Related by context. All words. (Click for frequent words.) 73 genetic susceptibility 70 predisposition 70 genetic predispositions 68 genetically predisposed 63 predispose 63 genetic mutations 63 heredity 62 inherited predisposition 62 genetically susceptible 62 genetic trait 62 hereditary predisposition 62 heritable 61 genetic mutation 61 genetic variations 61 genetic makeup 60 susceptibility genes 60 PTEN mutations 60 Genetic predisposition 59 gene mutation 59 gene variants 59 genetic variants 59 genetic variant 59 genes predisposing 58 APOE4 58 gene variant 58 genes 58 genetic 58 Genetic variants 58 susceptibility gene 57 genetic susceptibilities 57 biological predisposition 57 genetic determinants 57 insulin resistance 57 highly heritable 57 underlying pathophysiology 57 Heredity 56 mitochondrial mutations 56 de novo mutations 56 genetics 56 heritability 56 genetic abnormality 56 mtDNA mutations 56 MYH9 gene 56 genetic markers 56 genetic defect 56 personality traits 56 genetic variation 56 familial adenomatous polyposis 56 predisposed 56 APOE gene 56 LRRK2 mutations 56 epigenetic changes 56 predisposes 55 narcolepsy cataplexy 55 genetically inherited 55 familial pancreatic cancer 55 gene mutations 55 inherit predisposition 55 inherited mutations 55 dopamine receptor gene 55 familial predisposition 55 assortative mating 55 chromosomal alterations 55 Genetic variation 55 genetic abnormalities 55 susceptibility 55 BRCA mutation 55 potentially modifiable 54 metabolic syndrome 54 Hashimoto thyroiditis 54 predisposing factors 54 underactive thyroid gland 54 SE alleles 54 predisposing 54 genetically 54 metabolic abnormalities 54 penetrance 54 chromosomal anomaly 54 GABRA2 gene 54 familial clustering 54 Fragile X gene 54 subclinical hyperthyroidism 54 polygenic 54 mutated gene 54 phenotype 54 TCF#L# gene 54 untreated celiac disease 54 genetic polymorphisms 54 NAFLD 54 shorter telomeres 54 hyperinsulinemia 54 undiagnosed celiac disease 54 serotonin deficiency 54 causal pathway 54 MYH9 53 elevated CRP 53 CNTNAP2 53 underactive thyroid 53 APOE ε4 53 chromosomal disorders 53 APOE e4 53 apolipoprotein E gene 53 genetically predetermined 53 genetic defects 53 mutations 53 ApoE4 gene 53 mitochondrial dysfunction 53 etiology 53 gene 53 nongenetic factors 53 heritable genetic 53 chromosomal abnormalities 53 fatty liver disease 53 comorbid disorders 53 unmeasured factors 53 APOE genotype 53 causative gene 53 KIBRA 53 BRCA2 mutation 53 nongenetic 53 thyroid dysfunction 53 behavioral disinhibition 53 causative genes 53 BARD1 53 periodontal infection 53 subfertility 53 multifactorial 52 neuropsychological deficits 52 hypertrophic cardiomyopathy HCM 52 phenotypes 52 #q#.# deletion syndrome 52 gene variation 52 recessive trait 52 polycystic ovary syndrome 52 spontaneous mutations 52 recurrent miscarriages 52 psychiatric comorbidity 52 neurobiological 52 shorter telomere length 52 modifiable risk 52 phenotypic variation 52 developmental abnormalities 52 AAT deficiency 52 autistic traits 52 remnant lipoproteins 52 subclinical 52 alexithymia 52 HLA genes 52 TGFBR1 * 6A 52 folate deficiency 52 hormonal abnormalities 52 genetically disposed 52 defective gene 52 dysregulation 52 neurological abnormalities 52 GAB2 52 disease NAFLD 52 MHC genes 52 predisposing factor 52 mutant huntingtin protein 52 estrogen metabolism 52 G#S mutation 52 familial hypercholesterolemia 51 G6PD deficiency 51 germline