Related by context. All words. (Click for frequent words.) 75 dopamine receptor gene 73 DRD4 gene 70 gene DRD4 67 DRD2 gene 66 GABRA2 65 5 HTTLPR 65 DRD2 65 MAOA gene 65 CNTNAP2 65 dopamine D4 receptor 64 PTPN# 64 proband 64 dopamine transporter gene 64 APOE4 63 MAOA 63 apolipoprotein E 63 rs# [002] 63 rs# [001] 63 DQB1 * 63 rs# [003] 63 apolipoprotein E gene 62 KIF6 gene 62 homozygosity 62 BARD1 62 APOE ε4 62 missense mutations 62 CDKN2A 61 MSH2 61 TP# mutations 61 CYP#A# gene 61 OPRM1 gene 61 serotonin transporter gene 61 C#Y 61 genetic polymorphism 61 UGT#A# * 61 receptor gene 61 homozygotes 61 G allele 61 HLA DRB1 * 61 vasopressin receptor 61 repeat allele 61 heterozygotes 60 #q#.# [001] 60 Neuroticism 60 ABCB1 60 APOE genotype 60 ADH1B * 60 ApoE4 60 APOE gene 60 BDNF gene 60 allele frequencies 60 MLH1 60 susceptibility gene 60 gene APOE 60 genetic loci 60 SNP rs# [001] 60 IL#R 60 APOE allele 60 de novo mutations 59 chromosome #q# [002] 59 AVPR1A 59 TCF#L# gene 59 rs# [004] 59 monozygotic twins 59 PTEN mutations 59 SLC#A# [002] 59 microdeletion 59 VNTR 59 MC1R 59 HLA DRB1 59 MC4R gene 59 genes predisposing 59 gene polymorphisms 59 KLF4 59 WNK1 59 functional polymorphism 59 COMT gene 59 variant alleles 59 PON1 gene 59 ENPP1 58 MC1R gene 58 allele 58 ADRB2 58 monozygotic twin 58 TCF#L# 58 gene locus 58 UGT#B# 58 nicotinic receptor 58 Genetic variation 58 nondemented 58 Estrogen receptor 58 alexithymia 58 TGFBR1 * 6A 58 mosaicism 58 #q# deletion syndrome 58 FGFR2 58 CHEK2 58 IgA deficiency 58 autistic traits 58 APOC3 58 LPA gene 58 #p# [003] 58 ApoE gene 58 polymorphism 58 CHRNA5 58 Monoamine oxidase 58 promoter polymorphism 58 alpha synuclein gene 58 microcephalin 58 A1 allele 58 CYP#C# * 58 affective psychosis 58 KIAA# 58 narcolepsy cataplexy 58 MYH9 gene 58 COL#A# 58 MTHFR 58 APOE e4 58 behavioral disinhibition 57 schizotypal traits 57 germline mutations 57 apoE4 57 chromosome #p# [001] 57 #q# [002] 57 gene polymorphism 57 #q#.# deletion syndrome 57 KCNH2 57 KIBRA 57 C#BL/#J 57 SCN1A 57 intronic 57 Hashimoto thyroiditis 57 variant allele 57 genomic variants 57 mutant allele 57 missense mutation 57 OPRM1 57 genes CYP#C# 57 fewer dopamine receptors 57 CHD7 57 catechol O methyltransferase 57 CDH1 57 apolipoprotein E4 57 NR#A# gene 57 MEF2A 57 klotho 57 Genetic variants 57 monogenic 57 HLA DQ2 57 SNP rs# [002] 57 TT genotype 57 hypogonadotropic hypogonadism 57 HLA B# 57 heterozygous 57 CYP#B# 57 KRAS oncogene 57 heterozygosity 57 MECP2 gene 57 MLL2 57 GSTM1 56 adenylate cyclase 56 androgen receptor gene 56 DAT1 56 hypoactive 56 SHANK3 56 LRP5 56 alleles 56 hereditary hemochromatosis 56 LRRK2 gene 56 Clusterin 56 SE alleles 56 GLUT1 56 probands 56 chromosome #q# [001] 56 CYP#A# [002] 56 #p# [001] 56 genotype 56 GABRA2 gene 56 5 HTT gene 56 ESR1 56 ZNF# 56 heritable 56 BRAF V#E 56 indels 56 breast cancer genes BRCA1 56 seronegative 56 NPY gene 56 GAB2 56 caveolin 56 Single Nucleotide Polymorphisms 56 p# MAPK 56 #p#.