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(Click for frequent words.) 71 chromosome 69 X chromosomes 67 mutated gene 66 gene 66 chromosomal 65 Y chromosome 65 mutation 65 genes 64 FMR1 gene 64 chromosomes 63 alleles 63 gene mutation 63 mutations 63 mutant gene 61 allele 61 genetic mutation 61 X inactivation 60 imprinted genes 60 PALB2 60 Klinefelter syndrome 60 genetic variant 60 aY chromosome 60 SRY gene 60 mtDNA 59 defective gene 59 Chromosome 59 premutation 59 mutant genes 59 tumor suppressor genes 59 BRCA1 gene 59 tumor suppressor gene 59 polymorphism 58 mosaicism 58 genetic mutations 58 #p#.# [001] 58 gene variant 58 heritable 58 MECP2 gene 58 FMR1 58 genetic defect 58 IGF2 58 p# gene 58 breast cancer genes BRCA1 57 CNVs 57 heterozygous 57 gene mutations 57 centrosomes 57 myostatin gene 57 autosomal 57 centrosome 57 mutated genes 57 maternally inherited 57 PTEN gene 57 recessive gene 57 mammalian genome 57 COMT gene 57 germline 56 recessive trait 56 segmental duplications 56 phenotype 56 heterochromatin 56 de novo mutations 56 exons 56 homozygous 56 haplotype 56 BRCA2 gene 56 VHL gene 56 genetic 56 spontaneous mutations 56 autosomes 56 nucleotide 55 methylation 55 Y chromosomes 55 microdeletion 55 Fragile X gene 55 CFTR gene 55 FXTAS 55 CYP#E# gene 55 PTPN# 55 testis 55 APOE4 55 genetic abnormality 55 BRIP1 55 piRNAs 55 D. melanogaster 55 genome 55 #q# [001] 55 chromosome #q# [002] 55 MC1R 55 MLL gene 55 mRNAs 55 centromeres 55 mutant allele 55 intron 55 NF1 gene 55 genetic variants 55 PTCHD1 gene 54 introns 54 aneuploidy 54 Alu elements 54 MTHFR 54 gene variation 54 genomic instability 54 EZH2 54 chromosomal regions 54 progerin 54 genetic variation 54 paternally inherited 54 mitochondrial genome 54 DISC1 54 chromosome #q#.# [001] 54 SMN2 gene 54 EGFR gene 54 MECP2 54 MeCP2 gene 54 CHD7 54 inherited mutations 54 gene variants 54 BARD1 54 #q#.# [002] 54 miRNAs 54 homozygosity 54 FGFR2 54 Hox gene 54 protein p# 54 nucleotide sequence 54 microcephalin 54 BRCA2 54 mtDNA mutations 54 HMGA2 54 organism genome 54 noncoding 54 recessive genes 54 protein encoded 54 karyotype 54 genomic imprinting 53 gene expression 53 gene encoding 53 SMN2 53 germline mutations 53 apoE4 53 Rb gene 53 telomeric 53 TAp# 53 homologs 53 chromosome #q 53 chromosomal instability 53 chromosomal rearrangements 53 DNA methylation 53 p# protein 53 genetically 53 sporadic ALS 53 epigenetic 53 chromosome abnormality 53 LIS1 53 DNA sequences 53 agouti gene 53 polymorphisms 53 HGPS 53 autosomal dominant 53 MSH2 53 SNPs 53 autosomal recessive 53 susceptibility gene 53 chromosomal defect 53 IRAK1 53 alternatively spliced 53 radial glia 53 centromere 53 gene p# 53 receptor gene 53 chromatid 53 chromosomal abnormality 53 BRCA1 53 genes encoding 53 monozygotic twins 53 dizygotic 53 genomes 53 cohesin 53 mitochondrial gene 53 mitochondria 53 major histocompatibility complex 52 RNA molecule 52 mutant alleles 52 p# mutations 52 G#S mutation 52 frameshift mutation 52 isoform 52 mitochondrial DNA mtDNA 52 androgen receptor gene 52 loci 52 epigenetically 52 androgen receptor 52 mice lacking 52 APOE gene 52 cyclin D1 52 TCF#L# gene 52 recessive mutation 52 