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(Click for frequent words.) 76 Genetic 72 genes 72 genetics 71 gene 71 genomic 70 genetic makeup 68 genetically 68 genome 67 genetic markers 66 genomes 65 genetic mutations 65 genetic variation 64 genetic variations 64 chromosomal 63 genomewide 62 mutation 62 geneticists 61 epigenetic 61 mutations 61 genetic traits 60 human genome 60 mitochondrial DNA 60 DNA sequences 59 DNA 59 gene sequences 59 mtDNA 59 genetic abnormalities 59 genetic mutation 59 mitochondrial DNA mtDNA 59 gene mutation 58 gene mutations 58 Genetic testing 58 genetic variants 58 genetic susceptibility 58 chromosomes 58 gene expression 58 heritable 58 mutated genes 58 imprinted genes 58 genetic predisposition 58 gene variants 58 Y chromosome 57 genetic ancestry 57 chromosome 57 genetic defects 57 multigene 56 maternally inherited 56 phenotypic 56 SNPs 56 inheritable diseases 56 X chromosome 56 Mendelian 56 primate genomes 55 mutated gene 55 gene sequencing 55 biological 55 susceptibility genes 55 mitochondrial genome 55 recessive trait 55 aneuploidy 55 recessive mutations 55 alleles 55 haplotype 55 genetic trait 55 genomic imprinting 54 mutant gene 54 spontaneous mutations 54 genetic disorders 54 prion gene 54 breast cancer genes BRCA1 54 gene expression patterns 54 autosomal 54 heredity 54 Fragile X gene 54 genetic variant 54 genetic recombination 54 CHD7 54 Genes 54 VHL gene 54 epigenetic changes 54 nongenetic 54 phenotypes 54 microsatellite markers 54 mutant genes 54 genetic sequences 54 biochemical 54 transcriptome 54 CFTR gene 53 phenotypic expression 53 BRCA1 gene 53 germline 53 CYP#D# gene 53 gut microbes 53 genotyping 53 epigenome 53 haplotype map 53 genomics 53 MYH9 gene 53 phenotype 53 SRY gene 53 DNA deoxyribonucleic acid 53 paternally inherited 53 recessive genetic 53 quantitative trait loci 53 chromosomal anomalies 53 causative genes 53 yeast genome 53 genome sequence 53 genetic makeups 53 chromosomal abnormalities 53 CRISPR Cas 53 genetic imprinting 53 mtDNA mutations 53 recessive genes 53 Hox gene 53 microdeletion 53 immunological 53 human genome sequence 53 genomewide association studies 53 Genetic variation 53 aneuploid 53 genetic predispositions 53 genetic variability 53 transgenic 53 DNA methylation patterns 53 BARD1 52 nucleotide sequence 52 gene locus 52 molecular 52 genomic sequence 52 Venter genome 52 epistasis 52 LRRK2 gene 52 linkage disequilibrium 52 miRNAs 52 genome sequences 52 TCF#L# gene 52 APOE genotype 52 genetically identical 52 fungal genomes 52 genotype 52 chromatin structure 52 genetic determinants 52 single nucleotide polymorphism 52 cytogenetic 52 myostatin gene 52 methylation 52 Single Nucleotide Polymorphisms SNPs 52 Apobec3 52 spontaneous mutation 52 genetic defect 52 PALB2 52 autism susceptibility genes 52 Chromosomal 52 mosaicism 52 DNA methylation 52 mutational 52 epigenetic regulation 52 heritable genetic 52 phenotypic variation 52 multigenic 52 genetic underpinnings 52 miRNA 52 sequenced genomes 52 non coding RNA 52 exomes 51 CNVs 51 epigenetic alterations 51 