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(Click for frequent words.) 68 de novo mutations 67 spontaneous mutations 65 monogenic 65 genetic loci 65 somatic mutations 64 genomic rearrangements 64 histocompatibility 64 gene rearrangements 64 missense mutations 64 chromosomal anomalies 63 IL#R 63 narcolepsy cataplexy 63 anemias 63 microRNA expression 63 inherited genetic mutations 63 chromosome rearrangements 63 epigenetic alterations 62 KCNH2 62 autoinflammatory diseases 62 somatic mutation 62 non coding RNA 62 epigenetic changes 62 TGFBR1 * 6A 62 inherited mutations 62 chromosomal rearrangement 62 phenotypic expression 62 Genetic predisposition 62 Treg cell 62 neuropathologic 62 microdeletion 62 molecular abnormalities 62 pathogenic mutations 62 chromosome translocations 62 neuropsychiatric diseases 62 Clusterin 62 MGUS 62 underlying pathophysiology 62 epigenetic regulation 61 miRNA expression 61 genetic variants associated 61 microRNAs miRNAs 61 beta1 integrin 61 progranulin gene 61 microcephalin 61 BARD1 61 Cathepsin B 61 MYH9 gene 61 osteosarcomas 61 microarray experiments 61 VIPR2 61 multigenic 61 DNA demethylation 61 MEF2A 61 methylation markers 61 susceptibility loci 61 modifier genes 61 Genetic variations 61 indels 61 DNA rearrangements 61 CALHM1 60 lysosomal storage diseases 60 chromosome aberrations 60 engineered RAP peptides 60 degenerative neurological diseases 60 protein misfolding 60 HbF 60 germline mutations 60 microRNA molecules 60 transgenic mouse models 60 genetic heterogeneity 60 Prion diseases 60 genomic instability 60 ependymomas 60 amyloid cascade 60 mtDNA mutations 60 genetic aberrations 60 sickle cell hemoglobin 60 causative mutations 60 nongenetic 60 MC4R gene 60 hereditary predisposition 60 PTPN# 60 ALK mutations 60 KRAS oncogene 60 APOE ε4 60 epigenetic modification 60 phenotypic differences 60 PTEN mutations 60 JAK2 enzyme 60 mosaicism 60 splice variants 60 Inflammatory bowel diseases 60 sCJD 60 epigenetic markers 60 Arabidopsis genes 60 ataxias 60 mutated K ras 60 Genetic variants 60 GBA mutations 60 genomewide association studies 60 neuropsychiatric disorder 60 inherited neurological disorder 60 Chlamydia trachomatis infection 60 HLA alleles 60 CHD7 60 miRNA expression patterns 60 familial clustering 59 KIAA# 59 chromosomal aberrations 59 #beta HSD1 59 hypomethylation 59 nonhereditary 59 noncoding RNAs 59 Autoimmune disorders 59 immunoregulation 59 autoinflammatory 59 seminomas 59 progressive neurodegenerative disorder 59 herpesviruses 59 epigenetic modifications 59 multiplex assay 59 myopathies 59 aneuploidies 59 pilocytic astrocytomas 59 mitochondrial disorders 59 circulating endothelial cells 59 familial predisposition 59 genetic alterations 59 HGPS 59 epigenetic mechanisms 59 systemic amyloidosis 59 #q#.# [001] 59 Epileptic seizures 59 missense mutation 59 sequence homology 59 PARP inhibition 59 genetic syndromes 59 chromosomal anomaly 59 GPC5 59 pathogenic mechanisms 59 mRNA transcripts 59 Kufs disease 59 tumor suppressor protein 59 MDR1 59 G6PD deficiency 59 observable traits 59 Mendelian disorders 59 dyskeratosis congenita 59 M. pneumoniae 59 generalized vitiligo 59 CNTNAP2 59 brain lesions 59 phenotypic variation 59 genomic alterations 59 Polycomb proteins 59 genotoxic stress 59 #q# deletion 59 intercellular signaling 59 IgA deficiency 