Related by context. All words. (Click for frequent words.) 75 genes BRCA1 72 BARD1 72 mutated BRCA1 72 BRIP1 71 BRCA2 gene mutations 70 BRCA2 gene 70 PALB2 70 MSH2 70 MLH1 70 MLL2 69 BRCA1 BRCA2 69 BRCA2 68 CDKN2A 68 germline mutations 68 BRCA1 gene 68 MTHFR 67 BRCA2 gene mutation 67 BRCA2 carriers 67 C#Y 66 apolipoprotein E4 66 BRAC2 66 inherited mutations 66 BRCA2 genetic mutations 66 gene BRCA2 66 BRCA genes 66 PTPN# 65 CCR5 delta# 65 hypermethylated 65 CYP#D# gene 65 MYH9 gene 65 BRCA2 breast cancer 65 BRCA2 mutations 65 progranulin gene 65 KRAS oncogene 65 LRRK2 gene 65 microdeletions 64 PARP inhibition 64 ZNF# 64 genes BRCA 64 mutations 64 BRCA1 mutations 64 BRCA1 64 LRP5 64 TCF#L# gene 64 CDK4 64 testicular germ cell 64 CHEK2 64 CDH1 64 Li Fraumeni 64 EGFR gene 64 Genetic variation 64 HFE gene 64 FGFR2 63 BRCA gene mutation 63 p# mutations 63 mutation 63 aneuploidies 63 epigenetic changes 63 missense mutations 63 VHL gene 63 apolipoprotein E gene 63 GPC5 63 TP# mutation 63 KIF6 gene 63 #q#.# [001] 63 Polymorphisms 63 KCNQ1 63 ALK gene 63 TP# gene 63 mitochondrial DNA mtDNA 63 Germline 63 lung adenocarcinoma 63 KRAS mutations 63 BRAF V#E 63 CHD7 63 gene mutations 62 ABCB1 62 promoter hypermethylation 62 maternally inherited 62 somatic mutations 62 R#W [002] 62 rs# [002] 62 INF2 62 Fragile X gene 62 gene rearrangements 62 paternally inherited 62 RUNX3 62 rs# [001] 62 chromosomal aberrations 62 CpG island 62 LPA gene 62 mutated BRCA 62 GSTP1 62 atypical hyperplasia 62 Single Nucleotide Polymorphisms SNPs 62 mosaicism 62 GNAQ 62 SMN1 62 p# mutation 62 APOA5 62 CFTR gene 62 Chromosomal 62 STAT4 62 PIK3CA 62 cause cardiac channelopathies 62 Aneuploidy 62 CYP#C# [002] 62 MC1R 62 microcephalin 62 BRCA2 genes 62 BRAF gene 62 APOL1 61 androgen receptor gene 61 methylenetetrahydrofolate reductase 61 MECP2 gene 61 IL#R 61 V Leiden 61 Oncogenic 61 EGFR protein 61 BRCA1 mutation 61 NR#A# gene 61 Clusterin 61 abnormal methylation 61 de novo mutations 61 #q# [001] 61 succinate dehydrogenase 61 syngeneic 61 #p# [001] 61 MAP#K# 61 epigenetic regulation 61 HMMR 61 tumor suppressor protein 61 heterozygotes 61 VKORC1 61 KIAA# 61 c KIT 61 MC1R gene 61 abnormal p# 61 APOE e4 61 hypermethylation 61 E#F# 61 NF1 gene 61 TMEM#B 61 chromosomal rearrangement 61 herpesviruses 61 VIPR2 61 LRAT 61 mutated genes 61 NKX#.# 61 K ras mutations 61 mtDNA mutations 61 monogenic 61 cisplatin resistant 61 #q# deletion 61 FGFR2 gene 61 UGT#B# 61 gene mutation 61 BRCA2 mutation carriers 61 Epstein Barr Virus EBV 61 Endometrial 61 NR#A# 61 BRCA 61 Heterozygous 61 parkin gene 60 non mutated KRAS 60 genetic mutations 60 severe congenital neutropenia 60 TSC1 60 regulator CFTR gene 60 ERBB2 60 non coding RNA 60 poly ADP ribose polymerase 60 nonhereditary 60 HLA DQ2 60 dopamine D4 receptor 60 gene locus 60 germline mutation 60 genetic polymorphisms 60 BCL#A 