Related by context. All words. (Click for frequent words.) 68 MYH9 gene 68 APOE4 68 missense mutations 67 MTHFR 67 PTPN# 67 Li Fraumeni syndrome 67 germline mutations 67 ABCB1 67 proband 67 C#Y 67 MSH2 66 nondemented 66 apolipoprotein E gene 66 de novo mutations 66 autosomal recessive disease 66 TP# mutation 66 APOE e4 66 Fragile X gene 66 recessive mutations 66 mutated K ras 66 APOE gene 65 Genetic variants 65 apolipoprotein E 65 susceptibility alleles 65 HLA DQ2 65 PTEN mutations 65 ApoE gene 65 nonhereditary 65 inherited mutations 65 autosomal recessive 65 APOE ε4 65 shorter telomere length 64 penetrance 64 apolipoprotein E4 64 CCR5 delta# 64 TCF#L# gene 64 IgA deficiency 64 MTHFR gene 64 BARD1 64 #q# deletion 64 maternally inherited 64 dominantly inherited 64 spontaneous mutations 64 APOE genotype 64 MLH1 64 monogenic 64 susceptibility gene 64 NPC1 64 allele frequencies 63 HNPCC 63 leptin deficiency 63 LIS1 63 apoC III 63 BRCA1 mutations 63 PTEN gene 63 TT genotype 63 HLA B# 63 ApoE4 63 APOE epsilon 4 63 heterozygote 63 LRAT 63 heterozygous 63 APOE allele 63 prothrombotic 63 gene polymorphism 63 GABRA2 63 APOL1 63 Genetic mutations 63 SLC#A# [002] 63 OPRM1 gene 63 familial adenomatous polyposis FAP 63 PON1 63 CC genotype 63 LRRK2 gene 63 human leukocyte antigen HLA 63 heritable 63 mitochondrial mutations 62 gene locus 62 KIBRA 62 MYH9 62 monozygotic twins 62 p# mutations 62 BMPR2 62 HbF 62 genetic loci 62 COL#A# 62 gene APOE 62 SCN1A 62 APOE4 gene 62 CYP#B# 62 alpha synuclein gene 62 SHANK3 62 chromosomal alterations 62 LRP5 62 HLA DRB1 * 62 rs# [004] 62 apoE4 62 allelic variants 62 genetic polymorphisms 62 MEF2A 62 GPC5 62 PALB2 62 basal cell nevus syndrome 62 nongenetic 62 CYP#D# gene 62 monozygotic twin 62 DQB1 * 62 epigenetically 62 mutated gene 62 Leydig cell 62 homozygosity 62 sCJD 62 HFE gene 62 gene polymorphisms 62 mosaicism 62 GSTT1 62 syngeneic 62 hyper IgE syndrome 62 microsatellite instability 62 KRAS oncogene 62 CYP#C# gene 62 CDH1 62 NF1 gene 62 Homozygous 62 leptin receptor 62 ataxias 62 mGluR5 antagonist 62 ADPKD 62 heterozygotes 62 underlying pathophysiology 62 mutant allele 62 Genetic predisposition 61 narcolepsy cataplexy 61 CHD7 61 G#S mutation 61 IKZF1 61 thyrotropin levels 61 mutant gene 61 Meckel Gruber 61 phenotypic expression 61 genomic imprinting 61 DNA methylation patterns 61 FMR1 gene 61 metabolic abnormalities 61 KIF6 gene 61 galactosemia 61 transgenic mouse models 61 modifier genes 61 autopsied brains 61 recessive trait 61 UGT#B# 61 neuroligins 61 BRCA2 gene 61 MC1R gene 61 familial aggregation 61 hereditary predisposition 61 IL#R 61 ApoE 61 SLC#A# gene [001] 61 hypermethylated 61 autosomal dominant inheritance 61 MC4R gene 61 pathogenic mutations 61 microdeletions 61 CYP#C# [002] 61 #p#.