genetic variations

Related by string. genetic variation * genetics . Genetics . Genetic : journal Nature Genetics . Targeted Genetics . preimplantation genetic diagnosis PGD / Variations . Variation : variations thereof identify . seasonal variations * sensitivity genetic variation . correlate genetic variation . correlating genetic variation . genetic variation detection . Human Genetic Variation *

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(Click for frequent words.) 84 genetic variants 80 gene variants 77 genetic variation 74 genetic markers 73 genetic mutations 73 genes 73 gene mutations 71 SNPs 69 mutations 69 genetic variant 69 polymorphisms 68 susceptibility genes 68 genetic variants associated 68 mutated genes 67 CNVs 67 gene mutation 67 gene 67 gene variant 66 genetic makeup 66 genetic polymorphisms 66 genetic abnormalities 65 genetic mutation 65 genetic susceptibility 64 genetic 63 gene expression 63 gene expression patterns 62 genomewide 62 genetic alterations 62 mutation 62 genomes 61 autism susceptibility genes 61 chromosomal abnormalities 61 genetic determinants 61 susceptibility gene 61 biomarkers 61 MYH9 61 genetic predisposition 61 gene variation 60 causal variants 60 LRRK2 gene 60 phenotypes 60 biological pathways 60 chromosomal regions 60 miRNAs 60 genotype 60 mutated gene 60 genotypes 59 alleles 59 spontaneous mutations 59 narcolepsy cataplexy 59 Genetic variants 59 loci 59 MYH9 gene 59 microdeletions 59 genome 59 haplotypes 58 genetic underpinnings 58 gene expression profiles 58 causative genes 58 genes CYP#C# 58 EGFR mutations 58 familial pancreatic cancer 58 genomic 58 genetic disorders 58 methylation patterns 58 breast cancer metastasis 58 LQTS 58 epigenetic changes 58 genetic defect 58 sporadic ALS 58 molecular pathways 58 Genetic variations 58 epigenetic 58 metabolic syndrome 58 exomes 58 single nucleotide polymorphism 58 genetic ancestry 58 NAFLD 57 NPY gene 57 microRNAs 57 biomarker 57 enterotypes 57 #q# [001] 57 DNA methylation patterns 57 biologic pathways 57 micro RNA 57 MIF protein 57 gut microbes 57 inherited mutations 57 HLA DRB1 57 haplotype 57 microRNA molecules 57 APOE e4 57 familial ALS 57 SORL1 gene 57 MTHFR 57 BARD1 56 genetic abnormality 56 mutant gene 56 FTO gene 56 genetic loci 56 HLA genes 56 gene locus 56 chromosome #p# [001] 56 DNA sequences 56 PTEN mutations 56 TGFBR1 * 6A 56 chromosomal anomaly 56 imprinted genes 56 epigenetic alterations 56 VKORC1 56 molecular biomarkers 56 somatic mutations 56 chromosome #q# [001] 56 genetic traits 56 SORL1 56 germline mutations 56 APOE4 56 rs# [003] 56 genetic susceptibilities 56 methylation 56 insulin resistance 56 PTPN# 56 hereditary predisposition 56 molecular markers 55 epigenetic mechanisms 55 susceptibility locus 55 APOE gene 55 SLC#A# [002] 55 PICALM 55 molecular abnormalities 55 Genes 55 mtDNA mutations 55 gene fusions 55 molecular underpinnings 55 susceptibility loci 55 micro RNAs 55 MHC genes 55 LRRK2 mutations 55 APOL1 55 MGUS 55 phenotype 55 CYP#D# gene 55 clusterin 55 T2D 55 single nucleotide polymorphisms 55 hypermethylation 55 genetics 55 nonsense mutations 