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(Click for frequent words.) 64 familial aggregation 62 highly heritable 62 penetrance 62 heritable 61 monozygotic twins 61 phenotypic variation 59 Heritability 59 polygenic 58 endophenotypes 58 alexithymia 57 chromosomal alterations 57 genetic variants associated 57 familial clustering 57 Genetic predisposition 57 genetic variants 57 autistic traits 57 body fatness 57 #q# deletion 57 dizygotic twins 57 elevated CRP 57 CNVs 56 gene variants 56 genetic predisposition 56 etiology 56 subclinical 56 susceptibility genes 56 APOE genotype 56 #q#.# deletion syndrome 56 genetic susceptibility 56 assortative mating 55 sporadic ALS 55 chronicity 55 subclinical atherosclerosis 55 heterozygotes 55 genetic polymorphisms 55 MYH9 55 monozygotic 55 QTLs 55 genetic variation 55 moderately heritable 55 linkage disequilibrium 55 APOE e4 54 #q# [001] 54 CNTNAP2 54 genomewide association studies 54 etiologic 54 allele frequencies 54 phenotype 54 autosomal 54 missense mutations 54 allelic 54 genomewide 54 genetic determinants 54 Klinefelter syndrome 54 GSTM1 54 genetic loci 54 #p#.# [001] 54 aneuploidy 54 multivariable analysis 53 inbred strains 53 homozygosity 53 haplotype 53 recessive inheritance 53 somatoform disorders 53 folate intake 53 bivariate 53 probands 53 underlying pathophysiology 53 allelic variation 53 neurodevelopmental disorder 53 phenotypes 53 de novo mutations 53 colorectal neoplasia 53 ontogenetic 53 MetS 53 heterozygosity 53 comorbidity 53 neuroanatomical 53 chromosomal anomalies 53 phenotypic variability 53 loci 53 PTEN mutations 53 microdeletion 53 behavioral disinhibition 53 nondemented 53 GBA mutations 52 susceptibility loci 52 spontaneous mutations 52 prenatal testosterone 52 neurobiological 52 internalizing disorders 52 mosaicism 52 genetic relatedness 52 nongenetic 52 APOC3 52 prepubertal 52 germline mutations 52 cystatin C 52 Mendelian 52 adiposity 52 chromosomal deletions 52 euthymic patients 52 residual confounding 52 karyotype 52 alleles 52 genetic locus 52 epistasis 52 allergic sensitization 52 nucleotide sequence 52 evolvability 52 HMGA2 52 thyrotropin levels 52 C#Y 52 pathophysiological 52 logistic regression model 52 multifactorial 52 mtDNA mutations 52 APOE gene 52 subclinical hyperthyroidism 52 Neuroticism 52 LRRK2 gene 52 genetic polymorphism 52 sexual dimorphism 52 sequence homology 52 autosomal dominant disorder 52 hereditary hemochromatosis 52 birthweight 52 cognitive affective 51 susceptibility locus 51 callous unemotional traits 51 rs# [001] 51 CHD7 51 orthologs 51 developmental abnormalities 51 dietary intakes 51 monogenic 51 susceptibility gene 51 trait locus 51 syndromal 51 beta1 integrin 51 FeNO 51 etiological 51 proband 51 orthologous genes 51 IgA deficiency 51 modifier genes 51 dopamine transporter gene 51 mutant allele 51 TRAF1 C5 51 predisposing factor 51 quantitative trait loci 51 dysbindin 51 clinicopathological 51 genetic markers 51 schizophreniform disorder 51 rs# [002] 51 logistic regression analysis 51 nonfasting triglyceride levels 51 gene polymorphisms 51 monoclonal gammopathy 51 correlational 51 folate deficiency 51 Multivariate analysis 51 genetic variant 51 chromosome abnormality 51 genotype 51 TCF#L# gene 51 chromosomal regions 51 cryptorchidism 51 visceral adiposity 51 psychopathology 51 autism susceptibility genes 51 2D 4D ratio 51 LRRK2 mutations 51 telomere lengths 51 comorbid disorders 51 #q#.