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(Click for frequent words.) 73 chromosomes 73 chromosome 66 gene 66 X chromosome 65 mutations 65 methylation 65 mtDNA 64 genes 64 genetic 62 alleles 62 aneuploidy 62 telomeric 62 mutation 62 nucleotide 62 heterozygosity 61 MLL gene 61 Chromosomal 61 chromosomal rearrangements 61 imprinted genes 61 centromeres 61 genomic instability 61 allelic 61 germline 61 DNA methylation 61 Chromosome 61 microdeletion 61 mitochondrial gene 60 PTEN gene 60 intron 60 genome 60 cohesin 60 Y chromosome 60 gene expression 60 DNA rearrangements 60 mitochondrial DNA mtDNA 60 mRNAs 59 haplotype 59 tumor suppressor gene 59 breast cancer genes BRCA1 59 chromatin 59 chromosomal abnormalities 59 mosaicism 59 #p# [001] 59 chromosomal DNA 59 nucleosome 59 glycosylation 59 SNPs 59 mutational 59 heterochromatin 59 meiotic 59 genetic mutations 59 PALB2 59 chromosomal instability 58 phenotype 58 chromosome #q#.# [001] 58 transcriptome 58 PTPN# 58 #p#.# [001] 58 X inactivation 58 DNA sequences 58 mitochondrial 58 mRNA 58 homologous recombination 58 epigenetic 58 germline mutations 58 segmental duplications 58 chromosomal translocations 58 SRY gene 58 centrosome 58 #q#.# [002] 58 mitochondrial genome 58 autosomal 58 CNVs 57 FMR1 gene 57 chromosome #q# [002] 57 exons 57 #q# [001] 57 chromosome #q 57 E cadherin 57 gene expression patterns 57 microdeletions 57 CHD7 57 meiosis 57 polymorphisms 57 translocations 57 gene mutations 57 BRCA1 gene 57 chromosome #q# [001] 57 heritable 57 monozygotic twins 57 MLH1 57 FMR1 57 H#K#me# 57 nucleotide sequence 57 methylation patterns 57 chromatin structure 57 #q# [002] 57 introns 56 tumor suppressor genes 56 Jhdm2a 56 MSH2 56 paternally inherited 56 loci 56 genetic alterations 56 piRNAs 56 heterozygosity LOH 56 DSBs 56 microRNA molecules 56 karyotype 56 p# gene 56 chromosomal regions 56 Chromosomes 56 neural crest 56 proteins 56 telomere 56 chromosomal deletions 56 aneuploidies 56 microRNA expression 56 genetic recombination 56 CFTR gene 56 genomic imprinting 56 testis 56 mutated gene 56 LIS1 56 homologs 56 centrosomes 56 chromosomal aberrations 56 somatic mutations 56 p# mutations 56 de novo mutations 56 haplotypes 56 rs# [003] 55 radial glia 55 conformational 55 chromatid 55 X chromosome inactivation 55 miRNA expression 55 MECP2 gene 55 viral genome 55 epigenetic silencing 55 histone 55 recombination 55 genomes 55 hypermethylation 55 homologous chromosomes 55 mtDNA mutations 55 budding yeast 55 ubiquitylation 55 miRNAs 55 CYP#E# gene 55 CYP#D# gene 55 intergenic 55 D. melanogaster 55 epigenetic modification 55 CTCF 55 genetic variation 55 gene locus 55 Alu elements 55 aberrant methylation 55 #q#.# [001] 55 rDNA 55 somatic mutation 55 polymorphism 55 homozygosity 55 Hox gene 55 IGF2 55 array CGH 55 genomic 55 genetic abnormalities 55 vimentin 55 heterozygous 55 gene mutation 55 epithelial 55 VNTR 55 single nucleotide polymorphisms 55 CYP#B# 55 major histocompatibility complex 55 noncoding 55 quantitative trait loci 54 genetic variations 54 molecular 54 aneuploid 54 genetic variants 54 chromosome segregation 54 VHL gene 54 miRNA 54 inherited mutations 54 mutated genes 54 transmembrane 54 sister chromatid 54 mutant alleles 54 BARD1 54 indels 54 enzymatic activity 