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(Click for frequent words.) 73 genetic predisposition 66 genetic variants 65 genetically susceptible 65 genetic variations 64 genetic variation 64 gene variants 64 genetic mutations 63 epigenetic changes 63 susceptibility genes 63 genetic variant 63 gene mutations 62 genetic predispositions 62 Genetic predisposition 62 inherited predisposition 62 mtDNA mutations 61 mitochondrial dysfunction 61 hereditary predisposition 61 genetic makeup 61 genetic susceptibilities 61 Genetic variation 60 Genetic variations 60 Genetic variants 60 inherited mutations 60 susceptibility 60 causative genes 59 genetic polymorphisms 59 heredity 59 genetic alterations 59 genes 59 systemic inflammation 59 IDH mutations 59 genetic abnormalities 59 familial predisposition 59 gut microbes 59 Genetic mutations 59 folate deficiency 59 HLA DRB1 58 heritable 58 LRRK2 mutations 58 metabolic abnormalities 58 genetic 58 MYH9 58 insulin resistance 58 mitochondrial disorders 58 underlying pathophysiology 58 mitochondrial mutations 58 PTEN mutations 58 familial pancreatic cancer 58 gene mutation 58 genetic determinants 58 MYH9 gene 58 ovarian hormones 58 genetic mutation 58 susceptibility gene 58 STAT4 58 chromosomal instability 58 Heredity 58 TCF#L# gene 57 physiological mechanisms 57 genetic underpinnings 57 developmental abnormalities 57 FGFR2 gene 57 phenotypic variation 57 airway remodeling 57 genes predisposing 57 pathogenesis 57 chromosomal alterations 57 modifiable risk 57 HLA genes 57 APOE gene 57 epigenetic alterations 57 subclinical hyperthyroidism 57 epigenetic mechanisms 57 gene variation 57 nongenetic factors 56 APOE genotype 56 hyperinsulinemia 56 genetic variability 56 mutations 56 Bardet Biedl Syndrome 56 chromosomal abnormalities 56 gene variant 56 genetics 56 genetic variants associated 56 phenotypes 56 etiologic 56 neurodevelopmental 56 pathogenic mechanisms 56 coinfection 56 multifactorial 56 molecular underpinnings 56 CHD7 56 undiagnosed celiac disease 56 periodontal infection 56 folate intake 56 APOE e4 56 genetic markers 56 AAT deficiency 56 highly heritable 56 polygenic 56 environmental toxicants 56 testicular germ cell 56 SORL1 56 etiology 56 APOE4 56 epigenetic 56 PTPN# 56 heritability 56 G6PD deficiency 56 autoimmune thyroid 56 genetic heterogeneity 56 biologic pathways 56 APOE ε4 55 monozygotic twins 55 shorter telomeres 55 MTHFR 55 sporadic ALS 55 IgA deficiency 55 sCJD 55 multi factorial disease 55 predispose 55 genetically predisposed 55 estrogen metabolism 55 chromosomal anomaly 55 unmeasured factors 55 Hashimoto thyroiditis 55 dysregulation 55 spontaneous mutations 55 genomewide 55 PARP inhibition 55 airway hyperresponsiveness 55 BARD1 55 narcolepsy cataplexy 55 prion infection 55 IL#R 55 epigenetic regulation 55 DNA methylation patterns 55 Marc Weisskopf 55 mutated gene 55 NPY gene 55 FTLD 55 penetrance 55 LRRK2 gene 55 genomic imprinting 55 rhinovirus infection 55 #q#.