Related by context. All words. (Click for frequent words.) 77 BRCA1 73 BRCA1 gene 71 genes BRCA1 70 BRCA2 gene 70 PALB2 69 breast cancer genes BRCA1 67 BRCA genes 67 BRCA 65 mutated BRCA1 65 MSH2 64 BRCA1 mutations 64 BRCA mutations 64 BRCA2 mutation 63 BRCA2 gene mutations 63 tumor suppressor gene 62 BRCA2 mutations 62 BRAC2 62 BRCA2 carriers 62 mutated gene 62 gene mutations 62 aneuploidy 61 BRIP1 61 MLH1 61 BRCA mutation 61 BRCA gene mutation 60 mutations 60 PTEN gene 60 GSTP1 60 BRCA1 mutation 60 gene BRCA2 60 PTPN# 60 CDKN2A 60 BRCA2 gene mutation 60 BRCA2 mutation carriers 59 HNPCC 59 FGFR2 59 atypical hyperplasia 59 ovarian cancers 59 TCF#L# gene 59 APOE e4 59 estrogen receptor 59 CDH1 59 HER2 receptor 59 EGFR gene 59 gene variant 59 BARD1 59 somatic mutations 59 inherited mutations 59 mutation 59 MTHFR 59 CYP#D# 58 BRAF gene 58 p# gene 58 p# mutations 58 MSH6 58 MLL2 58 BRCA gene 58 chromosomal abnormalities 58 EZH2 58 GNAQ 58 IDH1 58 rs# [002] 58 microdeletions 58 cyclin D1 58 APOE4 58 ApoE4 58 CCR5 delta# 58 ERCC1 58 CHEK2 58 EGFR 58 miRNAs 57 TCF#L# 57 breast cancers 57 gene mutation 57 BRCA1 BRCA2 57 genetic variant 57 PIK3CA 57 testicular germ cell 57 atypia 57 caveolin 1 57 familial ALS 57 mtDNA mutations 57 germline mutations 57 mutated genes 57 p# protein 57 micro RNAs 57 APOE gene 57 Peutz Jeghers syndrome 57 WT1 57 GPC5 57 promoter methylation 56 MTHFR gene 56 BCR ABL 56 LKB1 56 tumor suppressor 56 NF kB 56 hereditary breast cancer 56 VHL gene 56 gene variants 56 FLT3 56 tumor suppressor protein 56 alleles 56 ovarian tumors 56 HER2 56 colorectal cancers 56 COX2 56 #q#.# [001] 56 CNVs 56 HMGA2 gene 56 variant allele 56 NF1 56 C#Y 56 BRCA2 breast cancer 56 NF1 gene 56 prostate cancers 56 G#S mutation 56 lobular carcinoma 56 CYP# [002] 56 heterozygous 56 CGG repeats 56 ZNF# 56 homozygosity 56 TMEM#B 56 Clusterin 56 chromosomal rearrangement 56 vimentin 55 TAp# 55 breast tumors 55 neuroligins 55 prostate specific 55 SHANK3 55 E#F# 55 ApoE gene 55 genetic mutations 55 KRAS oncogene 55 methylation 55 gene amplification 55 oncogenic 55 poly ADP ribose polymerase 55 PARP inhibition 55 p# mutation 55 hypermethylation 55 CHEK2 gene 55 PCa 55 IL#R 55 #q# [001] 55 Wwox 55 PTEN mutations 55 TGFBR1 * 6A 55 TACI mutations 55 p# [001] 55 tumorigenesis 55 penetrance 55 endometrial cancers 55 CaP 55 familial pancreatic cancer 55 ERBB2 55 ApoE4 gene 55 allele 55 KCNE2 55 FMR1 gene 55 tumor suppressor genes 55 HPV 55 Cyclin D1 55 androgen receptor 55 LQTS 55 human leukocyte antigen 55 non coding RNA 55 homozygotes 55 clusterin 55 polymorphism 55 APOE ε4 55 unmethylated 55 proto oncogene 55 CYP#C# [002] 55 Li Fraumeni 55 hereditary hemochromatosis 54 HGPIN 54 mosaicism 54 oncoprotein 54 KRAS mutations 54 autoantibodies 54 STAT3 54 methylated DNA 54 apolipoprotein E 54 maternally inherited 54 sporadic ALS 54 CYP#C# [001] 54 ABCB1 54 gene p# 54 HPV# 54 chromosomal rearrangements 54 methylenetetrahydrofolate reductase 54 HER2 gene 54 Akt1 54 allelic 54 chromosomal aberrations 54 SORL1 54 micro RNA 54 VKORC1 54 ALK mutations 54 lobular breast cancer 54 germline 54 FXTAS 54 sarcosine 54 rs# [003] 54 mtDNA 54 MLL gene 54 MDM2 54 IDH2 54 STAT4 54 homozygous 54 