55 mitochondrial dysfunction 55 de novo mutations 55 molecular pathway 55 tumor suppressor genes 55 BRCA mutations 55 BRCA1 gene 55 heritable 55 causative gene 55 chromosome #q# [002] 55 splice junctions 55 phenotypic variation 55 medulloblastomas 55 CHEK2 55 protein kinases 55 chromosomal alterations 55 Hakonarson 55 biochemical pathways 55 genetic defects 55 underlying pathophysiology 55 genetic trait 55 TCF#L# gene 54 chromosomal 54 molecular mechanism 54 alpha synuclein gene 54 BRCA1 mutations 54 noncoding RNAs 54 FTLD 54 Genetic variation 54 pathogenic mutations 54 aneuploidies 54 JAK2 mutation 54 underlying molecular mechanisms 54 mutant genes 54 cellular pathways 54 homozygosity 54 lung adenocarcinoma 54 #q# [002] 54 G#S mutation 54 breast cancer genes BRCA1 54 genomic variation 54 STK# gene 54 miRNA expression 54 CDH1 54 IL#R 54 tumor suppressor gene 54 subtypes 54 genes BRCA1 54 ZNF# 54 genetic polymorphism 54 chromosome rearrangements 54 defective gene 54 chromosome 54 CNTNAP2 54 endothelial dysfunction 54 genetic sequences 53 colorectal cancer CRC 53 colorectal neoplasia 53 histone modifications 53 gene polymorphisms 53 yeast genome 53 PALB2 53 breast cancer susceptibility genes 53 YKL 53 VHL gene 53 BRCA2 mutation 53 folate deficiency 53 basal cell nevus syndrome 53 biochemical mechanisms 53 monogenic 53 progranulin 53 HapMap 53 lipid abnormalities 53 microRNA 53 cardiac channelopathies 53 CYP#C# [002] 53 microRNA expression 53 human genome 53 parkin gene 53 molecular mechanisms 53 Froguel 53 FMR1 gene 53 CYP#C# [001] 53 CYP#E# gene 53 FGFR2 53 proteins 53 sortilin 53 GBA mutations 53 rs# [002] 53 microcephalin 53 missense mutations 53 mitochondrial mutations 53 HMGA2 53 #p# [001] 53 APOE ε4 53 generalized vitiligo 53 TCF#L# 53 metabolic abnormalities 53 rs# [001] 53 BRCA2 gene 53 miRNA genes 53 histone modification 53 causative mutations 53 epigenomes 53 MC1R gene 53 genetic locus 53 IKZF1 53 abnormalities 53 genetically 53 genetically susceptible 53 testicular germ cell 53 JAK mutations 53 NF1 gene 52 DNA methylation 52 cell signaling pathways 52 chromosomal translocations 52 quantitative trait loci 52 GSTP1 52 chromosome #p#.# 52 inflammatory bowel diseases 52 nicotine dependence 52 BRCA mutation 52 atherosclerosis 52 genomic variants 52 ADPKD 52 genomic alterations 52 DNA rearrangements 52 DQB1 * 52 genetic variability 52 5 hydroxymethylcytosine 52 QTLs 52 causative mutation 52 ALK mutations 52 phenotypic differences 52 Clusterin 52 MSH2 52 chromosome #q#.# [001] 52 ABCB1 52 inherited predisposition 52 colorectal cancer 52 RNA sequences 52 IDH1 mutation 52 CHD7 52 modifier genes 52 apolipoprotein E gene 52 LPA gene 52 physiologic mechanisms 52 monozygotic twins 52 polymorphism 52 Li Fraumeni 52 epigenome 52 elevated triglyceride levels 52 bile acid metabolism 52 autoantibodies 52 G6PD deficiency 52 Wwox 52 BRAF mutation 52 CCR3 52 linkage disequilibrium 52 p# mutations 52 neuroinflammation 52 genetic makeups 52 allele 52 dopamine receptor gene 52 prediabetes 52 chromosomal instability 52 prognostic markers 52 IgA deficiency 52 5 HTTLPR 52 ASDs 52 