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(Click for frequent words.) 79 mutations 78 genetic mutations 75 gene variants 75 gene mutation 74 genetic variants 73 mutated genes 73 genetic variations 73 mutation 73 genetic mutation 72 genetic abnormalities 71 genes 69 mutated gene 68 genetic defects 68 genetic variation 67 BRCA1 gene 67 genetic alterations 66 gene variant 66 susceptibility genes 66 genetic variant 66 polymorphisms 66 chromosomal abnormalities 65 alleles 65 gene 64 BRCA2 gene 64 miRNAs 64 BRCA mutations 64 genetic defect 64 inherited mutations 64 tumor suppressor gene 63 BRCA1 63 spontaneous mutations 63 SNPs 63 epigenetic 63 epigenetic changes 63 CNVs 63 BRCA1 mutations 63 LRRK2 gene 63 genetic susceptibility 63 mtDNA mutations 63 breast cancer genes BRCA1 62 mutant gene 62 chromosomal regions 62 somatic mutations 62 gene variation 62 micro RNAs 62 BRCA mutation 62 microdeletions 62 epigenetic alterations 62 germline mutations 62 noncoding RNAs 62 mitochondrial dysfunction 62 HLA genes 62 BRCA2 62 defective gene 61 gene expression patterns 61 G#S mutation 61 microRNAs 61 PTPN# 61 epigenetic mechanisms 61 genetic variants associated 61 haplotype 61 PTEN mutations 61 de novo mutations 61 APOE gene 61 PALB2 61 MSH2 61 susceptibility gene 61 proteins 61 genetic abnormality 61 BRCA2 mutation 61 genetic markers 61 missense mutations 61 familial ALS 61 MTHFR 61 genetic polymorphisms 61 mutant genes 61 BRAF gene 61 FGFR2 61 MLH1 61 p# mutations 61 protein kinases 61 loci 60 tumor suppressor genes 60 BRCA genes 60 DNA methylation 60 methylation 60 ApoE4 gene 60 familial pancreatic cancer 60 gene expression 60 chromosome rearrangements 60 aneuploidy 60 hypermethylation 60 phenotypes 59 genomes 59 chromosomal instability 59 molecular pathways 59 CDH1 59 genes encoding 59 microRNA molecules 59 HNPCC 59 spontaneous mutation 59 genetic alteration 59 HGPS 59 haplotypes 59 TACI mutations 59 chromosomal aberrations 59 chromosomal translocations 59 heterozygous 59 LQTS 59 chromosomal rearrangements 59 LIS1 59 SOD1 gene 59 sporadic ALS 59 nonsense mutations 59 imprinted genes 59 CHD7 59 APOE4 59 recessive mutations 59 C#Y 59 APOE e4 59 medulloblastomas 59 IgA deficiency 59 causative gene 59 mutated BRCA1 59 MECP2 gene 59 mRNAs 59 Genetic variants 59 molecular abnormalities 59 aneuploidies 58 genetic 58 MYH9 gene 58 genetic disorders 58 LRRK2 58 Skp2 58 overexpression 58 mutant protein 58 BRCA1 mutation 58 BRCA2 mutations 58 endometrial cancers 58 herpesviruses 58 genomewide 58 pathogenic mutations 58 #q# [001] 58 autoantibodies 58 miRNA genes 58 genes BRCA1 58 mutated protein 58 allele 58 PIK3CA 58 penetrance 58 clusterin 58 TGFBR1 * 6A 58 FMR1 gene 58 genotypes 58 abnormalities 58 WT1 58 malignant transformation 58 BRCA2 gene mutations 58 genotype 58 genetic polymorphism 58 CHEK2 58 PTEN gene 58 miRNA 58 EZH2 58 tyrosine kinases 58 narcolepsy cataplexy 58 cellular pathways 57 lung adenocarcinoma 57 NF1 57 basal cell nevus syndrome 57 mutant alleles 57 X chromosome 57 RNA molecules 57 palladin 57 apoC III 57 homozygosity 57 miRNA expression 57 Genetic variations 57 Six3 57 beta catenin 57 cancers 57 phenotype 57 GSTP1 57 VHL gene 57 neuroblastomas 57 JAK mutations 57 Notch1 57 CFTR gene 57 oncogenes 57 SORL1 57 causal variants 57 apolipoprotein E gene 57 TP# mutation 57 chromosomal anomaly 57 molecular pathway 57 gene locus 57 ALK mutations 57 chromosomal 57 MLL2 57 breast cancer metastasis 57 HMGA2 57 APOE allele 57 microcephalin 57 chromosomal alterations 57 RNAs 57 genetic trait 57 APOL1 57 transcription factors 57 #q#.