Related by context. All words. (Click for frequent words.) 77 gene variant 76 genetic variant 68 FTO gene 67 gene mutation 65 mutated gene 65 genetic mutation 65 gene variants 65 APOE gene 63 APOE4 63 genetic variants 62 gene mutations 62 BRCA1 mutations 61 genetic variation 61 APOE e4 61 ApoE4 gene 61 genetic variations 60 mutation 60 BRCA1 gene 59 G#S mutation 59 E4 variant 59 CNVs 59 FTO variant 59 GSTM1 gene 59 allele 59 genetic variants associated 59 genetic mutations 58 LRRK2 gene 58 apolipoprotein E gene 58 mutated genes 58 DQB1 * 58 G allele 58 ApoE4 58 TCF#L# gene 58 BRCA mutations 58 apoE4 58 postmenopausal breast cancer 58 FMR1 gene 58 familial pancreatic cancer 58 BRCA2 gene 57 COMT gene 57 5 HTT gene 57 susceptibility gene 57 BRCA mutation 57 HMGA2 57 MC1R 57 dopamine receptor gene 57 ApoE gene 57 genetic susceptibility 57 CYP#E# gene 57 Genetic variants 56 colorectal neoplasia 56 alpha synuclein gene 56 mutant gene 56 HLA B# 56 LQTS 56 ALDH2 56 GBA mutations 56 mutations 56 MC1R gene 56 defective gene 56 BRCA2 mutation 56 alleles 56 MC4R gene 56 SORL1 56 TGFBR1 * 6A 56 bowel polyps 56 microdeletions 56 mtDNA mutations 55 APOE 55 BRCA2 mutations 55 MYH9 gene 55 genomewide 55 gene 55 BARD1 55 apoC III 55 chromosomal regions 55 LIS1 55 CALHM1 55 V Leiden 55 vitamin B# deficiency 55 CDH1 55 CYP#C# [001] 55 Wwox 55 genetic trait 55 HPV# 55 GRK5 55 FASPS 55 shorter telomeres 55 LRP5 55 p# mutations 55 genetic defect 55 STAT4 55 inherited mutations 55 EGFR gene 55 HFE gene 55 TCF#L# 55 GSTT1 54 serotonin transporter gene 54 KIBRA 54 polymorphisms 54 lipin 54 CETP gene 54 PTPN# 54 elevated triglyceride levels 54 H. pylori 54 premenopausal breast cancer 54 C#Y 54 APOE e4 gene 54 NPY gene 54 X chromosome 54 genetic polymorphism 54 SNPs 54 familial ALS 54 mutated BRCA1 54 CETP VV 54 NAFLD 54 ApoE 54 cardioembolic stroke 54 type2 diabetes 54 Fragile X gene 54 subclinical hyperthyroidism 54 microcephalin 54 dopamine D4 receptor 54 sporadic ALS 54 folate deficiency 54 CHEK2 54 adiponectin levels 54 STK# gene 54 neuroglobin 54 MTHFR gene 54 genes 54 hormone adiponectin 54 disease NAFLD 54 number variations CNVs 54 APOE allele 54 BRCA2 54 rs# [002] 54 ABCB1 54 MTHFR 54 rs# [003] 53 MC4R 53 Meckel Gruber 53 IGF2 53 FTO allele 53 BRCA gene 53 CCL#L# 53 MYH9 53 genetic polymorphisms 53 parkin gene 53 spontaneous mutations 53 HGPS 53 chromosome #q# [002] 53 CFH gene 53 5 HTTLPR 53 clusterin 53 mitochondrial dysfunction 53 HLA genes 53 HMGA2 gene 53 CYP#C# gene 53 APOE ε4 53 PALB2 53 polycystic ovary syndrome PCOS 53 VHL gene 53 heterozygous 53 APOE4 gene 53 CNTNAP2 53 recessive mutation 53 genetic alterations 53 mutant allele 53 gene APOE 53 tumor suppressor gene 53 MIF protein 53 Obstructive sleep apnea 53 chromosomal abnormalities 53 DRD2 gene 53 APOE genotype 53 BRCA2 gene mutation 53 Neuregulin 1 53 genes predisposing 53 familial hypercholesterolemia 53 HER2 gene 53 PTEN mutations 53 Genetic variation 53 epigenetic changes 53 chromosomal translocations 53 untreated