Related by context. All words. (Click for frequent words.) 75 chromosome 65 #p# [001] 65 chromosome #q#.# [001] 63 #q# [001] 63 #q# [002] 63 #p#.# [001] 62 #p#.# [002] 62 #q#.# [001] 61 chromosomal 60 susceptibility gene 59 chromosome #p# [001] 59 #p# [003] 59 chromosomes 59 Chromosomes 59 X chromosome 59 chromosome #q# [002] 59 chromosome #q 59 tumor suppressor gene 59 Chromosomal 59 chromosome #q# [001] 58 HMGA2 58 gene 58 caveolin 58 Mitochondrial 57 exons 57 chromosomal regions 57 PTPN# 57 segmental duplications 57 FMR1 gene 57 MSH2 57 noncoding 57 CNVs 56 microdeletion 56 MLL2 56 Mutation 56 #q#.# [002] 56 genes BRCA 56 PALB2 56 genetic variant 56 MLH1 56 #S rRNA 56 BARD1 56 mutated genes 55 microdeletions 55 VHL gene 55 mtDNA 55 haplotype 55 MECP2 gene 55 intron 55 VNTR 55 cadherin 55 KLF4 55 chromosome deletion 55 CDKN2A 55 mitochondrial gene 55 miRNAs 55 FMR1 55 CDH# 55 loci 55 CYP#E# gene 55 MeCP2 gene 55 KIAA# 55 genetic variants 55 chromosome #p#.# 54 rs# [003] 54 breast cancer genes BRCA1 54 mutations 54 Germline 54 Transcriptome 54 susceptibility locus 54 Methylation 54 imprinted genes 54 mutation 54 genes encoding 54 gene mutation 54 Arabidopsis genome 54 Kinase 54 Caspase 54 genetic mutations 54 MYH9 gene 54 IRAK1 54 chromosome #q#.# [002] 54 polymorphisms 54 genes 54 Neuronal 54 protein encoded 54 neurofibromatosis type 54 presenilin 54 ribosomal DNA 54 MECP2 53 intronic 53 alternatively spliced 53 genomic instability 53 IRF6 53 EGFR gene 53 receptor gene 53 major histocompatibility complex 53 IDH1 53 TP# gene 53 matrix metalloproteinase 53 somatic mutations 53 glycogen synthase kinase 53 ribosomal protein 53 mitochondrial DNA mtDNA 53 genome 53 Genes 53 gene variants 53 NR#A# 53 microRNA miR 53 autosomal 53 mutated gene 53 intergenic 53 homeobox genes 53 nucleotide sequence 53 Wwox 53 centromere 53 Alu elements 53 autism susceptibility genes 53 BRCA1 gene 53 CHD7 53 Phosphorylation 53 heterochromatin 53 missense mutations 53 TACI 53 DISC1 53 IKZF1 52 IL#R 52 single nucleotide polymorphism 52 Cyclin D1 52 hypermethylation 52 micro RNA 52 aneuploidies 52 haplotypes 52 MicroRNAs 52 gene encodes protein 52 tumor suppressor genes 52 centrosome 52 huntingtin 52 genetic loci 52 CNTNAP2 52 SNPs 52 GTPase 52 phosphorylates 52 cell adhesion molecule 52 proto oncogene 52 uPAR 52 gene encoding 52 RNA splicing 52 Genetic 52 gene locus 52 ApoE 52 TSC1 52 GSTP1 52 V3 loop 52 mosaicism 52 SNP rs# [001] 52 apolipoprotein E gene 52 Tumor Suppressor 52 IGF2 52 R#W [002] 52 Protein Kinase 52 APOL1 52 cytokeratin 52 Mutational 52 PTEN gene 52 SLC#A# [001] 52 tyrosine kinase 52 microRNA molecules 52 NKX2 52 filaggrin gene 52 BRAF V#E 52 Prox1 52 p# mutations 52 Src 52 inherited mutations 52 transcriptional repressor 52 vimentin 52 HOTAIR 52 IDH1 gene 52 glycosylation 52 Haplotype 52 CDK4 52 X Chromosome 52 LRAT 52 retrotransposon 51 genes BRCA1 51 exon 51 methyltransferase 51 apolipoprotein E 51 X inactivation 51 microRNAs miRNAs 51 INF2 51 alpha synuclein gene 51 MLL gene 51 subcellular localization 51 miRNA genes 51 kilobase 51 PICALM 51 NF1 gene 51 sporadic ALS 51 BRAF gene 51 Dysregulation 51 MC4R gene 51 homozygosity 