heritable

Related by string. Heritable * * Heritable Bank . highly heritable . heritable traits . heritable trait . heritable disorders . heritable genetic . heritable diseases . heritable component . subsidiary Heritable . Heritable Disorders . heritable variation . moderately heritable . Caledonian Heritable *

Related by context. All words. (Click for frequent words.) 65 monozygotic twins 65 highly heritable 63 polygenic 63 genes predisposing 62 heritability 62 genetic predisposition 62 phenotype 62 gene variants 61 autosomal recessive 61 missense mutations 61 phenotypes 61 aneuploidy 61 Genetic variation 60 genes 60 mosaicism 60 inheritable 60 dizygotic twins 60 MHC genes 60 alleles 60 CHD7 60 gene locus 60 imprinted genes 59 PTPN# 59 spontaneous mutations 59 germline mutations 59 inherited mutations 59 #q# [001] 59 mutation 59 gene variant 59 heterozygotes 59 epigenetic changes 59 maternally inherited 59 APOE gene 59 autosomal dominant 59 genetically inherited 59 DRD2 gene 58 genetic susceptibility 58 phenotypic variation 58 MLH1 58 MC1R 58 genetic 58 dysbindin 58 X chromosome 58 genetic mutations 58 polymorphism 58 receptor gene 58 familial aggregation 58 genetic variant 58 assortative mating 58 heterozygous 58 Mendelian 58 DQB1 * 58 heritable traits 58 heredity 58 BARD1 58 PTEN mutations 58 genetic variants 58 causative genes 58 nongenetic 57 homozygosity 57 polymorphisms 57 evolutionarily conserved 57 aneuploid 57 de novo mutations 57 SRY gene 57 mutations 57 Genetic predisposition 57 gene mutation 57 #q#.# [002] 57 genetic loci 57 MSH2 57 p# mutations 57 gene 57 chromosomal anomalies 57 epistasis 57 PALB2 57 homeobox genes 57 OCA2 57 chromosomal 57 IKZF1 57 CNVs 57 microcephalin 57 OPRM1 gene 57 monogenic 57 autosomal dominant disorder 57 recessive trait 57 alexithymia 56 polyploid 56 spontaneous mutation 56 familial clustering 56 autosomal 56 genetic variation 56 heterozygosity 56 HLA genes 56 APOE4 56 Genetic variants 56 susceptibility genes 56 susceptibility gene 56 heritable trait 56 chromosomal deletions 56 genetic polymorphism 56 DRD4 56 recessive genes 56 FMR1 gene 56 apolipoprotein E gene 56 HNPCC 56 sexually dimorphic 56 genetic abnormality 56 DNA methylation patterns 56 holoprosencephaly 56 rs# [003] 56 mtDNA mutations 56 #q#.# [001] 56 germline 56 mutated gene 56 APOE ε4 56 genetic mutation 56 proband 56 phenotypic expression 56 penetrance 56 HGPS 56 inherited predisposition 56 dizygotic 56 MYH9 gene 56 eusociality 56 PON1 56 sporadic ALS 56 NF1 56 MECP2 gene 55 autosomal dominant inheritance 55 COMT gene 55 genetic alterations 55 APOE genotype 55 linkage disequilibrium 55 LIS1 55 genetic polymorphisms 55 CYP#A# gene 55 #p#.# [001] 55 microdeletion 55 FTO gene 55 HMGA2 55 CNTNAP2 55 rs# [002] 55 dopamine transporter gene 55 MTHFR 55 haplotype 55 #q#.