Related by context. All words. (Click for frequent words.) 70 DRD2 69 CYP#E# gene 68 DQB1 * 68 GABRA2 68 CYP#A# gene 68 dopamine receptor gene 68 gene DRD4 67 TCF#L# gene 67 KIF6 gene 67 dopamine D4 receptor 67 DRD4 66 CNTNAP2 66 BARD1 66 CYP#E# 66 GABRA2 gene 66 LPA gene 66 MYH9 gene 66 KIAA# 65 MC4R gene 65 Genetic variants 65 MAOA gene 65 DRD4 gene 65 ApoE gene 65 MTHFR 65 ABCB1 gene 65 apoE4 65 dopamine transporter gene 64 HFE gene 64 CYP#D# gene 64 serotonin transporter gene 64 OPRM1 gene 64 ENPP1 64 HLA DRB1 SE 64 SORL1 gene 64 genes CYP#C# 64 CHRNA5 64 SNP rs# [001] 64 rs# [003] 64 LRRK2 gene 64 proband 64 familial pancreatic cancer 64 PTPN# 64 TCF#L# 64 CYP#C# gene 64 COMT gene 63 APOE ε4 63 CALHM1 63 circadian clock genes 63 MC1R 63 dysbindin 63 chromosome #q#.# [002] 63 BDNF gene 63 5 HTTLPR 63 SLC#A# [002] 63 G allele 63 chromosome #q# [001] 63 KRAS oncogene 63 chromosome #q# [002] 63 5 HTT gene 62 androgen receptor gene 62 CETP VV 62 C#Y 62 APOE4 62 CETP gene 62 gene locus 62 GABA receptor 62 KCNH2 62 SCN1A 62 CNTNAP2 gene 62 H#K#me# 62 receptor gene 62 IL#R 62 CHRNA5 gene 62 AVPR1A 62 hypermethylated 62 ADH1B * 62 HLA DRB1 62 mu opioid 62 Apolipoprotein E 62 LRP5 62 ALDH2 62 intronic 62 G#S [002] 62 nondemented 62 serotonin transporter 62 genetic loci 61 #q# [001] 61 chromosome #p#.# 61 Genetic variation 61 GPC5 61 missense mutations 61 APOE gene 61 susceptibility gene 61 rs# [002] 61 susceptibility locus 61 dopamine D2 receptor 61 apolipoprotein E gene 61 gene APOE 61 GAB2 61 MC1R gene 61 Foxp2 61 rs# [004] 61 prodynorphin 61 Fragile X gene 61 apolipoprotein E4 61 mutant allele 61 narcolepsy cataplexy 61 VKORC1 61 folate metabolism 61 SORL1 61 apolipoprotein E APOE 61 c KIT 61 UGT#A# * 61 MSH2 61 serotonin 2A 61 homozygosity 61 gene polymorphisms 60 polymorphism 60 genes predisposing 60 CCR5 delta# 60 MLL2 60 APOE allele 60 CHEK2 60 NPC1 60 chromosome #q#.# [001] 60 catechol O methyltransferase 60 autosomal recessive disease 60 epigenetically 60 chromosome #q 60 meiotic recombination 60 MHC genes 60 MECP2 gene 60 germline mutations 60 APOC3 60 PDE#A 60 miRNA expression 60 STAT4 60 monozygotic twins 60 metabolizing enzymes 60 LRRK2 mutation 60 ADH1B 60 DAT1 60 APOE genotype 60 ERK signaling 60 CDH1 60 familial clustering 60 microsatellite markers 60 apoC III 60 number variations CNVs 60 MYH9 60 genetic variants associated 60 APOE4 gene 60 fewer dopamine receptors 60 FGFR2 60 KLF4 60 gene polymorphism 60 monozygotic twin 60 NR#A# 60 BRAF V#E 60 NPY gene 60 lysine residues 60 acetylcholine receptor 60 MEF2A 60 metabolizing enzyme 60 Genetic variations 60 aldehyde dehydrogenase 59 #p#.