Related by context. All words. (Click for frequent words.) 66 familial aggregation 66 phenotypic expression 66 familial clustering 66 de novo mutations 65 etiologic 64 pathogenic mutations 64 evolvability 64 APOE genotype 64 epistasis 64 allele frequencies 63 mtDNA mutations 63 phenotypic variation 63 spontaneous mutations 63 APOE ε4 63 germline mutations 63 nucleotide substitutions 63 differential gene expression 63 subfertility 63 genetic loci 63 missense mutations 63 Heavy menstrual bleeding 62 Genetic predisposition 62 bimodal distribution 62 K ras gene 62 penetrance 62 unmeasured confounding 62 MYH9 62 mosaicism 62 thyrotropin levels 62 sexually dimorphic 62 unmeasured factors 62 CYP#C# gene 62 inherited mutations 62 chromosomal rearrangement 62 GBA mutations 61 affective psychoses 61 spontaneous mutation 61 Bacterial vaginosis 61 hormone receptor status 61 T. vaginalis 61 tumor histology 61 evolutionary divergence 61 CYP#D# gene 61 Kaplan Meier curve 61 sequence homology 61 myocardial ischaemia 61 phenotypic differences 61 sexual dimorphism 61 histologic subtype 61 Candida species 61 monogenic 61 inhibin B 61 SRY gene 61 carcinoids 61 ovarian hormones 61 recombination hotspots 61 H#Y 61 maturational 61 deleterious mutations 61 psychiatric comorbidity 61 nongenetic 61 DNA demethylation 61 etiological 61 TCF#L# gene 61 heterozygotes 60 orthologous genes 60 MGUS 60 androgen deficiency 60 HER2 positivity 60 mutated K ras 60 mitochondrial mutations 60 chromosomal aberrations 60 phenotypic traits 60 K ras mutations 60 APOE e4 60 Genetic variation 60 pathophysiologic 60 motor neuron degeneration 60 EBV infection 60 HER2 expression 60 NNRTI resistance 60 albumin excretion 60 clade B 60 TGFBR1 * 6A 60 dizygotic twins 60 polygenic 60 IgA deficiency 60 sCJD 60 chromosomal alterations 60 phenotypic variability 60 Chronic pancreatitis 60 Telomere length 60 ABCB1 60 corticosterone levels 60 Cognitive impairment 60 serotonin deficiency 60 karyotypes 60 residual confounding 60 HbF 60 biochemical abnormalities 60 obstructive coronary artery 60 seminomas 60 thiopurine 60 hermaphroditism 60 chromosomal anomalies 60 gene duplications 60 arterial thickening 60 leiomyomas 60 silico prediction 60 fluoroquinolone resistance 60 pleiotropy 59 pathophysiological mechanisms 59 monoclonal gammopathy 59 modifier genes 59 genomic alterations 59 fetal malformations 59 XMRV infection 59 ascertainment bias 59 hamartomas 59 neurodevelopmental outcome 59 sociodemographic factors 59 H. pylori infections 59 prostate cancer CaP 59 SCN1A 59 G6PD deficiency 59 M. pneumoniae 59 testicular tumors 59 monozygotic twins 59 MYH9 gene 59 ABCB1 gene 59 TMPRSS2 ERG fusion 59 affective psychosis 59 underlying pathophysiology 59 #q# deletion 59 endometrial hyperplasia 59 genital HPV infections 59 periprocedural MI 59 nonvaccine 59 pharmacologic treatments 59 CAG repeats 59 Chlamydia trachomatis infection 59 autosomal 59 Genetic variants 59 selfing 59 androgen suppression 59 azoospermia 59 MLH1 59 thyroid dysfunction 59 CYP#D# genotype 59 aneuploid 59 rhinovirus infection 59 artifactual 59 epigenetic changes 59 TP# gene 59 autosomal dominant inheritance 59 prion infection 59 DNA methylation patterns 59 testicular dysgenesis syndrome 59 LVNC 59 Cytogenetic 59 dimorphic 59 prion gene 59 cis regulatory 59 amyloid plaque formation 59 oncogene addiction 59 splice variants 59 