Related by context. All words. (Click for frequent words.) 75 mitochondrial DNA 67 mtDNA 64 mitochondrial DNA mtDNA 64 maternal lineage 64 Y STR 62 maternally inherited 61 mitochondrial genome 60 paternal lineage 60 #S rRNA 59 Y chromosome 58 Y Chromosome 58 chromosomal anomalies 58 Arabidopsis genome 57 SRY gene 57 autosomal 57 paternally inherited 57 Y chromosomal 56 breast cancer genes BRCA1 56 microsatellite markers 56 paternal ancestry 56 BARD1 55 somatic mutations 55 IgA deficiency 55 methylation patterns 55 piRNAs 55 blastomeres 55 telomerase RNA 55 haplotype 55 Telomere length 55 haplogroups 55 VNTR 54 mitochondrial DNA sequence 54 paraffin embedded tissue 54 Transcriptome 54 genomic imprinting 54 deoxyribonucleic acid 54 MLL2 54 Chromosomal 54 MC1R 54 miRNA expression 54 mutant alleles 54 Haplogroup 54 Rh factor 54 non coding RNA 54 mitochondrial genomes 54 monozygotic twins 54 TP# gene 54 Neanderthal fossils 54 pseudogenes 54 mtDNA sequences 54 isotopic analysis 54 metazoan 54 epigenetic changes 54 abnormal prions 54 maternal lineages 54 proband 54 alternatively spliced 54 DNA 54 epigenetic modification 54 PTEN gene 54 phylogenetically 53 #S rRNA gene 53 chordate 53 MSH2 53 phylogenetic analysis 53 DNA methylation patterns 53 placental mammals 53 mutant allele 53 paternal lineages 53 NF1 gene 53 chromosomal DNA 53 gametophyte 53 Streptococcus agalactiae 53 Alu elements 53 mitochondrial gene 53 PALB2 53 Germline 53 Single Nucleotide Polymorphisms SNPs 53 Cytogenetic 53 abnormal chromosomes 53 mosaicism 53 TP# mutation 53 genes BRCA1 53 karyotype 53 HPRT gene 53 ALK mutations 53 X inactivation 53 genetic recombination 53 BRCA1 gene 53 FADS2 53 MTHFR gene 53 PCR amplified 53 TOMM# 53 germline cells 53 Mitochondrial 53 congenital CMV infection 53 plastid 53 methylated DNA 53 organism genome 53 genetic mutation 53 recessive trait 52 ribonucleic acid RNA 52 PKD1 52 mutated genes 52 mRNA transcripts 52 linkage disequilibrium 52 exome 52 ribosomal DNA 52 chromosomal disorders 52 mutation 52 Methylation 52 genetic lineages 52 tyrannosaurids 52 Y chromosomes 52 recessive mutations 52 nucleotide sequence 52 nucleotide sequences 52 missense mutations 52 multiprotein complex 52 epigenetic inheritance 52 jawed vertebrates 52 genetic mutations 52 noncoding 52 spontaneous mutations 52 proteomic analysis 52 DICER1 gene 52 allele frequencies 52 cytochrome b 52 p# mutations 52 Prevotella 52 epigenetically 52 causative genes 52 aneuploidy 52 aneuploidies 52 de novo mutations 52 maize genome 52 segmental duplications 52 ramidus 52 parkin gene 52 positional cloning 52 clades 52 Genetic testing 52 R#W [002] 51 CHD7 51 FMR1 gene 51 X Chromosome 51 MECP2 gene 51 X chromosome 51 amino acid sequences 51 germline mutations 51 Cora Crippen 51 5 hydroxymethylcytosine 51 BRIP1 51 orthologs 51 5 methylcytosine 51 protein fragment 51 Heterodontosaurus 51 virulence genes 51 X chromosome inactivation 51 sCJD 51 DNA rearrangements 51 Deoxyribonucleic