# [001] 59 phenotypic variation 59 vasopressin receptor 59 causal variants 59 AMACR 59 microdeletions 59 HLA DRB1 * 59 TOMM# 59 major histocompatibility complex 59 dopamine transporter 59 ORMDL3 59 variant rs# 59 Monoamine oxidase 59 monogenic 59 CDKN2A 59 APOE e4 59 HLA DQ2 59 ESR1 59 promoter polymorphism 59 synuclein 59 MnSOD 59 PTEN mutations 59 rs# [001] 59 PON1 gene 59 susceptibility loci 59 thyrotropin 59 genetic polymorphism 59 apolipoprotein E 59 IRS1 59 allele frequencies 59 MAOA 59 SNP rs# [002] 59 assortative mating 59 APOE epsilon 4 59 GSTP1 59 chromosomal regions 59 PALB2 59 polymorphisms 59 VIPR2 59 UGT#B# 59 methylation patterns 59 Alu elements 59 microdeletion 59 Brain derived neurotrophic 59 recessive mutation 59 recessive trait 59 chromosome #p# [001] 59 genomewide 59 MLH1 59 epigenetic alterations 59 HLA DR4 59 non coding RNA 59 vasopressin receptors 59 genetic polymorphisms 59 ABCA1 gene 59 #q#.# [001] 59 COX2 59 BRCA1 BRCA2 59 behavioral disinhibition 59 TMEM#B 59 ABCB1 59 heritable 59 KIBRA 59 Apobec3 58 chromatin structure 58 alexithymia 58 dopamine D2 receptors 58 serine threonine kinase 58 nicotinic receptor 58 DNA methylation patterns 58 globin genes 58 TMPRSS2 ERG fusion 58 gene variant 58 repeat allele 58 homozygote 58 cytochrome b 58 MDR1 58 caveolin 58 underlying pathophysiology 58 amyloid ß 58 BMPR2 58 apoE 58 multigenic 58 amyloid plaque formation 58 klotho gene 58 progranulin gene 58 PON1 58 microcephalin 58 segmental duplication 58 subcellular localization 58 human leukocyte antigen 58 microRNA expression 58 neuroD2 58 paternally inherited 58 mammary stem cells 58 beta1 integrin 58 PPARg 58 Clusterin 58 SCN5A 58 histone methylation 58 Froguel 58 promoter hypermethylation 58 TNFAIP3 58 de novo mutations 58 FGFs 58 #S rRNA 58 CDK4 58 cypin 58 D2 receptor 58 telomere lengths 58 neuroligins 58 prefrontal cortical 58 ADRB2 58 ZNF# 58 FKBP# 58 SE alleles 58 alternatively spliced 58 serotonin receptor 58 COL#A# 58 allelic variants 58 perirhinal cortex 58 TGFBR1 * 6A 58 epigenetic modification 58 Fc gamma receptor 58 mutated BRCA 58 ribosomal protein 58 epigenetic changes 58 MTHFR gene 58 PRNP 58 SLC#A# gene [001] 58 autosomal recessive 58 PDZ domain 58 alpha synuclein gene 57 #q# deletion 57 glucocorticoid receptor GR 57 GABAA 57 HLA B# 57 klotho 57 PcG proteins 57 CYP#A# [002] 57 APOL1 57 #p# [003] 57 haplotype 57 C. neoformans 57 C#T [002] 57 inherited mutations 57 transmembrane receptor 57 Histone 57 FOXP2 gene 57 #p# [001] 57 transcriptional repressor 57 ApoE 57 phylogenetically 57 NF1 gene 57 LIS1 57 breast cancer genes BRCA1 57 humanin 57 breast carcinogenesis 57 gene MECP2 57 phenotypes 57 oligomerization 57 alleles 57 VHL gene 57 JAK2 enzyme 57 CXCL5 57 CagA 57 D. melanogaster 57 heterozygous 57 histone acetylation 57 genetic variant 57 DRB1 57 regulates gene expression 57 haplotypes 57 testicular germ cell 57 HbF levels 57 monozygotic 57 deacetylation 57 thyrotropin levels 57 recessive mutations 57 transcriptional