# deletion syndrome 55 neuroendocrine 55 G#S mutation 55 recurrent miscarriages 55 potentially modifiable 55 bacterium Helicobacter pylori 55 genetic polymorphism 55 elevated CRP 55 TGFBR1 * 6A 55 familial clustering 55 thyrotropin levels 55 nongenetic 55 disregulation 54 prostate carcinogenesis 54 MHC genes 54 ORMDL3 54 chromosome rearrangements 54 microbiota 54 GAB2 54 neurodevelopmental disorders 54 imprinted genes 54 familial adenomatous polyposis 54 genetic imprinting 54 EBV infection 54 chromosomal regions 54 HLA B# gene 54 mutated genes 54 de novo mutations 54 clefting 54 predisposing factor 54 obesity insulin resistance 54 neuroinflammation 54 familial ALS 54 SHANK3 54 gene expression patterns 54 NAFLD 54 basal cell nevus syndrome 54 untreated celiac disease 54 genetic locus 54 reproductive abnormalities 54 atopy 54 fatty liver disease 54 gut microflora 54 gene locus 54 germline mutations 54 SE alleles 54 gallstone disease 54 utero exposure 54 predisposition 54 dopamine receptor gene 54 phenotypic expression 54 allergic sensitization 54 PON1 54 apoE 54 IKZF1 54 chromosomal translocations 54 Kufs disease 54 mutation 54 breast cancer metastasis 54 missense mutations 54 BRCA mutation 54 mitochondrial defects 54 phenotypic variability 54 epigenetic modification 54 causal pathway 54 prenatal exposure 54 shorter telomere length 54 causative gene 54 familial aggregation 54 adiponectin levels 54 underlying molecular mechanisms 54 molecular abnormalities 53 susceptibility locus 53 BRCA1 mutations 53 CNTNAP2 53 chlamydial infection 53 LIS1 53 bile acid metabolism 53 neurological abnormalities 53 lipid metabolism 53 NOD2 53 TMEM#B 53 persistent pulmonary hypertension 53 polymorphisms 53 subclinical 53 chromosome translocations 53 protein misfolding 53 breast endometrial 53 aneuploidy 53 CNVs 53 pathophysiological 53 IGF2 53 virulence genes 53 Helicobacter 53 FGFR2 53 pathophysiological mechanisms 53 COMT gene 53 assortative mating 53 neuroligins 53 PICALM 53 colorectal neoplasia 53 subclinical atherosclerosis 53 gut microbiota 53 neuropsychiatric diseases 53 periodontal disease 53 thyroid hormone levels 53 lipid abnormalities 53 uric acid levels 53 apoE4 53 TCF#L# 53 methylation patterns 53 genetic syndromes 53 progranulin 53 residual confounding 53 antenatal depression 53 DNA methylation 53 airway responsiveness 53 GBA mutations 53 Meckel Gruber 53 prenatal exposures 53 genetic loci 53 inherit predisposition 53 intestinal microflora 53 ApoE gene 53 CDH1 53 chromosomal anomalies 53 Chlamydia pneumoniae 53 Folic acid supplements 53 epigenetic inheritance 53 elevated triglyceride levels 53 Toxoplasmosis 53 Klinefelter syndrome 53 inflammatory bowel disease 53 thyroid function 53 ALDH2 53 heritable diseases 53 epigenetic markers 53 cholesterol metabolism 53 5 HTTLPR 53 breast cancer genes BRCA1 53 LRP5 53 biologically plausible 53 aneuploidies 53 gene 53 epigenetics 53 INF2 53 #q#.# [001] 53 metabolic 53 microdeletion 53 molecular pathways 53 apolipoprotein E gene 53 impair fertility 53 bowel cancers 53 nonalcoholic fatty liver 53 endothelial dysfunction 53 transcriptional repression 53 gene polymorphisms 53 Secondhand smoke exposure 53 atopic disease 52 phenotype 52 probiotic supplementation 52 Clusterin 52 chromosomal disorders 52 behavioral disinhibition 52 male infertility 52 metabolic disturbances 52 predisposing factors 52 neurodevelopment 52 molecular mechanisms underlying 52 alpha synuclein protein 52 mutant huntingtin protein 52 Six3 52 remnant lipoproteins 52 microbiome 52 gastric carcinogenesis 52 methylation markers 52 alpha synuclein gene 52 PB1 F2 52 pathophysiology 