Related by context. All words. (Click for frequent words.) 70 susceptibility loci 69 genetic loci 66 genetic polymorphisms 66 causal pathways 66 susceptibility locus 66 neuropathologic 65 genetic determinants 65 TCF#L# gene 65 chromosome #p#.# 65 underlying pathophysiology 65 LRRK2 gene 65 epigenetic regulation 65 etiologic 65 pathophysiological mechanisms 65 genetic variants associated 65 genetic underpinnings 65 molecular underpinnings 64 familial clustering 64 #q# deletion 64 somatic mutations 64 molecular abnormalities 64 etiologic factors 63 endophenotypes 63 APOE genotype 63 chromosomal regions 63 enterotypes 63 CSF biomarkers 63 genomewide 63 pleiotropic effects 63 beta1 integrin 63 differential gene expression 63 epigenetic modification 62 biologic pathways 62 causative mutations 62 molecular mechanisms underlying 62 pathogenic mechanisms 62 clinicopathological 62 MECP2 gene 62 LIS1 62 susceptibility gene 62 epigenetic changes 62 causative genes 62 DNA methylation patterns 62 chromosome #q# [001] 62 missense mutations 62 Genetic variants 62 epigenetic mechanisms 62 molecular subtypes 62 KIAA# 62 splice junctions 62 gene polymorphisms 62 GPC5 62 histone deacetylases 62 monogenic 62 circadian genes 62 biochemical abnormalities 62 genomic alterations 62 chromosome rearrangements 62 prospective longitudinal 62 histone modifications 62 prognostic significance 61 previously uncharacterized 61 #p#.# [001] 61 microRNA expression 61 motor neuron degeneration 61 amyloid deposition 61 pathogenetic 61 genomewide association study 61 bile acid metabolism 61 cAMP signaling 61 gene rearrangements 61 hypermethylated 61 methylation patterns 61 neuropsychiatric diseases 61 prognostic markers 61 GBA mutations 61 PALB2 61 aetiology 61 FGFR2 gene 61 neurotransmitter receptor 61 Singh Manoux 61 etiologic agent 61 stratifying patients 61 malaria parasite genome 61 FGFs 61 extramedullary 61 clefting 61 methylation markers 61 subclinical atherosclerosis 61 fronto temporal dementia 61 genetic modifiers 61 spontaneous regression 61 underlying molecular mechanisms 61 genomic variation 61 microdeletions 61 STK# gene 61 gene loci 61 genetic aberrations 61 modifier genes 61 PICALM 60 alpha synuclein gene 60 #S rRNA 60 distinct subtypes 60 IgA deficiency 60 chromosomal rearrangement 60 phylogenetic analyzes 60 lipoprotein metabolism 60 LRP5 60 ligand receptor 60 epigenetic markers 60 APOE e4 60 superior mesenteric artery 60 KRAS oncogene 60 de novo mutations 60 phenotypic expression 60 multi factorial disease 60 neuroanatomical 60 mitochondrial DNA mtDNA 60 HLA DRB1 60 nucleotide sequence 60 MYH9 60 microbiomes 60 p#/CBP 60 ABCB1 60 angiographically 60 ConclusionThis 60 previously undescribed 60 SCN1A 60 prognostic indicators 60 impaired insulin secretion 60 CALHM1 60 Sacktor 60 KCNQ1 60 cardioembolic stroke 60 Hutchinson Gilford progeria 60 sporadic ALS 60 susceptibility genes 60 hereditary predisposition 60 aberrant methylation 60 diathesis 60 SLC#A# [002] 60 SNP rs# [001] 60 PTEN gene 60 ADPKD 60 molecular determinants 60 diagnostic biomarker 60 ADAMTS# 60 genotype phenotype 60 genes differentially expressed 60 druggable targets 60 obesity insulin resistance 59 Dr. Pasinetti 59 prognostic marker 