Related by context. All words. (Click for frequent words.) 71 SNPs 70 genetic variants 70 polymorphisms 69 gene variants 68 susceptibility genes 68 microdeletions 67 genetic variations 66 loci 66 chromosomal regions 66 #q# [001] 66 sporadic ALS 66 mutations 65 genetic variant 65 medulloblastomas 65 haplotypes 64 alleles 64 haplotype 64 genetic variation 64 autism susceptibility genes 64 #p#.# [001] 63 genetic mutations 63 microRNA expression 63 mutated genes 63 somatic mutations 63 gene expression profiles 63 #q#.# [002] 63 genetic polymorphisms 63 gene mutations 63 miRNAs 63 #q#.# [001] 63 NF1 62 missense mutations 62 imprinted genes 62 segmental duplications 62 methylation patterns 62 germline mutations 62 genomic variation 62 chromosome #q#.# [001] 62 genetic variants associated 62 nucleotide sequence 62 ependymomas 62 polymorphism 62 spontaneous mutations 62 EGFR gene 62 genetic loci 62 single nucleotide polymorphism 62 inherited mutations 62 #p# [001] 61 gene expression patterns 61 CNTNAP2 61 Hakonarson 61 chromosomal rearrangements 61 genomewide 61 APOE e4 61 gene variant 61 allele 61 APOE4 61 autosomal 61 genomes 61 PALB2 61 genetic markers 61 mutation 61 rs# [003] 61 susceptibility loci 61 phenotypic variation 60 causal variants 60 number variations CNVs 60 heterozygosity 60 susceptibility gene 60 allelic 60 Alu elements 60 MLL2 60 chromosomal abnormalities 60 chromosomal translocations 60 mtDNA mutations 60 DNA sequences 60 single nucleotide polymorphisms 60 heterozygous 60 #q# [002] 60 mtDNA 60 chromosome #q# [002] 60 genotyped 60 mitochondrial dysfunction 60 splice junctions 60 exons 60 PTPN# 60 homozygosity 60 genetic determinants 60 SLC#A# [002] 60 rs# [002] 60 monozygotic twins 59 CDH1 59 chromosome #p#.# 59 non coding RNA 59 narcolepsy cataplexy 59 gene mutation 59 chromosome #p# [001] 59 chromosome 59 MYH9 59 SORL1 59 LRRK2 gene 59 MYH9 gene 59 familial ALS 59 #p#.# [002] 59 indels 59 FTLD 59 CDKN2A 59 MTHFR 59 mitochondrial gene 59 C#Y 59 gene variation 59 allele frequencies 59 paralogs 59 linkage disequilibrium 59 genes 59 TCF#L# gene 59 mitochondrial genome 59 miRNA expression 59 ALK mutations 59 microRNA molecules 59 micro RNA 59 mutated gene 59 miRNA genes 59 microRNAs 59 FMR1 gene 59 LIS1 58 DISC1 58 mammalian genomes 58 histone modifications 58 de novo mutations 58 DNA methylation patterns 58 gene expression 58 NF1 gene 58 exomes 58 dysbindin 58 noncoding 58 organism genome 58 genomic loci 58 BRCA1 mutations 58 proband 58 #S rRNA 58 MSH2 58 microcephalin 58 chromosome #q# [001] 58 aneuploidies 58 CYP#D# gene 58 protein kinases 58 TCF#L# 58 genome 58 5 HTTLPR 58 microdeletion 58 LRRK2 58 ORMDL3 58 IKZF1 58 genetic abnormalities 58 chromosome deletion 58 noncoding RNAs 58 genetic alterations 58 mitochondrial DNA mtDNA 58 monogenic 58 IL#R 58 IgA deficiency 58 APOE gene 58 CNTNAP2 gene 58 phenotype 58 EGFR mutations 58 gene 58 chromosomal 58 phenotypes 57 DNA methylation 57 FGFR2 57 Venter genome 57 orthologs 57 X chromosome 57 NAFLD 57 breast cancer genes BRCA1 57 number variants CNVs 57 micro RNAs 57 chromosomal deletions 57 Wwox 57 transcriptomes 57 apoE4 57 SLC#A# [001] 57 bacterial genomes 57 SNP rs# [001] 57 #q# deletion 57 clusterin 57 genotypes 57 variant allele 57 VNTR 57 microarray experiments 57 splice variants 57 haplogroups 57 PTEN gene 57 KIAA# 57 HLA genes 57 RNA sequences 57 BRCA1 gene 57 chromosomal alterations 57 