Related by context. All words. (Click for frequent words.) 73 DRD4 68 gene DRD4 67 dopamine receptor gene 67 MAOA gene 65 DRD2 gene 63 serotonin transporter gene 62 CNTNAP2 62 DQB1 * 62 behavioral disinhibition 61 GABRA2 61 5 HTT gene 61 COMT gene 61 androgen receptor gene 61 MAOA 60 5 HTTLPR 60 OPRM1 gene 60 BDNF gene 60 G allele 59 DRD2 59 dopamine transporter gene 59 dopamine D4 receptor 59 APOE gene 59 APOE4 59 MC1R 59 allele 58 prairie vole 58 nondemented 58 homozygosity 58 assortative mating 58 CYP#A# gene 57 APOE ε4 57 FTO gene 57 APOE allele 57 PTPN# 57 CYP#E# gene 57 KIBRA 57 CagA 56 MTHFR 56 C#Y 56 missense mutations 56 BARD1 56 heterozygotes 56 ApoE gene 56 gene APOE 56 SLC#A# [002] 56 MYH9 gene 56 repeat allele 56 rs# [001] 56 genes predisposing 56 TCF#L# gene 56 vasopressin receptor 56 activity MAOA 56 CYP#C# gene 56 receptor gene 56 hypoactive 55 assortative 55 UGT#A# * 55 narcolepsy cataplexy 55 mutant allele 55 ApoE4 55 ADH1B * 55 MHC genes 55 alleles 55 MHC molecules 55 NPY gene 55 APOE4 gene 55 APOC3 55 FTO variant 55 dopamine receptors 55 autistic traits 55 proband 54 extraversion 54 alpha synuclein gene 54 corticosterone levels 54 rs# [002] 54 methylation patterns 54 euthymic patients 54 allele frequencies 54 alexithymia 54 dyads 54 stereotypy 54 #q#.# deletion syndrome 54 MC4R gene 54 ALDH2 54 COMT 54 ABCB1 54 genotype 54 functional polymorphism 54 Neuregulin 1 54 externalizing disorders 54 PTEN mutations 54 Neuroticism 54 nicotinic receptor 54 catechol O methyltransferase 54 KIF6 gene 54 sporadic ALS 54 MECP2 gene 54 valine 53 mosaicism 53 apoE4 53 bulimia nervosa 53 CYP#B# 53 IgA deficiency 53 habitual snoring 53 aldehyde dehydrogenase 53 neuroimaging studies 53 psychopathy 53 genetic polymorphism 53 neuroD2 53 CHRNA5 53 PON1 gene 53 circadian clock genes 53 dopamine receptor 53 AVPR1A 53 SORL1 53 ENPP1 53 unipolar depression 53 APOE 53 heterozygous 53 Personality traits 53 GSTM1 53 LRRK2 gene 53 Alu elements 53 Hashimoto thyroiditis 53 inbred strains 53 familial clustering 53 gene locus 53 rs# [003] 53 overactivity 53 susceptibility gene 53 penile vaginal intercourse 53 antisocial traits 53 MSH2 53 TGFBR1 * 6A 53 gene variant 53 #q# deletion 53 APOE genotype 53 polymorphism 53 CHRNA5 gene 53 disinhibition 53 CHD7 53 telomere lengths 53 A1 allele 53 androgen deficiency 53 FGFR2 53 STAT4 53 vasopressin 52 GABRA2 gene 52 mu opioid 52 HLA DRB1 * 52 WNK1 52 deleterious mutations 52 homozygotes 52 underexpressed 52 HFE gene 52 gonadotropins 52 gut microbes 52 CDKN2A 52 Genetic variation 52 cyclin E 52 MC1R gene 52 shorter telomere length 52 major histocompatibility complex 52 APOE e4 52 affective disorders 52 microcephalin 52 genes encoding 52 germline mutations 52 gestational diabetes mellitus 52 Fragile X gene 52 Suicidal ideation 52 rs# [004] 52 neutralizing antibody responses 52 SRY gene 52 prepubertal 52 FXTAS 52 euthymic 52 ApoE 52 CYP#E# 52 #q#.