Related by context. All words. (Click for frequent words.) 71 TCF#L# gene 69 MC4R gene 68 gene DRD4 68 ENPP1 67 KCNH2 67 5 HTTLPR 67 SHANK3 67 GAB2 67 DRD2 gene 67 MLL2 66 BARD1 66 apolipoprotein E4 66 BDNF gene 66 LRP5 66 monogenic 66 apolipoprotein E APOE 65 SLC#A# [002] 65 chromosome #q# [002] 65 TCF#L# 65 apolipoprotein E gene 65 dopamine receptor gene 65 SORL1 65 CNTNAP2 65 CYP#D# gene 65 SLITRK1 65 COMT gene 65 androgen receptor gene 65 CYP#A# [002] 65 C#Y 65 LPA gene 65 IL#R 65 DRD4 64 MSH2 64 serotonin transporter gene 64 amyloid cascade 64 dysbindin 64 KIF6 gene 64 MAOA gene 64 MECP2 gene 64 KRAS oncogene 64 DQB1 * 64 microcephalin 64 UGT#A# * 64 inherited mutations 64 Genetic variation 64 CHRNA5 64 HLA DRB1 64 PTPN# 63 MYH9 gene 63 BRIP1 63 MTHFR 63 K ras mutations 63 CCR5 delta# 63 #q# deletion 63 GABRA2 63 SNP rs# [001] 63 CHD7 63 apoE4 63 SOD2 gene 63 de novo mutations 63 CDH1 63 JAK2 enzyme 63 SHANK3 gene 63 alpha synuclein gene 63 VHL gene 63 BRCA1 BRCA2 63 LRRK2 gene 63 microdeletion 62 NR#A# 62 HMGA2 62 MC1R 62 genes CYP#C# 62 ZNF# 62 MLH1 62 rs# [004] 62 Genetic variants 62 HFE gene 62 CYP#A# gene 62 Clusterin 62 hypomethylation 62 hypermethylated 62 CETP gene 62 rs# [002] 62 CHEK2 62 Apolipoprotein E 62 LRAT 62 #q#.# [001] 62 MEF2A 62 CYP#C# gene 62 FGFR2 62 catechol O methyltransferase 62 III EGFRvIII 62 5 HTT gene 62 GPC5 62 recessive mutation 62 STAT4 62 progranulin gene 62 CDKN2A 62 KIAA# 62 ABCB1 62 GNAQ 62 missense mutation 62 germline mutations 62 autosomal recessive 62 #q#.# deletion syndrome 62 HMGCR 61 Janus kinase 61 fewer dopamine receptors 61 PON1 gene 61 VNTR 61 CALHM1 61 APOL1 61 autosomal dominant disorder 61 Cryptococcus neoformans 61 Hashimoto thyroiditis 61 LKB1 61 APOE ε4 61 mosaicism 61 VKORC1 61 BRAF V#E 61 ORMDL3 61 5 HT1A 61 SCN1A 61 chromosome #q# [001] 61 causative mutations 61 DEC2 61 missense mutations 61 ADH1B * 61 FMR1 gene 61 SNCA 61 BCL#A 61 heterozygotes 61 genetic polymorphism 61 5 HT1A receptor 61 epigenetic modification 61 COX2 61 TRAF1 C5 60 protein encoded 60 Bacterial vaginosis 60 neuropsychiatric disorder 60 AVPR1A 60 Cathepsin B 60 breast cancer genes BRCA1 60 Treg cell 60 CYP#E# 60 Hutchinson Gilford progeria 60 ATG#L# 60 ALK gene 60 p# MAPK 60 IgA deficiency 60 MGUS 60 NF1 gene 60 ALDH2 60 gene locus 60 FUS1 60 nonhereditary 60 SLC#A# [001] 60 affective psychosis 60 gastric carcinogenesis 60 GSTP1 60 Wwox 60 SCN5A 60 genetic loci 60 KIBRA 60 neuroblastoma tumors 60 PALB2 60 gene APOE 60 prolonged QT interval 60 MLL gene 60 ESR1 60 rs# [003] 60 APOE4 60 G#S mutation 60 DRD2 60 mitogen activated protein kinases 60 F#del 60 DICER1 gene 60 APOE e4 60 CYP#C# [001] 60 chromosomal rearrangement 60 c KIT 60 promoter hypermethylation 60 methylenetetrahydrofolate reductase 60 Nf1 60 dyskeratosis congenita 60 promoter polymorphism 60 GABA receptor 60 mice lacking 60 cause cardiac channelopathies 60 KLF# 60 Suicidal tendencies 60 NKX#.