microRNA 51 genetic alteration 51 maize genome 51 mitochondrial 51 genetic abnormality 51 ALK gene 51 genetic alterations 51 epigenetic modifications 51 array CGH 51 microdeletions 51 ribonucleic acid RNA 51 NF1 gene 51 miRNA expression 51 modifier genes 51 A. thaliana 51 defective gene 51 P. patens 51 MC1R gene 51 causative gene 51 genotypic 51 polydactylism 51 chromosomal regions 51 mitochondrial mutations 51 gene variant 51 allelic 51 homozygosity 51 coding sequences 51 Genetic variants 51 genetic sequencing 51 enterotypes 51 epigenetic reprogramming 51 organism genome 51 Genetics 51 metabolic 51 sequenced genome 51 LMNA gene 51 Chromosome 51 physiological 51 chromosomal translocations 51 microbiomes 51 genetic loci 51 gene duplications 51 Y STR 51 genomic variation 51 ribosomal RNA 51 positional cloning 51 microRNAs miRNAs 51 genes predisposing 51 monozygotic twins 51 aneuploidies 51 noncoding RNAs 51 Mitochondrial DNA 51 platypus genome 51 inheritable genetic 51 sequencing 51 sea urchin genome 51 Y chromosomes 50 geneticist 50 somatic mutations 50 microRNA expression 50 abnormal chromosomes 50 Meckel Gruber 50 cardiac channelopathies 50 Alu elements 50 haploid 50 transgene 50 polymorphisms 50 BRCA gene 50 protein isoforms 50 genetic rearrangements 50 viral genomes 50 chromosomal instability 50 phylogenetic analysis 50 progranulin gene 50 MEF2A 50 mitochondrial gene 50 mammalian embryos 50 metabolome 50 MHC genes 50 epigenomes 50 genetic diversity 50 #S rRNA gene 50 histone code 50 DNA rearrangements 50 chimerism 50 coevolution 50 chromosome abnormality 50 inbred strains 50 Genetically 50 genomic alterations 50 noncoding DNA 50 heritable traits 50 histone modification 50 PTPN# 50 de novo mutations 50 #S rDNA 50 methylation patterns 50 gene expression profiles 50 DRD2 gene 50 BRCA1 50 epigenomic 50 loci 50 BRCA2 gene 50 epigenetic marks 50 uncharacterized genes 50 chromosomal anomaly 50 nucleotide substitution 50 mammalian genomes 50 sexually reproducing 50 generalized vitiligo 50 MECP2 gene 50 primordial germ cells 50 genomic proteomic 50 TP# gene 50 JAK2 mutation 50 genetic variants associated 50 genotypes 50 genome rearrangements 50 DNA sequencing 50 genetical 50 Arabidopsis genome 50 microbial genome 50 micro RNA 50 maternal lineage 49 CYP#E# gene 49 splice junctions 49 chromosomal defects 49 rDNA 49 Geneticists 49 BAC clones 49 susceptibility gene 49 germline cells 49 Neanderthal genes 49 Genomic 49 epigenetic inheritance 49 APOE e4 49 chromosome rearrangements 49 microarray 49 microRNAs 49 HNPCC 49 STK# gene 49 Kufs disease 49 microbial genomes 49 Arabidopsis genes 49 apolipoprotein E gene 49 genotyping arrays 49 germline mutations 49 nucleotide 49 micro RNAs 49 mitochondrial disorders 49 comparative genomics 49 LIS1 49 chromosomal DNA 49 telomere DNA 49 mitochondrial genomes 49 genomic loci 49 sRNA 49 segmental duplications 49 genetic polymorphisms 49 single nucleotide polymorphisms 49 MSH2 49 chromosomal disorders 49 Mendelian genetics 49 recessive traits 49 hereditary disorders 49 TOMM# 49 haplotypes 49 MIF protein 