silencing 57 ERBB2 57 sexually dimorphic 57 hereditary hemochromatosis 57 R#W [002] 57 GBA mutations 57 DARPP 57 transcriptional activation 57 PcG 57 atypical neuroleptics 57 BCL#A 57 KCNQ1 57 #HT#A receptor 57 MTHFD1L gene 57 heterozygotes 57 bacterial virulence 57 hepatoma 57 C1q 57 CCL#L# 57 GSTM1 gene 57 previously uncharacterized 57 ApoE4 57 segmental duplications 57 fruitflies 57 microRNA molecules 57 Wwox 57 TRIM5 57 SRY gene 57 glutamate signaling 57 intracellular signal transduction 57 HMGCR 57 MiRNAs 57 giant danio 57 CFTR gene 57 VNTR 57 p# mutation 57 SLC#A# [001] 57 LKB1 57 Cathepsin B 57 trans palmitoleate 57 protein isoforms 57 maternally inherited 57 WNK1 56 SNCA 56 KLF# 56 chromosomal rearrangement 56 CYP#B# 56 μ opioid receptor 56 transgenic mouse models 56 FTO gene 56 inbred strains 56 Hutchinson Gilford progeria 56 S. cerevisiae 56 POMC gene 56 SMAD4 56 outbred 56 Sonic Hedgehog 56 HMGA2 56 APOE e4 gene 56 variant alleles 56 mosaicism 56 epistasis 56 PB1 F2 56 MHC molecules 56 autosomal 56 histone modification 56 progressive neurodegenerative disorder 56 mutated K ras 56 serine protease 56 exfoliation glaucoma 56 apolipoprotein 56 Monoamine Oxidase 56 CFH gene 56 cyclin E 56 G#S mutation 56 N Myc 56 nicotine receptor 56 hydrolase 56 RNA binding 56 causative mutations 56 neuropsychiatric disorder 56 penetrance 56 apo E 56 tumor suppressor protein 56 CHD7 56 clade B 56 susceptibility alleles 56 posterior cingulate 56 FADS2 gene 56 5 HT1A 56 RRM1 56 CRISPR Cas 56 5alpha reductase 56 spontaneous mutations 56 MAPK pathway 56 excitatory synapses 56 intergenic 56 MIF protein 56 NAT2 56 transgene expression 56 kinase gene 56 neural progenitor 56 TEL AML1 56 drug metabolizing enzyme 56 histocompatibility 56 tumorigenicity 56 GPR# [002] 56 LDL receptor 56 functional polymorphism 56 NEIL1 56 tumor subtypes 56 HPA axis 56 Leukotriene 56 heterozygote 56 Neuregulin 1 56 circadian genes 56 lipid rafts 56 DRB1 * 56 quantitative trait loci 56 mRNA transcripts 56 Darapladib 56 inactive X chromosome 56 HMMR 56 MC4R 56 mitochondrial DNA mtDNA 56 molecular abnormalities 56 SCD1 56 chemically alters 56 PTEN gene 56 vitamin D receptors 56 SHANK3 56 lactase persistence 56 #q# [002] 56 differential gene expression 56 EGFR gene 56 allele 56 DISC1 gene 56 2 diabetes T2D 56 dopamine signaling 56 GLUT1 56 Oncogenic 56 Lafora disease 56 SHANK3 gene 56 cis regulatory 56 TAp# 56 neuroglobin 56 SMN2 gene 56 glucocorticoid receptors 56 chlamydial infection 56 FMR1 gene 56 NKX#.