52 autism susceptibility genes 52 Periodontal disease 52 selenium deficiency 52 ultra rapid metabolizer 52 Epstein Barr virus 52 chromosomal rearrangement 52 metabolizing enzymes 52 autosomal dominant disorder 52 metabolic abnormality 52 hormonally sensitive 52 neural tube defect 52 chromosome abnormality 52 polycystic ovary syndrome PCOS 52 Vitamin D insufficiency 52 thyroid dysfunction 52 inflammatory bowel diseases 52 neurodevelopmental disorder 52 neuronal dysfunction 52 Smad3 52 de ath 52 disease NAFLD 52 primary biliary cirrhosis 52 KIF6 gene 52 gut flora 52 amino acid homocysteine 52 neuropsychiatric disorders 52 enterotypes 52 osteopontin 52 Epidemiologic studies 52 mosaicism 52 causal pathways 52 evolvability 52 p# MAPK 52 carcinogenesis 52 intestinal microbiota 52 respiratory viral infections 52 BRCA2 mutations 52 FTO gene 52 neuropsychiatric disorder 52 Genetic mutation 52 nonhereditary 52 genetic defect 52 MIF protein 52 Prenatal exposure 52 promoter hypermethylation 52 serotonin transporter 52 hypovitaminosis D 52 GSTT1 52 plasma kallikrein 52 Socioeconomic status 52 inherited genetic mutations 52 p# activation 52 genetically inherited 52 metabolic syndrome MetS 52 BRCA2 gene mutation 52 chronic hepatitis cirrhosis 52 epistasis 52 Folic acid deficiency 52 ZNF# 52 Vitamin D deficiency 52 CYP#C# [002] 52 neuropsychological deficits 52 p# mutations 52 vitamin D deficiency 52 leptin deficiency 52 Coeliac disease 52 testicular dysgenesis syndrome 52 aetiological 52 folate metabolism 52 mutant genes 52 Maternal obesity 52 AUDs 52 clusterin 52 serum biomarkers 52 MGUS 52 monogenic 52 maternally transmitted 52 Cotinine 52 enteroviruses 52 mitochondrial fusion 52 GABRA2 gene 52 IgE antibody 52 elevated homocysteine 52 testicular tumors 52 microdeletions 52 HLA B# 52 GSTM1 52 aldehyde dehydrogenase 52 GRK5 52 organochlorine compounds 52 motor neuron degeneration 52 LPA gene 52 inhaled allergens 52 fatty liver 52 carbohydrate intolerance 52 PPAR γ 52 DHEAS 52 subclinical hypothyroidism 52 Fragile X gene 52 carotid atherosclerosis 52 IUGR 51 FGFs 51 TP# mutation 51 Male pattern baldness 51 WNK1 51 aetiology 51 genetic trait 51 HNPCC 51 parkinsonism 51 pathogenetic mechanisms 51 GSTP1 51 apoC III 51 trans palmitoleic acid 51 FASPS 51 predisposes 51 Fatty liver 51 Cognitive impairment 51 paraneoplastic 51 Neuregulin 1 51 endocrine dysfunction 51 CALHM1 51 Mycoplasma pneumoniae 51 CYP#D# gene 51 sortilin 51 cellular pathways 51 adrenal function 51 spontaneous mutation 51 antioxidant intake 51 cirrhosis liver failure 51 pathogenic mutations 51 DQB1 * 51 APOL1 51 ApoE4 gene 51 genomic instability 51 Oxidative stress 51 HGPS 51 body fatness 51 Zinc deficiency 51 serotonin deficiency 51 etiological 51 genetically 51 metabolic syndrome 51 hereditary breast cancer 51 pathogenetic 51 HER2 neu 51 nerve degeneration 51 atopic disorders 51 molecular pathogenesis 51 metabolic enzymes 51 channelopathies 51 GABRA2 51 homozygosity 51 adult neurogenesis 51 periodontal infections 51 epigenetic modifications 51 2D 4D ratio 51 benign proliferative breast 51 predisposing 51 FMRP protein 51 Gluten intolerance 51 adiponectin 51 lobular breast cancer 51 LQTS 51 liver scarring 51 regulates gene expression 51 oxidative stress 51 immunological mechanisms 51 Li Fraumeni syndrome 