Related by context. All words. (Click for frequent words.) 64 Heredity 63 genetic predisposition 62 genetics 61 hereditary 59 genetic susceptibility 58 epigenetic changes 58 heritable 55 nongenetic 55 polygenic 55 Genetic predisposition 55 Mendelian 55 assortative mating 55 genetic makeup 54 genetic 54 genes 53 inherited genetic mutations 53 biological predisposition 53 MYH9 53 genetic predispositions 52 genetically inherited 52 mitochondrial mutations 52 recessive genetic 52 recessive trait 52 genomic imprinting 52 Male pattern baldness 52 Helicobacter 51 phenotypic variation 51 autosomal dominant inheritance 51 mtDNA mutations 51 Genetic variation 51 autosomal recessive 51 SRY gene 51 mitochondrial defects 51 evolutionarily speaking 51 multifactorial 51 gut microbes 51 Lamarckian 50 genetic mutations 50 de novo mutations 50 monozygotic twins 50 dominantly inherited 50 unmeasured factors 50 subfertility 50 Oxidative stress 50 phenotypic expression 50 placental hormones 50 inherit predisposition 50 potentially modifiable 50 epigenetic inheritance 50 Genes 50 hippocampal function 49 Genetic variants 49 epigenetic modifications 49 Socioeconomic status 49 Eukaryotes 49 aetiological 49 genetic determinants 49 inbreeding depression 49 genetically predisposed 49 familial clustering 49 hereditary predisposition 49 maternally inherited 49 neural crest 49 nonhereditary 49 hormonal imbalances 49 phenotypic variability 49 TCF#L# gene 49 imprinted genes 49 recessive genes 49 inherited mutations 49 epigenetic regulation 49 causative genes 49 genetically predetermined 49 developmental abnormalities 48 Mendelian genetics 48 highly heritable 48 PTEN mutations 48 genetic susceptibilities 48 Hip dysplasia 48 intracellular signal transduction 48 Fragile X gene 48 cardiac fibrosis 48 CHD7 48 familial pancreatic cancer 48 inherited predisposition 48 APOE gene 48 evolvability 48 underlying pathophysiology 48 genes predispose 48 autosomal dominant disorder 48 predisposing factor 48 inborn 48 nephron 48 patrilineal 48 nongenetic factors 48 STAT4 48 fetal microchimerism 48 heritability 48 epigenetics 48 Chronic inflammation 48 biopsychosocial 48 periodontal infection 48 hereditary disorders 48 APOE ε4 48 pathophysiological 48 familial polyposis 48 MHC genes 48 Genetic mutations 48 ataxias 48 spontaneous mutation 48 familial aggregation 47 CNTNAP2 47 Bacterial vaginosis 47 menarche 47 developmental trajectories 47 chromosomal anomalies 47 mitochondrial dysfunction 47 airway remodeling 47 Dwarfism 47 mosaicism 47 hormone imbalances 47 socioeconomic status 47 genetic alterations 47 epigenetic alterations 47 genetic variation 47 genetically 47 TACI mutations 47 obesity sedentary lifestyle 47 spontaneous mutations 47 remains mystery Yairi 47 paternal lineage 47 homeobox genes 47 VHL gene 47 physiological mechanisms 47 intersexuality 47 gut microbiota 47 Telomere shortening 47 fatty liver disease 47 insulin signaling pathway 47 MC4R gene 47 estrogen metabolism 47 eusocial 47 HLA DRB1 47 epigenetic modification 47 testicular tumors 47 neurochemistry 47 Heritability 47 serotonin deficiency 47 STK# gene 47 recessive inheritance 47 genetic recombination 47 periodontal infections 47 Rh factor 47 CYP#A# gene 47 Bardet Biedl Syndrome 47 evolutionary origins 47 chorioamnionitis 47 shorter telomeres 47 epigenetic 46 