genetic variants

Related by string. genetic variant * genetics . Genetics . Genetic . GENETIC . GENETICS : journal Nature Genetics . Targeted Genetics . preimplantation genetic diagnosis PGD . Seattle Genetics . genetic diversity . sensitivity genetic variation / Variant . Variants . VARIANT : breakout variant . further breakout variant . gene variant . gene variants . variant CJD * genetic variants associated *

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(Click for frequent words.) 85 gene variants 84 genetic variations 76 genetic variation 75 genes 75 genetic variant 74 SNPs 74 gene mutations 73 genetic mutations 72 genetic variants associated 72 gene variant 72 polymorphisms 72 genetic markers 71 mutations 70 CNVs 69 susceptibility genes 69 genetic polymorphisms 68 gene 68 miRNAs 68 gene mutation 67 loci 66 mutated genes 66 gene expression 66 genetic susceptibility 64 haplotypes 64 chromosomal regions 64 genetic determinants 64 biomarkers 64 gene expression patterns 64 susceptibility gene 64 microRNAs 64 genotypes 64 genomes 64 alleles 64 autism susceptibility genes 64 genetic alterations 63 haplotype 63 genetic mutation 63 gene variation 63 genotype 63 FTO gene 62 exomes 62 micro RNA 62 genetic abnormalities 62 genomewide 62 sporadic ALS 62 susceptibility loci 62 EGFR mutations 62 genome 62 LRRK2 gene 61 phenotypes 61 epigenetic mechanisms 61 mutation 61 genetic makeup 61 somatic mutations 61 causative genes 61 spontaneous mutations 61 SORL1 61 microdeletions 61 mutated gene 61 genetic loci 61 PTEN mutations 60 APOE4 60 PICALM 60 rs# [003] 60 MYH9 60 molecular markers 60 Genetic variants 60 clusterin 60 methylation patterns 60 DNA sequences 60 APOE e4 60 gene expression profiles 60 familial pancreatic cancer 60 causal variants 60 allele 60 chromosomal abnormalities 60 chromosome #p# [001] 60 FGFR2 60 biological pathways 60 mtDNA mutations 60 APOE gene 60 genomic 59 #q# [001] 59 molecular pathways 59 breast cancer metastasis 59 biomarker 59 HLA genes 59 genetic predisposition 59 NPY gene 59 metabolic syndrome 59 SORL1 gene 59 methylation 59 MTHFR 59 inherited mutations 59 yeast genome 59 FMR1 gene 59 tumor suppressor genes 59 PALB2 59 HLA DRB1 59 epigenetic changes 59 chromosome 59 BRCA1 gene 59 gut microbes 59 noncoding RNAs 59 enterotypes 59 VKORC1 59 microRNA molecules 59 microRNA 59 BRCA1 mutations 59 familial ALS 59 biologic pathways 59 single nucleotide polymorphism 59 imprinted genes 58 PTPN# 58 BRCA mutations 58 genetic underpinnings 58 insulin resistance 58 genetic 58 DNA methylation 58 NAFLD 58 tumor suppressor gene 58 miRNA 58 HMGA2 58 MYH9 gene 58 gene locus 58 genes CYP#C# 58 missense mutations 58 pathogenic mutations 58 TCF#L# gene 58 genomewide association studies 58 TCF#L# 58 Nature Genetics 58 genes BRCA1 58 TGFBR1 * 6A 58 narcolepsy cataplexy 58 heritable 58 rs# [001] 58 chromosome #q# [001] 58 CYP#D# gene 58 LQTS 58 human genome 57 ApoE4 gene 57 polymorphism 57 phenotype 57 alpha synuclein gene 57 BARD1 57 germline mutations 57 #q# [002] 57 SLC#A# [002] 