Related by context. All words. (Click for frequent words.) 73 genetic loci 69 susceptibility genes 68 genetic variants associated 67 chromosomal regions 67 sporadic ALS 67 PALB2 66 neuroligins 66 FGFR2 66 splice junctions 66 INF2 66 gene loci 66 non coding RNA 65 neurexins 65 causal variants 65 splice variants 65 micro RNA 65 TMEM#B 64 BARD1 64 #q# [001] 64 ZNF# 64 causative genes 64 PTPN# 64 epigenetic regulation 64 mitochondrial DNA mtDNA 64 CNVs 64 genetic variants 64 chromosome #q#.# [001] 64 PICALM 63 chromosome #p#.# 63 missense mutations 63 #q#.# [002] 63 Arabidopsis genes 63 susceptibility gene 63 genetic polymorphisms 63 LRRK2 gene 63 susceptibility loci 63 ORMDL3 63 microdeletions 63 quantitative trait loci 63 gene locus 63 5 hydroxymethylcytosine 63 PIK3CA 63 microcephalin 63 microRNA expression 63 chromosome #q# [001] 62 genomic variation 62 biologic pathways 62 genomewide 62 transcriptional regulation 62 malaria parasite genome 62 chromatin immunoprecipitation ChIP 62 primate genomes 62 gene variants 62 endophenotypes 62 loci 62 chromosome #q# [002] 62 VIPR2 62 histone modifications 62 cellular pathways 62 metabolomic 62 somatic mutations 62 phenotypic differences 62 mRNA transcripts 62 #p#.# [001] 62 #p# [001] 62 spontaneous mutations 62 Wnt signaling pathway 62 QTLs 62 retinoid X 62 haplotype map 62 RNA sequences 62 lincRNAs 62 micro RNAs 62 Single Nucleotide Polymorphisms SNPs 62 intronic 61 A3 adenosine receptor 61 IL#R 61 protein kinases 61 homologs 61 chromosomal translocations 61 genes encoding 61 chromosome #q 61 DNA methyltransferases 61 SNP rs# [001] 61 underlying molecular mechanisms 61 KIAA# 61 chromosome #p# [001] 61 LIS1 61 genetic variations 61 #S rRNA 61 epigenetic mechanisms 61 PI3K AKT 61 CDH1 61 alpha synuclein gene 61 gene fusions 61 PGRN 61 tumor suppressor protein 61 TCF#L# 61 virulence genes 61 uncharacterized genes 61 PARP inhibition 61 Autism Genome Project 61 5 hmC 61 exomes 61 genome rearrangements 61 apoE 61 breast cancer subtypes 61 MECP2 gene 61 methylation markers 61 molecular biomarkers 61 TCF#L# gene 61 human microbiome 61 nucleotide sequence 60 polymorphisms 60 tRNA synthetase 60 germline mutations 60 histocompatibility 60 JAK3 60 Apobec3 60 Hakonarson 60 mutated genes 60 MLL2 60 maize genome 60 microRNA molecules 60 inactivating mutations 60 indels 60 CALHM1 60 KCNQ1 60 MYH9 60 GATA4 60 genomic biomarkers 60 clefting 60 gene rearrangements 60 previously undescribed 60 causative mutations 60 #p#.# [002] 60 gene expression assays 60 microRNA biomarkers 60 medulloblastomas 60 NF1 gene 60 molecular abnormalities 60 MYH9 gene 60 Brd4 60 Clusterin 60 microarray experiments 60 mtDNA mutations 60 n cofilin 60 dbSNP 60 NR#A# 60 gene polymorphisms 60 imprinted genes 60 International HapMap Project 60 neuropsychiatric diseases 60 #q#.