51 H#K#me# 51 methylation 51 entorhinal cortex 51 number variations CNVs 51 Epigenetic 51 thrombospondin 51 chemokine receptor 51 polymorphism 51 chromosomal aberrations 51 mutant gene 51 DNA sequences 51 dysbindin 51 susceptibility genes 51 LRRK2 gene 51 non coding RNAs 51 trinucleotide 51 IDH2 51 centromeres 51 genetic 51 CHEK2 51 neuregulin 51 gene variant 51 epigenetic modification 51 MicroRNA 51 TYMS 51 IRS1 51 SLITRK1 51 LIS1 51 CDH1 51 p# gene 51 tumor suppressor 51 chromatin structure 51 apoE4 51 causal variants 51 Aneuploidy 51 paternally inherited 51 Frizzled 51 CpG islands 51 mutant allele 51 COL#A# 51 CNTNAP2 gene 51 BRCA2 51 JAK STAT 51 introns 51 untranslated regions 51 caspase 51 SHANK3 51 causative genes 51 EZH2 50 protocadherin 50 Mutations 50 cohesin 50 RNA polymerase II 50 SORL1 50 Polymorphism 50 SLC#A# [002] 50 neuroligin 50 5 HTTLPR 50 GPC5 50 Argonaute 50 LMNA 50 human genome 50 maize genome 50 PKD1 50 Rearrangements 50 OCA2 50 maternally inherited 50 endogenous retroviruses 50 presynaptic 50 coding exons 50 3'UTR 50 mRNA transcripts 50 ADAM# 50 SLC#A# gene [001] 50 gene polymorphisms 50 ubiquitylation 50 genetic mutation 50 rs# [002] 50 mitochondrial genome 50 tRNA synthetase 50 transmembrane protein 50 ataxin 50 interferon pathway 50 Microtubule 50 HMGA2 gene 50 rRNA genes 50 chromosome abnormality 50 telomeric 50 CALHM1 50 endonuclease 50 homologs 50 genetic variations 50 epigenetic regulation 50 microcephalin 50 HFE gene 50 encodes protein 50 quantitative trait loci 50 GNAQ 50 cyclin dependent kinase 50 genetic abnormality 50 SCN5A 50 centromeric 50 spontaneous mutations 50 homodimer 50 Phosphatase 50 receptor tyrosine kinase 50 COMT gene 50 MEF2A 50 chromosomal abnormalities 50 UGT#B# 50 amino acid residues 50 rRNA 50 non coding RNA 50 TERT 50 PON1 50 methylation patterns 50 nucleotide 50 Gene Mutation 50 UTRs 50 Ph chromosome 50 allelic 50 Allele 50 heterozygous 50 Genetic variation 50 genetic variation 50 mutant genes 50 Premature Aging 50 cyclin D1 50 TGF ß 50 Genetic Variation 50 genomic deletions 50 Leukemias 50 human leukocyte antigen 50 regulator CFTR gene 50 Signaling Pathway 50 amino acid sequence 50 chromosomal instability 50 APOE gene 50 de novo mutations 50 pseudogenes 49 NOTCH1 49 Histone 49 catenin 49 TCF#L# gene 49 DNA rearrangements 49 SOD1 protein 49 chromosome #p# [002] 49 Klotho gene 49 FGFR2 49 rs# [004] 49 Sonic Hedgehog 49 Apolipoprotein E 49 tyrosine kinases 49 CYP#D# gene 49 gene MECP2 49 Fanconi Anemia 49 aneuploidy 49 Phenotypic 49 E cadherin 49 mutant protein 49 APOE 49 receptor protein 49 BRCA2 gene 49 demethylase 49 ERBB2 49 CagA 49 epigenome 49 catalytic subunit 49 HAR1 49 TCF#L# 49 epigenetic alterations 49 monozygotic twins 49 ALDH2 49 Transcription Factor 49 extracellular matrix protein 49 cytochrome b 49 proband 49 BMP2 49 LKB1 49 dopamine D4 receptor 49 C#Y 49 gp# [002] 49 euchromatin 49 dopamine transporter gene 49 linkage disequilibrium 49 Hepatocyte 49 leptin receptor 49 Haplogroup 49 neurodevelopmental disorder 49 FGFR3 49 regulates gene expression 49 MTHFR 49 membrane proximal 49 Inactivation 49 susceptibility loci 49 DRD2 49 nucleotide sequences 