# [001] 61 Apolipoprotein E 61 Klinefelter syndrome 61 JAK2 mutation 61 neurofibrillary 61 DLX5 61 chromosome #q# [002] 61 heritable genetic 61 MC1R 61 ABCB1 gene 61 chromosomal deletions 61 maternally transmitted 61 causative genes 61 K ras mutations 61 GSTM1 61 CYP#A# gene 61 CAG repeats 61 hippocampal function 61 cytopathic 60 5 HTTLPR 60 CFTR gene 60 HLA genes 60 chromosomal anomalies 60 sporadic ALS 60 DRD2 gene 60 endophenotypes 60 paternally inherited 60 dyskeratosis congenita 60 TMEM#B 60 dopamine receptor gene 60 congenital deficiency 60 APOC3 60 BCL#A 60 differential gene expression 60 familial adenomatous polyposis 60 familial ALS 60 ApoE4 gene 60 alleles 60 gastric carcinomas 60 Genetic variation 60 klotho 60 promoter polymorphism 60 huntingtin gene 60 orthologs 60 LRRK2 mutations 60 BRCA1 BRCA2 60 dysgenesis 60 hypertrophic cardiomyopathy HCM 60 HLA molecules 60 Alleles 60 familial clustering 60 TGFBR1 60 holoprosencephaly 60 MECP2 gene 60 virulence genes 60 aneuploid 60 cholesteryl ester transfer 60 predisposing factor 60 glutamic acid decarboxylase 60 monozygotic 60 autosomal recessive genetic 60 causative mutation 60 genetic makeups 60 Li Fraumeni 60 androgen receptor gene 60 testicular germ cell 60 polygenic 60 untreated celiac disease 60 ALK gene 60 Genetic variations 60 susceptibility locus 60 STAT4 60 inherited predisposition 60 idiopathic PAH 60 familial hypercholesterolemia 60 #q# [001] 60 FASPS 60 T1DM 60 klotho gene 60 genetically inherited 60 debilitating neurodegenerative disorder 60 C. neoformans 60 HLAs 60 germline mutation 60 phenotype 60 KCNH2 60 normal karyotype 60 gene MECP2 60 p#INK#a 60 autosomal dominant disorder 60 COMT gene 60 renal tubular 60 chromosome #q# [001] 60 insoluble plaques 60 highly heritable 60 p# mutation 60 IGF2 60 TGFBR1 * 6A 60 #q#.# [002] 60 chromosome #q#.# [001] 60 c KIT 60 HLA DRB1 59 chromosomal rearrangement 59 ENPP1 59 T. vaginalis 59 airway responsiveness 59 NOD2 59 multigenic 59 psychiatric comorbidity 59 CETP VV 59 maternally derived 59 neuroblastoma tumors 59 progranulin mutations 59 MTHFD1L gene 59 genetic variants associated 59 parkinsonism 59 homocystinuria 59 SMN1 59 circadian genes 59 BRCA2 carriers 59 Spinal muscular atrophy 59 Treg cell 59 constitutively expressed 59 metabolizing enzyme 59 Leydig cells 59 susceptibility genes 59 polycystin 59 von Hippel Lindau 59 N. gonorrhoeae 59 CDKN2A 59 Cowden syndrome 59 gene deletions 59 ORMDL3 59 genetic polymorphism 59 noncarriers 59 renal fibrosis 59 DAT1 59 fetal hemoglobin 59 #p#.# [002] 59 variant allele 59 β thalassemia 59 homozygote 59 GBA mutations 59 thyrotropin 59 MLL gene 59 null mice 59 MYCN amplification 59 autosomal dominant 59 G allele 59 gene rearrangements 59 receptor gene 59 methylation patterns 59 IPAH 59 familial polyposis 59 progressive neurodegenerative disorder 59 CFH gene 59 autonomic dysfunction 59 genomewide 59 immunodeficient 59 Clusterin 59 chromosomal regions 59 herpesviruses 59 DRD4 59 TACI mutations 59 phenotypes 59 ciliated 59 CNTNAP2 59 genetic variant 59 microdeletion 59 GSTP1 59 SORL1 gene 59 rs# [001] 59 haematopoietic 59 lymphoblastoid cell lines 59 familial pancreatic cancer 59 Neurofibromatosis type 59 metaplasia 59 pathological hallmark 59 SCD1 59 chromosome #q#.