Related by context. All words. (Click for frequent words.) 74 Y chromosomes 65 X chromosome 63 mtDNA 62 mitochondrial DNA 61 aY chromosome 60 chromosomal 59 mutation 59 Mitochondrial DNA 58 genetic 56 SRY gene 56 chromosome 55 chromosomes 55 genetic variant 55 maternal lineage 55 gene 54 mutations 54 Haplogroup 54 genes 54 genetic mutations 54 autosomal 53 Y chromosomal 53 gene mutation 53 X chromosomes 53 alleles 52 paternal ancestry 52 DNA 52 paternal lineage 52 haplogroup 52 mosaicism 52 paternally inherited 51 genetically 51 mitochondrial genome 51 homo erectus 51 Neanderthal genes 51 BRCA1 gene 51 genetic variation 51 genetic mutation 51 homozygosity 51 introns 51 mutated gene 51 mutated genes 51 lineages 51 haplotype 50 mutant gene 50 Neanderthal DNA 50 Y Chromosome 50 genetic lineages 50 FMR1 gene 50 D. melanogaster 50 heterochromatin 49 placental mammals 49 Homo neanderthalensis 49 karyotype 49 autosomes 49 haplogroups 49 Mitochondrial Eve 49 X inactivation 49 germline 49 nucleotide sequence 49 primordial germ cells 49 Homo sapiens 49 Chromosome 49 Hox gene 49 BRCA2 gene 49 epigenetic marks 49 centromeres 49 human genome 49 segmental duplications 48 Y STR 48 organism genome 48 defective gene 48 genetic markers 48 prairie vole 48 chordate 48 methylation 48 allele 48 mitochondrial DNA mtDNA 48 breast cancer genes BRCA1 48 MHC genes 48 lineage 48 gene variant 48 imprinted genes 48 genome 48 genetic makeup 48 HLA genes 48 platypus genome 48 mutant allele 48 Neanderthal 48 genetic abnormality 48 genomes 47 maternally inherited 47 noncoding 47 BRCA mutations 47 XY chromosome 47 genetic abnormalities 47 testis 47 eukaryote 47 aneuploidy 47 spontaneous mutations 47 mitochondrial Eve 47 pseudogenes 47 mtDNA mutations 47 ancestor 47 piRNAs 47 recombination hotspots 47 primate lineage 47 mutational 47 microcephalin 47 heritable 47 mammalian genomes 47 prokaryote 47 polymorphism 47 chromosome abnormality 47 chromosomal disorders 47 Deoxyribonucleic acid DNA 47 Alu elements 47 sporadic ALS 46 CYP#E# gene 46 myostatin gene 46 genetic ancestry 46 major histocompatibility complex 46 BRCA mutation 46 genetic variations 46 DNA sequences 46 telomeric 46 chromosomal abnormalities 46 germ cells 46 genetic defect 46 mtDNA sequence 46 recessive trait 46 FMR1 46 primate genomes 46 Neanderthals 46 MC1R 46 mammalian genome 46 homologs 46 homozygous 46 common ancestor 46 BRCA1 46 CNVs 46 mitochondrial genomes 46 BRCA2 46 genetic recombination 46 genetic trait 46 genetic alteration 46 yeast genome 46 Klinefelter syndrome 46 genetic variants 46 lactose tolerance 46 paternal lineages 46 primate evolution 46 TCF#L# gene 46 MC1R gene 46 FOXP2 46 hunter gatherer societies 46 gene mutations 46 IKZF1 46 Neandertal 46 VNTR 45 centrosomes 45 chromosomally 45 TP# mutation 45 MTHFR gene 45 maternal lineages 45 recessive genes 45 gut microbes 45 BRCA2 mutation 45 A. thaliana 45 genetically homogeneous 45 meiotic recombination 45 phylogenetic analysis 45 S. cerevisiae 45 heterozygous 45 H. habilis 45 blastomeres 45 BRCA gene 45 chordates 45 XX chromosomes 45 genus Homo 45 nematode worm 45 breast cancer gene mutation 45 outbred 45 hominid ancestors 45 haplotypes 45 genetic diversity 45 de novo mutations 45 BRCA1 mutations 45 Homo Sapiens 45 #p# [001] 45 gene variation 45 APOE gene 45 Homo ergaster 45 APOE4 45 HAR1 45 gene variants 45 endogenous retroviruses 45 patrilineal 45 chromosomal rearrangements 