# 59 TMPRSS2 ERG 59 pancreatic endocrine 59 progressive neurodegenerative disorder 59 phenothiazines 59 NRG1 59 ADPKD 59 TP# mutations 59 sporadic ALS 59 PDE#A 59 COL#A# 59 #p#.# [001] 59 AMACR 59 HPA axis 59 #p#.# [002] 59 Neuregulin 1 59 neuronal plasticity 59 DRD4 gene 59 hepatoma 59 dopamine transporter gene 59 Epstein Barr Virus EBV 59 APOC3 59 somatostatin 59 DRB1 59 PTEN mutations 59 DISC1 gene 59 herpesviruses 59 inherited neurological disorder 59 glutamic acid decarboxylase 59 thyrotropin 59 IL#B 59 Prox1 59 TGFBR1 * 6A 59 BMPR2 59 CNTNAP2 gene 59 Cyclin E 59 clomipramine 59 testicular germ cell 59 glucocorticoid receptors 59 frameshift mutation 59 G allele 59 serine threonine kinase 59 parkin gene 59 MIF gene 59 HLA DQ2 59 EBV infection 59 medulloblastomas 59 caveolin 59 Ras oncogene 59 Genetic predisposition 59 familial ALS 59 RASSF1A 59 methylation patterns 59 PTEN gene 59 rs# [001] 59 klotho 59 K#N 59 aldehyde dehydrogenase 59 genes BRCA1 59 susceptibility gene 59 KCNQ1 59 Li Fraumeni syndrome 59 beta1 integrin 59 variant rs# 59 affective psychoses 59 airway hyperresponsiveness 59 MTHFD1L gene 59 microRNA expression 59 HMMR 59 FGFR2 gene 59 CCL#L# 59 CYP#C# * 59 Folate deficiency 59 Ribavirin causes 59 BRAF gene 59 circadian clock genes 59 Epstein Barr virus EBV 59 Vidaza ® 59 STK# gene 59 Treponema 59 Brugada syndrome 59 chromosomal aberrations 59 synuclein 59 cell adhesion molecule 59 serum BDNF 59 sex hormones estrogen 58 MC1R gene 58 #q# [001] 58 Premature Aging 58 epigenetically 58 cytopathic 58 GBA mutations 58 severe congenital neutropenia 58 IRS1 58 mutated K ras 58 mRNA transcripts 58 HLA B# 58 ataxin 58 IDH mutations 58 TP# gene 58 CYP #A# 58 alternatively spliced 58 confusional arousals 58 excitatory neurotransmitter glutamate 58 miRNA expression 58 gene rearrangements 58 IKZF1 58 LRRK2 mutation 58 GSTT1 58 Klotho gene 58 OPRM1 gene 58 inverse agonist 58 Kabuki syndrome 58 somatic mutations 58 homozygosity 58 FASPS 58 NPY gene 58 IL #R 58 HER2 overexpression 58 CYP#C# [002] 58 Argonaute 58 GSTM1 gene 58 Ets2 58 inactive X chromosome 58 genomic deletions 58 CFTR cystic fibrosis transmembrane 58 NAT2 58 susceptibility loci 58 APOA5 58 C1 INH deficiency 58 xenotropic murine leukemia 58 HepG2 cells 58 genetic variants associated 58 VIPR2 58 leptin receptor 58 WAGR syndrome 58 MECP2 58 survival motor neuron 58 HGPS 58 MDR1 58 SMN1 58 E#F# 58 allelic variants 58 CagA 58 lymphocyte activation 58 oesophageal adenocarcinoma 58 FOXP2 gene 58 eotaxin 58 clefting 58 TMEM#B 58 FMR1 58 ApoE4 58 behavioral disinhibition 58 NKX2 58 Kufs disease 58 mutant allele 58 histone methylation 58 nicotinic receptor 58 polymorphisms 58 regulator CFTR gene 58 inhibitory receptor 58 MAPK pathway 58 Cognitive impairment 58 MMP# 58 CETP VV 58 epigenetic alterations 58 2 diabetes T2D 58 Irritable bowel syndrome IBS 58 UGT#B# 58 monozygotic twin 58 histone deacetylases 58 CEACAM1 58 WNK1 58 CREBBP 58 amnestic 58 EGFR gene 58 chromosomal rearrangements 58 IL 1Ra 58 receptor kinase 58 Subgroup analysis 58 receptor