Related by context. All words. (Click for frequent words.) 60 heritable 57 polygenic 55 highly heritable 53 inherited predisposition 53 heritable traits 53 nondemented 53 recessive trait 53 autosomal recessive 53 genes predisposing 53 familial aggregation 53 Genetic variations 53 recessive genetic 53 multigenic 53 APOE genotype 52 p# mutations 52 underlying pathophysiology 52 inherited mutations 52 Genetic variation 52 epigenetic changes 52 familial pancreatic cancer 51 genetic predisposition 51 Genetic predisposition 51 phenotypic expression 51 observable traits 51 susceptibility genes 51 psychiatric comorbidity 51 Meckel Gruber 51 nonhereditary 51 hereditary hemochromatosis 51 de novo mutations 51 chromosomal instability 51 autosomal dominant 50 potentially modifiable 50 MYH9 gene 50 heritable diseases 50 germline mutations 50 Mendelian 50 inherited genetic mutations 50 inheritability 50 LRRK2 mutations 50 autosomal dominant disorder 50 spastic paraplegia 50 p# mutation 50 assortative mating 50 Telomere length 50 biochemical imbalances 50 monogenic 50 Kufs disease 50 hereditary predisposition 49 endophenotypes 49 inherit predisposition 49 sporadic ALS 49 untreated celiac disease 49 IKZF1 49 hippocampal function 49 FTLD 49 phenotypic variation 49 PTEN mutations 49 multisystem disease 49 mitochondrial mutations 49 missense mutations 49 aetiological 49 Genetic variants 49 hereditary 49 modifier genes 49 Li Fraumeni syndrome 49 auditory neuropathy 49 cryptogenic 49 GSTM1 gene 49 nongenetic 49 Klinefelter syndrome 49 Lysosomal storage 49 chronicity 49 causal pathway 49 basal cell nevus syndrome 49 subfertility 49 familial adenomatous polyposis 49 familial ALS 49 TP# mutation 49 MC1R 49 atopic 49 predisposing factors 49 exfoliation glaucoma 49 phenotypic variability 49 dominantly inherited 49 hereditary blindness 48 obesity sedentary lifestyle 48 Lafora disease 48 monogenic disorders 48 apoC III 48 chromosomal rearrangement 48 Ets2 48 sociodemographics 48 intestinal polyps 48 testicular germ cell 48 familial adenomatous polyposis FAP 48 deleterious mutations 48 hyper IgE syndrome 48 Inherited 48 lysosomal storage diseases 48 primary ciliary dyskinesia 48 cardiac channelopathies 48 Heritability 48 hyperinsulinism 48 PON1 48 trustor 48 phenotype 48 metabolic abnormalities 48 causally linked 48 spontaneous mutations 48 LRRK2 gene 48 spastic diplegia 48 testicular tumors 48 Genetic mutations 48 Brugada syndrome 48 causative genes 48 autosomal dominant inheritance 48 chronic relapsing 48 autoinflammatory diseases 48 thiopurine 48 heritable component 47 genetically inherited 47 sociodemographic variables 47 arterial calcification 47 comorbid disorders 47 ataxias 47 neuropsychological impairments 47 MC1R gene 47 prothrombotic 47 maternally inherited 47 CCR5 delta# 47 familial clustering 47 Tay Sachs thalassemia 47 induced cardiomyopathy 47 neuropsychological deficits 47 heritable trait 47 biological predisposition 47 premorbid 47 leptin deficiency 47 PTEN gene 47 cyclin E 47 genetic abnormality 47 neural crest 47 Vitamin B# deficiency 47 alkalosis 47 alpha syn 47 hydrops 47 mitochondrial disorders 47 chromosome abnormality 47 androgen deficiency 47 evolvability 47 subclinical 47 airway responsiveness 47 APOE ε4 47 autosomal recessive disease 47 cardiac fibrosis 47 epileptogenic 47 psychosocial functioning 47 autosomal recessive genetic 47 chromosomal anomalies 47 observable characteristics 47 clefting 