Related by context. All words. (Click for frequent words.) 79 BRCA2 gene 77 BRCA1 74 mutated gene 73 BRCA2 71 mutated BRCA1 70 BRCA1 mutation 70 gene mutation 69 BRCA mutation 68 mutation 68 breast cancer genes BRCA1 68 BRCA1 mutations 68 mutated genes 67 PALB2 67 BRIP1 67 gene mutations 67 BRCA 67 BRCA gene mutation 66 BRCA mutations 66 genetic mutations 66 BRCA2 mutation 66 BRCA genes 65 p# gene 65 genes BRCA1 65 MSH2 65 defective gene 65 tumor suppressor gene 65 genetic mutation 65 mutant gene 65 mutations 65 p# protein 65 BRAF gene 64 inherited mutations 64 G#S mutation 64 EGFR gene 64 genes 64 gene 64 PTPN# 63 BRAC2 63 breast cancer gene mutation 63 ApoE4 gene 63 BRCA2 mutations 63 BRCA gene 63 PTEN gene 63 genetic variant 63 p# mutations 63 genetic abnormalities 63 BRCA2 gene mutation 63 CFTR gene 63 gene variant 62 gene BRCA2 62 ApoE4 62 APOE4 62 BRCA2 gene mutations 62 BRCA2 breast cancer 62 genetic alteration 62 SMN1 gene 61 APOE gene 61 LRRK2 gene 61 BARD1 61 Fragile X gene 61 HER2 gene 61 BRCA2 carriers 61 FMR1 gene 61 tumor suppressor genes 61 WT1 61 FGFR2 61 aneuploidy 60 TP# mutation 60 estrogen receptor 60 micro RNAs 60 TCF#L# gene 60 FTO gene 60 CYP#D# gene 60 somatic mutations 60 CDH1 60 gene variation 60 p# mutation 60 hereditary breast cancer 60 myostatin gene 60 VHL gene 60 NF1 gene 60 RUNX3 60 chromosomal abnormalities 60 genetic abnormality 60 epigenetic changes 60 SMN2 60 heterozygous 60 CDKN2A 59 BRCA1 gene mutation 59 androgen receptor gene 59 mammary cells 59 genes BRCA 59 TAp# 59 Foxp3 59 IKZF1 59 progerin 59 Rb gene 59 epigenetically 59 DISC1 gene 59 breast epithelial cells 59 MTHFR 59 X chromosome 59 Pten 59 SHANK3 59 mutated BRCA 59 NF1 59 endostatin 59 mosaicism 59 atypical hyperplasia 59 Akt1 59 HMGA2 59 GPC5 59 CCR5 delta# 59 BRCA1 BRCA2 59 Epstein Barr virus EBV 59 CHEK2 59 genetic variants 59 KRAS mutations 59 SORL1 59 MLH1 59 MECP2 gene 59 MC1R gene 59 APOE e4 59 miRNAs 59 microRNAs 58 genetic defect 58 cyclin D1 58 mtDNA mutations 58 mutant allele 58 TACI mutations 58 familial ALS 58 CDK4 58 ovarian tumors 58 HNPCC 58 TP# gene 58 genetic defects 58 GFP gene 58 MLL2 58 estrogen receptors 58 apolipoprotein E gene 58 HOTAIR 58 lung adenocarcinoma 58 FGFR2 gene 58 tumor suppressor protein 58 GBM tumors 58 maternally inherited 58 MTHFR gene 58 progranulin gene 58 LRAT 58 palladin 58 nonsense mutations 58 gene variants 58 APOE ε4 58 protein encoded 58 germline mutations 58 alpha synuclein gene 57 KRAS oncogene 57 ERBB2 57 CHD7 57 GNAQ 57 alleles 57 autoantibodies 57 EZH2 57 BRCA2 mutation carriers 57 Wwox 57 Li Fraumeni 57 MYH9 gene 57 epigenetic silencing 57 MeCP2 gene 57 NFKBIA 57 Cyclin D1 57 CCR5 gene 57 HER2 receptor 57 gene expression patterns 57 histone modification 57 gene amplification 57 LKB1 57 NF kB 57 MC1R 57 MEF2A 57 SATB1 57 genes predisposing 57 DICER1 gene 57 CNVs 57 ALK gene 57 CNTNAP2 57 homozygous 57 APOE4 gene 57 MLL gene 57 KRAS gene 57 imprinted genes 57 SRY gene 57 EGFR mutation 57 faulty BRCA1 gene 57 chromosomal 57 allele 57 missense mutations 57 SMN2 gene 57 APOL1 57 epigenetic mechanisms 57 breast cancers 57 oncogenes 57 apoE 57 GSTP1 57 endometrial cancers 57 HGPS 57 medulloblastomas 57 C#Y 57 HPV# 57 KIF6 gene 