epigenetic mechanisms 57 BARD1 57 rs# [001] 57 WDR# 57 mRNA transcripts 57 genes encoding 57 gene polymorphisms 57 transcriptome 57 genotype 57 HLA B# 57 APOE4 gene 57 CCL#L# 57 intron 57 alpha synuclein gene 57 chimpanzee genomes 57 heritable 57 PIK3CA 57 QTLs 57 genomic variants 57 chromosomal aberrations 57 neuroblastomas 57 heritability 57 genomic alterations 57 chromosome #q 57 familial pancreatic cancer 57 causative gene 57 protein isoforms 57 miR #b [002] 57 cDNAs 57 Chromosome 57 phylogenetically 57 mosaicism 57 TACI mutations 56 mutant allele 56 HNPCC 56 #p# [003] 56 genomic deletions 56 chromosome abnormalities 56 transcriptional regulation 56 methylation 56 intergenic 56 LQTS 56 MECP2 gene 56 somatic mutation 56 DQB1 * 56 MC1R 56 cytogenetic 56 enterotypes 56 APOE 56 IL#B 56 SNPs pronounced snips 56 epigenetic modification 56 gene rearrangements 56 heterozygotes 56 TGFBR1 * 6A 56 VHL gene 56 kilobase 56 RNA transcripts 56 PTEN mutations 56 HGPS 56 STAT4 56 activating mutations 56 T2D 56 apolipoprotein E gene 56 alternative splicing 56 LRRK2 mutation 56 breast cancer subtypes 56 GSTM1 56 maize genome 56 perilipin 56 familial aggregation 56 causative mutations 56 epigenomes 56 MC4R gene 56 BRCA2 56 MC1R gene 56 autosomal recessive 56 mutant alleles 56 HMGA2 56 genes CYP#C# 56 hamartomas 56 chromosomal rearrangement 56 hypermethylation 56 p# mutations 56 Meckel Gruber 56 genomic rearrangements 56 gene sequences 56 recombination hotspots 56 tumor suppressor genes 56 GPC5 56 FTO gene 56 genes BRCA1 56 penetrance 56 pseudogenes 56 autosomal dominant 56 evolutionarily conserved 56 genetic polymorphism 56 ABCB1 56 developmental abnormalities 55 yeast genome 55 pathogenic mutations 55 segmental duplication 55 CC genotype 55 coding sequences 55 apoE 55 insertions deletions 55 EoE 55 exon 55 Bardet Biedl syndrome 55 familial clustering 55 pilocytic astrocytomas 55 meningiomas 55 ultraconserved elements 55 FASPS 55 mammalian genome 55 TOP2A 55 SLITRK1 55 HOTAIR 55 VKORC1 55 gene APOE4 55 gene locus 55 5 hmC 55 ZNF# 55 IDH1 mutation 55 neuroligins 55 epigenetic 55 TMEM#B 55 phylogenetic analyzes 55 chromosome rearrangements 55 piRNAs 55 primate genomes 55 DLC1 55 telomere lengths 55 colorectal neoplasia 55 APOE genotype 55 rs# [004] 55 lincRNAs 55 diploid genome 55 epigenome 55 intronic 55 epigenetic changes 55 mitochondrial genomes 55 aberrant methylation 55 APOL1 55 genetic abnormality 55 DNA rearrangements 55 missense mutation 55 ncRNAs 55 genetic locus 55 nonsense mutations 55 miR #a [001] 55 MLH1 55 dopamine transporter gene 55 NF2 55 PDGFRA 55 major histocompatibility complex 55 CHD7 55 G#S mutation 55 CYP#C# [002] 55 PICALM 55 highly heritable 55 UGT#B# 55 ApoE gene 55 CALHM1 55 UGT#A# * 55 genomewide association studies 55 genetic syndromes 55 mRNA expression 55 maternally inherited 55 gene loci 55 Arabidopsis genome 55 Klinefelter syndrome 55 NPY gene 55 telomere length 55 epigenetically 55 fungal genomes 55 tumor suppressor gene 55 microsatellite markers 55 Y chromosomal 55 kinases 54 MAPK pathway 54 NFKBIA 54 histone modification 54 mutant protein 54 INF2 54 dizygotic twins 54 susceptibility locus 54 PARP inhibition 54 allelic variation 54 array CGH 54 MLL gene 54 HMGA2 gene 54 protein encoded 54 HPV# 54 promoter methylation 54 GBA mutations 54 causative mutation 54 genes predisposing 54 homozygous 54 TMPRSS2 ERG fusion 54 genetic mutation 54 non coding