57 APOL1 57 CHEK2 57 histone modifications 57 CNTNAP2 57 gene fusions 57 miRNA genes 57 Genetic variations 57 micro RNAs 57 heritability 57 GSTP1 57 DNA methylation patterns 57 lung adenocarcinoma 57 ApoE 57 BRCA mutation 57 mitochondrial dysfunction 57 APOE 57 EGFR gene 57 single nucleotide polymorphisms 57 chromosome #q# [002] 57 subtypes 57 proteins 57 virulence genes 57 mutant genes 57 IL#R 57 molecular pathway 56 lincRNAs 56 ALK mutations 56 autoantibodies 56 ORMDL3 56 apoE4 56 miRNA expression 56 molecular mechanism 56 elevated CRP 56 gene polymorphisms 56 genetic locus 56 genomic variation 56 KIAA# 56 IKZF1 56 cellular pathways 56 BRCA genes 56 susceptibility locus 56 hypermethylation 56 G#S mutation 56 Genes 56 telomere lengths 56 MGUS 56 microRNA expression 56 mitochondrial DNA mtDNA 56 gene loci 56 APOE genotype 56 non coding RNAs 56 modifiable risk 56 protein kinases 56 CDH1 56 genes encoding 56 apolipoprotein E gene 56 HNPCC 56 colorectal neoplasia 56 epigenetic alterations 56 telomere length 56 chromosomal alterations 56 CYP#C# [001] 56 p# mutations 56 mitochondrial mutations 56 epigenetic modification 56 rs# [002] 56 BRCA1 55 GBA mutations 55 journal Nature Genetics 55 MHC genes 55 genetic sequences 55 adiponectin 55 mutant gene 55 C#Y 55 FTLD 55 signaling pathways 55 progranulin 55 chimpanzee genomes 55 chromosome rearrangements 55 genomic alterations 55 molecular biomarkers 55 chromosome #p#.# 55 #q#.# [002] 55 monogenic 55 LPA gene 55 microcephalin 55 quantitative trait loci 55 mutant allele 55 STAT4 55 estrogen receptor 55 DQB1 * 55 ZNF# 55 penetrance 55 MIF protein 55 modifier genes 55 bile acid metabolism 55 physiological mechanisms 55 genotypic 55 BRCA2 gene 55 genotyped 55 monozygotic twins 55 genetic ancestry 55 SE alleles 55 genetic susceptibilities 55 #q#.# [001] 55 MSH2 55 ApoE gene 55 transcription factors 55 IgA deficiency 55 ultraconserved elements 55 T2D 55 #p#.# [001] 55 RUNX3 55 epigenetic 55 primate genomes 55 MC1R gene 55 breast cancer genes BRCA1 55 linkage disequilibrium 55 SIRT1 55 chromosomal translocations 55 5 HTTLPR 55 TMEM#B 55 gene APOE 55 IDH1 mutation 55 dysbindin 55 TRAF1 C5 55 LRRK2 mutation 55 Chromosome 55 phenotypic variation 55 JAK2 mutation 55 APOE ε4 55 transcriptome 55 PLoS Genetics 55 TP# mutation 55 hereditary predisposition 55 aberrant methylation 55 APOC3 55 causative gene 55 molecular underpinnings 55 X chromosome 55 genomic variants 55 Hakonarson 55 RNA sequences 55 postmenopausal breast cancer 55 APOE e4 gene 55 WTCCC 54 BRCA2 mutation 54 GSTM1 54 mutated BRCA1 54 EBV infection 54 chromosomal 54 folate deficiency 54 Genetic variation 54 Wwox 54 ependymomas 54 ApoE4 54 mammographic density 54 genes predisposing 54 chromosomal anomaly 54 haplogroups 54 metabolic pathways 54 de novo mutations 54 epigenome 54 #p# [001] 54 Lp PLA2 54 indels 54 splice junctions 54 mitochondrial genome 54 BRCA1 mutation 54 metabolic abnormalities 54 elevated triglyceride levels 54 APOE allele 54 promoter methylation 54 apoE 54 genetic trait 54 basal