haplotypes

Related by string. Haplotype . haplotype * * genetic markers haplotypes . haplotype map . Cohen Modal Haplotype *

Related by context. All words. (Click for frequent words.) 74 haplotype 72 haplogroups 71 SNPs 71 loci 71 linkage disequilibrium 70 polymorphisms 70 homozygosity 70 chromosome #q# [001] 69 microsatellite markers 69 alleles 69 allele frequencies 69 intergenic 68 rs# [003] 68 #q# [001] 68 missense mutations 68 VNTR 67 chromosome #q# [002] 67 intronic 67 #q# [002] 67 #S rRNA 66 heterozygous 66 orthologs 66 polymorphism 66 rs# [002] 66 rs# [004] 65 indels 65 CNVs 65 PTPN# 65 germline mutations 65 nucleotide sequence 65 single nucleotide polymorphism 65 quantitative trait loci 65 allelic 65 microdeletions 65 genotyped 64 chromosomal regions 64 genetic variants 64 segmental duplications 64 indel 64 MLH1 64 genotypes 64 heterozygotes 64 autosomal 64 genetic lineages 64 #p# [001] 64 #p#.# [001] 64 mtDNA 64 clades 64 gene variants 64 5 HTTLPR 64 haplogroup 64 genetic loci 64 chromosome #p# [001] 64 methylation patterns 64 gene locus 64 paralogs 64 UTRs 63 sporadic ALS 63 cytochrome b 63 MYH9 gene 63 mRNA expression 63 rs# [001] 63 phylogenetic analyzes 63 phenotype 63 genotype 63 C#Y 63 CAG repeats 63 homozygotes 63 genetic markers 63 genotypic 63 chromosome #q#.# [001] 63 A. thaliana 63 homozygote 62 LPA gene 62 chromosome #q#.# [002] 62 penetrance 62 amino acid sequences 62 exons 62 GSTM1 62 nucleotide substitutions 62 DNA sequences 62 ABCB1 62 GSTP1 62 chromosome #q 62 gene expression patterns 62 susceptibility loci 62 mitochondrial DNA mtDNA 62 spontaneous mutations 62 pseudogenes 62 homozygous 62 #q#.# [001] 61 segmental duplication 61 genetic polymorphisms 61 KIAA# 61 intron 61 genetic variants associated 61 #p#.# [002] 61 gene polymorphisms 61 #p# [003] 61 phylogenetically 61 CC genotype 61 PALB2 61 heterozygosity 61 MSH2 61 Alu elements 61 chromosomal rearrangements 61 Haplotype 61 monozygotic twins 61 coding sequences 61 microcephalin 61 kilobase 61 IKZF1 61 K ras mutations 61 intergenic regions 61 orthologous 61 HLA genes 61 variant allele 61 chromosome #p# [002] 61 NNRTI resistance 61 #q#.# [002] 61 phylogenies 61 ZNF# 60 R#W [002] 60 untranslated regions 60 genes encoding 60 Genotypes 60 mutations 60 subtype 60 QTLs 60 allelic variation 60 yeast genome 60 nucleotide sequences 60 functional polymorphism 60 frameshift mutation 60 VKORC1 60 mRNA transcripts 60 exon 60 BARD1 60 allelic variants 60 gene expression profiles 60 phenotypic variation 60 cyclin E 60 ORFs 60 histone modifications 60 bacterial genomes 60 IgA deficiency 60 heterozygote 60 synuclein 60 maternally inherited 60 subfamilies 60 noncoding 60 MC1R gene 60 CpG 60 logistic regression analysis 60 allele 60 rRNA 60 mutant allele 60 outbred 60 RNA sequences 60 protein isoforms 60 mitochondrial genomes 60 somatic mutations 60 International HapMap Project 60 susceptibility gene 60 splice junctions 60 genomes 59 hypermethylation 59 mitochondrial gene 59 DRD2 59 synteny 59 LRRK2 gene 59 miRNA expression 59 CpG islands 59 inbred strains 59 promoter methylation 59 amino acid sequence 59 genes CYP#C# 59 TCF#L# gene 59 MTHFR gene 59 genetic variation 59 ribosomal DNA 59 causal variants 59 KRAS mutations 59 D. melanogaster 59 unmethylated 59 IL#R 59 lineages 59 homologs 59 Polymorphisms 59 susceptibility genes 59 cDNA libraries 59 MTHFR 59 gene mutations 59 proband 59 telomere lengths 59 STAT4 59 SNP rs# [002] 59 PRNP 59 chromosome #p#.