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(Click for frequent words.) 84 genetic variant 77 gene variation 73 gene mutation 73 gene variants 72 genetic variants 72 allele 71 APOE4 70 mutated gene 70 FTO gene 69 genetic mutation 69 mutation 68 ApoE4 gene 68 APOE gene 68 genetic variation 67 APOE e4 67 genetic variations 67 gene 66 gene mutations 66 ApoE4 65 APOE4 gene 64 mutant gene 64 alleles 64 APOE 64 mutations 63 genetic mutations 63 polymorphisms 63 polymorphism 63 BRCA1 gene 63 susceptibility gene 63 G allele 62 haplotype 62 shorter telomeres 62 genotype 62 apoE4 62 SORL1 62 metabolic syndrome 62 BRCA1 mutations 62 ApoE 62 COMT gene 61 FMR1 gene 61 genes 61 Wwox 61 C#Y 61 MTHFR 61 CNVs 61 HFE gene 61 G#S mutation 61 APOE ε4 61 rs# [003] 61 mutated genes 61 defective gene 61 BRCA mutations 60 TCF#L# gene 60 insulin resistance 60 homozygous 60 TGFBR1 * 6A 60 FTO variant 60 APOE e4 gene 60 APOE allele 60 BRCA mutation 60 EGFR gene 59 heterozygous 59 serotonin transporter gene 59 BRCA2 mutation 59 apolipoprotein E gene 59 genetic trait 59 heritable 59 DQB1 * 59 genetic variants associated 59 PTEN mutations 59 TCF#L# 59 familial pancreatic cancer 59 BRCA2 59 SNPs 59 IGF2 59 clusterin 59 5 HTT gene 59 genetic polymorphisms 59 tumor suppressor gene 59 LRRK2 gene 58 rs# [002] 58 susceptibility genes 58 DRD2 gene 58 genetic defect 58 CFH gene 58 MYH9 gene 58 ApoE gene 58 MC1R gene 58 BRCA1 58 5 HTTLPR 58 genetic predisposition 58 PTPN# 58 X chromosome 58 LQTS 58 heterozygotes 58 NAFLD 58 BARD1 58 TP# mutation 58 DRD2 58 genetic abnormality 58 mutant allele 58 chromosome #q# [001] 58 genes BRCA1 58 KIF6 gene 58 #q# [001] 58 disease NAFLD 57 BRCA2 gene 57 CYP#C# [001] 57 dopamine receptor gene 57 narcolepsy cataplexy 57 apoC III 57 MAOA gene 57 GSTM1 57 Fragile X gene 57 #q# [002] 57 folate deficiency 57 haptoglobin 57 phenotype 57 p# mutations 57 FGFR2 57 alpha synuclein gene 57 Genetic variants 57 BRCA2 gene mutation 57 CALHM1 57 FTO allele 57 CDH1 57 ALDH2 56 STAT4 56 CETP gene 56 variant alleles 56 CNTNAP2 56 CDKN2A 56 CYP#E# gene 56 APOC3 56 UGT#A# * 56 chromosome #p# [001] 56 SLC#A# [002] 56 CHEK2 56 genetic susceptibility 56 genetic markers 56 inherited mutations 56 somatic mutations 56 postmenopausal breast cancer 56 KLF# 56 NPY gene 56 genes predisposing 56 mtDNA mutations 56 adiponectin levels 56 GBA mutations 56 HMGA2 56 dopamine D4 receptor 56 BDNF gene 56 penetrance 56 gene expression patterns 56 cognitively normal 56 colorectal neoplasia 56 EGFR mutations 56 subclinical hyperthyroidism 56 apolipoprotein E 56 HLA B# 56 chromosomal abnormalities 56 sporadic ALS 56 GSTP1 56 glucose metabolism 56 BRCA gene 56 chromosomal regions 56 tumor suppressor protein 56 mitochondrial dysfunction 56 SNP rs# [001] 55 germline mutations 55 CETP VV 55 lipin 55 rs# [001] 55 GSTM1 gene 