spontaneous mutation 52 Arabidopsis genome 52 haplotypes 52 X chromosome inactivation 52 UGT#B# 52 epigenetic changes 52 germ cells 52 Sox9 52 mutant protein 52 Dpp 52 abnormal hemoglobin 52 HFE gene 52 genetic alteration 52 chromosome #q# [001] 52 mRNA 52 neuroligins 52 genetic trait 52 receptor molecule 52 RNA splicing 52 PrP 52 gene MECP2 52 unmethylated 52 CDH1 52 chromosomal abnormalities 52 Rad# 52 #p# [001] 52 CDKN2A 52 heterozygosity 52 gametophyte 52 KCNQ1 52 transcriptional repression 52 HLA genes 52 CNTNAP2 52 Apert syndrome 52 germline stem cells 52 genetic makeup 52 SRY 52 A. thaliana 52 huntingtin 52 presenilin 52 SGK1 52 meiosis 52 MLH1 51 apolipoprotein E gene 51 Mitochondrial DNA 51 viral genome 51 SLC#A# gene [001] 51 ERK2 51 CCL#L# 51 Klotho gene 51 rs# [003] 51 HLA molecules 51 SHANK3 51 RhoA 51 thymine 51 vasopressin receptors 51 chromosomal translocations 51 PON1 51 number variations CNVs 51 MHC molecules 51 haploid 51 chromosomal DNA 51 genetic defects 51 microdeletions 51 single nucleotide polymorphism 51 C#Y 51 mutational 51 R#W [002] 51 p# mutation 51 epigenetic modifications 51 PKD1 51 ncRNAs 51 SMN1 gene 51 WAGR syndrome 51 gene expression patterns 51 chromatin structure 51 FTO gene 51 IKZF1 51 5 hydroxymethylcytosine 51 mitochondrial 51 COMT 51 ovule 51 DRD2 gene 51 chromosomal deletions 51 transgene 51 MAOA gene 51 telomere 51 tyrosine phosphorylation 51 acetylation 51 alternative splicing 51 evolutionarily 51 RUNX3 51 zebrafish genome 51 ovules 51 NFKBIA 51 transcriptome 51 HMGA2 gene 51 mitochondrial mutations 51 DICER1 gene 51 genetic alterations 51 regulates gene expression 51 Cyclin D1 51 evolutionarily conserved 51 neural tube defect 51 OCA2 51 Prox1 51 primordial germ cells 51 NR#A# gene 51 primary visual cortex 51 Dicer 51 DEC2 51 DLX5 51 melanocyte 51 NF2 51 disulfide bond 51 #q# [002] 51 BRCA1 mutations 51 mitochondrial DNA 51 GTPase 51 germline mutation 51 yeast genome 51 embryogenesis 51 dizygotic twins 51 C EBP alpha 50 mutated BRCA1 50 Math1 50 tumor suppressor 50 codons 50 mutant mouse 50 holoprosencephaly 50 blastomeres 50 susceptibility genes 50 granule cells 50 homolog 50 alpha synuclein gene 50 autosomal dominant disorder 50 ApoE4 50 endostatin 50 CNTNAP2 gene 50 heterozygote 50 estrogen receptor alpha 50 micro RNAs 50 FMRP 50 LRRK2 gene 50 Cx# [001] 50 organelle 50 SMN1 50 centromeric 50 huntingtin gene 50 H2AX 50 ApoE gene 50 constitutively 50 MTHFR gene 50 GSTT1 50 #p#.# [002] 50 RNA transcripts 50 RNA molecules 50 exon 50 somatic mutations 50 MC1R gene 50 Meckel Gruber 50 HOTAIR 50 OCA2 gene 50 E cadherin 50 encodes protein 50 missense mutations 50 p# [001] 50 MLL2 50 Akt1 50 genetic variations 50 Akt 50 diploid 50 helicase 50 suppressor gene 50 Notch signaling 50 genes predisposing 50 proband 50 spermatogenesis 50 mitochondrial genes 50 micro RNA 50 S#K# 50 Vpu 50 metabolic enzymes 50 aneuploid 50 MYH9 gene 50 intronic 50 transmembrane protein 50 orthologs 50 codon 50 KLF# 50 SORL1 50 LDL receptor 50 miRNA genes 50 telomere length 50 epigenetic modification 50 hyperactivation 50 helices 50 chordate 50 CGG repeats 50 antisense strand 50 primary ovarian insufficiency 50 LKB1 50 