Related by context. All words. (Click for frequent words.) 77 familial ALS 74 FTLD 71 missense mutations 69 NF1 69 PTPN# 69 medulloblastomas 69 ZNF# 69 APOE e4 68 alpha synuclein gene 68 genetic loci 68 MSH2 68 TMEM#B 68 molecular abnormalities 68 DNA methylation patterns 67 apoE4 67 GBA mutations 67 APOE4 67 MLH1 67 motor neuron degeneration 67 #q# [001] 67 autosomal dominant 67 apoE 67 Li Fraumeni syndrome 67 PTEN mutations 67 CNTNAP2 67 APOL1 67 FGFR1 67 autism susceptibility genes 67 genetic polymorphisms 66 ABCB1 66 chromosomal regions 66 heterozygotes 66 genetic variants associated 66 neurofibrillary tangles 66 IgA deficiency 66 neurodegenerative disorder 66 microdeletion 66 germline mutations 66 LRRK2 gene 66 mitochondrial dysfunction 66 SSc 66 familial clustering 66 pathogenic mechanisms 66 SOD1 66 tumor suppressor protein 66 ependymomas 66 underlying pathophysiology 66 HNPCC 66 synuclein 66 HLA DRB1 66 chromosomal translocations 66 microRNA expression 66 K ras mutations 66 CNVs 66 homozygosity 66 essential thrombocythemia 65 susceptibility gene 65 motor neuron diseases 65 Aß 65 STAT4 65 methylation patterns 65 sCJD 65 cyclin E 65 ApoE4 65 FLT3 65 narcolepsy cataplexy 65 mosaicism 65 PTEN gene 65 APOE gene 65 susceptibility genes 65 basal cell nevus syndrome 65 MYH9 gene 65 MECP2 gene 65 pilocytic astrocytomas 65 MGUS 65 PARP inhibition 65 LQTS 65 IDH1 65 aneuploidies 65 somatic mutations 65 causative genes 65 myeloproliferative diseases 65 ADAM# 65 NKX2 65 hypermethylated 65 mtDNA mutations 65 LRRK2 mutations 65 phenotype 65 inherited mutations 65 progranulin 65 TCF#L# 65 #p# [001] 65 rs# [002] 65 TCF#L# gene 65 familial pancreatic cancer 65 pathogenic mutations 65 gene locus 65 GSTP1 65 NF2 65 splice junctions 65 GISTs 65 rs# [004] 65 ADPKD 65 CDH1 65 adenocarcinomas 65 spontaneous mutations 65 β amyloid 65 ependymoma 65 MAPK pathway 65 ApoE gene 65 chromosome #q#.# [001] 65 chromosomal aberrations 65 #q#.# [002] 65 neuronal dysfunction 64 CHD7 64 frontotemporal dementia 64 clusterin 64 causal variants 64 FXTAS 64 atherosclerotic lesions 64 GBM tumors 64 hypermethylation 64 elevated triglyceride levels 64 FGFR2 64 #p#.# [002] 64 missense mutation 64 HLA B# 64 HMGA2 64 childhood leukemias 64 monogenic 64 demyelination 64 T2D 64 microRNA miR 64 epigenetic modification 64 NNRTI resistance 64 LRAT 64 dyskeratosis congenita 64 EBV infection 64 diabetes mellitus DM 64 myeloproliferative neoplasms 64 SORL1 64 genetic polymorphism 64 chromosome #q# [002] 64 nonsense mutations 64 TRAIL induced apoptosis 64 miRNA genes 64 SOD1 mutation 64 ALK mutations 64 paraganglioma 64 Cowden syndrome 64 #q# deletion 64 amyloid beta plaques 64 p# mutations 64 HGPS 64 breast carcinomas 64 GPC5 64 prostate cancer CaP 64 MLL2 64 Hashimoto thyroiditis 64 SCN5A 64 amyloid deposits 64 KLF4 64 Epstein Barr virus EBV 64 alpha synuclein 64 miR #a [001] 64 autosomal recessive 64 FSGS 64 autosomal dominant