# [001] 60 DNA methylation patterns 60 phylogenetic analyzes 60 Yamanaka recipe 60 susceptibility locus 60 Genetic variations 60 SH#B# 60 enterotypes 60 STK# gene 60 Alu elements 60 neuropathologic 60 ENPP1 60 chromosome rearrangements 60 epigenetic alterations 60 genetic determinants 60 tRNA synthetases 60 γ secretase 60 SLITRK1 60 sequence homology 60 HLA DQ2 60 Genetic variants 60 CHD7 60 phenotypic variation 60 ABCB1 60 segmental duplication 60 miRNA expression 60 LPA gene 60 androgen receptor gene 60 previously uncharacterized 60 CagA 60 noncoding RNAs 60 drug metabolizing enzymes 60 Akt3 60 protein encoded 59 RNA binding 59 chromatin immunoprecipitation 59 validate biomarkers 59 homeobox gene 59 intergenic regions 59 APOL1 59 FGFs 59 monogenic 59 USP# 59 mammalian genomes 59 epigenetic changes 59 gene expression patterns 59 genomewide association studies 59 familial ALS 59 HDACs 59 microbial genomes 59 phenotypic traits 59 ubiquitin ligases 59 methylation patterns 59 intergenic 59 maternally inherited 59 posttranslational modifications 59 transcriptional regulators 59 gene expression profiles 59 dysbindin 59 LDL receptor 59 proteins encoded 59 RRM1 59 modifier genes 59 chromatin structure 59 fungal genomes 59 OPHN1 59 HLA genes 59 multiprotein complex 59 causative gene 59 amino acid sequences 59 mutational analysis 59 CDKN2A 59 Karayiorgou 59 SIRT1 gene 59 VHL gene 59 epigenetic modification 59 generalized vitiligo 59 serine protease 59 transcriptomes 59 LRRK2 59 GPR# [002] 59 mRNA sequences 59 protein isoforms 59 potent inhibitors 59 tyrosine kinases 59 microbial genome 59 CCL#L# 59 ALK mutations 59 biomarker identification 59 engineered RAP peptides 59 TACI mutations 59 genetic markers 59 pathogenic mechanisms 59 noncoding RNA 59 primary cilia 59 miRNAs 59 FGFR1 59 rs# [001] 59 Arabidopsis genome 59 p#/CBP 59 Syllego system 59 biological pathways 59 transgenic mouse models 59 aCGH 59 IGFBP2 59 evolutionarily conserved 59 metabolomic profiles 59 SCN5A 59 genetic modifiers 59 hypermethylated 59 ribonucleic acids 59 orthologs 59 genomic alterations 59 exome sequencing 59 YKL 58 activate SIRT1 58 SNPs pronounced snips 58 p# mutations 58 sortilin 58 apoE4 58 microRNAs miRNAs 58 CCR3 58 CYP#C# [002] 58 ncRNA 58 protein misfolding 58 IDH1 58 genetically mapped 58 methylated DNA 58 molecular subtypes 58 aneuploidies 58 hypermethylation 58 HER2 HER3 58 HLA DRB1 58 miR #b [002] 58 cell signaling pathways 58 breast cancer genes BRCA1 58 Drosophila genome 58 paralogs 58 multisensory integration 58 MTHFR 58 mutations 58 microdeletion 58 body louse genome 58 evolutionary conserved 58 amyloidogenic 58 epigenetic markers 58 pathogenic mutations 58 chromosome #p# [002] 58 genetic polymorphism 58 PAR1 58 mitochondrial gene 58 Hinxton UK 58 Fibroblast Growth Factor Receptor 58 serine proteases 58 selective antagonists 58 targeted resequencing 58 HLA alleles 58 inherited mutations 58 SLC#A# [002] 58 CENP E 58 CNTNAP2 58 luminal cells 58 TGFBR1 * 6A 58 autosomal 58 ChIP chip 58 bisulfite sequencing 58 3'UTR 58 platypus genome 58 phosphorylates 58 PTEN mutations 58 histone