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(Click for frequent words.) 85 mutations 82 genetic mutation 79 mutated gene 78 gene mutation 74 genetic mutations 73 gene 73 gene mutations 72 genetic variant 72 alleles 71 mutant gene 70 spontaneous mutation 69 defective gene 69 gene variant 69 genes 68 BRCA1 gene 67 genetic defect 67 mutated genes 67 allele 66 genetic alteration 66 heterozygous 66 FMR1 gene 66 haplotype 66 polymorphism 66 phenotype 65 mutant alleles 65 germline mutations 65 tumor suppressor gene 65 X chromosome 65 polymorphisms 65 genetic abnormalities 64 BRCA2 gene 64 genetic variation 64 microcephalin 64 genetic abnormality 64 mutated 64 homozygous 64 CDH1 64 genotype 64 gene variants 64 CFTR gene 64 APOE4 64 spontaneous mutations 64 missense mutation 63 G#S mutation 63 autosomal recessive 63 breast cancer genes BRCA1 63 missense mutations 63 TP# mutation 63 MSH2 63 progranulin gene 63 mosaicism 63 NF1 gene 63 MC1R gene 63 huntingtin gene 63 C#Y 63 PTPN# 63 BRCA1 63 methylation 63 LIS1 62 germline mutation 62 genetic 62 LRRK2 gene 62 familial ALS 62 parkin gene 62 recessive mutations 62 recessive gene 62 mtDNA mutations 62 mutant protein 62 BRCA1 mutations 62 susceptibility gene 62 mutant allele 62 inherited mutations 62 genotypes 62 Mutation 62 VHL gene 62 genetic variations 62 chromosomal 62 BRCA2 mutation 61 apolipoprotein E gene 61 heterozygotes 61 mtDNA 61 ApoE4 gene 61 genetic variants 61 genetic alterations 61 mutational 61 RUNX3 61 endogenous retroviruses 61 miRNA genes 61 BRCA mutations 61 MLH1 61 chromosomal translocations 61 aneuploidy 61 somatic mutations 61 chromosome 61 heterozygote 61 PALB2 61 MECP2 gene 61 genetic defects 61 CNVs 61 LRAT 61 retrovirus 61 ZNF# 61 TACI mutations 61 FGFR2 61 overexpression 61 malignant transformation 60 KRAS gene 60 BRCA mutation 60 MTHFR 60 HLA B# 60 homozygosity 60 herpesviruses 60 amino acid substitution 60 H#Y 60 TCF#L# gene 60 gene variation 60 gene rearrangements 60 BRAF gene 60 chromosomal aberrations 60 Fragile X gene 60 autosomal dominant 60 genetic trait 60 ApoE4 60 SNPs 60 subtype 60 EGFR gene 60 HNPCC 60 microdeletions 60 tumor suppressor protein 60 sporadic ALS 60 maternally inherited 60 acetylation 60 suppressor gene 60 transgene 60 mitochondrial mutations 60 susceptibility genes 60 BRCA1 mutation 60 MLL gene 60 mutated protein 60 trypanosome 59 virulence genes 59 prion disease 59 p# mutations 59 CHEK2 59 HLA genes 59 homozygotes 59 BARD1 59 mice lacking 59 CCR5 delta# 59 hypermethylation 59 Foxp3 59 homologs 59 MTHFR gene 59 kinase gene 59 K ras gene 59 genes encoding 59 miRNAs 59 recessive trait 59 heritable 59 Akt1 59 mitochondrial dysfunction 59 chromosomal rearrangements 59 beta thalassemia 59 GNAQ 59 X inactivation 59 genomes 59 IKZF1 59 chromosome abnormality 59 HGPS 59 alternatively spliced 59 PTEN gene 59 multidrug resistance 59 DNA methylation 59 penetrance 59 IGF2 59 TP# gene 59 epigenetic silencing 59 Y chromosome 59 somatic mutation 59 genomic instability 59 CHD7 59 MLL2 59 K#R [002] 59 chromosomal abnormalities 59 activating mutations 59 BRCA2 59 IgA deficiency 59 protein encoded 59 proto oncogene 59 HFE gene 59 gene expression 59 HLA alleles 59 BRCA gene 58 