sleep apnea 53 de novo mutations 53 brain shrinkage 53 neuroligins 53 PICALM 53 cardiac hypertrophy 53 Klinefelter syndrome 53 telomere lengths 53 vasopressin receptors 53 medulloblastomas 53 homozygous 53 haplotypes 53 slow metabolizers 53 ApoE4 allele 53 narcolepsy cataplexy 53 IgA deficiency 52 gene locus 52 #q# deletion 52 heritable 52 HLA DRB1 52 Froguel 52 apolipoprotein E 52 DRD2 52 FGFR2 gene 52 FGFR2 52 haplotype 52 NKX2 52 metabolic syndrome MetS 52 genetic predisposition 52 GSTP1 52 colorectal adenomas 52 herpes simplex virus 52 #p# [001] 52 varicella zoster virus 52 mutant genes 52 TCF4 52 ADPKD 52 UGT#A# * 52 leptin hormone 52 SLC#A# [002] 52 gene expression patterns 52 chromosome #p# [001] 52 progranulin gene 52 CYP#D# gene 52 MHC genes 52 folate intake 52 arterial calcification 52 BRCA genes 52 fewer dopamine receptors 52 elevated CRP 52 postoperative delirium 52 Hashimoto thyroiditis 52 FMRP protein 52 pathogenic mutations 52 MAOA gene 52 lobular breast cancer 52 Sjögren syndrome 52 apoE 52 Alu elements 52 missense mutations 52 progranulin 52 KIF6 gene 52 chromosomal alterations 52 CHRNA5 gene 52 BDNF gene 52 chromosomal anomaly 52 basal cell nevus syndrome 52 GSTM1 52 SORL1 gene 52 CC genotype 52 endometrial cancers 52 systemic lupus erythematosus SLE 52 journal Nature Genetics 52 apolipoprotein E4 52 nongenetic factors 52 endometrial cancer 52 G6PD deficiency 52 bowel cancers 52 myotonic dystrophy 52 haptoglobin 52 susceptibility genes 52 chromosome #q# [001] 52 MSH2 51 HLA B 51 COX2 51 YKL 51 testicular germ cell 51 CCR5 delta# 51 familial adenomatous polyposis 51 proband 51 hereditary predisposition 51 metabolic syndrome 51 mitochondrial mutations 51 AAT deficiency 51 fasting glucose levels 51 somatic mutations 51 brain lesions 51 habitual snoring 51 TP# mutation 51 Helicobacter 51 mice lacking 51 Ets2 51 tumor suppressor protein 51 Genetic variations 51 T1DM 51 autoantibodies 51 EGFR mutations 51 polymorphism 51 aneuploidy 51 mammary stem cells 51 El Sohemy 51 NF1 51 GAB2 51 Clusterin 51 cholesterol metabolism 51 heterozygotes 51 TB bacterium 51 BRCA1 51 Leitzmann 51 2 diabetes T2D 51 SLC#A# [001] 51 variant alleles 51 SRBD 51 autosomal recessive disease 51 enteroviruses 51 chlamydial infection 51 BRCA1 mutation 51 #q# [001] 51 HNPCC 51 APOL1 51 Epstein Barr virus EBV 51 molecular pathway 51 EBV infection 51 DISC1 gene 51 FGFs 51 germline mutations 51 genetic determinants 51 vitamin D deficiency 51 cognitively normal 51 C. neoformans 51 PPAR gamma 51 CIB1 51 nongenetic 51 genetic abnormality 51 exfoliation glaucoma 51 Li Fraumeni syndrome 51 colon cancers 51 HMGCR 51 recurrent miscarriages 51 hypocretin 51 SHANK3 51 thyrotropin levels 51 nonmelanoma skin cancers 51 penetrance 51 fatty liver disease 51 nevi 51 endothelial dysfunction 51 lipoprotein 51 oxidized lipids 51 troponin T 51 LPA gene 51 resistin 51 Colorectal cancers 51 KIAA# 51 microdeletion 51 signaling molecule 51 sortilin 51 SMN2 51 modifiable risk 51 genetically susceptible 51 