Related by context. All words. (Click for frequent words.) 68 ApoE gene 67 MYH9 gene 64 C. pneumoniae 64 XLHED 64 MTHFD1L gene 63 UGT#A# * 63 PTPN# 63 ABCB1 63 rs# [004] 63 gene APOE 63 HLA DRB1 63 CYP#C# gene 63 HFE gene 63 APOE gene 63 CYP#D# gene 63 gene polymorphism 63 Genetic variants 62 LPA gene 62 heterozygotes 62 MTHFR 62 MC1R gene 62 missense mutations 62 APOE e4 62 APOE ε4 62 MTHFR gene 62 APOE4 61 heterozygous 61 C#Y 61 gene MECP2 61 microsatellite instability 61 neovascular 61 COL#A# 61 sporadic ALS 61 apolipoprotein E gene 61 G allele 61 gene locus 61 CETP gene 61 SHANK3 61 HLA DRB1 * 61 penetrance 61 homozygotes 61 CC genotype 61 missense mutation 61 chromosomal rearrangement 60 GSTM1 gene 60 GBA mutations 60 allelic variants 60 homozygote 60 susceptibility gene 60 rs# [003] 60 CDH1 60 TOP2A gene 60 UGT#B# 60 BRAF V#E 60 mutated K ras 60 Genetic variation 60 BDNF gene 60 TCF#L# gene 60 paternally inherited 60 narcolepsy cataplexy 60 ADAMTS# 60 ADPKD 60 variant alleles 60 C#T [002] 60 androgen receptor gene 60 C#BL/#J 60 de novo mutations 60 PTEN mutations 60 rs# [002] 59 elevated triglyceride levels 59 p# mutations 59 Homozygous 59 GSTT1 59 chromosome #q# [002] 59 nondemented 59 APOC3 59 autosomal recessive disease 59 alleles 59 genetic polymorphism 59 CHD7 59 Genetic predisposition 59 apoE4 59 PON1 gene 59 insulin resistance syndrome 59 hormone receptor negative 59 genes predisposing 59 monogenic 59 microdeletions 59 HLA B# 59 germline mutations 59 hereditary predisposition 59 TCF4 59 polymorphism 59 Beta thalassemia 59 IKZF1 59 ApoE4 gene 59 susceptibility alleles 59 allele 59 K ras mutations 59 DRD2 59 autosomal recessive 59 MetS 59 sCJD 59 LRRK2 gene 59 VHL gene 59 familial clustering 59 MeCP2 gene 59 progranulin gene 59 germline mutation 59 GSTP1 59 APOE allele 59 CCR5 delta# 59 Wwox 59 APOE genotype 58 neuropathologic 58 atopic disorders 58 distinct subtypes 58 KIF6 gene 58 gene variant 58 NNRTI resistance 58 BARD1 58 chromosome #q# [001] 58 DQB1 * 58 5 HTT gene 58 genetic loci 58 chromosomal alterations 58 normal karyotype 58 nonalcoholic steatohepatitis NASH 58 hyperplastic 58 haematopoietic 58 arterial calcification 58 5q 58 #q# [001] 58 Klinefelter syndrome 58 TMEM#B 58 homozygosity 58 autosomal dominant disorder 58 asplenia 58 genetic polymorphisms 58 IL#R 58 HMMR 58 monozygotic twin 58 inherited mutations 58 beta amyloid peptides 58 promoter polymorphism 58 genetic variant 58 LRAT 58 MLH1 58 carotid plaque 58 nonalcoholic steatohepatitis 58 prothrombotic 58 Vascular dementia 58 microcephalin 58 homozygous 58 c KIT 58 ALK gene 57 thyrotropin levels 57 genotype 57 demyelinating 57 Leydig cell 57 #q#.# [002] 57 familial pancreatic cancer 57 polymorphisms 57 variant allele 57 microdeletion 57 Magnesium deficiency 57 G6PD deficiency 57 Chlamydia pneumoniae 57 MC4R gene 57 gene rearrangements 57 #q#.