47 GBA mutations 47 genetic predispositions 47 IgA deficiency 47 G6PD deficiency 47 gallstone disease 47 narcolepsy cataplexy 47 TACI mutations 47 SRY gene 47 alexithymia 47 breast endometrial 47 genetic polymorphism 47 Von Willebrand disease 47 puerperal psychosis 47 remains mystery Yairi 47 hereditary spastic paraplegia 47 epigenetic markers 47 WAGR syndrome 47 HLA genes 47 genomic imprinting 47 CHD7 47 Cognitive impairment 47 G#S mutation 47 mosaicism 47 homozygosity 47 mtDNA mutations 47 alpha synuclein protein 46 motor neuron degeneration 46 etiologic 46 proband 46 Hashimoto thyroiditis 46 lysosomal storage disease 46 lung epithelium 46 GSTT1 46 neurobiological basis 46 confounding variables 46 monocots 46 genetic syndromes 46 renal fibrosis 46 socioeconomic deprivation 46 undiagnosed celiac disease 46 developmental abnormalities 46 advanced glycation endproducts 46 dementia praecox 46 heredity 46 chromosomal regions 46 familial hypercholesterolemia 46 behavioral disinhibition 46 ORMDL3 46 KIBRA 46 Male pattern baldness 46 radiosensitive 46 ABCB1 46 diabetic kidney 46 multifactorial 46 hypercoagulability 46 Vascular dementia 46 inter vivos trust 46 DQB1 * 46 hereditary disorders 46 pre malignant lesions 46 genetic alteration 46 regulates gene expression 46 MAOA gene 46 underactive thyroid gland 46 airflow limitation 46 genetic susceptibility 46 obstructive lung 46 genetically predetermined 46 myeloproliferative neoplasms 46 comorbid psychiatric 46 susceptibility gene 46 fatal neurodegenerative disorder 46 innate tendency 46 dyslipidemia hypertension 46 GABRA2 gene 46 neurodevelopmental disorder 46 Nicotine dependence 46 HNPCC 46 ABCB1 gene 46 BMPR2 46 heritable disorders 46 Hair follicles 46 uncharacterized 46 #q#.# deletion syndrome 46 shorter telomere length 46 neurogenetic 46 genetic loci 46 atrophic gastritis 46 referable 46 parkinsonism 46 metabolomic profiles 46 somatoform disorder 46 proximal colon 46 artifactual 46 #q# deletion 46 immunodeficiency disorder 46 noncognitive 46 somatoform disorders 46 Hurthle cell 46 mitochondrial defects 46 Spinal muscular atrophy 46 cystic fibrosis chronic pancreatitis 46 Joubert syndromes 46 Genetic abnormalities 46 FGFs 46 Predisposition 46 hormonal abnormalities 46 allelic variation 46 orthologous genes 46 olfactory dysfunction 46 ALI ARDS 46 gestational diabetes mellitus 46 APOE4 46 mitochondrial DNA mutations 46 ZNF# 46 thyroid dysfunction 46 neoplastic 46 recessive genes 46 inherited genetic mutation 46 DNA methylation patterns 46 #q#.# [001] 46 recessive inheritance 46 JAK2 mutation 46 metabolic disturbances 46 DHEAS 46 PTPN# 46 hypogonadotropic hypogonadism 46 genetic defects 46 HYPP 46 nonvascular 46 spinocerebellar ataxia 46 mutated K ras 45 retinitis pigmentosa RP 45 #q#.# [002] 45 dyskeratosis congenita 45 Von Hippel Lindau 45 genetic makeups 45 VHL gene 45 CYP#E# gene 45 congenital disorders 45 phenotypes 45 maternally transmitted 45 molecular abnormalities 45 MEF2A 45 autoimmune thyroid 45 chromosomal disorders 45 arteriosclerotic 45 transgene expression 45 neuropsychiatric disorder 45 digest lactose 45 FUS protein 45 correlated 45 incurable genetic 45 amenorrhoea 45 AAT deficiency 45 elevated triglyceride levels 45 eusociality 45 abnormal proteins 45 cohabiting relationships 45 immunodeficient 45 atopy 45 aneuploid cells 45 monozygotic twins 45 Uveal melanoma 45 allostatic load 45 eusocial 45 tertiary syphilis 45 UGT#B# 45 