Nature Genetics 51 Apobec3 51 PDE#A 51 epigenetic mechanisms 51 repeat allele 51 CRTC3 51 receptor gene 51 KLF# 51 BRCA gene mutations 51 allostatic load 51 MnSOD 51 genetic makeup 51 hereditary breast cancer 51 Ashkenazi Jewish 51 gut microbes 51 plasma kallikrein 51 hormone ghrelin 51 miRNA genes 51 DRD4 gene 50 OPRM1 gene 50 ADH1B * 50 GFP gene 50 chromosomal aberrations 50 genes BRCA1 50 onset Alzheimer disease 50 hormone leptin 50 intra abdominal fat 50 recessive trait 50 febrile seizure 50 apolipoprotein E APOE 50 gene APOE4 50 knee OA 50 genes CYP#C# 50 BRIP1 50 mosaicism 50 mutated protein 50 HLA DQ2 50 SOD2 gene 50 breast cancer genes BRCA1 50 RBP4 50 IGF1 50 epigenetic inheritance 50 gestational diabetes mellitus GDM 50 SMN2 gene 50 MIF gene 50 DRD4 50 WDR# 50 T2D 50 Autoimmune disorders 50 testicular tumors 50 ZNF# 50 recessive mutations 50 Akt1 50 fetuin 50 HLA gene variant 50 elevated depressive symptoms 50 serotonin receptor 50 SRY gene 50 behavioral disinhibition 50 TMEM#B 50 insulin resistance 50 clade B 50 MetS 50 Uterine cancer 50 Hormone pills 50 recessive gene 50 perimenopausal women 50 BRCA gene mutation 50 dopamine transporter 50 monogenic 50 molecular mechanism 50 epigenetic alterations 50 chromosomal disorders 50 microRNA molecules 50 missense mutation 50 ORMDL3 50 SIDS infants 50 colorectal polyps 50 neural tube defect 50 monozygotic twins 50 connexin 50 adiponectin 50 SE alleles 50 NF1 gene 50 IL#R 50 single nucleotide polymorphism 50 endogenous estrogen 50 thyroid hormone levels 50 CAG repeats 50 subclinical hypothyroidism 50 #p#.# [001] 50 MLL gene 50 atopy 50 metabolic abnormalities 50 nicotinic receptor 50 genetic abnormalities 50 atherosclerosis 50 JAK2 mutation 50 mitochondrial genome 50 APOC3 50 WNK1 50 alpha carotene 50 nestin 50 androgen receptor gene 50 alpha synuclein protein 50 venous thrombosis 50 mutant protein 50 IKZF1 50 LRRK2 mutation 50 adenoma 50 uric acid levels 50 aneuploidies 50 Kari Stefansson 50 mice genetically engineered 50 biologic pathways 50 uveal melanoma 50 Genetic mutation 50 klotho 50 neuropeptide Y NPY 50 insulin resistance syndrome 50 CYP#E# 50 histone modification 50 homozygosity 50 Six3 50 BRCA carriers 50 fatty acid synthase 50 achromatopsia 50 BRAF gene 50 MLL2 50 chronic prostatitis 50 synuclein 50 CFTR gene 50 persistent pulmonary hypertension 50 Treg cell 50 genetic alteration 50 KRAS gene 50 GPC5 50 SIRT6 50 endogenous retroviruses 50 molecular abnormalities 50 Apolipoprotein E 50 monozygotic twin 50 Calcium supplements 50 metabolic abnormality 50 encodes protein 50 SH#B# 50 mitochondrial fusion 50 epigenetically 50 heart disease 49 telomere length 49 familial hypercholesterolaemia 49 T. gondii 49 FANCD2 49 serotonin transporter 49 chromosomal rearrangement 49 CYP#C# * 49 colon tumors 49 non aspirin NSAIDs 49 abdominal obesity 49 inherit predisposition 49 FADS2 49 CYP# [002] 49 MHC molecules 49 chromosome abnormalities 49 HDL2 49 aldehyde dehydrogenase 49 oxysterols 49 breast cancer metastasis 49 gestational diabetes mellitus 49 Cryptococcus neoformans 49 abnormal glucose tolerance 49 ovulatory infertility 49 microbleeds 49 coronary calcification 49 trans palmitoleic acid 49 K ras mutations 49 cardiovascular disease 49 neurological abnormalities 49 dysbindin gene 49 FXTAS 49 chromosome translocations 49 amino acid homocysteine 49 prostate carcinogenesis 49 fructose diet 49 B7 H3 49 #q#.