gene 58 pathogenic mutations 58 schizophreniform disorder 58 drug metabolizing enzyme 58 Cyclin D1 58 DEAR1 58 human herpesvirus 58 APOE gene 58 segmental duplications 58 cyclin E 58 Fas ligand 58 hypermethylation 58 telomerase reverse transcriptase 58 CDK4 58 Creutzfeldt Jacob 58 chemically alters 58 SORL1 gene 58 MC4R 58 ADRB2 58 neuroD2 58 underlying pathophysiology 58 genetic variant 58 CYP#A# CYP#D# 57 colorectal carcinoma 57 HLA DRB1 * 57 demethylase 57 pDC 57 narcolepsy cataplexy 57 polymorphic ventricular tachycardia 57 NS5B polymerase 57 aneuploidies 57 Genetic mutations 57 Pten 57 folate metabolism 57 antibody mediated 57 CFTR gene 57 Wnt1 57 Estrogen receptor 57 SNP rs# [002] 57 chromosome #p#.# 57 TRAIL induced apoptosis 57 C#T [002] 57 giant danio 57 premenstrual syndrome PMS 57 Bardet Biedl syndrome 57 ribosomal protein 57 apoE 57 siRNA knockdown 57 mda 7 57 prodynorphin 57 recessive trait 57 autosomal dominant inheritance 57 Chlamydia pneumoniae 57 DLC1 57 Alu elements 57 Oxidative damage 57 brain lesions 57 HMG CoA reductase inhibitors 57 receptor inhibitor 57 recessive inheritance 57 number variations CNVs 57 LIS1 57 ERBB2 57 sequence homology 57 epigenetic changes 57 hepatic lipase 57 macrophage migration inhibitory 57 anaplastic lymphoma kinase 57 sporadic Creutzfeldt Jakob 57 #p# [003] 57 inherited maternally 57 KLF4 57 #q# deletion syndrome 57 gene polymorphism 57 genomewide 57 TET2 57 beta globin gene 57 unmutated 57 prostate carcinogenesis 57 microsatellite instability 57 hypothalamic pituitary adrenal axis 57 genomic variants 57 autosomal recessive disorder 57 glutamate signaling 57 Leukemias 57 promoter methylation 57 Selective Serotonin Reuptake Inhibitor 57 PLX STROKE targeting 57 lichen planus 57 Polymorphisms 57 DISC1 57 WDR# 57 APOE genotype 57 Avandia Actos 57 testicular tumors 57 prostate cancer CaP 57 ABCB1 gene 57 tics involuntary 57 breast carcinogenesis 57 postoperative delirium 57 coiled coil domain 57 superinfection 57 huntingtin gene 57 gene polymorphisms 57 DNA methylation patterns 57 Genetic Variation 57 missense 57 susceptibility locus 57 monozygotic twins 57 tau mutation 57 SH#B# 57 Acute pancreatitis 57 Selective serotonin reuptake inhibitors 57 RUNX3 57 idiopathic PAH 57 gene MECP2 57 dinucleotide 57 Valproic acid 57 p# activation 57 H#Y mutation 57 Amino acid 57 Froguel 57 ApoE gene 57 causal variants 57 Imprinted genes 57 p#INK#a 57 vasopressin receptor 57 genetic polymorphisms 57 ADAMTS# 57 somatic mutation 57 Karayiorgou 57 Thyroid disorders 57 tumor suppressors cytokines 57 Selective Inhibitor 57 glycogen synthase kinase 57 SGK1 57 dominantly inherited 57 melanocyte 57 myeloproliferative 57 amyloid plaque formation 57 IDH1 gene 57 PICALM 57 familial pancreatic cancer 57 APOE epsilon 4 57 RCAN1 57 constitutively expressed 57 transgenic mouse models 57 GLUT1 57 SLC#A# gene [001] 57 GABRA2 gene 57 Mg Usa 57 proband 57 Lafora disease 57 microRNA molecules 57 TOMM# 57 NPM1 gene 57 CYP#A# substrate 