# deletion syndrome 55 gene mutations 55 IL#R 55 neural crest 55 methylation patterns 55 heterozygote 55 chromosomal regions 55 inbred strains 55 MC1R gene 55 chromosomal instability 55 TCF#L# gene 55 G allele 55 sexual dimorphism 55 dopamine receptor gene 55 Klinefelter syndrome 55 autosomes 55 CYP#E# gene 55 genetic variations 55 multigenic 55 genetic trait 55 ontogeny 55 pathophysiological 55 mutant allele 55 androgen receptor gene 55 gene polymorphisms 55 DRD2 55 evolvability 55 TSC1 55 underlying pathophysiology 55 microdeletions 55 HFE gene 55 breast cancer genes BRCA1 54 phenotypically 54 heritable diseases 54 genetic alteration 54 endophenotypes 54 NF1 gene 54 recessive inheritance 54 Fragile X gene 54 MC4R gene 54 hereditary hemochromatosis 54 GABRA2 gene 54 p# mutation 54 NPY gene 54 monozygotic 54 piRNAs 54 behavioral disinhibition 54 LRRK2 gene 54 Angelman syndrome 54 QTLs 54 pathogenic mutations 54 TCF#L# 54 chromosomal rearrangements 54 MAOA gene 54 homozygous 54 HLA DRB1 * 54 loci 54 CALHM1 54 ataxias 54 neuroendocrine 54 KIF6 gene 54 epigenetic modification 54 5q 54 APOE e4 54 chromosome #q# [002] 54 FXTAS 54 deuterostomes 54 genomic imprinting 54 familial pancreatic cancer 54 Heredity 54 IgA deficiency 54 SLC#A# [002] 54 allele frequencies 54 developmental abnormalities 54 CCR5 delta# 54 genotype 54 vasopressin receptors 54 inherited genetic mutations 54 aetiological 54 alpha synuclein gene 54 genetically 54 GSTT1 54 #p#.# [002] 54 apoE4 54 CDKN2A 54 chromosome #q# [001] 54 FGFR2 54 missense mutation 54 aneuploidies 54 genomewide 54 indels 54 PTEN gene 54 Drosophila melanogaster 54 allele 54 MYH9 54 prion strains 54 5 HTTLPR 54 dysregulation 54 mitochondrial gene 54 TP# mutation 54 chromosome deletion 54 autistic traits 54 BRCA1 mutations 54 genotypic 54 Hsp# [001] 54 allelic variation 54 neuroligins 54 Meckel Gruber 54 ApoE 54 gene APOE 53 filaggrin gene 53 leptin receptor 53 IGF2 53 Li Fraumeni syndrome 53 synaptic function 53 WNK1 53 homozygote 53 #p# [001] 53 chromosome abnormality 53 selfing 53 virulence genes 53 SNPs 53 HLA B# 53 ABCB1 gene 53 CYP#D# gene 53 MAOA 53 D. melanogaster 53 metabolic abnormalities 53 RUNX3 53 Hox gene 53 HMGA2 gene 53 chromosome #q 53 Rb gene 53 MC4R 53 dominantly inherited 53 recessive mutations 53 #q# [002] 53 APOE4 gene 53 Sonic Hedgehog 53 FASPS 53 heritable component 53 chromosomal abnormalities 53 causally linked 53 IGF1 53 rs# [004] 53 suppressor gene 53 chromosome #p# [001] 53 intronic 53 epigenetic alterations 53 miRNA expression 53 genetic abnormalities 53 hippocampal function 53 genes BRCA1 53 orthologs 53 maladaptive 53 LPA gene 53 Leydig cell 53 cryptorchidism 53 Genetic mutations 53 conserved sequences 53 genetic makeup 53 TP# gene 53 BRCA1 gene 53 protein encoded 53 HbF 53 neurobiological 53 sphingolipid 53 Dysregulation 53 prefrontal cortical 53 A. thaliana 53 chordates 53 Genetic variations 53 monozygotic twin 53 metazoan 53 Chromosomal 53 Genes 53 APOE 53 Hashimoto thyroiditis 53 HLA DRB1 53 Wnt#b 53 genetic predispositions 53 estrogen metabolism 53 granule cells 53 CHEK2 53 odorant receptor 53 paraneoplastic 53 GSTM1 53 ribosomal proteins 53 nonhereditary 53 neuropsychiatric disorder 53 mutated genes 52 Alu elements 52 karyotype 52 maternally transmitted 52 LKB1 52 ApoE gene 52 circadian clock genes 52 UGT#B# 52 genetic defects 52 metabolizing enzymes 52 gene variation 52 miRNAs 52 premorbid 52 CFTR gene 52 polyploids 52 H#K#me# 52 SORL1 gene 52 DARPP 52 recessive genetic 52 narcolepsy cataplexy 52 outcrossing 52 Cowden syndrome 52 epigenetic modifications 52 neurodevelopmental 52 haplotypes 52 orthologous genes 52 mice lacking 52 BDNF gene 52 MEF2A 52 prion gene 52 chromosomal alterations 52 eukaryote 