# [002] 51 relatedness 51 genomic deletions 51 causative genes 50 chromosomal rearrangement 50 #mg/dL [001] 50 subclinical hypothyroidism 50 paternal discrepancy 50 HLA DRB1 50 fraternal twin pairs 50 5 HTTLPR 50 aetiology 50 #p#.# [002] 50 SRBD 50 genetic syndromes 50 polymorphism 50 comorbid anxiety 50 heritable traits 50 #q#.# [001] 50 monozygotic twin 50 PTPN# 50 MDRD 50 periprocedural MI 50 MAOA 50 univariate analyzes 50 FGFR2 gene 50 paternal lineages 50 DRD4 50 hippocampal volume 50 inherited mutations 50 Genetic variants 50 modifiable risk 50 subsyndromal 50 klotho 50 chromosomal aberrations 50 familial pancreatic cancer 50 neuropsychiatric disorder 50 biochemical abnormalities 50 multiple logistic regression 50 psychiatric comorbidity 50 airway hyperresponsiveness 50 genotypes 50 apoE 50 conditional logistic regression 50 androgen deficiency 50 central adiposity 50 Socioeconomic status 50 SNP rs# [002] 50 elevated triglycerides 50 Reynolds Risk Score 50 dopamine receptor gene 50 MYH9 gene 50 MTHFR 50 Multivariate analyzes 50 Darwinius 50 Cognitive impairment 50 mitochondrial dysfunction 50 maternally inherited 50 DRD2 50 causative gene 50 chromosomal anomaly 50 paralogs 50 #p# [001] 50 NAFLD 50 schizotypal traits 50 methylation patterns 50 orthologous 50 Apolipoprotein E 50 fasting glucose levels 50 dietary calcium intake 50 socioeconomic status SES 50 TGFBR1 * 6A 50 genetic variability 50 chromosome #q# [001] 50 SCA5 50 phthalate exposure 50 indels 50 genetic variations 50 multigenic 50 PALB2 50 susceptibility 50 STAT4 50 inherited predisposition 50 TOP2A 50 statistically significant correlation 50 UGT#A# * 50 Bonferroni correction 50 SRY gene 50 shorter telomere length 50 OPRM1 gene 50 MECP2 gene 50 heterogeneity 50 premorbid 50 extraversion 49 longitudinal studies 49 PICALM 49 NPY gene 49 insulin resistance 49 rs# [003] 49 sCJD 49 multivariate analyzes 49 genetic underpinnings 49 rs# [004] 49 RBP4 49 G#S mutation 49 unmeasured confounding 49 SLC#A# [002] 49 psychosocial variables 49 autonomic dysfunction 49 phenotypic expression 49 ELBW infants 49 apolipoprotein E gene 49 varicoceles 49 intelligence quotient IQ 49 neuropsychological deficits 49 predictive validity 49 causal pathways 49 impaired fasting glucose 49 dietary fiber intake 49 DRD2 gene 49 narcolepsy cataplexy 49 Y chromosomal 49 MDRD equation 49 serum biomarkers 49 NF1 49 antidepressant efficacy 49 subfertility 49 Meckel Gruber 49 tHcy 49 genomic variation 49 MLH1 49 meta analytic 49 DQB1 * 49 logistic regression analyzes 49 autosomal dominant inheritance 49 repeat allele 49 enterotypes 49 chromosome #q# [002] 49 BRCA1 mutation carriers 49 serum cholesterol 49 chromosome #q 49 Genetic variation 49 haplotypes 49 LPA gene 49 adiponectin levels 49 genotypic 49 chromosomal disorders 49 gonadal hormones 49 KLF4 49 mitochondrial disorders 49 MAOA gene 49 DNA methylation patterns 49 metabolic abnormalities 49 esophageal squamous cell carcinoma 49 splice junctions 49 nonfasting triglycerides 49 