RNAs 54 human leukocyte antigen 54 phenotypic 54 phenotypic differences 54 Genotypes 54 chromosome aberrations 54 malaria parasite genome 54 indel 54 euthymic patients 54 coding exons 54 platypus genome 54 BRCA1 54 BRAF mutation 54 chromosomes 54 MTHFR gene 54 BRCA2 gene 54 ApoE4 54 lung adenocarcinoma 54 BRCA mutations 54 ApoE4 gene 54 aneuploidy 54 mitochondrial disorders 54 kilobases 54 SMN2 54 HFE gene 54 chromosomal anomaly 54 X chromosome genes 54 HbF 54 microbial genomes 54 centrosome 54 atypical hyperplasia 54 COMT gene 54 SHANK3 54 DICER1 gene 54 miRs 54 number variation CNV 54 sCJD 54 CHEK2 54 RNA molecules 54 KRAS mutations 54 polygenic 54 ribosomal RNA rRNA 54 BRCA2 mutations 54 epilepsies 54 APOE ε4 54 KRAS variant 54 ASDs 54 probands 54 quantitative trait loci 54 CGG repeats 54 GSTP1 54 modifier genes 54 VIPR2 54 K ras mutations 54 Genetic variants 54 FMR1 54 miRNA 54 genomic instability 54 conserved sequences 54 small RNAs 54 Clusterin 54 nucleotide substitutions 54 metabolic abnormalities 54 gene fusions 54 SNCA 54 proteome 54 genomic 54 adenocarcinomas 54 amino acid sequences 54 chromosomal disorders 54 Li Fraumeni 54 LPA gene 54 FXTAS 54 BDNF gene 54 chromatin structure 54 #q#.# deletion syndrome 54 recessive inheritance 54 genotypic 54 MGUS 54 chromosome #p# [002] 54 SCN5A 54 hypermethylated 54 JAK mutations 54 CagA 54 5 hydroxymethylcytosine 54 androgen receptor gene 54 human genome 54 neurodevelopmental disorder 54 DISC1 gene 54 CYP#C# [001] 54 karyotypes 54 nondemented 54 neuroimaging studies 54 nucleotide sequences 54 YKL 54 methylated DNA 54 HLA DQ2 54 chromosomal instability 54 SNP arrays 54 neuropsychiatric disorder 54 epigenetic alterations 54 differentially expressed genes 54 microRNA miR 54 Li Fraumeni syndrome 53 TRIM5 53 mesotheliomas 53 bile acid metabolism 53 alternatively spliced 53 protein coding 53 BCL#A 53 ADAM# 53 KIBRA 53 medulloblastoma 53 mitochondrial 53 underlying pathophysiology 53 HER2 gene 53 CFTR gene 53 FTO variant 53 nonhereditary 53 genomic sequences 53 basal cell nevus syndrome 53 KCNQ1 53 mitochondrial diseases 53 dopamine D4 receptor 53 Mendelian disorders 53 STK# gene 53 vitamin D receptor 53 R#W [002] 53 apolipoprotein E 53 miRNA molecules 53 HLA molecules 53 TP# mutation 53 vertebrate genomes 53 gene amplification 53 synaptic proteins 53 genotyping arrays 53 mutant genes 53 genetic susceptibility 53 SMN2 gene 53 CpG islands 53 chimp genome 53 endophenotypes 53 dbSNP 53 molecular subtypes 53 synuclein 53 gut microbes 53 IDH1 53 GBM tumors 53 PLoS Genetics 53 LRRK2 mutations 53 autoantibodies 53 haplotype map 53 MIF protein 53 defective gene 53 molecular pathways 53 genetic makeup 53 MDM2 53 ERK2 53 DRD2 gene 53 orthologous genes 53 isotype 53 G allele 53 KCNH2 53 genomewide association study 53 rRNA 53 #S rRNA gene 53 homologs 53 MicroRNA 53 MHC genes 53 HMGCR 53 HLA alleles 53 elevated triglyceride levels 53 recessive mutation 53 CpG 53 5 methylcytosine 53 Nature Genetics 53 ADPKD 53 RUNX3 53 recessive mutations 53 HLA DRB1 53 CAG repeats 53 Prox1 53 intergenic regions 53 OGG1 53 MicroRNAs 53 white matter hyperintensities 53 subtypes 53 molecular biomarkers 53 heritable traits 53 placental mammals 53 Kabuki syndrome 53 microRNAs miRNAs 53 KIF6 gene 53 autistic traits 53 adenoma 53 HapMap 53 variant alleles 53 genetic underpinnings 53 chromosome abnormality 53 autism spectrum disorders 53 3'UTR 53 