genetic variant

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

Related by context. All words. (Click for frequent words.) 84 gene variant 76 gene variation 75 genetic variants 74 genetic variation 74 gene mutation 74 gene variants 73 mutated gene 73 genetic mutation 72 mutation 71 allele 70 FTO gene 69 genetic variations 69 APOE4 68 gene 68 alleles 68 haplotype 67 APOE gene 66 gene mutations 66 ApoE4 gene 66 mutant gene 66 mutations 66 ApoE4 65 genetic mutations 65 CNVs 65 APOE e4 65 APOE 65 susceptibility gene 64 genetic variants associated 64 polymorphisms 64 apolipoprotein E gene 64 genotype 63 C#Y 63 MTHFR 63 BRCA1 gene 63 TCF#L# gene 63 G#S mutation 63 genetic susceptibility 63 BARD1 63 rs# [003] 62 HFE gene 62 mutated genes 62 BRCA2 mutation 62 G allele 62 BRCA1 mutations 62 homozygous 61 ApoE 61 heterozygous 61 genes 61 EGFR gene 61 APOE4 gene 61 DQB1 * 61 SORL1 61 mtDNA mutations 61 HLA B# 61 chromosome #p# [001] 61 #q# [001] 61 FMR1 gene 61 BRCA mutations 61 polymorphism 61 rs# [002] 61 BRCA mutation 61 sporadic ALS 61 COMT gene 61 mutant allele 61 MYH9 gene 61 APOE ε4 60 #q# [002] 60 PTPN# 60 defective gene 60 alpha synuclein gene 60 KIF6 gene 60 MTHFR gene 60 BRCA2 gene 60 genetic defect 60 genetic polymorphisms 60 FTO variant 60 X chromosome 60 MC1R gene 60 TP# mutation 60 TCF#L# 60 mutated BRCA1 60 5 HTTLPR 60 IGF2 60 TGFBR1 * 6A 60 breast cancer genes BRCA1 60 DRD2 60 tumor suppressor gene 60 LRRK2 gene 60 #p# [001] 60 familial pancreatic cancer 60 MC1R 60 susceptibility genes 60 FGFR2 60 clusterin 60 CYP#C# [001] 60 STAT4 60 apoE4 59 haptoglobin 59 heterozygotes 59 phenotype 59 APOC3 59 PTEN mutations 59 HMGA2 59 chromosome #q# [001] 59 chromosome 59 p# mutations 59 microcephalin 59 IKZF1 59 genetic predisposition 59 HMGA2 gene 59 genes predisposing 59 CNTNAP2 59 SNPs 59 germline mutations 59 LIS1 59 EGFR mutations 59 serotonin transporter gene 59 CC genotype 59 JAK2 mutation 59 inherited mutations 59 GSTM1 59 OPRM1 gene 59 haplotypes 59 GRK5 58 SNP rs# [001] 58 PALB2 58 APOL1 58 Wwox 58 apolipoprotein E 58 BRCA1 mutation 58 genetic trait 58 colorectal neoplasia 58 ApoE gene 58 miRNA genes 58 mutant protein 58 folate deficiency 58 MAOA gene 58 genes BRCA1 58 parkin gene 58 CYP#C# gene 58 genetic markers 58 receptor gene 58 shorter telomeres 58 heritable 58 NF1 gene 58 NAFLD 58 BRCA1 58 penetrance 58 CFH gene 58 insulin resistance 58 Genetic variation 58 chromosome #q# [002] 58 MnSOD 58 apoC III 58 rs# [001] 58 apoE 58 epigenetic changes 58 metabolic syndrome 58 familial ALS 58 CYP#D# gene 58 dopamine D4 receptor 57 APOE e4 gene 57 genomewide 57 missense mutation 57 SLC#A# [002] 57 GSTP1 57 CHEK2 57 gene expression patterns 57 mutated protein 57 IgA deficiency 57 gene locus 57 BRCA2 57 GSTM1 gene 57 medulloblastomas 57 repeat allele 57 C#Y mutation 57 H. pylori 57 chromosomal regions 57 mitochondrial genome 57 HLA DRB1 57 HPV# 57 Nature Genetics 57 DRD2 gene 57 MIF protein 57 5 HTT gene 57 gene APOE4 57 NPY gene 57 HLA genes 57 disease NAFLD 57 elevated triglyceride levels 57 MSH2 57 #q#.