45 heterozygosity 45 IGF2 45 Neandertals 45 #S rRNA 45 Mendelian 45 globular clusters 45 HMGA2 gene 45 genetic rearrangements 45 evolutionary lineage 45 premutation 45 FXTAS 45 Fragile X gene 45 Paranthropus 45 radial glia 45 LRRK2 gene 45 epigenetic inheritance 45 SORL1 45 microsatellite markers 44 proband 44 Trichoplax 44 epistasis 44 chromosome abnormalities 44 PALB2 44 ape ancestors 44 microdeletion 44 interbred 44 microcephalic 44 mitochondrial gene 44 geneticists 44 linkage disequilibrium 44 noncoding regions 44 chromosome #p# [001] 44 meadow vole 44 BARD1 44 mitochondrial DNA lineages 44 causative genes 44 transposable elements 44 SOX3 gene 44 Venter genome 44 phylogenetically 44 recessive mutations 44 MLL2 44 NF1 gene 44 genomic imprinting 44 genotype 44 thymine 44 mutated BRCA1 44 SNPs 44 alpha synuclein gene 44 XX chromosome 44 genetic traits 44 chromosomal anomalies 44 hominoids 44 Oxford Ancestors 44 germline cells 44 monozygotic twins 44 epigenetic changes 44 tumor suppressor gene 44 Australopithecus 44 p# gene 44 sperm 44 genomewide 44 mutant alleles 44 hominid species 44 bdelloids 44 recessive gene 44 Neanderthal fossils 44 multicellular organism 44 KLF# gene 44 polydactylism 44 FOXP2 gene 44 TP# gene 44 endosymbiosis 44 penetrance 44 androgen receptor gene 44 retrotransposon 44 eukaryotes 44 methylation patterns 44 germline mutations 44 recessive mutation 44 noncoding DNA 44 germline stem cells 44 ancient hominid 43 orthologs 43 Australopithecines 43 nucleotide substitutions 43 feathered dinosaurs 43 Genetic 43 monotremes 43 frameshift mutation 43 nucleotide 43 Wolbachia 43 MHC molecules 43 genomic instability 43 5 hydroxymethylcytosine 43 MLL gene 43 allelic 43 mutant genes 43 chromosome #q 43 phenotype 43 ApoE4 43 MSH2 43 G#S mutation 43 lipoprotein 43 Darwinius 43 #p#.# [001] 43 gametophyte 43 telomere 43 chromosomal instability 43 DNA methylation patterns 43 apolipoprotein E gene 43 #q# [001] 43 H. sapiens 43 protein coding 43 telomere DNA 43 Genetic testing 43 Homo genus 43 recessive traits 43 PTPN# 43 familial ALS 43 phenotypically 43 Lamarckian 43 exons 43 aneuploidies 43 species Homo sapiens 43 haploid 43 primate ancestors 43 Arabidopsis genome 43 genetic alterations 43 clonally 43 DNA rearrangements 43 spontaneous mutation 43 X chromosome inactivation 43 centromere 43 phenotypic variation 43 chimp genome 43 codons 43 fruitflies 43 zebrafish genome 43 ZNF# 43 CNTNAP2 43 #q# [002] 43 ancestral lineage 43 ultraconserved elements 43 PTEN gene 43 Homo sapiens evolved 43 BRCA 43 alternatively spliced 43 chromosome #q# [001] 43 p# mutations 43 progerin 43 recombination 43 habilis 43 ramidus 43 Gigantopithecus 43 p# mutation 43 CYP#D# gene 43 RNA molecule 43 Mendelian disorders 43 CAG repeats 43 Paranthropus robustus 43 tumor suppressor genes 43 hair follicle stem cells 43 chimpanzee genome 43 genetic predisposition 43 OPRM1 gene 43 genetically identical 43 TRF1 43 genes BRCA1 43 cohesin 43 monozygotic 43 microdeletions 43 thylacine DNA 43 H. floresiensis 42 granule cells 42 CGG repeats 42 MYH9 gene 42 monkeys apes 42 sea urchin genome 42 progenitors 42 ribosomal DNA 42 hominins 42 DNA methylation 42 Harpending 42 asexual organisms 42 diploid 42 angiosperms 42 primitive organisms 42 Pax6 42 Homo sapiens sapiens 42 messenger RNA molecules 42 Chromosomes 42 kilobase 42 lactase persistence 42 chromosomal aberrations 42 homo sapiens 42 DRD2 gene 42 jawed