# [001] 57 beta1 integrin 57 alpha synuclein gene 57 tumor suppressor protein 57 kinases 57 familial adenomatous polyposis 57 cyclin D1 57 genomic instability 57 gene fusions 57 HbF 57 genetic aberrations 57 histone modifications 57 hereditary breast cancer 57 TMEM#B 57 CYP#E# gene 57 KIT mutations 57 medulloblastoma 57 SMN2 gene 57 mitochondrial disorders 57 NF1 gene 57 Li Fraumeni syndrome 57 histone modification 57 Li Fraumeni 57 virulence genes 57 causative genes 57 mosaicism 56 EGFR mutations 56 TCF#L# 56 FMRP protein 56 genomic rearrangements 56 non coding RNAs 56 microdeletion 56 ZNF# 56 FANCD2 56 HLA B# 56 estrogen receptor 56 chromosome aberrations 56 GPC5 56 BRAF mutation 56 TCF#L# gene 56 apoE4 56 epigenetic modification 56 ALK gene 56 genetic determinants 56 SIRT3 56 CNTNAP2 56 mammary cells 56 CNTNAP2 gene 56 APOE ε4 56 MYH9 56 colorectal neoplasia 56 chromosome abnormalities 56 PARP inhibition 56 SLC#A# [002] 56 BRIP1 56 BARD1 56 genetic syndromes 56 protein encoded 56 APOE 56 transcriptional repression 56 apolipoprotein E 56 mitochondrial mutations 56 TP# mutations 56 ovarian tumors 56 lincRNAs 56 progranulin 56 Fanconi anemia 56 ADPKD 56 genes predisposing 56 breast cancers 56 folate metabolism 56 acetylation 56 Src 56 MGUS 56 IL#R 56 FMR1 56 chromosomal defects 56 BRCA1 BRCA2 56 exomes 56 S#A# [002] 56 Foxp3 56 Wnt pathway 56 heterozygotes 56 testicular germ cell 56 epigenetic silencing 56 promoter hypermethylation 56 subtypes 56 deleterious mutations 56 proto oncogene 56 receptor protein 56 tumorigenesis 56 INF2 56 genetic loci 56 LRRK2 mutations 56 germline mutation 56 NAFLD 56 hereditary predisposition 56 brain lesions 56 epigenetic markers 56 apoE 56 EGFR gene 56 missense mutation 56 tumor suppressor 55 endostatin 55 maternally inherited 55 JAK2 mutation 55 genomic alterations 55 Epstein Barr virus 55 signaling cascades 55 ERBB2 55 CCR3 55 metabolic abnormalities 55 chromatin structure 55 biomarkers 55 signaling pathways 55 genetic predisposition 55 microRNAs miRNAs 55 JAK2 55 Clusterin 55 primary cilia 55 autosomal recessive 55 tyrosine phosphorylation 55 monogenic 55 BRCA2 gene mutation 55 PON1 55 DQB1 * 55 GBA mutations 55 KIBRA 55 Fragile X gene 55 biological pathways 55 developmental abnormalities 55 PICALM 55 deacetylation 55 shorter telomeres 55 rs# [003] 55 microRNA expression 55 synapse formation 55 splice junctions 55 nestin 55 autism susceptibility genes 55 ABCB1 55 LKB1 55 Hashimoto thyroiditis 55 CYP#D# 55 heritable 55 neuroligins 55 DNA methylation patterns 55 colorectal tumors 55 HLA molecules 55 STAT4 55 proteases 55 activating mutations 55 CDKN2A 55 ApoE4 55 SORL1 gene 55 Genes 55 chromosome translocations 55 GBM tumors 55 Genetic mutations 55 mammary cancers 55 #q#.