dentate gyrus 50 autism susceptibility genes 50 allelic 50 CALHM1 50 CAG repeats 50 progranulin 50 RPE# 50 NR#A# 50 genotype 50 Myc 50 chromosome #p# [001] 50 TEP1 50 transcriptional repressor 50 MHC genes 50 genital tract 50 IKKa 50 gamma globin gene 50 Golgi apparatus 50 epididymis 50 Beckwith Wiedemann syndrome 50 retrotransposons 50 microRNA molecules 50 epigenetic silencing 50 hypermethylation 50 genetic variability 50 globin 50 aromatase 50 heterozygotes 50 ectopic expression 50 germline cells 50 homologous chromosomes 50 MeCP2 50 progranulin gene 50 tumor suppressor protein 50 CagA 50 Chromosomes 50 H#K# methylation 50 TSC1 50 Spina bifida 50 molecular pathway 50 chromosome abnormalities 50 sex hormone estrogen 50 MnSOD 50 antisense RNA 50 overexpression 49 reproductive hormones 49 receptor protein 49 RNA binding 49 tetramers 49 mRNA transcripts 49 Li Fraumeni syndrome 49 BRCA mutation 49 Pax6 49 cadherin 49 KIAA# 49 VNTR 49 CYP#D# gene 49 recessive mutations 49 XY chromosome 49 chromosome deletion 49 ZNF# 49 ApoE 49 FASPS 49 Foxp3 49 Y chromosomal 49 DICER1 49 chromosomal aberrations 49 transposable elements 49 inactive X chromosome 49 mitochondrial dysfunction 49 BRCA gene mutation 49 FADS2 49 Cdk5 49 RPE# gene 49 FANCD2 49 Pten 49 Neuregulin 1 49 trisomy 49 untranslated regions 49 glycoproteins 49 Wolbachia 49 H#K# [002] 49 APOE4 gene 49 ectopic 49 fru 49 chromosome segregation 49 ubiquitination 49 pseudogenes 49 GATA4 49 telomerase RNA 49 genotoxic stress 49 STAT4 49 neural crest cells 49 guanine G 49 somatic mutation 49 chromatin 49 GAPDH 49 RNAs 49 polycystic ovary syndrome PCOS 49 Wnt signaling 49 ribosomal RNA 49 dystrophin gene 49 STAT3 49 ADAM# 49 intergenic 49 human genome 49 dopamine receptor 49 ubiquitylation 49 retrotransposon 49 dopamine D4 receptor 49 chromosomally 49 IGF1 49 5 methylcytosine 49 IDH1 49 GNAQ 49 TRF1 49 Pol IV 49 HSCs 49 leptin receptor 49 BDNF gene 49 causative genes 49 autosomal recessive disease 49 Leydig cells 49 neuroblasts 49 gene locus 49 #S rRNA 49 genetic abnormalities 49 signaling pathway 49 gut microbes 49 estrogen receptor 49 amino acid substitution 49 cyclin 49 phenotypic variation 49 TGF ß 49 microRNA miR 49 Pin1 49 palmitoylation 49 non coding RNAs 49 telomere DNA 49 gp# [002] 49 guanine 49 Peutz Jeghers syndrome 49 KCNE2 49 nonsense mutations 49 vasopressin 49 parkin gene 49 C. neoformans 49 SLC#A# [001] 49 methylated 49 causative gene 49 pRb 49 histone protein 49 TMEM#B 49 BMAL1 49 RCAN1 49 miR 49 melanocyte stem cells 49 DNA methylation patterns 49 5 HTT gene 49 genetic disorder 49 NHEJ 49 beta subunit 49 colocalization 49 endogenous retroviruses 49 Sir2 49 trinucleotide 49 proteins 49 chromosomal alterations 49 DSBs 49 primate evolution 48 adrenal cortex 48 microglial 48 APOE e4 48 GPC5 48 DNMT1 48 tau protein 48 transcription factors 48 heterochromatic 48 chromosomal rearrangement 48 oocyte 48 homologous recombination 48 globin genes 48 LRAT 48 EBNA1 48 epigenetic alterations 48 Skp2 48 genetic loci 48 FGF# 48 messenger RNA 48 maternally transmitted 48 PDGFRA 48 synapsis 48 #BP# 48 TFIIH 48 Notch pathway 48 apoE 48 vitamin D receptor 48 SLC#A# [002] 48 MIF protein 48 serine 48 NOTCH1 48 ovaries 48 familial ALS 48 Wwox 48 #q#.