# [001] 57 ultrastructural 57 metabolic abnormalities 57 mosaicism 57 T. vaginalis 57 karyotypes 57 clade B 57 PON1 57 gastrointestinal stromal tumors GISTs 57 rs# [001] 57 GSTM1 57 TMPRSS2 ERG fusion 57 coinfection 57 SMAD4 57 lysosomal storage diseases 57 dopamine receptor gene 57 protein tyrosine phosphatase 57 APOL1 57 testicular germ cell 57 SOD2 gene 57 susceptibility genes 57 underlying pathophysiology 57 COMT gene 57 Sjögren syndrome 57 #q# deletion 57 nonhereditary 57 cardioembolic stroke 57 lupus anticoagulant 57 TOMM# 57 genetic variants associated 57 gonorrhoeae 57 C1q 57 allele frequencies 57 geographic atrophy 57 null mice 57 receptor gene 57 MECP2 gene 57 MYH9 57 CAG repeats 57 hepatic lipase 57 Vitamin B# deficiency 57 gastric carcinogenesis 57 K ras gene 57 nonischemic 57 neuroligins 57 alpha synuclein protein 57 PDGFRA 57 Li Fraumeni syndrome 57 chronic hepatitis cirrhosis 57 hypothalamic amenorrhea 57 prion gene 57 MSH2 57 SORL1 57 indels 57 basal cell nevus syndrome 57 DNA methylation patterns 57 APOE e4 allele 57 V Leiden 57 ENPP1 57 gene polymorphisms 57 TGFBR1 * 6A 57 APOE4 gene 57 diabetes mellitus DM 57 genes CYP#C# 57 subclinical hyperthyroidism 57 MC1R 57 IGF1 57 predisposing factor 57 motor neuron degeneration 57 autosomal dominant inheritance 57 chromosomal aberrations 57 SNP rs# [001] 57 CYP #D# 56 Epstein Barr virus EBV 56 FLT3 56 related maculopathy 56 paraneoplastic 56 congenital deficiency 56 M#V 56 functional polymorphism 56 chorioamnionitis 56 CFTR gene 56 MIF gene 56 HSV1 56 Cognitive impairment 56 serum PTH 56 G#D 56 C#Y mutation 56 KRAS oncogene 56 HMGCR 56 autosomal dominant 56 CP CPPS 56 mitochondrial metabolism 56 exfoliation glaucoma 56 methylation patterns 56 MELAS 56 aetiological 56 C. trachomatis 56 somatic mutations 56 murine models 56 autosomal 56 prodynorphin 56 polymicrobial 56 MAOA gene 56 proband 56 SMN2 gene 56 DRD2 gene 56 APOE e4 gene 56 methylenetetrahydrofolate reductase 56 HbF 56 HLA DQ2 56 familial adenomatous polyposis FAP 56 autonomic dysfunction 56 neuronal dysfunction 56 aggrecan 56 LRRK2 mutations 56 squamous cell lung cancer 56 5 HTTLPR 56 hypercoagulable 56 GH deficiency 56 CDK4 56 filaggrin gene 56 idiopathic PAH 56 neuroD2 56 primary ciliary dyskinesia 56 MHC genes 56 SORL1 gene 56 BRCA1 BRCA2 56 Heritability 56 TP# mutation 56 TACI mutations 56 IgA deficiency 56 Hp2 2 56 activating mutation 56 Cowden syndrome 56 gene APOE4 56 biochemical abnormalities 56 neurological abnormalities 56 invasive lobular 56 hypogonadotropic hypogonadism 56 progressive neurodegenerative disorder 56 thiopurine 56 differential gene expression 56 carotid plaques 56 variant rs# 56 Acute myeloid leukemia 56 K#N 56 isoenzymes 56 MMP# 56 mutant allele 56 myostatin gene 56 chromosome #q#.