acid DNA 51 HAR1 51 aneuploid 51 cnidarians 51 Denisovan 51 genetic markers 51 rRNA 51 microdeletion 51 polydactylism 51 medulloblastomas 51 ZNF# 51 cell nuclei 51 genomewide 51 mtDNA sequence 51 Sanger sequencing 51 microdeletions 51 Comparative genomics 51 polyploid 51 PrPSc 51 bilaterians 51 MAOA gene 51 retrotransposon 51 gene expression patterns 51 5 hmC 51 methylation markers 51 microRNAs miRNAs 51 epigenetic reprogramming 51 eukaryote 51 BRCA genes 51 endogenous retroviruses 51 telomere DNA 51 IKZF1 51 APOE gene 51 chimp genomes 51 chromosomal aberrations 51 evolutionarily conserved 51 D. melanogaster 51 genetic fingerprint 51 prokaryote 51 chromosomally normal 51 CYP#E# gene 51 mutated BRCA1 51 inherited maternally 51 homozygosity 51 totipotent 51 chromosomally 51 animal phyla 51 genetic 51 #S ribosomal RNA 51 nucleotide substitutions 51 gene amplification 51 mtDNA mutations 51 HFE gene 51 fruitfly Drosophila 51 BRCA2 50 isotope ratios 50 gene mutation 50 noncoding DNA 50 chromosomal 50 miRNA expression profiles 50 louse genome 50 sporadic ALS 50 cohesin 50 homodimers 50 MLH1 50 Mammalian 50 Chlamydomonas reinhardtii 50 RNA sequences 50 microchimerism 50 RFLP 50 HLA genes 50 haplotypes 50 BRCA2 gene mutations 50 girl Hagemen 50 Serology 50 deleterious mutation 50 monozygotic 50 multigene 50 chromosomal abnormalities 50 epigenetic marks 50 placental tissue 50 Neanderthal genes 50 DNA deoxyribonucleic acid 50 phenotypic expression 50 imprinted genes 50 GSTP1 50 PCR RFLP 50 maternal serum 50 prion gene 50 FGFR2 gene 50 CYP#D# gene 50 roundworm C. elegans 50 viral nucleic acids 50 mutations 50 microbiomes 50 epigenetic modifications 50 conserved sequences 50 Mendelian 50 quantitative RT PCR 50 dizygotic twins 50 BRCA2 gene 50 human leukocyte antigen 50 CNVs 50 T. gondii 50 cDNA libraries 50 clefting 50 p# mutation 50 chromosome #q#.# [001] 50 chromosomal alterations 50 S. cerevisiae 50 chloroplast genome 50 Li Fraumeni syndrome 50 SLC#A# gene [001] 50 Viral RNA 50 cDNA microarray 50 radial glia 50 S. pombe 50 Phenotype 50 Genetic variation 50 extracted mitochondrial DNA 50 female gametophyte 50 chromosome #q# [002] 50 sequenced genomes 50 ornithischians 50 primitive meteorites 50 aY chromosome 50 #q#.# [001] 50 body louse genome 50 ribosomal RNA 50 gene expression profiles 50 Radiocarbon 50 vertebrate embryos 50 PTPN# 50 #p#.# [001] 50 autosomes 50 Simian Immunodeficiency Virus 50 Single Nucleotide Polymorphisms 50 genetic defects 50 yeast genome 50 BAC clones 50 NR#A# gene 49 dbSNP 49 metazoans 49 diploid 49 LRRK2 gene 49 hypermethylated 49 chromosomal imbalance 49 chromatin structure 49 lysine residues 49 #p# [001] 49 telomere lengths 49 gene sequences 49 chromosomal defect 49 X. laevis 49 archaeal 49 hominoids 49 MTHFR 49 homologous genes 49 Chlamydia pneumoniae 49 monotremes 49 Placental 49 ApoE gene 49 chromosome abnormality 49 prion infection 49 chromosomal regions 49 noncoding regions 49 CDH1 49 uPAR 49 