impaired glucose metabolism 45 Cowden syndrome 45 heritable variation 45 psychosocial variables 45 microdeletions 45 chromosomal deletions 45 immunodeficiencies 45 cartilage tendons 45 recessive mutations 45 heterozygote 45 abnormal lipids 45 nonalcoholic steatohepatitis 45 amyloid pathology 45 generalized epilepsy 45 psychosocial stressors 45 autosomal 45 presymptomatic 45 sociodemographic factors 45 herpesviruses 45 mental retardation syndromes 45 polyglutamine diseases 45 nephron 45 HLA molecules 45 EBV infection 45 tumoral 45 TCF#L# gene 45 Shy Drager syndrome 45 huntingtin gene 45 nucleosome positioning 45 modifiable 45 TPMT 45 CHD5 45 transcriptional silencing 45 channelopathies 45 genetically predisposed 45 Fatty liver 45 Celiac sprue 45 subclinical atherosclerosis 45 societal stigma 45 hyperinsulinemia 45 comorbid illnesses 45 prosopagnosia 45 chronic obstructive airway 45 distinct subtypes 45 myeloproliferative 45 incomplete penetrance 45 CHRNA5 gene 45 heterotaxy 45 genes predispose 45 outcrossing 45 systemic inflammation 45 Malignant mesothelioma 45 piRNAs 45 salivary amylase 45 HLA DRB1 45 Myostatin 45 Personality traits 45 epigenetically 45 androgenic hormones 45 CYP#A# gene 45 virulence genes 45 mammary gland tumors 45 unmeasured factors 45 CYP#D# gene 45 methylation patterns 45 chromosomal translocations 45 mGluR 45 5q 45 Settlor 45 malignant phenotype 45 gene locus 45 axonal damage 45 dysfunctioning 45 TRIM5 45 male reproductive tract 45 systemic amyloidosis 45 embryonal 45 nonischemic 45 incurable degenerative 45 homocystinuria 45 pericardial mesothelioma 45 hereditary pancreatitis 45 metabolic dysfunction 45 germline cells 45 druggable 45 metabolic abnormality 45 leaky gut 45 Hyperthyroidism 45 genetic polymorphisms 45 muscular dystrophies 45 alpha thalassemia 45 oligomeric 45 nerve degeneration 45 Rh factor 45 MYH9 45 compulsive hoarding 45 diffuse gastric 45 aldehyde dehydrogenase 45 Vitamin D insufficiency 45 neuroligins 45 synovial cells 45 primary biliary cirrhosis 45 genomic alterations 45 negative affectivity 45 inherited retinal degeneration 45 genetic abnormalities 45 paternally inherited 45 brain lesions 45 neurological abnormalities 45 bacteria Helicobacter pylori 45 internalizing disorders 45 temper dysregulation disorder 45 Rh incompatibility 45 thyroid hormone deficiency 45 coagulopathy 45 inheritable genetic 45 fat malabsorption 45 MTHFR 45 hereditary nonpolyposis colorectal cancer 45 neurodegenerative disorder 45 evolutionarily novel 45 motor neuron diseases 45 lactase deficiency 45 primary ovarian insufficiency 45 familial predisposition 45 APOE gene 45 dying intestate 45 Heredity 44 sociodemographic characteristics 44 Compulsive hoarding 44 predisposing 44 epigenetic reprogramming 44 periodontal infection 44 neurological degeneration 44 progressive neurodegenerative disorder 44 sexually dimorphic 44 maladaptive 44 oxidases 44 genetic variants associated 44 psychogenic 44 gastric carcinoma 44 concessionally taxed 44 hyperparathyroidism 44 polygynous 44 ADPKD 44 spongiform encephalopathies 44 BARD1 44 progressive neurodegenerative disorders 44 LIS1 44 airway remodeling 44 periodontal pathogens 44 #q# [001] 44 aY chromosome 44 insulin resistance syndrome 44 aniridia 44 incurable neurodegenerative disease 44 inherited neurological disorder 44 fatal neuromuscular disorder 44 apolipoprotein E4 44 Leber congenital amaurosis LCA 44 ontogenetic 44 extramedullary 