uric acid levels 52 SNPs pronounced snips 52 physiological mechanisms 52 hypermethylated 52 PIK3CA 52 APOE genotype 52 KIAA# 52 genetic syndromes 52 genotyped 52 transcription factors 52 gene loci 52 gene rearrangements 52 Velculescu 52 genetic aberrations 52 PTEN gene 52 SIRT1 52 ARID1A 52 lipid levels 52 MECP2 52 Bardet Biedl syndrome 52 Venter genome 52 recessive mutations 52 chromosome #q 52 TMEM#B 52 telomere length 52 K ras mutations 52 genes predisposing 52 genotypic 52 microRNAs miRNAs 52 BRCA genes 52 Genetic predisposition 52 cardiovascular disease 52 CYP#D# 52 TACI mutations 52 EBV infection 51 genetic predispositions 51 chromosomal disorders 51 HLA B# 51 GAB2 51 mitochondrial disorders 51 neuropsychiatric disorders 51 HNPCC 51 virulence genes 51 galectin 3 51 INF2 51 GSTT1 51 HLA DQ2 51 androgen receptor gene 51 apoE 51 causal pathways 51 signaling pathways 51 Nordestgaard 51 DRD2 gene 51 SMAD4 51 epigenetic modification 51 molecular mechanisms underlying 51 multigene 51 KIBRA 51 slow metabolizers 51 mitochondrial DNA mtDNA 51 primate genomes 51 #q#.# [001] 51 ApoE4 gene 51 CALHM1 51 aberrant methylation 51 lincRNAs 51 alternative splicing 51 LRRK2 51 SOD1 gene 51 drug metabolizing enzymes 51 phenotypic 51 MEF2A 51 CYP#E# 51 Brd4 51 sCJD 51 neurodevelopmental disorders 51 metabolic pathways 51 tyrosine kinases 51 primary biliary cirrhosis 51 fatty acid metabolism 51 chromosomal anomalies 51 HLA alleles 51 GATA4 51 penetrance 51 SE alleles 51 miRNA 51 non coding RNA 51 AAT deficiency 51 colorectal tumors 51 RUNX3 51 MECP2 gene 51 ion channels 51 allelic variation 51 cardiac hypertrophy 51 haplogroups 51 microbiomes 51 HGPS 51 brain lesions 51 Kari Stefansson 51 developmental abnormalities 51 KRAS mutation 51 ORMDL3 51 telomere lengths 51 endometrial cancers 51 pharmacogenetic 51 Mitochondrial diseases 51 ApoE gene 51 protein isoforms 51 Meckel Gruber 51 Genetic mutations 51 familial hypercholesterolemia 51 epigenetic markers 51 KRAS oncogene 51 NF1 51 C#Y 51 apoE4 51 plasma kallikrein 51 journal Nature Genetics 51 SIRT1 gene 51 genes encoding 51 exfoliation glaucoma 51 #p#.# [001] 51 nonalcoholic fatty liver 51 STAT4 51 systemic lupus erythematosus SLE 51 EGFR gene 51 vitamin D deficiency 51 MC1R 50 LRRK2 mutation 50 Genetic testing 50 CHI#L# 50 enteroviruses 50 metabolites 50 airway remodeling 50 DISC1 gene 50 malaria parasite genome 50 OCA2 50 KCNQ1 50 nongenetic factors 50 prion protein gene 50 allele frequencies 50 pilocytic astrocytomas 50 elevated CRP 50 Yamanaka recipe 50 cardiac progenitor cells 50 RNA molecules 50 APOE 50 kinases 50 GPC5 50 coronary artery disease 50 metabolic disorders 50 APOE e4 gene 50 TPMT 50 CHRNA5 50 Lp PLA2 50 adiponectin 50 heritable diseases 50 SH#B# 50 rhinoviruses 50 receptor protein 50 chromosomal rearrangement 50 gene sequences 50 TOMM# 50 chromosomal aberrations 50 GBM tumors 50 Kufs disease 50 microdeletion 50 serotonin transporter gene 50 Arabidopsis genes 50 GSTM1 50 metabolic enzymes 50 FASPS 50 tumor suppressor protein 50 cancers 50 X chromosome 50 gut microbiota 50 GRK5 50 HFE gene 50 clefting 50 coding exons 