54 microRNAs miRNAs 54 missense mutations 54 mitochondria 54 UTRs 54 Fragile X gene 54 heterochromatic 54 epigenetically 54 ribonucleic acid RNA 54 transposable elements 54 NF1 gene 54 LKB1 54 genetic mutation 54 ploidy 54 CHEK2 54 chromatin proteins 54 DNA methylation patterns 54 desmosomes 54 cytoplasmic 54 chromosomal anomalies 54 mRNA expression 54 subcellular localization 54 centromere 54 synaptogenesis 54 3'UTR 54 unmethylated 54 Y chromosomes 54 single nucleotide polymorphism 54 recessive mutation 54 genomic rearrangements 54 Wnt signaling 54 chromosome abnormalities 54 ALK gene 54 epithelial cell 54 histone modifications 54 Sonic Hedgehog 54 Cyclin D1 54 #BP# 54 genetic variant 54 CpG 54 DNMT1 54 CNTNAP2 gene 54 genes encoding 54 DNA replication 54 SLC#A# gene [001] 54 NR#A# gene 54 polymerase 54 MLL2 54 linkage disequilibrium 54 morphogens 54 untranslated regions 54 insertions deletions 54 orthologs 53 chromosomal rearrangement 53 ribosomal DNA 53 coding sequences 53 CpG islands 53 Genetic variation 53 subcellular 53 chromosome #p#.# 53 non coding RNA 53 chaperone proteins 53 cis regulatory 53 A. thaliana 53 allele 53 mutant protein 53 S. cerevisiae 53 TAp# 53 microglial 53 embryogenesis 53 blastomeres 53 antigenic 53 receptor gene 53 germ cells 53 retrotransposon 53 evolutionarily conserved 53 Drosophila 53 MSH6 53 transcriptional regulation 53 genomic loci 53 genomewide 53 RUNX3 53 exon 53 gene encoding 53 protein isoforms 53 maternally inherited 53 HOTAIR 53 Arp2 3 53 tRNA 53 histone H4 53 TOP2A gene 53 #p#.# [002] 53 chromosome condensation 53 intergenic regions 53 splice junctions 53 endonuclease 53 PIK3CA 53 genetically 53 genotoxic stress 53 #p# [003] 53 RNA polymerase II 53 autosomes 53 Mre# 53 centromeric 53 hypermethylated 53 gene rearrangements 53 morphogen 53 MC1R 53 mutant gene 53 codons 53 EGFR gene 53 PON1 53 gene amplification 53 epigenetic regulation 53 p# [001] 53 granule cells 53 epigenetic changes 53 mutant genes 53 LMNA gene 53 BAC clones 53 primate genomes 53 mitotic spindle 53 intronic 53 DISC1 53 BRCA2 53 nucleases 53 nucleosomes 53 mammary stem cells 53 DNA strands 52 proto oncogene 52 orthologous 52 beta1 integrin 52 CGG repeats 52 alternatively spliced 52 adherens junctions 52 mRNA transcripts 52 p# MAPK 52 micro RNA 52 gp# [002] 52 nucleotide substitution 52 p# mutation 52 DLX5 52 phenotypic variation 52 phenotypes 52 methylated 52 noncoding RNAs 52 Prox1 52 polyadenylation 52 HAR1 52 genetic markers 52 transgene 52 glycoproteins 52 cytosine 52 monozygotic 52 gene expression profiles 52 BRCA1 52 organelle 52 neuronal 52 MeCP2 gene 52 palladin 52 conformational changes 52 virulence genes 52 gene variants 52 IKKa 52 mammalian genomes 52 acetylation 52 IKZF1 52 Rb gene 52 cytogenetic 52 Methylation 52 methylated DNA 52 cytosine methylation 52 protein coding 52 MTHFR gene 52 helicase 52 X chromosomes 52 EBNA1 52 codon 52 activating mutations 52 catenin 52 immunoglobulin genes 52 dopamine transporter gene 52 overexpression 52 uracil 52 multiprotein complex 52 metabolic enzymes 52 ERCC1 52 fission yeast 52 BRAF gene 52 yeast genome 52 glycan 52 organism genome 52 malignant transformation 52 micro RNAs 52 ERK2 52 neuroligins 52 parkin gene 52 mitochondrial DNA 52 trophoblast 52 Golgi