60 HER2 HER2 60 BRCA1 gene mutation 60 microdeletion 60 COX2 60 COL#A# 60 SCN5A 60 promoter methylation 60 mutated K ras 60 BRCA2 mutation 60 CFTR cystic fibrosis transmembrane 60 FMR1 gene 60 BRCA mutations 60 Epidermal Growth Factor Receptor 60 missense mutation 60 filaggrin gene 60 ovarian pancreatic 60 Epstein Barr virus EBV 60 Genetic variants 60 nonsense mutations 60 HER2 neu 60 autosomal recessive 60 MEF2A 60 sequence homology 60 activating mutations 60 spontaneous mutation 60 transiently transfected 60 BRCA mutation 60 Kufs disease 60 causative mutations 60 FGFR3 60 genetic variant 60 #p# [003] 60 chromosome #q# [002] 60 endometrial cancers 60 Autoantibodies 60 DICER1 gene 60 apoC III 60 TCF#L# 60 allelic variants 60 intronic 60 SLC#A# [001] 60 SMAD4 60 epigenetic modification 60 IDH1 gene 60 homozygosity 60 IKZF1 60 activating mutation 60 aneuploidy 60 Genetic mutations 60 TGFBR1 * 6A 60 JAK2 mutation 59 PRNP 59 IgA deficiency 59 ApoE4 59 rs# [004] 59 recessive mutations 59 spontaneous mutations 59 virulence genes 59 uterine ovarian 59 protein encoded 59 HNPCC 59 PTEN gene 59 genes CYP#C# 59 chromosomal 59 SOD1 gene 59 rs# [003] 59 #q# [002] 59 HER2 gene 59 GSTT1 59 Histone 59 MDR1 59 vimentin 59 myopathies 59 susceptibility gene 59 invasive lobular 59 IRF6 59 mutated gene 59 LIS1 59 MIF protein 59 SNP rs# [001] 59 SRY gene 59 G#S mutation 59 chromosomal instability 59 APOE4 59 CYP#B# 59 HG PIN 59 familial ALS 59 Predisposition 59 tumor suppressor gene 59 methylated DNA 59 Cyclin D1 59 ARID1A 59 beta1 integrin 59 HMGA2 59 HER2 receptor 59 Drosha 59 Gene Mutation 59 narcolepsy cataplexy 59 mRNA transcripts 59 segmental duplication 59 Premature Aging 59 normal karyotype 59 chromosome #q# [001] 59 F#del 59 apoE 59 von Hippel Lindau 59 UGT#A# * 59 potent inducer 59 genetic polymorphism 59 LMNA 59 miRNA expression 59 Cytogenetic 59 breast carcinomas 59 Leydig cells 59 gastric carcinogenesis 59 eIF 4E 59 prostate carcinoma 59 frameshift mutation 59 #p#.# [002] 59 ovarian endometrial 59 Upregulation 59 c MYC 59 Trichomonas vaginalis 59 C#T [002] 59 K ras gene 59 Overexpression 59 Myostatin 58 APOE gene 58 endogenous retroviruses 58 JAK2 gene 58 retinoblastoma Rb 58 MC4R gene 58 Raf MEK ERK 58 TOP2A gene 58 SPINK1 58 BMPR2 58 Genetic variations 58 deacetylation 58 caveolin 1 58 TRIM5 58 genetic loci 58 autism susceptibility genes 58 #p#.# [001] 58 JAK2 enzyme 58 TP# mutations 58 genotoxic stress 58 neural progenitor 58 PTEN tumor suppressor 58 LKB1 58 familial pancreatic cancer 58 KCNE2 58 5 HTTLPR 58 micro RNAs 58 CpG DNA 58 Tay Sachs thalassemia 58 polyomavirus 58 TACI mutations 58 NOTCH1 58 genetic mutation 58 aneuploid 58 GAB2 58 breast endometrial 58 breast cancer metastasis 58 Prolactin 58 chromosome #p# [002] 58 MicroRNA 58 colorectal carcinoma 58 Alleles 58 ORMDL3 58 genomic rearrangement 58 Genetic