# [002] 56 IL#B 56 mutated K ras 56 CYP#E# gene 56 BMP2 56 CETP gene 56 neuroD2 56 allelic variants 56 CagA 56 plasma lipid 56 genetic polymorphisms 56 GSTP1 56 glucocorticoid receptors 56 dysbindin 56 FLT3 56 PALB2 56 CYP#D# 56 NAT2 56 TOP2A 56 apolipoprotein E APOE 56 Univariate analysis 56 metabolizing enzyme 56 antiphospholipid antibodies 56 MC4R 56 H#K#me# 56 susceptibility loci 56 IKZF1 56 #q# deletion 56 euthymic patients 55 Apolipoprotein E 55 sporadic ALS 55 V Leiden 55 MHC genes 55 orthologs 55 3'UTR 55 thyroglobulin 55 hyperinsulinemia 55 monozygotic 55 K#R [002] 55 CYP#C# gene 55 COMT 55 LKB1 55 CCR5 delta# 55 thrombospondin 55 CALHM1 55 FOXP2 gene 55 mRNA expression 55 K#N 55 univariate analyzes 55 CNTNAP2 gene 55 VKORC1 55 ApoE 55 R#W [002] 55 K ras mutations 55 ribosomal protein 55 extraversion 55 schizotypal 55 bivariate analyzes 55 APOE4 gene 55 #p#.# [001] 55 chromosome #q#.# [001] 55 recessive mutation 55 HLA DR4 immune 55 IL#B gene 55 thyrotropin 55 phenotype 55 chromosomal rearrangement 55 familial aggregation 55 melatonin receptor 55 LRRK2 mutation 55 GSTT1 55 KRAS mutations 55 NR#A# 55 homozygous 55 susceptibility genes 55 sequence homology 55 serotonin transporter 55 MGUS 55 assortative mating 55 V#F mutation 55 gestational diabetes mellitus 55 SLC#A# gene [002] 55 prefrontal cortical 55 homozygote 55 inherited mutations 55 autosomal recessive 55 polymorphisms 55 ABCB1 gene 55 prostate cancer CaP 55 BRCA1 BRCA2 55 apoC III 55 folate metabolism 55 HLA DRB1 SE 55 HFE gene 55 constitutively expressed 55 germline mutation 55 lipid abnormalities 55 Leukemias 55 CYP#D# gene 55 familial clustering 55 FTO gene 54 allelic variation 54 hypothalamic pituitary 54 TNFAIP3 54 Froguel 54 neuroimaging studies 54 TNFalpha 54 recessive trait 54 MDR1 54 airway hyperresponsiveness 54 Bonferroni correction 54 Heterozygous 54 SORL1 54 eotaxin 54 differentially expressed genes 54 transcriptional regulators 54 #q# [001] 54 CETP VV 54 endocannabinoid signaling 54 genes BRCA1 54 chromosomal anomalies 54 amygdala reactivity 54 multiple logistic regression 54 Sonic Hedgehog 54 PCa 54 GABA receptor 54 eIF4E 54 medial prefrontal 54 Personality traits 54 UGT#A# 54 hypermethylated 54 polygenic 54 phenotypes 54 microdeletions 54 microsatellite instability 54 COX2 54 susceptibility locus 54 chromosome #p#.