59 metaplasia 59 uPAR 59 CDH1 59 orthologs 59 allelic variation 59 TMPRSS2 ERG fusion 59 sCJD 59 inherited mutations 59 mitochondrial mutations 59 LRRK2 mutation 59 Chronic pancreatitis 59 TOMM# 59 Leydig cell 59 pre malignant lesions 59 exfoliative glaucoma 59 paralogs 59 KCNH2 59 etiology 59 metabolic abnormalities 59 #p# [001] 59 alexithymia 59 euthymic patients 59 hamartomas 59 5 hydroxymethylcytosine 59 virulence genes 59 gene amplification 59 ORMDL3 59 airway hyperresponsiveness 59 neuroimaging studies 59 IDH mutations 59 HLA DQ2 59 metabolic dysfunction 59 WDR# 59 MYH9 gene 59 MEF2A 59 neurofibrillary 59 Genetic variation 59 Wwox 59 Genetic predisposition 59 chromosome #q#.# [001] 59 genome rearrangements 59 miRNA expression 59 SCN5A 59 #p# [003] 59 hyperinsulinism 59 phenotypic variation 59 gene polymorphism 59 cytochrome b 59 mitochondrial gene 59 CagA 59 Brugada syndrome 59 apoE4 59 mutated K ras 59 prostate carcinogenesis 59 #q#.# [001] 59 genetic susceptibilities 59 meta regression 59 multigene 59 primate genomes 59 podocyte 59 mitochondrial defects 59 sequence homology 59 gene locus 59 colocalization 59 fungal genomes 59 maize genome 59 genomic biomarker 59 spontaneous mutations 59 splice variants 59 myopathies 59 germline mutations 59 antiphospholipid syndrome 59 chromosome #p# [002] 59 narcolepsy cataplexy 59 neuroendocrine 59 #q#.# [002] 59 esophageal squamous cell carcinoma 59 flow cytometric analysis 59 chronicity 59 colorectal adenoma 59 hypercalciuria 59 MAPK pathway 58 Sjögren syndrome 58 proteomes 58 chromosomal aberrations 58 genomewide association studies 58 noncoding RNAs 58 biopsychosocial 58 COL#A# 58 JAK mutations 58 pituitary adenomas 58 autonomic dysfunction 58 bacterial genomes 58 monoclonal gammopathy 58 aminotransferase 58 Genetic mutation 58 PIK3CA 58 neuritic 58 molecular biomarkers 58 genomic rearrangements 58 Multivariate analysis 58 SHANK3 58 chromosomal anomalies 58 electroencephalographic 58 inherited predisposition 58 causative gene 58 neuroligins 58 amyloid cascade 58 carotid atherosclerosis 58 pathogenic mutations 58 aetiological 58 promoter hypermethylation 58 penetrance 58 causative mutation 58 Clusterin 58 hematological relapse 58 comorbid depression 58 gp# protein [002] 58 apolipoprotein E gene 58 STAT4 58 pathophysiologic 58 aneuploidies 58 5 HTTLPR 58 epigenomic 58 CaM kinase II 58 susceptibility alleles 58 LRRK2 mutations 58 DQB1 * 58 ANCA associated 58 SHANK3 gene 58 pulmonary metastasis 58 FDG PET scans 58 multifactorial disease 58 neuronal dysfunction 58 mechanistic insights 58 ZNF# 58 exomes 58 predisposing factor 58 Immunohistochemical analysis 58 somatic mutation 58 nucleotide sequences 58 microdeletion 58 Lenzenweger 58 genetic polymorphism 58 perilipin 58 differentially expressed proteins 58 microRNA molecules 58 causal pathway 58 MTHFD1L gene 58 CNTNAP2 58 ERK signaling 58 transgenic mouse models 58 S. sanguinis 58 S. maltophilia 58 non coding RNA 58 BRCA1 BRCA2 58 NFTs 58 pathological hallmark 58 nonmelanoma 58 airway remodeling 58 familial aggregation 58 ncRNA 58 genomic deletions 58 HER2 HER3 58 microarray experiments 58 MMP# 58 tumor subtypes 58 silent myocardial ischemia 58 serum biomarkers 58 TCF#L# 58 prognostic