Variation 58 phenotypic expression 58 retinoic acid receptor 58 MYH9 58 Factor Receptor 58 gamma globin gene 58 sporadic ALS 58 HLA DRB1 58 FANCD2 58 SHANK3 58 micro RNA 58 polymorphisms 58 chromosomal rearrangements 58 ESR1 58 bacterium Mycobacterium tuberculosis 58 gastric carcinoma 58 epigenetic modifications 58 chromosomal abnormalities 58 receptor molecule 58 BRAF V#E mutation 58 ENPP1 58 splice variants 58 CYP#E# gene 58 mutant alleles 58 TRAIL induced apoptosis 58 cyclin E 58 STK# [002] 58 causal variants 58 anaplastic lymphoma kinase 58 mitochondrial gene 58 ADRB2 58 Vidaza ® 58 proto oncogene 58 TOMM# 58 murine leukemia virus 58 homozygotes 58 homozygous 58 androgen receptor AR 58 IDH1 58 histone acetylation 58 Prion Protein 58 NPC1 58 palladin 58 autosomal recessive disease 58 MeCP2 gene 58 methylation patterns 58 Leukemias 58 TNFAIP3 58 cells overexpressing 58 NFKBIA 58 DQB1 * 58 HPRT gene 58 CYP# [002] 58 Metastases 58 mutated p# 58 CETP VV 58 TTR gene 58 HOTAIR 58 PALB2 gene 58 IL#B 58 Meckel Gruber 58 somatic mutation 58 PDGFRA 58 p#INK#a 58 constitutively expressed 58 CALHM1 58 folate metabolism 58 GRNOPC1 contains 58 gene amplification 58 CREBBP 58 hereditary hemochromatosis 58 uPAR 58 FUS protein 58 HPV# 58 microRNA molecules 58 prostate cancer CaP 58 Cathepsin B 58 chromosome rearrangements 58 NFkB 58 Li Fraumeni syndrome 58 HER2 overexpression 58 phosphorylates 58 genomic imprinting 58 HGPS 58 MTHFR gene 58 telomerase reverse transcriptase 58 X chromosome 58 epigenetic silencing 58 SETDB1 58 granzyme B 58 Apolipoprotein E 58 chlamydial 57 single nucleotide polymorphism 57 #q#.# [002] 57 myoepithelial 57 TOP2A 57 SOD2 gene 57 modifier genes 57 breast cancer gene mutation 57 Tumor Suppressor 57 DNA rearrangements 57 Wnt signaling pathway 57 pool dies unwept 57 Activating mutations 57 CNVs 57 apolipoprotein E 57 Mutation Detection 57 mammary cells 57 genomic instability 57 MiRNAs 57 WT1 57 TRAF1 C5 57 adenomatous polyposis coli 57 transactivation 57 APOC3 57 HLA B# 57 CYP#D# 57 TYMS 57 prodynorphin 57 LDL receptor 57 cyclin D1 57 mutant allele 57 mutant genes 57 copper zinc superoxide 57 DRD2 gene 57 cystic fibrosis transmembrane conductance 57 chromosomal anomalies 57 M. genitalium 57 vanA gene 57 breast uterine 57 oligonucleotide ligation 57 haplotype 57 proband 57 Y chromosomal 57 germline 57 chromosome abnormalities 57 BRAF protein 57 ribosomal protein 57 IRF6 gene 57 overexpress 57 CYP#A# [002] 57 methyltransferase 57 RAR beta 57 Zinc deficiency 57 BRCA1 mutation carriers 57 splice junctions 57 Cytotoxic T 57 Pten 57 Transcriptome 57 microglial 57 tryptase 57 major histocompatibility complex 57 IRS1 57 allele frequencies 57 susceptibility genes 57 gene fusions 57 Fibroblast 57 adipogenic 57 breast carcinoma 57 eotaxin 57 hepatic lipase 57 IDH2 57 coding exons 57 neuroligins 57 gene MECP2 57 GPR# [002] 