49 nucleoli 49 HER2 neu 49 p# mutation 49 kilobases 49 #q 49 BRIP1 49 Homology 49 Nf1 49 5q 49 chromosomal DNA 49 signaling molecule 49 MC1R 49 forkhead 49 mRNA 49 dentate gyrus 49 HPRT gene 49 ApoE gene 49 heterochromatic 49 segmental duplication 49 disulfide bond 49 p# [001] 49 Hox gene 49 ALK gene 49 histone 49 Y chromosome 49 indel 49 palladin 49 Li Fraumeni syndrome 49 DQB1 * 49 histone H3 49 alleles 49 Mitochondrial DNA 49 claudin 49 RT qPCR 49 platypus genome 49 codons 49 A. thaliana 49 TP# mutation 49 LDLR 49 Smad 49 OCA2 gene 49 Adrenoleukodystrophy 49 TET2 49 gene mutations 49 miRNA 49 H#K# [002] 49 caveolae 49 dynamin 49 mutational 49 Epithelial 49 Synthase 49 viral genome 49 transcriptional regulation 49 Mitochondrial Dysfunction 49 mutant mouse 49 transcription factor 49 mice lacking 49 repeat allele 49 Notch signaling 49 Tumor Suppressor Gene 49 gene amplification 49 eotaxin 49 noncoding RNAs 49 RAD# [001] 49 centrosomes 48 aberrant methylation 48 proline rich 48 transcriptional repression 48 missense mutation 48 RUNX3 48 STAT4 48 CCR5 delta# 48 amino terminal 48 APOE e4 48 FTO gene 48 HLA DRB1 48 NFKBIA 48 Y Chromosome 48 COX2 48 SMAD4 48 chromosomal rearrangements 48 functional polymorphism 48 yeast genome 48 Cell Adhesion 48 genetic polymorphisms 48 At#g# 48 serotonin receptor 48 Transgenic Mice 48 homolog 48 genetic alterations 48 Metastases 48 SMN2 48 overexpression 48 locus coeruleus 48 WT1 48 methylated 48 glycan 48 mammalian genomes 48 micro RNAs 48 TMEM#B 48 MSH6 48 monogenic 48 fibronectin 48 lysine residues 48 granule cells 48 chromosomal deletions 48 Dystrophin 48 germline mutations 48 pseudogene 48 RNA binding 48 coding genes 48 epigenetic changes 48 PIK3CA 48 E#F# 48 rs# [001] 48 microRNA expression 48 subventricular zone 48 noncoding RNA 48 exonuclease 48 SWI SNF 48 ERK1 48 KLF# 48 DRD2 gene 48 mitogen activated protein kinase 48 SRY gene 48 polyglutamine 48 holoprosencephaly 48 molecular pathway 48 miR 48 D. melanogaster 48 Rab# 48 gag pol 48 heterozygosity 48 Clusterin 48 genomewide 48 Genetic Variations 48 autosomal recessive 48 allele 48 Protein Interactions 48 TOP2A gene 48 transcriptionally active 48 5 hmC 48 Wnt signaling pathway 48 DNA methylation patterns 48 Mammalian 48 overexpressed 48 trisomy 48 DGAT1 48 cis regulatory 48 myostatin gene 48 BDNF gene 48 chromatin 48 genome rearrangements 48 radial glia 48 transposable elements 48 Adiponectin 48 indels 48 genetic alteration 48 neurexin 48 guanine 48 Hutchinson Gilford progeria 48 Polymorphisms 48 karyotype 48 KRAS oncogene 48 LDL receptor 48 BRCA1 BRCA2 48 apoE 48 tumor suppressor protein 48 Genotypes 48 ERK2 48 Single Nucleotide Polymorphisms SNPs 48 gastric carcinogenesis 48 mutated BRCA1 48 sea urchin genome 48 adhesion molecule 48 RNA sequences 48 beta1 integrin 48 WNK1 48 medulloblastomas 48 Circadian Clock 48 genetic polymorphism 48 Telomere 48 protein p# 48 extracellular domains 48 Homozygous 48 Polycomb 48 chromosome rearrangements 48 succinate dehydrogenase 48 OCT4 48 subunit 48 serotonin transporter gene 48 Neural Circuits 48 nicotinic receptor 48 Cytogenetic 48 mRNAs 48 frameshift mutation 48 FANCD2 48 Protein