# [001] 49 gamma tocopherol 49 CMV infection 49 carotid atherosclerosis 49 exomes 49 dysbindin 49 TT genotype 49 herpes viruses 49 malignant lymphoma 49 GABRA2 49 metabolizing enzymes 49 Joubert syndromes 49 virulence genes 49 CYP#A# gene 49 genetic loci 49 metabolic disturbances 49 PTEN gene 49 malaria parasite Plasmodium falciparum 49 CagA 49 #q# [002] 49 Genital herpes 49 melatonin receptor 49 muscular dystrophies 49 LRRK2 mutations 49 FTLD 49 chromosome 49 genotype 49 Klotho gene 49 carotid plaque 49 bone thinning 49 G#D mutation 49 Framingham Offspring Study 49 OCA2 49 parkinsonism 49 untreated celiac disease 49 #q#.# [002] 49 lung adenocarcinoma 49 maternally transmitted 49 fetal hemoglobin 49 RUNX3 49 assortative mating 49 mitochondrial metabolism 49 PON1 49 PARP inhibition 49 TSC1 49 ductal breast cancer 49 genetic syndromes 49 serum selenium 49 genetic markers 49 body fatness 49 hsp# 49 elevated homocysteine 49 hereditary deafness 49 INF2 49 GATA4 49 underlying pathophysiology 49 vitamin D receptors 49 periodontitis 49 segmental duplications 49 BRAF mutation 49 Adiponectin 49 esophageal squamous cell carcinoma 49 MCAD deficiency 49 Sporadic CJD 49 LKB1 49 ependymomas 49 coronary artery calcium 49 ovarian hormones 49 FoxO3 49 Glucose Metabolism 49 physiological mechanisms 49 NOD2 49 NRG1 49 Li Fraumeni 49 cohesin 49 psychotic illnesses 49 febrile seizures 49 molecular pathways 49 VKORC1 49 Mycoplasma pneumoniae 49 NF2 49 Wnt#b 49 polycystic ovary syndrome 49 susceptibility locus 49 preterm delivery 49 RCAN1 49 indels 49 nondemented 49 Hakonarson 49 amyloid deposition 49 inherited predisposition 49 SNPs pronounced snips 49 poor metabolizers 49 gallstone disease 49 cystatin C 49 BMPR2 49 esophageal adenocarcinoma 49 causative genes 49 PTEN mutation 49 mammary cells 49 mitochondrial proteins 49 Stomach cancer 49 Vitamin D supplements 49 S#A# [002] 49 PCSK9 protein 49 3kg heavier 49 rs# [001] 49 #p#.# [002] 49 UCP2 49 atherosclerotic lesions 49 amyloid protein 49 Lafora disease 49 micronuclei 49 CYP#D# 49 p# mutation 49 SERT gene 49 DICER1 49 squamous cell carcinomas 49 chromosomal rearrangements 49 anal cancers 49 tau mutation 49 subclinical atherosclerosis 49 Single Nucleotide Polymorphisms 49 CHD7 49 lipid abnormalities 49 TPMT 49 BCL#A 49 atypical hyperplasia 49 IRF6 gene 49 hereditary nonpolyposis colorectal cancer 49 Male pattern baldness 49 Wnt pathway 49 KLF4 49 Apert syndrome 49 oesophageal adenocarcinoma 49 colorectal tumors 49 chromosome abnormality 49 PLoS Genetics 49 latent TB infection 48 HLA B# gene 48 filaggrin gene 48 sarcosine 48 Folate deficiency 