55 familial hypercholesterolemia 55 ABCB1 55 ε4 55 fasting glucose levels 55 microcephalin 55 IKZF1 55 breast cancer genes BRCA1 55 OPRM1 gene 55 elevated triglyceride levels 55 subclinical hypothyroidism 55 gene APOE 55 MSH2 55 MHC genes 55 CCR5 delta# 55 RUNX3 55 SE alleles 55 BRCA1 mutation 55 MC1R 55 mutant protein 55 LIS1 55 PALB2 55 mutated BRCA1 55 genetic alteration 55 MnSOD 55 ADPKD 55 breast cancer metastasis 55 genotypes 55 BRCA genes 55 signaling molecule 55 genomewide 55 #q#.# [001] 55 miRNA genes 55 microdeletions 55 CYP#C# * 55 number variations CNVs 55 telomere length 55 BRCA2 mutations 55 LKB1 55 missense mutation 55 serotonin transporter 55 cognitive impairment 55 PTEN gene 55 leptin hormone 55 CAG repeats 55 T2D 55 #p# [001] 55 familial ALS 55 CC genotype 55 GRK5 55 mice lacking 54 GSTT1 54 SHANK3 54 gene APOE4 54 MIF protein 54 C#Y mutation 54 SMN2 gene 54 e4 allele 54 miRNAs 54 gene locus 54 EBV infection 54 MC4R gene 54 aldehyde dehydrogenase 54 poorer prognosis 54 mice genetically engineered 54 MTHFR gene 54 NF1 54 repeat allele 54 serotonin receptor 54 KIBRA 54 neuroglobin 54 V Leiden 54 COMT 54 DRD4 54 spontaneous mutations 54 BRCA gene mutation 54 noncarriers 54 molecular mechanism 54 brain shrinkage 54 human leukocyte antigen 54 MAOA 54 CFTR gene 54 IgA deficiency 54 genetic determinants 54 HER2 gene 54 homozygosity 54 epigenetic changes 54 SMN2 54 endothelial dysfunction 54 NF1 gene 54 PICALM 54 polycystic ovary syndrome PCOS 54 APOE epsilon 4 54 single nucleotide polymorphism 54 YKL 54 de novo mutations 54 JAK2 mutation 54 rs# [004] 54 MetS 54 p# gene 54 T1DM 54 HNPCC 54 apoE 54 gene expression 54 SIRT1 54 FXTAS 54 apolipoprotein E4 54 BRAF mutation 54 APOE genotype 54 progranulin 54 HPV# 54 NKX2 54 adenoma 54 chromosome #q# [002] 54 CYP#D# gene 54 nestin 54 HGPS 54 androgen receptor gene 54 APOL1 54 E4 variant 54 impaired fasting glucose 53 ApoE4 allele 53 phenotypes 53 CYP#C# gene 53 genetic polymorphism 53 CYP#D# 53 medulloblastomas 53 CNTNAP2 gene 53 telomere lengths 53 Froguel 53 ACE2 gene 53 Sjögren syndrome 53 VHL gene 53 recessive trait 53 basal cell nevus syndrome 53 homozygotes 53 NF kB 53 parkinsonism 53 brain lesions 53 ADH1B * 53 COX2 53 dopamine transporter gene 53 lung adenocarcinoma 53 tumor suppressor genes 53 FASPS 53 leptin 53 mutant genes 53 aneuploidy 53 Li Fraumeni 53 protein encoded 53 transthyretin 53 metabolic abnormalities 53 HNSCC 53 proband 53 IL#R 53 autoantibody 53 DISC1 53 SIDS infants 53 HLA genes 53 atherosclerosis 53 melatonin receptor 53 Ashkenazi Jewish 53 methylation 53 parkin gene 53 ZNF# 53 Genetic variation 53 vitamin D deficiency 53 SORL1 gene 53 colorectal tumors 53 CatB 53 MC4R 53 chlamydial infection 53 genetic abnormalities 53 epigenetic mechanisms 53 DRD4 gene 53 molecular pathway 53 chromosome 53 gallstone