familial predisposition 59 autonomic dysfunction 59 Chlamydia pneumoniae 59 pleiotropic effects 58 microsatellite instability 58 viral etiology 58 breast cancer subtypes 58 heritable trait 58 phylogenetic analyzes 58 chronicity 58 microchimerism 58 chromosomal rearrangements 58 covariate 58 enteroviral 58 unmeasured confounders 58 phthalate syndrome 58 MSH2 58 hematopoietic cancers 58 MECP2 gene 58 genetic heterogeneity 58 TPMT 58 enterotypes 58 gene rearrangements 58 aetiological 58 clinico pathological 58 clinicopathologic 58 p# activation 58 oseltamivir resistance 58 lymphocytic 58 generalisable 58 observable traits 58 heritable traits 58 homologies 58 psychosocial stressors 58 intersexuality 58 oncogenic transformation 58 pathogenetic 58 prognostic indicators 58 hepatitis B immunoglobulin 58 androgen depletion 58 poor metabolizers 58 LRP5 58 neuroanatomical 58 KIBRA 58 causally linked 58 dimorphism 58 assortative mating 58 totipotent 58 FGFR2 gene 58 polyploid 58 HIV HCV coinfected 58 amyloid deposition 58 microdeletion 58 genotypic 58 polymicrobial 58 coexpression 58 Orthostatic hypotension 58 sporadic Creutzfeldt Jakob 58 gastric carcinoma 58 endogenous hormones 58 empiric 58 epigenetic modifications 58 comorbid disorders 58 gene locus 58 aneuploid cells 58 Aspergillus species 58 evolutionary lineages 58 multiplicative 58 haematologic 58 invasive carcinoma 58 cytologic 58 X4 viruses 58 Thyroid nodules 58 serum PTH 58 APOL1 58 serum estradiol 58 aneuploidies 58 radiographic findings 58 glycosylated 58 immunodeficiency 58 genetic relatedness 58 HER2 overexpression 58 immunomodulation 58 SHANK3 58 thyrotropin 58 causal inference 58 hypermethylated 58 causal variants 58 p# mutations 58 morphological traits 58 microdeletions 58 phthalate exposure 58 polygyny 58 postmenopausal estrogen 58 irregular menstrual cycles 58 phylogenetically 58 hemoglobins 58 GSTT1 58 DHEA supplementation 58 impair fertility 58 cellular prion protein 58 late onset hypogonadism 57 lymphocyte activation 57 FGFs 57 genes BRCA1 57 clefting 57 IPAH 57 metabolic abnormalities 57 Genetic mutations 57 KRAS mutations 57 pharmacokinetic interactions 57 generalisability 57 Zinc deficiency 57 neuropsychological impairments 57 SLNB 57 nonvascular 57 ADAMTS# 57 promoter methylation 57 apolipoprotein E4 57 neuronal dysfunction 57 adenomatous polyps 57 predisposing factor 57 HLA genes 57 Hip dysplasia 57 Subgroup analyzes 57 Leydig cell 57 hippocampal function 57 histopathological 57 Thalomid ® 57 subcellular compartments 57 vascular dysfunction 57 Hurthle cell 57 S. neurona 57 genital ulcer 57 androgenic hormones 57 leiomyoma 57 biologic plausibility 57 extracolonic 57 metastatic neuroendocrine tumors 57 breast endometrial 57 allelic 57 Socioeconomic status 57 Leydig cells 57 CVD mortality 57 Heritability 57 thyroid carcinoma 57 NR#A# gene 57 CD#c 57 glial tumors 57 familial pancreatic cancer 57 unmutated 57 #q#.