# 59 phenotypes 59 BAC clones 59 globin genes 59 familial clustering 59 monozygotic 59 CDH1 59 Haplogroup 59 BDNF gene 59 T2D 59 hypermethylated 59 HLA DR 59 differentially expressed genes 59 phenotypically 59 substrate specificity 59 FMR1 59 epistasis 59 phenotypic traits 59 rs# rs# 59 HLA DRB1 59 MetS 59 genetic variations 59 genome rearrangements 59 coding exons 59 dopamine transporter gene 59 monogenic 59 CGG repeats 59 apolipoprotein E gene 59 probands 59 genetic variant 59 proteomes 59 CNTNAP2 59 missense 58 amino acid residues 58 perilipin 58 amino acid substitutions 58 MYH9 58 ERBB2 58 mutation 58 autosomal recessive 58 KLF4 58 CCR5 delta# 58 microRNA molecules 58 IL#B 58 missense mutation 58 exomes 58 differential gene expression 58 cystatin 58 transcriptomes 58 microdeletion 58 BRAF V#E 58 MECP2 gene 58 clade B 58 sequence homology 58 TACI mutations 58 TT genotype 58 mtDNA sequences 58 variant alleles 58 HLA DRB1 * 58 alternatively spliced 58 cis regulatory 58 CHEK2 58 #S rRNA genes 58 apoE4 58 genomewide 58 GABRA2 58 allele frequency 58 codons 58 #S rRNA gene 58 GSTT1 58 HNPCC 58 EGFR mutations 58 virulence genes 58 paternal lineages 58 paternally inherited 58 microRNA expression 58 familial ALS 58 HLA B# 58 Single Nucleotide Polymorphisms SNPs 58 At#g# 58 SNPs pronounced snips 58 cM 58 APOL1 58 contigs 58 mammalian genomes 58 TCF#L# 58 DNA methylation patterns 58 methylenetetrahydrofolate reductase 58 SNP rs# [001] 58 lysine residues 58 coding genes 58 UGT#A# * 58 single nucleotide polymorphisms 57 transgene expression 57 #S rDNA 57 NF1 gene 57 isoforms 57 TP# mutations 57 ApoE gene 57 sequenced genomes 57 MRSA isolates 57 coexpression 57 gene sequences 57 PCR amplified 57 major histocompatibility complex 57 mitochondrial genome 57 ADRB2 57 mutated genes 57 distinct lineages 57 causative mutations 57 CpG island 57 noncoding RNAs 57 chromosomal DNA 57 DQB1 * 57 archaeal 57 AFLP 57 gene duplications 57 autism susceptibility genes 57 CDKN2A 57 karyotypes 57 telomere length 57 Single Nucleotide Polymorphism 57 APOC3 57 HMGA2 57 PTEN mutations 57 gene rearrangements 57 H#K#me# 57 Alleles 57 3'UTR 57 MLL2 57 Clusterin 57 genes differentially expressed 57 succinate dehydrogenase 57 APOE e4 57 Y chromosomal 57 hepatocellular carcinomas 57 KIF6 gene 57 BRAF protein 57 DRD2 gene 57 chromosome 57 breast carcinomas 57 subtypes 57 CNTNAP2 gene 57 endogenous retroviruses 57 monophyletic 57 3' UTR 57 gene polymorphism 57 genetic variability 57 chromosomal alterations 57 karyotype 57 splice variants 57 FMR1 gene 57 DLC1 57 mutant alleles 57 phylogenetic trees 57 TSC1 57 sensu lato 57 alpha synuclein gene 57 operons 57 Prevotella 57 amplicons 57 PIK3CA 57 subfamily 57 TERT 57 HLA DQ2 57 TP# mutation 57 ESR1 57 array CGH 57 hamartomas 57 Li Fraumeni syndrome 57 de novo mutations 57 RFLP 57 nondiabetic 57 deuterostomes 57 lactase persistence 57 chimpanzee genomes 57 breast cancer subtypes 57 p# mutation 57 dysbindin 57 genes 57 apolipoprotein E 57 Arabidopsis genome 57 subpopulations 57 NPY gene 57 nucleotide 57 isotype 57 ADPKD 57 K#N 57 P. falciparum 57 receptor gene 56 chromosomal deletions 56 TRAF1 C5 56 transcriptome 56 transfected 56 CYP#D# gene 56 amino