49 MC4R gene 49 genes CYP#C# 49 artificial chromosomes 49 whole genome sequencing 49 microcephalin 49 histocompatibility 49 CDH1 49 evolvability 49 genetically inherited 49 cis regulatory 49 RNA sequences 49 DeCODE 49 proband 49 chromosomal deletions 49 prion infection 49 HAR1 49 5 hydroxymethylcytosine 49 genetic susceptibilities 49 polyploid 49 metazoan 49 APOL1 49 lactose tolerance 49 hereditary 49 congenital disorders 49 CNTNAP2 49 MYH9 49 pharmacogenetic 49 molecular profiling 49 piRNAs 49 Genetic variations 49 chromosome translocations 49 malaria parasite genome 49 woolly mammoth genome 49 gene splicing 49 epigenetic modification 48 epigenetics 48 COMT gene 48 NR#A# gene 48 pea aphid 48 FOXP2 gene 48 recessive mutation 48 human leukocyte antigens 48 embryo biopsy 48 paternal lineage 48 genes BRCA1 48 genome mapping 48 SERT gene 48 mitochondrial genes 48 endogenous retroviruses 48 indels 48 INF2 48 molecular abnormalities 48 #p#.# [001] 48 UGT#B# 48 mammalian 48 genome sequenced 48 genomic DNA 48 genome sequencing 48 exons 48 Fanconi anemia 48 molecular markers 48 Stuttering tends 48 sporadic ALS 48 epigenetic silencing 48 Y chromosomal 48 FMR1 gene 48 familial pancreatic cancer 48 metabolic enzymes 48 heritable disorders 48 proteins 48 coding exons 48 bacterial genomes 48 morphological 48 epigenetic mechanisms 48 chromosomal rearrangements 48 mammalian evolution 48 Li Fraumeni 48 clonal 48 recessive gene 48 transcriptional regulation 48 aCGH 48 gut microbiota 48 Genetic mutations 48 transcriptome sequencing 48 somatic mutation 48 ApoE gene 48 ribosomal genes 48 exome sequencing 48 DeCode 48 mitochondrial proteins 48 Spinal muscular atrophy 48 HMGCR 48 causal variants 48 chloroplast DNA 48 Mycoplasma genitalium 48 NPM1 gene 48 LMNA 48 Trichoderma reesei 48 molecular pathways 48 proteomic analysis 48 ABCB1 gene 48 KIAA# 48 transcriptomes 48 allelic variation 48 genomic instability 48 noncoding 48 M. genitalium 48 Froguel 48 genetic polymorphism 48 alternative splicing 48 mutated BRCA 48 genetic syndromes 48 X chromosome inactivation 48 Sanger sequencing 48 inherited mutations 48 neurobiological 48 Hakonarson 48 body louse genome 48 evolutionary lineage 48 gene expression profiling 48 microRNA miRNA 48 NPY gene 48 Lynn Jorde 48 genome scans 48 Toxoplasma 48 cDNA microarray 48 metabolomic profiles 48 pseudogenes 48 HLA genes 48 cybrid 48 #S rRNA 48 cybrids 48 PTEN gene 48 phenotypic traits 48 epigenetically 48 #q#.# [001] 48 inbreeding depression 47 androgen receptor gene 47 zebra finch genome 47 microarray analysis 47 orthologs 47 causative mutation 47 number variation CNV 47 ZNF# 47 clefting 47 BRIP1 47 monogenic 47 disease juvenile nephronophthisis 47 Genetic predisposition 47 MLL2 47 aberrant methylation 47 VKORC1 47 MC1R 47 C. neoformans 47 evolutionary 47 IGF2 47 dbSNP 47 RNA Seq 47 ADRB2 47 HLAs 47 Velculescu 47 prion protein gene 47 Genome sequencing 47 familial ALS 47 chromosome #q 47 epigenetic markers 47 Genotypic 47 genomic rearrangements 47 BRCA genes 47 gene amplification 47 mtDNA sequence 47 histone