 uterine tumors 57 flavivirus 57 genomic deletions 57 Toxoplasmosis 57 mutant proteins 57 demethylation 57 gambiae 57 UGT#A# * 57 beta globin gene 57 HHV 6 57 spermidine 57 tumor suppressor protein 57 fruitfly Drosophila 57 Toxoplasma 57 genetic defect 57 transgenic rats 57 Apert syndrome 57 Enterobacter 57 X. laevis 57 dopamine receptor gene 57 neuron degeneration 57 aetiological 57 SLC#A# [001] 57 neuro endocrine 57 Treponema 57 Intussusception 57 recessive gene 57 CREBBP 57 A. phagocytophilum 57 PrP 57 Neisseria gonorrhoeae 57 spore formation 57 genetic abnormality 57 MYH9 gene 57 HLA alleles 57 nephrogenic 57 amyloid deposition 57 apolipoprotein E APOE 57 eukaryote 57 hydrops 57 familial clustering 57 Genetic predisposition 57 receptor gene 57 opportunistic pathogen 57 Arabidopsis plants 57 epigenetic regulation 57 Male pattern baldness 57 RNA polymerases 57 IDH mutations 57 alveolar epithelial cells 57 HbF 57 LVNC 57 aneuploid cells 57 BMPR2 57 Y chromosomal 57 KIAA# 57 microsatellite markers 57 placental function 57 homolog 57 inactive X chromosome 57 histologic subtype 57 H. influenzae 57 Ras oncogene 57 toxoplasma 57 fungal pathogen 57 leucocytes 57 Cockayne syndrome 57 inducible nitric oxide synthase 57 chromosomal regions 57 G6PD 57 mammary cells 57 NF1 57 Pathogenicity 57 metabolizing enzymes 57 Phytophthora sojae 57 pRb 57 kDa protein 57 cultured neurons 57 apoE 57 eukaryotic cell 57 hyperactivation 57 haploid 57 p# MAPK 57 HLA DQ2 57 GSTP1 56 genes predisposing 56 Sporadic CJD 56 peroxisome 56 Cyclin D1 56 Foxp3 56 Staphylococcus epidermidis 56 thrombophilia 56 S. maltophilia 56 cellular prion protein 56 distantly related species 56 ADH1B * 56 hyperactivated 56 heritable 56 ependymoma 56 chromosome abnormalities 56 airway remodeling 56 Escherichia coli Klebsiella pneumoniae 56 prokaryote 56 KRAS BRAF 56 neural crest cells 56 primordial germ cells 56 VKORC1 56 mitochondrial defects 56 Hox gene 56 gastric adenocarcinoma 56 premalignant lesions 56 Akt signaling 56 breast cancer subtypes 56 Wnt signaling 56 amyloid peptide 56 Infectivity 56 coevolution 56 NPC1 56 seminomas 56 SOD1 gene 56 COL#A# 56 ADRB2 56 bronchopulmonary dysplasia 56 chromatin structure 56 recessive traits 56 genetic relatedness 56 phenotype 56 Malaria parasite 56 quasispecies 56 Toxoplasma gondii 56 single celled parasite 56 glutamic acid decarboxylase 56 BRCA1 gene 56 corona virus 56 P aeruginosa 56 aneuploidy screening 56 mitochondrial dysfunction 56 sensu lato 56 allelic 56 HER2 positivity 56 homocystinuria 56 Mycoplasma genitalium 56 incomplete penetrance 56 Jhdm2a 56 prion protein PrP 56 neoplasias 56 NRTI resistance 56 genetic variation 56 embryonal 56 Phytophthora species 56 FGFR2 gene 56 pneumoniae 56 genetic heterogeneity 56 indel 56 gastrulation 56 B. subtilis 56 endocannabinoid signaling 56 APOA5 56 IFN gamma 56 Fig. 1E 56 RT PCR assay 56 BDNF protein 56 clonally 56 plectasin 56 microsporidia 56 CYP#C# * 56 clonal 56 chimerism 56 D#N 56 corticosterone levels 56 bacterium Neisseria meningitidis 56 rs# [004] 56 systemic amyloidosis 56 C. jejuni 56 BVDV 56 Trichinella 56 gastric carcinoma 56 phenotypic variability 56 membrane fusion 56 ribosomal protein 56 antiphospholipid antibodies 56 orthologous genes 56 BMP4 56 activin 56 telomere shortening 56 fetal malformations 56 splice junctions 56 hypoperfusion 56 sexually dimorphic 56 Bt toxin 56 dizygotic twins 56 mitochondrial enzyme 56 LKB1 