51 SHANK3 gene 51 atherosclerosis 51 unmeasured confounders 51 KIBRA 51 histone modifications 51 SORL1 gene 51 impaired insulin secretion 51 hereditary hemochromatosis 51 resistin 51 protein misfolding diseases 51 Ets2 51 CYP#D# 51 chromosomal aberrations 51 haplotype 51 Magnesium deficiency 51 Rb gene 51 modifiable lifestyle 51 hyperinsulinism 51 Froguel 51 UCP2 51 hypermethylation 51 GSTM1 gene 51 molecular mechanisms 51 neurobiological underpinnings 51 prothrombotic 51 subfertility 51 autosomal recessive 51 SLC#A# [002] 51 gastroesophageal reflux GERD 51 #q# deletion 51 endocannabinoid signaling 51 psychotic illnesses 51 gestational diabetes mellitus 51 BRCA mutations 51 commonly mutated genes 51 biochemical mechanisms 51 biological predisposition 51 multi factorial 51 tumor suppressor protein 51 alleles 51 synaptic function 51 Brd4 51 endocrine disrupting chemicals 51 ASDs 51 CYP#A# gene 51 inheritable diseases 51 carbohydrate metabolism 51 underactive thyroid gland 51 muscular dystrophy cystic fibrosis 51 matriptase 51 micro RNAs 51 ALK gene 51 ADAM# 51 nonmelanoma skin cancer 51 mito 51 MECP2 gene 51 endogenous retroviruses 51 IGF1 51 Nonalcoholic fatty liver 51 Viral infections 51 biopsychosocial 51 oncogenesis 51 chromosome deletion 51 IGFBP2 51 dyscalculia 51 genetic defects 51 PALB2 51 genes CYP#C# 51 chromosomal defects 51 genetic abnormality 51 thyrotropin 51 pathophysiologic 51 G allele 51 chronicity 51 Sjögren syndrome 51 bacterial virulence 51 prodynorphin 51 pathophysiologic mechanisms 51 H. pylori 51 underactive thyroid 51 maternally inherited 51 immune dysregulation 51 corona virus 51 innate immune 50 preterm delivery 50 HBx 50 ataxias 50 genetic makeups 50 heritable component 50 heterozygosity 50 GPx 50 NADPH oxidase 50 CYP#E# 50 abnormal proteins 50 intestinal biopsy 50 Brugada syndrome 50 familial hypercholesterolemia 50 mitochondrial proteins 50 abnormal glucose metabolism 50 spinocerebellar ataxia 50 type2 diabetes 50 polycystic ovary syndrome 50 biogeochemical cycles 50 BRCA carriers 50 filaggrin mutations 50 Epstein Barr virus EBV 50 tic severity 50 HbF 50 pilocytic astrocytomas 50 androgen excess 50 microvascular disease 50 molecular mechanism 50 facial clefts 50 vitamin B# deficiency 50 genetic aberrations 50 V Leiden 50 germline mutation 50 modifier genes 50 JAK2 mutation 50 Cryptococcus neoformans 50 KCNH2 50 galanin 50 SIRT3 50 ApoE 50 mitochondrial DNA mutations 50 anovulatory infertility 50 p#INK#a 50 herpesviruses 50 T1DM 50 gene APOE 50 nonsense mutations 50 BRCA2 gene 50 DRD2 50 Bacterial vaginosis 50 congenital abnormalities 50 fructose intake 50 SERT gene 50 asthma eczema 50 Irva Hertz Picciotto 50 dizygotic twins 50 phthalate exposure 50 causal variants 50 hereditary deafness 50 tau mutation 50 herpes simplex encephalitis 50 HER2 expression 50 brain neurochemistry 50 gestational diabetes mellitus GDM 50 HER2 overexpression 50 epigenetic silencing 50 diabetic kidney 50 PBDE exposure 50 circulating estrogens 50 genomic alterations 50 chlamydial 50 cyclin E 50 overactivation 50 aberrant methylation 50 defective gene 50 HFE gene 50 PTEN gene 50 genetic ancestry 50 vascular inflammation 50 recessive trait 50 fatty acid metabolism 50 CHRNA5 50 metabolic alterations 50 metabolic dysfunction 50 elevated triglycerides 