# [002] 59 G6PD deficiency 59 inherited maternally 59 R#W [002] 59 antiphospholipid antibodies 59 hepatic lipase 59 metabolic abnormality 59 etiologic 59 FXTAS 59 SNP rs# [001] 59 chromosomal anomaly 59 PALB2 gene 59 thyroid hormone deficiency 59 motor neuron degeneration 59 C. trachomatis 59 BRAF V#E 59 BDNF gene 59 autosomal dominant polycystic kidney 59 E selectin 59 GATA4 59 Chronic pancreatitis 59 chromosomal aberrations 59 missense mutation 59 genetic predisposition 59 LDL receptor 59 SNPs pronounced snips 59 subclinical hyperthyroidism 59 PTEN tumor suppressor 59 immunocompetent 59 androgen receptor AR 59 beta adrenergic receptor 59 cranial irradiation 59 comorbid disorders 59 homozygotes 58 Foxp3 58 mutation 58 sphingolipid 58 multisystem disease 58 CHEK2 58 DRD2 58 prion gene 58 embryonic tissues 58 SORL1 58 microcephalin 58 BRCA2 gene mutation 58 TCF#L# 58 amyloid peptide 58 antiphospholipid syndrome 58 neurocognitive impairment 58 #q#.# deletion syndrome 58 presymptomatic 58 deleterious mutation 58 Fas ligand 58 apoE 58 cryptogenic 58 e4 allele 58 progranulin gene 58 neonatal lupus 58 Lafora disease 58 airway hyperresponsiveness 58 chorioamnionitis 58 TOMM# 58 thrombophilia 58 Beta thalassemia 58 human leukocyte antigens 58 amyloid ß 58 Aß 58 ApoE4 allele 58 mitochondrial proteins 58 neuropathologic 58 enterocolitis 58 transgenic rats 58 GLUT1 58 FMR1 58 FGFR2 58 FGFs 58 SNP rs# [002] 58 gene APOE4 58 dizygotic 58 FMRP protein 58 autoimmune thyroiditis 58 alpha1 antitrypsin deficiency 58 FGFR2 gene 58 dizygotic twins 58 LMNA 58 molecular abnormalities 58 synovial cells 58 gallstone disease 58 potent inducer 58 normotensive 58 hereditary hemochromatosis 58 Asymptomatic 58 Sonic Hedgehog 58 histocompatibility 58 glycosylated 58 phenotypic variation 58 somatic mutations 58 suppressor gene 58 TOP2A gene 58 rs# [002] 58 epigenetic changes 58 hereditary nonpolyposis colorectal cancer 58 glucocorticoid receptors 58 estrogen receptor alpha 58 rRNA 58 hematopoietic cancers 58 ZNF# 58 thymic 58 gene loci 58 HGPS 58 β amyloid 58 sCD# 58 Hsp# [001] 58 GABRA2 gene 58 #q#.# [001] 58 defective gene 58 mitochondrial metabolism 58 LDLR 58 obstructive coronary artery 58 GRK5 58 chromosomal rearrangements 58 repeat allele 58 CpG island 58 recessive genetic 58 heterotaxy 58 recessive mutation 58 metabolize cholesterol 58 C1q 58 V Leiden 58 prostate cancer CaP 58 FTLD 58 epigenetic silencing 58 chromosome rearrangements 58 Rh factor 58 IL#B gene 58 GSTM1 gene 58 5q 58 CFTR gene mutations 58 puerperal psychosis 58 chromosome #p#.# 58 VKORC1 58 KRAS mutations 58 mutated BRCA1 58 ERK signaling 58 genetic abnormality 58 Epstein Barr virus EBV 58 muscular dystrophies 58 malignant phenotype 58 etiologic factors 58 beta globin 58 gastric carcinogenesis 58 deleterious mutations 58 multi infarct dementia 58 NNRTI resistant virus 58 LRRK2 mutation 58 elevated triglyceride levels 58 epithelial barrier 58 heterozygosity 58 evolutionarily conserved 58 beta1 integrin 58 NF1 58 bronchopulmonary