57 huntingtin gene 57 NPM1 gene 57 KLF4 57 HLA markers 57 Shortened telomeres 57 haematopoietic 57 thyroid peroxidase 57 autosomal dominant disorder 57 gene variants 57 commonly mutated genes 57 RRM1 57 SGK1 57 C. pneumoniae 57 ERCC1 57 variant allele 57 prion infection 57 FLT3 57 heterozygous 57 serine threonine kinase 57 genetic abnormalities 57 MLL gene 57 hepatoma 57 hereditary predisposition 57 Ets2 57 genes predisposing 57 CCL#L# 57 cholesteryl ester transfer 57 p# MAPK 57 Homozygous 57 shortened telomeres 57 MSH6 57 tyrosine phosphorylation 57 CYP#A# CYP#D# 57 transthyretin 57 cervical breast 57 genetic variants associated 57 FGFR1 57 GSTM1 57 DEAR1 57 CC genotype 57 fetal chromosomal 57 antisense strand 57 chromosomal aberration 57 heterozygosity 57 ductal carcinomas 57 TMPRSS2 ERG fusion 57 klotho gene 57 ubiquitinated 57 monozygotic twins 57 HLA DRB1 * 57 meiotic recombination 57 inactivating mutations 57 progerin 57 subcellular localization 57 EphB4 57 mammographic density 57 Arabidopsis genome 57 regulates gene expression 57 malignant phenotype 57 ADPKD 57 HER2 expression 57 Inactivation 57 inactive X chromosome 57 WDR# 57 OCT4 57 KIBRA 57 gastrointestinal stromal tumors GISTs 57 NFAT 57 interferon pathway 57 Dystrophin 57 immunohistochemical analysis 57 DNA methylation patterns 57 abnormal proteins 57 hormone receptor negative 57 AMACR 57 ovarian cancers 57 histone H4 56 A. thaliana 56 CIN2 + 56 mutant p# 56 gene polymorphism 56 TET2 56 LMNA gene 56 Genetic Variant 56 tadenovec Ad5FGF 4 56 dominantly inherited 56 Ovary removal 56 X Chromosome 56 PTEN mutations 56 monocyte chemoattractant protein 56 chromosome #p# [001] 56 miRNA genes 56 genomewide 56 receptor tyrosine kinase 56 HMGA2 gene 56 MAPK pathway 56 BRCA gene 56 rs# rs# 56 protein kinase C 56 IRAK1 56 tumor suppressors 56 chromosomal deletions 56 EZH2 56 phenotypic variation 56 N Myc 56 RASSF1A 56 medulloblastomas 56 ADAM# 56 Folate deficiency 56 ortholog 56 gestational diabetes mellitus 56 estrogen receptor alpha 56 ectopic expression 56 genotyped 56 GLI1 56 human leukocyte antigen 56 autosomal 56 SNPs pronounced snips 56 previously uncharacterized 56 SMN1 gene 56 Mitochondrial DNA 56 Sporadic CJD 56 recessive trait 56 CYP#A# gene 56 microRNA expression 56 ARF1 56 linkage disequilibrium 56 ADAMTS# 56 RNA ribonucleic acid 56 BMP2 56 PKD1 56 tumorigenicity 56 nephronophthisis 56 genes encoding 56 Phosphorylation 56 tyrosine kinase receptor 56 Trypanosoma brucei 56 Mitochondrial 56 androgen independent 56 Src kinase 56 protein isoforms 56 4E BP1 56 Squamous 56 Apc 56 mtDNA 56 Brugada Syndrome 56 Hashimoto thyroiditis 56 Sox9 56 ribonucleic acid RNA 56 apoE4 56 DRB1 * 56 gamma H2AX 56 dopamine receptor gene 56 chromosomal regions 56 RAD# [001] 56 hypomethylation 56 CYP#C# * 56 trypanosomes 56 lung adenocarcinomas 56 Fanconi anemia FA 56 Apobec3 