# [002] 55 IKZF1 55 homozygous 55 single nucleotide polymorphism 55 isoform 55 multidrug resistance 55 mitochondrial 55 MDM2 55 BMPR2 55 chromosomal anomalies 55 colorectal cancer CRC 55 polymorphism 55 vimentin 55 uPAR 55 TSC1 55 chromosomal rearrangement 55 IDH1 55 TP# gene 55 PKM2 55 LRRK2 mutation 55 alternative splicing 55 epigenetically 55 chromosome abnormality 55 MYCN amplification 55 MC1R gene 55 chromosomal defect 55 progranulin gene 55 cell signaling pathways 55 gut microbes 55 STAT3 55 gene amplification 55 translocations 55 histone deacetylases 55 HDACs 55 neurodegenerative disorder 55 tumors 55 gene rearrangements 55 huntingtin protein 55 Meckel Gruber 55 protein 54 ovarian cancers 54 gene polymorphisms 54 Alu elements 54 chromosomal disorders 54 methylated DNA 54 CYP#C# [002] 54 AAT deficiency 54 CYP#D# gene 54 GFP gene 54 recurrent miscarriages 54 SMN2 54 methylation patterns 54 Mitochondrial diseases 54 GSTT1 54 Wnt signaling pathway 54 insulin resistance 54 genome 54 dysbindin 54 MTHFR gene 54 dopamine receptor gene 54 telomere shortening 54 Akt1 54 CAG repeats 54 alternatively spliced 54 Peutz Jeghers syndrome 54 MeCP2 gene 54 splice variants 54 Prox1 54 PTP1B 54 genomic variants 54 FTLD 54 FLT3 54 LRP5 54 atypical hyperplasia 54 genomic deletions 54 APOE e4 gene 54 ion channels 54 grade gliomas 54 lymphomas 54 ubiquitination 54 WDR# 54 CCL#L# 54 PDGFR 54 mtDNA 54 RBP4 54 cystatin C 54 chromosomal abnormality 54 hedgehog pathway 54 BCL#A 54 inherited predisposition 54 gene loci 54 Treg cell 54 clefting 54 BRAF V#E 54 protein isoforms 54 microglial 54 cystic fibrosis transmembrane conductance 54 Aβ 54 promoter methylation 54 CGG repeats 54 BRCA gene mutation 54 oncogenic 54 SPINK1 54 colon cancers 54 Pten 54 NFkB 54 Stat3 54 mutant allele 54 gene expression profiles 54 caveolin 1 54 aldehyde dehydrogenase 54 mitochondrial proteins 54 BRCA gene 54 congenital anomalies 54 #q# deletion 54 serotonin receptor 54 IGF2 54 oncogene 54 Notch signaling 54 CALHM1 54 KIF6 gene 54 Cyclin D1 54 subclinical hyperthyroidism 54 pRb 54 rs# [001] 54 BRCA 54 NF2 54 mRNA expression 54 HLA DRB1 54 molecular mechanisms 54 nonsense mutation 54 beta thalassemia 54 epigenetic modifications 54 ApoE 54 DSBs 54 KIAA# 54 non coding RNA 54 ALDH2 54 chromosome #q# [001] 54 genetic makeup 54 poorer prognosis 54 microRNA 54 Dpp 54 faulty BRCA1 gene 54 telomere length 54 EBV infection 54 atherosclerotic lesions 54 urate 54 epigenetic regulation 54 chromosome #q#.# [001] 54 RUNX3 54 shRNAs 54 molecular mechanism 54 FOXP3 54 COMT 54 FGFR1 54 renin 54 neuroinflammation 54 NKX2 54 colon tumors 54 BRCA2 breast cancer 54 tumor suppressors 54 DNA rearrangements 54 ABCA1 54 GRP# 54 isoforms 54 genotoxic stress 54 hemochromatosis 54 exons 54 coding sequences 54 NR#A# gene 54 CXCL5 54 HPV# 54 matriptase 54 GRK5 54 H. pylori 54 CYP# [002] 54 piRNAs 54 rs# [004] 54 HSCs 54 APOE4 gene 54 KCNE2 54 adiponectin levels 53 activating mutation 53 ASDs 53 MAPK pathway 53 IGF1 53 oncoproteins 53 VKORC1 53 proband 53 p# protein 53 GSTM1 53 metabolic enzymes 53 RNA sequences 53 HLA alleles 53 ncRNAs 53 transcription factor 53 recessive genes 53 KLF# 53 trypanosomes 53 Wnt signaling 53 connexin 53 molecular underpinnings 53 TGF β 53 sortilin 53 Rb gene 53 GISTs 53 neurodevelopmental disorders 53 biochemical mechanisms 53 epithelial tissues 53 genes CYP#C# 53 breast tumors 53 small RNAs 53 HFE gene 53 GPR# [002] 53 GAB2 53 KRAS oncogene 53 neurofibromatosis type 53 DRD2 gene 53 thyroid hormone levels 53 NKT cells 53 biochemical signaling pathway 53 neuroendocrine 53 HLA DQ2 53 gene sequences 53 HER2 gene 53 susceptibility loci 53 C1q 53 allele frequencies 53 autoantibody 53 paralogs 53 p# activation 53 antibodies 53 Htt 53 