dysplasia 58 prion infection 58 thiopurine 58 perilipin 58 Hp2 2 58 ε4 58 genetic locus 58 myeloproliferative 58 diabetes mellitus DM 58 PTEN protein 58 replicase 58 tumor suppressor protein 58 HIV HCV coinfected 58 intestinal microbiota 58 allelic 58 susceptibility loci 58 5 HTT gene 58 metabolizing enzymes 58 ceruloplasmin 58 protein alpha synuclein 58 MHC genes 57 SSc 57 HER2 neu 57 immunodeficiencies 57 distinct subtypes 57 variant alleles 57 K ras gene 57 paralogs 57 multi factorial disease 57 microfilariae 57 DRB1 * 57 carbohydrate intolerance 57 gene variants 57 LPA gene 57 CYP#C# * 57 hepatoma 57 adiponectin levels 57 gene DRD4 57 Leukemias 57 colonic polyps 57 nonischemic 57 alpha synuclein protein 57 Entamoeba 57 karyotypes 57 mtDNA mutations 57 mutant huntingtin protein 57 dopamine transporter gene 57 indels 57 colorectal adenoma 57 systemic amyloidosis 57 colonic mucosa 57 WNK1 57 Phenotypic 57 HLA DRB1 SE 57 habitual snoring 57 cyclin E 57 aneuploidies 57 PRNP 57 Peutz Jeghers syndrome 57 subclinical 57 teratogens 57 epistasis 57 transgenic mouse model 57 haemochromatosis 57 Phenylketonuria 57 podocyte 57 euthymic patients 57 homodimers 57 chronic lymphocytic 57 fronto temporal dementia 57 pleiotropic effects 57 vasopressin receptor 57 steroidogenic 57 MeCP2 gene 57 ALI ARDS 57 M. pneumoniae 57 UGT#A# * 57 nicotinic receptor 57 #q# deletion syndrome 57 Dr. Bezprozvanny 57 causative gene 57 polyhydramnios 57 hydrops 57 primary ciliary dyskinesia 57 BRCA mutation 57 albumin excretion 57 neuritic 57 nephronophthisis 57 B7 H4 57 brain lesions 57 mutations 57 normal prion proteins 57 NSCLC tumors 57 vasopressin receptors 57 TOP2A 57 SCA5 57 Myotonic dystrophy 57 hypothalamic pituitary 57 beta globin gene 57 behavioral disinhibition 57 autoimmune thyroid 57 TMPRSS2 ERG fusion 57 pancreatic endocrine 57 #p# [003] 57 histological subtype 57 causative mutations 57 polymorphism 57 ankyrin B 57 MnSOD 57 JAK2 enzyme 57 IGFBP 57 NR#A# 57 Colon polyps 57 tumorigenicity 57 BRCA breast cancer 57 polyglutamine diseases 57 myopathies 57 protein tyrosine phosphatase 57 MT1 MMP 57 PAR1 57 Alport syndrome 57 CYP#E# gene 57 hypogonadotropic hypogonadism 57 filaggrin gene 57 BRCA1 gene 57 Amino acid 57 GFP gene 57 hormone receptor status 57 affective psychosis 57 VLDL cholesterol 57 cystic fibrosis muscular dystrophy 57 non mutated KRAS 57 Wwox 57 rs# [003] 57 haplotype 57 SMN1 gene 57 genetic susceptibility 57 murine models 57 gastrointestinal dysfunction 57 eotaxin 57 aldehyde dehydrogenase 57 lung epithelium 57 MGUS 57 prefrontal cortical 57 BRCA2 mutation 57 chronicity 57 p# Shc 57 IGFBP 3 57 dysbindin 57 CALHM1 57 neuronal dysfunction 57 AAT deficiency 57 cardiac channelopathies 57 myostatin gene 57 Pten 57 prostate carcinoma 57 SCN5A 57 nitrotyrosine 57 AVPR1A 57 p# activation 57 genomic instability 57 familial dysautonomia 57 ovarian hormones 57 histone modification 57 severe congenital neutropenia 57 APOE e4 gene 57 chromosomally 57 Kufs disease 57 estrone 57 pre