57 breast tumors 57 mutant protein 57 COMT gene 57 TMEM#B 57 FOXP3 57 androgen receptor 57 LIS1 57 chromosome abnormality 57 EGFR protein 56 germline 56 vimentin 56 PARP inhibition 56 placental function 56 oncoprotein 56 ApoE gene 56 spontaneous mutation 56 methylation 56 hypermethylated 56 Pin1 56 mutant genes 56 SOD1 gene 56 activating mutations 56 estrogen receptor alpha 56 Peutz Jeghers syndrome 56 APOE allele 56 microdeletions 56 abnormal prions 56 Genetic variants 56 MnSOD 56 PKM2 56 STAT4 56 Wnt signaling 56 chromosomal aberrations 56 IDH1 56 LRP5 56 TGFBR1 * 6A 56 PIK3CA 56 ApoE 56 germ cells 56 aneuploid 56 chromosomal rearrangement 56 susceptibility gene 56 caveolin 1 56 promoter hypermethylation 56 Ets2 56 de novo mutations 56 chromosomal regions 56 ovarian cancers 56 aromatase 56 MIF protein 56 DNA methylation patterns 56 micro RNA 56 MDM2 56 inherited gene mutation 56 kinase gene 56 STAT3 56 HLA genes 56 HCMV 56 suppressor gene 56 NFkB 56 virulence genes 56 p# [001] 56 HFE gene 56 K ras mutations 56 ZNF# 56 parkin gene 56 breast cancer metastasis 56 MC4R gene 56 nestin 56 SOCS1 56 FOXP3 gene 56 BRAF mutation 56 SMN protein 56 SCN5A 56 Meckel Gruber 56 familial pancreatic cancer 56 IGF1 56 filaggrin gene 56 KLF# 56 anaplastic lymphoma kinase 56 microcephalin 56 chromosome abnormalities 56 NF kB pathway 56 endometrial cells 55 germline mutation 55 HbF 55 TCF#L# 55 mitochondrial DNA mtDNA 55 genomic instability 55 SMN1 55 PKD1 55 primordial germ cells 55 Six3 55 miRNA genes 55 LQTS 55 gene rearrangements 55 leukaemic cells 55 mtDNA 55 CCL#L# 55 tumor suppressor p# 55 PTEN protein 55 GAB2 55 epigenetic modification 55 p# deficient 55 DISC1 55 mutated K ras 55 recessive gene 55 GBV C 55 gene p# 55 CYP#C# [001] 55 HER2 55 LPA gene 55 malignant transformation 55 SIRT6 55 breast carcinomas 55 BRCA gene mutations 55 testicular germ cell 55 E cadherin 55 BCR ABL protein 55 spontaneous mutations 55 recessive mutations 55 constitutively 55 HLA DQ2 55 missense mutation 55 tumorigenesis 55 MSH6 55 apolipoprotein E 55 SLC#A# gene [001] 55 oncogene 55 mitochondrial fusion 55 TSC1 55 SORL1 gene 55 genetic alterations 55 CHEK2 gene 55 UGT#B# 55 IL#R 55 blastomeres 55 Skp2 55 ADPKD 55 endocrine tumors 55 chromosomal rearrangements 55 genetic variations 55 neural tube defect 55 faulty BRCA2 gene 55 Sox9 55 primary cilia 55 #q#.# [001] 55 neuroblastomas 55 Epstein Barr virus 55 R#W [002] 55 Notch signaling 55 Klotho gene 55 Clusterin 55 poorer prognosis 55 FMR1 55 Wolbachia 55 apoE4 55 DICER1 55 IRS1 55 Notch pathway 55 molecular pathways 55 CIB1 55 sporadic ALS 55 molecular pathway 55 RNA splicing 55 Lrp5 55 Prox1 55 mutant alleles 55 SGK1 55 methylation patterns 55 ERCC1 55 mutant worms 55 IgA deficiency 55 FLT3 55 heterozygote 55 LMNA 55 IDH1 mutation 55 alpha synuclein 55 IKKa 55 BRCA1 mutation carriers 55 tumor suppressor 54 proto oncogene 54 hypermethylation 54 progranulin 54 tumors 54 ErbB2 54 FANCD2 54 BMP2 54 chromosomal instability 54 uPAR 54 Pten gene 54 MECP2 54 transthyretin 54 genetic polymorphisms 54 K ras gene 54 NR#A# 54 presenilin 54 RNA molecule 54 Stat5 54 CETP VV 54 telomerase gene 54 Heterozygous 54 K#R [002] 54 thyroid hormone levels 54 SPINK1 54 RPE# 54 