ORMDL3 53 inherited neurological disorder 53 familial clustering 53 Myc 53 evolutionarily conserved 53 chromosome #q# [002] 53 autosomal dominant disorder 53 BCR ABL 53 muscular dystrophies 53 allelic variants 53 mutant huntingtin protein 53 ARID1A 53 enzymatic activity 53 somatic mutation 53 phenotypic variation 53 EGFR 53 hypermethylated 53 YKL 53 protein misfolding 53 NRG1 53 Wwox 53 epigenome 53 linkage disequilibrium 53 CIB1 53 autosomal dominant 53 glutamate signaling 53 IDH1 mutation 53 E4 variant 53 parkin gene 53 p# gene 53 filaggrin 53 glycoproteins 53 T. gondii 53 selective inhibitors 53 TGF beta pathway 53 signaling pathway 53 JAK2 enzyme 53 chromosomal deletions 53 genomic 53 DLX5 53 ADAM# 53 genetic underpinnings 53 NPY gene 53 mitochondrial DNA mtDNA 53 SMN protein 53 SMAD4 53 thioredoxin 53 Methylation 53 VIPR2 53 Kufs disease 53 pathogenic mechanisms 53 tau mutation 53 biochemical pathway 53 SMN1 gene 53 germline cells 53 neurones 53 suppressor gene 53 HOTAIR 53 Epstein Barr virus EBV 53 MLL gene 53 SOD1 protein 53 neurological abnormalities 53 huntingtin gene 53 FTO gene 53 MnSOD 53 hereditary hemochromatosis 53 FGFs 53 cardiac channelopathies 53 biologic pathways 53 LRAT 53 mRNA molecules 53 hyperactivation 53 adiponectin 53 IDH2 53 transcriptional regulation 53 lipoprotein 53 5 hydroxymethylcytosine 53 underlying pathophysiology 53 CagA 53 TNFa 53 ependymoma 53 SIRT1 53 ribosomal proteins 53 TSP1 53 array CGH 53 Tregs 53 autosomal recessive disease 53 elevated triglyceride levels 53 CCR5 delta# 53 p# mutation 53 G allele 53 KCNH2 53 MSH6 53 WNK1 53 microsatellite instability 53 R#W [002] 53 micro RNA 53 inheritable diseases 53 serotonin transporter 53 #p#.# [002] 53 deleterious mutation 53 MHC genes 53 Aß 53 Stat5 53 caveolin 53 breast carcinomas 53 SIRT1 gene 53 myelination 53 malformations 53 yeast cells 53 NKX#.# 53 MIF protein 53 commonly mutated genes 53 substrate specificity 53 causative mutation 53 sequence homology 53 protein kinase C 53 SHANK3 53 nicotinamide 53 SOCS1 53 genome rearrangements 53 E#F# 52 transthyretin 52 untreated celiac disease 52 genetically susceptible 52 CYP#B# 52 G#S [002] 52 GPx 52 homozygotes 52 menin 52 SCN5A 52 coding genes 52 mitochondrial fusion 52 polyamines 52 gastrointestinal stromal tumors GISTs 52 epigenetic marks 52 heterozygote 52 SE alleles 52 TCF4 52 HPV infection 52 rs# [002] 52 sCJD 52 latent TB infection 52 FGFR2 gene 52 herpes viruses 52 calcineurin 52 osteopontin 52 myotonic dystrophy 52 SMN1 52 misfolding 52 telomere lengths 52 genomic imprinting 52 PDE#A 52 OGG1 52 mRNA transcripts 52 secretory pathway 52 amyloids 52 mammalian cells 52 neural tube defect 52 #q# [002] 52 prostate adenocarcinoma 52 mesothelin 52 PKCi 52 TACI 52 serotonin receptors 52 Genetic variation 52 ubiquitylation 52 chlamydial infection 52 receptor gene 52 PKD1 52 C. neoformans 52 neuroglobin 52 MAPCs 52 Wnts 52 TTR gene 52 prostate cancer CaP 52 leptin 52 familial hypercholesterolemia 52 melatonin receptor 52 amyloid deposits 52 alpha synuclein 52 VEGF receptor 52 regulator CFTR gene 52 ApoE gene 52 endogenous retroviruses 52 constitutively 52 SGK1 52 DISC1 52 homodimers 52 HOX genes 52 fatty acid synthase 52 nucleotide substitutions 52 synaptogenesis 52 leukaemic stem cells 52 Dravet syndrome 52 p# [001] 52 microglial cells 52 MC1R 52 cyclin E 52 GATA4 52 gene