LRRK2 gene 46 evolutionary adaptation 46 genetic makeups 46 synaptic function 46 Hereditary 46 genetic imprinting 46 intestinal microbiota 46 dizygotic twins 46 FASPS 46 hereditary deafness 46 eusociality 46 IRF6 46 congential 46 causal pathway 46 inheritable 46 APOE genotype 46 shorten telomeres 46 Pseudomonas syringae 46 neurobiological 46 hormonal abnormalities 46 genetic syndromes 46 apolipoprotein E gene 46 heritable variation 46 Ashkenazi Jews 46 epigenetic reprogramming 46 schizoid personality 46 paraneoplastic 46 genetic variations 46 genetic defect 46 vascular dysfunction 46 Imprinted genes 46 Autoimmune disorders 46 filaggrin gene 46 epistasis 46 physiology 46 microbiota 46 gonadal hormones 46 ApoE gene 46 aneuploidy 46 Kufs disease 46 modifier genes 46 pathophysiologic 46 mitochondrial proteins 46 ABCB1 gene 46 recessive traits 46 Von Hippel Lindau 46 telomere maintenance 46 causally linked 46 muscular dystrophy cystic fibrosis 46 Apert syndrome 46 heritable trait 46 genomic instability 46 Myotonic dystrophy 46 polydactylism 46 etiology 46 motor neuron degeneration 46 retinal dysfunction 46 genes predisposing 46 COMT gene 46 incompletely understood 46 degenerative neurological 46 GABRA2 gene 46 airborne fungal spores 46 androgen signaling 46 spatial cognition 46 lymphatic vasculature 46 Klinefelter syndrome 46 multi factorial disease 46 nucleus Chinnery 46 chromosomal instability 46 abnormal chromosomes 46 heritable disorders 46 Personality traits 46 Von Willebrand disease 46 Sarcopenia 46 SCA5 46 Fatty liver 46 p# mutations 45 phthalate syndrome 45 TP# mutation 45 MECP2 gene 45 FGFs 45 microcephalin 45 Dilated cardiomyopathy 45 dopamine receptor gene 45 clefting 45 inbred strains 45 microbiomes 45 pathophysiological mechanisms 45 metabolic 45 hormones neurotransmitters 45 aneuploidies 45 behavioral disinhibition 45 vitamin deficiency 45 Meckel Gruber 45 sexual dimorphism 45 prefrontal regions 45 IKZF1 45 Socioeconomic factors 45 Skeletal muscle 45 embryological 45 metabolic dysfunction 45 MEF2A 45 NOD2 45 Hashimoto thyroiditis 45 monogenic 45 inborn traits 45 Zinc deficiency 45 HLA genes 45 polydactyly 45 neurogenetics 45 facioscapulohumeral muscular dystrophy 45 phenotypic differences 45 bacteria Helicobacter pylori 45 lactose tolerance 45 LRRK2 mutations 45 predisposing factors 45 environmental toxicants 45 Paranthropus 45 cholesterol metabolism 45 morphogenetic 45 sexually dimorphic 45 familial adenomatous polyposis 45 masculinization 45 multigenic 45 klotho 45 biochemical imbalances 45 genetic mutation 45 savant syndrome 45 chromosomal imbalance 45 infantile amnesia 45 homophily 45 gene variants 45 chromosomal alterations 45 enterotypes 45 Mendelian disorders 45 osteodystrophy 45 LMNA 45 channelopathies 45 transgenerational 45 MYH9 gene 45 epigenetically 45 Y chromosomal 45 CYP#C# gene 45 genetic variants 45 endocannabinoid signaling 45 residual confounding 45 embryonic tissues 45 FGFR2 gene 45 terrestrial vertebrates 45 obesity insulin resistance 45 inflammatory bowel syndrome 45 predisposition 45 skeletal dysplasia 45 multi celled organisms 45 immuno deficiency 45 polyploidy 45 Societal norms 45 molecular underpinnings 45 thrifty gene 45 prostate carcinogenesis 45 genetic defects 45 misregulation 45 FTO gene 45 autism dyslexia 45 congenital disorders 45 hermaphroditism 