50 pharmacogenetics 50 SCN5A 50 subclinical atherosclerosis 50 transcriptomes 50 genetic biomarkers 50 SNP rs# [001] 50 segmental duplications 50 neuroligins 50 KIF6 gene 50 genetic modifiers 50 genomewide association study 50 BRCA1 50 protein biomarkers 50 CCL#L# 50 modifiable risk 50 KRAS mutations 50 familial adenomatous polyposis 50 SIRT3 50 nucleotide sequence 50 methylation markers 50 epigenetic regulation 50 type2 diabetes 50 IDH1 50 RBP4 50 Chromosome 50 chromosome abnormality 50 HOX genes 50 mutant allele 50 bowel cancers 50 ALK gene 50 subclinical hyperthyroidism 50 promoter hypermethylation 50 human leukocyte antigen 50 #q# deletion 50 receptors 50 phenotypic traits 50 respiratory viral infections 50 International HapMap Project 50 proband 50 acetylation 50 OGG1 50 WNK1 50 Wnt pathway 50 remnant lipoproteins 50 chimpanzee genomes 50 susceptibility alleles 50 inflammatory bowel disease 50 receptor gene 50 transcriptome 50 aneuploidy 50 VIPR2 50 shorter telomeres 50 aldehyde dehydrogenase 50 cholesterol metabolism 50 El Sohemy 50 LMNA 50 TCF4 50 periodontal disease 50 familial predisposition 50 heterozygotes 50 pathogenic mechanisms 50 Apobec3 50 vitamin D receptors 50 IGF2 50 hereditary hemochromatosis 50 cannabinoid receptors 50 FMR1 50 heritability 50 Fragile X gene 50 #q#.# [002] 50 SMN2 50 LIS1 50 Epstein Barr virus 50 STK# [002] 50 adaptive immunity 50 lipid metabolism 50 metabolic 50 epigenetics 50 PARP inhibition 50 small RNAs 50 MC4R gene 50 prostate carcinogenesis 50 Darapladib 50 CFH gene 50 breast cancers 50 gestational diabetes mellitus 50 chromosome aberrations 49 diagnostic biomarker 49 amyloid deposits 49 LRP5 49 abnormal growths 49 abdominal obesity 49 promoter methylation 49 PKM2 49 thrombophilia 49 KLF# 49 uncharacterized genes 49 psychiatric disorders 49 Li Fraumeni syndrome 49 HbF 49 DeCode Genetics 49 Alpha synuclein 49 epigenetic silencing 49 mutated protein 49 protein misfolding 49 C. pneumoniae 49 ApoE 49 primary cilia 49 serum biomarkers 49 evolutionary conserved 49 antigen PSA 49 UGT#B# 49 chromosomal defects 49 microalbuminuria 49 CYP#C# gene 49 orthologs 49 WT1 49 nicotinic receptors 49 IL#B 49 mitochondrial diseases 49 serotonin receptor 49 NSCLC tumors 49 indels 49 chromosome translocations 49 WDR# 49 prognostic marker 49 colorectal polyps 49 biologic pathway 49 onset Alzheimer disease 49 genotyping arrays 49 hereditary breast cancer 49 signaling molecule 49 DRD2 49 S#A# [002] 49 HNSCC 49 microbiota 49 CFTR gene 49 connexin 49 HLA molecules 49 paternal lineages 49 herpesviruses 49 chitinase 49 EGFR mutation 49 coding sequences 49 subpopulations 49 gastric carcinogenesis 49 EAAT2 49 HPV# 49 CETP gene 49 lactose tolerance 49 familial clustering 49 disease NAFLD 49 IGFBP2 49 apoC III 49 heterozygous 49 prodynorphin 49 autosomal 49 autism spectrum disorders 49 nicotinic receptor 49 estrogen receptors 49 HMGCR 49 metabolic abnormality 49 H. pylori infection 49 postmenopausal breast cancer 49 iron overload 49 neurological diseases 49 mammalian genomes 49 MLH1 49 Brugada syndrome 49 degenerative neurological diseases 49 X chromosome