59 genetic polymorphisms 59 telomere dysfunction 59 oncogenesis 59 SMAD4 59 TACI mutations 59 Bardet Biedl Syndrome 59 familial pancreatic cancer 59 neurexins 58 APOE genotype 58 myeloproliferative 58 FGFs 58 chromosomal disorders 58 Chronic pancreatitis 58 BMPR2 58 beta globin gene 58 hypermethylated 58 protein isoforms 58 HMGCR 58 etiologic 58 spontaneous mutation 58 Single Nucleotide Polymorphisms SNPs 58 Genetic profiling 58 SHANK3 58 Genetic mutations 58 gene locus 58 HLA B# 58 ZNF# 58 Genetic mutation 58 miRs 58 pathophysiological 58 motor neuron degeneration 58 squamous cell lung cancer 58 familial ALS 58 antibody mediated 58 Systemic lupus erythematosus SLE 58 neuro degenerative disorders 58 V#F mutation 58 pathogenetic 58 demyelinating diseases 58 inbred strains 58 mRNA molecules 58 VHL gene 58 aneuploid cells 58 gene APOE4 58 HLA molecules 58 fatty acid biosynthesis 58 microdeletions 58 genomewide 58 neuropsychological impairments 58 XMRV infection 58 BRCA1 BRCA2 58 mitochondrial dysfunction 58 cardiomyopathies 58 PML RARA 58 progressive neurodegenerative disorders 58 Alternative splicing 58 Wnt signaling pathway 58 alpha synuclein gene 58 histone deacetylase HDAC 58 MLL2 58 ciliopathies 58 spongiform encephalopathies 58 insertions deletions 58 chromosomal instability 58 Bardet Biedl syndrome 58 cytopathic 58 genomic loci 58 Alu elements 58 euthymic patients 58 ABCB1 gene 58 susceptibility gene 58 studies GWAS 58 KLF4 58 Dental caries 58 paralogs 58 Hereditary angioedema HAE 58 prognostic markers 58 clinically heterogeneous 58 microchimerism 58 glutamate signaling 58 distinct subtypes 58 dominantly inherited 58 TTR gene 58 neurosensory 58 Velculescu 58 K ras mutations 58 folate metabolism 58 ORMDL3 58 chromosomal rearrangements 58 previously uncharacterized 58 S. maltophilia 58 dedifferentiation 58 promoter hypermethylation 58 transgenic rats 58 endogenous retroviruses 58 FMR1 gene 58 Leukemias 58 biochemical abnormalities 58 methylated DNA 58 Hutchinson Gilford progeria 58 noncoding RNA 58 Genetic variation 58 inflammatory demyelinating 58 PALB2 58 kidney urologic 58 Atopic dermatitis 58 glial tumors 58 ABCB1 58 Myotonic dystrophy 58 ovarian hormones 58 prostate carcinogenesis 58 Mitochondrial dysfunction 58 lincRNA 58 microarray gene expression 58 sporadic ALS 58 quasispecies 58 epilepsies 57 genes BRCA1 57 nucleotide substitutions 57 3'UTR 57 fungal genomes 57 NF1 gene 57 hypermethylation 57 conserved sequences 57 recessive trait 57 TCF#L# gene 57 chromosomal deletions 57 neuroligins 57 vitamin D receptors 57 metabolic abnormalities 57 CETP gene 57 CNTNAP2 gene 57 retroviral vectors 57 BCL#A 57 gene duplications 57 carcinoid 57 primary cilia 57 primate genomes 57 neuronal dysfunction 57 chromosomal translocations 57 LRRK2 mutations 57 DLC1 57 phenotypic variability 57 NPM1 mutations 57 TP# gene 57 genetic polymorphism 57 p# activation 57 pathophysiologic 57 biologic pathways 57 paraneoplastic 57 immunopathology 57 autosomal dominant disorder 57 Induced pluripotent stem cells 57 NKX#.