biomarkers 58 CARDIA study 58 serotonin transporters 58 nicotinic receptor 58 histopathologic diagnosis 58 Wnt proteins 58 epigenetic alterations 58 TLE3 58 logistic regression analysis 58 Six3 58 colonic polyps 58 arterial calcification 58 neuro developmental disorders 58 RNA sequences 58 Mechanistic studies 58 genes predisposing 58 intracellular bacteria 58 glutamic acid decarboxylase 58 K ras mutations 58 neuropsychiatric disorder 58 Univariate analysis 57 microRNAs miRNAs 57 histone H4 57 pilocytic astrocytomas 57 chromosomal deletions 57 mRNA transcripts 57 antiphospholipid antibodies 57 immunohistochemical 57 prognostic biomarker 57 Single Nucleotide Polymorphisms SNPs 57 replicase 57 SH#B# 57 GSTP1 57 CD# expression [002] 57 Apolipoprotein E 57 nodal metastasis 57 tumor suppressor protein 57 neurobiological underpinnings 57 #S rRNA gene 57 BARD1 57 histone methylation 57 PTPN# 57 ankyrin repeat 57 autistic enterocolitis 57 channelopathies 57 posterior cingulate 57 TGFBR1 * 6A 57 diabetes dyslipidemia 57 serine threonine kinase 57 leiomyomas 57 protein coding RNAs 57 Hurthle cell 57 proto oncogene 57 neuroinflammatory 57 intergenic 57 ABCB1 gene 57 MSH2 57 nongenetic 57 APOL1 57 hyperacute 57 infantile hemangioma 57 demyelinating 57 thrombophilia 57 polygenic 57 NOD2 57 microsatellite instability 57 metalloprotease 57 metabolomic profiles 57 genetic heterogeneity 57 homolog 57 CYP#D# gene 57 autism susceptibility genes 57 mGluR2 NAM 57 validate biomarkers 57 DARPP 57 retrovirus XMRV 57 insertional 57 #S rDNA 57 somatic symptoms 57 metabolizing enzymes 57 multiprotein complex 57 protein misfolding 57 CYP#C# [002] 57 Phylogenetic analysis 57 kinase inhibition 57 neurological abnormalities 57 paraneoplastic 57 repolarization 57 mGluR5 antagonist 57 PCA3 gene 57 genes CYP#C# 57 atherothrombotic 57 morphological traits 57 pharmacodynamic biomarkers 57 VKORC1 57 molecular pathogenesis 57 ortholog 57 GABAB receptors 57 CHEK2 57 ALK mutations 57 herpesviruses 57 serine protease 57 proteinases 57 Cyclin E 57 osteocalcin protein 57 Bardet Biedl Syndrome 57 proteomic analysis 57 Heritability 57 intestinal permeability 57 IL 7R 57 cDNA microarray 57 B7 H3 57 thyrotropin levels 57 IGFBP2 57 biochemical signaling pathway 57 etiological 57 MC1R 57 transgenic mouse model 57 autosomal dominant inheritance 57 nondemented 57 yeast genome 57 liver metastasis 57 synaptic function 57 cellular pathways 57 epithelial barrier 57 Brodmann Area 57 Mycobacterium smegmatis 57 chromosomal alterations 57 comorbid anxiety 57 neuroligin 57 outer membrane proteins 57 Caenorhabditis 57 serum GGT 57 urolithiasis 57 chromosome #q# [002] 57 #q# [001] 57 epigenetic inheritance 57 highly heritable 57 autosomal 57 gene fusions 57 clinicopathologic 57 genetic biomarkers 57 ADAM# 57 potent inhibitors 57 telomere DNA 57 NSCLC tumors 57 Multiple logistic regression 57 apoE 57 antioxidant supplementation 57 BCL#A 57 DLX5 57 transcriptional regulation 57 papillary renal cell carcinoma 57 TP# mutation 57 atopic diseases 57 DNA methylation markers 57 proteins misfold 57 histone demethylase 57 C. neoformans 57 pathophysiologic mechanism 57 LRP6 57 Boston DbTechNo Results 57 unmeasured confounders 57 NPM1 gene 57 #F