genes 49 colon tumors 49 Epidemiologic studies 49 poor metabolizers 49 Fragile X syndrome 49 splice variants 49 chromatin structure 49 PGRN 49 huntingtin gene 49 TP# mutation 49 ubiquitin ligases 49 mutant protein 49 alpha synuclein protein 49 autoantigens 49 heart disease 49 folate metabolism 49 haplotype map 49 liver fibrosis 49 familial hypercholesterolaemia 49 genomewide association studies 49 MTHFR gene 49 hormone adiponectin 49 BRCA2 gene mutations 49 palladin 49 SNCA 49 chromosome abnormalities 49 MLL2 49 G allele 49 mtDNA 49 NNRTI resistance 49 FMRP protein 49 mitochondrial gene 49 nestin 49 MAPK pathway 49 epigenetic marks 49 intestinal microbiota 49 persistent pulmonary hypertension 49 zebrafish 49 KLF# gene 49 airway hyperresponsiveness 49 dietary patterns 49 chromosomal deletions 49 BRCA2 mutations 49 biomarker assay 49 cognitively normal 49 endocannabinoids 49 Drosophila genome 49 MSMB 49 SLC#A# [001] 49 Sjögren syndrome 49 Jhdm2a 49 Wnt signaling pathway 49 cystatin C 49 preeclampsia 49 PDE#A 49 DeCode 49 Sox2 49 inflammatory biomarkers 49 Single Nucleotide Polymorphisms SNPs 49 psychotic illnesses 49 NF2 49 #q#.# deletion syndrome 49 metabolizing enzymes 49 CAG repeats 49 lipoprotein 49 achromatopsia 49 metabolic disturbances 49 prion diseases 49 #p#.# [002] 49 p#/CBP 49 KCNH2 49 latent TB infection 49 CYP#C# genotype 49 atherosclerotic lesions 49 mutated BRCA1 49 albuminuria 49 obesity insulin resistance 49 LXRs 49 CYP#B# 49 nongenetic 49 neuroendocrine 48 breast tumors 48 RNA transcripts 48 epilepsies 48 dopamine transporter 48 unmeasured factors 48 microRNA biomarkers 48 HER2 gene 48 HDACs 48 C. neoformans 48 humanin 48 LRAT 48 GFP gene 48 HMGA2 gene 48 COX enzymes 48 selective inhibitors 48 gene APOE4 48 proteins encoded 48 inheritable diseases 48 myeloproliferative neoplasms 48 sarcosine 48 ADAM# 48 BCL#A 48 essential thrombocythemia 48 IRF6 gene 48 CCR5 delta# 48 FGFs 48 subclinical hypothyroidism 48 dopamine D4 receptor 48 GABRA2 48 gene APOE 48 coding genes 48 chromosomal rearrangements 48 neuropsychiatric disorder 48 pharmacogenetic test 48 mRNA molecules 48 BRIP1 48 HPV genotypes 48 white matter hyperintensities 48 serotonin transporter 48 sequenced genomes 48 tau protein tangles 48 non coding RNAs 48 genomic markers 48 IGF1 48 podocytes 48 IgE antibody 48 mitochondrial genome 48 COMT gene 48 biochemical markers 48 metabolic syndrome MetS 48 neuroglobin 48 plasma lipid 48 BRAF gene 48 microsatellite instability 48 Wolbachia infection 48 repeat allele 48 Ashkenazi Jewish 48 ERBB2 48 highly heritable 48 BMPR2 48 genetically engineered mice 48 motor neuron degeneration 48 gene expression profiling 48 MTHFD1L gene 48 Mendelian diseases 48 Parkinson disease PD 48 epigenetically 48 Hashimoto thyroiditis 48 PITX2 48 Y chromosomes 48 glucose metabolism 48 Her2/neu 48 Treg cell 48 neuroblastomas 48 neuronal stem cells 48 dysbindin 48 CC genotype 48 poorer prognosis 48 BRCA1 mutation 48 muscular dystrophies 48 SOX3 gene 48 WTCCC 48 progranulin gene 48 mRNA transcripts 48 EGFR mutation status 48 DHEAS 48 gene expression assays 48 CpG islands 48 fatty