# deletion syndrome 57 KRAS oncogene 57 Rh factor 57 pituitary adenomas 57 univariate analyzes 57 LRAT 57 hepatocellular carcinomas 57 liver metastasis 57 HPV subtypes 57 CYP #D# 57 BRCA1 mutation carriers 57 renal cysts 57 behavioral disinhibition 57 proximal colon 57 CYP #A# 57 endocannabinoid signaling 57 monozygotic 57 advanced neoplasia 57 tyrosine phosphorylation 57 dentinal hypersensitivity 57 quasispecies 57 carotid plaque 57 antioxidant supplementation 57 eusociality 57 introgression 57 serologic 57 polyploidy 57 Assisted reproduction 57 alexithymia 57 FGFR2 57 bivariate 57 sonographic diagnosis 57 Treg cell 57 serum folate concentrations 57 indels 57 gestational diabetes mellitus GDM 57 IDH mutations 57 amino acid substitution 57 neurosensory 57 CHD7 57 parasitaemia 57 PTEN mutations 57 teratogens 57 pancreatic endocrine 57 adrenocorticotropic hormone 57 resistant isolates 57 paralogs 57 adiponectin levels 57 allelic variation 57 PCOD 57 multivariate logistic regression 57 Multivariate analysis 57 pharmacologic intervention 57 KCNH2 57 statistical correlations 57 plasma lipid 57 chlamydial infection 57 intracellular signal transduction 57 prodynorphin 57 postnatally 57 abnormal chromosomes 57 BubR1 57 vitamin B# folic acid 57 orthologs 57 airborne fungal spores 57 NIHSS score 57 antiphospholipid antibodies 57 ± SEM 57 maternally inherited 57 amyloid cascade 57 neurodevelopmental impairment 57 bivariate analysis 57 S. maltophilia 57 asplenia 57 hyperplastic 57 apolipoprotein E gene 57 airway responsiveness 57 anovulation 57 correlational 57 BARD1 57 vertebrate embryos 57 androgen deprivation 57 gonadotropins 57 Kufs disease 57 neonatal morbidity 57 colorectal carcinogenesis 57 arterial calcification 57 hormonal stimulation 57 clinicopathological 57 GH deficiency 57 syndromic 57 progranulin gene 57 hypovitaminosis D 57 proteolytic processing 57 hyper IgE syndrome 57 BCL#A 56 intracytoplasmic 56 empiric therapy 56 neuritic 56 Plasmodium infection 56 Myocardial infarction 56 phylogeographic 56 transgene expression 56 GBM tumors 56 morphologic 56 FASPS 56 inherited predisposition 56 elevated LDH 56 subclinical hypothyroidism 56 heterozygosity 56 masculinization 56 autosomal recessive 56 epistatic 56 seropositivity 56 HLA DRB1 56 silent myocardial ischemia 56 inherit predisposition 56 Eukaryotes 56 Disordered eating 56 hormonal abnormalities 56 #q#.# [002] 56 GSTM1 gene 56 chimp genomes 56 comorbid conditions 56 advanced adenoma 56 photoreceptor cell 56 incidentalomas 56 herpesviruses 56 cybrid 56 psychogenic 56 anatomic abnormalities 56 ontogenetic 56 inbred strains 56 coinfection 56 somatic mutations 56 enteroviral infection 56 MYCN amplification 56 Synovial sarcoma 56 neurocognitive deficits 56 UGT#B# 56 mechanistic explanation 56 thrombophilia 56 prevalences 56 nonmelanoma skin cancers 56 PTEN gene 56 Malignant tumors 56 olfactory dysfunction 56 ENPP1 56 irregular menstrual periods 56 adrenocortical 56 Y chromosomal 56 pathognomonic 56 mammary cancers 56 synovial cells 56 germline cells 56 Genetic variations 56 hypometabolism 56 interindividual variability 56 etiological factors 56 mitochondrial defects 56 potentially modifiable 56 nonhereditary 56 IUGR 56 gastric cardia 56 neuropsychological impairment 56 meta analytic 56 phylogenetic relationships 56 silibinin 56 neurocognitive impairment 56 internalizing disorders 56 molecular abnormalities 56 p#INK#a 56 shorter telomere length 56 epigenetic modification 56 Male infertility 56 prothrombotic 56 mitochondrial DNA mutations 56 prostate carcinogenesis 56 bilaterians 56 highly heritable 56 atherothrombotic disease 56 terminally differentiated 56 STAT4 56 cervical secretions 56 primary ovarian insufficiency 56 comorbid depression 56 constitutively expressed 56 recurrent tonsillitis 56 Vitamin D insufficiency 56 X inactivation 