TP# mutations 54 genetically engineered mice 54 RPE# gene 54 Myc 54 ovaries 54 mitochondrial mutations 54 mRNA transcripts 54 mouse embryos 54 Apert syndrome 54 Src 54 mutant proteins 54 EGFR 54 C EBP alpha 54 IGF2 54 thalassemia trait 54 APOE e4 gene 54 FOXP2 gene 54 TOP2A gene 54 medulloblastoma 54 germline stem cells 54 chromosome 54 gene expression 54 HLA B# 54 NEIL1 54 recessive mutation 54 Wnt#b 54 clusterin 54 BDNF gene 54 mice lacking 54 receptor protein 54 epigenetic 54 causal variants 54 dopamine receptor gene 54 BCL#A 54 rs# [002] 54 hormone estrogen 54 IRF5 54 V Leiden 54 microRNA molecules 54 heterotaxy 54 mesenchymal cells 54 IRF6 54 tumor cells 54 ABCB1 54 MMP9 54 NKX#.# 54 herpes viruses 54 Sonic Hedgehog 54 Wnt signaling pathway 54 prion gene 54 microRNA miR 54 mitochondrial gene 54 mitochondrial genome 54 IDH2 54 GPR# [002] 54 E#F# 54 mutated protein 54 sarcosine 54 GSTT1 54 chimeric mice 54 FHIT 54 beta catenin 54 HLA molecules 54 enzymatic activity 54 apoC III 54 breast carcinoma 54 dystrophin gene 54 genes encoding 54 Dpp 54 polycystic ovary syndrome PCOS 54 prostate cancers 54 KIAA# 54 pRb 54 variant allele 54 chitinase 54 HER2 neu 54 RASSF1A 54 gene sequences 54 colorectal tumor 53 recessive genes 53 Li Fraumeni syndrome 53 chromosomal defects 53 tumor suppressing 53 mitochondrial DNA 53 ependymomas 53 genetic 53 DEC2 53 Neuregulin 1 53 alternatively spliced 53 neuroblastoma tumors 53 interferon pathway 53 lipin 53 penetrance 53 5 HTT gene 53 malignant prostate 53 EGFR mutations 53 transgenic mouse model 53 homozygosity 53 Id1 53 aneuploidies 53 number variations CNVs 53 atypia 53 OCA2 gene 53 CXCL5 53 hair follicle stem cells 53 miRNA expression 53 oncogenic 53 chromatin structure 53 Bcr Abl 53 BRAF protein 53 ADAM# 53 connexin 53 epigenetic modifications 53 MHC genes 53 CNTNAP2 gene 53 LRRK2 53 Vpu 53 holoprosencephaly 53 #q# [002] 53 female hormone estrogen 53 mRNAs 53 bowel cancers 53 Genes 53 genotoxic stress 53 methylated DNA 53 gene predisposing 53 MiRNAs 53 H2AX 53 microdeletion 53 mutated BRAF gene 53 variant alleles 53 BRAF V#E 53 HER2 protein 53 protein p# 53 EGFRvIII 53 PCSK9 protein 53 NOD2 53 genetic variation 53 ductal breast cancer 53 IRAK1 53 exons 53 Ras oncogene 53 Cx# [001] 53 TRIM5 53 Hashimoto thyroiditis 53 SMAD4 53 Wnt pathway 53 LRP6 53 NR#A# gene 53 pre eclamptic 53 colon tumors 53 regulate gene expression 53 JAK2 mutation 53 BRCA breast cancer 53 overexpression 53 APOE 53 MHC molecules 53 shorter telomeres 53 beta1 integrin 53 GSTM1 gene 53 trophoblasts 53 RKIP 53 DNA methylation 53 p# activation 53 RAR beta 53 TGF beta pathway 53 K#N 53 mice genetically engineered 53 Genetic mutations 53 overexpress 53 estrogen receptor negative 53 nonsense mutation 53 adenoma 53 mammalian genome 53 thyroid hormones 53 X chromosome genes 53 hematopoetic stem cells 53 signaling pathway 53 c MYC 53 HMMR 53 causative genes 53 PALB2 gene 53 senescent cells 53 FMRP protein 53 ovaries removed 53 APOC3 53 Mitochondrial DNA 53 regulator CFTR gene 53 RCAN1 53 heritable 53 polymorphism 53 dopamine D4 receptor 53 haplotype 53 apolipoprotein E4 53 chromosomal anomalies 53 melanoma tumors 53 ApoE4 allele 53 Ashkenazi Jewish 53 axillary lymph nodes 