M. pneumoniae 49 Amborella 49 defective mitochondria 49 RNA Seq 49 Western blotting 49 autosomal recessive 49 microRNA molecules 49 SOX3 gene 49 Microarrays 49 genetically homogeneous 49 isotope composition 49 methylation 49 regulates gene expression 49 biopsied tissue 49 inherited mutations 49 MC1R gene 49 somatic mutation 49 penetrance 49 CCR5 delta# 49 epigenetic markers 49 aneuploid cells 49 GPC5 49 HLA G 49 chromosomal rearrangement 49 Klotho gene 49 mammary cells 49 lineages 49 unmethylated 49 atypical hyperplasia 49 heritable 49 mitochondrial genome sequence 49 suppressor gene 49 major histocompatibility complex 49 M. genitalium 49 mutated gene 49 genetic ancestry 49 formalin fixed 49 tissue biopsies 49 monogenic 49 Neandertal 49 chromosome rearrangements 49 immunochemical 49 mitochondrial genes 49 disulfide bond 49 homologies 49 alleles 49 phylogenetic analyzes 49 Analysis Backlog Elimination 49 inhibin B 49 haploid 49 theropod 49 genetic syndromes 49 haplogroup 49 Bacteroides 49 holoprosencephaly 49 SIR2 49 Haplotype 49 anterior pituitary 49 Amniotic fluid 49 bioengineered mice 49 Alleles 49 Eukaryotic 49 H2AX 49 collagen VII 49 urease 49 messenger RNAs mRNAs 49 multi celled organisms 49 astrocyte cells 49 progranulin gene 49 Activating mutations 49 chromosome aberrations 49 trophoblasts 49 ultra rapid metabolizer 49 promoter hypermethylation 49 Serologic 49 budding yeast 49 histone modifications 49 SGK1 49 endogenous retrovirus 49 thylacine DNA 49 sarcosine 49 CDKN2A 49 Alu RNA 49 Chromosome 49 choroid plexus 49 microRNA expression 49 KRAS BRAF 49 KRAS oncogene 49 sequence homology 49 heritable traits 49 flavivirus 49 embryonal 49 outbred 49 androgen receptor gene 49 Wnt protein 49 Infectivity 49 hereditary hemochromatosis 49 IGF2 49 Neandertal DNA 49 PRNP 49 HSPCs 49 monophyletic 49 iPSC lines 49 KRAS mutation 49 APOE4 49 Embryos 49 nucleosome positioning 49 sensu lato 49 GBM tumors 49 centromeric 49 FOXP2 49 nucleases 49 viral genomes 49 pathogenic mutations 49 Phosphatase 49 Oxidative Stress 49 primate genomes 49 Paranthropus 49 TCF#L# gene 49 haem 48 eukaryotic organisms 48 A. thaliana 48 ultrastructure 48 DRD2 gene 48 genomic sequence 48 bisulfite sequencing 48 Pax6 48 differential gene expression 48 human leukocyte antigens 48 T. vaginalis 48 mammalian genome 48 #BP# 48 transcriptomes 48 genome rearrangements 48 splice junctions 48 genetically identical 48 Phenotypic 48 chromosome abnormalities 48 Rickettsia 48 genetic sequences 48 intergenic regions 48 cybrid 48 phenotypic characteristics 48 ependymomas 48 transcriptional machinery 48 nematode worm 48 heterochromatin 48 globin 48 astatine 48 HMGA2 48 Rb gene 48 OCA2 gene 48 Antigens 48 myostatin gene 48 UGT#B# 48 chromatin proteins 48 mitochondrial DNA mutations 48 Orrorin tugenensis 48 deoxyribonucleic acid DNA 48 Paranthropus robustus 48 Proteobacteria 48 abnormal hemoglobin 48 protein p# 48 Phylogenetic analysis 48 colorectal neoplasia 48 karyotypes 48 