# [001] 56 subtype 56 muscular dystrophy cystic fibrosis 56 oesophageal adenocarcinoma 56 P aeruginosa 56 haplogroups 56 Haptoglobin 56 hypermethylated 56 FMR1 gene 56 Genetic mutation 56 BRAF V#E mutation 56 MGUS 56 orthologs 56 p# mutation 56 microRNA expression 56 mtDNA mutations 56 coagulation abnormalities 56 telomere lengths 56 clinicopathological 56 type2 diabetes 56 #p# [001] 56 HIBM 56 immunodeficiencies 56 IL#B 56 EGFR gene 56 ADRB2 56 NEIL1 56 prefrontal regions 56 pathophysiologic 56 spontaneous mutations 56 susceptibility locus 56 IPAH 56 heritable variation 56 TPMT 56 dopamine transporter gene 55 OPRM1 gene 55 gastric carcinoma 55 FMR1 55 HIV HCV coinfected 55 MYCN amplification 55 karyotype 55 nitrotyrosine 55 multifactorial disease 55 neuritic 55 etiologic agent 55 #p#.# [002] 55 HDL2 55 CpG island 55 cranial irradiation 55 gallstone disease 55 transgenic mice expressing 55 BRCA2 gene 55 APOE epsilon 4 55 murine leukemia virus 55 miRNAs miR 55 IDH1 mutation 55 HBV genotype 55 SSc 55 TGFBR1 55 STAT4 55 Haplotype 55 haplotypes 55 xeroderma pigmentosum 55 T2D 55 inactivating mutations 55 phenotypic variation 55 cystic fibrosis muscular dystrophy 55 chromosome #p#.# 55 DRB1 * 55 #p#.# [001] 55 Impaired glucose tolerance 55 HBeAg negative 55 Hashimoto thyroiditis 55 neuropathological 55 MLL gene 55 LV ejection fraction 55 affective psychosis 55 hamartomas 55 GABRA2 55 systemic amyloidosis 55 breast endometrial 55 T2DM 55 LRP5 55 subclinical 55 causative mutation 55 genital ulcer 55 ER alpha 55 SCN1A 55 SLC#A# [001] 55 osteosarcomas 55 FADS2 gene 55 causative genes 55 FTO variant 55 recessive trait 55 esophageal squamous cell carcinoma 55 autoimmune thyroiditis 55 airway hyperresponsiveness 55 unmutated 55 serotonin transporter gene 55 Chronic lymphocytic leukemia 55 poorer prognosis 55 enteroviral 55 Nonalcoholic fatty liver 55 SCN5A 55 DGAT1 55 metaplasia 55 chromosomal deletions 55 colorectal tumor 55 fibulin 55 mutated gene 55 sequence homology 55 CNTNAP2 55 BRCA1 mutation carriers 55 seropositivity 55 hereditary hemochromatosis 55 transgenic mouse models 55 ductal breast cancer 55 anemia neutropenia 55 genetic makeups 55 apolipoprotein E4 55 NF1 gene 55 PALB2 gene 55 gene variants 55 R#W [002] 55 Severe Primary IGFD 55 JAK2 mutation 55 haplotype 55 ß = 55 pancreatic endocrine 55 orchitis 55 kDa protein 55 Aß 55 lymphocytic 55 AAT deficiency 55 proliferative retinopathy 55 CYP#C# [002] 55 familial ALS 55 CALHM1 55 Trichophyton rubrum 55 TCF#L# 55 ApoE4 55 Nf1 55 ApoE 55 Sarcopenia 55 overt hypothyroidism 55 HMGA1 55 HMPV 55 PTEN gene 55 ESR1 55 transcriptional repressor 55 apolipoprotein E APOE 55 cognitively normal 55 anemias 55 amnestic MCI 55 apoC III 55 astrocytomas 55 gene amplification 55 gene deletions 55 aldehyde dehydrogenase 55 pathogenic mutations 55 del 5q 55 Fragile X gene 55 stratifying patients 55 Sporadic CJD 55 airway hyper responsiveness 55 hemagglutinin gene 55 SE alleles 55 NFKBIA 55 clefting 55 autosomal recessive disorder 55 phenotype 55 transgenic rats 55 beta carotene supplementation 55 M. genitalium 55 CDKN2A 55 gastric adenocarcinoma 55 folate deficiency 55 Bacterial vaginosis 55 genotypes 55 KIBRA 55 dyskeratosis congenita 55 immunocompetent 55 collagen VI 55 G#S mutation 55 immunopathology 54 CagA 54 IDH1 mutations 54 activin 54 GPC5 54 susceptibility loci 54 NRF2 gene 54 alpha2 54 Amino acid 