apparatus 52 telomere length 52 APOL1 52 recombination hotspots 52 CDH1 52 gene duplications 52 frameshift mutation 52 ectopic expression 52 methyltransferase 52 transgene expression 52 primordial germ cells 52 chromosome #p# [001] 52 coding genes 52 HOX genes 52 MHC genes 52 pRb 52 cadherin 52 proband 52 Mitochondrial 52 epistasis 52 neurogenesis 52 aCGH 52 telomere DNA 52 FXTAS 52 heterozygote 52 pseudogenes 52 enzyme 52 PARP inhibition 52 subventricular zone 52 neuromuscular junction 52 ADRB2 52 protein p# 51 non coding RNAs 51 neural crest cells 51 #S rRNA 51 endonucleases 51 CDH# 51 Pten 51 spontaneous mutation 51 protein 51 RNA polymerases 51 sister chromatids 51 transgenic mice expressing 51 neuroepithelial cells 51 nucleotides 51 epigenetic alterations 51 OGG1 51 extracellular domains 51 MC4R gene 51 BRCA2 gene 51 H#K# [002] 51 KRAS oncogene 51 mitosis 51 ectoderm 51 BDNF gene 51 genetic defects 51 SMN2 gene 51 histone acetylation 51 RNA molecules 51 BRCA1 BRCA2 51 chromosome rearrangements 51 KIAA# 51 spontaneous mutations 51 nucleic acid sequence 51 NFKBIA 51 androgen receptor 51 ssDNA 51 HSF1 51 heterozygotes 51 acinar 51 E3 ubiquitin ligase 51 genomic rearrangement 51 genetic loci 51 microcephalin 51 beta globin gene 51 mesoderm 51 transcription factor 51 Germline 51 estrogen receptor 51 susceptibility genes 51 microsatellite instability 51 RNAs 51 disulfide bond 51 metaphase 51 TP# gene 51 telomeres 51 tumor suppressor protein 51 TMPRSS2 ERG fusion 51 Foxp3 51 MTHFR 51 suppressor gene 51 GATA4 51 genetic defect 51 histone modification 51 RNA splicing 51 progerin 51 MECP2 51 HER2 neu 51 GAPDH 51 FGF signaling 51 constitutively 51 cDNA 51 phenotypically 51 phenotypic expression 51 uPAR 51 human genome 51 multigene 51 H2AX 51 C. neoformans 51 regulates gene expression 51 clefting 51 Wnt pathway 51 p# protein 51 hyperactivation 51 kilobase 51 IDH1 51 DEAR1 51 filaggrin gene 51 Dictyostelium 51 HPRT gene 51 nucleolar 51 DNA polymerases 51 colocalization 51 prion gene 51 homologous 51 chromosomally 51 Dpp 51 mitochondrial mutations 51 Drosophila melanogaster 51 HLA molecules 51 mitotic 51 amino acid 51 germline mutation 51 HMGA2 51 clonal 51 SMN1 51 tumorigenesis 51 guanine G 51 trinucleotide 51 protein conformation 51 melanocyte 51 nucleolar dominance 51 rRNA 51 cerebellar 51 KCNE2 51 helicases 51 eukaryotic cell 51 microtubule 51 uncharacterized genes 51 myelination 50 NR#A# 50 TFIIH 50 homodimers 50 guanine 50 TSC1 50 functional polymorphism 50 CHI#L# 50 LRRK2 gene 50 BMP signaling 50 neuroblasts 50 Mitochondrial DNA 50 protein complexes 50 immunoreactivity 50 epithelial tissues 50 primary cilia 50 ribosomal RNA 50 karyotypes 50 membrane proximal 50 autism susceptibility genes 50 DLC1 50 gut microbes 50 cyclin E 50 mutant proteins 50 c Myb 50 genomic DNA 50 transcriptional repressor 50 transcriptional activation 50 phosphorylation 50 amino terminal 50 polymerases 50 PKD1 50 haploid 50 gene MECP2 50 amino acid substitutions 50 chromosome deletion 50 OCA2 50 FGFR2 50 tRNA synthetase 50 isoform 50 Genetic 50 KLF4 50 Cx# [001] 50 CNTNAP2 50 trypanosome 50 GLI1 50 protein encoded 50 OCA2 gene 50 substrate specificity 50 Foxp2 50 RT qPCR 50 multigenic 50 STAT4 50 genomic deletions 50 molecular pathways 50 