# 56 autosomal dominant inheritance 56 OCA2 56 gene variants 56 virulence genes 56 COMT 56 ALK gene 56 epigenetic regulation 56 kinesin motor 56 PrPC 56 neurocognitive dysfunction 55 A. thaliana 55 hypothalamic pituitary 55 chromosomal aberrations 55 tau gene 55 IL6 55 protein p# 55 folate deficiency 55 PD# [005] 55 STK# gene 55 IKZF1 55 GPx 55 protein encoded 55 CpG island 55 PTP1B 55 M. pneumoniae 55 p#/CBP 55 APOE e4 allele 55 gene deletions 55 HepG2 cells 55 flavopiridol 55 Nicotine dependence 55 underexpressed 55 genomic variants 55 BRAF gene 55 multigene 55 GSTT1 55 cyclic AMP cAMP 55 adult neurogenesis 55 G6PD 55 GSTM1 55 hereditary predisposition 55 inverse agonist 55 PKMzeta 55 JAK STAT 55 A1 allele 55 fig. S4 55 dehydrogenases 55 gene loci 55 cAMP signaling 55 serotonin transporters 55 indels 55 tumor suppressor PTEN 55 ABL kinase 55 valine 55 chromosomal anomalies 55 constitutively 55 colorectal neoplasia 55 proline rich 55 Foxp3 55 HMGA2 gene 55 nucleus Chinnery 55 ApoE4 gene 55 salivary amylase 55 susceptibility genes 55 lysyl oxidase 55 genome rearrangements 55 lacZ 55 QTLs 55 cysteines 55 Kir#.# 55 kinase domain 55 evolutionarily conserved 55 sporadic ALS 55 FUS1 55 dopamine receptor 55 missense mutation 55 periodontal pathogens 55 basal forebrain 55 effector protein 55 uncharacterized genes 55 ALK mutations 55 Cyclin D1 55 TP# mutation 55 CYP#D# 55 Karayiorgou 55 O methyltransferase 55 fibrillin 1 55 USP# 55 prion gene 55 SOD2 gene 55 SGK1 55 haplogroups 55 sphingolipid 55 variant allele 55 TOP2A gene 55 CYP#C# [002] 55 GABAA receptor 55 IRF6 gene 55 orthologs 55 HMPV 55 AMPA receptor 55 Polymorphism 55 lipid homeostasis 55 C. pneumoniae 55 CC genotype 55 APOA5 55 BRIP1 55 drug metabolizing enzymes 55 C#BL/#J 55 microbiomes 55 pathogenic mutations 55 genes encoding 55 mammalian brains 55 mutant alleles 55 neurexins 55 HOTAIR 55 VMAT2 55 tyrosine phosphorylation 55 CHI#L# 55 polygenic 55 selective antagonists 55 Immunohistochemical analysis 55 ataxias 55 Rap1 55 mammary cancers 55 MECP2 55 leptin receptor 55 Single Nucleotide Polymorphisms 55 somatic mutation 55 pre mRNA splicing 55 splice variants 55 Yamanaka recipe 55 orthologous genes 55 mitogen activated protein kinase 55 familial aggregation 55 synapse formation 55 obesity insulin resistance 55 mitogen activated protein kinases 55 heterozygosity 55 WAGR syndrome 55 RCAN1 55 allelic variation 55 phenotypic expression 55 K ras mutations 55 endophenotypes 55 EP3 receptor 55 Alpha synuclein 55 ribosomal RNA rRNA 55 HLA genes 55 predisposing factor 55 TGF beta pathway 55 Li Fraumeni syndrome 55 myo inositol 55 mtDNA mutations 55 gamma aminobutyric acid 55 proteinases 55 noncoding 55 histone deacetylases 55 coexpression 55 RNA polymerases 55 evolutionary conserved 55 protein kinase C 55 #q#.