56 serum biomarkers 56 cranial irradiation 56 DNA rearrangements 56 chromosomal translocations 56 mutant allele 56 embryo biopsy 56 C. neoformans 56 induce ovulation 56 homozygotes 56 ERK2 56 TACI mutations 56 cervicitis 56 prostate carcinoma 56 genes predisposing 56 neoplastic 56 neurologic complications 56 surrogate markers 56 immune dysregulation 56 PON1 gene 56 amenorrhoea 56 chorioamnionitis 56 emotional dysregulation 56 genetic polymorphism 56 Glucocorticoids 56 cortisol secretion 56 BMPR2 56 pleiotropic 56 abnormal Pap smears 56 Acute pancreatitis 56 moderately heritable 56 SCN5A 56 CSF biomarkers 56 chimpanzee genomes 56 multicellularity 56 plasma pharmacokinetics 56 cytochrome b 56 DNA hypomethylation 56 BDNF protein 56 C1 INH deficiency 56 Severe hypersensitivity reactions 56 folate deficiency 56 alternatively spliced 56 prenatal exposures 56 bronchopulmonary dysplasia BPD 56 pre malignant lesions 56 H pylori 56 androgen receptor gene 56 elevated CRP 56 HER2 neu 56 methylation patterns 56 Osteoporotic fractures 56 subfertile 56 Excessive daytime sleepiness 56 genotype phenotype 56 TT genotype 56 outcrossing 56 precursor lesions 56 spermidine 56 Preterm delivery 56 Male pattern baldness 56 nondemented 56 CYP#C# [002] 56 sex hormones estrogen 56 TOP2A gene 56 phenotypic characteristics 56 schistosome 56 developmental abnormalities 56 telomerase activation 56 hypoperfusion 56 p# mutation 56 malabsorptive 56 Hashimoto thyroiditis 56 underdiagnosis 56 ovulatory cycles 56 transgenic mice expressing 56 MMSE score 56 neuro developmental disorders 56 posttranslational modifications 56 somatoform disorders 56 involution 56 metabolomic profiles 56 virological response 56 lethal arrhythmias 56 gonadal 56 ovarian endometrial 56 morphological abnormalities 56 thyroid hormone levels 56 multivariate Cox 56 comorbid psychiatric 56 abdominal adiposity 56 osteogenic differentiation 56 Amino acid 56 neuropsychiatric disorder 56 neuropathologic 56 mechanistic studies 56 G. biloba 56 hypothalamic pituitary 56 leptin receptor 56 multi factorial disease 56 urethritis 56 genital herpes infections 56 paratuberculosis 56 schizophreniform disorder 56 psychiatric comorbidities 56 serum aminotransferase levels 56 subclinical hyperthyroidism 56 CFH gene 56 Brugada syndrome 56 pituitary hormone 56 WNV infections 56 allogeneic HSCT 55 paternal discrepancy 55 linear pharmacokinetics 55 SIRT1 activation 55 Alu elements 55 Grass tetany 55 TEAEs 55 MC1R 55 probiotic supplementation 55 chromosomal disorders 55 neurologic abnormalities 55 Chronic Lyme disease 55 homozygosity 55 recurrent miscarriage 55 overt hypothyroidism 55 neurological abnormalities 55 prognostic indicator 55 cardiogenic 55 impaired cognition 55 Mycobacterium bovis 55 diathesis 55 psychosocial variables 55 clinically insignificant 55 clonal expansion 55 ADPKD 55 aneuploidy 55 CYP#A# gene 55 premenopause 55 haematopoietic 55 Lactose intolerance 55 pCR 55 CHD mortality 55 pathophysiological 55 proton MR spectroscopy 55 mutant huntingtin protein 55 androgen signaling 55 GABRA2 gene 55 immunodeficiencies 55 telomere lengths 55 virulence genes 55 TMEM#B 55 causative genes 55 recurrent venous thromboembolism 55 telomere dysfunction 55 #q# deletion syndrome 55 mitochondrial DNA mtDNA 55 cytopathic 55 circulating endothelial cells 55 myocardial fibrosis 55 beta carotene supplementation 55 