cell nevus syndrome 54 nucleotide sequence 54 genetic variability 54 ABCB1 54 QTLs 54 KLF4 54 medulloblastomas 54 LRRK2 mutations 54 microarray experiments 54 GPC5 54 platypus genome 54 physiologic mechanisms 54 LRRK2 54 VIPR2 54 palladin 54 parkin gene 54 Alu elements 54 epigenetic regulation 54 mitochondrial gene 54 sCJD 54 heterozygous 54 Clusterin 54 FGFR2 gene 54 PIK3CA 54 PTEN gene 54 #q# deletion 54 gene sequences 54 genetic biomarkers 54 non coding RNA 54 genomic rearrangements 54 genetic abnormality 54 5 hydroxymethylcytosine 54 cardiovascular disease 54 RNA molecules 54 endometrial cancers 54 DISC1 gene 54 genetic polymorphism 54 familial clustering 54 INTERHEART study 54 Genetic predisposition 54 cognitively normal 54 causative mutations 54 gene APOE4 54 HLA molecules 54 APOE4 gene 54 RBP4 54 BRAF mutation 54 atherosclerosis 54 Neanderthal genes 54 IL#B 54 aneuploidies 54 mitochondrial 54 IDH1 54 heterozygotes 53 CFH gene 53 CCL#L# 53 KLF# 53 C. pneumoniae 53 MC1R 53 HapMap 53 HLA B# 53 Wellcome Trust Case 53 cell signaling pathways 53 meta analysis 53 Brd4 53 protein isoforms 53 TACI mutations 53 HMGA2 gene 53 ncRNAs 53 miR 53 inflammatory markers 53 homozygosity 53 epidemiological studies 53 FASPS 53 NF1 gene 53 chromosomal aberrations 53 ALDH2 53 microRNAs miRNAs 53 cystatin C 53 K ras mutations 53 prognostic markers 53 SOD1 gene 53 molecular subtypes 53 serotonin transporter 53 histone deacetylases 53 allele frequencies 53 pathogenic mechanisms 53 subclinical atherosclerosis 53 aneuploidy 53 histone modification 53 MC4R gene 53 lipid abnormalities 53 bacterial genomes 53 small RNAs 53 genetic modifiers 53 mammalian genomes 53 genome sequences 53 microbiomes 53 BDNF gene 53 subclinical hyperthyroidism 53 transcriptomes 53 chromosome #q#.# [001] 53 telomere shortening 53 serotonin receptor 53 CC genotype 53 BRCA2 53 promoter hypermethylation 53 receptor gene 53 molecular mechanisms 53 STK# gene 53 LRP5 53 DRD2 53 CYP#C# [002] 53 CCR3 53 SIRT3 53 genetic traits 53 INF2 53 chromosomal instability 53 signaling molecule 53 underlying pathophysiology 53 gene rearrangements 53 genetically susceptible 53 white matter hyperintensities 53 DRD2 gene 53 genetic aberrations 53 transcription factor 53 uric acid levels 53 colorectal cancer CRC 53 chromatin structure 53 KIF6 gene 53 G allele 53 drug metabolizing enzymes 53 coronary calcification 53 chromosome aberrations 53 VHL gene 53 Fragile X gene 53 NNRTI resistance 53 HPV# 53 primary cilia 53 isoforms 53 metabolic 53 MTHFR gene 53 mRNA expression 53 alpha synuclein protein 53 TOMM# 53 ADAM# 53 CALHM1 53 TCF4 53 fasting glucose levels 53 albuminuria 53 hypermethylated 53 ERBB2 53 underlying molecular mechanisms 53 hereditary breast cancer 53 nicotinic receptor 53 cholesterol metabolism 53 genetic syndromes 53 exome sequencing 53 CYP#E# gene 53 acetylation 53 nonsense mutations 53 EAAT2 53 preeclampsia 53 malaria parasite genome 53 chromosomal rearrangement 53 WT1 52 disease NAFLD 52 CDKN2A 52 Froguel 52 prognostic marker 52 GBM tumors 