45 neurobiological basis 45 monozygotic 45 genetic aberrations 45 GAB2 45 infertility miscarriages 45 bowel cancers 45 auditory neuropathy 45 sickle cell hemoglobin 45 Notch signaling 45 Cognitive impairment 45 mutations 45 heritable genetic 45 epigenetic marks 45 vertebrate embryos 45 allergic airway 45 rhinovirus infection 45 maternal lineage 45 epigenetic mechanisms 45 chromosomal 45 ontogeny 45 Nicotine dependence 45 hormonal disorders 44 gene 44 Vitamin D insufficiency 44 Hypertrophic cardiomyopathy 44 untreated celiac disease 44 Periodontal disease 44 Folic acid deficiency 44 microbial ecology 44 progranulin 44 Hyperthyroidism 44 susceptibility gene 44 telomere shortening 44 Hutchinson Gilford progeria 44 underactive thyroid gland 44 neuritic 44 SLC#A# gene [001] 44 mito 44 DICER1 44 maternally transmitted 44 evolutionary genetics 44 inheritable genetic 44 modifiable lifestyle 44 physiological 44 DNA methylation patterns 44 primate lineage 44 adult neurogenesis 44 autosomal dominant 44 diathesis 44 FMRP protein 44 FOXM1 44 Genetic mutation 44 mammary gland tumors 44 dysgenesis 44 telomere dysfunction 44 Genetic variations 44 Picky eating 44 Oxidative damage 44 etiological 44 peptic ulcer disease 44 gene mutation 44 morphological traits 44 lactase deficiency 44 Androgenetic alopecia 44 psychobiological 44 striated muscle 44 psychogenic 44 neurogenetic 44 histone methylation 44 lymphocyte activation 44 disregulation 44 neurodevelopmental disorder 44 gene duplications 44 podocyte 44 achondroplasia 44 Maternal obesity 44 leptin deficiency 44 chromosomal rearrangement 44 anatomic abnormalities 44 orthologous genes 44 induced cardiomyopathy 44 IGF1 44 APOL1 44 chromosome deletion 44 hormone aldosterone 44 chronicity 44 neuro endocrine 44 Chlamydia pneumoniae 44 speciation 44 cardiovascular disease hypertension 44 A. ramidus 44 predisposing 44 BRIP1 44 marsupial mammals 44 angiosperms 44 prion gene 44 epigenetic markers 44 gut flora 44 NF1 gene 44 Neanderthal extinction 44 ovarian hormones 44 mental retardation syndromes 44 HNPCC 44 hyperinsulinism 44 arteriosclerotic 44 lipid metabolism 44 structural abnormalities 44 extramedullary 44 bile acid metabolism 44 Dr. Abhimanyu Garg 44 Thyroid hormone 44 familial 44 SCN9A gene 44 genetically susceptible 44 nerve degeneration 44 Secondhand smoke exposure 44 mitochondrial DNA mtDNA 44 polycystic ovary 44 thyroid dysfunction 44 muscular dystrophies 44 Radiographic findings 44 genetic polymorphisms 44 G6PD deficiency 44 chromosomal deletions 44 cretinism 44 mutated gene 44 #q#.# deletion syndrome 44 hypertrophic cardiomyopathy HCM 44 CYP#D# gene 44 hyperinsulinemia 44 airway hyperresponsiveness 44 Excessive sweating 44 KIBRA 44 multisystem disease 44 neural plasticity 44 mechanotransduction 44 congenital abnormalities 44 microbiome 44 folate deficiency 44 socioeconomic deprivation 44 systemic inflammation 44 lipoprotein metabolism 44 apoE4 44 NRF2 gene 44 Toxoplasmosis 44 psychosocial stressors 44 neuropsychiatric disorder 44 olfactory dysfunction 44 GBA mutations 44 Inbreeding 44 undiagnosed celiac disease 44 familial predisposition 44 cryptorchidism 44 amyloid cascade 44 heritable diseases 43 GATA4 43 MC1R 43 metazoan 43 asexual reproduction 43 parasitic flatworms 43 classical CJD 43 Irva Hertz Picciotto 43 Ets2 43 bacterial flora 