terminal 56 GSTM1 gene 56 multigenic 56 BRCA1 mutations 56 germline mutation 56 hepatoma 56 mtDNA sequence 56 IGFBP 56 clusterin 56 neuroligins 56 trinucleotide 56 mosaicism 56 causative mutation 56 distinct subtypes 56 primate genomes 56 cDNAs 56 homologues 56 kilobases 56 differentially expressed proteins 56 SCN5A 56 transposable elements 56 Supplementary Table 56 lymphoblastoid cell lines 56 mutated gene 56 generalized vitiligo 56 Phylogenetic analysis 56 colorectal neoplasia 56 BMAL1 56 immunoreactive 56 dinucleotide 56 CCL#L# 56 COL#A# 56 genetic polymorphism 56 activating mutations 56 LRAT 56 rDNA 56 subcellular localization 56 valine 56 micro RNA 56 chromosomal rearrangement 56 ependymomas 56 ADH1B * 56 Arabidopsis genes 56 microarray experiments 56 activating mutation 56 SLC#A# [002] 56 amino acid substitution 56 chromosome rearrangements 56 gene amplification 56 genes predisposing 56 ALDH2 56 Bacteroides 56 ortholog 56 mammalian genome 56 PON1 56 variant rs# 56 Karayiorgou 56 inherited mutations 56 atopy 56 Single Nucleotide Polymorphisms 56 prion gene 56 ribosomal protein 56 CYP#C# [001] 56 APOE ε4 56 T2DM 56 micro RNAs 56 mtDNA mutations 56 heterochromatic 56 UGT#B# 56 #q# deletion 56 SLC#A# [001] 56 seropositivity 56 FGFR2 56 tyrosine kinases 56 Mendelian 56 genomic sequence 56 breast cancer genes BRCA1 56 sCJD 56 C#T [002] 56 gene loci 56 microsatellite instability 56 clinicopathological 56 ancestries 56 susceptibility locus 56 PFGE 56 forkhead 56 taxa 56 MAPT 56 homology 56 serum leptin 56 chromosomal 56 Trypanosoma brucei 56 falciparum 56 HLA B 56 familial pancreatic cancer 55 catechol O methyltransferase 55 apoE 55 genetic relatedness 55 tRNA synthetase 55 protein encoded 55 prion protein gene 55 caveolin 55 repeat allele 55 FLT3 55 miRNA genes 55 autosomal dominant 55 hypervariable 55 vimentin 55 oxytocin receptor 55 vertebrate genomes 55 SORL1 55 causative genes 55 GLUT1 55 ORMDL3 55 transgenic mouse model 55 uPAR 55 Genotypic 55 constitutively expressed 55 Polymorphism 55 RRM1 55 miR #a [001] 55 conserved sequences 55 proline rich 55 HLA molecules 55 viral genome 55 EGFR gene 55 CFH gene 55 Multivariate analysis 55 kDa protein 55 LRRK2 mutation 55 homologous 55 paramyxoviruses 55 genetic mutations 55 epitope 55 IDH1 gene 55 dopamine receptor gene 55 cytokeratin 55 #S ribosomal RNA 55 orthologous genes 55 brain lesions 55 constitutively 55 Phenotypic 55 metabolomic profiles 55 evolutionarily conserved 55 homodimers 55 methylated 55 serum concentrations 55 fig. S1 55 homologous genes 55 TMEM#B 55 serine 55 etiologic 55 unmutated 55 Enterobacteriaceae 55 aneuploidy 55 hyperintense lesions 55 histone modification 55 G#S [002] 55 MLL gene 55 cytosine 55 landraces 55 cDNA microarray 55 Volvox 55 basal cell nevus syndrome 55 Eukaryotes 55 serotype 55 genetic aberrations 55 N acetyltransferase 55 C. neoformans 55 TGFBR1 * 6A 55 adenoma 55 multivariate Cox 55 PICALM 55 EphB4 55 amyloidogenic 55 epitopes 55 Sp1 55 telomeric 55 inactivating mutations 55 familial aggregation 55 dizygotic 55 APOE allele 55 cysteines 55 HMGA1 55 Phylogenetic 55 fungal genomes 55 carotid plaque 55 T. brucei 55 adenocarcinomas 55 CDK4 55 tyrosine phosphorylation 55 immunodominant 55 KRAS oncogene 55 HapMap 55 cystatin C 55 ribosomal RNA rRNA 55 bcl 2 55 circadian genes 55 KLF# 55 Yamanaka recipe 55 