psychobiological 49 Logistic regression 49 CYP#D# genotype 49 differential gene expression 49 Lenzenweger 49 heritable variation 49 prevalences 49 phenotypic differences 49 microdeletions 49 FGF2 49 prenatally exposed 49 cardiovascular mortality 49 BRCA carriers 49 genes predisposing 49 polycystic ovary syndrome PCOS 49 pathogenic mutations 49 obstructive coronary artery 49 C. neoformans 49 fractional anisotropy 49 TOMM# 49 5q 49 meta analyzes 49 thyroid dysfunction 49 neurological abnormalities 49 neuropathological 49 cerebellar vermis 49 aetiological 49 SNPs 49 menarche 49 BARD1 49 Dr. Edward Giovannucci 49 generalizability 49 Pearson correlation coefficients 49 genetic susceptibilities 49 pathophysiological mechanisms 49 gene APOE 49 prevalence 49 Univariate analysis 49 covariate 49 microsatellite instability 49 convergent validity 49 D. melanogaster 49 platypus genome 49 diabetes dyslipidemia 49 potentially modifiable 49 seropositivity 48 allostatic load 48 laterality 48 DLC1 48 HNPCC 48 autosomal dominant 48 correlation coefficients 48 APOE4 48 neurodevelopmental 48 Bacterial vaginosis 48 T2D 48 Hashimoto thyroiditis 48 uric acid levels 48 medulloblastomas 48 genes 48 dizygotic 48 microRNA expression 48 serotonin deficiency 48 S#A# [002] 48 density lipoprotein cholesterol 48 paraneoplastic 48 KIBRA 48 NNRTI resistance 48 chromosome #p# [001] 48 KRAS variant 48 neurodevelopmental disorders 48 Venter genome 48 TCF4 48 inverse association 48 2D 4D 48 genetic trait 48 causative mutation 48 chromosome #p#.# 48 cortical thickness 48 nonadherence 48 singleton babies 48 Longitudinal studies 48 corticosterone levels 48 SLC#A# [001] 48 chorioamnionitis 48 genotype phenotype 48 meta analysis 48 biological underpinnings 48 SNP rs# [001] 48 unmeasured factors 48 familial predisposition 48 LDL HDL 48 heterozygous 48 heritable component 48 neuropsychological functioning 48 allele frequency 48 epigenetic changes 48 aneuploidies 48 Alu elements 48 Simon Baron Cohen 48 adiponectin concentrations 48 seroprevalence 48 albumin excretion 48 homozygotes 48 familial ALS 48 elevated triglyceride levels 48 unmeasured confounders 48 prion gene 48 clinically insignificant 48 placental mammals 48 multivariate logistic regression 48 MSH2 48 miR #a [001] 48 ADRB2 48 intraclass correlation coefficient 48 fetuin 48 gallstone disease 48 bile acid metabolism 48 heredity 48 plasma lipid 48 Cochrane reviewers 48 lactose malabsorption 48 resistin 48 chromosome abnormalities 48 prognostic markers 48 arterial thickening 48 HMGA1 48 confounder 48 prenatally diagnosed 48 chimpanzee genomes 48 FTO variant 48 externalizing behaviors 48 multivariable adjusted 48 gene variant 48 genetic alterations 48 APOL1 48 phenotypic traits 48 homology 48 nucleotide substitutions 48 ADH1B * 48 trans palmitoleate 48 inbreeding coefficient 48 homozygote 48 coronary artery calcification 48 hydroxyvitamin D levels 48 lipid abnormalities 48 cryptogenic 48 CNTNAP2 gene 48 IGF2 48 chromosomal abnormalities 48 pathogenesis 48 BRCA2 mutation carriers 48 alternative splicing 48 ORMDL3 48 nucleotide substitution 48 neuroimaging studies 48 IL#B 48 #S rRNA 48 Logistic regression analysis 48 fructose intake 48 pathophysiology 48 ADAM# 48 