# 57 KIBRA 57 cisplatin resistant 57 dopamine D4 receptor 57 heritable disorders 57 Pancreatic neuroendocrine tumors 57 differential gene expression 57 CYP#D# gene 57 validating biomarkers 57 RNA ribonucleic acid 57 clefting 57 DQB1 * 57 DRD4 57 methylation patterns 57 SOD1 gene 57 micro RNA 57 cDNAs 57 susceptibility genes 57 Prostatitis 57 MC1R 57 sphingolipid 57 fatal neuromuscular disorder 57 synuclein 57 excitotoxicity 57 nonsense mutations 57 colorectal carcinogenesis 57 Thyroid nodules 57 T1DM 57 HLAs 57 virulence genes 57 haematopoietic 57 gene loci 57 hematopoietic cancers 57 Foxp3 57 genetic rearrangements 57 Brd4 57 Colon polyps 57 UGT#B# 57 genomic deletions 57 presymptomatic 57 molecular mimicry 57 gastrointestinal dysfunction 57 Autoimmune diseases 57 autosomal recessive 57 familial aggregation 57 amyloid formation 57 alpha synuclein protein 57 allelic variation 57 chromatin structure 57 Zinc deficiency 57 mitochondrial metabolism 57 MTHFR 57 FLT3 57 SLITRK1 57 nondemented 57 diagnostic biomarkers 57 basal cell nevus syndrome 57 SORL1 57 protein coding RNAs 57 MECP2 gene 57 piRNAs 57 Six3 57 myelofibrosis polycythemia vera 57 protein tyrosine phosphatase 57 p#INK#a 57 iPSC 57 functional polymorphism 57 CXCL5 57 STAT4 57 transcriptional regulators 57 genetic abnormalities 57 MAPK pathway 57 Telomere shortening 57 CNVs 57 posttranslational modifications 57 lymphoblasts 57 embryonal 57 epithelial tumors 57 ApoE gene 57 costimulatory 57 TEL AML1 57 abnormal proteins 57 pathophysiological mechanisms 57 monozygotic twins 57 LIS1 57 cause cardiac channelopathies 57 CDH1 57 PCNSL 57 CpG island 57 mitochondrial mutations 57 endostatin 57 Peutz Jeghers syndrome 57 Froguel 57 filoviruses 57 TMPRSS2 ERG 57 sporadic Creutzfeldt Jakob 57 pre malignant lesions 57 neuroimaging studies 57 muscular dystrophies 57 gastric carcinoma 57 Systemic lupus erythematosus 56 multifactorial disease 56 nanobacteria 56 assortative mating 56 Mitochondrial diseases 56 leukaemias 56 Rh incompatibility 56 ribosomal RNA rRNA 56 susceptibility alleles 56 proton MR spectroscopy 56 apolipoprotein E gene 56 causative genes 56 hemoglobinopathies 56 Male pattern baldness 56 FGFR2 56 Epstein Barr virus EBV 56 fluoroquinolone resistance 56 autosomal dominant 56 malignant transformation 56 RNA polymerases 56 granule cells 56 neurofibrillary 56 antisense therapies 56 cardiac progenitor cells 56 eotaxin 56 synovial cells 56 pharmacogenomic tests 56 gene fusions 56 serous ovarian cancer 56 GPx 56 IL 1ß 56 PIK3CA 56 phenotypes 56 miRNA molecules 56 Prox1 56 APOL1 56 retinoblastoma Rb 56 OGG1 56 intracellular bacteria 56 JAK mutations 56 pathological hallmark 56 PGRN 56 transcriptional regulation 56 transcriptomes 56 genomic variation 56 NR#A# gene 56 genetic recombination 56 fronto temporal dementia 56 epigenetic reprogramming 56 abnormal glucose metabolism 56 HFE gene 56 involuntary tics 56 filaggrin 56 miRNA genes 56 CETP VV 56 #p# [003] 56 lysosomal storage disease 56 murine models 56 nonmelanoma skin cancers 56 genetic susceptibilities 56 humanin 56 multigene 56 thrombophilia 56 insertional mutagenesis 56 PCA3 gene 56 obesity insulin resistance 56 heritable diseases 56 LRP5 56 H#K#me# 56 GAB2 56 genomic markers 56 Cyclin D1 56 LRRK2 mutation 56 aetiological 56 viral genomes 56 CHRNA5 56 autism spectrum disorders ASDs 56 tRNA synthetases 56 DLX5 56 leptin deficiency 56 HMGA2 56 Cyclin E 56 huntingtin gene 56 inheritable diseases 56 clinico pathological 56 SCN5A 56 Hereditary angioedema 56 homocystinuria 56 desmosomes 56 NPY gene 56 Folate deficiency 56 chronic granulomatous disease 56 A3 adenosine receptor 56 ADPKD 56 glucocorticoid receptors 56 histone methylation 56 PICALM 56 K ras gene 56 BRAF protein 56 L. pneumophila 56 phenotyping 56 sirtuin activators 56 KCNQ1 56 MIF protein 56 transgene expression 56 MLL gene 56 Brugada syndrome 56 pDCs 56 carcinoids 56 holoprosencephaly 56 #q#.