acetylation 58 monozygotic twins 58 VKORC1 58 genetic mutations 58 KLF4 58 FGFR3 58 neuroligin 58 metabolic enzymes 58 GPC5 58 vimentin 58 synthetases 58 WTCCC 58 coding sequences 58 array CGH 58 Phylomer ® 58 folate metabolism 58 rs# [004] 58 short hairpin RNAs 58 cis regulatory 58 multigene 58 viral genomes 58 GSTP1 58 kinome 58 yeast genome 58 prognostic markers 58 virulence determinants 58 genetic underpinnings 58 MAPK pathway 58 lipoprotein metabolism 58 cytosine methylation 58 STK# [002] 58 ankyrin repeat 58 genotypic 58 STAT4 58 Gene Ontology terms 58 kidney urologic 58 #p# [003] 58 untranslated regions 58 UTRs 58 prostate carcinogenesis 58 chromosomal alterations 58 substrate specificity 57 topoisomerases 57 colonic mucosa 57 DNA rearrangements 57 molecular pathway 57 clusterin 57 segmental duplications 57 tumor suppressor genes 57 Transcription factors 57 transcriptome sequencing 57 Li Fraumeni 57 promoter methylation 57 alternative splicing 57 histone modification 57 genes BRCA1 57 ribosomal protein 57 ribosomal RNA rRNA 57 nicotinic receptor 57 genetic biomarkers 57 ribonucleic acid RNA 57 mutant genes 57 noncoding 57 TRAF1 C5 57 Consortium ICGC 57 K ras mutations 57 ribosomal proteins 57 nicotinic receptors 57 molecular biomarker 57 COX enzymes 57 Dr. Pasinetti 57 TLR8 57 EMBL EBI 57 WDR# 57 causal pathways 57 haplotypes 57 glycolipid 57 fibrocytes 57 ERBB2 57 cathepsins 57 SILAC 57 cell adhesion molecule 57 LRP5 57 Six3 57 adipogenic 57 VEGF receptor 57 druggable targets 57 gene expression microarrays 57 genetic locus 57 LMNA 57 chemokine receptor 57 recombination hotspots 57 miRNA genes 57 IL#B 57 biochemical mechanisms 57 #S ribosomal RNA 57 CpG island 57 PI3 kinase 57 genes 57 epigenomic 57 CHRNA5 57 hypomethylation 57 SMAD4 57 fruitfly Drosophila 57 THR beta agonist 57 genomic rearrangement 57 proteomes 57 uPAR 57 CXCL5 57 NS4B 57 microRNAs 57 HbF 57 bacterial genomes 57 DNA demethylation 57 HHMI investigator 57 miRs 57 single nucleotide polymorphism 57 microarray gene expression 57 mitochondrial dysfunction 57 M. pneumoniae 57 miRNA molecules 57 molecular pathways 57 Neuregulin 1 57 embryonic germ 57 C1q 57 functional polymorphism 57 Ets2 57 protein phosphorylation 57 secreted proteins 57 FLT3 57 eukaryotic genomes 57 small molecule modulators 57 bioinformatic analysis 57 Kinases 57 BRIP1 57 genomic proteomic 57 SNP arrays 57 MAP kinases 57 JAK2 mutation 57 quantitative proteomics 57 tyrosine kinase receptor 57 ncRNAs 57 C#T [002] 57 SOD1 gene 57 riboswitches 57 zebra finch genome 57 DLX5 57 C#Y 57 SIRT3 57 transmembrane receptor 57 UGT#B# 57 gastric carcinogenesis 57 serine threonine kinase 57 allelic variation 57 genomic loci 57 familial clustering 57 coding exons 57 NEDD9 57 Drosha 57 Janus kinase 57 vitamin D receptors 57 eotaxin 57 narcolepsy cataplexy 57 tyrosine phosphorylation 57 RNA splicing 57 microbiomes 57 FTLD 57 HDAC3 57 linkage disequilibrium 57 genes CYP#C# 57 ADAM# 57 genomewide