44 shortened lifespan 44 muscle dysmorphia 44 vascular cognitive impairment 44 obstructive coronary artery 44 hypercalciuria 44 carbohydrate intolerance 44 androgen depletion 44 neurosensory 44 hormonally sensitive 44 Li Fraumeni 44 germline 44 autosomal recessive disorder 44 imprinted genes 44 HGPS 44 hypertrophic 44 debilitating neurodegenerative 44 NPM1 gene 44 myotonic dystrophy 44 predisposed 44 Myotonic dystrophy 44 familial hypercholesterolemia FH 44 APOE e4 44 determinates 44 gut microbes 44 metabolic derangement 44 Canavan Disease 44 differential gene expression 44 habitual snoring 44 Lactose intolerance 44 holoprosencephaly 44 nonmarital 44 pathogenic mutations 44 genetically disposed 44 myopathies 44 Postnatal depression 44 elevated serum ALT 44 epigenetic alterations 44 debilitating neurodegenerative disorder 44 T1DM 44 polyp recurrence 44 misregulation 44 unfavorable prognostic 44 fronto temporal dementia 44 neural substrates 44 chromosomal alterations 44 premature ovarian 44 epigenetic marks 44 genetically homogeneous 44 therapeutically beneficial 44 ovarian hormones 44 metaplasia 44 GABRA2 44 MLH1 44 MGUS 44 Protein Kinase C 44 progranulin gene 44 Dysregulation 44 leptin resistant 44 Retinitis pigmentosa 44 Congenital Adrenal Hyperplasia 44 PHLPP 44 hamartomas 44 granulosa cell 44 Sjögren syndrome 44 gene APOE4 44 muscular dystrophy cystic fibrosis 44 SORL1 gene 44 MSH2 44 von Hippel Lindau 44 leukemia inhibitory 44 modifiable lifestyle 44 Chronic pancreatitis 44 hypovitaminosis D 44 non polyposis colorectal 44 variable immunodeficiency 44 liver metastasis 44 β amyloid 44 pathogenetic 44 progranulin mutations 44 paraneoplastic 44 elevated fasting glucose 44 odorant receptor 44 irregular menses 44 genetically susceptible 44 Angelman syndrome 44 LQTS 44 QPRT 44 Menkes disease 44 Socioeconomic factors 44 Polycomb proteins 44 excitotoxic 44 psychotic illnesses 44 Dwarfism 44 penetrance 44 Neuroticism 44 Neuregulin 1 44 Hip dysplasia 44 alpha catenin 44 carbohydrate polymers 44 gastric atrophy 44 cognitively intact 44 mutations 44 plasma lipid 44 abnormal glucose metabolism 44 neurogenerative diseases 44 Hutchinson Gilford progeria 44 totipotent 44 TNF blocker therapy 44 microdeletion 44 hypertension diabetes mellitus 44 estrogen metabolism 44 vasopressin receptors 44 etiological 44 genetic determinants 44 gene polymorphisms 44 gastric carcinomas 44 Bacteroides 44 heterozygous 44 Prostate enlargement 44 Chronic Lyme disease 44 unmeasured confounders 44 clinico pathological 44 SIRT3 44 parkinsonian 44 nonworking spouse 44 conserved sequences 44 MECP2 gene 44 frontotemporal 44 genetic alterations 44 filaggrin 44 Severe Combined Immunodeficiency 44 anosognosia 44 Usher Syndrome 44 biochemical imbalance 44 de ath 44 cause cardiac channelopathies 44 cystic kidney 44 susceptibility alleles 44 circadian clock genes 44 Diverticulosis 44 #q# deletion syndrome 44 Caspases 44 Androgenetic alopecia 44 modifiable risk 44 transgenic mice expressing 44 uncurable 44 underlying molecular mechanisms 44 frontotemporal dementia 44 familial polyposis 44 APOL1 44 megacolon 44 adenomatous polyps 44 impaired insulin secretion 44 STAT4 44 pleiotropic effects 44 selfing 44 hereditary deafness 44 heritability 44 Polymorphic Ventricular Tachycardia CPVT 44 chronic hepatitis cirrhosis 44 Coeliac disease 44 alpha synuclein gene 44 sporadic Creutzfeldt Jakob 44 pulmonary hypertension PH 43 dopamine receptor gene 43 monogenic diabetes 43 Modifiable risk 43 bone marrow mesenchymal stem 43 maternally derived 43 leukodystrophies 43 androgen excess 43 AUDs 43 hereditary diseases 43 BRCA1 mutations 43 ichthyosis vulgaris 43 prostate carcinogenesis 43 multiorgan 43 cystic fibrosis sickle cell 43 #p#.