modifications 47 human leukocyte antigen 47 SORL1 gene 47 methylation markers 47 trypanosome 47 noncoding RNA 47 5 hmC 47 phylogenetic analyzes 47 polymorphism 47 genomic variants 47 muscular dystrophy cystic fibrosis 47 gene rearrangements 47 #q# [001] 47 Brachypodium 47 outbred 47 HMGA2 47 HapMap 47 HLA DRB1 47 preimplantation genetic 47 molecular biology genetics 47 genetically mapped 47 proteome 47 protein 47 nucleosome positioning 47 HLA DQ2 47 highly heritable 47 FOXP2 47 comparative genomic hybridization 47 alternatively spliced 47 aY chromosome 47 heritability 47 MAPCs 47 receptor gene 47 FMR1 47 missense mutations 47 Haplotype 47 chimpanzee genomes 47 undiagnosed celiac disease 47 functional genomics 47 Leptospira 47 chromatin immunoprecipitation ChIP 47 glycan 47 heritable diseases 47 human microbiome 47 proteomes 47 cytosine methylation 47 chimp genome 47 metabolomic profiling 47 Neanderthal DNA 47 insertions deletions 47 lentivirus 47 mitochondrial dysfunction 47 introgression 47 toxicogenomic 47 LPA gene 47 HFE gene 47 mutant alleles 47 GAB2 47 MetaChip 47 monozygotic 47 Deoxyribonucleic acid DNA 47 bacterial genome 47 OCA2 47 APOE4 47 gastric carcinomas 47 filaggrin gene 47 Trichomonas 47 STAT4 47 genomic sequencing 47 biomarker 47 Genome 47 chromosome #p# [001] 47 diploid 47 glycosylation 47 gamete donors 47 chromosome #q#.# [001] 47 parkin gene 47 SNPs pronounced snips 47 CHEK2 47 methylated DNA 47 dizygotic twins 47 CRISPR 47 IKZF1 47 gene loci 47 Brd4 47 genes BRCA 47 autosomal recessive 47 metagenomics 47 small RNAs 47 mutant allele 47 parthenogenetic 47 honeybee genome 47 embyros 47 protein conformation 46 landraces 46 protein coding RNAs 46 biochemical mechanisms 46 autosomal dominant inheritance 46 QTLs 46 CCL#L# 46 deoxyribonucleic acid 46 evolutionary relatedness 46 mutagenesis 46 microRNA molecules 46 nucleic acid sequence 46 polygenic 46 underlying molecular mechanisms 46 heterologous expression 46 planarian 46 functional annotation 46 FGFR2 gene 46 iPS cells 46 chromatin proteins 46 HLA DQ 46 Amborella 46 mitochondrial defects 46 PARP inhibition 46 genome decoded 46 G#S mutation 46 stem cells 46 evolutionary genomics 46 HOTAIR 46 RNA splicing 46 shotgun sequencing 46 TACI mutations 46 HLA molecules 46 deoxyribonucleic acid DNA 46 lactase gene 46 RNA molecules 46 DNA Deoxyribonucleic Acid 46 Heredity 46 amino acid sequence 46 breast cancer metastasis 46 karyotype 46 genomic profiling 46 alpha synuclein gene 46 APOE gene 46 virulence genes 46 chromosomal aberrations 46 K ras gene 46 RNA viruses 46 sCJD 46 apoE 46 non coding RNAs 46 observable traits 46 budding yeast 46 sequence homology 46 von Hippel Lindau 46 SMN2 gene 46 MLH1 46 TP# mutation 46 MTHFR gene 46 FUS protein 46 tammar wallaby 46 BRCA breast cancer 46 Aneuploidy 46 Telomere length 46 pancreatic tissue 46 molecular underpinnings 46 homologs 46 microchimerism 46 nucleases 46 allele 46 DNA fingerprinting 46 TRIM5 46 SLC#A# gene [001] 46 homeobox genes 46 HMGA2 gene 46 microsatellite instability 46 allele frequencies 46 OCA2 gene 46 Brugada