56 abnormal chromosomes 56 penile cancers 56 genomic rearrangements 56 Cx# [001] 56 susceptibility locus 56 Microarray analysis 56 DRD4 56 pathogenic mutations 56 E cadherin expression 56 sickle cell cystic fibrosis 56 Dr. Bezprozvanny 56 fronto temporal dementia 56 fruitfly Drosophila 56 cyclin dependent kinase inhibitor 56 SOD2 56 ASCUS 56 CNTNAP2 56 tensin homolog 56 hereditary breast cancer 56 SCD1 56 c Myb 56 causative genes 56 clade B 56 Gene Mutations 56 HLA molecules 56 encodes protein 56 SORL1 56 Macrophage 56 SNP rs# [002] 56 PCA3 gene 56 inhibin B 56 HepG2 cells 56 SMN protein 56 ApoE4 gene 56 micrometastasis 56 sporadic Creutzfeldt Jakob 56 mitogen activated protein kinase 56 neuroblastoma tumors 56 DSBs 56 EGFR mutation 56 autosomes 56 Leydig cell 56 p# protein 56 endogenous retrovirus 56 leukaemias 56 histone modification 56 BRAF gene mutations 56 gene 56 survival motor neuron 56 APOE ε4 56 prion gene 56 Protein Kinase 56 β1 56 CNTNAP2 gene 56 castration resistant 56 Yamanaka recipe 56 Hepatocellular 56 oncogenic mutations 56 HLA DR4 immune 56 klotho 56 HLA DR 56 SMN2 56 gametophyte 56 multiply uncontrollably 56 eIF4E 56 peroxisome 56 Six3 56 MECP2 56 variant alleles 56 hereditary breast 56 prion protein PrP 56 SIRT3 56 piRNAs 56 Alzheimer's linked 56 suppressor gene 56 telomere dysfunction 56 VNTR 56 DNMT1 56 catechol O methyltransferase 56 G6PD 56 demethylase 56 Transcription Factor 56 PCR RFLP 56 ribonucleic acids 56 alternatively spliced 56 ERalpha 56 sFlt 1 56 ABCB1 gene 56 virulence determinants 56 EBNA1 56 DU# [002] 56 kinase gene 56 LQTS 56 transcriptional regulation 56 Selective Inhibitor 56 genes 56 GSTM1 gene 56 chromosome translocations 56 mammary stem cells 56 gene polymorphisms 56 CXCL5 56 polyploid 56 Tuberous sclerosis 56 mRNA expression 56 H#K# methylation 56 PCa 56 Cell Proliferation 56 ubiquitylation 56 CEACAM1 56 Haplotype 56 chromatin immunoprecipitation ChIP 56 vesicular stomatitis virus 56 haplotypes 56 macrophage migration inhibitory 56 forkhead 56 cagA 56 Id1 56 WNK1 56 C EBP alpha 56 CagA 56 hemagglutinin H 56 multigene 56 Creutzfeld Jakob disease 56 AML MDS 56 methylation markers 56 JAK STAT 56 human leukocyte antigens 56 endostatin 56 chromatin structure 56 Rb gene 56 gene predisposing 56 Cryptococcus neoformans 56 heterozygote 56 K#R [002] 56 Oncogenes 56 BRCA mutation carriers 56 lysine residues 56 steroidogenic 56 primordial germ cells 56 FMR1 56 cyclin dependent kinase 56 Lymphocytes 56 Dpp 56 CFTR gene mutations 56 TT genotype 56 heritable genetic 56 dopamine transporter gene 55 alferminogene tadenovec 55 MMP9 55 Methylation 55 ubiquitin ligases 55 functional polymorphism 55 poorer prognosis 55 III EGFRvIII 55 transgenic mice expressing 55 HLA DRB1 SE 55 diagnostic biomarker 55 DEC2 55 castrate resistant 55 Jhdm2a 55 pleiotropic 55 genetic syndromes 55 AGTR1 55 DNA