vertebrates 42 chimpanzee genomes 42 CpG islands 42 genetic variability 42 evolutionarily 42 evolutionarily conserved 42 RNA sequences 42 hunter gatherer populations 42 polyploidy 42 fungal genomes 42 ribosomal RNA 42 genetically inherited 42 indels 42 copulatory 42 XY chromosomes 42 ancestry 42 thalassemia trait 42 somatic stem cells 42 rDNA 42 dwarf galaxy 42 Rb gene 42 spermatozoa 42 histone code 42 Lynn Jorde 42 male prairie voles 42 genetically programmed 42 Rh factor 42 humans Homo sapiens 42 gene expression patterns 42 non coding RNA 42 BRCA2 gene mutations 42 placentals 42 neural crest 42 phylogeny 42 orthologous genes 42 epigenetic 42 evolutionary origins 42 theropod 42 microRNA expression 42 globin 42 MAOA gene 42 mammalian ancestor 42 maleness 42 Apobec3 42 rs# [002] 42 allelic variants 42 undifferentiated cells 42 australopithecines 42 sexual dimorphism 42 sapiens 42 epigenetically 42 Geneticists 42 bdelloid rotifers 42 ontogeny 42 laforin 42 rs# [003] 42 mitochondrial mutations 42 tyrannosaur 42 deoxyribonucleic acid 42 telomeric DNA 42 pluripotent cells 42 Darwinopterus 42 Ashkenazi Jews 42 subfamily 42 chromosomal abnormality 42 Denisovan 42 heredity 42 telomeres shorten 42 virulence genes 42 medulloblastomas 42 HNPCC 42 diploid genome 42 vasopressin receptors 42 Rad# 42 SLC#A# gene [001] 42 choanoflagellates 42 beta globin 42 COMT gene 42 CDH1 42 clades 42 antisense strand 42 APOE e4 42 Cohen Modal Haplotype 42 BRCA1 mutation 42 evolutionary 42 progenitor 42 assortative mating 42 androgen receptor 41 segmental duplication 41 unmethylated 41 Negroid 41 H. erectus 41 Klotho gene 41 vertebrate evolution 41 genomic 41 Archaeopteryx 41 LQTS 41 chromosomal deletions 41 maternal ancestor 41 meiosis 41 trypanosome 41 globular star 41 matrilineal 41 heterochromatic 41 dizygotic 41 PRNP 41 evolutionary lineages 41 PGCs 41 hereditary 41 genetic defects 41 homozygote 41 extinct mammals 41 Neuregulin 1 41 neural crest cells 41 dizygotic twins 41 chimp genomes 41 faulty BRCA1 gene 41 vertebrate embryos 41 PTCHD1 gene 41 PKD1 41 centromeric 41 deleterious mutations 41 miRNAs 41 flagellum 41 positional cloning 41 doublesex 41 SRY 41 allele frequencies 41 RNA transcripts 41 epigenome 41 guanine 41 sexually reproducing 41 colugos 41 Chromosomal 41 prion gene 41 mitochondrial genes 41 BRCA gene mutations 41 VHL gene 41 CETP VV 41 genetics 41 exon 41 Male pattern baldness 41 evolutionary psychologists 41 selfing 41 ribozyme 41 calpastatin 41 #q#.# [001] 41 translocations 41 STK# gene 41 dopamine transporter gene 41 FTO gene 41 cytosine methylation 41 chromatids 41 micro RNA 41 disulfide bond 41 MECP2 gene 41 genotyped 41 APOE4 gene 41 orangutan genome 41 hominid fossils 41 HPRT gene 41 phylogenies 41 bacterial symbiont 41 p# protein 41 ES cells 41 chimerism 41 O. tugenensis 41 unisexual 41 missense mutations 41 interbreeding 41 microchimerism 41 aneuploid 41 causative gene 41 SGK1 41 multicellular organisms 41 genetic determinism 41 KCNQ1 41 neuronal circuitry 41 diploid cells 41 single nucleotide polymorphism 41 euchromatin 41 susceptibility gene 41 gene locus 41 epigenetic modifications 41 LMNA gene 41 chromosome #q# [002] 41 facial attractiveness 41 indel 41 blastomere 41 MECP2 41 mammalian embryos 41 somatic mutations 41 CNTNAP2 gene 41 epigenetic modification 41 autosomal recessive 41 MLH1 41 splice junctions 41 Pierolapithecus 41 BRCA genes 41 tubule 41 chromosomal