CHD7 54 missense mutations 54 receptor tyrosine kinase 54 LRAT 54 LRRK2 gene 54 rs# [001] 54 cyclin E 54 FANCD2 54 androgen receptor gene 54 breast cancer gene mutation 54 Hashimoto thyroiditis 54 IKKa 54 apolipoprotein E gene 54 Src 54 TP# gene 54 K ras mutations 54 IRF6 54 CFTR gene 54 CDK4 54 tumor suppressors 54 adenocarcinomas 54 HMGA2 54 MYH9 gene 54 colon cancers 54 X chromosome 54 gene variation 54 SMN2 54 polymorphisms 54 susceptibility gene 54 EGFR mutation 54 uterine ovarian 54 EGFR protein 54 TCF4 54 BRAF mutation 54 chromosomal instability 54 genes BRCA 54 KIF6 gene 53 tyrosine phosphorylation 53 single nucleotide polymorphism 53 heterozygotes 53 R#W [002] 53 IKZF1 53 LRP5 53 HLA B# 53 Stat5 53 LPA gene 53 estrogen receptors 53 HFE gene 53 germline mutation 53 breast carcinomas 53 TOMM# 53 c KIT 53 E cadherin 53 lung adenocarcinoma 53 spontaneous mutations 53 ADAM# 53 Epstein Barr virus EBV 53 hTERT 53 estrogen receptor negative 53 oncogene 53 MnSOD 53 nestin 53 mutant gene 53 BRCA1 gene mutation 53 IgA deficiency 53 APOE 53 HOTAIR 53 FOXP3 53 genetic variants 53 apolipoprotein E4 53 defective gene 53 PDGFR 53 coding genes 53 microRNAs 53 breast cancer metastasis 53 ApoE 53 SRY gene 53 Pten 53 folate metabolism 53 microRNA 53 causal variants 53 RAR beta 53 MC1R 53 DISC1 gene 53 estrogen receptor ER 53 ductal cancer 53 #q# [002] 53 p#INK#a 53 UGT#B# 53 number variation CNV 53 haplotype 53 anaplastic lymphoma kinase 53 beta catenin 53 activating mutations 53 ETV1 53 RAD# [001] 53 GLI1 53 medulloblastomas 53 Hedgehog pathway 53 methylated 53 BMP2 53 neurofibromin 53 PICALM 53 chromosomal 53 BRAF V#E 52 uPAR 52 piRNAs 52 genetic abnormalities 52 SGK1 52 TSC1 52 CNTNAP2 gene 52 NR#A# 52 monozygotic twins 52 HER-2/neu 52 GISTs 52 JAK2 mutation 52 alpha synuclein 52 CIN2 + 52 adenomatous polyps 52 polyomavirus 52 FMR1 52 HER2 neu 52 ribonucleic acid RNA 52 telomere dysfunction 52 SOD1 52 Methylation 52 ccRCC 52 DISC1 52 valine 52 BRCA1 mutation carriers 52 shortened telomeres 52 LDL receptor 52 thyroglobulin 52 Six3 52 apoE4 52 homologous recombination 52 shorter telomeres 52 enzymatic activity 52 GRP# 52 mutant alleles 52 miRNA 52 genetic polymorphism 52 overexpress 52 colorectal cancer CRC 52 MicroRNA 52 colorectal carcinoma 52 hamartomas 52 protein kinases 52 CETP VV 52 miRNAs miR 52 gene fusions 52 progranulin 52 mitochondrial gene 52 Aromatase 52 ADPKD 52 TP# mutation 52 LRRK2 52 genes encoding 52 EGFR mutations 52 mammary cells 52 substrate specificity 52 IDH1 mutation 52 TRAF1 C5 52 specific antigen 52 MMP9 52 SNPs 52 Pin1 52 PAR1 52 advanced adenoma 52 commonly mutated genes 52 tyrosine kinases 52 CYP#D# gene 52 GPR# [002] 52 c MYC 52 follicle stimulating hormone FSH 52 connexin 52 precursor lesions 52 apoE 52 pRb 52 pancreatic cancers 52 exons 52 neuroblastomas 52 genomic instability 52 MECP2 gene 52 NFkB 52 NF κB 52 B7 H3 52 breast ovarian 52 HER2/neu 52 DNA replication 52 microdeletion 52 APOE allele 52 HPVs 52 aneuploid 52 RUNX3 52 Dystrophin 52 Akt 52 microcephalin 52 GSTT1 52 Aneuploidy 52 Notch signaling 52 ependymomas 52 TOP2A 52 PSA velocity 52 miR #a [001] 52 sequence homology 52 CagA 52 sCJD 52 KIAA# 52 VIPR2 52 genetic