HMGA2 gene 48 cell lysate 48 Caenorhabditis elegans 48 quantitative reverse transcriptase 48 Homo neanderthalensis 48 germline 48 HLA molecules 48 SMN2 gene 48 HNPCC 48 B. henselae 48 ribosomal RNA rRNA 48 VHL gene 48 quantitative trait loci 48 recessive inheritance 48 Genetic 48 subfamilies 48 MicroRNA 48 single celled yeast 48 proto oncogene 48 DEAR1 48 genes 48 morphological traits 48 RNA splicing 48 Linheraptor 48 miRNA genes 48 somatic cells 48 receptor molecule 48 RT qPCR 48 KCNQ1 48 SORL1 48 cybrids 48 Repenomamus robustus 48 chromatid 48 gene mutations 48 #S rDNA 48 modifier genes 48 breast cancer gene mutation 48 telomere maintenance 48 IDH1 48 BRAC2 48 Polymerase Chain Reaction PCR 48 chromosomal anomaly 48 Denisova Cave 48 Igf2 48 Serological 48 C1q 48 nondemented 48 euchromatin 48 neuroblastomas 48 epigenome 48 unicellular 48 faulty BRCA1 gene 48 promoter methylation 48 oviraptors 48 ncRNAs 48 heterozygosity 48 fungal genomes 48 maternally derived 48 Immune Responses 48 mitochondrial 48 CETP VV 48 pseudogene 48 ubiquitylation 48 thrifty gene 48 centromeres 48 tumor biopsies 48 gut microbes 48 chromosomal mutations 48 chromatin immunoprecipitation ChIP 48 intronic 48 methyltransferase 48 mucins 48 hemoglobins 48 HMPV 48 ORMDL3 48 Tr DNA 48 cardiac channelopathies 48 DNA Methylation 48 rDNA 48 genetic abnormalities 48 Hox gene 48 HLAs 48 seminiferous tubules 48 Fc gamma receptor 48 LIS1 48 histocompatibility 48 IRAK1 48 Massospondylus 48 nucleotide substitution 48 macaque genome 48 CTCF 48 bases adenine 48 CRISPR Cas 48 MYH9 gene 48 chorionic villi 48 transcriptional activation 48 Chromosomes 48 Yamanaka recipe 48 centrosomes 48 Hsp# [001] 48 amino acid sequence 48 Neanderthal genome sequence 48 Indohyus 48 HLA B# 48 mRNA molecules 48 FDG PET scans 48 klotho 48 CRISPR 48 GenBank accession 48 breast carcinomas 48 primitive organisms 48 microbiota 48 mutated K ras 48 centrioles 48 differentially expressed genes 48 TMPRSS2 ERG fusion 48 epigenetic regulation 48 chromosome translocations 48 chloroplast DNA 48 #q#.# deletion syndrome 48 PON1 48 primate lineage 48 genetic abnormality 48 CTVT 48 gene BRCA2 48 CALHM1 48 chromosomally abnormal 48 herbivorous dinosaurs 48 coding exons 48 genetically 48 Leptospira 48 Phosphorylation 48 BRCA2 mutations 47 chromosomal instability 47 mitochondrial metabolism 47 Genetic Variation 47 Pollen grains 47 DNA Fingerprinting 47 dopamine transporter gene 47 laforin 47 Genotypic 47 MECP2 47 lymphoblastoid cell lines 47 telomeres shorten 47 microcephalin 47 recessive genes 47 coprolites 47 noncoding RNAs 47 Leukemias 47 RUNX3 47 Lynn Jorde 47 gene p# 47 ploidy 47 evolutionary lineage 47 Biopsies 47 luminal cells 47 Siberian mammoths 47 SLC#A# [001] 47 serum samples 47 chromosome #q#.