54 colorectal carcinoma 54 colorectal adenoma 54 2 diabetes T2D 54 mRNA transcripts 54 dietary glycemic index 54 constitutively active 54 chromosome #p# [001] 54 synuclein 54 myeloproliferative neoplasms 54 Fas ligand 54 alternatively spliced 54 elevated LDH 54 gestational diabetes mellitus GDM 54 T1DM 54 P. aeruginosa infection 54 chromosome abnormality 54 untreated celiac disease 54 aneuploidies 54 amyloid beta plaques 54 histologic subtype 54 immunodeficient 54 autosomal recessive genetic 54 Prox1 54 genomewide 54 modifier genes 54 dysbindin 54 inherited retinal degeneration 54 transgenic mouse model 54 normotensive 54 substrate specificity 54 obstructive coronary artery 54 abnormal chromosome 54 missense 54 FGFR2 gene 54 recessive inheritance 54 BMP2 54 de novo AML 54 PALB2 54 familial predisposition 54 heterozygote 54 HPV subtypes 54 nephropathy 54 atypical hemolytic uremic syndrome 54 #q#.# deletion syndrome 54 lysophosphatidic acid 54 F#del mutation 54 COX2 54 γ secretase 54 KCNQ1 54 epistasis 54 chromosome #q#.# [002] 54 gamma globin gene 54 caveolin 54 FTLD 54 vWD 54 progranulin 54 nonmelanoma 54 MIF protein 54 ribosomal protein 54 K#R [002] 54 gene mutation 54 brain lesions 54 Polymorphisms 54 telomere dysfunction 54 plasminogen activator inhibitor 54 JAK2 enzyme 54 allelic 54 atherosclerotic lesion 54 Relapsing remitting MS 54 SLC#A# [002] 54 cyclin E 54 neurofibrillary 54 atherosclerotic vascular disease 54 hypothalamic pituitary 54 CREBBP 54 parkinsonism 54 M. pneumoniae 54 antiphospholipid antibodies 54 GBM tumors 54 Zinc deficiency 54 familial adenomatous polyposis 54 multisystem disease 54 hemorrhagic colitis 54 Aortic stenosis 54 Subtype 54 metabolizing enzymes 54 immunodeficiency 54 phthalate syndrome 54 ε4 54 Ets2 54 isoenzyme 54 QTLs 54 melanocortin receptor 54 TT genotype 54 neurofibromas 54 PI3K signaling 54 klotho gene 54 radiosensitive 54 Androgenetic alopecia 54 Dilated cardiomyopathy 54 leiomyomas 54 hepatocellular carcinomas 54 homolog 54 testicular dysgenesis syndrome 54 smoldering myeloma 54 monozygotic twins 54 bile acid metabolism 54 globin 54 HLA DRB1 SE 54 allele frequency 54 coronary calcification 54 transgene expression 54 elevated CRP 54 Heterozygous 54 prostate cancer CaP 54 ZNF# 54 AUDs 54 Multivariate analyzes 54 ectodermal dysplasia 54 HMGA2 gene 54 nongenetic 54 hematopoietic cancers 54 serum ferritin 54 ABCB1 gene 54 Alu elements 54 Myelodysplastic syndrome 54 recessive genetic 54 CHEK2 54 dominantly inherited 54 parkinsonian 54 metabolic abnormality 54 lactose malabsorption 54 serous ovarian cancer 54 intestinal microflora 54 muscular dystrophies 54 Cockayne syndrome 54 HNPCC 54 mutation 54 E4 variant 54 CYP#A# gene 54 BRAF protein 54 CHRNA5 54 recessive mutation 54 osteochondrosis 54 ANCA associated 54 C#BL 6 mice 54 RRM1 54 promoter hypermethylation 54 proto oncogene 54 fluoroquinolone resistance 54 D#N 54 albumin excretion 54 Myotonic dystrophy 54 alpha synuclein gene 54 #p# [003] 54 nicotinic receptor 54 familial