association study 57 phenotypes 57 NPM1 57 RNA transcripts 57 DLC1 57 HLA markers 57 BGI Shenzhen 57 predictive biomarkers 57 phenotyping 57 neurodevelopmental disorders 57 RNAi therapeutic targeting 57 mutated K ras 57 bile acid metabolism 57 DQB1 * 57 glycan 57 hedgehog signaling pathway 56 regulates gene expression 56 genetic variation 56 CYP#D# gene 56 cyclin E 56 PITX2 56 signaling cascades 56 ALK gene 56 proteomics bioinformatics 56 synaptic proteins 56 genomic deletions 56 PCA3 gene 56 histone demethylase 56 MEF2A 56 synuclein 56 HLA B# 56 protein tyrosine phosphatase 56 Fas ligand 56 pathophysiological 56 galectin 56 subcellular localization 56 HMGCR 56 prion strains 56 chromosomal aberrations 56 haplogroups 56 meganuclease 56 TLE3 56 IKZF1 56 immunoregulatory 56 neuropsychiatric disorders 56 human leukocyte antigens 56 alpha7 56 ubiquitin ligase 56 CDH# 56 sigma receptors 56 herpesviruses 56 perilipin 56 WNK1 56 acetylation 56 tau aggregates 56 G Protein Coupled 56 intracellular signaling pathways 56 neurexin 56 Wwox 56 nucleic acid sequence 56 pre mRNA splicing 56 Th# cells 56 doublecortin 56 CGEMS 56 chromosomal instability 56 beta lactamases 56 molecular markers 56 MAPCs 56 immunoregulation 56 muscular dystrophies 56 glycoproteins 56 LRAT 56 bNAbs 56 exons 56 BRAF V#E 56 proteomic analysis 56 DARPP 56 exome 56 biomarkers 56 Rosetta Genomics microRNA 56 comparative genomic hybridization 56 preclinically 56 amino acid substitutions 56 comparative genomic 56 pharmacodynamic biomarkers 56 KIF6 gene 56 allelic 56 genotype phenotype 56 alpha synuclein protein 56 rs# [002] 56 Cancer Genome Project 56 cDNAs 56 E3 ubiquitin ligase 56 S#A# [002] 56 transmembrane proteins 56 MLH1 56 differentially expressed proteins 56 centromeres 56 transcriptional profiling 56 CD# CEA 56 microRNA miR 56 #S rRNA gene 56 APOE e4 56 melanocortin receptors 56 ARID1A 56 Cathepsin B 56 ankyrin B 56 studies GWAS 56 miRNAs miR 56 sCJD 56 MIF protein 56 ependymomas 56 biologic pathway 56 histone H4 56 IgA deficiency 56 homologues 56 proto oncogene 56 ABCB1 gene 56 ligand binding 56 etiologic 56 myelin repair 56 cytogenetic 56 MALAT1 56 endogenous retroviruses 56 B Raf 56 EGFR mutations 56 ChIP seq 56 MSH2 56 PML RARA 56 P#X# 56 subcellular compartments 56 neuroinflammation 56 HLA molecules 56 heterodimers 56 eukaryotic organisms 56 telomere DNA 56 biochemical pathways 56 lymphangiogenesis 56 molecular pathology 56 ChIP Seq 56 salivary proteins 56 sRNA 56 OGG1 56 mitochondrial disorders 56 genotyping arrays 56 MTHFR gene 56 multiplex assay 56 SORL1 gene 56 SNPs 56 bioinformatic 56 miRNA expression profiles 56 virulence factors 56 Genizon 56 NS5A 56 differentially regulated 56 mRNA molecules 56 immunoglobulin genes 56 progranulin gene 56 diagnostic biomarker 56 intracellular signaling 56 genomic variants 56 PB1 F2 56 R#W [002] 56 apoptotic pathway 56 Genetics Consortium 56 nucleolar 56 prokaryotic 56 number variation CNV 56 intercellular