50 protein kinase C 50 blood clotting disorders 50 TOMM# 50 circadian genes 50 muscular dystrophies 50 gene rearrangements 50 neuroglobin 50 gallstone formation 50 calcium excretion 50 COX enzymes 50 biochemical abnormalities 50 dietary sodium 50 VHL gene 50 PIK3CA 50 cortisol hormone produced 50 prenatal testosterone 50 alexithymia 50 ALK mutations 50 psychobiological 50 androgenic hormones 50 H. pylori infection 50 Alzheimer disease vascular dementia 50 amyloid plaque formation 50 RIP1 50 gene expression 50 dietary interventions 50 phytoestrogens 50 chromosome abnormalities 50 promoter methylation 50 autistic traits 50 plasma lipid 50 Lp PLA2 50 oestrogens 50 precursor lesions 50 anal cancers 50 MTHFR gene 50 Chronic inflammation 50 Genetic testing 50 recurrent miscarriage 50 misregulation 50 diabetic microvascular complications 50 cardiac fibrosis 50 B# deficiency 50 serum selenium 50 bacteria Streptococcus pneumoniae 50 Rh factor 50 cardiovascular disease hypertension 50 melatonin receptor 50 ADAMTS# 50 IKK2 50 PTEN protein 50 BCL#A 50 CHEK2 50 RUNX3 50 multigenic 50 autism spectrum disorders ASDs 50 neurobiological mechanisms 50 CaM kinase II 50 coronary calcification 50 impaired glucose metabolism 50 evolutionarily conserved 50 biologic plausibility 50 leaky gut 50 El Sohemy 50 dysbindin 50 Li Fraumeni 50 methylation 50 vitamin D insufficiency 50 atopic 50 lupus scleroderma 50 glucocorticoid hormones 50 APOE allele 50 human microbiome 50 airborne fungal spores 50 T2D 50 neuropathologic 50 GPC5 50 autosomal dominant inheritance 50 atherogenesis 50 C. neoformans 50 RBP4 50 Hakonarson 50 Contagious yawning 50 S#A# [002] 50 vitamin D receptors 50 epigenome 50 folic acid intake 50 microRNA expression 50 unmeasured confounding 50 estrogen deficiency 50 estrogenic effects 50 MEF2A 50 trans palmitoleate 50 MC1R gene 50 signaling pathways 50 SRBD 50 placental hormones 50 clinically heterogeneous 50 dominantly inherited 50 molecular pathway 50 BRCA2 gene mutations 50 Ovary removal 50 genomic variation 50 DRD2 gene 50 Cowden syndrome 50 fetal malformations 50 myeloproliferative disorders 50 sexual dimorphism 50 dysregulated 50 myopathies 50 liver fibrosis 50 ABCB1 50 synaptogenesis 50 rs# [002] 50 adiposity 50 albuminuria 50 monoclonal gammopathy 50 #q#.# [002] 50 BRCA2 mutation 50 ACE2 50 lactose malabsorption 50 cotinine levels 50 C. pneumoniae 50 gene predisposing 50 histone methylation 50 MTHFD1L gene 50 allelic variation 50 YKL 50 chitinase 50 subsyndromal 50 BRIP1 50 hydrops 50 Genes 50 telomere shortening 50 proband 50 olfactory dysfunction 50 uncharacterized genes 50 endocrine disruption 50 ADPKD 50 MC1R 50 underdiagnosis 49 neurofibrillary tangles 49 biochemical pathways 49 p# mutation 49 familial polyposis 49 genotype 49 teratogens 49 CYP#B# 49 microglial 49 neurexins 49 physiological 49 STK# gene 49 CYP#E# gene 49 precancerous tumors 49 cryptogenic 49 imatinib resistance 49 cardioprotective effects 49 lignan intake 49 male hormone androgen 49 hemochromatosis 49 proinflammatory 49 KIAA# 49 podocyte 49 intestinal inflammation 49 biochemical imbalance 49 lymphocyte activation 49 autistic regression 49 degenerative neurological diseases 49 ApoE4 49 Dravet syndrome 49 histocompatibility 49 chorioamnionitis 49 Postnatal depression 49 colorectal