48 denser breasts 48 elevated triglycerides 48 p# gene 48 selenium supplementation 48 Darapladib 48 microRNA miR 48 CYP#C# [002] 48 X chromosome genes 48 C#Y mutation 48 Vitamin D supplementation 48 abdominal fat 48 spontaneous preterm delivery 48 Oral contraceptives 48 Genes 48 BRCA2 carriers 48 unmeasured factors 48 adrenal function 48 Scarmeas 48 toxoplasma 48 enterovirus infection 48 C. pneumoniae 48 gastric carcinogenesis 48 autosomal 48 pneumococcal infection 48 Hypertrophic cardiomyopathy 48 familial clustering 48 fatty acid metabolism 48 colorectal cancer 48 SCA5 48 DISC1 48 EGFR mutation 48 H. pylori infection 48 CatB 48 breast cancers 48 micro RNAs 48 hereditary hemochromatosis 48 Vitamin B# deficiency 48 cannabinoid receptors 48 GABRA2 gene 48 KCNH2 48 gene amplification 48 SGK1 48 FMR1 48 anovulatory infertility 48 colorectal cancer CRC 48 APOE e4 allele 48 heterozygote 48 inflammatory polyarthritis 48 autistic regression 48 cTnT 48 adrenal cortex 48 chronic heartburn 48 Akt3 48 NR#A# 48 JAK2 enzyme 48 Chronic insomnia 48 cortisol levels 48 PPARγ 48 abnormal hemoglobin 48 coronary artery calcification 48 MSMB 48 dysglycemia 48 thrombophilia 48 miRNA expression 48 ADAM# 48 SIRT1 48 recurrent miscarriage 48 bile acid metabolism 48 LRAT 48 causative gene 48 CYP#B# 48 humanin 48 colorectal adenoma 48 pRb 48 spontaneous mutation 48 TOMM# 48 germline mutation 48 Ashkenazi Jews 48 DNA methylation patterns 48 MGUS 48 MEF2A 48 TYMS 48 polycystic disease 48 CHRNA5 48 HbF 48 Peutz Jeghers syndrome 48 lipid levels 48 Genetic predisposition 48 HLA DRB1 * 48 choline intake 48 transthyretin 48 folate metabolism 48 ABCA1 48 hippocampal function 48 vitamin B6 48 G#S [002] 48 Abdominal fat 48 impaired fasting glucose 48 chromosomal abnormality 48 faulty BRCA2 gene 48 familial adenomatous polyposis FAP 48 DEC2 48 pneumococci 48 glycemic diet 48 INTERHEART study 48 NSAIDS 48 inherited genetic mutation 48 prothrombotic 48 homocysteine levels 48 advanced adenomas 48 cortisol secretion 48 Prox1 48 autoantibody 48 PPAR γ 48 HPV strains 48 silent myocardial ischemia 48 Foxp3 48 parasite Toxoplasma gondii 48 hormone therapy estrogen 48 A1 allele 48 primary cilia 48 chitinase 48 GNAQ 48 herpesviruses 48 precancerous colon polyps 48 autistic traits 48 Excessive daytime sleepiness 48 glutamate signaling 48 gene expression 48 M. pneumoniae 48 advanced adenoma 48 autoantigens 48 poorer prognosis 48 Epstein Barr virus 48 Folic acid supplements 48 BRAF mutations 48 dyskeratosis congenita 48 BRCA breast cancer 48 splice junctions 48 nicotinamide 48 restless legs 48 pathogenic mechanisms 48 MYCN amplification 48 Abdominal aortic aneurysms 48 corticosterone levels 48 orexin 48 Haptoglobin 48 vascular dysfunction 48 IKKa 48 anaplastic lymphoma kinase 48 ACAT2 48 contagious yawning 48 obestatin 48 genetically predisposed 48 SNP rs# [001] 48 Cowden syndrome 48 G6PD 48 SLC#A# gene [001] 48 premenstrual syndrome PMS 48 rhinoviruses 48 genomic deletions 48 attention-deficit/hyperactivity