52 polyploidy 52 mammary gland tumors 52 lactase persistence 52 STAT4 52 disease NAFLD 52 nicotinic receptor 52 gene DRD4 52 gametophyte 52 epigenetic 52 genes encoding 52 IL#B gene 52 apoE 52 C#Y 52 presenilin 52 allelic 52 genotypes 52 VHL gene 52 karyotypes 52 causal pathway 52 NOD2 52 affective psychoses 52 mutant gene 52 aberrant methylation 52 prodynorphin 52 serotonin transporter gene 52 genetic defect 52 SMAD4 52 Apert syndrome 52 apolipoprotein E APOE 52 neurodevelopmental disorder 52 AVPR1A 52 chromosomal rearrangement 52 chromosomal disorders 52 dysregulated 52 LRP5 52 somatic mutation 52 recessive gene 52 chromosomal translocations 52 nondemented 52 TMEM#B 52 methylenetetrahydrofolate reductase 52 exfoliation glaucoma 52 quantitative trait loci 52 non coding RNA 52 progerin 52 DLC1 52 familial ALS 52 hereditary 52 SOD1 protein 52 MeCP2 gene 52 mutational 52 chromosomal anomaly 52 mutant alleles 52 Activating mutations 52 TRIM5 52 Leydig cells 52 SHANK3 52 epigenetically 52 cybrid 52 DISC1 52 hypermethylated 52 TOP2A 52 PTEN protein 52 DAT1 52 predisposing factor 52 CNTNAP2 gene 52 COMT 52 TYMS 52 genetic determinants 52 mitochondrial mutations 52 neural substrates 52 SLC#A# gene [001] 52 BRIP1 52 mutant genes 52 ploidy 52 genetic markers 52 gut microbes 52 herpesviruses 52 DRD4 gene 52 testicular germ cell 52 FGFR2 gene 52 metazoans 52 UGT#A# * 52 genetically predetermined 52 sexually reproducing 52 somatic mutations 52 epigenetic reprogramming 52 Dpp 52 germline cells 52 ABCB1 52 radial glia 52 hypermethylation 52 APOL1 51 5 HTT gene 51 heritable variation 51 chromosome #q#.# [001] 51 GSTP1 51 CYP#C# gene 51 Clusterin 51 meiotic recombination 51 sequence homology 51 VNTR 51 reproductively isolated 51 nucleotide substitution 51 Neuregulin 1 51 body fatness 51 PrPC 51 functional polymorphism 51 fruitflies 51 multifactorial 51 chromosomal abnormality 51 pathophysiologic 51 SORL1 51 rs# [001] 51 amphioxus 51 ultraconserved elements 51 NR#A# 51 Bardet Biedl Syndrome 51 gene MECP2 51 paralogs 51 KIBRA 51 giant danio 51 Heterozygous 51 homozygotes 51 miRNA genes 51 T. vaginalis 51 Meckel Gruber syndrome 51 MLL2 51 vasopressin receptor 51 paternally inherited 51 mitochondrial disorders 51 G#S mutation 51 bile acid metabolism 51 ZNF# 51 gallstone disease 51 cognitive affective 51 epigenetic inheritance 51 evolutionarily 51 nucleotide sequence 51 gastric carcinomas 51 PRNP 51 morphological 51 parthenogenetic 51 CYP# [002] 51 telomere maintenance 51 mammalian genome 51 mtDNA 51 fewer dopamine receptors 51 KLF4 51 Heritability 51 nonidentical 51 JAK2 mutation 51 ENPP1 51 ectopic expression 51 LRRK2 mutations 51 FGFs 51 dysgenesis 51 Hypothalamic 51 aY chromosome 51 CYP#B# 51 deleterious mutations 51 hyperinsulinemia 51 transcriptional coactivator 51 TCF4 51 homologs 51 incomplete penetrance 51 TGFBR1 * 6A 51 COL#A# 51 apoC III 51 APOE allele 51 micro RNAs 51 Dwarfism 51 transcriptional regulation 51 NR#A# gene 51 cerevisiae 51 FTLD 51 metabolizing enzyme 51 mitochondrial dysfunction 51 motor neuron degeneration 51 Neuronal 51 HOX genes 51 IDH1 51 neurological abnormalities 51 nephronophthisis 51 Lamarckian 51 GSTM1 gene 51 hyper IgE syndrome 51 VIPR2 51 KIAA# 51 Male pattern baldness 51 apolipoprotein E 51 INF2 51 