amyloidogenic 55 chemosensitivity 55 PNH patients 55 male reproductive tract 55 MetS 55 epigenetic alterations 55 gallstone disease 55 conserved sequences 55 eusocial 55 prodromal phase 55 mesenchymal cell 55 neural crest stem cells 55 lactational 55 Trichophyton rubrum 55 chronic hepatitis cirrhosis 55 stone formers 55 endophenotypes 55 BRCA2 mutation carriers 55 etiologic agent 55 WNK1 55 elevated homocysteine 55 HFE gene 55 biochemical imbalance 55 NP CRNs 55 serologic testing 55 chromosomal deletions 55 amenorrhea 55 unicellular organisms 55 chromosome translocations 55 MeCP2 gene 55 ERK signaling 55 CNTNAP2 55 endogenous estrogen 55 SLITRK1 55 inferential statistics 55 acute rheumatic fever 55 MLL2 55 Vitamin B# deficiency 55 causative mutations 55 dysbindin 55 Sarcopenia 55 adnexal mass 55 Drospirenone 55 putative biomarkers 55 trans palmitoleate 55 transfusion transmitted 55 autistic regression 55 hereditary predisposition 55 brain lesions 55 gene deletions 55 thyroid nodules 55 pathogenic mechanisms 55 genomic variation 55 body fatness 55 familial AF 55 premenstrual syndrome PMS 55 histological subtype 55 allele frequency 55 E. histolytica 55 dietary folate 55 marsupial mammals 55 Listeria infections 55 anthracycline induced 55 prion strains 55 proinflammatory mediators 55 Mycoplasma pneumoniae 55 endometrial thickness 55 Jhdm2a 55 chi squared 55 Fragile X gene 55 nonalcoholic steatohepatitis 55 DLC1 55 colorectal adenomas 55 APOE4 55 multivariable analysis 55 Prostatitis 55 GABRA2 55 genomic deletions 55 ontogeny 55 mitochondrial proteins 55 CP CPPS 55 inbreeding depression 55 cholinergic tone 55 presymptomatic 55 multivariate analyzes 55 neuropsychiatric diseases 55 metabolite concentrations 55 metabolizing enzymes 55 PTPN# 55 Kabuki syndrome 55 Calcium intake 55 Testosterone deficiency 55 apneic episodes 55 atherothrombotic 55 fungal genomes 55 APOC3 55 neurologic dysfunction 55 hormone therapy estrogen 55 colorectal neoplasia 55 SORL1 gene 55 osteosarcomas 55 growth hormone secretion 55 homochirality 55 aminotransferase levels 55 N. gonorrhoeae 55 antiandrogen 55 TNF blocker therapy 55 asymptomatic carriers 55 P. falciparum malaria 55 generalizability 55 prostate gland mammary gland 55 granulosa cell 55 neuropsychiatric symptoms 55 dietary antioxidants 55 evolutionarily novel 55 mammographic breast density 55 myopathies 55 histocompatibility 55 apoptosis pathway 55 postmenopausal hormone replacement 55 suppress ovulation 55 squamous cell lung cancer 55 RET PTC rearrangements 55 intracranial hemorrhage ICH 55 aberrant methylation 55 histopathologic diagnosis 55 conditional logistic regression 55 Phenotypic 55 Androgenetic alopecia 55 generalized epilepsy 55 syndromal 55 Previous epidemiological studies 55 GSTM1 55 HIV tropism 55 β amyloid 55 autosomes 55 isoenzyme 55 prolonged QT interval 55 analgesic medications 55 lamivudine resistant 55 physiologic mechanisms 55 coagulopathy 55 causal pathway 55 parous women 55 prefrontal regions 55 Proximate cause 55 corpus luteum 55 functional polymorphism 55 E. faecalis 55 biopsied embryos 55 Trichomonas 55 S. enterica 55 metaplasia 55 airway hyperresponsiveness 55 FKBP# 55 penile vaginal intercourse 55 congenital adrenal hyperplasia CAH 55 heritable disorders 55 DQB1 * 55 antigenic shift 55 HMGCR 55 neutrophil counts 55 genetic susceptibilities 55 Postoperative complications 