53 mutant SOD1 53 HER2/neu 53 NOTCH1 53 gamma globin gene 53 ncRNAs 53 Chromosome 53 normal karyotype 53 noncoding 53 TB bacterium 53 PTEN 53 Notch1 53 p# tumor suppressor 53 gene BRCA1 53 PTEN mutations 53 caveolin 53 non coding RNAs 53 Ras pathway 53 genomic rearrangements 53 uterine ovarian 53 intestinal polyps 53 #q# [001] 52 PTP1B 52 pancreatic islet 52 HLA B 52 cyclophilin D 52 S#K# 52 ADAMTS# 52 allelic variants 52 piRNAs 52 HER2 positive tumors 52 Stat3 52 Smad3 52 TYMS 52 CEACAM1 52 E1A 52 FUS protein 52 Genetic variation 52 TH# cells 52 prostate tumors 52 colon cancers 52 VKORC1 52 telomere lengths 52 EphA2 52 mammary tumors 52 cyclin E 52 ERK2 52 dystrophin 52 ubiquitylation 52 polymorphisms 52 IFNg 52 SOX3 gene 52 TRAF1 C5 52 DHFR 52 ETV1 52 toxoplasmosis 52 chromosomes 52 pathogenic mutations 52 normal prion protein 52 FXTAS 52 miR #b [001] 52 ES cells 52 protein kinases 52 Irs2 52 mitochondrial function 52 postmenopausal breast cancer 52 methylated genes 52 HOX genes 52 X chromosomes 52 colorectal tumors 52 chromosomal translocations 52 LDLR 52 sFlt 1 52 valine 52 androgen receptor AR 52 estrogen receptor ER 52 UGT#A# * 52 polycystic ovary syndrome 52 antisense RNA 52 proteins 52 BRCA mutation carriers 52 RAD# [001] 52 ribonucleic acid RNA 52 neural crest cells 52 mitochondrial disorders 52 CYP#C# [002] 52 DLC1 52 5 HTTLPR 52 serotonin transporter gene 52 SNPs 52 gene encoding 52 chlamydial infection 52 Joubert syndrome 52 mRNA decay 52 HER2 positivity 52 KRAS mutation 52 neuroligins 52 invasive carcinoma 52 HMGA2 gene 52 aneuploid cells 52 PHLPP 52 PDGFR 52 germline cells 52 HPVs 52 miR 52 COX2 52 PCa 52 CYP#C# * 52 non coding RNA 52 CALHM1 52 miRNA 52 microRNA expression 52 Hsp# [001] 52 Math1 52 melanocyte 52 X inactivation 52 miR #a [001] 52 ovary 52 FGFR3 52 GATA4 52 human leukocyte antigen 52 uterine cancers 52 OGG1 52 deleterious mutation 52 neural crest 52 mutant mouse 52 Single Nucleotide Polymorphisms SNPs 52 M. genitalium 52 endogenous retroviruses 52 Helicobacter 52 tyrosine phosphorylation 52 DEAR1 52 vesicular stomatitis virus 52 crystallin 52 Mcl 1 52 KCNE2 52 Wnt1 52 genetic polymorphism 52 PrPSc 52 LDL receptor 52 HMGCR 52 C1q 52 ε4 52 tau gene 52 prostate adenocarcinoma 52 epigenetic marks 52 SHBG 52 mitochondrial metabolism 52 cypin 52 chromosome #q#.# [001] 52 neuroglobin 52 Transcription factors 52 p#INK#a 52 somatic mutation 52 genomic imprinting 52 DNA rearrangements 52 sortilin 52 overexpressing 52 monozygotic twins 52 pneumococci 52 leptin receptor 52 epigenetic regulation 52 premature menopause 52 susceptibility genes 52 S#A# [002] 52 AGTR1 52 CAG repeats 52 prion protein 52 isoform 52 micrometastases 52 medulloblastoma tumors 52 salpingo oophorectomy 52 haematopoietic 52 CGG repeats 52 miR #b [002] 52 myelomeningocele 52 beta catenin protein 52 SIRT3 52 telomerase 52 abnormal chromosomes 52 ER alpha 52 Leydig cells 52 mitochondrial dysfunction 52 MeCP2 protein 52 GLI1 52 c Myb 52 CYP#B# 52 HeLa 52 TCF4 52 NRG1 52 FGFR1 52 messenger RNAs 52 ARF1 52 telomere dysfunction 52 KSHV 52 ovarian hormones 52 mammary cancers 52 epigenetic alterations 52 cystic fibrosis transmembrane conductance 52 spinocerebellar ataxia 52 miR #a [002] 52 