# [001] 52 GABA receptor 52 thyrotropin 52 GSTT1 52 homozygous 52 ESR1 52 ε4 52 TCF#L# 52 chromosomal anomalies 52 TNFAIP3 52 CAG repeats 52 antisocial personality 52 parkinsonism 52 CYP#D# gene 52 non affective psychosis 52 amino acid valine 52 HPA axis 52 familial pancreatic cancer 52 hypomania 52 D. melanogaster 52 CETP gene 52 APOE epsilon 4 52 alpha amylase 52 heritable 52 impulsivity 52 apolipoprotein E gene 52 AUDs 52 PON1 52 inhibin B 52 vasopressin receptors 52 SNP rs# [002] 52 miRNA expression 52 recessive trait 52 cytopathic 51 MnSOD 51 outbred 51 nondepressed 51 H#K#me# 51 allelic variation 51 apolipoprotein E 51 externalizing behaviors 51 subclinical hyperthyroidism 51 Apolipoprotein E 51 pseudogenes 51 dopamine signaling 51 C#BL/#J 51 SE alleles 51 chromosomal rearrangement 51 Hsp# [001] 51 onset diabetes mellitus 51 plasma folate 51 HLA DRB1 51 epigenetic modification 51 MLH1 51 antisocial behaviors 51 alternatively spliced 51 hyperinsulinemia 51 promoter polymorphism 51 SCN1A 51 serotonin transporter 51 HGPS 51 atypical neuroleptics 51 DARPP 51 fruitflies 51 Klinefelter syndrome 51 autosomal recessive 51 MGUS 51 CALHM1 51 HLA B# 51 SNP rs# [001] 51 transgene expression 51 genetic variant 51 mice lacking 51 #S rRNA 51 aY chromosome 51 hippocampal neurons 51 Leydig cell 51 telomere length 51 VHL gene 51 GSTM1 gene 51 cognitively normal 51 mtDNA mutations 51 neurocognitive impairment 51 DLPFC 51 LRP5 51 probands 51 subclinical hypothyroidism 51 psychopathology 51 hereditary hemochromatosis 51 anterior cingulate 51 imprinted genes 51 overt hypothyroidism 51 NNRTI resistance 51 HMGA2 51 glutamate signaling 51 orbital frontal cortex 51 DAT1 51 maternally inherited 51 lymphocyte activation 51 fewer dopamine receptors 51 APOE4 variant 51 prairie voles 51 amygdalas 51 glucocorticoid receptors 51 FOXP2 gene 51 VNTR 51 seronegative 51 mRNA transcripts 51 prosocial 51 p# mutation 51 circadian genes 51 CCR7 51 mitochondrial mutations 51 D2 receptors 51 folate deficiency 51 apoC III 51 chlamydial infection 51 atopic 51 2 diabetes T2D 51 male prairie voles 51 CCR5 delta# 51 orthologous genes 51 ApoE4 gene 51 estrogenic effects 51 X inactivation 51 polycystic ovary syndrome PCOS 51 SHANK3 51 monozygotic twins 51 CETP VV 51 genotypic 51 muscle dysmorphia 51 TT genotype 51 indels 51 urethritis 51 gene variation 51 epigenetic changes 50 selfing 50 NF1 gene 50 premenstrual syndrome PMS 50 follicular phase 50 schizotypal traits 50 FMR1 gene 50 antiphospholipid antibodies 50 excitatory synapses 50 monozygotic 50 recessive mutation 50 untreated hypothyroidism 50 LC#m# vaccine 50 familial aggregation 50 Th2 50 evolutionarily conserved 50 variant alleles 50 dopamine transporter 50 OPRM1 50 proinflammatory cytokine 50 prosocial behavior 50 GRK5 50 estrone 50 PALB2 50 heritable traits 50 salivary amylase 50 fast metabolizers 50 nonpregnant women 50 ADH1B 50 