disease 53 Akt1 53 recessive gene 53 TMEM#B 53 abdominal obesity 53 adiponectin 53 CHD7 53 2 diabetes T2D 53 CIB1 53 TCF4 53 hereditary hemochromatosis 53 metabolic syndrome MetS 53 imprinted genes 53 impaired glucose tolerance 53 DEC2 53 G#S [002] 53 S#A# [002] 52 gene polymorphism 52 TOMM# 52 PTEN mutation 52 Prox1 52 colon tumors 52 ovarian hormones 52 elevated CRP 52 H. pylori 52 autosomal recessive 52 familial adenomatous polyposis 52 DAT1 52 HDL2 52 elevated triglycerides 52 AAT deficiency 52 white matter hyperintensities 52 IGF1 52 MHC molecules 52 CRTC3 52 Hashimoto thyroiditis 52 HLA DRB1 52 GPC5 52 methylation patterns 52 cardiovascular disease 52 GAB2 52 SOD2 gene 52 Genes 52 autoantibodies 52 variant allele 52 HLA B 52 premenopausal breast cancer 52 autistic traits 52 progranulin gene 52 heterozygote 52 dysbindin 52 KLF4 52 subtype 52 untreated sleep apnea 52 TT genotype 52 recessive mutations 52 histone modification 52 CCL#L# 52 hereditary predisposition 52 LRRK2 mutation 52 colorectal adenomas 52 CagA 52 hypermethylation 52 EGFR mutation 52 modifiable risk 52 GRK2 52 fetuin 52 chromosomal aberrations 52 estrogen receptor 52 PON1 52 MIF gene 52 glucose intolerance 52 DISC1 gene 52 trans palmitoleic acid 52 IDH1 52 tumor suppressor 52 endometrial cancer 52 BRCA2 breast cancer 52 B7 H3 52 TLR3 52 FTLD 52 genetic makeup 52 Wnt#b 52 UCP2 52 knee OA 52 MECP2 gene 52 coronary artery calcium 52 MGUS 52 gastric carcinogenesis 52 hormone leptin 52 genetically engineered mice 52 coronary calcification 52 loci 52 fewer dopamine receptors 52 LRP5 52 receptor gene 52 esophageal squamous cell carcinoma 52 Li Fraumeni syndrome 52 monozygotic twins 52 HOTAIR 52 hormone ghrelin 52 fatty liver disease 52 heart disease 52 neuroD2 52 elevated homocysteine 52 NR#A# 52 PDE#A 52 genotyped 52 brain derived neurotrophic 52 cardiac hypertrophy 52 estrogen receptor alpha 52 CXCL5 52 Nrf2 52 hypocretin 52 neuroblastoma tumors 52 p# protein 52 frontotemporal dementia 52 systemic lupus erythematosus SLE 52 STK# gene 52 HMGA2 gene 52 atypical hyperplasia 52 resistin 52 MLL2 52 cardiovascular mortality 51 X chromosome genes 51 CCR5 mutation 51 KRAS gene 51 UGT#B# 51 C. pneumoniae 51 missense mutations 51 nondemented 51 LRRK2 51 C reactive protein 51 SLC#A# [001] 51 Akt 51 El Sohemy 51 overexpression 51 TSP1 51 esophageal adenocarcinoma 51 SH#B# 51 p#INK#a 51 vimentin 51 untreated celiac disease 51 Ets2 51 lipid levels 51 estrogen receptors 51 lipoprotein 51 PTP1B 51 hormone adiponectin 51 IL#B 51 haplotypes 51 journal Nature Genetics 51 IGFBP 51 RIP1 51 Neuregulin 1 51 Apolipoprotein E 51 BACE1 51 CYP# [002] 51 major histocompatibility complex 51 LRAT 51 causal variants 51 atherosclerotic lesions 51 heterozygosity 51 Nature Genetics 51 apolipoprotein E APOE 51 carotid atherosclerosis 51 NOD2 51 latent TB infection 51 TYMS 51 gestational diabetes mellitus 51 dopamine receptors 51 Klotho gene 51 mutated protein 51 VKORC1 51 encodes protein 51 A1 allele 51 neuroblastomas 51 NF2 51 ependymomas 51 colorectal cancer CRC 51 dentate gyrus 51 HbF 51 AUDs 51 genetic 51 pathogenic mutations 51 DRB1 * 51 EZH2 51 mitochondrial mutations 51 anaplastic lymphoma kinase 51 BRCA2 carriers 51 #p#.