SMN1 51 Foxp2 51 mammary stem cells 51 microsatellite instability 51 meadow vole 51 serotonin transporter 51 CHRNA5 gene 51 chromosome rearrangements 51 neoplastic 51 outbred 51 neuroanatomical 51 insulin resistance 51 GBA mutations 51 gene polymorphism 51 CDH1 51 Wolbachia 51 Homozygous 51 DNMT1 51 olfactory receptor 51 p# MAPK 51 adiponectin 51 Germline 51 Personality traits 51 amyloid peptide 51 genetically identical 51 FOXP2 gene 51 CagA 51 glycosylated 51 allelic variants 51 mammalian brains 51 DLX5 51 APOC3 51 LQTS 51 evolutionary conserved 51 SCA5 51 C. neoformans 51 susceptibility locus 51 intron 51 BRCA2 mutation 51 homeobox gene 51 phenotypic 51 metaplasia 51 RCAN1 51 major histocompatibility complex 51 Notch1 51 ApoE4 51 reciprocal altruism 51 KRAS oncogene 51 K ras gene 51 Phytophthora species 51 plasma lipid 51 malignant transformation 50 frameshift mutation 50 Prevotella 50 subfertility 50 sCJD 50 situs inversus 50 PDGFR 50 Brain derived neurotrophic 50 Froguel 50 monophyletic 50 hypothalamic pituitary 50 KCNQ1 50 bilaterians 50 neural crest cells 50 globin genes 50 synuclein 50 Pten 50 digest lactose 50 TGFBR1 50 subclinical hyperthyroidism 50 M. pneumoniae 50 masculinization 50 Lafora disease 50 ribosomal protein 50 p#INK#a 50 genetics 50 BRCA2 gene 50 allele frequency 50 GABRA2 50 colugos 50 cerebellar 50 histone modifications 50 folate metabolism 50 chromosome abnormalities 50 moderately heritable 50 genomic instability 50 subclinical 50 heritable genetic 50 hepatic lipase 50 X chromosomes 50 miR #a [001] 50 Mitochondrial 50 CETP VV 50 CHD5 50 TACI mutations 50 GNAQ 50 DICER1 50 chaperone proteins 50 RAR beta 50 cytochrome b 50 autosomal recessive disease 50 nonsense mutations 50 cis regulatory 50 tumor suppressor gene 50 Bardet Biedl syndrome 50 modifier genes 50 chromosome 50 eukaryotic cell 50 tumor suppressor protein 50 X. laevis 50 nongenetic factors 50 #q# deletion 50 DRB1 50 LDL receptor 50 pathogenetic 50 metabolic enzymes 50 CYP#C# [002] 50 caveolin 50 orthologous 50 Ets2 50 noncoding RNAs 50 genetic syndromes 50 sortilin 50 leaky gut 50 homologous chromosomes 50 histone modification 50 multigene 50 mitochondrial defects 50 #p# [003] 50 Neuroticism 50 Neurofibromatosis type 50 progranulin 50 hereditary predisposition 50 Chlamydia pneumoniae 50 mitochondrial genome 50 chordate 50 folate deficiency 50 relatedness 50 inactive X chromosome 50 promoter methylation 50 autophagic 50 EF Tu 50 parkin gene 50 vitamin D receptor VDR 50 SLC#A# [001] 50 Drosophila 50 gonadotropins 50 TP# mutations 50 D2 receptors 50 genetic variants associated 50 evolutionarily novel 50 Hh pathway 50 genetic relatedness 50 apolipoprotein E4 50 etiologic agent 50 methylation 50 genetic recombination 50 epigenetic regulation 50 nucleus Chinnery 50 MTHFR gene 50 Socioeconomic status 50 Nf1 50 genomic variation 50 NAFLD 50 ERK signaling 50 myeloproliferative 50 Bacteroides 50 Volvox 50 airway hyperresponsiveness 50 protein isoforms 50 Y chromosomal 50 Hutchinson Gilford progeria 50 MetS 50 MLL gene 50 cyclin E 50 thyrotropin levels 50 hypothalamic 50 mammalian species 50 β amyloid 50 inherited maternally 50 phylogenetically 50 regulates gene expression 50 germline mutation 50 testicular tumors 50 internalizing disorders 50 