DNA 41 uncharacterized genes 41 unicellular 41 Amborella 41 miRNA genes 41 FASPS 41 telomere length 41 microbiomes 41 sediba 41 erectus 41 retrovirus 41 APOE 41 offspring 41 sister chromatids 41 speciation 41 homo habilis 41 SATB1 41 human genome sequence 41 Denisovans 41 ApoE4 gene 41 CRISPR Cas 41 HOTAIR 41 BRIP1 41 causal variants 41 C. neoformans 41 hominid 41 Rickettsia 41 D. simulans 41 eusociality 41 mitochondrial 41 FGFR2 41 Austria Gruner Veltliner 41 viral genome 41 primate cousins 41 HLA gene 41 palladin 41 PCR amplified 41 mammalian evolution 41 anthropoids 41 hereditary hemochromatosis 41 human leukocyte antigen 41 APOE ε4 41 prehistoric ancestors 41 archaeal 41 Ardipithecus 41 Hox genes 41 differentially methylated 41 CYP#A# gene 41 abnormal hemoglobin 41 var genes 41 antisense RNA 41 Ui Neill 41 SIR2 41 #S rRNA genes 41 Ashkenazi Jewish 41 A. sediba 41 coding sequences 41 autosomal dominant 41 Homo erectus 40 bilaterians 40 SIVcpz 40 Sanger sequencing 40 somatic cells 40 Mongol empire 40 mitochondrial DNA mutations 40 polyandry 40 placental mammal 40 Homo erectus evolved 40 mutated 40 evolutionarily speaking 40 PrPSc 40 BRCA gene mutation 40 chromatid 40 OCA2 40 Europasaurus 40 promoter methylation 40 GQ Lupi 40 Evolutionary biologists 40 planarian 40 HLA gene variant 40 Fragile X 40 Dicer 40 mitochondrial genome sequence 40 ribonucleic acid RNA 40 cilium 40 LB1 40 recessive 40 nestin 40 rhesus 40 rRNA 40 fertilized ovum 40 histone modification 40 SLC#A# [001] 40 NPY gene 40 gene duplications 40 hypospadias 40 honey bee genome 40 adenine 40 untranslated regions 40 Saqqaq 40 metazoan 40 intron 40 deoxyribonucleic acid DNA 40 parkin gene 40 inbred strains 40 gene amplification 40 Sir Francis Galton 40 messenger RNA 40 poly dA 40 UGT#B# 40 genetic susceptibility 40 extra centrosomes 40 P. reichenowi 40 KLF4 40 horned dinosaurs 40 Neanderthals Homo neanderthalensis 40 FADS2 40 CCR5 delta# 40 amniocentesis 40 woolly mammoth genome 40 protein encoded 40 fruitfly Drosophila 40 seminiferous tubules 40 eusocial 40 multi celled organisms 40 amino acid sequences 40 LMNA 40 Australopithecus anamensis 40 Neanderthal genome 40 somatic mutation 40 LIS1 40 Single Nucleotide Polymorphisms SNPs 40 embryonic stem ES 40 genome sequenced 40 maize genome 40 chromosomal translocations 40 DNA strands 40 HMGA2 40 chromosomal alterations 40 CFTR gene 40 chromosomal defects 40 nucleotide sequences 40 BAC clones 40 HSCs 40 pea aphid 40 enzymatic activity 40 planet habitability 40 enterotypes 40 huntingtin 40 endogenous retrovirus 40 NR#A# gene 40 OCA2 gene 40 apoE4 40 A. ramidus 40 Pol IV 40 nucleotide substitution 40 vaginal canal 40 cell nuclei 40 aberrant methylation 40 abnormal chromosomes 40 Semitic 40 paternal 40 transcriptional machinery 40 parthenogenetic 40 animal phyla 40 maternally 40 fission yeast 40 luminal cells 40 genetically coded 40 iPSCs 40 Simian Immunodeficiency Virus 40 MHC dissimilar 40 Homo species 40 monophyletic 40 histone modifications 40 intergenic 40 Eston Hemings 40 Hominids 40 epigenetic reprogramming 40 genomic sequence 40 adenoma 40 KIAA# 40 giant danio 40 PtERV1 40 ApoE gene 40 paralogs 40 valine 40 messenger RNAs mRNAs 40 mitochondria 40 CHEK2 40 species interbred 40 microsporidia 40 DHEAS 40 Pääbo 40 totipotent 40 hunter gatherer 40 diagnosis PGD 40 H2AX 40 genetic sequences 40 unicellular organism 40 exome 40 cytochrome b 40 ultraconserved 40 