aggregation 54 C#T [001] 54 poor metabolizers 54 IGF2 54 dopamine D4 receptor 54 hematopoietic progenitor cells 54 N. gonorrhoeae 54 autoantibodies 54 CNTNAP2 gene 54 lung epithelial cells 54 oncogenic mutations 54 TRAF1 C5 54 LV dysfunction 54 Uterine cancer 54 aminotransferase 54 G#S [002] 54 mitochondrial mutations 54 atrophic 54 Thyroid hormone 54 TYMS 54 idiopathic myelofibrosis 54 vascular dysfunction 54 maternally inherited 54 Chronic pancreatitis 54 splice variants 54 cagA 54 hyperinsulinemic 54 EBV infection 54 CRTAP 53 genetic variants 53 myopathies 53 FTO gene 53 Sezary syndrome 53 JAK mutations 53 Myostatin 53 triglyceride concentrations 53 Apolipoprotein E 53 metabolizing enzyme 53 PDE#A 53 alpha1 antitrypsin deficiency 53 NF1 53 IRF6 53 chromosomal translocations 53 proapoptotic 53 prostate carcinoma 53 invasive carcinoma 53 T1c 53 HepG2 cells 53 etiologic factors 53 breast carcinoma 53 MnSOD 53 NKX2 53 S. maltophilia 53 cytogenetic abnormalities 53 leptin receptor 53 Niemann Pick disease 53 calcium oxalate stones 53 Neuregulin 1 53 cystatin 53 HIV seropositive 53 mutations 53 GABRA2 gene 53 histopathological 53 thyroid carcinoma 53 A. thaliana 53 chromosomal anomalies 53 gene variation 53 antiphospholipid syndrome 53 ERK signaling 53 monozygotic 53 #q# [002] 53 supratentorial 53 frameshift mutation 53 von Willebrand 53 metabolic syndrome MetS 53 generalized vitiligo 53 constitutively expressed 53 coexpression 53 RET PTC rearrangements 53 NNRTI resistant virus 53 prion protein PrP 53 urolithiasis 53 lichen planus 53 SOD1 gene 53 HIV coinfected 53 urethritis 53 genetically inherited 53 proline rich 53 mesotheliomas 53 mice lacking 53 cytochrome b 53 CYP#C# * 53 Brugada syndrome 53 thyrotropin 53 comorbid disorders 53 MEF2A 53 polygenic 53 lignan intake 53 Papillary 53 psychiatric comorbidity 53 exocrine glands 53 retrocyclin 53 apoE 53 inherited maternally 53 endocrine dysfunction 53 fibrillin 1 53 BCL#A 53 unfavorable prognostic 53 LIS1 53 hyperhomocysteinemia 53 aneuploid 53 non syndromic 53 wildtype 53 malignant lymphoma 53 paralogs 53 ORFs 53 morphologic 53 neurodevelopmental disorder 53 tau gene 53 VNTR 53 MAOA 53 frontotemporal dementia 53 isoleucine 53 glycosylated 53 H#D 53 pleiotropic 53 diagnostic biomarker 53 ischemic vascular 53 apolipoprotein E 53 diabetes dyslipidemia 53 chromosome #q 53 cytopathic 53 neoplasias 53 filaggrin 53 asymptomatic carriers 53 EGFR mutations 53 hereditary deafness 53 pituitary hormone 53 thrombocytopenic patients 53 heterozygosity 53 genes encoding 53 androgen deficiency 53 BRAF mutation 53 MRSA isolates 53 affective disorders 53 MLL2 53 Klotho gene 53 cellular prion protein 53 neuropsychiatric disorder 53 premutation 53 fasting plasma 53 SLITRK1 53 genetically altered mouse 53 adiponectin concentrations 53 pathological hallmark 53 GG genotype 53 serum BDNF 53 FUS protein 53 SMN1 53 phenotypic expression 53 fascin 53 microbiomes 53 colorectal neoplasia 53 XMRV infection 53 hypocretin neurons 53 neurologic