assortative 48 mesotheliomas 48 postnatally 48 KCNH2 48 cytochrome b 48 latent celiac disease 48 CVD mortality 48 multivariable Cox 48 K ras mutation 48 Subgroup analyzes 48 nicotinic receptor 48 serum IGF 48 microcephaly 48 shorter telomeres 48 obesity insulin resistance 48 anogenital distance 48 autosomal recessive 48 TT genotype 48 CYP#D# 48 C. pneumoniae 48 mammographic density 48 prion strains 48 virulence genes 48 HER2 expression 48 autistic regression 48 Haptoglobin 48 ortholog 48 retinol binding protein 48 coinfection 48 gene polymorphism 48 nonhereditary 48 pelvic inlet 48 Lp lipoprotein 48 pathogenetic 48 MGUS 48 confidence intervals CIs 48 CC genotype 48 somatic mutations 48 neurodevelopment disorder 48 Heterogeneity 47 Multiple linear regression 47 BRCA1 mutations 47 chimp genome 47 phthalate syndrome 47 Bardet Biedl Syndrome 47 hereditary predisposition 47 causative mutations 47 hypercalciuria 47 GSTT1 47 JAK mutations 47 PITX2 47 interindividual variability 47 protein isoforms 47 nNOS 47 neuroligins 47 lignan intake 47 pathogenetic mechanisms 47 testosterone supplementation 47 linkage disequilibrium LD 47 telomere length 47 gene mutations 47 maternal lineage 47 BRCA2 mutations 47 dietary folate 47 Multiple logistic regression 47 androgen depletion 47 prenatal exposures 47 evolutionary psychologists 47 histologic subtype 47 abdominal obesity 47 Kozyrskyj 47 HGPS 47 bivariate analysis 47 invasive lobular 47 LRP5 47 chi squared 47 miRNAs miR 47 univariate analysis 47 multivariate Cox 47 GSTP1 47 TMPRSS2 ERG fusion 47 dysbindin gene 47 non syndromic 47 sociodemographic variables 47 chromosome deletion 47 cM 47 pathogenic mechanisms 47 Descriptive statistics 47 anorexia sufferers 47 thyrotropin 47 covariance 47 microscopic colitis 47 multiple linear regression 47 haplogroups 47 elevated homocysteine 47 pseudogenes 47 atopy 47 remnant lipoproteins 47 HbF levels 47 SHANK3 47 gestational diabetes mellitus 47 LVNC 47 SLITRK1 47 ischemic lesions 47 generalized estimating 47 abdominal adiposity 47 genetic predispositions 47 CYP#D# gene 47 biological plausibility 47 serum concentrations 47 microcephalin 47 etiologic agent 47 pharmacological interventions 47 piRNAs 47 bimodal distribution 47 FTLD 47 splice variants 47 NIHSS score 47 underdiagnosis 47 Supplementary Table 47 CYP#C# gene 47 FTO gene 47 neurodevelopmental outcomes 47 mtDNA 47 β = 47 null hypothesis 47 genes BRCA1 47 thyroid hormone levels 47 correlations 47 EN2 47 Mustanski 47 #q# [002] 47 HLA DRB1 SE 47 clinico pathological 47 genetic 47 PTEN gene 47 HFE gene 47 polyploid 47 mitochondrial DNA mtDNA 47 multivariate regression 47 phenotypic 47 ASD prevalence 47 transcriptomes 47 unipolar depression 47 undiagnosed celiac disease 47 neuroticism 47 #F FDG PET 47 2 diabetes T2D 47 metabolic dysfunction 47 airway responsiveness 47 psychiatric morbidity 47 somatoform disorder 47 Low birthweight 47 utero exposure 47 odds ratios ORs 47 EBVs 47 serum vitamin D 47 inhibin 47 subfamily 47 Telomere length 47 interobserver 47 apolipoprotein E APOE 47 dysregulation 47 chromosomal instability 47 Pearson correlation coefficient 47 causal pathway 47 flavonoid intake 47 generalisability 47 mitochondrial proteins 47 cardioprotective