HMGA2 58 genes predisposing 58 medulloblastomas 58 chromosomal rearrangement 58 APOE gene 58 haplotypes 58 H#K# methylation 58 recessive mutation 58 alpha synuclein gene 58 Prox1 58 Alu elements 58 causal variants 58 herpes viruses 58 APOE e4 58 mitochondrial genome 58 enzymatic activity 58 mutant genes 58 IGF1 58 recessive genes 58 genetically 58 CCR5 mutation 58 histone modification 58 APOL1 58 loci 58 tumor suppressor genes 58 #q# [001] 58 allelic variants 58 de novo mutations 58 orthologs 58 epigenetically 58 epigenetic alterations 58 PrPSc 58 genomic rearrangements 58 APOE 58 myostatin gene 58 oncogenic 58 proband 58 intron 58 germline 58 P. falciparum 58 genetic makeup 58 evolutionarily conserved 58 Helicobacter 58 CDKN2A 58 STAT4 58 pathogenic mutations 58 Six3 58 cyclin D1 58 tyrosine phosphorylation 58 mutant strain 58 mRNAs 58 ALK gene 58 SOD1 gene 58 HCMV 58 EBV infection 58 gene locus 58 JAK2 gene 58 TMEM#B 58 NF1 58 MeCP2 gene 57 frameshift mutation 57 p# gene 57 HTLV 57 #q#.# [001] 57 tumor suppressor 57 autosomal 57 HbF 57 uPAR 57 estrogen receptor 57 imprinted genes 57 genes BRCA1 57 Vpu 57 endostatin 57 ApoE 57 MC1R 57 microdeletion 57 autosomal dominant disorder 57 apoE4 57 EBNA1 57 chromosomal instability 57 isoform 57 translocations 57 variant alleles 57 ubiquitination 57 MAPK pathway 57 phenotypes 57 Wwox 57 progerin 57 globin 57 epigenetic changes 57 SMN1 57 mRNA transcripts 57 transcriptional repressor 57 Li Fraumeni syndrome 57 Mycobacterium tuberculosis 57 SOD1 protein 57 genome 57 ERBB2 57 BRAF V#E 57 homozygote 57 chromosomal abnormality 57 AAV2 57 epigenetic 57 nucleotide sequence 57 transgene expression 57 SRY gene 57 SORL1 57 ADPKD 57 nonsense mutation 57 measles virus 57 T. gondii 57 PTEN mutation 57 RNAs 57 SGK1 57 SCN5A 57 LKB1 57 SMN1 gene 57 CNTNAP2 gene 57 IDH2 57 linkage disequilibrium 57 Epstein Barr virus EBV 57 BRIP1 57 N Myc 57 MYH9 gene 57 H. pylori 57 promoter methylation 57 breast carcinomas 57 IDH1 57 G#S [002] 57 single nucleotide polymorphism 57 FLT3 57 SMN2 gene 57 Wolbachia 57 Pten 57 outer membrane proteins 57 genetic recombination 57 PB1 F2 57 nonsense mutations 57 karyotypes 57 herpes virus 57 prion protein gene 57 CGG repeats 57 genetic polymorphism 57 pneumococci 57 GSTP1 57 CCL#L# 57 mammary cells 57 CYP#E# gene 57 PrP 57 defensin 57 APOE4 gene 57 KIF6 gene 57 constitutively 57 Kufs disease 57 serotype 56 Plasmodium falciparum 56 gene encoding 56 CYP#D# gene 56 BRCA1 BRCA2 56 KRAS oncogene 56 PAX5 56 mutated BRCA1 56 NF2 56 mitochondrial 56 FMR1 56 prion gene 56 CagA 56 MnSOD 56 causative gene 56 gene expression patterns 56 anaplastic lymphoma kinase 56 PON1 56 MC4R gene 56 Toxoplasma 56 progranulin 56 transgenic mouse model 56 protein p# 56 apoE 56 CDK4 56 X chromosomes 56 #q# [002] 56 PIK3CA 56 micro RNAs 56 recombination 56 FASPS 56 Htt 56 RPE# 56 WT1 56 palladin 56 Rickettsia 56 Skp2 56 DSBs 56 regulator CFTR gene 56 EZH2 56 Cyclin D1 56 NF κB activation 56 Wnt signaling 56 LRRK2 56 breast cancer metastasis 56 BRCA genes 56 chromosome rearrangements 56 receptor gene 56 E#F# 56 autosomal recessive disease 56 viral genome 56 Genetic variation 56 LQTS 56 nucleotide substitution 56 C. neoformans 56 