mutation 52 Skp2 52 APOL1 52 thyroid cancers 52 TP# mutations 52 HLA B 52 lobular cancer 52 NFKBIA 52 HeLa 51 estrogen receptor alpha 51 ubiquitinated 51 Prolactin 51 protein encoded 51 DNA methylation 51 HLA genes 51 alternatively spliced 51 transthyretin 51 PTEN protein 51 genetic abnormality 51 breast carcinoma 51 genes CYP#C# 51 Epidermal Growth Factor Receptor 51 mutated BRCA 51 LRP6 51 variant alleles 51 KCNQ1 51 5 HTTLPR 51 BRCA mutation carriers 51 dopamine D4 receptor 51 SMN1 51 hereditary breast 51 situ LCIS 51 H2AX 51 CXCR4 51 ErbB2 51 apoC III 51 presenilin 51 haematopoietic 51 GSTM1 51 cystic fibrosis transmembrane conductance 51 genes 51 TRIM5 51 JAK2 51 mutant allele 51 beta subunit 51 Cyclin E 51 gene 51 protein kinase C 51 genetic polymorphisms 51 de novo mutations 51 pheochromocytomas 51 DICER1 gene 51 promoter hypermethylation 51 HER2 overexpression 51 regulating gene expression 51 telomere lengths 51 FGFR3 51 anal cancers 51 major histocompatibility complex 51 oncogenes 51 PARP inhibitor 51 constitutively 51 Wnt signaling pathway 51 colon tumors 51 homodimer 51 miR #a [002] 51 CFTR cystic fibrosis transmembrane 51 overexpressed 51 TMPRSS2 ERG fusion 51 TGF beta 51 Activating mutations 51 imprinted genes 51 protein p# 51 IL#B 51 ALK gene 51 antisense oligonucleotides 51 DHFR 51 mitochondrial fusion 51 crystallin 51 loci 51 HLA DQ2 51 sFlt 1 51 DEAR1 51 renal cell carcinomas 51 Hedgehog signaling 51 karyotype 51 APOE4 gene 51 chromosomal translocations 51 overexpression 51 segmental duplications 51 UGT#A# * 51 KRAS 51 CCL#L# 51 qRT PCR 51 malignant prostate 51 paternally inherited 51 KRT# 51 CNTNAP2 51 bladder cancers 51 SMN1 gene 51 adenoma 51 GPx 51 neoplastic 51 HbF 51 BRAF protein 51 SLC#A# [001] 51 virulence genes 51 epigenetic silencing 51 COMT gene 51 MGMT gene 51 androgen receptor AR 51 RBP4 51 FGFR1 51 hypermethylated 51 chromosome segregation 51 normal karyotype 51 c Myb 51 oncoproteins 51 progranulin gene 51 kinases 51 Her2 51 APOC3 51 Bcr Abl 51 rs# [004] 51 Th# cells 51 MSMB 51 ABCA1 51 uterine cancers 51 collagen VII 51 protein isoforms 51 prostate pancreatic 51 COL#A# 51 pancreatic adenocarcinoma 51 autosomal 51 Telomerase 51 desmosomes 51 encodes protein 51 epigenetic modification 51 eotaxin 51 HPV infection 51 allele frequencies 51 CpG island 51 cause cardiac channelopathies 51 deleterious mutation 51 Smad3 51 allelic variants 51 ovarian cancer 51 Drosha 51 Polymorphisms 51 mitochondrial dysfunction 51 BMP4 51 MicroRNAs 51 Heterozygous 51 Chromosome 51 Stat3 51 endostatin 51 colorectal neoplasia 51 Phosphorylation 51 nonsense mutations 51 #p#.# [001] 51 TLR3 51 activin 51 FGFR2 gene 51 parkin gene 51 mitochondrial function 51 gene APOE 51 malignant transformation 51 Mitochondrial DNA 51 X inactivation 51 ubiquitylation 51 aneuploidies 51 MiRNAs 51 SMN protein 50 noncoding 50 medulloblastoma 50 Myc 50 STK# [002] 50 SPINK1 50 chromosome abnormalities 50 haplotypes 50 deacetylation 50 aromatase 50 Rb gene 50 RNA splicing 50 Rh factor 50 Vpu 50 BRCA gene mutations 50 PALB2 gene 50 hepatic stellate cells 50 SMAD4 50 breast cancer subtypes 50 CXCL5 50 forkhead 50 autosomal recessive 50 colorectal tumors 50 Fanconi anemia 50 Sanger sequencing 50 antigen PSA 50 serous ovarian cancer 50 missense mutation 50 homodimers 50 LDLR 50 ε4 50 chromosome #q#.