# 54 abdominal adiposity 54 human leukocyte antigen HLA 54 Leydig cell 54 hypermethylation 54 GPR# [002] 54 gene variant 54 miRNA expression 54 frameshift mutation 54 paraneoplastic 54 HMGA2 54 SLC#A# [001] 54 apoE 54 SOD2 gene 54 airway hyper responsiveness 54 nongenetic 54 ERalpha 54 mtDNA mutations 54 adiponectin concentrations 54 progranulin gene 54 cyclin E 54 neuropathologic 54 CC genotype 54 subclinical hyperthyroidism 54 isoenzymes 54 Her2/neu 54 μ opioid receptor 54 underlying pathophysiology 54 ALDH2 54 DARPP 54 amyloid cascade 54 autosomes 54 MLL gene 54 activity MAOA 54 HMGCR 54 miR #a [001] 54 subclinical atherosclerosis 54 assortative 54 SRY gene 54 APOE 54 APOA5 54 ORMDL3 54 multivariate analyzes 54 PTHrP 54 gene loci 54 comorbid anxiety 54 atopy 54 serotonin receptor 54 circadian clock genes 54 MMP# 54 Neuregulin 1 54 onset diabetes mellitus 54 amino acid substitutions 54 clinicopathological 54 glutamic acid decarboxylase 54 VHL gene 54 externalizing disorders 54 missense 54 multivariable Cox 54 oxytocin receptor 54 adrenoceptor 54 Fragile X gene 54 Genotype 54 kDa protein 54 c KIT 54 K ras gene 54 homodimers 53 mRNA transcripts 53 PIGF 53 gonadal 53 TNF α 53 dopamine signaling 53 synuclein 53 tyrosine phosphorylation 53 ε4 53 TRAF1 C5 53 neutralizing antibody responses 53 lupus anticoagulant 53 dopamine receptors 53 etiologic 53 GSTM1 gene 53 X inactivation 53 seropositivity 53 mu opioid 53 posterior cingulate 53 CREBBP 53 mutant huntingtin protein 53 comorbid disorders 53 RRM1 53 DRB1 53 rheumatoid factor 53 p# mutation 53 GNAQ 53 BRCA1 mutations 53 MYH9 53 histocompatibility 53 IGFBP 53 GBA mutations 53 overactivation 53 adipogenic 53 HDL2 53 genomewide 53 spontaneous mutation 53 ABO blood 53 noncarriers 53 CYP#E# 53 BMPR2 53 subcellular localization 53 HMGA1 53 lymphocyte activation 53 AMACR 53 virulence genes 53 JAK2 enzyme 53 autosomal dominant disorder 53 KCNQ1 53 BRCA2 mutations 53 number variations CNVs 53 overt hypothyroidism 53 NKX#.# 53 CYP#C# [001] 53 APOE e4 gene 53 SCN5A 53 leptin receptor 53 Haplogroup 53 BCL#A 53 human herpesvirus 53 Hutchinson Gilford progeria 53 T2D 53 estrogen receptor ER 53 PARP inhibition 53 SLITRK1 53 susceptibility alleles 53 STAT4 53 somatic mutations 53 herpesviruses 53 steroidogenic 53 paraoxonase 53 G#S mutation 53 HNPCC 53 arterial thickening 53 tHcy 53 Polymorphisms 53 dopamine transporter 53 FTO variant 53 aldehyde dehydrogenase 53 HLA DR 53 TOP2A gene 53 elevated triglyceride levels 53 genes encoding 53 HLA B 53 dyads 53 T2 lesions 53 Alu elements 53 hypothalamic pituitary adrenal axis 53 evolutionarily conserved 53 KRAS gene 53 NNRTI resistance 53 ADAM# 53 DNA methyltransferase 53 SCD1 53 paternally inherited 53 epigenetic alterations 53 serum estradiol 53 protein phosphatase 53 allelic 53 Suicidal ideation 53 IGF2 53 Homozygous 53 ApoB 53 circadian genes 53 2D 4D ratio 53 HLA DR4 53 predisposing factor 53 prodynorphin 53 Prefrontal 53 histone H4 53 intergenic 53 habitual snoring 53 GABAB receptors 53 beta1 integrin 53 homologs 53 5 HT1A receptor 53 Androgen receptor 53 meiotic recombination 53 genetic variants associated 53 apo E 53 Li Fraumeni syndrome 53 endophenotypes 53 dizygotic 53 haplotypes 53 