monogenic 56 FTLD 56 tau gene 56 unmutated 56 Jhdm2a 56 GSTM1 gene 56 sequence homology 56 ALK mutations 56 Plasmodium 56 MSH6 56 IDH1 gene 56 genetic markers 56 trypanosomes 56 phenotypic variation 56 melanocyte 56 germline cells 56 EGFR mutations 56 pRb 56 Mutations 56 chromosomal alterations 56 COX2 56 Notch1 56 TGFBR1 * 6A 56 KLF# 56 aneuploid 56 unmethylated 56 HLA molecules 56 chromosome #q# [002] 56 genomic imprinting 56 TRIM5 56 phosphorylation 56 neuroblastomas 56 autoantibodies 56 Dpp 56 C1q 56 APOE ε4 56 RNA viruses 56 CAG repeats 56 JAK2 mutation 56 coding sequences 56 G6PD 56 major histocompatibility complex 56 K ras mutations 56 prion infection 56 chromosome #q# [001] 56 haplogroup 56 methylation patterns 56 transcriptional repression 56 beta globin 56 transgenes 56 achromatopsia 56 phosphorylate 56 gene MECP2 56 substrate specificity 56 sCJD 56 mycobacterium 56 transactivation 56 FANCD2 56 phenotypically 56 genetic rearrangements 56 Heterozygous 56 germ cells 56 APOE e4 gene 56 cystic fibrosis transmembrane conductance 56 Pin1 56 GBM tumors 56 p# protein 56 activin 55 deacetylation 55 HLA DQ2 55 presenilin 55 #p#.# [002] 55 chromosome #p# [001] 55 E1A 55 COMT gene 55 SMN2 55 receptor protein 55 RPE# gene 55 telomere shortening 55 heterozygosity 55 myotonic dystrophy 55 NFkB 55 mycobacterium tuberculosis 55 ncRNAs 55 familial pancreatic cancer 55 chromosome #q#.# [001] 55 amino acid sequence 55 BRAF mutation 55 neuroblastoma tumors 55 BCL#A 55 globin genes 55 LMNA 55 karyotype 55 Plasmodium parasites 55 primordial germ cells 55 mutant proteins 55 receptor molecule 55 exons 55 KCNE2 55 corona virus 55 deleterious mutations 55 ubiquitylation 55 huntingtin protein 55 variant allele 55 kinases 55 epistasis 55 NPC1 55 CNTNAP2 55 GSTT1 55 BRAF protein 55 apolipoprotein E 55 APOC3 55 nucleotide 55 ectopic expression 55 transthyretin 55 UGT#B# 55 BRCA gene mutation 55 malaria parasite Plasmodium falciparum 55 exon 55 DNA rearrangements 55 mammary cancers 55 phenotypic expression 55 TAp# 55 hypermethylated 55 transcriptional regulation 55 transcription factor 55 K#N 55 protein fragment 55 dopamine receptor gene 55 SLC#A# [001] 55 conformational 55 CYP# [002] 55 SATB1 55 PKD1 55 homologue 55 A. thaliana 55 medulloblastoma 55 HPV# 55 genomic deletions 55 pseudogenes 55 APOE allele 55 MIF protein 55 GPR# [002] 55 homolog 55 FOXP2 gene 55 V#F mutation 55 genetic variability 55 MHC genes 55 synuclein 55 BRCA 55 chromosomes 55 protein 55 SLC#A# gene [001] 55 mutant worms 55 microglial 55 endosymbiosis 55 familial adenomatous polyposis 55 proteins 55 Fanconi anemia 55 tumor suppressor p# 55 catenin 55 clade B 55 malaria parasite 55 rs# [003] 55 LRRK2 mutation 55 chromatin structure 55 TTR gene 55 DNMT1 55 vimentin 55 proteolytic cleavage 55 DNA methylation patterns 55 PKM2 55 oncoprotein 55 Y chromosomes 55 gene sequences 55 kinase 55 SHANK3 55 ovarian tumors 55 aneuploidies 55 Hox gene 55 mitochondrial DNA mtDNA 55 SLC#A# [002] 55 phenotypic 55 CYP#C# * 55 noncoding RNAs 55 viral genomes 55 LRP5 55 Immunohistochemical analysis 55 RAR beta 55 fusion protein 55 caveolin 55 p# [001] 55 antisense RNA 55 bacterium 55 M. pneumoniae 55 overexpress 55 CEACAM1 55 C EBP