C. neoformans 50 neuropathologic 50 eating disordered 50 psychopathic traits 50 microdeletion 50 dysthymia 50 MetS 50 HLA gene 50 dysregulated 50 serotonin receptor 50 lipid abnormalities 50 BDNF protein 50 pyrimidines 50 LPA gene 50 T2D 50 #p# [003] 50 genetic loci 50 comorbid disorders 50 inherited mutations 50 ABCB1 gene 50 bivariate analyzes 50 cytochrome b 50 beta endorphin 50 inverse agonist 50 metabolizing enzyme 50 prenatal testosterone 50 Kaplan Meier curve 50 HepG2 cells 50 KLF4 50 Foxp3 50 chromosomal alterations 50 monozygotic twin 50 coprolalia 50 covariate 50 GBA mutations 50 T. vaginalis 50 depressive symptomatology 50 synuclein 50 Fig. 3a 50 anti inflammatory cytokine 50 orthologs 50 differentially expressed genes 50 neurodevelopmental disorder 50 HMGA1 50 neuroticism 50 manic depressive illness 50 chromosomal regions 50 S#A# [002] 50 mRNA expression 50 phenotype 50 germline cells 50 amygdalae 50 HNPCC 50 subcellular localization 50 overactivated 50 ovarian hormones 50 hippocampal 50 downregulated 50 heritable trait 50 asexuals 50 Froguel 50 HLA DR 50 chromosome #q#.# [001] 50 constitutively 50 chromosome #q# [001] 50 hormone vasopressin 50 activin 50 tyrosine phosphorylation 50 ORMDL3 50 fru 50 pDCs 50 GAB2 50 atopy 50 Wernicke Korsakoff syndrome 50 basal cell nevus syndrome 50 KCNH2 50 tau gene 50 adenylate cyclase 50 gene variants 50 extraverts 50 adult neurogenesis 50 MDR1 50 HLA gene variant 50 oxytocin receptor 50 cybrid 50 microglial 50 deacetylation 50 Th1 50 hormone therapy estrogen 50 recessive inheritance 50 folate metabolism 49 abstainers 49 miR #a [001] 49 beta subunit 49 normotensive 49 gene polymorphism 49 poorer prognosis 49 equol 49 autoimmune thyroiditis 49 acamprosate 49 microchimerism 49 dimorphism 49 abstainer 49 SERT gene 49 CFH gene 49 subclinical 49 pathogenic mutations 49 psychobiological 49 missense mutation 49 klotho gene 49 ADRB2 49 casual flings 49 intronic 49 BRCA1 mutation 49 familial ALS 49 metabolizing enzymes 49 constitutively expressed 49 hyperactivity inattention 49 RCAN1 49 masculinization 49 nonpsychotic 49 dizygotic 49 polymorphisms 49 behavioral abnormalities 49 PTEN gene 49 physiological arousal 49 antisocial personality traits 49 Li Fraumeni syndrome 49 MAOA genotype 49 nonexposed 49 Toxoplasma 49 NRF2 gene 49 K ras mutations 49 SLC#A# [001] 49 JAK2 enzyme 49 dysregulation 49 virulence genes 49 p#INK#a 49 HLA molecules 49 menarche 49 metabolic abnormalities 49 dysthymic 49 de novo mutations 49 ovulatory cycles 49 sexually dimorphic 49 HLA DRB1 SE 49 heterozygosity 49 CYP#C# [002] 49 syndromal 49 polyploid 49 sex hormone estrogen 49 amyloid ß 49 sex hormones estrogen 49 miRNA genes 49 callous unemotional traits 49 temporoparietal junction 49 S. cerevisiae 49 untranslated regions 49 hypothalamic pituitary 49 NAT2 49 BRCA1 mutations 49 affective psychosis 49 anhedonia 49 LKB1 49 CCL#L# 49 Adiponectin 