# [002] 56 tau protein tangles 56 LRRK2 gene 56 ALK inhibitors 56 genes predisposing 56 MDSCs 56 tyrosine phosphorylation 56 chromosome #p#.# 56 histone modification 56 Tay Sachs thalassemia 56 untranslated regions 56 TMPRSS2 ERG fusion 56 congenital disorders 56 C#Y 56 neuronal plasticity 56 Aortic stenosis 56 neuro developmental disorder 56 Acute lymphoblastic leukemia 56 TÎ ² 4 56 NOD mice 56 Systemic lupus 56 MYH9 56 autism susceptibility genes 56 insulin resistance syndrome 56 Progenitor cells 56 Sporadic CJD 56 genomewide association study 56 chromatin immunoprecipitation ChIP 56 COX2 56 Aortic aneurysms 56 Polymorphic Ventricular Tachycardia CPVT 56 previously undescribed 56 FUS1 56 HYPP 56 bone marrow mesenchymal stem 56 cystic fibrosis chronic pancreatitis 56 Fragile X gene 56 INF2 56 overactivation 56 demyelinating disorders 56 biologic pathway 56 immunodeficiencies 56 tau aggregates 56 CCR5 delta# 56 proliferative disorders 56 protein alpha synuclein 56 prodynorphin 56 MTHFR gene 56 thiopurine 56 lymphoblastoid cell lines 56 Hypertrophic cardiomyopathy 56 spontaneous remission 56 muscular dystrophy cystic fibrosis 56 JAK2 56 LPA gene 56 GRK5 56 peroxisome 56 DISC1 gene 56 druggable targets 56 neural degeneration 56 rifamycins 56 medulloblastomas 56 genes encode proteins 56 gene deletions 56 primordial germ cells 56 recessive genetic 56 CCR7 56 LRAT 56 klotho 56 hepatocellular carcinomas 56 causal variants 56 hereditary hemochromatosis 56 mda 7 56 Muscular dystrophies 56 mutations 56 autistic enterocolitis 56 WDR# 55 arthritis lupus 55 Haptoglobin 55 KRAS variant 55 neurofibromas 55 DNA methylation patterns 55 synaptogenesis 55 STK# [002] 55 HLA DRB1 55 Excessive daytime sleepiness 55 Parkinson disease Alzheimer disease 55 vaso occlusive crisis 55 COL#A# 55 endophenotypes 55 siRNA knockdown 55 comorbid disorders 55 MAP kinases 55 tumorigenicity 55 GRNCM1 55 familial hypercholesterolemia 55 pneumococcal serotypes 55 neural progenitor 55 cutaneous lupus 55 recessive mutation 55 shRNAs 55 bexarotene 55 SNCA 55 Alport syndrome 55 uncharacterized 55 autosomal 55 DRD2 gene 55 atopic march 55 autoantigens 55 homozygosity 55 androgen receptor gene 55 respiratory viral infections 55 neoplastic transformation 55 incurable neurodegenerative disease 55 coding sequences 55 hematologic disorders 55 aneuploidy screening 55 neurodevelopmental disorder 55 non alcoholic steatohepatitis 55 predisposing factor 55 human leukocyte antigens 55 transgenic mouse model 55 phylogenetic analyzes 55 RNA transcripts 55 neurologic disorders 55 Ets2 55 Spinal muscular atrophy 55 Yamanaka recipe 55 TCF#L# 55 telomere DNA 55 HER2 overexpression 55 metaplasia 55 PTEN gene 55 Hashimoto thyroiditis 55 genetic biomarkers 55 allelic 55 alternative splicing 55 neuroinflammatory 55 genetic locus 55 insulin signaling pathway 55 adipokines 55 transfusion syndrome 55 debilitating neurodegenerative disorder 55 putative biomarkers 55 PrPSc 55 IGFBP2 55 allelic variants 55 ABO blood 55 prolonged QT interval 55 dysbindin