57 PCSK9 gene 57 5 HT2A serotonin 57 CYP#D# 57 predisposing factor 57 autoinflammatory diseases 57 lactate dehydrogenase LDH 57 ataxias 57 spontaneous mutations 57 TSC1 57 intronic 57 C. neoformans 57 neuroimaging studies 57 SMAD4 57 S. sanguinis 57 aneuploid cells 57 Epigenetics refers 57 CD#c 57 genotoxic stress 57 CYP#E# gene 57 evolutionary conserved 57 selective modulator 57 R#W [002] 57 mutated BRCA 57 overactivation 57 Cyclooxygenase 2 57 androgen receptor AR 57 virulence genes 57 Fragile X gene 57 uPAR 57 El Sohemy 57 TGFBR1 57 maternally transmitted 57 chlamydial infection 57 DRB1 * 57 schizotypal 57 stress cardiomyopathy 57 Leydig cell 57 ependymomas 57 Peptide YY 57 COMT 57 dysbindin gene 56 neural progenitor 56 CpG DNA 56 XMRV infection 56 histone acetylation 56 gene loci 56 Foxp3 56 diabetic kidney 56 transcriptional repressor 56 MeCP2 gene 56 Htt 56 CYP #D# 56 histone H4 56 Cytotoxic T 56 deacetylation 56 IGF2 56 Foxp2 56 alexithymia 56 activin 56 TNFalpha 56 PDGFR 56 MnSOD 56 unprovoked seizures 56 folate deficiency 56 Male pattern baldness 56 #S rRNA 56 colorectal carcinogenesis 56 TEL AML1 56 glutamatergic 56 genes predisposing 56 upregulates 56 telomere dysfunction 56 oseltamivir resistant 56 allogeneic HSCT 56 fibrillin 1 56 lipid abnormalities 56 atypical hyperplasia 56 squamous cell lung cancer 56 apo E 56 transthyretin 56 mGluR 56 nondemented 56 #S ribosomal RNA 56 IGF binding 56 chromosomal anomalies 56 humanin 56 mRNA expression 56 TPMT 56 gene APOE4 56 TTR gene 56 thyrotropin levels 56 NFkB 56 DNA methyltransferase 56 alpha2 56 familial aggregation 56 LMNA gene 56 PDGFRA 56 genomewide association study 56 mitotic catastrophe 56 Genetic variations 56 functional polymorphism 56 H#K#me# 56 haloperidol Haldol 56 DUX4 56 Six3 56 IDH1 mutation 56 unmeasured confounders 56 gastroenteritis conjunctivitis 56 Nilotinib 56 Apobec3 56 neurite outgrowth 56 FGFR1 56 PPARγ 56 neurofibroma 56 Immunohistochemical analysis 56 CaMKII 56 nephronophthisis 56 LDLR 56 Teriflunomide 56 impaired glucose metabolism 56 neuritic 56 sFlt1 56 BMP2 56 euthymic patients 56 endoplasmic reticulum stress 56 sCJD 56 JAK mutations 56 autosomal dominant 56 exocrine 56 TOP2A 56 Nedd4 56 leptin deficiency 56 alleles 56 circadian genes 56 Systemic lupus erythematosus SLE 56 Androgen receptor 56 CYP#B# 56 apoC III 56 virus XMRV 56 Inappropriate activation 56 IDH2 56 TACI mutations 56 meiotic recombination 56 Glucocorticoids 56 Monoamine oxidase 56 autosomal 56 Haptoglobin 56 IKK beta 56 epigenetic regulation 56 GRP# 56 indels 56 familial clustering 56 gene variant 56 TrkB 56 K ras gene 56 tumor suppressor PTEN 56 Darapladib 56 #q# [002] 56 Leber hereditary optic neuropathy 56 Cancer Incidence Mortality 56 CYT# potent vascular disrupting 56 thymidylate synthase 56 aneuploid 56 BRAF V#E mutation 56 steroidogenic 56 FKBP# 56 included exfoliative dermatitis 56 Predisposition 56 gestational diabetes mellitus 56 IRF6 56 Tasigna prolongs 56 cystic fibrosis transmembrane