liver disease 48 environmental toxicants 48 histone deacetylases 48 autism spectrum disorders ASDs 48 gut flora 48 validate biomarkers 48 FGFR1 48 tumor suppressors 48 metalloprotease 48 biochemical pathway 48 heritable disorders 48 MiRNAs 48 Hp2 2 48 gene deletions 48 p# activation 48 adiponectin hormone 48 array CGH 48 uPAR 48 diseases 48 Autoimmune disorders 48 virulence determinants 48 TP# gene 48 MIF gene 48 polycystic ovary syndrome PCOS 48 T1DM 48 ependymomas 48 triglyceride levels 48 UTRs 48 dysglycemia 48 oxysterols 48 biochemical processes 48 inflammatory markers 48 Neanderthal genes 48 CIB1 48 NFkB 48 phytoestrogens 48 beta1 integrin 48 atopy 48 epithelial tissues 48 cardiovascular mortality 48 mosaicism 48 ApoE4 48 cytogenetic 48 bucindolol 48 genotyping 48 GPR# [002] 48 male infertility 48 colon cancers 48 C#Y mutation 48 MCAD deficiency 48 Nature Genetics 48 CGG repeats 48 Vitamin D insufficiency 48 ataxias 48 commonly mutated genes 48 Observational studies 48 SERT gene 48 BRCA gene 48 vitamin B# deficiency 48 sirtuin 48 autoimmune diseases 48 studies GWAS 48 cytomegalovirus CMV 48 Wolbachia 48 ciliopathies 48 intestinal polyps 48 mitochondrial 48 resistin 48 molecular 48 ancestries 48 mammary cells 48 protein kinase C 48 melatonin receptor 48 dopamine transporter gene 48 genetically inherited 48 G#S [002] 48 maternal lineage 48 sirtuin enzymes 48 CNTNAP2 gene 48 Pericak Vance 48 prostate cancer CaP 48 endophenotypes 48 neurodegenerative disease 48 mammographic density 48 familial hypercholesterolaemia FH 48 phenotypic variability 48 autosomal dominant inheritance 48 progressive neurodegenerative disorder 48 CagA 48 maize genome 48 gallstone disease 48 mammary cancers 48 osteopontin 48 MC4R 48 cardioembolic stroke 48 sequenced genome 48 RASSF1A 48 presymptomatic 48 synaptic function 48 lipid disorders 48 autosomal dominant disorder 48 genomic rearrangements 48 P. falciparum 48 urate 48 neural tube defect 48 ALDH2 48 pathophysiological 48 syndromes 48 transcription factor 48 methyltransferases 48 leptin deficiency 48 body louse genome 48 estrogen receptor 48 systemic inflammation 48 Methylation 48 Pseudomonas syringae 48 neural circuitry 48 DARPP 48 recessive trait 48 lactase persistence 48 sudden cardiac death 47 diagnose Alzheimer disease 47 untreated celiac disease 47 myeloproliferative disorders 47 DISC1 47 genetic heterogeneity 47 endogenous retroviruses 47 Phylomer ® 47 variant rs# 47 ncRNAs 47 SMN2 gene 47 personality traits 47 epigenetic modifications 47 gonadal hormones 47 major histocompatibility complex 47 Wnt proteins 47 PTP1B 47 transcriptional 47 G#D 47 Neuregulin 1 47 virulence factors 47 KLF4 47 CYP#A# gene 47 recurrent miscarriages 47 maternally inherited 47 TTR gene 47 geneticists 47 hormone leptin 47 vasopressin receptors 47 NRF2 gene 47 genomic deletions 47 circadian clock genes 47 Six3 47 estrogen receptor alpha 47 mitochondrial metabolism 47 periodontal pathogens 47 nonsense mutation 47 genetic alteration 47 Plasmodium falciparum 47 Heredity 47 BRCA2 gene mutation 47 KRAS gene

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