Function 48 thymine T 48 DNA methylation 48 autosomal dominant disorder 48 IDH1 mutation 48 KIF6 gene 48 protein isoforms 48 MTHFR gene 48 hypermethylated 48 transcription factors 48 fibrillin 1 48 thymine 47 mRNA expression 47 H2AX 47 Genetic Mutation 47 collagen VII 47 catechol O methyltransferase 47 ribosomal proteins 47 amyloid peptide 47 activating mutation 47 ultraconserved elements 47 laminin 47 LMNA gene 47 Nup# 47 Abnormalities 47 splice junctions 47 guanine G 47 NF2 47 Cerebral Cortex 47 CHD5 47 globin genes 47 BCR ABL 47 MYH9 47 transmembrane domain 47 VIPR2 47 Gene Mutations 47 heterozygotes 47 protein kinases 47 G#S mutation 47 Antigens 47 pathogenic mutations 47 number variation CNV 47 microRNA 47 podocyte 47 iNOS 47 transmembrane 47 genetic variants associated 47 receptor molecule 47 WDR# 47 codon 47 pRb 47 VEGF receptor 47 ORFs 47 BCL#A 47 IgA deficiency 47 amyloid precursor protein 47 inherited neurological disorder 47 circadian genes 47 Small RNAs 47 HPV# 47 CpG 47 DLX5 47 SMN1 gene 47 FHIT 47 DISC1 gene 47 chromosomal anomaly 47 Meckel Gruber 47 MiRNAs 47 PTEN mutations 47 gene rearrangements 47 miR #a [002] 47 familial ALS 47 epigenetic silencing 47 cytoplasmic 47 genetic determinants 47 progerin 47 HGPS 47 genomic rearrangements 47 CFTR gene 47 EphB4 47 ZNF# 47 Htt 47 nephronophthisis 47 DNA Methylation 47 EBNA1 47 TAp# 47 SH#B# 47 mtDNA mutations 47 chromosome translocation 47 Adenoma 47 alternative splicing 47 chimpanzee genome 47 GATA4 47 FGFR1 47 tubule 47 chromosomal rearrangement 47 missense 47 neuroblastoma tumors 47 ribonucleic acids 47 serine threonine kinase 47 ncRNA 47 Epstein Barr Virus EBV 47 adenocarcinomas 47 Genetic Variant 47 piRNAs 47 IGFBP2 47 beta defensin 47 MIF protein 47 cystic fibrosis transmembrane conductance 47 β 47 rs# rs# 47 Kv#.# 47 G6PD 47 antisense strand 47 tumor suppressor p# 47 gene polymorphism 47 Heredity 47 C#T [002] 47 homeobox gene 47 SOD1 47 #q deletion 47 ubiquitinated 47 chromosomal abnormality 47 transmembrane receptor 47 genetic markers 47 generalized vitiligo 47 genes differentially expressed 47 ortholog 47 NF1 47 MC4R 47 FOXP2 47 BRCA1 47 allelic variants 47 SNP rs# [002] 47 blastomeres 47 PTP1B 47 Human Leukocyte Antigen 47 Drosha 47 Genotype 47 ectopic expression 47 Kinesin 47 mitochondrial 47 colorectal carcinoma 47 Heterozygous 47 RNA polymerase 47 budding yeast 47 HTLV 47 tyrosine phosphorylation 47 colocalization 47 unmethylated 47 gene expression patterns 47 NFkB 47 STAT3 47 causative gene 47 promoter methylation 47 EGFR protein 47 Genome 47 SMN1 47 Lymphocytes 47 estrogen receptor alpha 47 microRNAs 47 LRP6 47 DNMT1 47 chromosomal translocations 47 huntingtin gene 47 KCNQ1 47 miR #b [002] 47 APOE4 47 ORMDL3 46 kinase domain 46 kinase gene 46 CFH gene 46 BRAF protein 46 heritable 46 ubiquitin ligase 46 Rap1 46 Pten 46 FoxO1 46 Klinefelter Syndrome 46 single nucleotide polymorphisms 46 Oncogenic 46 intergenic regions 46 phenotype 46 RCAN1 46 synuclein 46 neural crest 46 glycoproteins 46 Breast Ovarian Cancer 46 Alleles 46 FGF signaling 46 nicotinic receptors 46 MAPK pathway 46 Mutagenesis 46 cyclin E 46 neuroligins 46 adherens junctions 46 parkin