# [001] 57 lipoprotein 57 proband 57 APOE allele 57 ABCB1 57 epigenetic mechanisms 57 genetic makeup 57 microdeletions 57 genotypes 57 gene expression 57 variant alleles 57 GSTT1 57 CDH1 57 genetic abnormality 57 CFTR gene 57 subclinical hyperthyroidism 57 postmenopausal breast cancer 57 recessive gene 57 lung adenocarcinoma 57 SHANK3 57 CYP#E# gene 57 homozygosity 57 LQTS 57 Genetic variants 57 genetic polymorphism 57 subtype 57 narcolepsy cataplexy 57 gene encoding 57 autosomal recessive 56 missense mutations 56 dopamine receptor gene 56 somatic mutations 56 KLF# 56 serotonin transporter 56 mtDNA 56 SLC#A# [001] 56 TMEM#B 56 autosomal 56 TT genotype 56 progranulin 56 ALDH2 56 genetic determinants 56 CCL#L# 56 IL#R 56 CNTNAP2 gene 56 apolipoprotein E4 56 ZNF# 56 CAG repeats 56 chromosomal alterations 56 haplogroup 56 RUNX3 56 CETP gene 56 MC4R gene 56 hypermethylation 56 PARP inhibition 56 familial hypercholesterolemia 56 heterozygosity 56 haplogroups 56 LRRK2 mutation 56 MIF gene 56 T2D 56 Chromosome 56 spontaneous mutations 56 CCR5 mutation 56 BRCA2 mutations 56 SE alleles 56 recessive mutations 56 PTEN gene 56 DNA methylation 56 Six3 56 molecular mechanism 56 V Leiden 56 ADH1B * 55 ADPKD 55 aldehyde dehydrogenase 55 p# gene 55 genetic alteration 55 chromosomal aberrations 55 adiponectin levels 55 chromosomal abnormalities 55 aneuploidies 55 #p#.# [001] 55 PLoS Genetics 55 signaling molecule 55 autosomal dominant disorder 55 endogenous retroviruses 55 de novo mutations 55 FASPS 55 KIAA# 55 genetic alterations 55 causal variants 55 tumor suppressor protein 55 BRCA gene 55 telomere lengths 55 CCR5 delta# 55 Fragile X gene 55 BDNF gene 55 lipin 55 MECP2 gene 55 methylation patterns 55 Y chromosome 55 imprinted genes 55 loci 55 heterozygote 55 myostatin gene 55 Akt1 55 vimentin 55 mitochondrial DNA mtDNA 55 mitochondrial dysfunction 55 breast cancer metastasis 55 rs# [004] 55 VKORC1 55 protein encoded 55 EBV infection 55 ADAM# 55 CYP#C# * 55 BRCA2 gene mutation 55 LRRK2 mutations 55 #p#.# [002] 55 aneuploidy 55 TOP2A 55 autosomal dominant 55 basal cell nevus syndrome 55 UGT#A# * 55 uPAR 55 SMN2 55 APOE genotype 55 gene polymorphism 55 journal Nature Genetics 55 ε4 55 adiponectin 55 estrogen receptor 55 LRAT 55 COMT 55 IL#B 55 endothelial dysfunction 55 CDKN2A 55 WNK1 55 NRG1 55 FMR1 55 VHL gene 55 sCJD 55 recessive mutation 55 causative genes 55 HLA DRB1 * 55 defensin 55 e4 allele 55 major histocompatibility complex 55 MHC genes 54 mutant genes 54 RBP4 54 genetically 54 nicotinic receptor 54 HNSCC 54 HER2 gene 54 genetic variability 54 single nucleotide polymorphism 54 Ashkenazi Jewish 54 methylation 54 T1DM 54 K ras mutations 54 telomere length 54 chromosomal instability 54 mosaicism 54 CALHM1 54 elevated CRP 54 adenoma 54 FXTAS 54 gestational diabetes mellitus 54 homozygotes 54 phenotypic variation 54 CYP#D# 54 GAB2 54 protein p# 54 EGFR mutation 54 HGPS 54 melatonin receptor 54 UCP2 54 PICALM 54 transcription factor 54 E4 variant 54 LRP5 54 MLL2 54 BRCA genes 54 CYP#C# [002] 54 hereditary hemochromatosis 54 SGK1 54 mice lacking 54 COX2 54 MGUS 54 Li Fraumeni 54 synuclein 54 micro RNA 54 chromosome abnormalities 54 HNPCC 54 genes encoding 54 chromosome #q 54 genetic 54 NR#A# 54 CYP#E# 54 parkinsonism 54 SMN2 gene 54 polycystic ovary syndrome PCOS 54 FTLD 54 FTO allele 54 GBA mutations 54 Epstein Barr virus EBV 54 CHRNA5 gene 54 nestin 54 HbF 54 Plasmodium falciparum 54 YKL 54 Hashimoto thyroiditis 54 autism susceptibility genes 54 IGF1 54 Alu elements 54 osteopontin 54 colorectal tumors 54 progranulin gene 54 C. neoformans 54 