mutations 51 Male pattern baldness 51 FTO gene 51 leptin deficiency 51 inheritable 51 puerperal psychosis 51 hormonal imbalances 51 IDH mutations 51 chromosomal anomalies 51 recessive genetic 51 genetic underpinnings 51 FTLD 51 hemochromatosis 51 BRCA2 gene mutation 51 autosomal dominant inheritance 51 SORL1 51 heritable component 51 chromosomal regions 51 hippocampal function 51 mutation 51 mutated genes 51 hereditary 51 Cowden syndrome 51 EBV infection 51 TP# mutation 51 phenotypic expression 51 familial aggregation 51 BRCA gene mutations 51 genetic variants associated 51 subclinical atherosclerosis 51 leptin resistance 51 neurobiological disorder 51 atopy 51 basal cell nevus syndrome 51 glucose intolerance 51 chromosomal instability 51 dominantly inherited 51 autosomal dominant disorder 51 intestinal polyps 51 insulin resistance syndrome 51 Li Fraumeni syndrome 51 nonhereditary 50 sporadic ALS 50 allergic sensitization 50 inherited genetic mutations 50 Genetic variations 50 chromosomal rearrangement 50 socioeconomic status 50 mitochondrial defects 50 carbohydrate intolerance 50 HNPCC 50 spastic paraplegia 50 nonalcoholic fatty liver 50 DRD4 50 metabolic disturbances 50 #q# deletion 50 brain lesions 50 predispositions 50 thyroid abnormalities 50 thrombophilia 50 metabolic abnormality 50 placental hormones 50 primary biliary cirrhosis 50 periodontal infections 50 neophobia 50 molecular abnormalities 50 Hip dysplasia 50 neuropsychiatric disorder 50 multi factorial disease 50 hormonal fluctuations 50 psychosocial variables 50 hormone imbalances 50 serotonin transporter 50 Vitamin B# deficiency 50 uric acid levels 50 ultra rapid metabolizer 50 MAOA gene 50 etiologic 50 chromosome abnormality 50 Klinefelter syndrome 50 periodontal disease 50 underlying molecular mechanisms 50 olfactory dysfunction 50 nerve degeneration 50 genetic syndromes 50 genetically programmed 50 BRCA1 mutation 50 APOE e4 gene 50 recessive genes 50 alleles 50 biochemical imbalance 50 autoimmune thyroid 50 monozygotic twins 50 thyrotropin levels 50 genetic alterations 50 obesity insulin resistance 50 GABRA2 50 antenatal depression 50 IgA deficiency 50 HGPS 50 FGFR2 gene 50 subclinical hypothyroidism 50 heart disease 50 GBA mutations 50 autosomal recessive 50 pathophysiological mechanisms 50 mitochondrial disorders 50 heritable variation 50 STAT4 50 aldehyde dehydrogenase 50 Tay Sachs disease 50 inborn 50 dopamine D2 receptors 50 abnormal lipids 50 gut microbes 50 genomic imprinting 50 abnormalities 50 mammary cancers 50 epigenetic mechanisms 50 susceptibility locus 50 proband 50 Fatty liver 50 MC1R 50 intersexuality 50 genetic traits 50 BRCA1 mutations 50 endothelial dysfunction 50 MEF2A 50 SLC#A# [002] 50 inbreeding depression 50 lupus scleroderma 50 ApoE4 50 MTHFR 50 physiological mechanisms 50 gallstone disease 50 genes predispose 50 genetic makeups 50 autosomal recessive disease 50 systemic inflammation 50 ovarian hormones 50 BRCA2 gene 49 neural substrates 49 testicular tumors 49 circulating estrogens 49 LRRK2 gene 49 degenerative neurological diseases 49 body fatness 49 prenatal testosterone 49 gestational diabetes mellitus 49 recessive mutations 49 familial polyposis 49 neurodevelopmental disorder 49 recessive gene 49 Socioeconomic status 49 modifier genes 49 Heritability 49 Kufs disease 49 monogenic 49 cognitive deficits 49 compulsive hoarding 49 MAOA 49 heritable diseases 49 testicular germ cell 