gene 46 BOULE 46 DRD4 46 ssDNA 46 Smad3 46 gene expression 46 VKORC1 46 Mouse Genome 46 serotonin transporter 46 telomere DNA 46 Cancer Cells 46 chaperone proteins 46 CAG repeats 46 KRAS mutations 46 Loeys Dietz syndrome 46 HLA B# 46 chromosome abnormalities 46 G#S [002] 46 K#R [002] 46 TP# mutations 46 von Hippel Lindau 46 meiotic recombination 46 p# protein 46 CRISPR 46 IL#B 46 dopamine receptor gene 46 primary cilia 46 genes encode proteins 46 array CGH 46 Nature Genetics 46 endoplasmic reticulum 46 genes CYP#C# 46 metalloprotease 46 cytoplasmic tail 46 progranulin gene 46 premutation 46 Plasmodium vivax 46 FGF2 46 RNA molecule 46 NFAT 46 germline mutation 46 glucocorticoid receptor GR 46 transcriptional activation 46 globin 46 melanocyte 46 HNPCC 46 ribonucleic acid RNA 46 gene deletions 46 phosphorylation 46 conserved sequences 46 TrkB 46 nucleotides 46 APOC3 46 genetic defect 46 Dpp 46 aneuploid 46 androgen receptor 46 Conserved 46 FXTAS 46 NRG1 46 receptor kinase 46 autosomal dominant 46 Neuroimmunology 46 polyadenylation 46 Scientists Identify 46 PAX5 46 Kinases 46 nonsense mutations 46 SEQ ID 46 NPM1 gene 46 IGF1 46 mesoderm 46 SIRT1 46 IGFBP 46 RNAs 46 Testis 46 retrotransposons 46 telomerase RNA 46 Epstein Barr Virus 46 c Myb 46 JAK mutations 46 Cx# [001] 46 Jhdm2a 46 virulence genes 46 Recombination 46 ependymomas 46 Gene Variants 46 TSLP 46 HLA DQ2 46 Golgi apparatus 46 Akt 46 lacZ 46 Cytoplasmic 46 genetic abnormalities 46 MDM2 46 Phenotype 46 miRNA expression 46 Cockayne syndrome 46 FLT3 46 cilium 46 bcl 2 46 Cortical 46 oncoprotein 46 ALK mutations 46 OGG1 46 Whole Genome 46 Eukaryotic 46 hTERT 46 CYP#E# 46 biogenesis 46 nucleic acid sequence 46 NF kB 46 Nedd4 46 serine 46 mammalian genome 46 Bile Acid 46 histone methylation 46 mitochondrial mutations 46 lincRNAs 46 protein fragment 46 PrP 46 Supplementary Table 46 gene BRCA2 46 cDNAs 46 breast carcinomas 46 orthologous 46 kinases 46 HLA B 46 autoantibodies 46 HER2 receptor 46 PDGFR 46 Ubiquitin 46 Fibroblasts 46 RNA transcripts 46 Bardet Biedl syndrome 46 TG2 46 trypanosome 46 Glial 46 Neuregulin 1 46 CpG island 46 recessive mutation 46 GSK 3ß 46 transcriptional coactivator 46 Transcriptional 46 estrogen receptor 46 C. neoformans 46 connexin 46 rDNA 46 5 hydroxymethylcytosine 46 somatic mutation 46 evolutionarily conserved 46 corpus callosum 46 ZBP1 46 Oxidative Stress 46 chromosomal disorders 46 MYCN 46 TOP2A 46 chromosomal defect 46 messenger RNAs mRNAs 46 histone proteins 46 dysgenesis 46 lamin 46 Susceptibility Gene 46 Sjögren syndrome 46 Caenorhabditis 46 ENPP1 46 LRRK2 46 ribosomal RNA rRNA 46 CCL#L# 46 UCP2 46 Pancreatic 46 cM 46 PAK1 45 DICER1 45 Estrogen Receptor 45 ESR1 45 NKX#.# 45 TRF1 45 protein phosphorylation 45 Wnt pathway 45 Fragile X 45 anterior pituitary 45 Therapeutic Effects 45 membrane protein 45 pheochromocytomas 45 caspases 45 Epitopes 45 mitochondrial dysfunction 45 genomes 45 polypeptide 45 microsatellite markers 45 cytosine 45 #BP# 45 Mouse Model 45 differentially methylated 45 CD8 + 45 Epigenetics 45 mitotic spindle 45 #S ribosomal RNA 45 insertions deletions 45 spontaneous mutation 45 TFIIH 45 Six3 45 telomere 45 fascin