52 CagA 52 CHD7 52 MC4R 52 Drosophila genome 52 SNPs pronounced snips 52 human microbiome 52 HER2 gene 52 uncharacterized genes 52 HLA alleles 52 gene amplification 52 coding sequences 52 apolipoprotein E 52 sarcosine 52 breast cancer susceptibility genes 52 haptoglobin 52 HFE gene 52 Klotho gene 52 JAK mutations 52 serotonin transporter gene 52 chromosomal rearrangements 52 colorectal tumors 52 UCP2 52 genomewide association study 52 epigenomes 52 biochemical markers 52 cardiovascular mortality 52 GSTT1 52 methylation markers 52 PARP inhibition 52 Velculescu 52 polycystic ovary syndrome PCOS 52 lipoprotein 52 lipid levels 52 alternative splicing 52 HDACs 52 genetic alteration 52 HLA DQ2 52 DeCode 52 Autism Consortium 52 cardioembolic stroke 52 causal pathways 52 NF2 52 neuroinflammation 52 Li Fraumeni 52 clefting 52 dopamine receptor gene 52 impaired fasting glucose 52 germline mutation 52 SIRT1 gene 52 rhinoviruses 52 muscular dystrophies 52 dietary patterns 52 enteroviruses 52 molecular abnormalities 52 #S rRNA 52 KIF6 gene variant 52 leptin 52 osteopontin 52 recessive mutations 52 chromosomal deletions 52 autosomal 52 nonalcoholic fatty liver 52 breast cancers 52 shorter telomeres 52 microalbuminuria 52 vitamin D receptors 52 Bardet Biedl syndrome 52 MicroRNA 52 WNK1 52 chromosomal disorders 52 LIS1 52 CHI#L# 52 allelic variation 52 SMN2 52 SH#B# 52 allelic 52 familial predisposition 52 SMAD4 52 brain lesions 52 #p#.# [002] 52 IL 7R 52 pharmacogenetic 52 Li Fraumeni syndrome 52 primary biliary cirrhosis 52 prediabetes 52 molecular mechanisms underlying 52 protein misfolding 52 PTP1B 52 neuroligins 52 KRAS mutation 52 YKL 52 DNA rearrangements 52 IGF2 52 mammalian genome 52 amyloid deposits 52 splice variants 52 MAPK pathway 52 Wolbachia 52 beta1 integrin 52 mutant protein 52 familial adenomatous polyposis 52 microbial genomes 52 PKM2 52 prostate cancer CaP 52 androgen receptor gene 52 cardiac progenitor cells 52 endophenotypes 52 uPAR 52 defective gene 52 melatonin receptor 52 CHRNA5 52 obesity insulin resistance 52 benign breast 52 miR #b [002] 52 mammary cells 52 KRAS mutations 52 SLC#A# [001] 52 nicotinic receptors 52 highly heritable 52 epigenetic markers 52 studies GWAS 52 apoC III 52 array CGH 52 metabolites 52 rs# [004] 52 nucleotide 52 tumor suppressor protein 52 MicroRNAs 52 gut microbiota 52 lipid metabolism 52 subtype 52 paralogs 52 androgen receptor 51 abdominal obesity 51 generalized vitiligo 51 HOTAIR 51 DISC1 51 genetically engineered mice 51 metabolic syndrome MetS 51 COX enzymes 51 genetically 51 coding exons 51 coding genes 51 Wnt pathway 51 miR #a [001] 51 urate 51 mtDNA 51 KIBRA 51 ACE2 51 STAT3 51 ADPKD 51 multigene 51 herpesviruses 51 phenotypic differences 51 biochemical pathway 51 phenotypic 51 SNP rs# [001] 51 microsatellite markers 51 MLL2 51 mitochondrial proteins 51 protein encoded 51 C. neoformans 51 T. gondii 51 SPINK1 51 variant alleles 51 genomic instability 51 sortilin 51 receptors 51 International HapMap Project 51 microRNA biomarkers 51 HIV HCV