Syndrome 46 preimplantation 46 Oxford Ancestors 46 exome 46 microarray gene expression 46 genetic manipulations 46 promoter hypermethylation 46 environmental toxicants 46 TGFBR1 * 6A 46 BRCA mutation 46 MECP2 46 Navigenics #andMe 46 bacterial symbiont 46 IDH1 46 transgenesis 46 abnormal prions 46 fruitflies 46 Rh factor 46 bdelloid rotifer 46 chromosome abnormalities 46 Illumina genotyping 46 macaque genome 46 number variations CNVs 46 CYP#C# [002] 46 LRP5 46 vertebrate embryos 46 Ets2 46 agronomically important 46 Neandertal DNA 46 DNAPrint TM 46 UTRs 46 Phenotypic 46 DNA samples 46 diploid genome 46 blastomeres 46 PCR RFLP 46 vasopressin receptor 46 TCF4 46 fruitfly Drosophila 46 retroviral 46 Jhdm2a 46 suppressor gene 46 orthologous genes 46 International HapMap Project 46 Folic acid deficiency 46 SHANK3 gene 46 SNP genotyping 46 diagnosis PGD 46 genetically susceptible 46 D. melanogaster 46 molecular determinants 46 familial clustering 46 Comparative genomics 46 underlying pathophysiology 46 prion strains 46 heterozygosity 46 transcriptome profiling 46 HLA typing 46 biologic 46 phylogenetic trees 46 microbiota 46 meganuclease 46 retrovirus 46 prion diseases 46 pharmacogenetic testing 46 tumor suppressor protein 46 selective breeding 46 laforin 46 neural crest 46 CFTR gene mutations 46 pathogenic mutations 46 HLA markers 46 Drosophila genome 46 DNA testing 46 viral genome 46 intronic 46 filoviruses 46 CNTNAP2 gene 46 genetic lineages 46 bovine genome 46 RNA ribonucleic acid 46 IVF embryos 46 5 methylcytosine 46 pathogen interactions 46 transgenic rats 46 chordate 46 hereditary diseases 46 Y Chromosome 46 Li Fraumeni syndrome 46 malarial parasites 46 genotype phenotype 46 Germline 45 mitochondrial DNA mutations 45 intergenic 45 tumor suppressor gene 45 IRAK1 45 segmental duplication 45 metagenomic 45 pathophysiological 45 Rhesus D 45 CSHL scientists 45 MLL gene 45 genomic deletions 45 conserved sequences 45 transgenes 45 lincRNAs 45 nucleolar dominance 45 chromatid 45 Neanderthal fossils 45 Randy Jirtle 45 Levy Lahad 45 nucleotide substitutions 45 sympatric speciation 45 Mitochondrial 45 HLA G 45 susceptibility locus 45 genes encoding 45 glycan microarray 45 heterozygote 45 Tischfield 45 embryological 45 neoplastic 45 VNTR 45 muscular dystrophies 45 adult neurogenesis 45 Transcriptome 45 massively parallel sequencing 45 SNP Array #.# 45 HOX genes 45 Apert syndrome 45 Deoxyribonucleic acid 45 prodynorphin 45 mRNA transcripts 45 Chromatin 45 FGF signaling 45 predisposition 45 T. gondii 45 orangutan genome 45 HPRT gene 45 genotyped 45 telomere dysfunction 45 transdifferentiation 45 SMN1 gene 45 homozygote 45 Rb gene 45 UGT#A# 45 BRCA2 gene mutations 45 fully sequenced genomes 45 neurogenetics 45 interactome 45 preimplantation genetic diagnosis PGD 45 testicular germ cell 45 messenger RNAs mRNAs 45 biological pathways 45 KIBRA 45 Wolbachia infection 45 proteomic 45 huntingtin gene 45 chromosomal alterations 45 DNA microarray 45 tandem mass spectrometry 45 P. infestans 45 phylogenies 45 S. cerevisiae 45 spermatogonial cells 45 Congenital Adrenal Hyperplasia 45 M. pneumoniae 45 genetic modifiers 45 #p#.