estrogen receptor alpha 50 contigs 50 indel 50 EZH2 50 monogenic 50 beta globin 50 hierarchical clustering 50 Rad# 50 PALB2 gene 50 agouti gene 50 neuronal cell 50 dimer 50 actin cytoskeleton 50 gene p# 50 Argonaute proteins 50 MC1R gene 50 nuclease 50 mammalian 50 COL#A# 50 Mendelian 50 ubiquitination 50 ciliated 50 FANCD2 50 proteolysis 50 placental 50 RNA sequences 50 mutant allele 50 embryoid bodies 50 number variations CNVs 50 transcriptional 50 tetramer 50 Saccharomyces cerevisiae 50 tumor suppressor p# 50 HLA genes 50 chromosomal anomaly 50 chromosomal alterations 50 orthologous genes 50 isogenic 50 allele frequencies 50 morphologic 50 gonadal 50 fibrillin 1 50 genetic makeup 50 tau protein 50 FGFR2 gene 50 epigenetic marks 50 receptor molecule 50 dizygotic twins 50 polyglutamine 50 globin genes 50 autosomal recessive 50 genital tract 50 motor neuron 50 causative genes 50 spermatogenesis 50 Single Nucleotide Polymorphisms SNPs 50 morphological 50 myocyte 50 Arabidopsis 50 SLC#A# [002] 50 PDGFR 50 embryological 50 messenger RNA 50 synapsis 50 nucleoli 50 CFTR proteins 50 genomic alterations 50 dimers 50 SCN5A 50 promoter methylation 50 S. pombe 50 phylogenetic 50 cilium 50 endoplasmic reticulum 50 dizygotic 50 Skp2 50 transposon 50 mRNA molecules 50 histone protein 50 MAPK pathway 50 centrioles 50 miRNA genes 50 ZNF# 50 histone proteins 50 transcriptional coactivator 50 sequence homology 50 inbred strains 50 susceptibility gene 50 epigenetic modifications 50 lacZ 50 ectopic 50 tubule 50 yeast cells 50 paralogs 50 MMP9 50 HLA DQ2 50 histones 50 BMAL1 50 neuron 50 TCF#L# gene 50 polyploidy 50 familial clustering 50 protein phosphorylation 50 genetic alteration 50 polygenic 50 CDKN2A 50 HER2 receptor 50 amino acid sequence 50 basal cells 50 kinetochores 50 CFTR 50 transcription elongation 50 MDM2 50 fru 50 autosomal dominant 50 spliceosome 50 meiotic recombination 50 Arabidopsis genome 50 rRNA genes 49 JAK2 49 5q 49 number variation CNV 49 5 hydroxymethylcytosine 49 mitochondrial genes 49 dynamin 49 membrane protein 49 preimplantation 49 transcriptionally active 49 Hox genes 49 genetic rearrangements 49 adenine 49 #S rRNA gene 49 mutated protein 49 CpG island 49 actin 49 chimerism 49 autophagic 49 genes predisposing 49 AMACR 49 p# activation 49 retrotransposons 49 CEACAM1 49 sporadic ALS 49 histopathological 49 Notch signaling 49 chromosome #p# [002] 49 ependymomas 49 gene polymorphisms 49 premutation 49 exonuclease 49 Leydig cells 49 proline rich 49 oligomer 49 MEF2A 49 homolog 49 coiled coil 49 Immunohistochemical analysis 49 UGT#B# 49 cellular senescence 49 fruit fly Drosophila 49 immunological 49 PCR RFLP 49 chordate 49 phenotypic 49 6S RNA 49 ectodermal 49 antibody antigen 49 genetic underpinnings 49 DNA helix 49 recessive mutations 49 Sox2 49 TGF ß 49 RASSF1A 49 molecular abnormalities 49 Sox9 49 mammary cells 49 IRF6 49 Cytogenetic 49 thymine 49 disulfide bonds 49 eukaryotic cells 49 F actin 49 alpha synuclein gene 49 STAT1 49 IRAK1 49 haematopoietic 49 metabolomic profiles 49 genotypic 49 SNP rs# [001] 49 GSTP1 49 BMP4 49 biochemical 49 caveolae 49 doublesex 49 WT1 49 rs# [002] 49 acrosome 49 homozygous 49 huntingtin 49 breast epithelial cells 49 cysteines 49 fluorescently labeled 49 Hsp# [001] 49 