eclamptic 57 CD#c 57 Joubert syndromes 57 prodynorphin 57 HepG2 cells 57 aneuploid cells 57 cerebellar 57 sickle cell hemoglobin 57 sexually dimorphic 57 Chlamydia pneumoniae 57 HLA identical 57 endostatin 57 sequence homology 57 bronchoalveolar 57 Aldosterone 57 5 HT1A receptor 57 FGF2 57 pancreatic islet 57 glial tumors 57 lysosomal storage disease 57 monoclonal gammopathy 57 peroxisomal 57 breast cancer genes BRCA1 57 NF κB activation 57 functional polymorphism 57 HLA matched 57 TP# mutations 57 Smad3 57 intestinal microflora 57 obesity insulin resistance 57 idiopathic pulmonary arterial hypertension 57 Hutchinson Gilford progeria 57 non coding RNA 57 exfoliation glaucoma 57 coinfection 57 CHD5 57 enteroviral 57 Becker muscular dystrophy 57 overt hypothyroidism 57 cybrid 57 premorbid 57 neurodevelopmental impairment 57 TNFAIP3 57 CIB1 57 Hurthle cell 57 genes BRCA 57 hippocampal atrophy 57 dopamine signaling 57 polymorphisms 57 amyloid beta plaques 57 chronic granulomatous disease 57 Hereditary angioedema 57 mutated genes 57 leptin receptors 57 hypothalamic amenorrhea 57 inhibitory receptor 57 familial hypercholesterolemia FH 57 breast endometrial 57 neurocognitive dysfunction 57 abnormal hemoglobin 57 affective psychoses 57 TSC1 57 Runx1 57 cell adhesion molecule 57 BRIP1 57 SLC#A# [001] 57 autosomal 57 molecularly defined 57 chromosome abnormality 57 Apert syndrome 57 melanocortin receptor 57 pDCs 57 Alu elements 57 lung adenocarcinomas 57 clefting 57 paraneoplastic 57 autosomal recessive disorder 57 gastric carcinoma 57 C. pneumoniae 57 COX2 57 Notch receptor 57 Wolbachia strains 57 IGF1 57 mRNA decay 57 intestinal polyps 57 Hypothalamic 57 Estrogen Receptor 57 MLL2 57 progranulin 57 comorbid anxiety 57 LKB1 57 adipogenic 57 neuropsychological impairments 57 supratentorial 57 CYP# [002] 57 toxic amyloid beta 57 TP# gene 57 Telomere length 57 cystatin 57 MSH6 57 enkephalin 57 ADAMTS# 57 chromosome #q 56 resistin 56 spontaneous mutation 56 myo inositol 56 leiomyomas 56 inherit predisposition 56 KRAS mutant 56 Pdx1 56 metabolic dysfunction 56 CYP #D# 56 paraoxonase 56 Rb gene 56 genomic alterations 56 mitochondrial gene 56 biochemical abnormalities 56 CEACAM1 56 tyrosine phosphorylation 56 Gorlin syndrome 56 G6PD 56 imprinted genes 56 Heritability 56 microchimerism 56 hemoglobinopathies 56 mutated BRCA 56 premature ovarian 56 μ opioid receptor 56 Igf2 56 ADH1B * 56 picornavirus 56 atherothrombotic 56 synuclein 56 chemokine receptor 56 mucins 56 phenothiazines 56 inverse agonist 56 tryptase 56 ankyrin repeat 56 phylogenetically 56 histologic subtype 56 KLF4 56 Hashimoto thyroiditis 56 chromosome deletion 56 gene predisposing 56 gametocytes 56 transgene expression 56 L. pneumophila 56 Genotypes 56 SERT gene 56 retinol binding protein 56 dopamine D4 receptor 56 Abeta# 56 incomplete penetrance 56 latent celiac disease 56 mesenchymal cell 56 MELAS 56 causally linked 56 protein encoded 56 insulin resistance syndrome 56 homozygous FH 56 transthyretin 56 seropositivity 56 