FDG PET 57 proteoglycan 57 seminomas 57 Phenotype 57 dysgenesis 57 ciliopathies 57 Genetic variations 57 CpG island 57 MTHFR gene 57 microcephalin 57 functional polymorphism 57 Kraepelin 57 Lambris 56 nanobacteria 56 PTEN protein 56 indels 56 CRISPR Cas 56 gut microbiota 56 ultrastructural 56 VNTR 56 cortical thinning 56 HER2 expression 56 SNP rs# [002] 56 picornavirus 56 HGPS 56 IPAH 56 serologic tests 56 cytosine methylation 56 PON1 56 IDH1 mutation 56 abnormal glucose metabolism 56 phylogenetically 56 PALB2 gene 56 INF2 56 TMEM#B 56 longitudinal cohort study 56 pathogenetic mechanisms 56 HLA genes 56 Epidemiologic studies 56 obstructive coronary 56 protein conformation 56 kallikrein 56 incidentalomas 56 allelic variants 56 Prox1 56 Subtypes 56 gene APOE 56 MAP kinase pathway 56 ipRGCs 56 idiopathic pulmonary 56 biochemical marker 56 Hp2 2 56 Confocal microscopy 56 SLC#A# [001] 56 CSHL scientists 56 electrophysiologic 56 neurobiological basis 56 coinfection 56 HFE gene 56 neuropsychological deficits 56 hippocampal atrophy 56 genetic variants 56 SIRT1 gene 56 ependymomas 56 precancerous tumors 56 activated microglia 56 residual confounding 56 subcellular localization 56 Functional neuroimaging 56 Angiotensin converting enzyme 56 Lp PLA 2 56 Electrophysiological 56 NR#A# 56 MTHFR 56 Transcriptome 56 prodynorphin 56 neurocognitive dysfunction 56 diabetic polyneuropathy 56 periodontal pathogens 56 PMR1 56 histologic subtypes 56 SLC#A# gene [001] 56 Cognitive impairment 56 sea urchin genome 56 K ras mutation 56 Li Fraumeni syndrome 56 amyloidogenic 56 gastro esophageal reflux 56 miRNA genes 56 3'UTR 56 hypermethylation 56 Histologically 56 MetAP2 56 neuronal circuitry 56 comorbid psychiatric disorders 56 PB1 F2 56 telomere lengths 56 causal variants 56 ncRNAs 56 epistasis 56 neuroinflammation 56 vitamin D receptor 56 epigenetic modifications 56 NKX#.# 56 androgen receptor gene 56 SSc 56 SERT gene 56 CHD7 56 familial pancreatic cancer 56 cardioprotective effects 56 activating mutation 56 BDNF gene 56 coding exons 56 quantitative trait loci 56 evolutionarily conserved 56 hyperactivation 56 anterior pituitary 56 neurocognitive impairment 56 allele frequencies 56 demethylase 56 coding RNA 56 mutational analysis 56 Chlamydia pneumoniae 56 MGUS 56 macaque genome 56 cypin 56 osteosarcomas 56 protein encoded 56 PARP inhibition 56 coding genes 56 thyroid hormone deficiency 56 pathophysiological 56 gallstone disease 56 HG PIN 56 HLA B# 56 chromosomal translocations 56 comorbid disorders 56 p# activation 56 laforin 56 BRAF V#E 56 Chapkin 56 receptor ligand 56 mRNA expression 56 calcium homeostasis 56 laterality 56 transient elastography 56 molecular signaling pathways 56 astrocytomas 56 NPHP 56 MC4R gene 56 pressure natriuresis 56 gene APOE4 56 cerebellar vermis 56 biomarker identification 56 Wnt signaling pathway 56 differentially expressed genes 56 histone modification 56 chromosome aberrations 56 FGFR2 56 Froguel 56 carcinoid tumor 56 chromosome #q 56 TP# gene 56 Genetic mutations 56 breast cancer subtypes 56 plasma kallikrein 56 Multivariate analyzes 56 tRNA synthetase 56 neuropsychiatric illnesses 56 metabolite concentrations 56 circulating endothelial cells 56 amyloid plaque formation 