BRCA2 52 chromosome 52 histone acetylation 52 commensal bacteria 52 synuclein 52 phenotypic 52 methyltransferases 52 leukaemias 52 metastasis 52 CDK4 52 Genetic predisposition 52 overexpress 52 APOC3 52 SOD1 52 ubiquitin ligases 52 inherited genetic mutations 52 neuropsychiatric disorders 52 mesotheliomas 52 genetic traits 52 receptor molecule 52 Th# cells 52 BRAC2 52 transgenic mouse model 52 Bardet Biedl syndrome 52 glucocorticoids 52 protein fragment 52 N Myc 52 progerin 52 lung tumors 52 granule cells 52 placental function 52 microRNA miR 52 nonmelanoma skin cancers 52 motor neuron degeneration 52 intestinal polyps 52 regulates gene expression 52 gallstone disease 52 COMT gene 52 Sjögren syndrome 52 PI3K pathway 52 Fibroblast Growth Factor Receptor 52 segmental duplications 52 myeloproliferative disorders 52 indels 52 monozygotic twins 52 podocytes 52 adenomatous polyps 52 achromatopsia 52 LPA gene 52 AAV2 52 homologs 52 BMP4 52 chromosomes 52 telomere dysfunction 52 oxysterols 52 RANKL 52 orthologs 52 ovarian hormones 52 BRAF protein 52 oncogenesis 52 CYP#C# [001] 52 chitinase 52 V#F mutation 52 BRCA2 carriers 52 signaling molecule 52 CatB 52 PALB2 gene 52 dysbindin gene 52 pDCs 52 hereditary deafness 52 folate deficiency 52 H#K# [002] 52 MMP9 52 Wnt1 52 subtype 52 CISH 52 miR #b [001] 52 myeloproliferative neoplasms 52 G6PD deficiency 52 breast cancer subtypes 52 ataxin 52 ApoE4 allele 52 PPARγ 52 chromosome #p# [001] 52 thrombophilia 52 cysteines 52 gene encoding 52 MC4R gene 52 TH# cells 52 thyroid hormones 52 MetAP2 52 ADDLs 52 recessive gene 52 homeobox gene 52 RASSF1A 52 mutational 52 MCAD deficiency 52 Velculescu 52 genetically 52 Immunohistochemical analysis 52 STK# [002] 52 KRAS mutations 52 cardiac hypertrophy 52 enterotypes 52 amino acid substitutions 52 TOMM# 52 IGFBP2 52 IL 1β 52 cyclins 52 ERCC1 52 enteroviruses 52 dysregulation 52 E selectin 52 DARPP 52 OCT4 52 genetic disorder 52 FASPS 52 miR 52 fetal hemoglobin 52 enterovirus infection 52 metabolizing enzymes 52 LDL receptor 52 synaptic function 52 colorectal polyps 52 G6PD 52 NF kB 52 uric acid levels 52 prion proteins 52 malignant prostate 51 SLC#A# [001] 51 MECP2 51 circadian genes 51 LRP6 51 physiological mechanisms 51 frameshift mutation 51 cytokine 51 COX2 51 HDAC inhibitors 51 Sonic Hedgehog 51 TAp# 51 RPE# 51 mitochondrial DNA mutations 51 fronto temporal dementia 51 amyloid deposition 51 phenotypic variability 51 Stuttering tends 51 IGFBP 51 K ras gene 51 ubiquitinated 51 short hairpin RNAs 51 subclinical atherosclerosis 51 KLF4 51 gene p# 51 cell signaling pathway 51 JAK2 gene 51 LMNA 51 C. pneumoniae 51 epithelial cancers 51 presenilin 51 MAPK 51 melanopsin 51 IGF 1R 51 splice variant 51 overactivation 51 malaria parasite Plasmodium falciparum 51 neuronal dysfunction 51 hedgehog signaling 51 APOE genotype 51 SATB1 51 metabolic pathways 51 coinfection 51 nAChR 51 transgene expression 51 mitochondrial diseases 51 ε4 51 activin 51 RNA viruses 51 recessive trait 51 causative mutations 51 proteins encoded 51 neurodevelopmental disorder 51 genetic manipulations 51 aberrant methylation 51 downregulation 51 c myc 51 nucleotide sequence 51 filaggrin gene 51 beta catenin protein 51 bacterial strains 51 CMV infection 51 Smad3 51 messenger RNAs mRNAs 51 Ashkenazi Jewish 51 Mutations 51 perilipin 51 gamma globin gene 51 viral proteins