ORMDL3 54 genetic abnormalities 54 neural tube defect 54 DISC1 54 TLR3 54 serotonin receptor 54 huntingtin gene 54 MetS 54 phenotypes 54 autoantibody 54 Neuregulin 1 54 chromosomal 54 G6PD 54 gut microbes 54 UGT#B# 54 klotho 54 gene APOE 54 LPA gene 54 Prox1 54 AAT deficiency 54 MC4R 54 neuroblastoma tumors 54 receptor protein 54 GPC5 54 filaggrin gene 54 human leukocyte antigen 54 subclinical hypothyroidism 54 monogenic 54 clade B 54 PB1 F2 54 HLA B 54 KIBRA 54 BRAF gene 54 MHC molecules 54 NKX2 54 MAOA 53 micro RNAs 53 coronary calcification 53 Apolipoprotein E 53 prognostic marker 53 chromosomal translocations 53 BCL#A 53 Vpu 53 MEF2A 53 retrovirus 53 miRNAs 53 BRAF mutation 53 HLA alleles 53 overexpression 53 autoantibodies 53 PON1 53 IDH1 53 herpes simplex virus 53 atherosclerosis 53 #q# deletion 53 mice genetically engineered 53 poorer prognosis 53 HLA DQ2 53 KLF4 53 CHD7 53 MAPK pathway 53 microRNA molecules 53 epigenetic silencing 53 CYP#A# gene 53 MLH1 53 GNAQ 53 mitochondrial mutations 53 2 diabetes T2D 53 LDL receptor 53 monozygotic twins 53 TOMM# 53 FGFR2 gene 53 hormone leptin 53 progerin 53 genes CYP#C# 53 OCA2 53 S#A# [002] 53 DISC1 gene 53 HLA molecules 53 KRAS gene 53 activin 53 gastric carcinogenesis 53 SORL1 gene 53 NF kB 53 promoter methylation 53 CagA 53 microdeletion 53 TP# gene 53 CETP VV 53 Li Fraumeni syndrome 53 dopamine transporter 53 activating mutations 53 germline mutation 53 exomes 53 caveolin 53 genetic underpinnings 53 TCF4 53 GATA4 53 mutant alleles 53 deleterious mutation 53 alpha synuclein 53 FOXP2 gene 53 SOD1 protein 53 susceptibility locus 53 epigenetic modification 53 X chromosome genes 53 AUDs 53 insulin secretion 53 atypical hyperplasia 53 TSC1 53 LRP6 53 ependymomas 53 KRAS mutations 53 mammary stem cells 53 CYP# [002] 53 vitamin D deficiency 53 neuroglobin 53 chromosome abnormality 53 hereditary predisposition 53 INF2 53 systemic lupus erythematosus SLE 53 resistin 53 HDL2 53 CXCL5 53 lactose tolerance 53 chromosome #q#.# [001] 53 familial clustering 53 metabolic abnormalities 53 SLC#A# gene [001] 53 inherited predisposition 53 androgen receptor 53 ApoB 53 P. falciparum 53 encodes protein 53 PIK3CA 53 genomic instability 53 Helicobacter 53 abnormal hemoglobin 53 modifiable risk 53 ApoE4 allele 53 Clusterin 53 p# protein 53 microRNA miR 53 Ashkenazi Jews 53 fetal hemoglobin 53 cardiovascular mortality 53 Y chromosomes 53 familial adenomatous polyposis 53 intron 53 Klinefelter syndrome 53 folate intake 53 non coding RNA 53 recessive genes 53 Rhes 53 MYH9 53 fasting glucose levels 53 GPR# [002] 52 SCN5A 52 PPAR gamma 52 bowel polyps 52 variant allele 52 BMPR2 52 mitochondrial 52 virulence genes 52 5q 52 coronary artery calcium 52 number variations CNVs 52 cardiac hypertrophy 52 endostatin 52 MLL gene 52 glucose metabolism 52 cardioembolic stroke 52 dopamine receptor 52 chromosomal abnormality 52 #p# [003] 52 NNRTI resistance 52 gene expression profiles 52 medulloblastoma 52 atherosclerotic lesions 52 Froguel 52 dysbindin 52 Genes 52 Foxp3 52 homozygote 52 progressive neurodegenerative disorder 52 TTR gene 52 GRK2 52 estrogen receptor alpha 52 genotyped 52 abdominal obesity 52 PKM2 52 Meckel Gruber 52 chimpanzee genomes 52 colorectal adenomas 52 androgen receptor gene 52 PTEN mutation 52 IDH1 mutation 52 APOE e4 allele 52 BRCA gene