56 logistic regression model 56 oncogenesis 56 renal cysts 56 impaired glucose metabolism 56 gastric cardia 56 MLL2 56 BCL6 gene 56 STAT3 signaling 56 cofactors 56 transfusion syndrome 56 MALAT1 56 Haptoglobin 56 amino acid substitutions 56 psychobiological 56 synaptogenesis 56 HepG2 cells 56 mtDNA mutations 56 neural correlates 56 TXNIP 56 achromatopsia 56 glaucomatous 56 mitochondrial toxicity 56 kinome 56 affective disorders 56 fibroma 56 metabolic disturbances 56 lipid abnormalities 56 autosomal dominant disorder 56 Wernicke Korsakoff syndrome 56 immunohistochemical staining 56 gamma oscillations 56 Bartonella species 56 genetic syndromes 56 posttranslational modifications 56 transcriptome 56 gastric carcinoma 56 hypoperfusion 56 multiple logistic regression 56 Convit 56 biochemical imbalances 56 cortisol secretion 56 microvascular disease 56 subcellular 56 Helicobacter 56 C1q 56 membrane fusion 56 R#W [002] 56 endocrine dysfunction 56 Cathepsin B 56 annexin 56 viral etiology 56 prothrombotic 56 metaanalysis 56 FTLD 56 epigenetic silencing 56 filaggrin mutations 56 chromatin structure 56 chromosome #p# [001] 56 X chromosome inactivation 56 podocytes 56 subsyndromal 56 organogenesis 56 microbiome 56 Hox gene 56 allelic 56 NF1 gene 56 γ secretase 56 Hypothalamic 56 myocardial fibrosis 56 β amyloid 56 heritable component 56 epigenome 55 Longitudinal studies 55 KRAS BRAF 55 C. trachomatis 55 intact parathyroid hormone 55 Irritable bowel syndrome IBS 55 antagomirs 55 type2 diabetes 55 glycogen metabolism 55 biochemical markers 55 apoptotic pathway 55 rs# [004] 55 neurosensory 55 Cochrane reviewers 55 histologic subtype 55 germline mutation 55 chromosomal mutations 55 Epstein Barr Virus EBV 55 #beta HSD1 55 calculi 55 ovarian endometrial 55 phylogenetic analysis 55 histological subtypes 55 Mycoplasma pneumoniae 55 isotype 55 HH GLI 55 Histological 55 EBV infection 55 chromosome #q#.# [002] 55 MLH1 55 remnant lipoproteins 55 Estrogen Receptor 55 sphingolipid 55 aMCI precursor 55 protein tyrosine phosphatase 55 Drosophila genome 55 Pseudomonas syringae 55 hemoglobinopathies 55 Phenotypic 55 recessive mutation 55 Kufs disease 55 Entamoeba histolytica 55 ribosomal protein 55 Subgroup analysis 55 hypercoagulable 55 inverse agonist 55 viral pathogenesis 55 metabolic abnormality 55 synapse formation 55 Dr. Loeken 55 microRNA miR 55 M. pneumoniae 55 chromosomal imbalance 55 NAT2 55 micro RNA 55 glial tumors 55 RNA binding 55 lipid metabolism 55 body louse genome 55 obese postmenopausal 55 methyltransferase 55 homologous genes 55 occipital regions 55 human microbiome 55 hyperplastic 55 ANGPTL4 55 prion infection 55 tyrosine phosphorylation 55 VHL gene 55 serum antibodies 55 Dietary calcium 55 monozygotic twins 55 immunofluorescent 55 STEP BD 55 fruitfly Drosophila 55 quasispecies 55 KLF4 55 protein phosphorylation 55 Polymorphisms 55 Genetics Consortium 55 ApoE gene 55 progressive neurodegenerative disorder 55 DNA demethylation 55 prostate cancer CaP 55 genomic variants 55 Logistic regression analysis 55 lobular breast cancer 55 G6PD deficiency 55 RNA polymerases 55 cDNAs 55 Wnts 55 atherothrombosis 55 sequenced genomes 55 N. gonorrhoeae 55 viral genomes 55 leaky gut 55 rs# [001] 55 haplotype map 55 Arabidopsis genome 55 RRM1 55 conformational changes 55 genomic sequence 55 genetic markers 55 eotaxin 55 psychosocial variables 55 ribosomal RNA rRNA 55 gene predisposing 55 assortative mating 55 EP3 receptor 55 white matter hyperintensities 55 ductal adenocarcinoma 55 C#Y 55 TERT 55 FCGR3A 55 physiologic mechanisms 55 Amino acid 55 syndromal 55 retrospective cohort 55 Kv#.