coinfected 51 IGFBP 51 biochemical mechanisms 51 coronary artery calcium 51 Getzenberg 51 MEF2A 51 trans palmitoleic acid 51 breast cancer subtypes 51 mRNAs 51 CYP#D# genotype 51 vitamin D receptor 51 conserved sequences 51 COMT gene 51 CYP#C# gene 51 Sanger sequencing 51 CYP#E# 51 vitamin D deficiency 51 MLH1 51 OGG1 51 GATA4 51 DARPP 51 S#A# [002] 51 PI3K pathway 51 neurodevelopmental disorders 51 Dr. Victor Velculescu 51 adiponectin levels 51 selective inhibitors 51 NF1 51 epigenetic marks 51 pseudogenes 51 AAT deficiency 51 miRNA molecules 51 HNSCC 51 neuroendocrine 51 chromosome #q 51 miRNA expression patterns 51 prion protein gene 51 BCL#A 51 BRCA2 mutations 51 chromosome abnormalities 51 mutational 51 chromosomal anomalies 51 IGFBP2 51 endogenous retroviruses 51 glucose metabolism 51 genetics 51 ALK gene 51 CYP#D# 51 sirtuins 51 endothelial dysfunction 51 oxysterols 51 airway remodeling 51 orthologs 51 globin genes 51 FGFR1 51 mitochondrial disorders 51 PTEN protein 51 Meckel Gruber 51 oncogenes 51 Apobec3 51 thyrotropin levels 51 Observational studies 51 cardiovascular disease CVD 51 BMPR2 51 body louse genome 51 GRK5 51 TSC1 51 COX2 51 methylated genes 51 genotyping 51 serum biomarkers 51 number variations CNVs 51 SMN2 gene 51 cancers 51 Genetic mutations 51 KRAS oncogene 51 organism genome 51 subclinical hypothyroidism 51 BRAF gene 51 hormone leptin 51 epistasis 51 MetS 51 RASSF1A 51 proteins encoded 51 chitinase 51 PDE#A 51 genomic loci 51 genetic predispositions 51 5 HTT gene 51 TSP1 51 sequenced genomes 51 missense mutation 51 unmeasured factors 51 chromosome abnormality 51 Dr. Pasinetti 51 proteins misfold 51 periodontal disease 51 variants 51 protein alpha synuclein 51 ovarian hormones 51 neurogenesis 51 receptor 51 intron 51 genotyping arrays 51 autosomal dominant disorder 51 Ashkenazi Jews 51 tyrosine kinases 51 autoantibody 51 NKX2 51 signaling pathway 51 metabolic enzymes 51 CAG repeats 51 odorant receptors 51 Akt3 51 chimp genome 50 cardioprotective effects 50 humanin 50 remnant lipoproteins 50 body fatness 50 Pericak Vance 50 KIF6 50 pilocytic astrocytomas 50 galectin 3 50 APOE e4 allele 50 periodontal infections 50 BRAF V#E 50 EGFR mutation 50 PGRN 50 somatic mutation 50 mitochondrial genomes 50 MeCP2 gene 50 mRNA molecules 50 colorectal adenomas 50 major histocompatibility complex 50 noncoding RNA 50 alpha synuclein 50 CNTNAP2 gene 50 TLR3 50 proto oncogene 50 type2 diabetes 50 microdeletion 50 fungal genomes 50 homozygote 50 ion channels 50 DLX5 50 RNAs 50 MECP2 gene 50 Skp2 50 H. pylori infection 50 enterovirus infection 50 inherited predisposition 50 testicular germ cell 50 genetic defects 50 colon cancers 50 SERT gene 50 NR#A# 50 epigenomics 50 causative mutation 50 FOXP3 50 slow metabolizers 50 neuroglobin 50 cyclin D1 50 FMR1 50 phenotypic traits 50 gallstone disease 50 FTO variant 50 Karayiorgou 50 mRNA transcripts 50 SCN5A 50 PKCi 50 obstructive coronary artery 50 dietary glycemic index 50 receptor protein 50 microglial cells 50 LRAT 50 perilipin 50 HGPS 50 El