# deletion syndrome 55 T. vaginalis 55 rRNA 55 protein tyrosine phosphatase 55 vitamin D receptor 55 highly heritable 55 neurodevelopmental disorder 55 noncoding regions 55 gene expression patterns 55 DLC1 55 carotid plaques 55 adipogenic 55 chromosomal translocations 55 proto oncogene 55 DISC1 55 Genetic predisposition 55 linkage disequilibrium 55 NR#A# gene 55 shorter telomere length 55 podocyte 55 retinoid X 55 hypothalamic pituitary adrenal HPA 55 CYP#C# [001] 55 PIK3CA 55 airway hyperresponsiveness 55 micro RNA 55 mutated genes 55 MMP9 55 olfactory receptor 55 noncoding RNA 55 homodimers 55 plasma lipid 55 cytopathic 54 LRP6 54 Igf2 54 DLX5 54 PAK1 54 FTO variant 54 endogenous opioid 54 microglial 54 glutamatergic 54 TRAF1 C5 54 p# mutations 54 COMT genotype 54 UCRs 54 Adiponectin 54 vacuolar 54 squamous cell lung cancer 54 IGF2 54 pleiotropic effects 54 sequence homology 54 kDa protein 54 HSF1 54 FUS protein 54 differentially expressed genes 54 Amino acid 54 chromatin remodeling 54 miRNA genes 54 dopamine receptors 54 CAG repeats 54 dopamine D2 54 inhibit platelet aggregation 54 aberrant methylation 54 histone modifications 54 cryptoxanthin 54 IgA deficiency 54 serum GGT 54 Trypanosoma brucei 54 alpha synuclein protein 54 amine oxidase 54 IRF6 54 tryptase 54 PPARγ 54 alcohol dehydrogenase 54 clinicopathological 54 autosomes 54 promoter methylation 54 SOD2 54 isoenzymes 54 #S ribosomal RNA 54 HGPS 54 Arabidopsis genome 54 estrogen metabolism 54 interferon induced 54 somatic mutations 54 Dpp 54 lymphocyte activation 54 autistic traits 54 NFkB 54 microglial activation 54 Metabolites 54 C EBP alpha 54 T#M 54 Rho GTPases 54 loci 54 receptor gamma 54 euthymic patients 54 aetiological 54 NOD2 54 TRAF1 54 secretory pathway 54 MSMB 54 endogenous ligands 54 anterior pituitary 54 maternally transmitted 54 TOP2A 54 IL#B 54 paralogs 54 cisplatin resistant 54 constitutively expressed 54 cdk5 54 HMGA1 54 kappa opioid receptor 54 ADPKD 54 inhibitory receptor 54 corticosterone levels 54 lincRNA 54 downregulated 54 E#F# 54 metabolic syndrome MetS 54 HLA gene 54 genetically inherited 54 orthologous 54 constitutively active 54 Polymorphisms 54 prostate carcinogenesis 54 chromosomal rearrangements 54 murine models 54 metaplasia 54 paternal lineages 54 transgenic mouse model 54 5 HT1A receptor 54 microsatellite instability 54 Hsp# [001] 54 laforin 54 impaired glucose metabolism 54 FASPS 54 stimulate neurogenesis 54 ankyrin B 54 ncRNAs 54 2D 4D ratio 54 unmethylated 54 Wnt#b 54 methylenetetrahydrofolate reductase 54 Suicidal ideation 54 antisense therapies 54 condensin 54 GABAB receptors 54 modifier genes 54 receptor tyrosine kinase 54 ERalpha 54 polymorphic 54 Prefrontal 54 SLITRK1 54 frameshift mutation 54 mu opioid receptor 54 ploidy 54 TP# gene 54 cholesteryl ester transfer 54 EBNA1 54 Heritability 54 neuropeptide Y NPY 54 HBx 54 clefting 54 receptor molecule 54 amino acid substitutions 54 hypermethylation 54 Genetic mutations 54 bronchoalveolar 54 histone H4 54 HbF 54 mitochondrial mutations 54 perilipin 54 polyadenylation 54 NRF2 gene 54 genetic makeups 54 transmembrane protein 54 CFTR gene mutations 