# [002] 45 sickle cell hemoglobin 45 bone marrow transplants 45 germline mutation 45 proteomic analyzes 45 ultra rapid metabolizer 45 DRD4 45 pharmacogenetics 45 Dr. Maren Scheuner 45 luminal cells 45 preimplantation genetic diagnosis 45 Sexual Attraction 45 neurodevelopmental disorder 45 PRNP 45 metabolomics 45 iPS derived 45 neural circuitry 45 mammalian genome 45 SOD1 gene 45 genes predispose 45 primate evolution 45 mitochondrial DNA sequence 45 microbiome 45 #q# [002] 45 RUNX3 45 abnormal hemoglobin 45 p# mutations 45 morphological characteristics 45 cardiac progenitor cells 45 phylogenetic 45 induced pluripotent cells 45 transcriptomics 45 PTEN mutations 45 dopamine transporter gene 45 causative mutations 45 intergenic regions 45 coding RNA 45 gene deletions 45 aneuploidy screening 45 desiccation tolerance 45 multi celled organisms 45 maternally transmitted 45 genetically engineered mouse 45 Prevotella 45 neuroligins 45 immunoglobulin genes 45 mitochondrial diseases 45 Wnt#b 45 cell nuclei 45 nucleus Chinnery 45 malaria parasite Plasmodium falciparum 45 polyploidy 45 neurogenetic 45 mammary stem cells 45 protein phosphorylation 45 BRCA2 45 louse genome 45 transposable elements 45 miRNA molecules 45 DeCode Genetics 45 archaeal 45 chromatin immunoprecipitation 45 mutant mouse 45 antisense RNA 45 achromatopsia 45 synthases 45 beta globin gene 45 mRNA molecules 45 H#Y 45 intestinal microbiota 45 Neandertal 45 herpesviruses 45 NFKBIA 45 epiblast stem cells 45 untranslated regions 45 miRNA genes 45 MTHFR 45 FTO gene 45 microRNA genes 45 molecular mimicry 45 SMN2 45 Sequencing 45 TMPRSS2 ERG fusion 45 transcriptional machinery 45 PALB2 gene 45 chromosome #q# [001] 45 transcriptomic 45 obligate intracellular 45 identifying genetic markers 45 chromosome aberrations 45 biomarkers 45 outer membrane proteins 45 TBC#D# 45 palladin 45 genetic blueprints 45 STK# [002] 45 transcriptional coactivator 45 sister chromatid 45 dedifferentiation 45 gen sequencing 45 GATA4 45 glycoproteins 45 miRNA sequences 45 cDNAs 45 murine leukemia virus 45 implantation genetic 45 mRNA decay 45 gene predisposing 45 evolutionary lineages 45 Alleles 45 Genetics Consortium 45 Reijo Pera 45 chimpanzee genome 45 antisense strand 45 embryonic stem ES 45 molecule sequencing 45 Assisted reproduction 45 gene BRCA2 45 Pääbo 45 primate lineage 45 Preimplantation Genetic Diagnosis PGD 45 phenotypic differences 45 FGFR2 45 cytoplasmic hybrids 45 ALCLS 45 amniotic stem cell 45 SORL1 45 gene expression microarray 45 TMEM#B 45 MeCP2 protein 45 DNA profiling 45 galactosemia 45 Induced pluripotent stem cells 45 IDH2 45 X inactivation 45 genetic aberrations 45 gene therapy 45 lactase persistence 45 FTLD 45 molecular biomarkers 45 hypermethylation 45 genetic heterogeneity 45 diploid cells 45 pilocytic astrocytomas 45 evolutionary origins 45 mtDNA sequences 45 therapeutically useful 44 HeLa cell 44 dopamine receptor gene 44 inherited maternally 44 aminoacyl tRNA synthetases 44 opossum genome 44 PCA3 gene