myeloproliferative 53 resistin 53 NF1 gene 53 PB1 F2 53 apolipoproteins 52 Parkinsonian 52 apolipoprotein 52 downregulated 52 penetrance 52 dopamine D2 receptors 52 NFkB 52 modifier genes 52 renal fibrosis 52 immunodominant 52 transgenic mouse models 52 ERBB2 52 miR #b [001] 52 ataxias 52 Haptoglobin 52 serum triglycerides 52 impaired glucose metabolism 52 familial ALS 52 mutated BRCA1 52 cell adhesion molecule 52 genotypic 52 causative mutations 52 DLC1 52 Avandia Actos 52 chromosome #q#.# [002] 52 nitrotyrosine 52 Predisposition 52 telomere lengths 52 hepatic lipase 52 TP# mutation 52 prepubertal 52 aneuploidy 52 QTLs 52 #q#.# [002] 52 HER2 overexpression 52 IgG1 52 normotensive 52 nonalcoholic steatohepatitis NASH 52 PON1 52 shorter telomere length 52 MIF protein 52 CYP#C# [002] 52 CHRNA5 gene 52 miRs 52 metabolizing enzymes 52 pathogenic mutations 52 transcriptional repressor 52 gonadotrophin releasing hormone 52 emotional lability 52 ADPKD 52 phenotypic expression 52 genetic variant 52 uPAR 52 chromosome deletion 52 cagA 52 autoantibody 52 PGC 1α 52 HbF levels 52 cardioprotective effects 52 CRF1 receptor 52 loci 52 TMEM#B 52 BRCA1 mutation carriers 52 Dysregulation 52 chromosomal aberrations 52 apolipoprotein B 52 gene variants 52 epigenetic modification 52 2 diabetes T2D 52 diabetes mellitus DM 52 Polymorphism 52 phospholipase A2 52 prairie vole 52 type2 diabetes 52 hepatoma 52 HPA axis 52 TEL AML1 52 immunoreactivity 52 LDLR 52 human leukocyte antigen 52 TYMS 52 TrkB 52 APOE e4 allele 52 IFN γ 52 ADAMTS# 52 lateralized 52 MnSOD 52 neurocognitive impairment 52 PCNSL 52 cysteines 52 replicase 52 tryptase 52 LPS induced 52 syndromal 52 nucleotide sequence 52 C#Y mutation 52 c fos 52 urocortin 52 C. pneumoniae 52 cardioembolic stroke 52 thiopurine 52 endogenous opioid 52 sensory gating 52 mice lacking 52 BRAF V#E mutation 52 atopic 52 genotyped 52 LRAT 52 promoter methylation 52 neuroblastoma tumors 52 fasting glucose levels 52 heritable trait 52 chlamydial infection 52 disinhibition 52 extramedullary 52 p# activation 52 Foxp3 52 logistic regression model 52 ApoE4 gene 52 biochemical imbalance 52 orthologous 52 dinucleotide 52 PDGFR alpha 52 TIMP 1 52 logistic regression analysis 52 inverse agonist 52 astrocytic 52 epigenetic changes 52 protein isoforms 52 BRCA2 mutation 52 metabolic disturbances 52 epistasis 52 isoenzyme 52 mitochondrial disorders 52 DRB1 * 52 PTP1B 52 corticosterone levels 52 lincRNA 52 gene rearrangements 52 tumor suppressor protein 52 CDK4 52 spontaneous mutations 52 Genotypes 52 hypochondriasis 52 tumor histology 52 PPARg 52 T#I [002] 52 5 HT1A 52 covariate 52 pDCs 52 K ras mutation 52 amino terminal 52 pathophysiological effects 52 anterior cingulate 52 γ secretase 52 C#T [002] 52 ovarian hormones 52 Bcl XL 52 protein encoded 52 Leukotriene 52 haptoglobin 52 Nf1 52 