Sohemy 50 STK# [002] 50 pathophysiological mechanisms 50 p# activation 50 nongenetic factors 50 HHMI investigator 50 GSTM1 gene 50 faulty BRCA2 gene 50 Epidemiologic studies 50 colon tumors 50 dopamine D4 receptor 50 liver fibrosis 50 coronary heart 50 systemic inflammation 50 Yamanaka recipe 50 hypomethylation 50 Kari Stefansson 50 biochemical pathways 50 Framingham Offspring Study 50 gene expression profiling 50 atypical hyperplasia 50 susceptibility alleles 50 Single Nucleotide Polymorphisms SNPs 50 transcriptional regulation 50 SNCA 50 microRNA miR 50 folate intake 50 UGT#A# * 50 Pin1 50 CDK4 50 familial hypercholesterolemia 50 metabolic disturbances 50 tumor biopsies 50 MetAP2 50 carotid atherosclerosis 50 CFTR gene 50 carcinoid 50 protein coding RNAs 50 genomic rearrangement 50 mutated protein 50 PITX2 50 RNA transcripts 50 #p# [003] 50 dopamine transporter 50 Hedgehog pathway 50 genetic defect 50 beta catenin 50 advanced adenomas 50 sea urchin genome 50 kinases 50 Neuregulin 1 50 HbF 50 comorbidity 50 genetically modified mice 50 hydroxyvitamin D levels 50 segmental duplications 50 colorectal polyps 50 HCV infection 50 gene predisposing 50 TGF β 50 UTRs 50 LMNA 50 deleterious mutation 50 esophageal squamous cell carcinoma 50 circadian genes 50 eotaxin 50 genomic markers 50 transthyretin 50 dysbindin gene 50 synaptic proteins 50 endostatin 50 nondiabetic 50 epigenetic silencing 50 Wnt#b 50 myeloproliferative disorders 50 Arabidopsis genes 50 LDL receptor 50 neural circuits 50 protein 50 protein biomarkers 50 chromosome translocations 50 serum BDNF 50 methylated DNA 50 airway hyperresponsiveness 50 chromosome #p# [002] 50 gene encoding 50 Arabidopsis genome 50 activating mutations 50 chromosomes 50 hormone adiponectin 50 ARID1A 50 tyrosine phosphorylation 50 genome rearrangements 50 subpopulations 50 HDAC inhibitors 50 circadian clock genes 50 PPAR gamma 50 microbiota 50 HSF1 50 PON1 50 inflammatory bowel diseases 50 E4 variant 50 gut bacteria 50 cytogenetic 50 haplotype map 50 polygenic 50 triglyceride levels 50 phytoestrogens 50 PALB2 gene 50 genetic makeups 50 MEF2D 50 FXTAS 50 MTHFD1L gene 50 GPR# [002] 50 SGK1 50 Epstein Barr virus 50 maternally inherited 50 coronary artery disease 50 BRIP1 50 A1 allele 50 vimentin 50 Hashimoto thyroiditis 50 BRCA gene 50 estrogen receptors 50 Indian origin boffin 50 methylenetetrahydrofolate reductase 50 Venter genome 50 tau mutation 50 obestatin 50 heterologous expression 50 developmental abnormalities 50 previously uncharacterized 50 adenoma 50 ribosomal proteins 50 exons 50 metabolic disorders 50 CYP#A# gene 50 intergenic 50 mammary cancers 50 lobular breast cancer 50 potentially modifiable 50 bioactive compounds 50 NF kB 50 dopamine transporter gene 50 BACE1 50 metabolic parameters 50 neuroblastoma tumors 50 variant rs# 50 estrogen receptor alpha 50 cAMP signaling 50 homozygous 50 CGG repeats 49 GABRA2 49 gene expression assays 49 mutant alleles 49 carcinogenesis 49 genomic deletions

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