43 socioeconomics 43 chromosomal disorders 43 SORL1 43 chordate 43 clinicopathological 43 alpha thalassemia 43 macrovascular complications 43 etiologic 43 neuroendocrine 43 X chromosome 43 Chronic fatigue 43 thyroid hormone deficiency 43 gametophyte 43 enteroviruses 43 primate ancestors 43 multigene 43 genetic loci 43 leaky gut 43 autonomic nerve 43 evolutionarily ancient 43 dyscalculia 43 intestinal ulcers 43 neoplastic 43 genetic relatedness 43 oral cleft 43 impaired insulin secretion 43 Kapha 43 primate evolution 43 cardiomyopathies 43 Mendelian diseases 43 C. pneumoniae 43 MGUS 43 teleost fish 43 Evolutionary psychologists 43 African cichlid fish 43 involuntary tics 43 Hox gene 43 piRNAs 43 atopic disease 43 hormone adiponectin 43 genetic trait 43 Michael Kaplitt Parkinson 43 testicular dysgenesis syndrome 43 giant danio 43 cerebellar 43 deuterostomes 43 DRD2 gene 43 atopic 43 Dental caries 43 hydrops 43 KCNQ1 43 debilitating neurodegenerative disorder 43 missense mutations 43 mtDNA 43 lactase persistence 43 carcinogenesis 43 pyloric stenosis 43 masculinizing 43 ectodermal dysplasia 43 monogenic diabetes 43 congenital muscular dystrophies 43 germline mutations 43 Mitochondrial 43 microchimerism 43 breast cancer genes BRCA1 43 gene locus 43 Modifiable risk 43 sexually reproducing 43 underlying molecular mechanisms 43 Epileptic seizures 43 determinates 43 sociodemographics 43 organismal 43 Nutritional deficiencies 43 metabolic abnormality 43 pyelonephritis 43 intestinal microflora 43 HGPS 43 Chromosomal 43 Magnesium deficiency 43 genes BRCA1 43 micro RNAs 43 Tay Sachs thalassemia 43 inherited retinal degeneration 43 allergic sensitization 43 Viral infections 43 selenium deficiency 43 mammalian embryos 43 eukaryotic cell 43 Levy Lahad 43 APOE4 43 multifactorial disease 43 neurosensory 43 sphingolipids 43 Olmecs 43 DiGeorge syndrome 43 hormone secretion 43 chloroplast DNA 43 filamentous fungus 43 predestination 43 undescended testes 43 CHI#L# 43 CaM kinase II 43 cerebral hemispheres 43 Telomere length 43 hunter gatherer societies 43 genetical 43 causal 43 epithelial tissues 43 PI3K signaling 43 Beta thalassemia 43 recurrent miscarriages 43 IGF2 43 SORL1 gene 43 genetic abnormality 43 galactosemia 43 metazoans 43 multicellularity 43 phenotypic plasticity 43 irregular menstruation 43 Klotho gene 43 comorbid disorders 43 Alport syndrome 43 genetically disposed 43 estrogenic effects 43 Paneth cells 43 Marfan syndrome connective tissue 43 desmosomes 43 personality traits 43 HFE gene 43 chronic obstructive airway 43 chromosomes 43 sporadic Creutzfeldt Jakob 43 RUNX3 43 PTEN gene 43 chordates 43 chronologic age 43 HOX genes 43 genetic polymorphism 43 genetic variability 43 Beckwith Wiedemann syndrome 43 MSH2 43 assortative 43 Iron deficiency anemia 43 protein conformation 43 chemosensory 43 eukaryote 43 neurasthenia 43 chromosomal defects 43 ORMDL3 43 etiological factors 43 Frontal lobe 43 familial adenomatous polyposis FAP 43 matrilineal 43 animal phyla 43 observable traits 43 Vascular dementia 43 C. neoformans 43 PON1 43 WAGR syndrome 43 gut microflora 43 body fatness 43 epiphenomenon 43 evolutionary genomics 42 Hox genes 42 Lafora disease 42 incomplete penetrance 42 neuropsychological deficits 42 allelic variation 42 polyandry 42 SLC#A# [001] 42 synovial cells 42 sickle cell cystic