conductance 56 neuropsychiatric symptoms 56 intensive statin therapy 56 cyclin dependent kinase inhibitor 56 Wnt#b 56 IRF6 gene 56 Upregulation 56 tryptase 56 apolipoprotein E 56 SSc 56 radial glia 56 DNMT1 56 Brd4 56 EGFR protein 56 PCNSL 56 X inactivation 56 TOP2A gene 56 Epileptic seizures 56 PARP inhibition 56 gene BRCA2 56 dystrophin gene 56 autistic enterocolitis 56 γ secretase 56 intracellular bacteria 56 hematopoietic cancers 56 non cirrhotic portal 56 maternally inherited 56 Sjögren syndrome 56 constitutive activation 56 comorbid anxiety 56 polymorphism 56 epigenetic silencing 56 inflammatory PDE 56 NRF2 gene 56 tyrosine phosphorylation 56 human leukocyte antigens 56 antidepressants fluoxetine 56 Gleevec resistant 56 endocannabinoid signaling 56 pharmacokinetic interactions 56 beta carotene supplementation 56 Inactivation 56 phospholipase A2 56 Myostatin 56 PTP1B 56 #q#.# [002] 56 MSMB 56 TGF beta pathway 56 PTEN tumor suppressor 56 progerin 56 p# deficient 56 isomerase II 56 fluoxetine Prozac 56 medulloblastoma tumors 56 serous ovarian cancer 56 SETDB1 56 Dehydrogenase 55 FXTAS 55 mitochondrial metabolism 55 PPAR γ 55 chromosome #q#.# [002] 55 T. vaginalis 55 hereditary nonpolyposis colorectal cancer 55 GlaxoSmithKline Plc Paxil 55 scombroid poisoning 55 tumor suppressor protein 55 epigenetic markers 55 chromosome #p# [002] 55 polycystic ovary syndrome PCOS 55 extrapyramidal symptoms 55 IGFBP2 55 torsade de pointes 55 HSV1 55 venlafaxine Effexor 55 T#I [002] 55 transgenic rats 55 CHRNA5 gene 55 chitinase 55 TGF ß 55 Peutz Jeghers syndrome 55 demyelinating disease 55 SLC#A# gene [002] 55 FADS2 55 dysglycemia 55 costimulatory 55 β1 55 NFKBIA 55 esophageal squamous cell carcinoma 55 CAG repeats 55 subcellular localization 55 Prolactin 55 cisplatin resistant 55 diploid genome 55 CXCL5 55 HbF levels 55 TMPRSS2 ERG fusion 55 Male infertility 55 neurodevelopmental disorder 55 podocyte 55 OPRM1 55 APOE allele 55 allelic variation 55 progesterone receptor negative 55 Yamanaka recipe 55 chromosome #p# [001] 55 cholinergic tone 55 NNRTI resistance 55 metapneumovirus 55 NQO1 55 chromosomal translocations 55 inducible nitric oxide synthase 55 p#/CBP 55 Atopic dermatitis 55 cyclin dependent kinases 55 type2 diabetes 55 Brain derived neurotrophic 55 human leukocyte antigen 55 nongenetic factors 55 PIK3CA 55 perilipin 55 coinfection 55 Korsakoff syndrome 55 dopamine signaling 55 Mg Uk 55 CD# expression [001] 55 glucose abnormalities 55 copper zinc superoxide 55 neuroblastomas 55 urocortin 55 V Leiden 55 sulphonylureas 55 GRK5 55 TNFAIP3 55 DLX5 55 plasma lipid 55 mitochondrial dysfunction 55 Variant Creutzfeldt Jakob 55 neuropsychiatric diseases 55 TNFα 55 ApoE 55 molecular abnormalities 55 proto oncogene 55 HER2 positivity 55 protein p# 55 SRY gene 55 unstable detrusor muscle 55 compulsive hoarding syndrome 55 IGF1 55 antiphospholipid antibodies 55 protein conformation 55 testicular dysgenesis syndrome 55 T1DM 55 BRCA2 breast cancer 55 HBx 55 