# [001] 48 CHEK2 48 transcription factor 48 nucleosome 48 CFH gene 48 MDM2 48 neural crest 48 neurones 48 catenin 48 Aβ 48 poorer prognosis 48 parathyroid glands 48 G allele 48 corpus luteum 48 molecular pathways 48 ribosomal DNA 48 enzymatic activity 48 karyotypes 48 polymerase 48 neurexin 48 biochemical pathway 48 BMP signaling 48 trypanosome 48 c Myc 48 Drosophila 48 HPRT gene 48 transcriptionally active 48 leptin receptors 48 LMNA 48 fibrillin 1 48 platypus genome 48 PrPSc 48 TCF#L# 48 haplogroup 48 podocytes 48 SIR2 gene 48 neuroD2 48 dopamine transporter gene 48 basal forebrain 48 proto oncogene 48 monozygotic 48 arrestin 48 klotho 48 dynamin 48 GPR# [002] 48 sister chromatid 48 gene encodes protein 48 HNPCC 48 Hox genes 48 virulence genes 48 recombination 48 endosymbiosis 48 myelination 48 Fragile X syndrome 48 LMNA gene 48 non coding RNA 48 SHANK3 gene 48 mammary cells 48 premature ovarian 48 Six3 48 CIB1 48 phenotypes 48 fetal hemoglobin 48 seminiferous tubules 48 chromosomal disorder 48 polyploidy 48 missense mutation 48 KLF4 48 euchromatin 48 beta globin 48 DNA polymerases 48 catalytic subunit 48 Th# cells 48 HOX genes 48 WNK1 48 maternal antibodies 48 Htt 48 TRIM5 48 C1q 48 hypospadias 48 dystrophin protein 48 genetically identical 48 aneuploidies 48 RNA polymerase II 48 hypothalamus 48 HLA B# 48 dystrophin 48 hTERT 48 valine 48 OPRM1 gene 48 genetic predisposition 48 apolipoprotein E 48 cytochrome b 48 genomic rearrangements 48 HER2 gene 48 causal variants 48 mammary cancers 48 NPY gene 48 Genetic variation 48 palladin 48 thrombospondin 48 SCN5A 48 extracellular matrix protein 48 G6PD 48 FOXP2 48 TP# mutation 48 IL#R 48 collagen VI 48 ventral 48 GABAergic neurons 48 p# MAPK 48 endonuclease 48 endogenous retrovirus 48 superior colliculus 48 HLA gene variant 48 mitochondrial genomes 48 Single Nucleotide Polymorphisms SNPs 48 messenger RNAs mRNAs 48 genomic deletions 48 severe congenital neutropenia 48 penetrance 48 rs# [002] 48 alanine 48 ovary 48 rDNA 48 XY chromosomes 48 GRK2 48 AMPA receptors 48 mutated protein 48 E1A 48 SOX9 48 autoantibodies 48 genetic markers 48 thyroid hormones 48 polydactylism 48 Sp1 48 olfactory receptor 48 situs inversus 48 microRNAs 48 Jhdm2a 48 APOC3 47 Igf2 47 deleterious mutations 47 Nrf2 47 phenotypic expression 47 postsynaptic 47 collagen VII 47 outcrossing 47 alpha catenin 47 morphogen 47 Immunohistochemical analysis 47 prairie vole 47 BRAF V#E 47 Dicer enzyme 47 5 HTTLPR 47 splice junctions 47 Klinefelter Syndrome 47 gene amplification 47 medulloblastomas 47 mammary stem cells 47 phosphorylate 47 dendritic spines 47 human leukocyte antigen 47 Wnt pathway 47 nucleotide sequences 47 BMP4 47 CD8 + 47 protein coding 47 transactivation 47 BRCA mutations 47 C. elegans 47 aberrant methylation 47 tumor suppressing 47 Th2 47 PKM2 47 beta globin gene 47 Sonic Hedgehog 47 transposon 47 somatic stem cells 47 NF1 47 chromosome #p#.