methyltransferases 55 ploidy 55 genus Plasmodium 55 HPV vaccine protects 55 MnSOD 55 MMP# 55 Brugada syndrome 55 beta subunit 55 alleles 55 Fas ligand 55 pancreatic endocrine 55 mitochondrial metabolism 55 gastric carcinomas 55 monozygotic twin 55 prostate pancreatic 55 Mutation 55 PICALM 55 H#K# [002] 55 nucleotide substitutions 55 gene DRD4 55 T#M 55 pre mRNA splicing 55 non polyposis colorectal 55 telomere maintenance 55 chemoresistant 55 paratuberculosis 55 leiomyomas 55 FOXP3 55 SLITRK1 55 thyrotropin 55 Hoxb8 55 MDM2 55 Cytochrome P# 55 survivin expression 55 thrombospondin 55 Single Nucleotide Polymorphisms 55 H#K#me# 55 mutant gene 55 Epigenomics proprietary 55 alpha defensin 55 Apolipoprotein E4 55 gene variant 55 resistin 55 gene expression patterns 55 Rap1 55 Genotypes 55 miR #a [001] 55 5 HT2A serotonin 55 variant rs# 55 CAG repeats 55 Helicobacter 55 monocytic 55 abnormal prions 55 GISTs 55 dysbindin 55 ε4 55 genotypic 55 colorectal tumor 55 deleterious mutation 55 Enterobacter 55 GRP# 55 C. trachomatis 55 HbF 55 oligodendrogliomas 55 myostatin gene 55 pancreatic lung 55 JAK mutations 55 Mcl 1 55 granulosa cell 55 collagen VII 55 segmental duplications 55 mitotic catastrophe 55 pancreatic prostate 55 SOX3 gene 55 quantitative trait loci 55 molecular abnormalities 55 epigenetic inheritance 55 alpha synuclein protein 55 nucleus Chinnery 55 upregulates 55 TMPRSS2 ERG 55 caveolin 55 Immunohistochemical analysis 55 intracellular pathogens 55 uracil 55 EGFR mutant 55 #:#-# [023] 55 Uterine cancer 55 gene expression microarrays 55 CYP#C# [001] 55 TSC2 55 lymphomas leukemias 55 conductance regulator 55 NF kB signaling 55 synuclein 55 gene APOE 55 downstream effector 55 transcriptional repression 55 progranulin 55 chromosome aberrations 55 FGFs 55 NSCLC tumors 55 Akt1 55 transgene expression 55 renal cell carcinomas 55 mitogen activated protein kinases 55 chromosome #q#.# [001] 55 amino terminal 55 Secretase 55 #S rRNA 55 V#F mutation 55 splice variant 55 PI3K AKT 55 susceptibility loci 55 chromosomal translocations 55 proapoptotic 55 TEL AML1 55 candidate alferminogene tadenovec 55 paraoxonase 55 Breast Ovarian Cancer 55 inherited predisposition 55 impair fertility 55 haplogroups 55 COMT gene 55 Protein Kinase C 55 gallstone disease 55 non coding RNAs 55 XLHED 55 Igf2 55 genomic alterations 55 orthologs 55 mitochondrial mutations 55 lupus anticoagulant 55 Dysregulation 55 cytopathic 55 Folic acid deficiency 55 genetic alteration 55 cytochrome b 55 Simian Immunodeficiency Virus 55 hnRNP 55 p# Shc 55 Rh factor 55 proto oncogenes 55 Fibroblasts 55 asymptomatic carriers 55 antisense therapies 55 Prox1 55 nucleoli 55 Hepatitis B Virus 55 Human papillomavirus 55 HGPIN 55 ADDLs 55 Peutz Jeghers syndrome 55 fibrillin 1 55 genomic deletions 55 KIT mutations 55 thrombophilia 55 miRNAs miR 55 amyloidogenic 55 Mutational