signaling 56 toxicogenomic 56 heterologous expression 56 isotypes 56 airway remodeling 56 metazoan 56 Li Fraumeni syndrome 56 genetic abnormalities 56 Bardet Biedl Syndrome 56 antibody reagents 56 alleles 56 familial pancreatic cancer 56 filoviruses 56 diagnostic biomarkers 56 beta amyloid peptides 56 BRAF mutation 56 CRISPR Cas 56 beta1 integrin 56 CHAVI 56 Skp2 56 #q# deletion 56 gene APOE 56 TCF4 56 KRAS mutations 56 cAMP signaling 56 p# biomarker 56 ribosomal DNA 56 serpin 56 forkhead 56 inbred strains 56 ortholog 56 chromosomal deletions 56 NPHP 56 LRRK2 mutation 56 transgenic mouse model 56 protein coding RNAs 56 tumor suppressors 56 BCL#A 56 Cytomegalovirus CMV 56 antisense inhibitors 56 Meckel Gruber 56 epigenomics 56 mammalian organisms 56 FGF2 56 viral pathogenesis 56 Notch signaling pathway 56 ADAMTS# 56 human proteome 56 SNP rs# [002] 55 cytokine receptor 55 miR #a [001] 55 oncogenesis 55 adrenergic regulation 55 cholesterol metabolism 55 nicotinic alpha 7 55 phosphate S1P 55 de novo mutations 55 epigenome 55 KRAS oncogene 55 genomic instability 55 HG PIN 55 outer membrane proteins 55 lymphoblastoid cell lines 55 protein homeostasis 55 microsatellite markers 55 paternally inherited 55 transcriptomics 55 Htt 55 metalloprotease 55 GPCR targets 55 GnRH neurons 55 protein kinase C 55 Kohwi Shigematsu 55 chromosomal anomalies 55 phosphatases 55 beta globin gene 55 Eg5 55 IRF6 55 A. thaliana 55 GPx 55 interactome 55 siRNA knockdown 55 genomics proteomics 55 APOE genotype 55 orthologous 55 clade B 55 chromosomal rearrangement 55 subfamilies 55 ErbB3 55 differentially expressed genes 55 receptor ligand 55 ORFs 55 myogenesis 55 GPR# [001] 55 CCR1 55 plasma kallikrein 55 CYP#B# 55 splice variant 55 estrogen receptor alpha 55 genomic sequence 55 Transcriptome 55 sPLA2 55 computational methods 55 tau gene 55 DEC2 55 ENCODE 55 antiviral compounds 55 FGF signaling 55 Protein Kinase C 55 mitochondrial genome 55 PPARγ 55 CCR5 delta# 55 DNA sequences 55 OCT4 55 transcriptome analysis 55 Cytogenetic 55 CHEK2 55 myeloproliferative disorders 55 SNCA 55 Autism Consortium 55 gene mutations 55 neuropilin 55 NSCLC tumors 55 human leukocyte antigen 55 PTEN gene 55 promoter hypermethylation 55 lipoprotein associated phospholipase 55 sphingolipid 55 CSHL scientists 55 intracellular pathways 55 SHANK3 gene 55 EphA2 55 microRNA miRNA 55 MAP#K# 55 MeCP2 protein 55 ABL1 55 resistin 55 methyltransferases 55 c Myb 55 MCPIP 55 N glycan 55 Aravinda Chakravarti 55 major histocompatibility complex 55 ENaC 55 glycosylation 55 RNase L 55 SH2 B 55 immunohistochemical 55 Cancer Genome 55 microglial 55 novel peptides 55 IRAK1 55 NNRs 55 positional cloning 55 NKT cells 55 MC1R 55 5 HTTLPR 55 triterpenoids 55 chimpanzee genome 55 FMR1 gene 55 metabonomics 55 EDRN 55 TSC1 55 antisense oligonucleotides 55 childhood leukemias 55 biomarker 55 L. pneumophila 55 subventricular zone 55 pathogen interactions 55 neuronal cell 55 gamma globin gene 55 genetic