49 Binge eating 49 Chlamydia pneumoniae 49 C#BL 6 mice 49 monogenic 49 TMEM#B 49 pre eclamptic 49 agonism 49 binge eating 49 apolipoprotein E4 49 p# mutations 49 homozygote 49 hippocampal function 49 BDNF 49 thyrotropin levels 49 FADS2 49 chromosome #q# [002] 49 spontaneous mutations 49 chromosome #p# [001] 49 lymphocytic 49 neuroligins 49 highly heritable 49 CD#c 49 COL#A# 49 transgenic mouse models 49 gene polymorphisms 49 homosexually 49 PPARγ 49 hepatoma 49 HIV uninfected 49 frameshift mutation 49 esterase 49 HbF levels 49 amino acid substitutions 49 MTHFR gene 49 5 HT1A receptor 49 IGFBP 49 eotaxin 49 nonobese 49 HIV seronegative 49 virginity pledgers 49 melanogaster 49 frontotemporal dementia 49 CYP# [002] 49 SRBD 49 elevated CRP 49 heritable variation 49 Bacteroides 49 loci 49 histone H4 49 leptin deficient mice 49 Wistar rats 49 epigenetically 49 FGFs 49 lincRNA 49 DSM IV Axis 49 amyloid plaque formation 49 urinary bowel 49 allelic variants 49 UGT#B# 49 chromosomally 49 lactis 49 GSTP1 49 C1q 49 Monoamine oxidase 49 CYP#C# * 49 airway responsiveness 49 apoE 49 valproic acid 49 estrogen metabolism 49 metabolic dysfunction 49 #q# [001] 49 autosomal 49 cyclophilin D 49 hormonal surges 49 autosomal dominant disorder 49 genetically inherited 49 IL#R 49 BMPR2 49 Wwox 49 urocortin 49 rhesus 49 DRB1 * 49 mitochondrial metabolism 49 gonadal 49 DLX5 49 microRNA expression 49 cognitive affective 49 amygdala activation 48 extraverted 48 CDH1 48 neuroglobin 48 adrenal cortex 48 A. thaliana 48 TOMM# 48 glutamatergic 48 psychostimulant 48 superinfection 48 glucocorticoids 48 Treg cell 48 ADPKD 48 homodimers 48 suppressor gene 48 orexin receptors 48 epigenetic reprogramming 48 psychiatric comorbidity 48 BCL#A 48 D2 receptor 48 juvenile idiopathic arthritis JIA 48 T1DM 48 uPAR 48 serum estradiol 48 vivax 48 herpesviruses 48 monoamines 48 LIS1 48 autosomal dominant 48 SLC#A# gene [002] 48 suicide attempters 48 neurotransmitters serotonin 48 neuroendocrine 48 unprotected receptive anal 48 comorbid anxiety 48 premutation 48 colorectal neoplasia 48 phenotypes 48 prodynorphin 48 sexual dimorphism 48 impulsive behaviors 48 phenotypic variation 48 CC genotype 48 c KIT 48 genetically predetermined 48 histone acetylation 48 Imprinted genes 48 cdk5 48 Lactobacillus 48 MYH9 48 #ß 48 aneuploid 48 homologs 48 pathophysiological effects 48 NF1 48 hypermethylation 48 hypochondriasis 48 predisposing factor 48 K#N 48 TrkB 48 predisposing 48 M. pneumoniae 48 allostatic load 48 germline mutation 48 vermis 48 potent inhibition 48 iron deficient 48 CDK4 48 shorter telomeres 48 atypical hyperplasia 48 DNMT1 48 anabolic androgenic steroid 48 sequence homology 48 cytokine IL 48 polycystic ovarian syndrome PCOS 48 depressive symptoms 48 genotyped 48 aneuploidy 48 EBV infection 48 genotypes 48 Personality disorders 48 prostate cancer CaP 48 SHBG levels 48 NAc 48 QTLs 48 cholinergic 48 Bed wetting 