effects 47 mitochondrial mutations 47 carotid stenosis 47 Heredity 47 FASPS 47 CagA 47 clinicopathologic 47 genital abnormalities 47 cerebellar 47 causal variants 47 Observational studies 47 #q# deletion syndrome 47 borderline statistical significance 47 Denisovan 47 genetically inherited 47 SNPs pronounced snips 47 anovulatory infertility 47 modifiable lifestyle 47 X chromosome inactivation 47 CALHM1 47 hepatocellular carcinomas 47 ascertainment bias 47 antenatal depression 47 bivariate analyzes 47 chromosomal imbalance 47 INF2 47 psychiatric comorbidities 47 SLC#A# gene [002] 47 T1D 47 epigenetic modification 47 serum BDNF 47 prion infection 47 magnesium intake 47 hepatic lipase 47 B7 H3 47 distinct subtypes 47 vegetable intake 47 genes encoding 47 atherogenic dyslipidemia 47 underlying molecular mechanisms 47 intraobserver 47 synuclein 47 prospective longitudinal 47 gene loci 47 atypical hyperplasia 47 affective psychoses 47 hypospadias 47 DAT1 47 VNTR 47 #OHD 47 APOE ε4 47 metabolic syndrome 47 cardioembolic stroke 47 hyperinsulinemia 47 nonfatal MI 47 type2 diabetes 47 G allele 47 IL 7R 47 HRQL 47 neuroglobin 47 IKZF1 47 ultra rapid metabolizer 47 synaptic proteins 47 urinary excretion 47 intact parathyroid hormone 47 EoE 47 metabolic disturbances 46 vitamin D inadequacy 46 COMT gene 46 homologies 46 molecular mechanisms underlying 46 HER2 overexpression 46 chromosomal rearrangements 46 methodological rigor 46 MC4R gene 46 heterosis 46 GPIHBP1 46 Singh Manoux 46 interobserver reliability 46 Haplogroup 46 genetics 46 univariate 46 fatness 46 puerperal psychosis 46 miRNAs 46 dietary folate intake 46 hitherto unrecognized 46 osteopenic 46 pathophysiologic 46 TCF#L# 46 ConclusionThis 46 subtypes 46 gastric carcinoma 46 MHC genes 46 PON1 46 apoE4 46 auditory neuropathy 46 methylenetetrahydrofolate reductase 46 Psychosomatic Research 46 bulimia nervosa 46 Genetic variations 46 AUDs 46 recurrent miscarriages 46 salivary cortisol 46 microsatellite markers 46 transcriptomics 46 neurofibromatosis type 46 MSMB 46 A. sediba 46 genetic ancestry 46 randomized controlled trials RCTs 46 intergenic 46 ZNF# 46 eotaxin 46 Depressive symptoms 46 overdiagnosis 46 C#BL/#J 46 neuropsychiatric disorders 46 neuro developmental disorder 46 genetic heterogeneity 46 gene duplications 46 nonparametric 46 dopamine D2 receptors 46 HRCT 46 eosinophil count 46 immunohistochemical staining 46 viral etiology 46 paraoxonase 46 previously undescribed 46 chromosomal translocations 46 mammographically 46 ASDs 46 SMAD4 46 functional polymorphism 46 Prochlorococcus 46 hallux valgus 46 Cronbach 46 Chlamydia pneumoniae 46 cortex thickness 46 gene locus 46 trans palmitoleic acid 46 APOE allele 46 coronary calcification 46 emotional dysregulation 46 cellularity 46 chlamydial infection 46 serum homocysteine 46 IGF1 46 mtDNA sequence 46 COMT genotype 46 recombination hotspots 46 epistatic 46 aneuploid 46 Mitochondrial DNA 46 testicular germ cell 46 cyclin E 46 cytologic 46 allele 46 morphological 46 fetal aneuploidy 46 mRNA expression 46 logistic regression models 46 atopic 46 DHEAS 46 dysmorphic features 46 recessive trait 46 Insulin sensitivity 46 CDH1 46 codon usage 46 mg BID dose 46 inhibin B 46 SORL1 46 neurobiological