# [001] 43 prion infection 43 SMAD4 43 DICER1 gene 43 lactational 43 revocable trusts 43 epigenetic modification 43 C. neoformans 43 myeloproliferative neoplasms MPNs 43 genetically wired 43 sickle cell cystic fibrosis 43 nonspousal 43 constitutively expressed 43 karyotypes 43 gallstone formation 43 renal scarring 43 fibrodysplasia ossificans progressiva FOP 43 BRCA mutation 43 IPAH 43 etiologic agent 43 congential 43 atherothrombotic 43 Pdx1 43 predispose 43 TCF#L# 43 CNTNAP2 43 sibling grandparent 43 autistic traits 43 epididymitis 43 dyscalculia 43 DICER1 43 Nutritional deficiencies 43 leptin resistance 43 Neurofibromatosis type 43 recurrent UTI 43 related maculopathy 43 dysregulated 43 Worthingtons testified 43 Pulmonary hypertension 43 epigenetic modifications 43 MHC genes 43 microvascular dysfunction 43 genomewide 43 dischargeable 43 teratogens 43 epigenetic inheritance 43 Agreeableness 43 multivariable analysis 43 pleiotropy 43 transitivity 43 Wernicke Korsakoff syndrome 43 Pernicious anemia 43 Imprinted genes 43 IHT liability 43 synaptogenesis 43 heterozygosity 43 genital ulcer 43 inbred strains 43 pilocytic astrocytomas 43 P. aeruginosa infection 43 Mitral regurgitation 43 BRCA2 breast cancer 43 multifactorial disease 43 dysfunctional voiding 43 Immediate annuities 43 VUR 43 β cell 43 elevated CRP 43 Bacterial vaginosis 43 terminally differentiated 43 cardiomyopathies 43 Leydig cell 43 nucleus Chinnery 43 Bardet Biedl Syndrome 43 constitutively active 43 CDH1 43 ARID1A 43 neuroinflammation 43 elevated IOP 43 premalignant 43 IDH mutations 43 deficiency syndrome 43 myalgic encephalomyelitis ME 43 FMRP protein 43 genetic traits 43 SSc 43 epigenetic 43 XMRV infection 43 CHI#L# 43 aneuploidies 43 dizygotic twins 43 ribosomal genes 43 metastatic lymph nodes 43 IL#R 43 neuro degenerative 43 Treg cell 43 pretransplant 43 apolipoprotein E gene 43 ploidy 43 invasive carcinoma 43 Eukaryotes 43 viral etiology 43 Severe acne 43 compulsive hoarding syndrome 43 e4 allele 43 HFE gene 43 multiplicative 43 SE alleles 43 obstructive CAD 43 body fatness 43 Psychiatric disorders 43 gene APOE 43 allergic sensitization 43 prostate cancer CaP 43 glycated 43 BRCA1 BRCA2 43 negatively correlated 43 testamentary trusts 43 etiologic factors 43 fluid shear 43 genetic trait 43 progressive neurodegenerative 43 genetic mutations 43 coinfection 43 Ovary removal 43 endogenous hormones 43 genetic susceptibilities 43 neurodegenerative disorder characterized 43 Hormonal imbalance 43 cardiac insufficiency 43 Leber Congenital Amaurosis LCA 43 extracolonic 43 settlors 43 hyperactivated 43 causal variants 43 Endocannabinoids 43 socioeconomic status 43 Oxidative stress 43 TTR amyloidosis 43 BRCA2 gene 43 Mental retardation 43 nicotinic receptor 43 neurocognitive impairment 43 coma convulsions 43 polyploid 43 HIV HCV coinfected 43 immunocompromised individuals 43 human leukocyte antigens 43 hypochondriasis 43 annuitize 43 OPRM1 gene 43 Hurler syndrome 43 alzheimer disease 43 nonconscious 43 Socioeconomic status 43 pathophysiological mechanisms 43 pattern baldness 43 M. catarrhalis 43 HLAs 43 immunologically matched 43 microscopic colitis 