induced phosphorylation 56 SE alleles 56 congenital adrenal hyperplasia CAH 56 serum BDNF 56 serotonin 2A 56 endogenous retroviruses 56 diathesis 56 inbred strains 56 EBV infection 56 G#S [002] 56 1 diabetes T1D 56 catechol O methyltransferase 56 ductal breast cancer 56 neurological abnormalities 56 neoplastic 56 TTR amyloidosis 56 Cryptococcus neoformans 56 FGFR4 56 beta thalassemia 56 peptide antigens 56 heritable traits 56 adenylate cyclase 56 abnormal lipids 56 TRAF1 C5 56 striatal neurons 56 ligand receptor 56 osteopontin 56 beta amyloid peptides 56 hormonal abnormalities 56 Opportunistic infections 56 fraternal twin pairs 56 ERBB2 56 recurrent acute pancreatitis 56 parkin gene 56 thyroid carcinoma 56 neutralizing antibody responses 56 Single Nucleotide Polymorphisms 56 NR#A# gene 56 PIGF 56 glomerular 56 HMGA1 56 Severe Combined Immunodeficiency 56 mitochondrial defects 56 mineralocorticoid 56 MIF gene 56 KIAA# 56 TRIM5 56 pg ml 56 autoantibodies 56 medium chain acyl 56 mammary stem cells 56 LPS induced 56 Balamuthia 56 Bardet Biedl Syndrome 56 gestational diabetes mellitus 56 testicular tumors 56 constitutively active 56 globin genes 56 capsular polysaccharide 56 histone H4 56 adiponectin concentrations 56 pathogenic mechanisms 56 MHC molecules 56 telomere dysfunction 56 autoreactive 56 cisplatin resistant 56 Brugada syndrome 56 Rh incompatibility 56 chromosome #p# [002] 56 hyperplastic 56 metabolomic profiles 56 Orthostatic hypotension 56 chemically inactivated 56 cystic fibrosis Duchenne muscular 56 Lesch Nyhan syndrome 56 SRY gene 56 NPY gene 56 H#K# [001] 56 impaired insulin secretion 56 retinoic acid receptor 56 miR #a [001] 56 deletion 5q 56 hepatocellular carcinomas 56 genes CYP#C# 56 multivariate Cox 56 Th2 56 mammary cancers 56 parkinsonian 56 Smith Lemli Opitz syndrome 56 premutation 56 Angiotensin converting enzyme 56 orchitis 56 PKCi 56 GLI1 56 β cell 56 DGAT1 56 haplotypes 56 gene mutations 56 HHV 6 56 BRCA1 mutation 56 MetS 56 neuro developmental disorders 56 coexpression 56 hypermethylation 56 causal pathway 56 BCG vaccinated 56 granulocyte 56 primordial germ cells 56 tau protein 56 HMGCR 56 gene variant 56 mutant genes 56 HLA G 56 clade B 56 heritable variation 56 globin 56 serotonin transporter gene 56 lymphoblasts 56 serum PTH 56 alpha1 56 huntingtin protein 56 PARP inhibition 56 hyperlipidemic 56 diabetic kidney 56 humoral responses 56 astrocytic 56 homozygous 56 genomic variants 56 hyperinsulinism 56 lymphoid cells 56 antibody titer 56 cytidine 56 seronegative 56 NKT cell 56 NNRTI resistance 56 etiologic agent 56 transmembrane protein 56 Fibroblasts 56 isoenzymes 56 dysbindin gene 56 microglial 56 dedifferentiation 56 recessive gene 56 proximal colon 56 NFKBIA 56 cellular prion protein 56 TNF blocker therapy 56 SMAD4 56 ß amyloid 56 evolvability 56 hyperactivated 56 innate immune responses 56 SHANK3 gene 56 gamma globin gene 56 upregulates 56 coding genes 56 sFlt 1 56 postnatally 56 #p# [001] 56 autistic enterocolitis 56 SOD2 gene 56 SOD1 gene