gene 55 enterotypes 55 adrenal hormones 55 evolutionary conserved 55 dissociative disorders 55 molecularly defined 55 activating mutation 55 germline mutation 55 cybrid 55 arterial calcification 55 SHANK3 gene 55 BRAF gene 55 kinase inhibition 55 c Myb 55 multi celled organisms 55 neuropsychiatric disorders 55 immunological responses 55 intracellular protein 55 segmental duplications 55 myotonic dystrophy 55 microRNA biomarkers 55 FOXM1 55 p#/CBP 55 myeloproliferative disorders 55 renal fibrosis 55 diagnostic biomarker 55 blood coagulation disorders 55 inactive X chromosome 55 clinicopathological 55 Symadex 55 TOP2A 55 KRAS BRAF 55 alternatively spliced 55 chromosomal regions 55 lymphomas leukemias 55 NNRTI resistant 55 SNPs pronounced snips 55 parkin gene 55 underdiagnosis 55 NF2 55 genomic biomarkers 55 airway hyperresponsiveness 55 neurodegenerative disorder 55 Heritability 55 exomes 55 cnidarians 55 HLA genes 55 PON1 55 biomolecular interactions 55 MAPCs 55 uPAR 55 ribonucleic acids 55 lung cancer NSCLC 55 EBV infection 55 histologies 55 Inflammatory bowel disease 55 metabolomic profiles 55 misregulation 55 demyelinating 55 lysosomal diseases 55 SNP rs# [001] 55 Wnts 55 C. neoformans 55 MC1R gene 55 elevated triglyceride levels 55 CCR3 55 atherothrombotic disease 55 adrenocortical cancer 55 neuroblastomas 55 cyclophilin D 55 neural crest stem cells 55 hormonal abnormalities 55 molecular biomarkers 55 clonal expansion 55 Dental fluorosis 55 activate p# 55 Wwox 55 homozygous FH 55 neurodevelopmental disorders 55 Cytogenetic 55 micro RNAs 55 neoplastic 55 proteomic analysis 55 genes CYP#C# 55 neurologic disorder 55 intracellular signal transduction 55 chitinase 55 neural crest 55 oligonucleotide probes 55 gene amplification 55 proliferative diseases 55 Klotho gene 55 inherited predisposition 55 molecular determinants 55 genetic modifiers 55 Contagious yawning 55 comparative genomic hybridization 55 metabolic dysfunctions 55 genetic determinants 55 sphingolipids 55 M. genitalium 55 RNA viruses 55 nonviral 55 mental retardation epilepsy 55 CHI#L# 55 IgG4 55 AAT deficiency 55 embryonic stem ES 55 Neurodegenerative diseases 55 unprovoked seizures 55 thalassemia sickle cell 55 neurobehavioral disorder 55 glucose abnormalities 55 antigenic epitopes 55 anticancer therapeutics 55 Colorectal cancers 55 1 diabetes T1D 55 Neuregulin 1 55 amnestic 55 number variations CNVs 55 breast cancer subtypes 55 GABRA2 55 BRAF V#E 55 experimentally validated 55 Jhdm2a 55 Imprinted genes 55 immunocompetent 55 chromosome #q#.# [001] 55 Myelodysplastic syndromes 55 5 methylcytosine 55 signaling cascades 55 LPA1 receptor 55 Aravinda Chakravarti 55 polycystin 1 55 Pichia pastoris 55 Polymorphisms 55 antisense oligonucleotides 55 uncharacterized genes 55 Premature menopause 55 LQTS 55 evolvability 55 multiprotein complex 55 redox reactions 55 biomarker identification 55 autosomal dominant inheritance 55 small RNAs encoded 55 ANGPTL4 55 structural rearrangements 55 cAMP signaling 55 metabolic dysfunction 55 multipotent 55 Androgenetic alopecia 55 Chlamydia trachomatis 55 beta amyloid peptides 55 inherited retinal degeneration 55 chromosome condensation 55 cognitive dysfunctions 55 Mendelian diseases 55 Relapsing remitting MS 55 Phylomer ® 55 channelopathies 55 potent inhibitors 55 Cognitive impairment 55 