# [002] 47 CYP#A# gene 47 JAK2 mutation 47 methyltransferases 47 mammalian genomes 47 heterozygous 47 Oncogenic 47 Evidence Clears 47 micro RNA 47 genes BRCA 47 RQ PCR 47 Hepatocyte 47 receptor gene 47 TRF1 47 serologically 47 spontaneous mutation 47 genetic fingerprinting 47 genetic makeups 47 Mycoplasma genitalium 47 mitochondrial proteins 47 NPM1 gene 47 Toxoplasmosis 47 proteomes 47 Ninad Place Mumbai 47 LRP5 47 genetic rearrangements 47 biochemical assays 47 nonbiological 47 Cytotoxicity 47 chromosome #q# [001] 47 KIAA# 47 mitochondrial DNA lineages 47 subfamily 47 HbF 47 HLA DQ 47 oxygen isotope ratios 47 BRCA1 47 FMR1 47 eukaryotic cells 47 diploid genome 47 sexually reproducing 47 congenital disorders 47 bacterium E. coli 47 malaria parasite genome 47 endosymbiosis 47 embryoid bodies 47 comparative genomic hybridization CGH 47 palladin 47 phenotypic variation 47 mutated BRCA 47 transcriptional repressor 47 HLA gene 47 micro RNAs 47 medullary bone 47 Neuregulin 1 47 H. habilis 47 Trypanosoma brucei 47 missense mutation 47 paralogs 47 chromosomal deletions 47 familial ALS 47 orangutan genome 47 bdelloid rotifers 47 TGFBR1 * 6A 47 gametocytes 47 chimpanzee genomes 47 Kufs disease 47 PCR amplification 47 HLA DRB1 47 telomere length 47 Trichoplax 47 Apobec3 47 KLF4 47 Asilisaurus 47 synuclein 47 #S rRNA genes 47 genomic alterations 47 BRCA mutation 47 apoE 47 mutant genes 47 vesicular stomatitis virus 47 hemagglutinin gene 47 Epstein Barr virus EBV 47 Situ Hybridization 47 extinct mammoths 47 chromosome #q 47 IRS1 47 Deoxyribonucleic acid 47 prokaryotic 47 sulfur isotopes 47 apoE4 47 progenitor stem cells 47 Dicer enzyme 47 genetic aberrations 47 biochemical signaling pathway 47 histone demethylase 47 exons 47 deacetylation 47 microglial 47 fission yeast 47 hyper IgE syndrome 47 CCL#L# 47 intestinal biopsy 47 AFLP 47 cDNAs 47 induced pluripotent cells 47 Mammalian Cells 47 causal variants 47 SHANK3 47 C#Y 47 primitive vertebrates 47 Microscopic examination 47 Radiocarbon dating 47 DNA methylation 47 buccal swabs 47 Deoxyribonucleic Acid DNA 47 MEF2A 47 Meckel Gruber 47 Inactivation 47 Human Leukocyte Antigen 47 DGGE 47 genetic trait 47 FFPE tissue samples 47 Klinefelter syndrome 47 PFGE 47 morphologic 47 coding genes 47 primordial germ cells 47 ovule 47 genetic variant 47 HLA typing 47 testicular germ cell 47 CFTR gene 47 Jhdm2a 47 naturally occurring histatin protein 47 isotopic 47 #q# deletion 47 Circulating Tumor Cells 47 Dikika 47 KCNE2 47 trypanosome 47 cerevisiae 47 multigenic 47 Placentas 47 immunohistochemical staining 47 Dalradian Resources Inc. 47 embryonic germ 47 genetic alteration 47 Toxoplasma gondii 47 BRCA1 mutations 47 highly heritable 47 mitochondrial DNA sequences 47 breast epithelial cells 47 Neanderthal DNA 47 sequenced genome 47 STAT4 47 homologs 47 morphogen 47 magnetic resonance NMR spectroscopy 47 macromolecule 47 Cytoplasmic 47 epigenomes 47 inbred strains 47 Protein Interactions 47 #q# [001] 47 epistasis 47 ncRNA 47 lipoprotein 47 neural crest 47 CNTNAP2 47 cynomolgus macaques 47 M. leprae 47 transcriptome profiling 47 genetic makeup 47 chromosomes 47 PHLPP 47 protein encoded 47 Hypophosphatasia 