NNRTI resistance 53 Genetic variation 53 folate deficiency 53 neuropsychiatric disorders 53 T1DM 53 presenilin 53 C. neoformans 53 dysbindin gene 53 sequence homology 53 mRNA molecules 53 Genomes Project 53 B7 H3 53 APOE allele 53 ciliopathies 53 lincRNA 53 TAp# 53 isoforms 53 mice lacking 53 SHANK3 gene 53 progranulin 53 microRNA 53 epigenetic markers 53 chromosomal DNA 53 cognitively normal 52 thyrotropin levels 52 mutational 52 cohesin 52 Sanger sequencing 52 clefting 52 protein coding RNAs 52 receptor gene 52 neurofibromatosis type 52 miRNA expression patterns 52 promoter hypermethylation 52 NPM1 mutations 52 TRAF1 C5 52 Single Nucleotide Polymorphisms SNPs 52 TP# gene 52 prognostic markers 52 sortilin 52 adiponectin 52 EBNA1 52 c Myb 52 epigenetic regulation 52 fraternal twin pairs 52 inbred strains 52 endogenous retroviruses 52 eukaryotic 52 GSTM1 gene 52 Jhdm2a 52 monozygotic 52 S#A# [002] 52 molecular abnormalities 52 GPR# [002] 52 GISTs 52 biological pathways 52 karyotype 52 demyelinating diseases 52 untranslated regions 52 genome rearrangements 52 lymphoblastoid cell lines 52 atherosclerotic lesions 52 uPAR 52 uncharacterized 52 p# mutation 52 Genetic variations 52 RBP4 52 phenotypically 52 WAGR syndrome 52 T2DM 52 virulence genes 52 ataxias 52 Fragile X gene 52 dietary intakes 52 UTRs 52 cardiac progenitor cells 52 epistasis 52 causative genes 52 gene deletions 52 cyclin E 52 M. pneumoniae 52 journal Nature Genetics 52 L1 retrotransposons 52 Karayiorgou 52 mitochondrial genes 52 estrogen receptor alpha 52 gonadal hormones 52 MeCP2 gene 52 herpesviruses 52 unmethylated 52 mRNAs 52 eukaryote 52 essential thrombocythemia 52 DRD2 52 nevi 52 parkin gene 52 FUS TLS 52 TSC1 52 viral genomes 52 Fragile X syndrome 52 Arabidopsis genes 52 CYP#C# gene 52 macaque genome 52 eukaryotic genomes 52 transcriptome sequencing 52 Klotho gene 52 BRCA2 mutation 52 generalized vitiligo 52 KLF4 52 SH#B# 52 exome 52 Neuregulin 1 52 mutant gene 52 APOE e4 gene 52 FLT3 52 chromosomal abnormality 52 chromosomal anomalies 52 SOD1 52 WT1 52 Mendelian diseases 52 ependymoma 52 chromosome translocations 52 LRP5 52 cytochrome b 52 genetic aberrations 52 polyploidy 52 methylated 52 proteomes 52 sequenced genomes 52 genetic ancestry 52 megabases 52 autoantibody 52 cystatin C 52 hepatocellular carcinomas 52 noncoding RNA 52 V#F mutation 52 E4 variant 52 uncharacterized genes 52 mutant mouse 52 IRAK1 52 inherited neurological disorder 52 progranulin gene 52 aneuploid cells 52 IGF2 52 p# gene 52 HCMV 52 OCA2 52 genomic imprinting 52 nucleotide 52 CFH gene 52 APOC3 52 epithelial tumors 52 NOMID 52 BMPR2 52 congenital anomalies 52 Drosophila genome 52 splice variant 52 SORL1 gene 52 nucleotide substitution 52 microsatellite instability 52 microbiomes 52 systemic lupus erythematosus SLE 52 mutated BRCA1 52 GRP# 52 homozygotes 52 autosomal dominant disorder 52 Wellcome Trust Case 52 Htt 52 PGRN 52 cellular pathways 52 Hutchinson Gilford progeria 52 breast carcinomas 52 GATA4 52 pathogenic mechanisms 52 GNAQ 52 Alleles 52 neuropilin 52 autism spectrum disorder 51 genetic 51 A. thaliana 51 primary biliary cirrhosis 51 ApoE 51 EAAT2 51 genomic DNA 51 lipoprotein 51 APOA5 51 M. leprae 51 breast cancer susceptibility genes 51 superinfection 51 KLF# 51 GSTT1 51 Akt 51 amino acid substitutions 51 frontotemporal dementia 51 miR 51 messenger RNAs mRNAs 51 overexpression 51 substrate specificity 51 