serum BDNF 52 FADS2 52 DSM IV diagnosis 52 fasting plasma 52 neuronal dysfunction 52 X Chromosome 52 isoprostane 52 folate deficiency 52 primary aldosteronism 52 TEAEs 52 rCBF 52 pulvinar 52 serum lipid 52 PDGFR 52 overactivity 52 MyoD 52 APOL1 52 somatoform disorders 52 activin 52 Cytogenetic 52 epigenetically 52 5alpha reductase 52 colorectal neoplasia 52 matrix metalloproteinase 52 #β estradiol 52 parkin gene 52 PUFA intake 52 B7 H4 52 Prehypertension 52 phenotypic variation 52 TSC1 52 monoclonal gammopathy 52 ERCC1 52 single nucleotide polymorphism 52 β actin 52 FSHR 52 fetuin 52 antibody titer 52 CYP#D# genotype 52 recessive inheritance 51 demethylase 51 ABL kinase 51 Mendelian disorders 51 ANCOVA 51 autism susceptibility genes 51 SMAD4 51 Prox1 51 idiopathic PAH 51 bivariate 51 SCN9A 51 FOXM1 51 extrapyramidal symptoms 51 Wwox 51 prothrombotic 51 multivariate adjustment 51 NPC1 51 acetylcholine receptor 51 parkinsonism 51 K ras 51 #ß 51 Heritability 51 ALK gene 51 mutation 51 neuro endocrine 51 maternally inherited 51 transgene expression 51 affective disorders 51 BRIP1 51 hereditary predisposition 51 von Hippel Lindau 51 juvenile idiopathic arthritis JIA 51 Overexpression 51 S#A# [002] 51 Multivariate analysis 51 muscarinic receptor 51 DNMT1 51 urethritis 51 elevated triglycerides 51 kidney allograft 51 receptor tyrosine kinase 51 interleukin IL 51 inactive X chromosome 51 esterase 51 Excessive daytime sleepiness 51 beta carotene supplementation 51 Amino acid 51 plasminogen activator inhibitor 51 genetic modifiers 51 fraternal twin pairs 51 #S rRNA 51 premorbid 51 HepG2 cells 51 premenstrual syndrome PMS 51 vermis 51 GRK5 51 haplotype 51 p tau 51 alternatively spliced 51 glutathione S transferase 51 G6PD deficiency 51 CCL#L# 51 deacetylation 51 MTHFR gene 51 APOE epsilon 4 51 Upregulation 51 Kufs disease 51 plasma folate 51 receptor kinase 51 histone methylation 51 Chronic pancreatitis 51 recessive mutations 51 X chromosome inactivation 51 homologue 51 presymptomatic 51 monocyte chemoattractant protein 51 MetS 51 #HT#A receptor 51 thyrotropin levels 51 haematopoietic 51 Genetic predisposition 51 mitogen activated protein kinase 51 neurodevelopmental outcome 51 chromosomal alterations 51 TMPRSS2 ERG fusion 51 methylenetetrahydrofolate reductase 51 hypomethylation 51 ACER paper 51 serum leptin 51 NRF2 gene 51 GPR# [001] 51 CIN2 + 51 masculinization 51 huntingtin gene 51 HER2 expression 51 typical antipsychotics 51 JAK STAT 51 NKX2 51 parietal cortices 51 human leukocyte antigens 51 VIPR2 51 neuronal plasticity 51 HMGA2 gene 51 Selective serotonin reuptake inhibitors 51 avoidant personality disorder 51 transcriptional silencing 51 periprocedural MI 51 GlcNAc 51 airway responsiveness 51 Chlamydia pneumoniae 51 methylation patterns 51 serine protease 51 major histocompatibility complex 51 poor metabolizers 51 osteoprotegerin 51 MAPK pathway 51 D2 receptors 51 C1q 51 syngeneic 51 confidence interval #.