inheritance 64 LRRK2 63 phenotypic differences 63 IL#R 63 supratentorial 63 ERBB2 63 herpesviruses 63 PICALM 63 amyloid deposition 63 progressive neurodegenerative disorder 63 haplotypes 63 HER2 overexpression 63 myotonic dystrophy 63 tau protein 63 chromosomal instability 63 SLC#A# [002] 63 primary biliary cirrhosis 63 allelic variants 63 gene rearrangements 63 spinocerebellar ataxia 63 Sjögren syndrome 63 SNP rs# [001] 63 systemic amyloidosis 63 MC1R 63 renal fibrosis 63 sortilin 63 NF1 gene 63 Huntingtin 63 PDGFR 63 OGG1 63 Haptoglobin 63 serous ovarian cancer 63 EGFR mutations 63 alpha synuclein protein 63 LRP5 63 gene expression patterns 63 PON1 63 HbF 63 GSTT1 63 #q#.# [001] 63 mitochondrial mutations 63 familial hypercholesterolemia 63 NAFLD 63 neuropilin 63 mesotheliomas 63 leukaemias 63 endophenotypes 63 gastric carcinogenesis 63 BMPR2 63 nicotinic receptor 63 mRNA expression 63 neurofibrillary 63 tyrosine phosphorylation 63 chromosome #q 63 pancreatic adenocarcinoma 63 E#F# 63 IDH2 63 chromosomal rearrangement 63 PCa 63 eotaxin 63 CYP#B# 63 ataxias 63 de novo mutations 63 causative gene 63 JAK mutations 63 nondemented 63 microdeletions 63 chromosomal alterations 63 nonalcoholic steatohepatitis NASH 63 astrocytomas 63 BRAF V#E 63 Clusterin 63 neuropathologic 63 lymphoid cells 63 demyelinating 63 neuroblastoma tumors 63 airway hyperresponsiveness 63 arterial calcification 63 neoplasm 63 substrate specificity 63 non coding RNA 63 T1D 63 CagA 63 colorectal tumor 63 biologic pathways 63 gene polymorphisms 63 chromosomal rearrangements 63 XMRV infection 63 beta amyloid peptides 63 lymphoid 63 autosomal dominant disorder 63 ERK2 63 amnestic MCI 63 INF2 63 PKCi 63 IGF2 63 brain lesions 63 JAK2 enzyme 63 proband 63 Brugada syndrome 63 KIBRA 63 T2DM 62 IKZF1 62 MDM2 62 T#I [002] 62 TP# mutation 62 subclinical atherosclerosis 62 evolutionarily conserved 62 lymphocytic 62 splice variants 62 DLC1 62 ALDH2 62 APOC3 62 p# mutation 62 chromosome #p#.# 62 neoplastic 62 JAK2 62 LDL receptor 62 CFTR gene 62 BCL#A 62 SOD1 gene 62 transgenic mouse model 62 autosomal 62 activated microglia 62 renal cell carcinomas 62 tau pathology 62 Leydig cell 62 pheochromocytoma 62 gastric carcinoma 62 Genetic variants 62 telomere lengths 62 FGFs 62 G#S mutation 62 familial aggregation 62 V#F mutation 62 colorectal carcinoma 62 pDCs 62 maternally inherited 62 squamous cell lung cancer 62 penetrance 62 micro RNA 62 melatonin receptor 62 gene polymorphism 62 WDR# 62 Neuregulin 1 62 genetic determinants 62 virulence genes 62 prostate carcinogenesis 62 GNAQ 62 progranulin mutations 62 proto oncogene 62 medulloblastoma 62 susceptibility loci 62 neuronal cell 62 nonhereditary 62 phenotypic expression 62 ataxin 62 BARD1 62 receptor gene 62 mutant protein 62 MC4R gene 62 miRNA expression 62 EoE 62 indels 62 amyloid peptide 62 myeloma cells 62 APOE genotype 62 BRAF gene 62 genetic variants 62 neuroblastomas 62 S#A# [002] 