48 PPARg 48 developmental trajectories 48 Nf1 48 intestinal microflora 48 ApoB 48 polyadenylation 48 perilipin 48 protein isoforms 48 XMRV infection 48 paternally inherited 48 sCJD 48 etiologic 48 endophenotypes 48 SOD2 gene 48 genetic polymorphisms 48 Sexual arousal 48 kDa protein 48 Agreeableness 48 gamma aminobutyric acid 48 5 HT1A 48 neuropeptide 48 PrPSc 48 K#R [002] 48 ACE2 gene 48 neuronal dysfunction 48 locomotor activity 48 inherited maternally 48 muscarinic 48 arterial thickening 48 cirrhotic 48 monophyletic 48 cortisol secretion 48 CYP#D# 48 HLA genes 48 Aldosterone 48 proto oncogene 48 suppressor cells 48 psychosocial functioning 48 immunocompetent 48 elevated triglyceride levels 48 underlying pathophysiology 48 FKBP# 48 endogenous retrovirus 48 meadow vole 48 KCNQ1 48 chromosomal aberrations 48 AMACR 48 Klotho gene 48 FGF# 48 HMPV 48 rheumatoid factor 48 genetic variants associated 48 NAFLD 48 neuroleptic 48 polygenic 48 piRNAs 48 endogenous estrogen 48 autosomes 48 diploid 48 HBx 48 ribosomal protein 48 MLL gene 48 androstenone 48 CNTNAP2 gene 48 slow metabolizers 48 elevated serum creatinine 48 extroversion 48 genital arousal 48 endoxifen 48 amyloid peptide 48 psychopathic personality 48 epigenetic silencing 48 univariate analyzes 48 palmitoylation 48 glucocorticoid 48 prodromal phase 48 unprotected anal intercourse 48 hyperactive impulsive 48 BRAF V#E 48 V#F mutation 48 hypogonadotropic hypogonadism 48 elevated cortisol 48 penetrance 48 C. trachomatis 48 ZNF# 48 orthologous 48 SORL1 gene 48 attention-deficit/hyperactivity disorder ADHD 48 NPY expression 48 RIP1 48 neurocognitive dysfunction 48 Apobec3 48 haplotypes 48 leptin deficient 48 subtype 48 S. sanguinis 48 psychotic disorders 48 genetic determinants 48 impaired glucose metabolism 48 parkinsonian 48 luteal phase 48 use disorders AUDs 48 Estrogen receptor 48 TNFalpha 48 viremic 48 isoform 48 Kozyrskyj 48 exfoliation glaucoma 47 clade B 47 neurological abnormalities 47 placental function 47 Rh factor 47 epigenetic alterations 47 V Leiden 47 parous women 47 fig. S1 47 cortical thinning 47 PrPC 47 diabetes mellitus DM 47 isoenzyme 47 GH deficiency 47 Sacktor 47 pre pubertal 47 borderline personality disorders 47 serotonin receptors 47 dopaminergic 47 BRCA2 gene 47 allelic 47 KLF# 47 huntingtin gene 47 chlorpromazine 47 excitatory neurotransmitter glutamate 47 transcriptional repressor 47 MMP# 47 ataxias 47 Bacterial vaginosis 47 Immunohistochemical analysis 47 internalizing disorders 47 TMPRSS2 ERG fusion 47 inattention hyperactivity 47 Individual Differences 47 BRCA gene mutation 47 elevated triglycerides 47 monoamine 47 polyploidy 47 promoter methylation 47 flavopiridol 47 Mustanski 47 Nicotine dependence 47 GABAergic 47 phenotypic expression 47 ouabain 47 BRIP1 47 neurofibrillary 47 NRTI resistance 47 serum lipid levels 47 nongenetic 47 hydroxylase 47 neurobiological 47 TP# mutations 