genetic variants 55 CagA 55 dopamine receptor gene 55 von Hippel Lindau 55 Carcinoid tumors 55 IgE antibody 55 transcriptional profiles 55 neuronal stem cells 55 Kabuki syndrome 55 HPV genotypes 55 mutant huntingtin protein 55 microarray datasets 55 splice junctions 54 gamma globin gene 54 amyloid deposition 54 Leber hereditary optic neuropathy 54 cardioembolic stroke 54 mitochondrial toxicity 54 short hairpin RNAs 54 Prevotella 54 lupus multiple sclerosis 54 genotype phenotype 54 hereditary deafness 54 plasmacytoid 54 causative mutation 54 monogenic disorders 54 facioscapulohumeral muscular dystrophy 54 Chronic Lyme disease 54 MeCP2 protein 54 gastric carcinomas 54 Friedreich ataxia 54 connexin 54 Apobec3 54 synaptic proteins 54 KIF6 gene 54 Transcriptome 54 NPC1 54 International HapMap Project 54 neuroendocrine cancers 54 peptide antigens 54 BDNF gene 54 Plasmodium parasites 54 coding exons 54 germline cells 54 neurobiological underpinnings 54 clade B 54 epigenetic inheritance 54 multisensory integration 54 mutated genes 54 nucleotide variations 54 etiologic factors 54 airway responsiveness 54 multicenter trials 54 pathogenetic mechanisms 54 aT cell 54 microbiomes 54 Darapladib 54 EoE 54 gene mutations 54 humanized mouse 54 APOE4 54 Magnesium deficiency 54 miR #b [001] 54 P. falciparum parasites 54 NSCLC tumors 54 ENMD # 54 recombination hotspots 54 Fibroblast growth 54 mRNA sequences 54 antagomirs 54 inherit predisposition 54 DEAR1 54 prion infection 54 Pier Paolo Pandolfi 54 Depressive disorders 54 behavioral disinhibition 54 multisystem disease 54 leiomyoma 54 resistin 54 nociceptive pain 54 stem cell transplantations 54 Sjögren syndrome 54 transgenic mice expressing 54 amyloid deposits 54 podocyte 54 immune dysregulation 54 GBM tumors 54 histone modifications 54 suppressor gene 54 UCRs 54 Beta thalassemia 54 deleterious mutations 54 COX enzymes 54 S1P receptor 54 Mycoplasma pneumoniae 54 Shortened telomeres 54 FTLD 54 Gorlin syndrome 54 OPRM1 gene 54 HSF1 54 gene expression 54 follicular adenoma 54 gene polymorphisms 54 SORL1 gene 54 fusion enhancers 54 genetic manipulations 54 Gleevec resistant 54 MMP inhibitors 54 chromosome abnormalities 54 coding genes 54 Marc Weisskopf 54 H#Y 54 splice variant 54 apoE 54 protein conformation 54 alexithymia 54 lymphocyte activation 54 genetic mutations 54 subclinical atherosclerosis 54 constitutively expressed 54 protein tyrosine phosphatases 54 Th2 responses 54 CNPs 54 microglial cells 54 PON1 gene 54 mGluR5 antagonist 54 nerve degeneration 54 heritable variation 54 adult neurogenesis 54 dopamine transporter gene 54 hereditary disorders 54 behavioral disturbances 54 Penile cancer 54 ENPP1 54 CYP#C# gene 54 demyelinating disease 54 monocyte chemoattractant protein 54 NOMID 54 extramedullary 54 Loeys Dietz syndrome 54 S. sanguinis 54 lung adenocarcinoma 54 synthases 54 Skeletal muscle 54 differentially expressed genes 54 mesenchymal cell 54 fetal chromosomal 54 segmental duplication 54 intergenic 54 myeloproliferative neoplasms 54 GIST tumors 54 biochemical imbalances 54 developmental neurotoxicity 54 Polycythemia vera 54 TLE3 54 microsatellite instability 54 persistent pulmonary hypertension 54 nucleic acid sequence 54 bioengineered mice 54 mutant proteins 54 eukaryotic cells 54 TTR amyloidosis 54 Ischemic strokes 54 podocytes 54 TXNIP