54 chromosomal alterations 54 neuropathologic 54 single nucleotide polymorphism 54 palladin 54 enolase 54 genotype 54 Myostatin 54 neuroendocrine 54 X Chromosome 54 anti inflammatory cytokine 54 GPR# [001] 54 microchimerism 54 dimeric 54 cyclin dependent kinase inhibitor 54 p#NTR 54 TACI mutations 54 NR2B 54 elevated serum ALT 54 homologs 54 bile acid metabolism 54 gene APOE4 54 GATA4 54 TT genotype 54 oxidant stress 54 glycosylated 54 genetic susceptibilities 54 inhibiting COX 54 fraternal twin pairs 54 cagA 54 endogenous estrogen 54 ribosomal genes 54 genotyping arrays 54 inherit predisposition 54 chromatin proteins 54 tumor subtype 54 oxytocin receptor 54 virulence determinants 54 SERT gene 54 sortilin 54 Multivariate analyzes 54 Hashimoto thyroiditis 54 FGF2 54 parkin gene 54 Univariate analysis 54 amyloid cascade 54 glycosyltransferase 54 FXTAS 54 comorbid disorders 54 monoamines 54 protein CETP 54 number variation CNV 54 neuropsychiatric diseases 54 nucleoli 54 chromosome #p# [002] 54 Klotho gene 54 orexin receptors 54 SNPs pronounced snips 54 K ras gene 54 impaired insulin secretion 54 MLL gene 54 messenger RNAs mRNAs 54 AUDs 54 LRRK2 mutations 53 ERa 53 GABAergic 53 neurone 53 Mustanski 53 HNPCC 53 mutation 53 Aldosterone 53 NFTs 53 endoxifen 53 El Sohemy 53 Gleevec inhibits 53 hypomethylation 53 cultured neurons 53 HER2 neu 53 X chromosome inactivation 53 adrenal cortex 53 serum BDNF 53 receptor inhibitor 53 fascin 53 eotaxin 53 neurocognitive impairment 53 miR #b [002] 53 Hp2 2 53 FADS2 53 dizygotic 53 Cryptococcus neoformans 53 miRNA molecules 53 medial prefrontal 53 mitochondrial gene 53 untranslated regions 53 neuroanatomical 53 Treg cell 53 vitamin D receptor VDR 53 peroxisome 53 TSC1 53 coreceptor 53 Dopaminergic 53 MGUS 53 oncogenic transformation 53 ob ob 53 neuro endocrine 53 syntaxin 53 S#A# [002] 53 CYP #D# 53 alpha synuclein toxicity 53 #p#.# [002] 53 epigenetic 53 receptor mediated endocytosis 53 HOX genes 53 calcium homeostasis 53 uPAR 53 prostate cancer CaP 53 gene mutations 53 Arabidopsis thaliana 53 GNAQ 53 epigenetic mechanisms 53 CaM kinase II 53 Androgen receptor 53 sCJD 53 psychobiological 53 circulating estrogens 53 methylated 53 GRP# 53 transgenic mice expressing 53 gene BRCA2 53 condensin II 53 parthenolide 53 invasive lobular 53 alternative splicing 53 Haplogroup 53 morphogen 53 nitrotyrosine 53 WT1 53 fru 53 beta globin gene 53 conditional logistic regression 53 NFKBIA 53 ApoE4 allele 53 receptor subtypes 53 TYMS 53 T2D 53 actin polymerization 53 V Leiden 53 CD#c 53 HLA molecules 53 estrogen receptor alpha 53 lung adenocarcinoma 53 clusterin 53 gene rearrangements 53 Aromatase 53 gene amplification 53 ADAM# 53 extramedullary 53 MYBPC3 53 Neuroticism 53 effector molecules 53 receptor subunits 53 probands 53 gastric carcinogenesis 53 ROP#