# [001] 50 M. pneumoniae 50 miR 50 neoplasia 50 epithelial tissues 50 amino terminal 50 chromosome 50 chromosomes 50 K#R [002] 50 RASSF1A 50 thrombophilia 50 linkage disequilibrium 50 NOTCH1 50 EphB4 50 proline rich 50 Foxp3 50 G6PD 50 Adiponectin 50 mRNA transcripts 50 colorectal cancer 50 trisomy 50 polyadenylation 50 carcinoembryonic antigen 50 Oncogenic 50 mitochondrial DNA mtDNA 50 GATA4 50 Rap1 50 SCN5A 50 TGF β 50 chromosome #q# [001] 50 #p# [003] 50 genetic alterations 50 epigenetic changes 50 Endometrial 50 HGPS 50 atypical ductal hyperplasia 50 miRNA genes 50 narcolepsy cataplexy 50 cystatin C 50 array CGH 50 SATB1 50 Germline 50 chromatin structure 50 NR#A# gene 50 neuroblastoma tumors 50 alternative splicing 50 dizygotic twins 50 familial adenomatous polyposis 50 c myc 50 NFAT 50 genetic variants associated 50 miR #b [001] 50 SOD1 gene 50 ERK2 50 microRNAs miRNAs 50 intronic 50 lipoprotein 50 IGF2 50 chromosomal deletions 50 Genetic variants 50 transcriptional regulation 50 vaginal cancers 50 progesterone receptor 50 hematopoetic stem cells 50 genomic alterations 50 interferon pathway 50 Klinefelter syndrome 50 colorectal tumor 50 mRNAs 50 TET2 50 T#I [002] 50 coding sequences 50 causative genes 50 palladin 50 autism susceptibility genes 50 β catenin 50 chlamydial infection 50 number variations CNVs 50 thioredoxin 50 thymosin 50 microRNA miR 50 suppressor gene 50 Dicer 50 PKD1 50 K ras gene 50 cell adhesion molecule 50 Raf MEK ERK 50 H#K# methylation 50 N. gonorrhoeae 50 invasive breast cancer 50 hormone therapy estrogen 50 NMP# 50 DQB1 * 50 epigenetic regulation 50 mutated K ras 50 gene rearrangements 50 globin 50 bcl 2 50 pre eclamptic 50 genomic rearrangement 50 PDE#A 50 Protein Kinase 50 Li Fraumeni syndrome 50 oophorectomy 50 ductal breast cancer 50 JAK2 gene 50 estrogen receptor positive 50 ncRNAs 50 familial hypercholesterolemia 50 dysbindin 50 MEF2A 50 CYP#B# 50 BRAF mutations 50 mesotheliomas 50 prostate carcinoma 50 LIS1 50 Meckel Gruber 50 endometrial cancer 50 Alu elements 50 NF2 50 oncogenesis 50 TOP2A gene 50 epithelial ovarian cancer 50 methylation patterns 50 copper zinc superoxide 50 KLF4 50 isoform 50 herpesviruses 50 Dpp 50 XMRV 49 HER2 expression 49 genetic alteration 49 beta1 integrin 49 microsatellite instability 49 MGUS 49 proto oncogenes 49 VEGF receptor 49 mRNA expression 49 splice junctions 49 NF kB pathway 49 BubR1 49 cervical carcinoma 49 HMMR 49 androgens 49 #p# [001] 49 carcinogenesis 49 caveolin 49 indels 49 pathogenic mutations 49 cervical breast 49 IFN gamma 49 E1A 49 xenograft tumors 49 LMNA 49 ER alpha 49 Smad7 49 Karlseder 49 ovarian pancreatic 49 FTO gene 49 cervical intraepithelial neoplasia 49 progerin 49 Notch1 49 c Myc 49 SORL1 gene 49 axillary lymph nodes 49 NRG1 49 HER2 protein 49 evolutionarily conserved 49 heterozygosity 49 alpha synuclein gene 49 IGFBP2 49 Chromosomal 49 tau protein 49 HER2 positive cancers 49 kinase 49 KIBRA 49 MIF protein 49 lung adenocarcinomas 49 polynucleotide 49 Chlamydia trachomatis 49 subclinical hyperthyroidism 49 NKX#.