49 poorer prognosis 49 atherosclerosis 49 unhealthy diets 49 impaired glucose metabolism 49 APOE4 gene 49 testicular dysgenesis syndrome 49 CYP#A# gene 49 CYP#D# gene 49 microvascular disease 49 polycystic ovary syndrome PCOS 49 mitochondrial DNA mutations 49 behavioral traits 49 environmental toxicants 49 epigenetic 49 genetic polymorphism 49 PTPN# 49 DRD2 gene 49 pathophysiologic 49 mutant allele 49 ApoE 49 mosaicism 49 SRY gene 49 airway hyperresponsiveness 49 ApoE gene 49 gene APOE 49 neurodevelopmental disorders 49 Wernicke Korsakoff syndrome 49 AUDs 49 Vitamin D insufficiency 49 neurological degeneration 49 retinal dysfunction 49 impair fertility 49 chronicity 49 fatty liver 49 breast endometrial 49 obesity sedentary lifestyle 49 GRK5 49 sexual dimorphism 49 parkinsonism 49 DNA methylation patterns 49 slow metabolizers 49 adiponectin levels 49 HLA DRB1 49 biologically plausible 49 nutritional deficiency 49 hereditary hemochromatosis 49 SORL1 gene 49 multi factorial 49 deleterious mutations 49 biochemical imbalances 49 cardiac fibrosis 49 MGUS 49 CYP#E# gene 49 p# mutations 49 autonomic dysfunction 49 biochemical abnormalities 49 type2 diabetes 49 genetic disorders 49 utero exposure 49 DQB1 * 49 synaptic function 49 IL#R 49 congenital disorders 49 2D 4D ratio 49 neuroinflammation 49 aetiological 49 COMT gene 49 epigenetic markers 49 ectodermal dysplasia 49 disregulation 49 antisocial behaviors 49 CHRNA5 gene 49 congenital abnormalities 48 glutamate signaling 48 epigenetic alterations 48 prostate carcinogenesis 48 LQTS 48 overactive thyroid gland 48 ataxias 48 imprinted genes 48 biologically predisposed 48 hardened arteries 48 monozygotic twin 48 abdominal obesity 48 primary ovarian insufficiency 48 nonalcoholic steatohepatitis 48 congenital deficiency 48 somatic symptoms 48 PTEN gene 48 bowel cancers 48 physiological 48 aneuploidy 48 dizygotic twins 48 GSTM1 gene 48 spontaneous mutation 48 airway responsiveness 48 postnatally 48 causally linked 48 Nicotine dependence 48 GSTM1 48 neuro developmental disorder 48 mood disorders 48 neurodevelopment disorder 48 insulin resistance precursor 48 Meckel Gruber 48 metabolic dysfunction 48 thyroid hormone levels 48 microdeletion 48 clefting 48 inflammatory rheumatic 48 impaired insulin secretion 48 habitual snoring 48 misregulation 48 maladaptive behavior 48 BRCA mutations 48 endophenotypes 48 elevated triglyceride levels 48 ADPKD 48 FMRP protein 48 Dravet syndrome 48 prothrombotic 48 GSTT1 48 progranulin 48 SERT gene 48 rhinovirus infection 48 Bacterial vaginosis 48 IKZF1 48 cardiovascular disease hypertension 48 #q#.# [001] 48 diathesis 48 Toxoplasmosis 48 vitamin B# deficiency 48 vmPFC 48 arterial thickening 48 JAK2 mutation 48 hydrops 48 genotype 48 Nordestgaard 48 TCF#L# 48 Coeliac disease 48 polymorphism 48 neurobiological mechanisms 48 FGFR2 48 hereditary nonpolyposis colorectal cancer 48 susceptibility alleles 48 familial adenomatous polyposis FAP 48 arterial calcification 48 #q# [001] 48 metabolizing enzymes 48 lactose malabsorption 48 epigenetic modification 48 impaired cognition 48 irregular menstrual cycles 48 phenotypic variability 48 maternally inherited 48 epigenetic inheritance 48 X chromosome 48 Personality traits 48 Neuroticism 48 antisocial tendencies 48 neuronal dysfunction 48 benign proliferative breast 48 psychotic illnesses 48 Maternal obesity 48 CNVs 48 cardiac insufficiency 48 Genetic mutations 48 