alterations 55 inactive X chromosome 55 PTP 1B 55 V3 loop 55 TTR gene 55 enolase 55 homologous chromosomes 55 Dysregulation 55 miR #a [002] 55 CD# ligand 55 observable traits 55 piRNAs 55 GABAB receptors 55 kinase gene 55 PDE#A 55 whole genome genotyping 55 LRRK2 mutations 55 transcriptome profiling 55 PKM2 55 allele frequencies 55 interleukins 55 cohesin 55 CFTR cystic fibrosis transmembrane 55 EVGN 55 palladin 55 dAbs 55 sea urchin genome 55 indel 55 mutant proteins 55 somatic mutation 55 p# mutation 55 viral genome 55 protein conformation 55 protein tyrosine kinase 55 phenotypic expression 55 serine threonine kinases 55 CYP#E# gene 55 lipid metabolites 55 superfamily 55 RAF kinase VEGFR 55 glutamic acid decarboxylase 55 binds selectively 55 ultraconserved elements 55 druggable 55 gene sequences 55 JAK STAT 55 epitopes 55 genotypes 55 CIB1 55 functional annotation 55 sequenced genome 55 therapeutic monoclonal antibody 55 breast cancer metastasis 55 atherothrombosis 55 metabolomics 55 biologic therapeutics 55 retinoic acid receptor 55 modENCODE 55 BAC clones 55 biosynthetic pathways 55 EAAT2 55 Prox1 55 Epstein Barr Virus EBV 55 uncharacterized 55 C. pneumoniae 55 signal transduction pathways 55 peroxisomal 55 plexin D1 55 mutant allele 55 genomic profiling 55 bioinformatic approaches 55 apolipoprotein E 55 CEACAM1 55 cytochromes P# 55 nestin 55 norepinephrine reuptake inhibition 55 Nanobodies ® 55 neuronal stem cells 55 haplotype 55 V#F mutation 55 carboxy terminal 55 APOA5 55 copper zinc superoxide 55 ApoE gene 55 p# MAPK 55 CEP# 55 SNP genotyping 55 distinct subtypes 55 SIgN 55 CpG islands 55 SORL1 55 epigenetic marks 55 TMPRSS2 ERG fusion 55 polymorphism 55 proteomic analyzes 55 variant rs# 55 nucleotide sequences 55 chromosomal abnormalities 55 histone deacetylase HDAC 55 detection reagents 55 heritable disorders 55 amyloid deposits 55 A2 Lp PLA2 55 TP# gene 55 coding genes 55 periodontal infections 55 NPM1 gene 55 demethylase 55 amino acid residues 55 NS4A 55 CXCR7 55 endostatin 55 epigenetic therapies 55 QTL mapping 55 MHC genes 55 ERK2 55 HOTAIR 55 dysbindin gene 55 Nanobody ® 55 haematopoietic 55 eukaryotic 55 nongenetic factors 55 BCR ABL1 55 comparative genomic hybridization CGH 55 H#K#me# 55 methyltransferase 54 OGAP R 54 intron 54 ERK1 54 cystatin 54 podocytes 54 calcineurin 54 neurofibrillary tangles 54 DEAR1 54 chromosome #q#.# [002] 54 histone H3 54 myopathies 54 validating biomarkers 54 #S rDNA 54 genotyped 54 TH# cells 54 MDR1 54 CB2 receptor 54 transmissible spongiform encephalopathies TSEs 54 chromosomal DNA 54 bone marrow mesenchymal stem 54 TLR9 agonists 54 HCV replication 54 pharmacogenetic 54 synapse formation 54 multiplex ligation dependent 54 post transcriptional 54 prodynorphin 54 multigenic 54 APOC3 54 MLL gene 54 vitro pharmacology 54 molecular underpinnings 54 genes predisposing 54 Velculescu 54 HapMap 54 microbial pathogenesis 54 biochemical signaling pathways 54 PKCi 54 PON1 54 genomic