estrogen receptor positive 52 Klinefelter syndrome 52 chromosomal defect 52 beta thalassemia 52 BCR ABL 52 N. gonorrhoeae 52 lobular carcinoma 52 c Myc 52 sequence homology 52 transcription factors 52 mitochondrial genes 52 microRNA 52 neurofibromin 52 hTERT 52 fronto temporal dementia 52 retinoic acid 52 homozygotes 52 ribosomal RNA 52 cultured cells 52 transcriptional repressor 52 oophorectomy 52 genetically modified mice 52 Apobec3 52 interferon gamma 52 KCNQ1 52 Jhdm2a 52 nonmelanoma skin cancers 52 antisense oligonucleotides 52 mutant huntingtin protein 52 OCT4 52 chromosomal anomaly 52 recessive trait 52 epigenome 52 leptin receptors 52 male hormone androgen 52 defective mitochondria 52 toxoplasma 52 PPAR alpha 52 receptor molecule 52 heterozygotes 52 RNA transcripts 52 Pax6 52 cybrids 52 epithelial tissues 51 Alu elements 51 PDE#A 51 ovarian cancer 51 dyskeratosis congenita 51 ependymoma 51 endogenous estrogen 51 JAK2 51 insulin secreting cells 51 RNAs 51 PICALM 51 Mdm2 51 HER2 positive cancers 51 BRCA carriers 51 Atoh1 51 TOMM# 51 transcriptional repression 51 Kufs disease 51 lung tumors 51 eukaryotic cells 51 lobular involution 51 NKT cells 51 BRAF V#E mutation 51 Akt 51 apoptotic pathway 51 excitatory synapses 51 TSP1 51 gp# [002] 51 huntingtin gene 51 neural cells 51 Akt3 51 telomerase enzyme 51 chromosome segregation 51 herpes virus 51 BRAF mutations 51 GATA3 51 thymosin 51 podocytes 51 overexpressed 51 TGF ß 51 syngeneic 51 genes CYP#C# 51 BMP4 51 H#K# methylation 51 chromosomal abnormality 51 MCAD deficiency 51 N Myc 51 EBNA1 51 TEL AML1 51 segmental duplications 51 chromosomal alterations 51 inactive X chromosome 51 klotho 51 myelination 51 hedgehog pathway 51 TGF beta 51 paternally inherited 51 colorectal neoplasia 51 Yamanaka recipe 51 recessive genetic disorders 51 HER-2/neu 51 E4 variant 51 atherosclerotic lesions 51 E cadherin expression 51 haplotypes 51 mesotheliomas 51 gene expression profiles 51 metastasis 51 insulin receptors 51 JAK2 gene 51 CXCL# 51 protein isoforms 51 C. neoformans 51 promoter methylation 51 adenocarcinomas 51 protein fragment 51 polyomavirus 51 luminal cells 51 chromosomal DNA 51 glandular tissue 51 cohesin 51 collagen VI 51 folate metabolism 51 inherited predisposition 51 cytomegalovirus CMV 51 genetic syndromes 51 calcineurin 51 SOD1 protein 51 endometrial cancer 51 ARID1A 51 premalignant lesions 51 Bt toxin 51 retrovirus 51 herpesviruses 51 STK# [002] 51 cholesterol metabolism 51 familial adenomatous polyposis 51 prostate cancer CaP 51 #p# [001] 51 metastatic melanomas 51 Myc protein 51 tau protein 51 mutant huntingtin 51 tyrosine kinases 51 abnormal chromosome 51 xenograft tumors 51 nematode worms 51 Y chromosome 51 EAAT2 51 alternative splicing 51 autosomes 51 cell signaling pathways 51 Fanconi anemia 51 SERT gene 51 OPRM1 gene 51 C. pneumoniae 51 mammary stem cells 51 Aβ 51 Th# cells 51 ALK mutations 51 genetic variants associated 51 Nrf2 51 pancreatic lung 51 pyruvate kinase 51 GSTM1 51 astrocyte 51 autoantibody 51 Bcl 2 51 GISTs 51 PKCi 51 serous ovarian cancer 51 BRCA deficient 51 GRP# 51 Immunohistochemical analysis 51 Plasmodium 51 globin 51 acetylation 51 transgenic mice 51 proband 51 DUX4 51 neural progenitor cells