adrenal function 48 MSH2 48 dyscalculia 48 TACI mutations 48 fewer dopamine receptors 48 syndromes 48 chromosomal translocations 48 CYP#C# gene 48 neuroblastomas 48 gestational diabetes mellitus GDM 48 somatoform disorder 48 nondemented 48 fructose intolerance 48 homozygosity 48 comorbid anxiety 48 untreated sleep apnea 48 recessive inheritance 48 apoC III 48 genetic alteration 48 inborn traits 48 BRCA1 gene 48 estrogenic effects 48 sCJD 48 muscular dystrophies 48 ASDs 48 chromosomal disorder 48 polycystic ovarian syndrome PCOS 48 V Leiden 48 promoter hypermethylation 48 dietary habits 48 Hypertrophic cardiomyopathy 48 klotho 48 chromosomal abnormality 47 polydactylism 47 mammary tumors 47 Hyperthyroidism 47 exfoliative glaucoma 47 G allele 47 autoimmune thyroiditis 47 thyroid deficiency 47 SRBD 47 autoimmune disorders 47 endogenous estrogen 47 leaky gut 47 CHD7 47 chromosome #q# [002] 47 motor neuron degeneration 47 etiological factors 47 Oxidative stress 47 genetic ancestry 47 autosomal dominant 47 El Sohemy 47 gene predisposing 47 epigenetic marks 47 polycystic ovaries 47 causal pathways 47 HLA B# gene 47 macrovascular complications 47 unmeasured confounders 47 hormonal disturbances 47 endocannabinoid signaling 47 WNK1 47 IGF2 47 autoimmune 47 paraneoplastic 47 recurrent miscarriage 47 evolvability 47 metabolic syndrome MetS 47 premenopausal breast cancer 47 cryptogenic 47 obstructive lung 47 BRCA2 mutations 47 neurodevelopmental 47 MTHFR gene 47 gene locus 47 digest lactose 47 causal 47 psychopathological disorders 47 coinfection 47 prenatal exposure 47 ZNF# 47 CDH1 47 abnormal lipid levels 47 etiological 47 neurobiological basis 47 DRD4 gene 47 postmenopausal breast cancer 47 cardiovascular disease 47 pituitary tumors 47 endocrinological 47 multisystem disease 47 arteriosclerotic 47 overactivation 47 HLA B# 47 Imprinted genes 47 hormone aldosterone 47 Chronic pancreatitis 47 heritable disorders 47 IUGR 47 cardio vascular disease 47 Brugada syndrome 47 nicotinic receptor 47 developmental trajectories 47 ABCB1 gene 47 impulsive behaviors 47 elevated triglycerides 47 psychopathic traits 47 pathogenetic mechanisms 47 FXTAS 47 BRCA genes 47 colorectal neoplasia 47 B# deficiency 47 Malignant mesothelioma 47 Lafora disease 47 galactosemia 47 Telomere length 47 coronary heart 47 BRCA2 gene mutations 47 neurochemistry 47 unhealthier lifestyles 47 CaM kinase II 47 ORMDL3 47 dysregulated 47 residual confounding 47 OCA2 47 rs# [002] 47 autism dyslexia 47 genomewide 47 compensatory mechanisms 47 chromosome deletion 47 epigenetic modifications 47 unmeasured confounding 47 Postnatal depression 47 LPA gene 47 Cognitive impairment 47 maladaptive 47 BRCA gene mutation 47 apoE4 47 thicker carotid arteries 47 galanin 47 atopic disorders 47 inflammatory bowel syndrome 47 mito 47 male hormone androgen 47 lipin 47 genetic variability 47 paternal lineages 47 fetal malformations 47 polycystic ovarian syndrome 47 LRP5 47 OPRM1 gene 47 inherited genetic mutation 47 CFH gene 47 cognitive impairment 47 coronary disease 47 lethal arrhythmias 47 familial ALS 47 mutant genes 47 bulimia nervosa 47 genetic loci 47 protein kinase C 47 metabolic alterations 47 unhealthy dietary habits 47 hereditary deafness 47 androgen deficiency 47 IGF1 47 germline mutation 47 STK# gene 47 Li Fraumeni 47 silent myocardial ischemia 47 osteopontin 47 diabetic kidney 47 sedentary lifestyle 47 hereditary disorders 47 