# 55 microsatellite markers 55 affective psychoses 55 randomized controlled trials RCTs 55 Oxidative damage 55 polymorphic ventricular tachycardia 55 catechol O methyltransferase 55 mammary stem cells 55 IL#R 55 adiponectin levels 55 mediated inhibition 55 endocrinologic 55 DEAR1 55 inherited neurological disorder 55 Alpha synuclein 55 cell adhesion molecule 55 dissociative disorders 55 membrane proximal 55 HbF 55 Plasmodium vivax 55 homodimers 55 VIPR2 55 RUNX3 55 diploid genome 55 XMRV infection 55 trait locus 55 epigenetically 55 serous ovarian cancer 55 neuronal synapses 55 biochemical mechanisms 55 BEXXAR Therapeutic Regimen 55 virus XMRV 55 cryptogenic 55 eosinophilic 55 polymorphisms 55 Colon polyps 55 somatoform disorders 55 diabetes mellitus DM 55 colonic mucosa 55 methylated genes 55 MYCN amplification 55 left ventricular diastolic 55 enolase 55 VADT 55 T. vaginalis 55 #S ribosomal RNA 55 sonographic appearance 55 endogenous ligands 55 parathyroid 55 carotid artery thickness 55 Dr. Rafii 55 hemoglobins 55 FOXO3a 55 gene expression patterns 55 sonographic diagnosis 55 cnidarians 55 homologies 55 normal karyotype 55 Alu elements 55 CNVs 55 thyroid carcinoma 55 GPx 55 testicular germ cell 55 dysbindin 55 recessive trait 55 PER2 55 multigenic 55 moderately heritable 55 potentially modifiable 55 PCNSL 55 pilocytic astrocytoma 55 autopsied brains 55 chromatin remodeling complex 55 Dental caries 55 Vgontzas 55 Klotho gene 55 metabolizing enzyme 55 perfusion CT 55 cardiolipin 55 Darapladib 55 Methylation 55 Genotypes 55 TRAF1 C5 55 positional cloning 55 Single Nucleotide Polymorphisms 55 leukocyte counts 55 murine models 55 mitochondrial genomes 55 Mathematical modeling 55 sortilin 55 predictive validity 55 β1 55 granulomatous 55 dysautonomia 55 mosaicism 55 PROactive study 55 etiological factors 55 Schunkert 55 copper zinc superoxide 55 metabolic parameters 55 bilaterians 55 eczema asthma 55 C. pneumoniae 55 alternans 55 Joubert syndromes 55 intestinal microbiota 55 USP# 55 atopic march 55 tumor subtype 55 Prostatitis 55 trimers 55 precursor lesions 55 T1DM 55 nucleosome positioning 55 protein tyrosine kinase 55 synaptic proteins 55 mammographically 55 HCV replication 55 Prefrontal 55 rRNA 55 microbiota 55 transthyretin 55 clinically heterogeneous 55 TIMP 55 dietary interventions 55 karyotype 55 allergic airway inflammation 55 Hashimoto thyroiditis 55 Micro RNAs 55 vitamin D receptors 55 S#A# [002] 55 ovarian hormones 55 rs# [002] 55 functional neuroimaging 55 gastric adenocarcinoma 55 transcriptomics 55 neurocognitive deficits 55 subclinical disease 55 evolvability 55 gastric carcinogenesis 55 GRP# 55 Skeletal muscle 55 androgen deficiency 55 #q#.# deletion syndrome 55 QTLs 55 FASPS 55 schizophreniform disorder 55 phosphorylated tau 55 CP CPPS 55 Sleep disordered breathing 55 dysglycemia