carcinogenesis 49 metabolites 49 mammary gland tumors 49 Leydig cell 49 serotonin transporter gene 49 occupational exposures 49 nonalcoholic steatohepatitis NASH 49 preeclampsia 49 NF1 49 VLDL cholesterol 49 XMRV infection 49 lactose tolerance 49 MAOA gene 49 mitochondrial function 49 multifactorial disease 49 intestinal polyps 49 Vitamin B# deficiency 49 BMPR2 49 caveolin 49 oxysterols 49 polyamines 49 enterovirus infection 49 receptor gene 49 insulin resistance precursor 49 hypocretin 49 IGFBP 3 49 HPA axis 49 hydroxyvitamin D levels 49 tryptase 49 acetylation 49 mitochondrial DNA mtDNA 49 immunological 49 dietary acrylamide 49 glucocorticoids 49 elevated serum ALT 49 genus Plasmodium 49 dysbindin gene 49 APOE 49 cystatin C 49 biochemical imbalances 49 multidrug resistance 49 toxoplasma 49 CFTR gene 49 Treg cell 49 postmenopausal breast cancer 49 overactivated 49 toxoplasmosis 49 physiologic mechanisms 49 STK# [002] 49 Imprinted genes 49 diffuse gastric 49 CETP gene 49 TRAF1 C5 49 heritable disorders 49 hypertrophic cardiomyopathy HCM 49 Genetic Variation 49 maintaining cardiorespiratory fitness 49 synapse formation 49 Familial hypercholesterolemia 49 IRAK1 49 JAK mutations 49 corticosterone levels 49 Irritable bowel syndrome IBS 49 Notch signaling 49 UVB induced 49 lymphatic cancers 49 allergic diseases 49 death syndrome SIDS 49 orofacial clefts 49 abnormal lipid levels 49 E4 variant 49 Atopic dermatitis 49 ciliopathies 49 dietary patterns 49 nNOS 49 genes BRCA1 49 dopamine D2 receptors 49 pleiotropic effects 49 genes predispose 49 act synergistically 49 periodontal diseases 49 glutamate signaling 49 chromatin structure 49 bowel polyps 49 folic acid deficiency 49 2 diabetes T2D 49 macrovascular complications 49 ABO blood 49 metabolic pathways 49 DNA demethylation 49 pressure natriuresis 49 periodontitis 49 mucins 49 arterial calcification 49 Wwox 49 MSH2 49 paternal lineages 49 hormone disrupting 49 SSc 49 linkage disequilibrium 49 oncogenic 49 mammary cells 49 platelet activation 49 neuro developmental disorder 49 journal Nature Genetics 49 Karayiorgou 49 intracellular signal transduction 49 receptor gamma 49 obstructive lung 49 NNRTI resistance 49 DISC1 49 Apobec3 49 immunopathology 49 susceptibility alleles 49 exomes 49 parkin gene 49 Notch1 49 haemochromatosis 49 Stress hormones 49 gut bacteria 49 Wolbachia 49 tumor suppressor gene 49 leukaemias 49 hypothalamic pituitary adrenal axis 49 tyrosine phosphorylation 49 progranulin mutations 49 dermatomyositis 49 glucose intolerance 49 Bardet Biedl syndrome 49 psychiatric comorbidity 49 miRNA genes 49 IDH1 mutations 49 CEACAM1 49 CA MRSA infections 49 hippocampal function 49 abnormal growths 49 glucose abnormalities 49 allergic dermatitis 49 neurochemistry 49 gynecologic malignancy 49 telomere dysfunction 49 dietary antioxidants 49 immunodeficiency diseases 49 demethylation 49 hormone cortisol 49 SNPs 49 endotoxin exposure 49 neuropathological 49 bronchopulmonary dysplasia 49 nucleus Chinnery 49 beta HCH 49 immunodeficiency 49 caffeine intake 49 bacteria Helicobacter pylori 49 mammary tumors 49 genotoxic stress 49 confounding factors 49 allostatic load 49 alpha thalassemia 49 Alzheimer Disease AD 49 observable traits 49 progranulin gene 49 selenium intake 49 Raf MEK ERK 49 abnormal methylation