# 49 APOE e4 gene 49 Smoothened 49 PCA3 49 tyrosine kinase 49 RCAN1 49 CIB1 49 autoantibody 49 proband 49 immunohistochemical 49 endogenous retroviruses 49 OCT4 49 SLITRK1 49 gastrointestinal stromal tumors GISTs 49 Homozygous 49 HNSCC 49 NOD2 49 polymerases 49 exfoliation glaucoma 49 regulator CFTR gene 49 granzyme B 49 Fragile X gene 49 transcriptional repressor 49 catenin 49 regulate gene expression 49 malignant lesions 49 genes predisposing 49 CYP#C# * 49 epigenetically 49 K#N 49 p# activation 49 Mcl 1 49 beta amyloid peptides 49 Ras oncogene 49 susceptibility genes 49 FMRP protein 49 APOE genotype 49 IGFBP 49 epithelial cancers 49 human leukocyte antigens 49 HPV types 49 Sox9 49 MAPK pathway 49 PML RARA 49 nonmelanoma skin cancers 49 Wnt signaling 49 Oncogenes 49 KLF# 49 breast epithelial cells 49 colorectal carcinomas 49 transcription factor 49 miRNA expression 49 ERK1 49 Jagged1 49 β amyloid 49 mutant protein 49 chromosomal regions 49 frameshift mutation 49 Prox1 49 hereditary nonpolyposis colorectal cancer 49 genetic defects 49 CAG repeats 49 Gene Mutation 49 noncoding RNAs 49 superoxide 49 KRAS mutation 49 Aβ 49 ADRB2 49 mammographic density 49 adipogenic 49 recurrent miscarriages 49 RPE# 49 apoptotic pathway 49 VNTR 49 metalloprotease 49 filaggrin gene 49 spermatogenesis 49 hepatocellular carcinomas 49 ARF1 49 C. pneumoniae 49 TGFBR1 49 microRNA expression 49 amino acid residues 49 PKM2 49 abnormal prions 49 BCL#A 49 estrogen receptor beta 49 epithelial tumors 49 HCMV 49 non coding RNAs 49 eIF 4E 49 apolipoprotein E APOE 49 GTPase 49 #S rRNA 49 recessive genetic disorders 49 gp# [002] 49 spinocerebellar ataxia 49 SNP rs# [001] 49 PARP inhibitors 49 cytokeratin 49 receptor molecule 49 MetS 49 variant rs# 49 ASCUS 49 H#K#me# 49 splice variants 49 clade C 49 centrosomes 49 PCSK9 protein 49 prostate cancer CaP 49 SH#B# 49 DLC1 49 GAPDH 49 micrometastases 49 pCR 49 mitochondrial 49 RNA sequences 49 transcriptional repression 49 transactivation 49 HLA DRB1 49 gastric carcinoma 49 cyclophilin D 49 Leydig cells 49 GSTM1 gene 49 eukaryotic cells 49 ADAMTS# 49 faulty BRCA2 gene 49 blastomeres 49 breast endometrial 49 postmenopausal breast cancer 49 methyltransferase 49 tumorigenic 49 activating mutation 49 chromosomal defect 49 G allele 49 CALHM1 49 MMP# 49 chromosome #p#.# 49 eukaryotic 49 dysglycemia 49 invasive carcinoma 49 squamous cell carcinomas 49 NKX2 49 cell signaling pathways 49 genetic syndromes 49 somatic mutation 49 allele frequency 49 prostate adenocarcinoma 49 uPA 49 Ashkenazi Jewish 49 Neuregulin 1 49 TACI 48 atherosclerotic lesions 48 oropharyngeal cancer 48 dystrophin gene 48 Bcl xL 48 FGFR4 48 introns 48 leiomyomas 48 ovarian 48 Fc gamma receptor 48 differentially expressed genes 48 diffuse gastric 48 RNAs 48 EGFR receptor 48 OPRM1 gene 48 ORMDL3 48 cohesin 48 mitochondrial DNA 48 telomerase 48 endonuclease 48 klotho 48 genital tract infections 48 prion protein 48 nucleotide 48 HDACs 48 antisense RNA 48 KIT mutations 48 MALAT1 48 monogenic 48 spontaneous mutation 48 advanced adenomas 48 NGAL 48 hair follicle stem cells 48 ADDLs 48 KRAS gene 48 SNP genotyping 48 beta catenin protein 48 sortilin 48 BMPR2 48 SOX9 48 telomere maintenance 48 dopamine receptor gene