47 inhibitory receptor 47 unmutated 47 paralogs 47 cholinergic tone 47 hormone secretion 47 irregular menstrual cycles 47 glucocorticoid receptor 47 pea aphid 47 perimenopausal women 47 non pledgers 47 γ secretase 47 mGluR 47 TLR4 47 TEL AML1 47 2D 4D ratio 47 GH secretion 47 histone modification 47 schizophrenia schizoaffective disorder 47 IL#B gene 47 negative affectivity 47 d amphetamine 47 polyglutamine diseases 47 FMR1 47 differential gene expression 47 metabolomic profiles 47 SCA5 47 genetic predisposition 47 ALDH 47 genetic relatedness 47 alcohol dehydrogenase 47 GNAQ 47 HLA B 47 varicocele 47 cDNAs 47 logistic regression model 47 cryptorchidism 47 adiponectin concentrations 47 breast cancer genes BRCA1 47 genes CYP#C# 47 neuroanatomical 47 prenatal exposures 47 masculinised 47 hypocretin 47 oestradiol 47 susceptibility genes 47 Antisocial Personality Disorder 47 olfactory receptor 47 WAGR syndrome 47 phenotypic characteristics 47 luteolin 47 haplotype 47 dysbindin gene 47 dietary intakes 47 HbF 47 abnormal lipid 47 intergenic 47 serum BDNF 47 IGF1 47 alpha2 47 IFN γ 47 asexuality 47 apolipoprotein 47 endocannabinoid signaling 47 IFN alpha 47 nongenetic factors 47 epigenetic mechanisms 47 transferrin saturation 47 asexual reproduction 47 IKZF1 47 NKT cell 47 #q#.# [002] 47 radial glia 47 ribosomal genes 47 autosomal dominant inheritance 47 Excessive daytime sleepiness 47 human leukocyte antigens 47 mitochondrial DNA mtDNA 47 SHANK3 gene 47 neural substrates 47 bronchopulmonary dysplasia 47 coinfection 47 EGFR gene 47 testicular germ cell 47 gastric carcinogenesis 47 Clusterin 47 phosphatases 47 human leukocyte antigen 47 fMRI scans 47 EoE 47 tau mutation 47 defensin 47 personality traits 47 vasopressin receptor gene 47 modifier genes 47 SGK1 47 neutralizing antibody 47 cell adhesion molecules 47 tubby husbands 47 lateralisation 47 urinary concentrations 47 mIU L 47 coexpression 47 CCL5 47 mitochondrial dysfunction 47 prothrombotic 47 neuroblastoma tumors 47 endogenous opioid 47 regulates gene expression 47 Pathological gambling 47 TGF ß 47 osteoblast 47 Parkinsonian 47 premorbid 47 postmenopausal breast cancer 47 masculinizing 47 abnormal proteins 47 dizygotic twins 47 #HT#A receptor 47 unmethylated 47 DRB1 47 abstinent alcoholics 47 cholecystokinin CCK 47 serotonin synthesis 47 mammary tumors 47 KRAS gene 47 androgen excess 47 spontaneous preterm birth 47 androgen depletion 47 causally linked 47 mood disorders 47 serum HBV DNA 47 herpes viruses 47 serum IGF 47 variant rs# 47 apo E 47 mutant huntingtin protein 47 myo inositol 47 parous 47 prodromal 47 constitutively active 47 homophily 47 aromatase 47 karyotype 47 genetic variation 47 neurodevelopmental disorders 47 mammary gland tumors 47 PBMCs 47 collected saliva samples 47 coronary calcification 47 SIRT1 gene 47 parasitized 47 PTP1B 47 neurotypical 47 Schaffir 47 disease NAFLD 47 mammalian brains