62 LIS1 62 mitochondrial disorders 62 JAK2 gene 62 Akt3 62 TGF β 62 nucleotide sequence 62 beta amyloid peptide 62 huntingtin gene 62 PNET 62 androgen receptor AR 62 osteopontin 62 NPHP 62 rs# [001] 62 neurodegenerative disease 62 germline mutation 62 chromosome abnormality 62 nNOS 62 Prox1 62 demyelinating diseases 62 vimentin 62 phenotypic variation 62 SOD1 protein 62 epigenetic markers 62 uPAR 62 ARVD 62 microsatellite instability 62 Genetic variation 62 paralogs 62 osteosarcomas 62 mutated K ras 62 R#W [002] 62 NR#A# 62 cell adhesion molecule 62 cystatin C 62 1 diabetes T1D 62 familial adenomatous polyposis 62 gene mutation 62 microcephalin 62 Li Fraumeni 62 Myotonic dystrophy 62 myeloid 62 synaptogenesis 62 huntingtin 62 clinicopathological 62 micro RNAs 62 extramedullary 62 dysbindin 62 CXCR2 62 carcinoid 62 Hedgehog pathway 62 IDH1 mutation 62 monozygotic twins 62 metabolic abnormalities 62 rs# [003] 62 heterozygous 62 cardioembolic stroke 62 FMR1 gene 62 Alzheimer pathology 62 amyloid cascade 62 microRNA molecules 61 genetic mutations 61 EAAT2 61 KIAA# 61 HDACs 61 apolipoprotein E 61 RNA sequences 61 acute leukemias 61 infarcts 61 transgenic mouse models 61 protein isoforms 61 mutated gene 61 severe congenital neutropenia 61 CAG repeats 61 MEF2A 61 ERK signaling 61 histone acetylation 61 PALB2 61 hereditary predisposition 61 chromosomal abnormalities 61 euthymic patients 61 MELAS 61 NFTs 61 microglial activation 61 DQB1 * 61 MYH9 61 Kufs disease 61 CISH 61 COL#A# 61 MYCN amplification 61 homozygotes 61 FGFR3 61 p# activation 61 pancreatic endocrine 61 JAK2 mutation 61 BRCA1 mutations 61 #beta HSD1 61 glutamic acid decarboxylase 61 hepatocellular carcinomas 61 etiologic 61 ccRCC 61 hamartomas 61 PIK3CA 61 myeloproliferative disorders 61 Lewy bodies 61 epigenetic alterations 61 Six3 61 TTR gene 61 WNK1 61 PAOD 61 presenilin 61 orthologs 61 methylated genes 61 VIPR2 61 genetic heterogeneity 61 genetic syndromes 61 C1q 61 chromosome translocations 61 phenotypes 61 serine protease 61 CFH gene 61 TRAF1 C5 61 Becker muscular dystrophy 61 ciliopathies 61 muscular dystrophies 61 BRCA1 BRCA2 61 genetic abnormalities 61 MeCP2 gene 61 epigenetic silencing 61 protein kinase C 61 HNSCC 61 leukemias lymphomas 61 MIF protein 61 mRNA transcripts 61 myeloproliferative 61 nonmelanoma skin cancers 61 cellular prion protein 61 UGT#A# * 61 MTHFR gene 61 MTHFR 61 GSTM1 61 plasma kallikrein 61 ADRB2 61 PCNSL 61 FMR1 61 palladin 61 tyrosine kinases 61 monoclonal gammopathy 61 ADAMTS# 61 genetic abnormality 61 chromosome #p# [001] 61 C. pneumoniae 61 T1DM 61 metabolomic profiles 61 subclinical 61 gene MECP2 61 chromosomal deletions 61 LRP6 61 Chlamydia pneumoniae 61 isoenzymes 61 Hsp# [001] 61 amino acid substitutions 61 Lafora disease 61 Wiskott Aldrich syndrome 61 probands 61 histone modifications 61 genetic variant 61 progranulin gene 61 genomewide 61 amyloid ß 61 neuroinflammation 61 NADPH