spontaneous mutation 55 atypical hyperplasia 55 CYP#D# 55 condensin 55 enterotypes 55 extracellular domain 55 guanine G 55 pyrimidine 55 BRCA genes 55 genetically divergent 55 EGFP 55 genomic sequences 55 V#F mutation 55 proto oncogene 55 Supplementary Fig 55 miRNAs 55 B. cereus 55 phylogenetic analysis 55 catechol O methyltransferase COMT 55 imprinted genes 55 SNCA 55 KCNH2 55 Leptospira 55 gene deletions 55 ribosomal proteins 55 Nilo Saharan 55 polygenic 55 t# c# CLA 55 Amino acid 55 epigenetic modification 55 WNK1 55 TIMP 1 55 organism genome 55 YKL 55 atopic 55 MGUS 55 diploid genome 55 GPx 55 BMPR2 55 maize genome 55 MC1R 55 logistic regression analyzes 55 autosomes 55 TNFR1 55 tau gene 55 N Myc 55 PGCs 55 transmembrane 55 Hsp# [001] 55 cDNA 55 EAAT2 55 HLA alleles 54 transgenic mouse models 54 triacylglycerol 54 multivariable analysis 54 gene 54 MHC genes 54 SMAD4 54 APOE4 54 Cytogenetic 54 univariate 54 morphologic 54 LRP5 54 PKD1 54 extracellular domains 54 C1q 54 chimp genomes 54 APOE genotype 54 gene expression 54 modifier genes 54 LIS1 54 methyltransferase 54 phenotypic characteristics 54 ncRNAs 54 uncharacterized genes 54 cytogenetic 54 microglial 54 tetramers 54 proapoptotic 54 AMACR 54 phylogenetic 54 K#R [002] 54 defensin 54 histologically 54 fascin 54 lung adenocarcinomas 54 deacetylation 54 BRCA mutations 54 Wwox 54 pathogenic mutations 54 fig. S4 54 S. maltophilia 54 genomic DNA 54 QTL mapping 54 disulfide bond 54 drug metabolizing enzymes 54 microbiomes 54 matrix metalloproteinase 54 heritable traits 54 haplotype map 54 eotaxin 54 MIF protein 54 Anopheles gambiae 54 CagA 54 peptide sequences 54 pressor response 54 homologue 54 ankyrin repeat 54 SOCS3 54 IPAH 54 logistic regression model 54 dizygotic twins 54 Recurrence Scores 54 KCNQ1 54 vivax 54 linkage disequilibrium LD 54 Foxp3 54 mutational 54 clefting 54 eukaryote 54 euchromatin 54 TIMP 54 proteolytic cleavage 54 clonally 54 protein tyrosine phosphatase 54 Bonferroni correction 54 ultraconserved elements 54 serum PTH 54 pairwise 54 PTEN gene 54 ALK mutations 54 alpha synuclein protein 54 herpesviruses 54 ribosomal RNA 54 tetramer 54 genetic sequences 54 Transcriptome 54 centromeres 54 melatonin receptor 54 ncRNA 54 site directed mutagenesis 54 gene encoding 54 Vps# 54 T#I [002] 54 dbSNP 54 recombination hotspots 54 beta globin 54 syngeneic 54 EoE 54 synthases 54 PAX5 54 PCa 54 mutated K ras 54 transmembrane protein 54 fraternal twin pairs 54 INF2 54 DRB1 * 54 hierarchical clustering 54 H#Y mutation 54 MAOA 54 FASPS 54 Logistic regression 54 colorectal tumor 54 ataxias 54 posttranslational modifications 54 polyadenylation 54 genetic alterations 54 deletion mutant 54 chromosomes 54 Apolipoprotein E 54 microsatellite loci 54 genetic locus 54 methylation 54 ChIP seq 54 Mutational 54 centromeric 54 Bos taurus 54 Venter genome 54 RASSF1A 54 lipoprotein 54 gene mutation 54 genetic determinants 54 immunoblotting 54 PrPSc 54 E#F# 54 RNA transcripts 54 RNA binding 54 insertion deletion 54 translocations 54 deleterious mutation 54 binding affinity 54 Haptoglobin 54 serine protease 54 epigenetically 54 FTLD 54 postsynaptic 54 genome 54 neutralizing antibody 54 NR#A# 54 binding affinities 54 exome 54 mutated protein 54 histone acetylation 54 BRCA2 mutation 54 CRISPR 54 pRb 54 GNAQ 54 polyploid 54 gp# [002] 54 nonsynonymous 54 