homozygote 51 β amyloid 51 myostatin gene 51 melatonin receptor 51 CCR5 delta# 51 Haplotype 51 MiRNAs 51 JAK2 51 ribosomal protein 51 vimentin 51 epitope 51 BRCA genes 51 DEC2 51 nondiabetic 51 MDR1 51 epigenetic modifications 51 peptide sequences 51 superfamily 51 ortholog 51 variant rs# 51 activating mutation 51 coding genes 51 haplogroup 51 subclinical hyperthyroidism 51 alexithymia 51 X chromosome inactivation 51 PON1 51 Cyclin D1 51 KRAS gene 51 SOD1 gene 51 TP# mutations 51 ERBB2 51 Hedgehog pathway 51 alpha synuclein 51 exome sequencing 51 Autism Consortium 51 cnidarians 51 alpha synuclein protein 51 BRAF gene 51 BRCA mutation 51 allelic variants 51 MAOA gene 51 International HapMap Project 51 chromatin immunoprecipitation ChIP 51 homology 51 endostatin 51 MHC molecules 51 CDH# 51 metabolic syndrome MetS 51 hypomethylation 51 genomic sequence 51 genetic heterogeneity 51 microglial cells 51 ORFs 51 gene encoding 51 bilaterians 51 transposable elements 51 biomarker 51 NSCLC tumors 51 SLC#A# gene [001] 51 infarcts 51 biomarkers 51 astrocytomas 51 Foxp2 51 Joubert syndromes 51 subcellular localization 51 evolutionary conserved 51 Phenotype 51 COMT 51 neurodevelopmental disorders 51 functional polymorphism 51 heterochromatin 51 thrombophilia 51 transcription factors 51 vasopressin receptors 51 fascin 51 proteins encoded 51 histocompatibility 51 FOXP2 51 LKB1 51 subtype 51 MECP2 51 miR #a [002] 51 microbleeds 51 Plasmodium falciparum 51 trisomy 51 amino acid residues 51 codons 51 hereditary hemochromatosis 51 familial hypercholesterolemia 51 amyloid deposits 51 subpopulations 51 gastric carcinogenesis 51 INTERHEART study 51 monogenic diabetes 51 PTP1B 51 eukaryotic cells 51 previously undescribed 51 amino acid substitution 51 brain lesions 51 euchromatin 51 MYCN amplification 51 LDL particle 51 DARPP 51 BRIP1 51 comorbidity 51 HCV infection 51 sarcosine 51 LRAT 51 neoplasms 51 KIF6 51 eotaxin 51 genetic variability 51 osteosarcomas 51 glycoproteins 51 genetic alteration 51 prostate cancer CaP 51 lysosomal storage diseases 51 tumor biopsies 51 neuroblastoma tumors 51 methyltransferases 51 CREBBP 51 Alternative splicing 51 Sjögren syndrome 51 ribonucleic acid RNA 51 ADRB2 51 drug metabolizing enzymes 51 Kari Stefansson CEO 51 H2AX 51 biochemical mechanisms 51 autism spectrum disorders ASDs 51 messenger RNAs 51 guanine G 51 testicular germ cell 51 acetylation 51 genetic sequences 51 FGFR2 gene 51 KRAS oncogene 51 ENPP1 51 WNK1 51 PALB2 gene 51 MetS 51 PKM2 51 SRY gene 51 differential gene expression 51 qRT PCR 51 RNA molecule 51 periodontal pathogens 51 defensin 51 SERT gene 51 clades 51 ccRCC 51 phosphatases 51 glycosylation 51 mitochondrial proteins 51 germline mutation 51 ALK gene 51 CYP#E# gene 51 lymphomas 51 Lp PLA2 51 C#Y mutation 51 granule cells 51 clade B 51 subfamilies 51 paternal lineages 50 DRD4 50 serotonin receptor 50 genetic defects 50 SGK1 50 distinct subtypes 50 mutated K ras 50 NPM1 gene 50 amplicon 50 5 HTT gene 50 evolutionary lineage 50 HLA loci 50 gene duplications 50 prion gene 50 microRNA genes 50 dysglycemia 50 histologic 50 hereditary predisposition 50 tRNA synthetase 50 colorectal polyps 50 apolipoprotein E4 50 FUS1 50 inactivating mutations 50 Argonaute 50 Cytogenetic 50 evolutionary lineages 50 sRNA 50 Hh 50 sequenced genome 50 p#INK#a 50 FGFR3 50 zebrafish genome 50 taxa 50 GBMs 50 cytosine methylation 50 fasting glucose levels