fibrosis 42 male prairie voles 42 G#S mutation 42 allostatic load 42 klotho gene 42 Aortic stenosis 42 sensory receptors 42 Negroid 42 cybrid 42 pathogenic mechanisms 42 malarial parasites 42 spongiform encephalopathies 42 Dietary fats 42 polycystic ovary syndrome 42 mammalian brains 42 bioengineered mice 42 psycholinguistics 42 V Leiden 42 morbid jealousy 42 methylation patterns 42 Spinal muscular atrophy 42 genetically coded 42 pattern baldness 42 T. vaginalis 42 hyperstimulation 42 morphogen 42 leptin resistance 42 proband 42 hemochromatosis 42 Cryptococcus neoformans 42 Spina bifida 42 susceptibility 42 holoprosencephaly 42 chromosomal disorder 42 neophobia 42 genetic underpinnings 42 metabolic enzymes 42 narcolepsy cataplexy 42 mutational 42 hypersensitivities 42 autosomal dominant polycystic kidney 42 TP# gene 42 mitochondrial DNA 42 spontaneous remission 42 irreducibly complex 42 symbioses 42 uro genital 42 chromosome abnormality 42 reciprocal altruism 42 causation 42 facial clefts 42 cystic fibrosis sickle cell 42 Insulin resistance 42 pathological manifestations 42 progressive degenerative neurological 42 endocrinological 42 coevolution 42 Foxp2 42 atherogenesis 42 FOXP2 gene 42 abnormal hemoglobin 42 Neo Darwinian 42 hereditary blindness 42 blindness paralysis 42 reproductive abnormalities 42 biopsychosocial model 42 FOXP2 42 synaesthesia 42 regulating gene expression 42 Circadian rhythm 42 Male infertility 42 hunter gatherer ancestors 42 Myths abound 42 lichen planus 42 chromosomal aberrations 42 telomere DNA 42 Workaholism 42 paternal discrepancy 42 immunological mechanisms 42 non coding RNA 42 evolutionary lineages 42 neurobiological mechanisms 42 behavioral traits 42 pathogenetic mechanisms 42 aberrant methylation 42 endosymbiosis 42 congenital cataract 42 premorbid 42 VCFS 42 laterality 42 Uveal melanoma 42 pleiotropy 42 jawed vertebrates 42 androgen excess 42 Cowden syndrome 42 mutated genes 42 aetiology 42 genital abnormalities 42 2D 4D ratio 42 Vitamin B# deficiency 42 unmeasured confounders 42 dyskeratosis congenita 42 Mitochondrial DNA 42 podocytes 42 amyloid plaque formation 42 laforin 42 heritable traits 42 reproductive hormones 42 hereditary hemochromatosis 42 genetic locus 42 socioeconomic 42 aneuploid cells 42 bipedalism 42 outcrossing 42 axon guidance 42 inhaled fibers 42 eczema hay fever 42 tubule 42 sociodemographic variables 42 LKB1 42 bacterial pathogenesis 42 prehuman 42 abnormal glucose metabolism 42 autonomic dysfunction 42 nucleolar dominance 42 Rh incompatibility 42 abnormal proteins 42 vertebral subluxation 42 Lenzenweger 42 fruitfly Drosophila 42 somatic motility 42 GPC5 42 LRP5 42 unhealthy diets 42 neuroendocrinology 42 chromosomal translocations 42 penetrance 42 BCL#A 42 nephronophthisis 42 evolutionary 42 genetically programmed 42 neuronal dysfunction 42 transcriptional regulation 42 plausible hypothesis 42 Paleolithic diet 42 susceptibility genes 42 lactase gene 42 psychosomatic 42 methodological individualism 42 testicular germ cell 42 brain frontal lobes 42 menstrual irregularity 42 circadian disruption 42 primary cilia 42 alexithymia 42 morphogens 42 sporadic ALS 42 neonatal herpes 42 neurocognitive dysfunction 42 endogamous 42 saju 42 Kornelia Polyak 42 nonrational 42 dizygotic 42 Genetic susceptibility 42 anatomical abnormalities 