Homozygous 54 S. pyogenes 54 polyglutamine 54 serine threonine kinase 54 logistic regressions 54 tumor suppressor protein 54 parkin gene 54 gambiae 54 Huntingtin 53 L1 retrotransposons 53 amplicon 53 synthetic analogues 53 fluoroquinolone resistance 53 morphological traits 53 insertions deletions 53 UGT#A# 53 homodimer 53 genotyping arrays 53 introns 53 NFKBIA 53 diploid 53 ciliated 53 airway responsiveness 53 thymine T 53 codon 53 G allele 53 amphioxus 53 microarray datasets 53 histone H3 53 somatic mutation 53 MAPK pathway 53 hypomethylation 53 methylated DNA 53 Genetic variants 53 beta amyloid peptides 53 HFE gene 53 FKBP# 53 Linear regression 53 GlcNAc 53 serotypes 53 SHANK3 53 phenotypic differences 53 isotypes 53 Neuregulin 1 53 aneuploidies 53 fig. S2 53 serum antibodies 53 morphogen 53 eukaryotic genomes 53 thymine 53 APOE gene 53 CHD7 53 operon 53 TET2 53 N. gonorrhoeae 53 ApoE 53 CYP#C# [002] 53 Plasmodium vivax 53 apo AI 53 non coding RNA 53 PCR RFLP 53 S. cerevisiae 53 amyloid deposition 53 prevalences 53 RAR beta 53 male Wistar rats 53 genes BRCA1 53 nucleotide substitution 53 dentate gyrus 53 blastomeres 53 DARPP 53 SLITRK1 53 Figure 2C 53 GBA mutations 53 differentially regulated 53 supratentorial 53 nucleic acid sequence 53 receptor subtypes 53 kinase domain 53 CCR7 53 PBMCs 53 TRIM5 53 MC4R gene 53 transgenic mice expressing 53 protein kinases 53 ChIP chip 53 proteins encoded 53 c Myb 53 Genotype 53 constitutively active 53 parkinsonism 53 chromosomal aberrations 53 molecular subtypes 53 multivariate analyzes 53 Recurrence Score 53 HBV genotype 53 CISH 53 zebrafish genome 53 suppressor gene 53 immunohistochemical 53 nucleotide variations 53 androgen receptor gene 53 MYBPC3 53 mRNA molecules 53 susceptibility alleles 53 IgG1 53 BRCA2 mutations 53 MSH6 53 gene fusions 53 NS5B 53 KRAS mutation 53 Plasmodium 53 cagA 53 catenin 53 p# mutations 53 Brugada syndrome 53 subcellular compartments 53 seroprevalence 53 palladin 53 SPINK1 53 OCT4 53 Typhi 53 cognitively normal 53 phosphorylated tau 53 genomic variation 53 racemic baclofen 53 immunohistochemical staining 53 Hox gene 53 ANOVA 53 mRNAs 53 APOA5 53 cellular prion protein 53 SRY gene 53 MDM2 53 carcinoembryonic antigen 53 lymph node metastasis 53 prothrombotic 53 Drosophila genome 53 DNA demethylation 53 H#N# isolates 53 mammographic density 53 evolutionary conserved 53 mutant gene 53 morphological characteristics 53 LDL receptor 53 transcriptional activation 53 p tau 53 LRP6 53 Rap1 53 colorectal carcinoma 53 LDL cholesterol concentrations 53 CYP#C# gene 53 trimer 53 phosphorothioate 53 phylogeny 53 mice lacking 53 Matthew Hurles 53 bivariate 53 DICER1 gene 53 metagenomes 53 haematopoietic 53 TOP2A 53 DNA rearrangements 53 IgG4 53 Proteobacteria 53 ALK gene 53 GenBank accession 53 WT1 53 human leukocyte antigen 53 TTR gene 53 phylogenetic relationships 53 HOTAIR 53 eukaryotic 53 linear regression analyzes 53 TOMM# 53 Xenopus 53 Jhdm2a 53 poor metabolizers 53 polynucleotides 53 FGFR1 53 MMP9 53 lactobacilli 53 parasitaemia 53 nondemented 53 apolipoproteins 53 Immunohistochemical analysis 53 chromatin structure 53 explanatory variables 53 clinicopathologic 53 transcriptional repressor 53 gene variation 53 SCA5 53 apolipoprotein B 53 RUNX3 53 haploid 53 TMPRSS2 ERG fusion

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