mutagenesis 49 PTEN protein 49 transcriptional repression 49 Aneuploidy 49 bisulfite sequencing 49 BRIP1 49 HER2 gene 49 mitochondrial dysfunction 49 ribosomal genes 49 bacterial genomes 49 Wnt signaling pathway 49 peroxisomes 49 homodimer 49 telomere maintenance 49 RhoA 49 tumor suppressor 49 MeCP2 49 LDLR 49 Western blotting 49 causal variants 49 valine 49 melanogaster 49 coding exons 49 odorant receptor 49 cyclin 49 noncoding DNA 49 V3 loop 49 anterior pituitary 49 prostatic 49 RNA transcripts 49 penetrance 49 RNA viruses 49 abnormal chromosomes 49 tyrosine phosphorylation 49 alpha synuclein protein 49 mammalian cells 49 morphogenesis 49 Pol IV 49 presynaptic 49 genetic imprinting 49 alpha catenin 49 ovules 49 ultrastructural 49 oncogenes 49 folate metabolism 49 genome rearrangements 49 dopamine receptor 49 genotype 49 PrP 49 immunohistochemical 49 osteoclast 49 Six3 49 holoprosencephaly 49 WDR# 49 ligand binding 49 cell motility 49 G#S mutation 49 forkhead 49 ErbB4 49 striatal 49 phytochrome 49 ERBB2 49 superfamily 49 DRD2 gene 49 #S rDNA 49 transactivation 49 recessive trait 49 phthalate syndrome 49 carboxy terminal 49 polyploid 49 NPY gene 49 dinucleotide 49 androgen receptor gene 49 alanine 49 nuclei 49 myostatin gene 49 telomerase RNA 49 beta subunit 49 H#K# methylation 49 conserved sequences 49 platypus genome 49 SLC#A# [001] 49 Dysregulation 49 nucleosome positioning 49 Mutational 49 cyclin D1 49 deacetylation 49 microRNAs 49 mutant huntingtin protein 49 human leukocyte antigens 49 RAR beta 49 PIP2 49 prion protein 49 diploid 49 genetic polymorphisms 49 RNA strand 49 ADAM# 49 genes BRCA1 49 metabolites 49 male hormone androgen 49 antisense strand 49 ribozyme 49 FGFR3 49 BCL#A 49 gene sequences 49 vesicle fusion 49 Ago2 49 plasminogen 49 chromosomal translocation 49 rs# [004] 49 ALK mutations 49 sRNA 49 COMT gene 49 ERK signaling 49 CCR5 gene 49 hexamer 49 TP# mutations 49 C. elegans 49 RNA molecule 49 cardiac fibroblasts 49 HNPCC 49 metabolic 49 collagen VII 49 SMN1 gene 49 Wwox 48 transcription factors 48 segmental duplication 48 MMP# 48 β catenin 48 BRAF protein 48 phylogenetic analysis 48 MIF protein 48 transcriptomes 48 PCR amplified 48 matrix metalloproteinase 48 Y chromosomal 48 MYH9 gene 48 podocyte 48 RNAP 48 P. patens 48 neurexins 48 ncRNAs 48 FGFs 48 hindbrain 48 TMEM#B 48 ribosomal proteins 48 alternative splicing 48 thymine T 48 chromophore 48 hair follicle stem cells 48 apoE4 48 helices 48 GSK 3ß 48 epigenome 48 recessive genetic 48 primary cilium 48 autoantibodies 48 microRNA 48 aneuploidy screening 48 gastric carcinomas 48 genetic abnormality 48 cytochrome b 48 proteomes 48 Phenotypic 48 Phylogenetic analysis 48 SMAD4 48 coevolution 48 Fc receptor 48 neoplastic cells 48 vertebrate embryos 48 polypeptides 48 embryo biopsy 48 maize genome 48 proteolytic 48 chromosome aberrations 48 lymphatic vasculature 48 microsatellite markers 48 PAX5 48 prokaryote 48 gastrulation 48 parthenogenetic 48 Math1 48 chromatin immunoprecipitation ChIP 48 gene variant 48 QTLs 48 protein fragment 48 PcG 48 IL#B 48 phylogenetically 48 lysine residues 48 sequenced genomes 48 tetramers 48 lincRNAs 48 IGF1 48 structural rearrangements 48 filaggrin 48 neural progenitor 48 mammary tissue 48 MYH9 48 promoter hypermethylation