47 theropods 47 histone modification 47 follicle stimulating hormone FSH 47 B. cereus 47 lincRNA 47 Nucleic acid 47 Estrogen Receptor 47 PTEN mutations 47 Argonaute 47 beta globin 47 aberrant methylation 47 ptau 47 Sox9 47 evolutionary relatedness 47 S. sanguinis 47 Scientists Decode 47 orthologous 47 CHEK2 47 lymphatic tissue 47 chaperone proteins 47 FUS protein 47 lactase gene 47 ectoderm 47 ALK gene 47 embryo biopsy 47 Coelophysis 47 Treponema pallidum 47 Phylogenetic 47 genome decoded 47 genotoxic stress 47 RT PCR assay 47 geoneutrinos 47 fetal microchimerism 47 ChIP Seq 47 gDNA 47 breast cancer subtypes 47 Polymorphisms 47 breast lobules 47 severe congenital neutropenia 47 thymine T 47 amphioxus 47 placental mammal 47 vasopressin receptors 47 GSTT1 47 DNA sequences 47 RNA molecule 47 TSC1 47 Archaea 47 immunohistochemical 47 vimentin 46 β amyloid 46 distantly related species 46 neuroblastoma tumors 46 Mycobacterium leprae 46 gene rearrangements 46 Bos taurus 46 Homo species 46 viral genome 46 Progenitor Cells 46 genes CYP#C# 46 genomic rearrangements 46 A. ramidus 46 capillary sequencing 46 sexually dimorphic 46 recessive mutation 46 urinary calculi 46 chondritic meteorites 46 suborder 46 Leydig cells 46 mammographic density 46 Histone 46 C EBP alpha 46 admixed 46 frameshift mutation 46 genes predisposing 46 defective gene 46 phthalate syndrome 46 Chromosome Aneuploidy Screening 46 semen saliva 46 spore formation 46 mammalian embryo 46 Anomalocaris 46 MCADD 46 synthesizing proteins 46 Xenopus 46 DNA profiling 46 Hadar Ethiopia 46 neural crest stem cells 46 Paranthropus boisei 46 FTLD 46 simian virus 46 FFPE samples 46 abnormal methylation 46 infectious prions 46 sister chromatid 46 magnetite crystals 46 neural tube defect 46 morphologically 46 MCAD deficiency 46 Notch signaling 46 HCMV 46 prion disease 46 differentially methylated 46 gene predisposing 46 miRNA molecules 46 HLA markers 46 reassortants 46 HPV genotypes 46 granule cells 46 beta1 integrin 46 selfing 46 exonuclease 46 genomic sequences 46 Tumor Suppressor Gene 46 CSHL scientists 46 centrosome 46 Gene Mutation 46 Mendelian disorders 46 Hair follicle 46 murine leukemia virus 46 NFKBIA 46 anti microbial peptides 46 FGFR2 46 causative mutation 46 MnSOD 46 non coding RNAs 46 MLL gene 46 accelerator mass spectrometry 46 phenotypically 46 dermal papilla cells 46 CDK4 46 estrogen metabolites 46 heritability 46 allelic variants 46 Homozygous 46 lincRNAs 46 TMEM#B 46 buffy coat 46 WAGR syndrome 46 PGCs 46 radiocarbon tests 46 ADAMTS# 46 reaction PCR 46 GNAQ 46 chloroplasts 46 S. enterica 46 mutational analysis 46 Karlseder 46 developmental abnormalities 46 enterotypes 46 sea urchin genome 46 Falcarius 46 hereditary nonpolyposis colorectal cancer 46 SMN1 46 phthalate metabolites 46 Quantitation 46 HHV 6 46 BCL#A 46 Culturing 46 HIV tropism 46 familial aggregation 46 spermatogonia 46 fetal fibronectin 46 parthenogenetic 46 Inkayacu 46 hominoid 46 epigenetic silencing