oxidase 61 TACI mutations 61 BDNF gene 61 neuron degeneration 61 G#S [002] 61 myelofibrosis polycythemia vera 61 FMRP protein 61 CALHM1 61 normal karyotype 61 CHEK2 61 familial adenomatous polyposis FAP 61 TOMM# 61 BRAF mutation 61 circadian clock genes 61 SLC#A# [001] 61 obstructive coronary artery 61 KRAS mutations 61 imatinib resistance 61 SHANK3 61 protein alpha synuclein 61 TTR amyloidosis 61 homeobox gene 61 regulates gene expression 61 PPARγ 61 promoter methylation 61 elevated CRP 61 mutated protein 61 prion protein PrP 61 IRAK1 61 Foxp3 61 ORMDL3 61 spontaneous mutation 61 Dpp 61 chromosomal anomalies 61 molecular subtypes 61 basal cell carcinoma BCC 61 CDK4 61 coding sequences 61 breast cancer subtypes 61 #S rRNA 61 γ secretase 61 aneuploidy 61 lymphomas 61 mitochondrial gene 61 alternatively spliced 61 Dysregulation 61 GPR# [002] 61 seminomas 61 circadian genes 61 IGFBP2 61 NOTCH1 61 chromosomal DNA 61 N Myc 61 SIRT3 61 parkin gene 60 neurofibromatosis type 60 CC genotype 60 sequence homology 60 #p#.# [001] 60 intronic 60 MIF gene 60 COX2 60 Wwox 60 transgene expression 60 CXCL# 60 generalized vitiligo 60 nondiabetic 60 genes predisposing 60 white matter hyperintensities 60 homozygote 60 Wnt signaling pathway 60 mutant proteins 60 VEGF receptor 60 AAT deficiency 60 TGFBR1 * 6A 60 protein kinases 60 prognostic biomarker 60 atypical hyperplasia 60 miRs 60 alternative splicing 60 neuroligins 60 hyperplastic 60 transmembrane protein 60 haematopoietic 60 HLA DRB1 * 60 Alu elements 60 H#K#me# 60 LDLR 60 Leber congenital amaurosis 60 idiopathic PAH 60 epigenetic changes 60 CNTNAP2 gene 60 NR2B 60 ApoE 60 tumoral 60 tHcy 60 autoantibodies 60 cognitively normal 60 VHL gene 60 perilipin 60 circulating endothelial cells 60 isoforms 60 HLA DR 60 mTOR inhibitors 60 inactivating mutations 60 kinase inhibition 60 YKL 60 BRAF protein 60 aggregated Abeta 60 ApoE4 gene 60 HSV1 60 previously undescribed 60 nonischemic 60 inherited retinal degeneration 60 GBMs 60 protein tau 60 pRb 60 hyperinsulinemia 60 PrPSc 60 genomewide association studies 60 cardiac hypertrophy 60 Cholangiocarcinoma 60 genomic instability 60 LPA gene 60 TERT 60 myocyte 60 PKM2 60 mutated genes 60 mutant SOD1 60 hepatoma 60 Leukemias 60 inherited predisposition 60 diagnostic biomarker 60 arrhythmogenic 60 defensin 60 synaptic function 60 MMP# 60 piRNAs 60 allele frequencies 60 HG PIN 60 JMML 60 functional polymorphism 60 SLITRK1 60 histone deacetylases 60 NF kB pathway 60 fatty acid synthase 60 serotonin receptor 60 protein encoded 60 IDH mutations 60 DLX5 60 PTHrP 60 gene APOE 60 prostate adenocarcinoma 60 dominantly inherited 60 fibrotic disease 60 telomere shortening 60 myopathies 60 microbleeds 60 CaM kinase II 60 biochemical abnormalities 60 KRAS oncogene 60 VKORC1 60 NKX#.