# [002] 51 klotho 51 thyrotropin levels 51 dopamine D2 receptors 51 microRNAs 51 osteopontin 51 BRCA gene mutations 51 VIPR2 51 #p#.# [001] 51 myostatin gene 51 Klinefelter syndrome 51 #q# deletion 51 LDLR 51 RBP4 51 bowel polyps 51 hippocampal volume 51 autosomal dominant disorder 51 vitamin B# deficiency 51 Alzheimer disease pathology 51 APOE e4 allele 51 microalbuminuria 51 Chromosome 51 PP2A 51 cholesterol metabolism 51 neuroligins 51 HDL cholesterol 51 PDGFRA 51 GATA4 51 leptin resistance 51 silent myocardial ischemia 51 CCR3 51 enterovirus infection 51 genetic alterations 51 CYP#A# gene 51 urate 51 colon cancers 51 SHBG 51 progerin 51 gene expression profiles 51 habitual snoring 51 Fragile X syndrome 51 periodontitis 51 receptor protein 51 FMRP protein 51 FMR1 51 Clusterin 51 protein p# 51 type2 diabetes 51 molecular pathways 51 LXRs 51 chromosomal translocations 51 behavioral disinhibition 51 JAK2 51 causative gene 51 nondiabetic 51 HLA DQ2 51 recessive genes 51 GABRA2 51 MECP2 51 CYP#E# 51 chromosomal instability 51 exfoliation glaucoma 51 triglyceride levels 51 abdominal fat 51 chromosome rearrangements 51 breast cancers 51 WNK1 51 KIAA# 51 mutant mice 51 Ashkenazi Jews 51 IDH1 mutation 51 K ras mutations 51 BCL#A 51 WT1 51 FGFR2 gene 51 nonalcoholic fatty liver 51 nicotinic receptor 50 MSMB 50 SCN5A 50 cyclin D1 50 endometrial cancers 50 testicular germ cell 50 CaMKII 50 DNA methylation 50 gene polymorphisms 50 TOP2A 50 cardioembolic stroke 50 hereditary breast cancer 50 p# mutation 50 herpes simplex virus 50 MAPK pathway 50 gene encoding 50 SNCA 50 folate intake 50 germline mutation 50 leptin receptor 50 NPY 50 MLH1 50 NFkB 50 genetically susceptible 50 hemochromatosis 50 phenotypic variation 50 genes encoding 50 PPAR γ 50 androgen receptor 50 PIK3CA 50 KIF6 gene variant 50 inflammatory markers 50 MEF2A 50 DICER1 gene 50 glucocorticoid receptors 50 SIRT6 50 mosaicism 50 receptor 50 insulin secretion 50 sCJD 50 ORMDL3 50 neurexin 50 BRAF mutations 50 fat hormone leptin 50 synapse formation 50 CGG repeats 50 depressive symptoms 50 Six3 50 mammary cancers 50 GPR# [002] 50 dopamine transporter 50 oropharyngeal cancer 50 β amyloid 50 transgenic mouse model 50 hippocampal function 50 C EBP alpha 50 filaggrin gene 50 chromosomal alterations 50 Irs2 50 chromosomal rearrangement 50 receptors 50 G6PD 50 albuminuria 50 PPAR gamma 50 BRAF gene 50 hypovitaminosis D 50 TSC1 50 BRCA1 BRCA2 50 cognitive decline 50 