42 mycobacterium 42 Hormonal imbalance 42 germline cells 42 Ischaemic heart 42 renal fibrosis 42 inbreeding 42 molecular pathways 42 bacterial flagellum 42 hormones leptin 42 presbycusis 42 LIS1 42 selfing 42 extra centrosomes 42 pathophysiologic mechanisms 42 emotional dysregulation 42 cardiac channelopathies 42 thale cress Arabidopsis thaliana 42 Glymour 42 diseases 42 biogenesis 42 human microbiome 42 congenital deformity 42 abiotic 42 chronic degenerative diseases 42 placental mammals 42 corneal dystrophy 42 Smad3 42 Li Fraumeni syndrome 42 chromosomal abnormalities 42 synaptogenesis 42 SCN5A 42 Multivariate analyzes 42 Y chromosome 42 insulin resistance 42 chromosome #p#.# 42 brain lesions 42 spinal muscle atrophy 42 mutant genes 42 papillomaviruses 42 epigenome 42 neuroinflammation 42 sortilin 42 Prevotella 42 fungal genomes 42 Nasal allergies 42 neurodegenerative disorder 42 innate predisposition 42 #q# deletion 42 OCA2 42 P. falciparum parasites 42 MAOA gene 42 progerin 42 sociality 42 neural progenitor 42 heterosis 42 Mitochondrial Eve 42 familial ALS 42 impaired glucose metabolism 42 MC1R gene 42 biochemical abnormalities 42 BRAF gene 42 CHRNA5 gene 42 prenatal exposure 42 phenotype 42 Severe acne 42 hereditarily 42 superorganism 42 Toxoplasma infection 42 Raynaud disease 42 Froguel 42 SLC#A# [002] 42 placental function 42 primary biliary cirrhosis 42 dimorphism 42 metabolic syndrome MetS 42 neurofibroma 42 ontogenetic 41 atopy 41 male pattern baldness 41 Paranthropus robustus 41 leptin receptor 41 Proteus syndrome 41 chromosomal aberration 41 oncogenesis 41 circadian cycles 41 exfoliative glaucoma 41 genes encode proteins 41 causative factors 41 placental mammal 41 Gregor Mendel 41 Bardet Biedl syndrome 41 orofacial 41 Osteogenesis imperfecta 41 IL#R 41 hay fever allergic rhinitis 41 spastic paraplegia 41 Austria Gruner Veltliner 41 hypotonia 41 histone code 41 genetic heterogeneity 41 Pier Paolo Pandolfi 41 fibrosing cardiomyopathy 41 Leitzmann 41 consanguineous marriage 41 genetically identical twins 41 microdeletion 41 phenotypic characteristics 41 hindbrain 41 digest lactose 41 Wynshaw Boris 41 homozygosity 41 Treacher Collins 41 transcriptional repression 41 GSTM1 gene 41 paternal 41 Prenatal diagnosis 41 genetic traits 41 pathogenesis 41 Leydig cell 41 circadian rhythmicity 41 organogenesis 41 biogeochemical cycles 41 RSPO2 41 chromosomal anomaly 41 neuro developmental 41 Marc Weisskopf 41 determinants 41 apoE 41 simulans 41 atypical parkinsonism 41 Marambaud 41 genetic determinism 41 SAPAP3 41 neuroligins 41 androgenetic alopecia 41 UGT#B# 41 brain neurochemistry 41 aldehyde dehydrogenase 41 nonsense mutations 41 vitamin D receptor VDR 41 allele frequencies 41 PALB2 41 FTLD 41 neural substrates 41 Atopic dermatitis 41 Essential tremor 41 neuro degenerative diseases 41 transitivity 41 tricuspid atresia 41 chromatin structure 41 infectious prion proteins 41 maternally derived 41 temporal arteritis 41 neurological abnormalities 41 recessive gene 41 meadow vole 41 filaggrin 41 fatal neuromuscular disorder 41 fossilization 41 transfusion syndrome 41 antagonistic pleiotropy 41 prokaryotes 41 asperger syndrome 41 protein folding misfolding 41 VUR 41 incurability 41 probiotic supplementation 41 CHRNA5 41 vascular cognitive impairment 41 Worthingtons testified 41 ancestry