# 47 adiponectin 47 recessive 47 viral genomes 47 neuron 47 JAK2 mutation 47 SIRT3 47 mutant worms 47 CXCL# 47 Hutchinson Gilford progeria 47 TYMS 47 nestin 47 monogenic 47 transmembrane 47 allelic variants 47 CCR5 delta# 47 hypermethylated 47 Her2 gene 47 cortex 47 histone 47 translocations 47 CTCF 47 clonally 47 amino acid residues 47 telomeres 47 indel 47 SIRT6 47 follistatin 47 oxidative lesions 47 FOXP2 gene 47 beta catenin 47 ultraconserved elements 47 GSTM1 gene 47 RNA sequences 47 budding yeast 47 quantitative trait loci 47 histone modification 47 filaggrin 47 Ago2 47 LPA gene 47 herpesviruses 47 microRNAs miRNAs 47 uPAR 47 MDMX 47 INF2 47 GSK 3ß 47 Src 47 signaling molecule 47 kinetochores 47 constitutively active 47 huntingtin protein 47 lipin 47 hippocampal neurons 47 phytochrome 47 TACI mutations 47 ribosomal proteins 47 methylation patterns 47 activin 47 laforin 47 GAB2 47 abnormal chromosomes 47 fruitflies 47 HLA B 47 RNA strand 47 nucleolar dominance 47 ubiquitin ligase 47 neural circuitry 47 subunit 47 mesenchyme 47 mesoderm 47 epigenetic marks 47 cofilin 47 HER2 neu 47 E4 variant 47 HbF 47 kilobase 47 amino acid 47 CFTR 47 E#F# 47 SIRT1 47 Smad7 47 eukaryote 47 genetic susceptibility 47 enzyme 47 astrocyte 47 Broca area 47 BRCA2 mutation 47 neural stem cells 47 cysteines 47 transposons 47 HAR1 47 messenger RNA mRNA 47 male reproductive organs 47 klotho gene 47 Rap1 47 KRAS oncogene 47 DISC1 gene 47 NKX2 47 JAK STAT 47 polyadenylation 47 SIR2 47 epigenome 47 glycosylation 47 temporoparietal junction 47 protein fragment 47 synapse formation 47 prolactin 47 promoter methylation 47 retinal ganglion cells 47 isoforms 47 myelomeningocele 47 hereditary hemochromatosis 47 gene transcription 47 ALDH2 47 beta defensin 47 lymphocyte 47 corpus callosum 47 prion gene 47 cyclins 47 mammalian genomes 47 locus coeruleus 47 lamin 47 conformational 47 ciliated 47 APOE ε4 47 APOL1 47 Hh 47 transcriptional activation 47 IRF6 47 phenotypically 47 transgenic mice 47 chromosome rearrangements 47 chloroplasts 47 X. laevis 47 protein 47 thymus 47 telomeric DNA 47 cryptochrome 47 tumor suppressor p# 47 epigenetic regulation 47 E3 ubiquitin ligase 47 hemoglobin molecule 47 MC4R gene 47 mRNA expression 47 TCF4 47 IRF6 gene 47 BRCA gene 47 BRCA1 mutation 47 Cdc# 47 ribosomal protein 47 differentially methylated 47 STAT1 47 GSTP1 47 endometrial cells 47 ERK1 47 #p# [003] 47 dimer 47 knockout mice 47 CHEK2 gene 47 androgens 47 eukaryotic cells 47 genetic recombination 47 asymptomatically 47 male hormone androgen 46 selfing 46 kilobases 46 SMN protein 46 genotypes 46 forebrain 46 familial adenomatous polyposis 46 ApoE4 gene 46 erythrocytes 46 HCMV 46 Wnt 46 ABCB1 46 tRNA 46 cytoplasmic 46 Bardet Biedl syndrome 46 calpastatin 46 overexpress 46 meiotic recombination 46 aldehyde dehydrogenase 46 nematode worm 46 adhesion molecule 46 entorhinal cortex 46 parietal lobes 46 Nf1 46 hemochromatosis 46 Transcription factors 46 phenotypic 46 placental function 46 defective mitochondria 46 neural progenitor 46 c Myb 46 POMC neurons 46 UCP2 46 pattern baldness 46 GFP gene 46 plasminogen 46 ssDNA 46 Genes 46 TH# cells 46 caspase 46 genomic rearrangement 46 phylogenetically 46 neurodevelopmental disorder 46 WT1 46 mice genetically engineered 46 Sonic hedgehog 46 XPB 46 miRNA expression 46 epigenetic inheritance 46 membrane protein 46 homodimers 46 egg follicles