56 homologs 56 bacterium E. coli 56 Volvox 56 C#Y 56 GSTT1 56 Enterobacter cloacae 56 serotype 56 commensal bacteria 56 protein encoded 56 HCMV 56 Leukemias 56 Prevotella 56 falciparum 56 parasite Toxoplasma gondii 56 microsatellite instability 56 ß1 56 GABHS 56 mycobacterial 56 S. aureus infection 56 ERK1 2 56 CNTNAP2 gene 56 serogroup 56 neurodegenerative disorder 56 parainfluenza virus 56 PAX5 56 familial aggregation 56 human herpesvirus 56 hamartomas 56 PML RARA 56 Single Nucleotide Polymorphisms SNPs 56 C. trachomatis 56 nonsense mutations 56 IRS1 56 valine 56 transgenesis 56 amyloid cascade 56 lymphangiogenesis 56 P falciparum 56 G#S mutation 56 caveolin 56 BRCA1 mutations 56 replicon 56 fig. S4 56 fungus infects 56 eusociality 56 mutated BRCA1 56 mammalian genomes 56 dimorphic 56 FLT3 56 nucleotide sequence 56 syngeneic 56 posttranslational modification 56 Plasmodium falciparum 56 melanocyte 56 Drosophila melanogaster 56 K ras mutations 56 LRP6 56 M. catarrhalis 56 villous atrophy 56 #S rRNA gene 56 PFGE 56 V. cholerae 56 inherited predisposition 56 GBM tumors 56 arterial calcification 56 biogenesis 56 transcriptional activation 56 synapse formation 56 serotype #A 56 brain lesions 56 Trichomonas 56 ductal adenocarcinoma 56 CYP#A# gene 56 LQTS 56 previously uncharacterized 56 phenotypic plasticity 56 Deinococcus 56 ortholog 56 BRCA2 gene mutation 56 OGG1 56 esophageal squamous cell carcinoma 56 Fig. 3b 56 structural rearrangements 56 H pylori 56 TRAF1 C5 56 globin 56 substrate specificity 56 MMP9 56 oesophageal adenocarcinoma 56 recessive inheritance 56 Typhimurium 56 myocardial fibrosis 56 DLX5 56 epithelial barrier 56 #S rRNA 56 chromosomal abnormalities 56 constitutively expressed 56 hydrolase 56 transmembrane protein 56 clades 56 DEC2 56 Pten 56 PCV2 56 karyotype 56 situs inversus 56 Oncogenic 56 parasitaemia 56 predisposing factor 56 PCNSL 56 eukaryotic organisms 56 sporulation 56 medium spiny neurons 56 MnSOD 56 ubiquitylation 56 genome rearrangements 56 thyroid dysfunction 56 cerebral vasospasm 56 linkage disequilibrium 56 Pseudomonas syringae 56 Meckel Gruber 56 superinfection 56 mutagenesis 56 myotonic dystrophy 56 abnormal prion protein 56 sympatric speciation 56 clostridium 56 striated muscle 56 #BP# 56 tetraploid 56 morphological traits 56 hypermethylation 56 colorectal tumor 56 Germline 56 tumor regressions 56 M. leprae 56 Sonic hedgehog 56 ApoE gene 56 immunoreactivity 56 APOE e4 56 immunoblotting 56 NQO1 56 hemoglobins 56 cellularity 56 Drosophila genome 56 untranslated regions 56 intronic 56 metazoans 56 #q# [001] 56 orthologous 56 myeloid 56 toxoplasma gondii 56 TET2 56 germline 56 parthenogenetic 56 teratoma 56 CMV infections 56 regulator CFTR gene 56 APOE4 56 CagA 56 pH#N# 56 MC1R 56 mitochondrial DNA mtDNA 56 variant alleles 56 Listeria infections 56 transmembrane receptor 56 severe congenital neutropenia 56 tetramer 56 CDK4 56 constitutive activation 56 metabolomic profiles 55 FMRP protein 55 Bt toxins 55 polygenic 55 carcinoid tumor 55 pDC 55 QTL mapping 55 IDH1 55 abnormal prions 55 hepatic metastasis 55 H#K# [002] 55 mitochondrial fusion 55 familial adenomatous polyposis 55 IGF2 55 microfilariae 55 NEIL1 55 fronto temporal dementia 55 ciliated 55 aortic atherosclerosis 55 somites 55 malignant phenotype 55 parasite Plasmodium 55 resistant mutants 55 MAP#K# 55 infectious prion proteins 55 albicans 55 ubiquitination 55 P. reichenowi 55 tau mutation