disorder ADHD 48 impaired glucose tolerance 48 melanosomes 48 MECP2 gene 48 ACE2 gene 48 adenomas 48 MLH1 48 prairie vole 48 herpes zoster 48 heterozygosity 48 NFkB 48 magnesium intake 48 epigenetic marks 48 asymptomatically 48 mammary cancers 48 autism susceptibility genes 48 Genetic mutations 48 preeclampsia 48 FOXP2 gene 48 DRB1 * 48 SCN5A 48 HNSCC 48 underactive thyroid gland 48 Candida species 48 Kozyrskyj 48 Grodstein 48 SHBG 48 BRAF V#E 48 Alzheimer pathology 48 nonalcoholic steatohepatitis NASH 48 chromosome rearrangements 48 osteopontin 48 cardiovascular disease CVD 48 vitamin D receptor 48 eotaxin 48 herpes infection 48 tau protein tangles 48 overt hypothyroidism 48 rs# [004] 48 nicotine dependence 48 huntingtin gene 48 CDKN2A 48 human leukocyte antigen 48 infective agent 48 HIV HCV coinfected 47 fibrillin 1 47 intermittent exotropia 47 fructose intolerance 47 Clinical Endocrinology & 47 gene predisposing 47 methylation patterns 47 chromosomal instability 47 nonmelanoma skin cancer 47 APOE4 variant 47 melanopsin 47 prediabetes 47 fungus Cryptococcus neoformans 47 HLA molecules 47 PGDH 47 pre menopausal 47 TACI mutations 47 oropharyngeal cancer 47 BRAF protein 47 number variants CNVs 47 primary biliary cirrhosis 47 atopic disease 47 dopamine receptor 47 polymorphic ventricular tachycardia 47 non coding RNA 47 hedgehog signaling 47 CXCL5 47 neuroblastomas 47 chromosome #q 47 remnant lipoproteins 47 LC#m# vaccine 47 LRP6 47 Nordestgaard 47 herpes virus 47 Wolbachia 47 NF kB 47 BRCA1 BRCA2 47 #q#.# deletion syndrome 47 colon polyps 47 undiagnosed sleep apnea 47 mammographic density 47 mitochondrial function 47 C1q 47 HER2 expression 47 cardiovascular mortality 47 klotho gene 47 metabolic dysfunction 47 progressive neurodegenerative disorder 47 genetically altered mice 47 thyrotropin 47 Dr. Edward Giovannucci 47 coronary heart 47 gastrointestinal stromal tumors GISTs 47 journal Psychosomatic Medicine 47 hemochromatosis 47 irreversible blindness 47 UGT#B# 47 insulin resistant 47 onset Alzheimer 47 endocrine tumors 47 sex hormone estrogen 47 glucose intolerance 47 Cockayne syndrome 47 HPVs 47 TZDs 47 SIR2 47 F#del mutation 47 FOXP2 47 DHFR 47 lactose tolerance 47 chromosome aberrations 47 N. gonorrhoeae 47 hippocampal volume 47 Wnt signaling pathway 47 Polycystic ovary syndrome PCOS 47 Chlamydia trachomatis 47 subtype 47 cardio vascular disease 47 causal variants 47 knee osteoarthritis 47 BDNF protein 47 FCGR3A 47 variant allele 47 beta carotene supplementation 47 epigenetic markers 47 protein p# 47 DeCode Genetics 47 p#INK#a 47 impaired glucose metabolism 47 nicotinic receptors 47 gene fusions 47 basal cell carcinomas 47 tuberculosis bacterium 47 nNOS 47 Kari Stefansson CEO 47 MDM2 47 untreated hypothyroidism 47 chromosome #q#.# [001] 47 extrapyramidal symptoms 47 haemochromatosis 47 estrogen deficiency 47 AUDs 47 SOX3 gene 47 autosomal recessive 47 tibolone 47 vimentin 47 metapneumovirus 47 mitochondrial gene 47 lactase persistence 47 Notch signaling 47 LDLR