Periodontal disease 47 Genetic mutation 47 alcoholic fatty liver 47 menarche 47 alpha thalassemia 47 LIS1 47 androgen excess 47 modifiable lifestyle 47 immunodeficiencies 47 CHRNA5 47 auditory neuropathy 47 Magnesium deficiency 47 cardiomyopathies 47 intestinal biopsy 47 unprovoked seizures 47 multisystem disorder 47 cardiac abnormality 47 pathophysiologic mechanisms 47 CETP gene 47 SCA5 47 dysbindin gene 47 mammary gland tumors 46 FASPS 46 gallstone formation 46 aspergers 46 chromosome #q# [001] 46 insulin resistant 46 BRCA carriers 46 subclinical infection 46 reproductive abnormalities 46 subsyndromal 46 aneuploidies 46 progranulin mutations 46 XMRV infection 46 missense mutations 46 nucleus Chinnery 46 teratogens 46 C#Y 46 bipolar illness 46 chromosome translocations 46 pathophysiological 46 estrogen deficiency 46 allele 46 anosognosia 46 TMEM#B 46 e4 allele 46 prediabetes 46 chromosomal aberrations 46 genes BRCA1 46 hypovitaminosis D 46 lactose tolerance 46 hypertension diabetes mellitus 46 Obsessive compulsive disorder 46 Excessive daytime sleepiness 46 psychosocial stressors 46 gene DRD4 46 benign breast 46 metabolic 46 neurocognitive impairment 46 Bardet Biedl syndrome 46 KIF6 gene 46 tic severity 46 carotid atherosclerosis 46 intestinal inflammation 46 spastic diplegia 46 vitamin D deficiency 46 multigenic 46 dyslipidemia hypertension 46 hypertension 46 serum selenium 46 pathogenesis 46 carotid bruit 46 neuroendocrine 46 Wnt#b 46 FGF2 46 eczema hay fever 46 Korsakoff syndrome 46 BRCA gene 46 Celiac sprue 46 selenium deficiency 46 serotonin transporter gene 46 bowel polyps 46 epistasis 46 Proteus syndrome 46 biochemical pathways 46 pathogenic mutations 46 molecular pathways 46 muscular dystrophy cystic fibrosis 46 premature ovarian 46 multifactorial disease 46 hypothyroid 46 Multivariate analyzes 46 breast cancer genes BRCA1 46 Epstein Barr virus 46 non pharmacological interventions 46 hyperexcitability 46 amyloid plaque formation 46 neurodegenerative disorder 46 Sjögren syndrome 46 childhood disintegrative disorder 46 Prenatal exposure 46 chorioamnionitis 46 prion infection 46 spontaneous remission 46 ambiguous genitalia 46 A1 allele 46 lipid abnormalities 46 thrifty gene 46 atopic 46 obsessive compulsive behaviors 46 Secondhand smoke exposure 46 Angelman syndrome 46 dyskeratosis congenita 46 CIB1 46 autoimmune pancreatitis 46 osteodystrophy 46 amino acid homocysteine 46 prosopagnosia 46 SHANK3 46 bronchitis emphysema 46 VLDL cholesterol 46 NF1 46 Toxoplasma 46 hypothyroidism 46 Abdominal fat 46 NOD2 46 apolipoprotein E4 46 CYP#D# 46 MECP2 gene 46 underactive thyroids 46 vascular cognitive impairment 46 cancers 46 lipid levels 46 neuropsychiatric disorders 46 neuroglobin 46 FTO variant 46 ABO blood 46 HPA axis 46 inhaled allergens 46 huntingtin gene 46 Bardet Biedl Syndrome 46 mutated BRCA1 46 diabetes cardiovascular disease 46 de ath 46 persistent pulmonary hypertension 46 adiposity 46 abnormal glucose tolerance 46 hyperemesis gravidarum 46 evolutionarily speaking 46 molecular underpinnings 46 coronary calcification 46 vascular dysfunction 46 post natally 46 subclinical cardiovascular disease 46 neoplastic 46 Modifiable risk 46 Von Willebrand disease 46 cerebral infarction 46 BRCA1 gene mutation 46 congential 46 airway remodeling 46 lactase persistence 46 stressors 46 aetiology 46 Chronic fatigue 46 late onset hypogonadism 46 fructose intolerant 46 premorbid 46 