mutation 52 microRNA expression 52 DRD4 52 VIPR2 52 protein fragment 52 NAT2 52 Notch signaling 52 EphA2 52 G#S [002] 52 tumor suppressor genes 52 genomes 52 EAAT2 52 brain lesions 52 spontaneous mutation 52 CRTC3 52 p# mutation 52 NOD2 52 Nrf2 52 chlamydial infection 52 herpes virus 52 LRRK2 52 colon cancers 52 APOE epsilon 4 52 dopamine D2 receptors 52 airway hyperresponsiveness 52 HLA DRB1 SE 52 IL# [001] 52 amino acid methionine 52 Plasmodium vivax 52 PP2A 52 alpha synuclein protein 52 HDL cholesterol 52 oropharyngeal cancer 52 BRCA2 carriers 52 genetically susceptible 52 transgenic mouse model 52 Apobec3 52 genetic loci 52 Klotho gene 52 molecular pathway 52 SMN1 52 El Sohemy 52 Ascherio 52 SH#B# 52 isoform 52 beta thalassemia 52 histone modification 52 coinfection 52 downregulation 52 pathogenic mutations 52 atopy 52 amino acid substitution 52 fatty liver disease 52 #q#.# [002] 52 leptin hormone 52 TAp# 52 LKB1 52 biologic pathways 52 colorectal cancer CRC 52 preterm delivery 52 allelic variants 52 Cockayne syndrome 52 vitamin D receptor 52 KIF6 gene variant 52 cell adhesion molecule 52 protein 52 hypocretin 52 G6PD deficiency 52 SIDS infants 52 chromosomal rearrangement 52 mitochondrial gene 52 eotaxin 52 ERBB2 52 causative gene 52 cyclin E 52 premenopausal breast cancer 52 Adiponectin 52 esophageal squamous cell carcinoma 52 Neanderthal genes 52 genetic traits 52 genotypic 52 nonalcoholic fatty liver 52 noncarriers 52 DRB1 * 52 modifier genes 52 H. pylori infection 52 GBM tumors 52 glucose intolerance 52 A1 allele 52 BACE1 52 NF1 52 adiponectin concentrations 52 hydroxyvitamin D levels 52 molecular pathways 52 FCGR3A 52 neuroblastomas 52 PTP1B 52 filaggrin 52 SERT gene 52 SOD1 gene 52 HDL particles 52 ALK mutations 52 autoimmune thyroid 52 SIRT1 52 fatty acid synthase 52 aldosterone 52 SRY gene 52 Fragile X syndrome 52 nNOS 52 IGFBP 3 52 BRIP1 52 ADRB2 52 Pten 52 hemochromatosis 51 gene amplification 51 breast cancers 51 poor metabolizers 51 autosomal recessive disease 51 enteroviruses 51 ACE2 gene 51 mammary cancers 51 alternatively spliced 51 TP# mutations 51 behavioral disinhibition 51 signaling pathway 51 suppressor gene 51 transcriptional repression 51 GABRA2 51 STK# gene 51 nonmelanoma skin cancer 51 JAK2 enzyme 51 acetylation 51 Skp2 51 chromosomal anomaly 51 herpesviruses 51 ubiquitylation 51 TRIM5 51 Getzenberg 51 LDLR 51 gene polymorphisms 51 CYP#B# 51 Ets2 51 HIV HCV coinfected 51 chromosomal rearrangements 51 DNMT1 51 fetuin 51 Nrf2 gene 51 latent TB infection 51 underlying pathophysiology 51 serum BDNF 51 aY chromosome 51 sortilin 51 trans palmitoleic acid 51 enterovirus infection 51 tumor suppressor 51 JAK mutations 51 neuroligins 51 DICER1 gene 51 lactase persistence 51 karyotype 51 tau mutation 51 NKT cells 51 bile acid metabolism 51 cyclin D1 51 estrogen metabolism 51 endometrial cancers 51 CCR3 51 K ras gene 51 metabolic disturbances 51 prion disease 51 mRNA expression 51 JAK2 51 Smad3 51 malaria parasite Plasmodium falciparum 51 indels 51 nonsense mutations 51 hypermethylated 51 allele frequencies 51 gallstone disease 51 C. pneumoniae 51 maternally inherited 51 HPV infection 51 K#R [002] 51 serous ovarian cancer 51 impaired glucose tolerance 51 DEC2 51 mammary cells 51 DRD4 gene 51 histone deacetylases 51 PrP 51 subclinical atherosclerosis 