55 abnormal cytology 55 chromosomal instability 55 Cardiorespiratory fitness 55 clinically meaningful differences 55 trophoblast cells 55 toxicologic 55 mitochondrial enzyme 55 aneuploidy screening 55 microbiologic 55 G allele 55 enterovirus infection 55 Colon polyps 55 serum lipid 55 biochemical imbalances 55 tumorigenicity 55 adjuvant systemic 55 Uncontrolled hypertension 55 nucleosome positioning 55 lobular involution 55 testicular biopsy 55 Poisson regression 55 null hypothesis 55 multigenic 55 autistic traits 55 apolipoprotein E APOE 55 allelic variants 55 selenium supplementation 55 ataxias 55 ncRNA 55 lactase persistence 55 serum creatinine levels 55 hormone deprivation 55 leptin resistant 55 dopamine receptor gene 55 varicocele 55 generalized vitiligo 55 hemagglutinin gene 55 leukaemias 55 Diverticulosis 55 estrogenic effects 55 Cyclin E 55 aetiology 55 genomic biomarker 55 ovulatory 55 genomic imprinting 55 proteomes 55 empiric treatment 55 morphologically distinct 55 somatic mutation 55 osteoblastic 55 polygynous 55 affective disorders 55 tumor subtypes 55 serologically 55 cardioprotective effect 55 gene polymorphisms 55 regression equations 55 hepatoma 55 Helicobacter 55 Socio demographic 55 p# Shc 55 eukaryote 55 clinicopathological features 54 murine models 54 genomically 54 CpG island 54 HRCT 54 autoimmune pancreatitis 54 molecularly defined 54 oncologic outcomes 54 Ovarian cysts 54 GPx 54 fusiform 54 Contagious yawning 54 HPAI H#N# 54 invasive lobular 54 atypical scrapie 54 choline intake 54 lipid elevations 54 imatinib resistance 54 HNSCC 54 excitatory synapses 54 lipid lowering medications 54 Alternative splicing 54 SRBD 54 differentially expressed genes 54 osteochondromas 54 hypochondriasis 54 Plasmodium falciparum malaria 54 Rectal cancer 54 NRTI resistance 54 androgen excess 54 pH#N# 54 epigenetic reprogramming 54 dysfunctional voiding 54 UCP2 54 mutant alleles 54 embryonic lethality 54 Nod1 54 T1DM 54 orofacial clefts 54 dysbindin gene 54 Entamoeba 54 abnormal pap smears 54 hypovolemia 54 LQTS 54 nonmelanoma 54 MMP# 54 congenital toxoplasmosis 54 BRCA1 BRCA2 54 lymph node metastasis 54 TP# mutations 54 adrenal hormone 54 laterality 54 antemortem 54 preoperative diagnosis 54 gut microbiota 54 MHC genes 54 cytochrome P# enzyme 54 genotoxic stress 54 MC1R gene 54 shortened telomeres 54 Plasmodium vivax 54 therapeutically beneficial 54 candidemia 54 autosomal dominant disorder 54 adrenal suppression 54 commensal bacteria 54 colorectal adenoma 54 chromosome #q# [002] 54 distinct subtypes 54 Ovary removal 54 convergent validity 54 LRRK2 mutations 54 etiologic factors 54 Insulin sensitivity 54 intact parathyroid hormone 54 adenomatous 54 puerperal psychosis 54 microsaccades 54 Li Fraumeni syndrome 54 demyelinating 54 impaired glucose metabolism 54 multiple logistic regression 54 microcephalin 54 Adjuvant chemotherapy 54 bioprosthetic valve 54 P falciparum 54 serotonin transporters 54 SOCS2 54 multifactorial disease 54 asexual organisms 54 morphological similarities 54 nephrolithiasis 54 lichen planus 54 benign thyroid nodules 54 protein tyrosine phosphatase 54 Gaussian distribution 54 genetic rearrangements 54 sarcomatoid 54 carotid bruit 54 limiting generalizability 54 HIV uninfected 54 placental mammals 54 generalizable 54 gonococcal infection 54 debilitating neurodegenerative disorder 54 gonococcal infections