hyperthyroidism 46 cardiac hypertrophy 46 contagious yawning 46 debilitating neurodegenerative disorder 46 lactase deficiency 46 food intolerances 46 BRCA1 BRCA2 46 PON1 46 neuropsychological functioning 46 MYCN amplification 46 hepatitis B infection 46 autosomal dominant polycystic kidney 46 allostatic load 46 MetS 46 hippocampal volume 46 Mitochondrial diseases 46 dysbindin 46 Ovary removal 46 Polycystic ovarian syndrome 46 irregular menstruation 46 periodontitis 46 polymorphisms 46 BMPR2 46 NAT2 46 endometrial cancers 46 thimerosal exposure 46 rs# [003] 46 organochlorine compounds 46 DRD2 46 circadian disruption 46 oxidative stress 46 neurogenerative diseases 46 abnormal growths 46 prenatal exposures 46 lobular breast cancer 46 abnormal proteins 46 UGT#B# 46 glucocorticoid receptors 46 INF2 46 prodynorphin 46 APOE e4 allele 46 gassiness 46 APOL1 46 endogenous opioid 46 MC1R gene 46 precocious puberty 46 SNPs 46 fructose intake 46 chromosomal deletions 46 structural abnormalities 46 rheumatoid arthritis lupus 46 recessive traits 46 homocystinuria 46 hormonal disorder 46 colon polyps 46 neurologic disorder 46 Neuregulin 1 46 varicocele 46 monoclonal gammopathy 46 airborne fungal spores 46 dysautonomia 46 physical inactivity 46 hyperinsulinism 46 activity MAOA 46 biologic plausibility 46 endometrial hyperplasia 46 chronic obstructive airway 46 hypertension cardiovascular disease 46 BRCA1 46 neurobiological underpinnings 46 nonmelanoma skin cancers 46 tumor histology 46 biologically programmed 46 Neurofibromatosis type 46 Pathological gambling 46 Apert syndrome 46 hematopoietic cancers 46 chromosomal defects 46 genomic instability 46 elevated homocysteine 46 induced cardiomyopathy 46 heritable traits 46 familial hypercholesterolaemia FH 46 heterozygosity 46 C. pneumoniae 46 congenital adrenal hyperplasia CAH 46 Sedentary lifestyles 46 anatomic abnormalities 46 genetic locus 46 SLC#A# [001] 46 spinocerebellar ataxia 46 Colon polyps 46 liver scarring 46 causal relation 46 oropharyngeal cancer 46 GPC5 46 obese postmenopausal 46 undiagnosed untreated 46 airway constriction 45 hypochondriasis 45 microdeletions 45 CALHM1 45 chlamydial infection 45 hypothesized 45 cardioprotective effects 45 neuropsychological impairments 45 androgenic hormones 45 corticosterone levels 45 prefrontal regions 45 cardiac channelopathies 45 asthmatic airways 45 premature senility 45 Androgenetic alopecia 45 Heavy menstrual bleeding 45 metabolizing enzyme 45 chromosome rearrangements 45 Dwarfism 45 experimentally induced 45 heritable trait 45 TGFBR1 45 biopsychosocial 45 TNFAIP3 45 haemochromatosis 45 Froguel 45 cardioembolic stroke 45 Mendelian disorders 45 HFE gene 45 microglial cells 45 psychotic illness 45 Lactose intolerance 45 preterm delivery 45 ovulatory dysfunction 45 Marc Weisskopf 45 NADPH oxidase 45 porphyria 45 Vitamin D deficiency 45 ApoE4 allele 45 elevated fasting glucose 45 p# activation 45 DAT1 45 congenital abnormality 45 2 diabetes T2D 45 inherited neurological disorder 45 allele frequencies 45 behavioral abnormalities 45 occupational exposures 45 exfoliation glaucoma 45 adult neurogenesis 45 comorbidity 45 premenstrual syndrome PMS 45 untreated hypothyroidism 45 toxoplasmosis 45 Cockayne syndrome 45 klotho gene 45 vasopressin receptors 45 prosocial behavior 45 BRCA2 breast cancer 45 amnestic MCI 45 Rh incompatibility 45 observable traits 45 Autoimmune disorders 45 Apert 45 stereotypy