51 chromosome rearrangements 51 TB bacterium 51 HSF1 51 MMP# 51 microglial 51 methylated DNA 51 uric acid levels 51 telomere shortening 51 endometrial cancer 51 impaired fasting glucose 51 protein kinase C 51 Obstructive sleep apnea 51 mitochondrial DNA 51 Hakonarson 51 CatB 51 proto oncogene 51 GBV C 51 DNA sequences 51 CIB1 51 STAT1 51 STAT3 51 gene loci 51 EZH2 51 microRNAs 51 homologs 51 ferritin 51 cystatin C 51 receptor 51 oncogenic 51 elevated triglycerides 51 DAT1 51 PKC beta 51 prion gene 51 anaplastic lymphoma kinase 51 ultraconserved elements 51 ovarian hormones 51 Sjögren syndrome 51 DICER1 51 thyrotropin 51 nucleotide 51 FOXP2 51 CISH 51 linkage disequilibrium 51 pDCs 51 adrenal function 51 nonhereditary 51 Cowden syndrome 51 chemokine receptor 51 ALK gene 51 heritability 51 E selectin 51 BRAF V#E 51 mutant worms 51 tyrosine phosphorylation 51 microalbuminuria 51 transthyretin 51 T2DM 51 glucocorticoid receptor 51 leukaemias 51 amyloidogenic 51 palladin 51 serum selenium 51 adiposity 51 familial predisposition 51 molecular abnormalities 51 51 BRCA2 gene mutations 51 G#D 51 dopamine transporter gene 51 progranulin protein 51 epigenetic 51 cholesterol metabolism 51 Smad7 51 predisposing factor 51 Brugada syndrome 51 epigenetically 51 leptin 51 thyrotropin levels 51 dizygotic twins 51 fewer dopamine receptors 51 KIF6 51 recessive trait 51 amyloid protein 51 SIRT3 51 mutated K ras 51 prognostic factor 51 SHBG 51 PrPSc 51 Jhdm2a 51 type2 diabetes 51 OGG1 51 prion protein gene 51 Homozygous 51 TACI mutations 51 circadian clock genes 51 colon tumors 51 BRCA gene mutations 51 FANCD2 51 pRb 51 neutralizing antibody 51 β amyloid 51 H2AX 51 familial aggregation 51 Chlamydia pneumoniae 51 airway remodeling 51 dentate gyrus 51 MUC1 51 Cyclin D1 51 collagen VI 51 Akt 51 squamous cell lung cancer 51 causative mutations 51 HLA B# gene 51 asymptomatically 51 breast cancer gene mutation 50 corticosterone levels 50 huntingtin protein 50 prostate cancer CaP 50 trypanosomes 50 Argonaute 50 polygenic 50 MECP2 50 demethylase 50 albumin excretion 50 susceptibility loci 50 IRAK1 50 HMMR 50 phenotypic expression 50 unmutated 50 metabolic abnormality 50 RASSF1A 50 IKK beta 50 Mcl 1 50 CRISPR Cas 50 DHEAS 50 habitual snoring 50 DGAT1 50 homolog 50 TNFα 50 apolipoprotein E APOE 50 genome 50 FGF2 50 obstructive coronary artery 50 Candida species 50 CMV infection 50 receptor molecule 50 EGFR protein 50 SMAD4 50 transmembrane receptor 50 orthologs 50 IGFBP 50 metabolic syndrome MetS 50 TRAF1 C5 50 beta carotene supplementation 50 IRS1 50 GPx 50 white matter hyperintensities 50 oxidative stress 50 miR #a [001] 50 Helicobacter pylori 50 advanced adenomas 50 IDH mutations 50 chromosome deletion 50 B7 H3 50 ER alpha 50 Genotype 50 Folate deficiency 50 hyperinsulinemia 50 DNA methylation patterns 50 PTEN protein 50 NF2 50 insulin receptors 50 gene MECP2 50 CXCL# 50 NFkB 50 BRAF mutations 50 beta1 integrin 50 hormone adiponectin 50 myo inositol 50 hypomethylation 50 X inactivation 50 dopamine receptors 50 brain derived neurotrophic 50 haemochromatosis 50 HLA DR 50 HCMV 50 estrogen receptors 50 MUC1 * 50 genomewide association study 50 N Myc 50 MetAP2 50 Bcl xL 50 SOD2 gene 50 C EBP alpha 50 M. pneumoniae 50 VNTR 50 preeclampsia 50 frontotemporal dementia 50 glutamate signaling

Back to home page