mtDNA 50 LDL receptor 50 GBM tumors 50 TACI mutations 50 STAT3 50 RASSF1A 50 alpha synuclein protein 50 GNAQ 50 Pin1 50 autism susceptibility genes 50 HLA gene variant 50 progressive neurodegenerative disorder 50 lipid metabolism 50 dysregulation 50 brain atrophy 50 virulence genes 50 JAK2 enzyme 50 deleterious mutations 50 abdominal adiposity 50 chromosomal anomaly 50 highly heritable 50 aldosterone 50 perimenopausal women 50 LPA gene 50 BRCA 50 HLA alleles 50 T2DM 50 BRAF V#E 50 telomere shortening 50 neuropeptide Y NPY 50 genes CYP#C# 50 Aβ 50 beta1 integrin 50 genetically modified mice 50 pre menopausal 50 Notch signaling 50 signaling pathway 50 cryptorchidism 50 coronary disease 50 PLoS Genetics 50 dopamine receptor 50 mutant alleles 50 KCNE2 50 estrogen receptor negative 50 caveolin 50 factor BDNF 50 corticosterone levels 50 PCSK9 protein 50 NKT cells 50 progranulin protein 50 MYH9 50 Alu elements 50 genetic loci 50 adiponectin concentrations 50 vasopressin receptors 50 PKM2 50 hereditary deafness 50 gene amplification 50 transcription factors 50 estrogen metabolism 50 PPARγ 50 G#D mutation 50 postoperative delirium 50 microglial 50 thyrotropin 50 abnormalities 50 autosomal dominant 50 prostate cancer CaP 50 causative genes 50 chromosomal disorders 50 CHRNA5 gene 50 LRRK2 mutations 50 melanopsin 50 subclinical atherosclerosis 50 protein kinase C 50 preeclampsia 50 Meckel Gruber 50 uric acid levels 50 intra abdominal fat 50 cannabinoid receptors 50 cyclin E 50 breast cancer gene mutation 50 microbleeds 50 Foxp3 50 fetal hemoglobin 50 biologic pathways 50 HLA DRB1 * 50 CYP#C# [002] 50 ApoB 50 alpha synuclein 50 miR 50 insulin sensitivity 50 SGK1 50 systolic dysfunction 50 genetic traits 49 BRCA2 mutation carriers 49 gene DRD4 49 chromosome abnormality 49 nicotinic receptors 49 insulin resistant 49 coronary artery disease 49 S#K# 49 autosomal 49 vitamin D insufficiency 49 recessive mutation 49 BMPR2 49 Lp PLA2 49 Treg cell 49 Brd4 49 Peutz Jeghers syndrome 49 uPAR 49 onset Alzheimer disease 49 Cowden syndrome 49 aneuploidies 49 promoter methylation 49 Skp2 49 neuropeptide Y 49 serum uric acid 49 postnatally 49 retrovirus 49 glutamate signaling 49 cortisol levels 49 transcription factor 49 subclinical 49 TAp# 49 NAT2 49 thyroid function 49 plasma kallikrein 49 breast tumors 49 protein 49 BRCA carriers 49 genetically inherited 49 osteocalcin 49 vasopressin 49 genetically predisposed 49 medulloblastoma 49 dizygotic twins 49 synuclein 49 ADAM# 49 SCA5 49 mitochondrial 49 amyloid deposits 49 lobular breast cancer 49 uveal melanoma 49 Adiponectin 49 ERCC1 49 PB1 F2 49 primary ovarian insufficiency 49 neuroendocrine 49 SIRT1 gene 49 CYP#B# 49 CEACAM1 49 insulin resistance syndrome 49 fatty acid metabolism 49 prediabetes 49 sex hormone estrogen 49 FOXP2 gene 49 H. pylori infection 49 arterial