Drosophila fruit 40 ovules 40 mRNA transcripts 40 heterozygotes 40 viral genomes 40 DNA testing 40 mutant worms 40 mosasaurs 40 DICER1 gene 40 CHD7 40 JAK2 mutation 40 mtDNA sequences 40 Leydig cells 40 hominin species 40 transposon 40 MeCP2 gene 40 presenilin 40 BRAC2 40 mouse ESCs 40 fru 40 bdelloid rotifer 40 thrifty gene 40 choosiness 40 microcephaly 40 Paranthropus boisei 40 trisomy 40 Mitochondrial 40 mammary cancers 40 TOMM# 40 loci 40 genetically wired 40 defective mitochondria 40 transcriptome 40 distinct lineages 40 planaria 40 Neanderthal genome sequence 40 evolvability 40 Mycoplasma species 40 Volvox 40 intronic 40 Micromonas 40 Drosophila melanogaster 40 progranulin gene 39 microsatellite instability 39 RNA molecules 39 XLHED 39 reproduce asexually 39 hypermethylated 39 Neanderthals interbred 39 apoE 39 APOC3 39 Alu sequences 39 familial pancreatic cancer 39 neural crest stem cells 39 monotreme 39 bacterial genome 39 oropharyngeal cancer 39 suppressor gene 39 S. pombe 39 telomeres 39 TRIM5 39 microcephalics 39 SCN5A 39 messenger RNA mRNA 39 progranulin 39 pathogenic mutations 39 masculine traits 39 polymerases 39 radiocarbon dating 39 Argonaute proteins 39 genome rearrangements 39 mutant mouse 39 RUNX3 39 chromosome #q#.# [001] 39 cytoplasmic tail 39 codon 39 C#BL/#J 39 APOE epsilon 4 39 GNAQ 39 adherens junctions 39 biogeographic 39 morphogen 39 homologous chromosomes 39 Cdk5 39 Neandertal DNA 39 tRNAs 39 telomere lengths 39 Kadanuumuu 39 C#Y 39 inbreeding 39 protein p# 39 heterozygote 39 mitochondrial DNA sequence 39 exonuclease 39 ovarian tumors 39 Cora Crippen 39 gene expression 39 unfertilised egg 39 Drosophila 39 phenotypic expression 39 C. elegans worm 39 MTHFR 39 preimplantation genetic diagnosis 39 5 methylcytosine 39 immunoglobulin genes 39 SMN1 39 microRNA molecules 39 RNA Seq 39 melanogaster 39 galaxies 39 prairie voles 39 earliest tetrapods 39 Myc 39 corpus callosum 39 MEF2D 39 Caulobacter 39 gene p# 39 AU Mic 39 histone protein 39 homeobox genes 39 genetic makeups 39 mouse embryonic fibroblasts 39 nucleases 39 M. leprae 39 genetic sequencing 39 mutated BRCA 39 genotoxic stress 39 amphioxus 39 lactase gene 39 PTEN mutations 39 Haast eagle 39 microevolution 39 centrosome 39 eukaryotic cells 39 sexually dimorphic 39 ncRNAs 39 LRRK2 mutation 39 M. genitalium 39 retrosexual 39 forebrain 39 Falcarius 39 neural circuitry 39 BRCA2 mutations 39 premature ovarian 39 cardiac fibroblasts 39 microRNAs miRNAs 39 globular cluster 39 hunter gatherer ancestors 39 deuterostomes 39 melanocyte stem cells 39 Drosophila genome 39 mammalian 39 Daevi 39 civilization 39 synuclein 39 maternally transmitted 39 X. laevis 39 Neanderthal skeletons 39 HLA alleles 39 Meckel Gruber 39 epigenetic silencing 39 asexual reproduction 39 susceptibility genes 39 TAp# 39 DISC1 39 supercolony 39 epigenetic regulation 39 Prox1 39 methylated 39 eukaryotic cell 39 Marfan syndrome 39 cyclin 39 malignancy 39 prion protein gene 39 Aß# 39 CALHM1 39 mouse embryo 39 flatworm 39 testes 39 homo sapiens sapiens 39 Svante Paabo 39 autism susceptibility genes 39 Homo 39 L1s 39 asexuals 39 ray finned fishes 39 insertions deletions 39 retrotransposons 39 rotifer 39 melanocyte 39 CDKN2A 39 recessive inheritance 39 chromosome segregation 39 embryoid bodies 39 quantum particle 39 mitochondrial DNA sequences 39 Heterodontosaurus 39 ape ancestor 39 melanosomes 39 phthalate syndrome 39 Comparative genomics