alpha 55 deleterious mutation 55 E cadherin 55 histone modifications 55 EGFRvIII 55 Leptospira 55 TB bacterium 55 JAK2 55 DLX5 55 enteroviruses 54 chromosome abnormalities 54 mRNA 54 abnormal chromosomes 54 microRNA molecules 54 Bcl2 54 poxvirus 54 NR#A# gene 54 genotyped 54 dyskeratosis congenita 54 neural crest 54 glycosylation 54 DHFR 54 transfected cells 54 transmembrane protein 54 MDM2 54 Clusterin 54 Chlamydia trachomatis 54 downregulation 54 GFP gene 54 RASSF1A 54 CRISPR Cas 54 RNA molecules 54 leukemic stem cells 54 gene amplification 54 nestin 54 clusterin 54 epigenetic mechanisms 54 chromosomal defect 54 FTO gene 54 Nf1 54 IL#R 54 succinate dehydrogenase 54 SOX3 gene 54 commensal bacteria 54 IDH1 mutation 54 Src 54 hTERT 54 chromosomal regions 54 transcription factors 54 Cockayne syndrome 54 HER2 gene 54 HLA DRB1 54 EGFR mutation 54 segmental duplications 54 LPA gene 54 meiotic recombination 54 TCF#L# 54 beta1 integrin 54 chromosome #q 54 oncogene 54 Peutz Jeghers syndrome 54 SMAD4 54 SORL1 gene 54 dystrophin gene 54 parainfluenza virus 54 lactase persistence 54 neurodegenerative disorder 54 rs# [002] 54 Methylation 54 cyclin E 54 Apobec3 54 polyomavirus 54 H#Y mutation 54 transmembrane receptor 54 microsatellite instability 54 alternative splicing 54 mutant huntingtin protein 54 endogenous retrovirus 54 JAK2 enzyme 54 antigenic shift 54 P. infestans 54 genetically identical 54 virulence determinants 54 causative genes 54 varicella zoster virus 54 H#N# viruses 54 Cx# [001] 54 ApoE4 allele 54 protein kinases 54 JAK mutations 54 MECP2 54 miRNA expression 54 adipogenic 54 SCN1A 54 STAT1 54 mitochondrial gene 54 mRNA decay 54 polyploidy 54 ABCB1 54 Candida species 54 Hepatitis B virus 54 Chromosome 54 Arabidopsis genome 54 activating mutation 54 MIF gene 54 Ets2 54 transgenic rats 54 piRNAs 54 ras gene 54 proteolysis 54 heterochromatin 54 colorectal tumors 54 agouti gene 54 H2AX 54 KLF4 54 genetic heterogeneity 54 MAOA gene 54 premutation 54 RCAN1 54 constitutively active 54 RNA splicing 54 molecular mechanism 54 variant 54 abnormal hemoglobin 54 p# MAPK 54 M. leprae 54 regulates gene expression 54 GISTs 54 N. gonorrhoeae 54 retroviruses 54 mutant 54 #q#.# [002] 54 abnormal prions 54 KIAA# 54 Smad3 54 VIPR2 54 3'UTR 54 holoprosencephaly 54 mutant p# 54 NKT cells 54 phosphorylated 54 prion protein 54 COL#A# 54 beta globin gene 54 downregulated 54 Epstein Barr virus 54 Argonaute 54 TET2 54 genetic susceptibility 54 YKL 54 DLC1 54 lentivirus 54 Meckel Gruber 54 ERK2 54 claudin 54 PDGFR 54 cytoplasmic tail 54 miRNA 54 prion proteins 54 tau mutation 54 retroviral 54 CFH gene 54 inherited neurological disorder 54 Mitochondrial 54 p# mutation 54 signaling pathway 54 NOTCH1 54 rotaviruses 54 gene p# 54 genomewide 54 mutated K ras 54 aldehyde dehydrogenase 54 OPRM1 gene 54 IL# [001] 54 ALDH2 54 microRNA expression 54 clade C 54 LRP6 54 dedifferentiation 54 ALDH2 enzyme 54 Rap1 54 syngeneic 54 methyltransferases 54 PTP1B 54 epigenetic modifications 54 Dystrophin 54 Cryptococcus neoformans 54 mitochondrial DNA mutations 54 Brugada syndrome 54 synaptogenesis 54 CD#c 54 mitochondrial genomes 53 Bcl xL 53 toxoplasmosis 53 CCR5 gene 53 DRD2 gene 53 H#K# [001] 53 