disorder 53 gestational diabetes mellitus 53 neuroblastoma tumors 53 IGFBP 53 hypovitaminosis D 53 CFTR gene mutations 53 mucinous 53 Lafora disease 53 NPY gene 53 lymphoblastoid cell lines 53 alkaline phosphatase 53 HMGA2 53 ortholog 53 Autoimmune hepatitis 53 WDR# 53 hyperinsulinemia 53 serovar 53 PBMCs 53 TP# gene 53 CEACAM1 53 PCNSL 53 euthymic patients 53 molecular abnormalities 53 dysglycemia 53 paraganglioma 53 S#A# [002] 53 human leukocyte antigens 53 TNFAIP3 53 microscopic colitis 53 spontaneous mutation 53 behavioral disinhibition 53 clade C 53 CYP#B# 53 autism susceptibility genes 53 tryptase 53 scintigraphic 53 Venous thromboembolism 53 Atopic dermatitis 53 p#NTR 53 serine protease 53 Geographic Atrophy 53 VKORC1 53 BMPR2 53 Coxsackievirus 53 cerebral microbleeds 53 pathogenetic 53 alpha thalassemia 53 ependymomas 53 lesional 53 Genetic variations 53 H pylori 53 hepatic enzymes 53 familial polyposis 53 prion protein gene 53 phylogenetic analyzes 53 haplogroup 53 cell adhesion molecule 53 schizophreniform disorder 53 intracranial hemorrhage ICH 53 FXTAS 53 causative mutations 53 isoprostane 53 mitochondrial gene 53 trophoblast cells 53 ErbB2 positive 53 carotid IMT 53 RASSF1A 53 maternally transmitted 53 Colon polyps 53 neurocognitive impairment 53 leukaemias 53 obesity insulin resistance 53 KCNH2 53 number variations CNVs 53 FGFR2 53 LMNA 53 bronchial epithelial cells 53 autoantibody 53 receptor inhibitor 53 PAOD 53 ADA SCID 53 cardiac hypertrophy 53 V#E 53 benign neoplasms 53 spongiform encephalopathies 53 colonic polyps 53 basal cell carcinoma BCC 53 fig. S4 53 impaired cognition 53 hepatic renal 53 Typhimurium 53 phenotypes 53 fluconazole resistant 53 HPV# 53 herpesviruses 53 hemoglobinopathies 53 potent inhibition 53 BRAF gene 53 elevated triglycerides 53 leptin deficiency 53 β amyloid 53 folic acid deficiency 53 IRF6 gene 53 NF2 53 Diabetic nephropathy 53 endocannabinoid signaling 53 ERK2 53 orthologous genes 53 gene loci 53 1 diabetes T1D 52 B7 H3 52 IDH mutations 52 mitochondrial proteins 52 mutated BRCA1 52 amyloidogenic 52 NAFLD 52 chromosomal instability 52 Kufs disease 52 papillary renal cell carcinoma 52 Leydig cells 52 HER2 overexpression 52 Irritable bowel syndrome 52 BALB c mice 52 nonmelanoma skin cancers 52 goblet cells 52 HeFH 52 medulloblastoma tumors 52 NR#A# gene 52 H. influenzae 52 TP# mutations 52 TGF ß 52 TMPRSS2 ERG 52 p# activation 52 transaminase elevations 52 P falciparum 52 hepatoma 52 chromosome #p# [002] 52 epithelial tissues 52 TMPRSS6 52 PIK3CA 52 Alzheimer pathology 52 severe congenital neutropenia 52 lung adenocarcinoma 52 postmenopausal estrogen 52 extramedullary 52 precancerous cervical 52 chromosome rearrangements 52 Aromatase 52 Wernicke Korsakoff syndrome 52 progranulin mutations 52 miRNA genes 52 abnormal proteins 52 PDGFR 52 SMN protein 52 mycosis fungoides 52 endometrial thickness 52 dizygotic twins 52 GISTs 52 ALI ARDS 52 periventricular 52 AAT Deficiency 52 oligomeric 52 Entamoeba 52 mitochondrial disorders