chromatin structure 55 UCRs 55 TCF4 55 paraneoplastic 55 Wnt signaling pathway 55 c Myb 55 chromosomal alterations 55 pleiotropic 55 Cowden syndrome 55 neuroleptic 55 EEG abnormalities 55 spontaneous mutation 55 HLA DRB1 SE 55 p# mutation 55 autosomes 55 hereditary predisposition 55 Fc receptor 55 Mendelian disorders 55 Chlamydia trachomatis 55 Raf MEK ERK 55 germline mutation 55 DAT1 55 microdeletions 55 papillary RCC 55 Electroconvulsive therapy 55 modifier genes 55 lysosomal storage disease 55 MAP kinases 55 Lymphocytic 55 lymphoblastoid cell lines 55 inhibiting COX 55 Mycoplasma pneumoniae 55 Meckel Gruber 55 inhibit CYP#A# 55 transgenic mouse model 55 Strong inducers 55 Heritability 55 assortative mating 55 lactose malabsorption 55 interferon IFN 55 Effexor venlafaxine 55 PTEN protein 55 SAPAP3 55 Angelman syndrome 55 elevated triglyceride levels 55 Anti depressant 55 SOD2 55 dopamine D2 receptor 55 misregulation 55 MYBPC3 55 mutated p# 55 protein secreted 55 Angiotensin converting enzyme 55 Listeria infections 55 inherit predisposition 55 pathogenic mechanisms 55 Magnesium deficiency 55 hormones leptin 55 MIF protein 55 MAPKs 55 Chlamydia psittaci 55 fatty acid synthase 55 GABAergic 55 TRIM5a 55 regulates gene expression 55 inherited genetic mutations 55 Rho GTPases 55 hormonally sensitive 55 Psychotic depression 55 subtyped 55 chromosomal anomaly 55 Wernicke Korsakoff syndrome 55 amyloid ß 55 microchimerism 55 major histocompatibility complex 55 circulating endothelial cells 55 metabolizing enzymes 55 neurexins 55 insulin resistance syndrome 55 tryptophan depletion 55 affective disorders 55 histone modification 55 neuropathologic 55 bacteria Pseudomonas aeruginosa 55 P. falciparum parasites 55 certain protein tyrosine 55 P. reichenowi 55 cortisol secretion 55 nNOS 55 dihydrofolate reductase 55 superoxide dismutase 55 untranslated regions 55 pool dies unwept 55 alcohol dehydrogenase 55 FGF2 55 Chlamydia trachomatis infection 55 H pylori 55 nucleoli 55 Long acting beta2 55 Trypanosoma brucei 55 chlamydial infections 55 adenomatous polyposis coli 55 Systemic lupus erythematosus 55 #p# [001] 55 mutated genes 55 multi factorial disease 55 NF1 55 Microarray analysis 55 cis regulatory 55 obesity insulin resistance 55 extramedullary 55 Pancreatic neuroendocrine tumors 55 alternative splicing 55 hippocampal function 55 cholesteryl ester transfer 55 hereditary hemochromatosis 55 endoxifen 55 MAOA 55 neurocognitive impairment 55 E cadherin expression 55 ERCC1 55 CYP#D# genotype 55 RNA sequences 55 tumor subtype 55 rifamycins 55 tipranavir ritonavir 55 chromatin remodeling 55 interferon induced 55 SOD1 protein 55 serum lipid 55 serotonin transporter 55 Am J Clin 55 colorectal adenoma 55 Smad3 55 Alleles 55 Klinefelter syndrome 55 tricyclic antidepressants TCAs 55 tensin homolog 55 SCHIZOPHRENIA DISORDERS SUPPORT GROUP 55 transgenic mice expressing 55 estrogen receptor alpha 55 GPx 55 SOX3 gene 55 ankyrin B 55 anticholinergic effects 55 phosphatases