# 60 Friedreich ataxia 60 systemic lupus erythematosus SLE 60 Karayiorgou 60 lung metastasis 60 gene variants 60 gastric adenocarcinoma 60 chronic myeloid 60 activating mutations 60 nicotinic receptors 60 CYP#C# gene 60 epithelial tumors 60 chromosome #q# [001] 60 activin 60 RIP1 60 estrogen receptor alpha 60 biochemical marker 60 karyotype 60 tRNA synthetase 60 UGT#B# 60 dizygotic twins 60 Angiotensin converting enzyme 60 amyloid plaque formation 60 dysregulated 60 genomic deletions 60 ribosomal proteins 60 gene expression profiles 60 del 5q 60 meningiomas 60 APOE ε4 60 Janus kinase 60 carotid plaque 60 gliosis 60 Cockayne syndrome 60 airway remodeling 60 nephronophthisis 60 autoinflammatory diseases 60 prion infection 60 C#Y 60 IL 1ß 60 untreated celiac disease 60 PAR1 60 unmutated 60 potent inhibition 60 lung adenocarcinoma 60 IGF1 60 genetic locus 60 Wnt#b 60 GSTM1 gene 60 motor neurones 60 G6PD 60 microarray experiments 60 p tau 60 β cells 60 CYP#C# [001] 60 genetic variation 60 fronto temporal dementia 60 JAK3 60 CYP# [002] 60 pre malignant lesions 60 cardiac fibrosis 60 ribosomal protein 60 phosphatases 60 iNOS 60 alleles 60 ultraconserved elements 60 catechol O methyltransferase 60 p#INK#a 60 CDKN2A 60 nestin 60 RUNX3 60 androgen receptor gene 60 Gleevec resistant 60 transgenic rats 60 KCNH2 60 SIRT1 gene 60 Peutz Jeghers syndrome 60 FGFR2 gene 60 uveal melanoma 60 IL 1β 60 TIMP 60 mutation 60 breast cancer susceptibility genes 60 GPx 60 amyloid plaque 60 mGluR5 antagonist 60 paraneoplastic 60 Relapsing remitting MS 60 cardioprotective effects 60 filaggrin 60 MMPs 60 Wnt pathway 60 endostatin 60 #p# [003] 60 SMAD4 60 Aβ 60 teratoma 60 inhibitory receptor 60 Glioblastoma multiforme GBM 60 syngeneic 60 PPAR γ 60 SGK1 60 Neurofibromatosis type 60 mutated p# 60 enzymatic activity 60 Retinitis pigmentosa 60 Cyclin E 60 mucinous 60 E3 ligase 60 myotonic muscular dystrophy 60 abnormal proteins 60 APOE allele 60 KIF6 gene 60 TrkB 60 p# MAPK 60 amyloids 60 chemokine receptor 60 HMGA2 gene 60 amyloid pathology 60 Hutchinson Gilford progeria 60 SNPs 60 apolipoprotein E gene 60 neuropsychiatric diseases 60 atherothrombosis 60 RPE# 60 thyroid carcinoma 60 HMGCR 60 colorectal adenoma 60 IGFBP 3 60 clefting 60 miRNAs miR 60 mice lacking 60 IGFBP 60 TP# gene 60 endogenous retroviruses 60 sarcomatoid 60 genetic alterations 60 lymphoproliferative disorders 59 glioblastoma tumors 59 neuropathological 59 presymptomatic 59 dysglycemia 59 telomere length 59 vWF 59 inflammatory bowel diseases 59 inherited genetic mutations 59 Kabuki syndrome 59 B7 H3 59 intergenic 59 spinocerebellar ataxia type 59 gene amplification 59 CpG island 59 hypertrophic cardiomyopathy HCM 59 UCP2 59 promoter hypermethylation 59 ductal adenocarcinoma 59 pathophysiologic 59 GRP# 59 commonly mutated genes 59 hepatocellular carcinoma HCC 59 apolipoprotein E APOE 59 CHD5 59 XLHED 59 thyroglobulin 59 mutations 59 DICER1 59 cellular pathways 59 Abeta# 59 CYP#C# [002] 59 transgenic mice expressing 59 isoform 59 SOD2 gene 59 dopamine D4 receptor 59 thrombophilia 59 microglial 