stiffness 49 visceral fat 49 impaired glucose metabolism 49 exomes 49 cystatin C 49 Ras pathway 49 ALK mutations 49 mRNAs 49 nonmelanoma skin cancer 49 TP# mutations 49 protein tau 49 BDNF 49 micro RNA 49 PPARg 49 slow metabolizers 49 EGFR 49 monogenic 49 IGFBP 3 49 nonsense mutations 49 susceptibility locus 49 metabolic abnormality 49 sortilin 49 nicotine dependence 49 autosomal recessive disease 49 genetic defects 49 genetically altered mice 49 MeCP2 gene 49 MDM2 49 PKC beta 49 activin 49 Vpu 49 tau mutation 49 mild cognitive impairment 49 nonmelanoma skin cancers 49 bile acid metabolism 49 GBV C 49 epigenetic silencing 49 colorectal carcinoma 49 ACE2 49 glucose tolerance 49 genetic syndromes 49 epigenetic alterations 49 PDGFR 49 micro RNAs 49 karyotype 49 SRBD 49 endostatin 49 eNOS 49 GABRA2 gene 49 premutation 49 adrenal function 49 vitamin D receptors 49 neural tube defect 49 p# [001] 49 hyperinsulinemia 49 metabolic 49 albumin excretion 49 KIF6 49 klotho gene 49 chromosome abnormalities 49 GFP gene 49 Notch1 49 hydroxyvitamin D levels 49 familial adenomatous polyposis FAP 49 5q 49 tyrosine phosphorylation 49 hypermethylated 49 presenilin 49 Folate deficiency 49 Niemann Pick disease 49 Obstructive sleep apnea 49 DICER1 49 Epstein Barr virus 49 beta thalassemia 49 SLC#A# gene [001] 49 cerebral infarction 49 serum selenium 49 gene p# 49 central adiposity 49 prenatal testosterone 49 homolog 49 impaired cognition 49 D2 receptors 49 colorectal cancer 49 miR #a [001] 49 neurological abnormalities 49 dietary glycemic index 49 latent TB 49 deleterious mutation 49 HLA DRB1 SE 49 SOD1 protein 49 fatty liver 49 cardiac insufficiency 49 XLHED 49 HER2 receptor 49 microdeletion 49 NNRTI resistance 49 testosterone supplementation 49 BMP2 49 PARP inhibition 49 DLX5 49 lipid abnormalities 49 NOMID 49 proto oncogene 49 HLA molecules 49 placental function 49 sleep disordered breathing 49 atopy 49 chromosome #q#.# [001] 49 MetAP2 49 mutant worms 49 KRAS mutations 49 Bcl xL 49 FGF2 49 orexin 49 hypertension 49 transferrin saturation 49 neural circuitry 49 obesity insulin resistance 49 periodontal disease 49 ovarian tumors 49 cardiorespiratory fitness 49 apelin 48 sirtuin 48 ncRNAs 48 insulin receptors 48 inherited neurological disorder 48 IKKa 48 diabetes mellitus T2DM 48 DNA methylation patterns 48 polycystic ovary syndrome 48 dysbindin gene 48 Ascherio 48 intensive statin therapy 48 mammary cells 48 Wnt signaling pathway 48 BMP signaling 48 POMC neurons 48 AMPK 48 neurodevelopmental outcome 48 serum cholesterol 48 promoter polymorphism 48 ENPP1 48 thyroid hormone levels 48 gut microbes 48 OCA2 48 SIRT3 48 microRNA molecules 48 underlying pathophysiology 48 oesophageal adenocarcinoma 48 oxidative stress 48 HMGCR 48 biomarker 48 vitamin D receptor 48 neurodegenerative disorder 48 nongenetic factors