43 Down syndrome spina bifida 43 oncogenic mutations 43 ApoE gene 43 pituitary tumors 43 Eisenmenger syndrome 43 incompletely understood 43 Dilated cardiomyopathy 43 Runx1 43 hormone imbalances 43 untreated hypothyroidism 43 Stress hormones 43 Dental caries 43 osteoporosis brittle bones 43 representative payees 43 MetS 43 epigenetic mechanisms 43 Viral infections 43 D3 receptors 43 Grantor Retained Annuity Trusts 43 carcinoids 43 predisposition 43 pathophysiological 43 hormone aldosterone 43 beta adrenergic receptor 43 recessive 43 FOXO3a 43 cryptorchidism 43 testamentary trust 43 renal tubular 43 colorectal carcinogenesis 43 cardiovascular disease hypertension 43 microvascular disease 43 apoptosis pathway 43 hypercholesterolaemia 43 Soy isoflavones 43 2D 4D ratio 43 histological subtype 43 apoptosis induced 43 Pelvic inflammatory 43 determinants 43 syndromic 43 asymptomatic bacteriuria 43 herpes viruses 43 LHON 43 abnormal prion protein 43 serum BDNF 43 genomic variants 43 Multivariate analysis 43 Froguel 43 amyloidogenic 43 lichen planus 43 apoE 43 retinal dysfunction 43 telomere DNA 43 affective psychoses 42 subclinical hyperthyroidism 42 androgen signaling 42 PI3K signaling 42 Fragile X gene 42 Hypertensive heart 42 decompensated cirrhosis 42 infants Sundlof 42 diabetes insipidus 42 nosology 42 hypoxemia 42 Gestational 42 facioscapulohumeral muscular dystrophy 42 euthymic patients 42 Serum calcium 42 G#S [002] 42 poorer prognosis 42 oxidized phospholipids 42 Helicobacter 42 microbiota 42 bronchopulmonary dysplasia BPD 42 neuropathological 42 serum IGF 42 congenital anomalies 42 elevated LDH 42 TP# mutations 42 autoinflammatory 42 diabetes hypertension hyperlipidemia 42 VCFS 42 estrogenic effects 42 TGFBR1 * 6A 42 Or#b 42 synaptic function 42 congenital deficiency 42 polycystic kidneys 42 Mendelian disorders 42 multisystemic 42 withholdable payment 42 testicular dysgenesis syndrome 42 socioeconomic variables 42 allelic 42 Pleural plaques 42 M. pneumoniae 42 imperfecta 42 medically unexplained 42 ovarian dysfunction 42 autonomic dysfunction 42 immunodeficiency diseases 42 Alpha synuclein 42 Longitudinal studies 42 spontaneous remission 42 IUGR 42 molecular determinants 42 genus Plasmodium 42 hypertrophic cardiomyopathy HCM 42 breast cancer genes BRCA1 42 atopic disorders 42 mediastinitis 42 myelodysplasia 42 maturational 42 extrinsically 42 coinfections 42 NAFLD 42 meiotic recombination 42 MAOA 42 TMPRSS2 ERG fusion 42 inheritable diseases 42 resistin 42 Genetic mutation 42 Mitochondrial dysfunction 42 somatic symptoms 42 chromosomal rearrangements 42 prodynorphin 42 non ulcer dyspepsia 42 CETP gene 42 communicable chronic 42 neuritic 42 homozygous 42 stimulate neurogenesis 42 severe periodontitis 42 hormonal imbalances 42 pathophysiologic 42 H pylori 42 thyrotropin 42 Multivariate analyzes 42 morphologic 42 neurologic dysfunction 42 mutated gene 42 BRCA2 mutations 42 nephritis 42 hypercoagulable 42 malignant transformation 42 lactose malabsorption 42 systemic scleroderma 42 Cystic fibrosis CF 42 pleiotropic 42 hippocampal dysfunction 42 epithelial barrier 42 haemochromatosis 42 TT genotype 42 collagen vascular 42 degenerative neurological 42 Genetic susceptibility 42 post transplant lymphoproliferative 42 deafness neurological 42 K ras mutation 42 AAT Deficiency 42 metazoan 42 survial 42 consanguineous marriage 42 aetiology 42 insulin resistant 42 degenerative disorder 42 A. thaliana