59 MAOA gene 59 TOP2A 59 cytopathic 59 prognostic marker 59 homozygous 59 TLR3 59 hereditary hemochromatosis 59 claudin 59 disease NAFLD 59 lysosomal storage diseases 59 colorectal tumors 59 cranial irradiation 59 Hurler syndrome 59 Upregulation 59 A3 adenosine receptor 59 parkinsonism 59 COMT 59 Immunohistochemical analysis 59 cardiac dysfunction 59 breast cancer metastasis 59 TAp# 59 PrP 59 EphA2 59 Fibroblast Growth Factor Receptor 59 ErbB2 59 gene fusions 59 5q 59 sphingolipid 59 metabolic enzymes 59 eosinophilic esophagitis 59 neuropsychiatric disorders 59 mitogen activated protein kinase 59 cardiac myocytes 59 exomes 59 suppressor gene 59 transcriptional regulation 59 klotho 59 micrometastases 59 Cyclin D1 59 histological subtype 59 differentially regulated 59 pharmacologic intervention 59 malignant transformation 59 c myc 59 mutant allele 59 miRNAs 59 mutational status 59 GATA4 59 uPA 59 metastatic tumors 59 idiopathic myelofibrosis 59 oxysterols 59 leukemia AML 59 adipogenic 59 hepatic steatosis 59 congenital muscular dystrophies 59 beta1 integrin 59 MDR1 59 neuropsychiatric disorder 59 synovial sarcoma 59 karyotypes 59 Acute myeloid leukemia 59 immunoregulatory 59 ATG#L# 59 paragangliomas 59 collagen VI 59 HBx 59 coding genes 59 chromosome abnormalities 59 Alzheimers disease 59 autosomal recessive disease 59 tryptase 59 telomere dysfunction 59 neuroblastoma cells 59 epigenetic inheritance 59 pleural mesothelioma 59 ANCA associated 59 beta amyloid plaques 59 CYP#D# 59 c KIT 59 glycogen synthase kinase 59 immunoreactivity 59 mtDNA 59 calcineurin 59 Chronic lymphocytic leukemia 59 papillary renal cell carcinoma 59 GRK2 59 polymorphisms 59 haptoglobin 59 fibrous tangles 59 TSC1 59 cell signaling pathways 59 FGF# 59 neuronal function 59 aneuploid cells 59 liver metastasis 59 inherited neurological disorder 59 excitotoxicity 59 DISC1 gene 59 distinct subtypes 59 costimulatory 59 antibody mediated 59 basal cell carcinomas 59 Meckel Gruber 59 microvascular disease 59 apoptotic pathway 59 chronic lymphocytic leukemia CLL 59 prion disease 59 IL#B 59 endometrioid 59 dopamine signaling 59 APOE e4 gene 59 monocytic 59 pathological hallmark 59 remyelination 59 bcl 2 59 metaplasia 59 cyclophilin D 59 epigenetic regulation 59 tumor suppressor gene 59 BRCA2 gene 59 cardiolipin 59 beta globin gene 59 subcellular compartments 59 cisplatin resistant 59 Fanconi anemia 59 Hh 59 colorectal neoplasia 59 modifier genes 59 FANCD2 59 autoantibody 59 superoxide dismutase 59 ependymal cells 59 amnestic mild cognitive impairment 59 SORL1 gene 59 MALAT1 59 phospholipase A2 59 parainfluenza virus 59 eNOS 59 somatic mutation 59 protein tyrosine phosphatase 59 granzyme B 59 cAMP signaling 59 monocyte chemoattractant protein 59 HGPIN 59 Bcr Abl 59 chromosomal translocation 59 neuro degenerative disease 59 linkage disequilibrium 59 troponin T 59 gene mutations 59 phylogenetically 59 SCD1 59 immunopathology