mechanisms 46 abnormal lipid levels 46 SOD2 46 EBV infection 46 Ascherio 46 Contagious yawning 46 mammary gland tumors 46 MC1R 46 allelic variants 46 BRCA gene mutations 46 calcium intakes 46 conserved sequences 46 ultraconserved elements 46 advanced neoplasia 46 late onset hypogonadism 46 transcriptional regulation 46 endometrial thickness 46 cardiometabolic risk 46 neuropathologic 46 bilaterians 46 dyscalculia 46 MTHFR gene 46 gene expression patterns 46 leptin deficiency 46 KIAA# 46 prolactin levels 46 Froguel 46 APOA5 46 fewer dopamine receptors 46 #p# [003] 46 affective disorders 46 N acetylaspartate 46 nongenetic factors 46 thimerosal exposure 46 Psychiatric disorders 46 ORFs 46 genetic abnormalities 46 histone code 46 polymorphisms 46 ApoE gene 46 heritable trait 46 abnormal glucose metabolism 46 Selembu shows 46 Stuttering tends 46 epigenetic reprogramming 46 extramedullary 46 thrombophilia 46 intersexuality 46 insulin resistance syndrome 46 incomplete penetrance 46 cardio respiratory fitness 46 hydroxyvitamin D concentrations 46 hamartomas 46 predisposing factors 46 transcriptome 46 white matter hyperintensities 46 nondepressed 46 IL#B gene 46 CHEK2 46 psychosocial stressors 46 Dr. Pasinetti 46 autoimmune thyroid 46 HOXB# 46 acrylamide intake 46 serum urate levels 46 confounding variables 46 Clusterin 46 neural correlates 46 PARP inhibition 46 KRAS mutation status 46 habitual snoring 46 VADT 46 Kay Tee Khaw 46 Math LD 46 T. hallae 46 avoidant personality disorder 46 IgE antibody 46 glycated hemoglobin levels 46 LIS1 46 vitamin D receptor 46 5 methylcytosine 46 neutrophil counts 46 haplotype map 46 Klotho gene 46 regression coefficient 46 prostate carcinogenesis 46 lymphocytic 46 CFH gene 46 molecular abnormalities 46 neurofibrillary 46 Neuregulin 1 46 ApoE4 46 COMT 46 miRNA expression 46 BLLs 46 mitochondrial genomes 46 cDNAs 46 differentially expressed proteins 46 silent myocardial ischemia 46 regression coefficients 46 methodologic 46 histone modifications 46 follicular adenoma 46 myopathies 46 evolutionarily conserved 46 nmol L 46 serum calcium 46 stereochemical 46 HOMA IR 46 GABRA2 46 neurobiological basis 46 prognostic indicators 46 ABCB1 46 neuropsychological impairment 46 abnormal chromosomes 46 ontogeny 46 scrotal circumference 46 LQTS 46 baseline HbA1c 46 differentially regulated 46 statistical correlations 46 polycystic ovary syndrome 46 demyelinating 46 dermatomyositis 46 homocysteine concentrations 46 dysfunctional voiding 46 androgenic hormones 46 single nucleotide polymorphism 46 promoter polymorphism 46 circadian genes 46 atopic disorders 46 autosomes 46 neurobiological underpinnings 46 Redei 46 Hublin 46 artifactual 46 prefrontal cortical 46 ectodermal dysplasia 46 human microbiome 46 polyploidy 45 genomic imprinting 45 hyperactivity inattention 45 p# mutations 45 endotoxin exposure 45 hippocampal volumes 45 statistical significance p 45 SE alleles 45 disc degeneration 45 toxoplasma 45 phenotypic characteristics 45 Brzustowicz 45 mechanistic explanation 45 homeobox genes 45 hypovitaminosis D 45 molecular subtypes 45 multigene 45 parasitaemia 45 MC4R 45 haptoglobin 45 epigenetic regulation 45 K ras mutations 45 TSC1 45 nematode worm 45 #.# df =