#-#.# 51 persistent pulmonary hypertension 51 Phenotypic 51 HOMA IR 51 hyper IgE syndrome 51 arrhythmogenic 51 vasopressin receptors 51 transferrin saturation 51 negative affectivity 51 testicular germ cell 51 microglial 51 HLA DR2 51 pre eclamptic 51 OCA2 51 beta endorphin 51 chemokine receptor 51 selective antagonists 51 constitutively 51 BRCA mutations 51 breast cancer subtypes 51 multivariate logistic regression 51 PDE#A 51 JAK mutations 51 outbred 51 BRCA2 gene 51 Brugada syndrome 51 Mendelian 51 hydroxylase 51 baseline HbA1c 51 metabolizer 51 MHC molecules 51 del 5q 51 PcG proteins 51 gastric carcinogenesis 51 cognitive affective 51 SAPAP3 51 ataxin 51 transcriptional profiles 51 alpha2 51 variant rs# 51 constitutively active 51 ORFs 51 BRCA2 carriers 51 IL 1ß 51 nonsynonymous 51 klotho gene 51 globin genes 51 lactose malabsorption 51 folate concentrations 51 Sjögren syndrome 51 DLPFC 51 chromosome #q 51 leptin deficiency 51 GPC5 51 brain lesions 51 cerebellar 51 nAChR 51 NRTI resistance 51 muscarinic receptors 51 subclinical hypothyroidism 51 PIK3CA 51 extraverts 51 fasting insulin 51 Prolactin 51 TP# gene 51 multigenic 51 involuntary tics 51 HbF 51 familial pancreatic cancer 51 unipolar depression 51 kinase gene 51 agonist antagonist 51 mutant alleles 51 inhibin 51 CAG repeats 51 subthreshold 51 chromosomal regions 51 prolactin levels 51 cytopathic 51 Cytotoxic T 51 autosomal dominant inheritance 51 karyotype 51 EoE 51 salivary amylase 51 inherited genetic mutations 51 aneuploidies 51 lipoprotein cholesterol 51 TRAF1 51 insulin resistance syndrome 51 E selectin 51 amnestic 51 D. melanogaster 51 pathophysiological 51 Karayiorgou 51 lysine residues 51 CFH gene 51 nonprogressive 51 neurohormonal 51 serum HBV DNA 51 cryptogenic 51 moderately heritable 51 β = 51 VEGF receptor 51 triacylglycerol concentrations 51 proto oncogene 51 FGFs 51 cystatin C 50 CNVs 50 pheochromocytoma 50 TAp# 50 HBx 50 nonischemic 50 chromosomal disorders 50 elevated CRP 50 glutamyl 50 Cyclin E 50 CIN3 50 c Myb 50 transcriptional activation 50 subclinical 50 transcriptionally 50 prognostic markers 50 deletion 5q 50 multivariate Cox 50 poorer prognosis 50 aminotransferase levels 50 activating mutations 50 dizygotic twins 50 HDL cholesterol triglycerides 50 cytochrome b 50 variant 50 FMR1 50 neurodevelopmental disorder 50 somatic mutation 50 autosomal dominant 50 testicular tumors 50 LIS1 50 CYP# [002] 50 Brodmann Area 50 myeloperoxidase 50 genetic predisposition 50 mutated gene 50 femoral neck BMD 50 antibody titers 50 GLI1 50 Cognitive impairment 50 BRCA1 gene 50 clade B 50 serine 50 OGG1 50 soluble fms 50 hematopoietic cancers 50 sCJD 50 Apobec3 50 mineralocorticoid 50 polyadenylation 50 adult neurogenesis