transposable elements 53 FUS TLS 53 murine leukemia virus 53 OCA2 53 mRNA expression 53 promoter hypermethylation 53 ADAM# 53 HMGA2 gene 53 PDGFRA 53 fetal hemoglobin 53 R#W [002] 53 tumorigenesis 53 BMP2 53 GPC5 53 caveolin 1 53 rifamycins 53 genetic disorder 53 molecular pathway 53 TP# mutations 53 iNOS 53 short hairpin RNAs 53 autoantibody 53 tubercle bacillus 53 splice junctions 53 malarial parasite 53 asymptomatically 53 HAR1 53 Neanderthal genes 53 histone deacetylases 53 peroxisome 53 centromeres 53 homodimers 53 transgenic mice 53 MEF2A 53 dephosphorylation 53 PARP inhibition 53 #p# [001] 53 Myc 53 hereditary deafness 53 Leydig cells 53 serine threonine kinase 53 KCNQ1 53 miR 53 olfactory receptor 53 #S rRNA gene 53 osteopontin 53 genomic alterations 53 P. vivax 53 eukaryote 53 Trypanosoma brucei 53 nucleotide substitutions 53 molecular abnormalities 53 colorectal carcinoma 53 coexpression 53 neural crest cells 53 DNA sequences 53 CLL cells 53 CHIKV 53 MyoD 53 M. genitalium 53 GSTM1 53 vesicular stomatitis virus 53 ChR2 53 immunoglobulin genes 53 Plasmodium vivax 53 filaggrin gene 53 beta galactosidase 53 BDNF gene 53 RNA polymerase II 53 sRNA 53 staphylococci 53 outcrossing 53 short hairpin RNA 53 gut microbes 53 genetic polymorphisms 53 resistant isolates 53 palmitoylation 53 IL#B 53 epigenetic modification 53 GAB2 53 FXTAS 53 DNMT3A 53 KSHV 53 gene APOE4 53 Brugada Syndrome 53 nucleotide variations 53 mitochondrial DNA 53 genotypic 53 follistatin 53 trisomy 53 Dicer enzyme 53 amino acid substitutions 53 intronic 53 epitope 53 dystrophin 53 gamma globin gene 53 viral proteins 53 leptin receptors 53 mitochondrial proteins 53 SLITRK1 53 lineages 53 yeast genome 53 oncogenes 53 ARID1A 53 hereditary disorder 53 S. cerevisiae 53 codons 53 transcriptional activation 53 microRNAs 53 CFTR protein 53 BRCA2 gene mutation 53 metazoan 53 CXCL# 53 simian virus 53 malignancy 53 microRNA miR 53 demethylation 53 Inactivation 53 BRCA2 mutations 53 CIB1 53 ApoE gene 53 codon 53 severe congenital neutropenia 53 lamin 53 CD8 + 53 Angelman syndrome 53 morphogen 53 lung adenocarcinoma 53 S. enterica 53 ε4 53 genetic traits 53 allele frequencies 53 ABCA1 53 inactive X chromosome 53 G allele 53 Genetic mutations 53 #p#.# [001] 53 H5 viruses 53 microsporidia 53 dopamine D4 receptor 53 transgenic mouse models 53 SOD2 gene 53 DICER1 gene 53 NRTI resistance 53 IDH mutations 53 T#I [002] 53 bacterium Listeria 53 RhoA 53 encodes protein 53 NKX#.# 53 thrombospondin 53 androgen receptor 53 GRP# 53 leukemic cell 53 CD1d 53 DICER1 53 ES cells 53 valine 53 fusogen 53 non coding RNA 53 NPM1 gene 53 mesotheliomas 53 beta catenin 53 Mycoplasma pneumoniae 53 GAPDH 53 FMRP protein 53 epigenetic inheritance 53 CALHM1 53 NR#A# 53 gp# [002] 53 D#G 53 ribosomal protein 53 PTEN mutations 53 paralogs 53 MHC molecules 53 chitinase 53 human leukocyte antigen 53 FGFR4 53 HLA B 53 RNA molecule 53 miR #b [001] 53 SMN protein 53 intergenic 53 EGFR 53 Rad# 53 genotoxic stress 53 RKIP 53 mesenchymal cell 53 HOX genes 53 cofilin 53 testis 53 oncoproteins 53 GBV C 53 histocompatibility 53 lacZ 53 Pax6 53 c KIT 53 leukemic cells 53 coding genes 53 antibodies 53 prion diseases 53 replicase 53 metalloprotease