eusocial 50 recessive mutation 50 chromosomal aberrations 50 schizotypal 50 tyrosine phosphorylation 50 telomere dysfunction 50 BMAL1 50 hydrolase 50 pilocytic astrocytomas 50 FGF2 50 SCN5A 50 Klotho gene 50 biogenesis 50 nephron 50 unmutated 50 MSH6 50 causal variants 50 KRAS gene 50 Telomere length 50 WAGR syndrome 50 subfamily 50 prokaryote 50 constitutively active 50 beta1 integrin 50 zygotic 50 axon guidance 50 hamartomas 50 pulvinar 50 repeat allele 50 Kufs disease 50 inherit predisposition 50 genetic imprinting 50 encodes protein 50 unmethylated 50 uncharacterized genes 50 dopamine D4 receptor 50 ortholog 50 neurobiological basis 50 serum BDNF 50 Treg cell 50 protein kinase C 50 terrestrial vertebrates 50 cytopathic 50 Rh factor 50 GATA4 50 auditory neuropathy 50 leptin receptors 50 Foxp3 50 placental mammals 50 neuroD2 50 CC genotype 50 Jhdm2a 50 diploid 50 temper dysregulation disorder 50 monocots 50 salivary amylase 50 Pol IV 50 IUGR 50 dopamine signaling 50 DICER1 gene 50 phenotypic variability 49 mRNA expression 49 ovarian dysfunction 49 neurodevelopment disorder 49 ALK gene 49 NFKBIA 49 sympatric speciation 49 ectodermal dysplasia 49 atopic 49 noncoding regions 49 ciliated 49 cerebellar hypoplasia 49 p# activation 49 Oxidative stress 49 FMR1 49 APOA5 49 APOE e4 gene 49 SNP rs# [001] 49 neurofibromatosis type 49 etiologic 49 c KIT 49 personality traits 49 yeast Saccharomyces cerevisiae 49 prepubertal 49 homolog 49 genetically predisposed 49 TMPRSS2 ERG fusion 49 causative gene 49 centrosome 49 untranslated regions 49 Wernicke Korsakoff syndrome 49 genetic traits 49 epigenetic mechanisms 49 airway remodeling 49 chromosome #p#.# 49 bacterial virulence 49 missense 49 normal karyotype 49 thymine 49 SLC#A# gene [002] 49 mGluR 49 postnatally 49 CYP#D# 49 circadian genes 49 inheritable genetic 49 chromosomal disorder 49 dysbindin gene 49 transgenic mice expressing 49 embryonic tissues 49 FOXP2 49 chronicity 49 alanine 49 PI3K signaling 49 calcium homeostasis 49 genes CYP#C# 49 gene duplications 49 acetylation 49 LMNA 49 synaptogenesis 49 regulator CFTR gene 49 heterotaxy 49 COX2 49 ontogenetic 49 hypothalamic pituitary adrenal axis 49 Brugada syndrome 49 Sox9 49 CEACAM1 49 preeclamptic 49 amino acid substitution 49 epigenetic silencing 49 psychotic illnesses 49 brain lesions 49 neuronal dysfunction 49 causative mutations 49 epithelial tissues 49 leptin deficiency 49 KCNE2 49 primordial germ cells 49 catechol O methyltransferase 49 renal fibrosis 49 valine 49 microbiota 49 NPM1 gene 49 behavioral traits 49 haplogroups 49 aldehyde dehydrogenase 49 progranulin gene 49 epigenetic markers 49 fronto temporal dementia 49 adult neurogenesis 49 myopathies 49 efferent 49 AUDs 49 HLA G 49 APOE epsilon 4 49 nucleotide substitutions 49 masculine traits 49 CFH gene 49 microcephaly 49 phenotypic traits 49 haematopoietic 49 KCNH2 49 mammary cancers 49 segmental duplications 49 transcriptional repressor 49 potentially modifiable 49 testis 49 TRAF1 C5 49 thale cress 49 alpha synuclein protein 49 homologues 49 Mitochondrial DNA 49 centromeres 49 androgenic hormones 49 IL#B 49 translocations 49 BRCA2 gene mutation 49 mitochondrial proteins 49 neuritic 49 adiposity 49 single nucleotide polymorphism 49 Argonaute 49 V Leiden 49 shortened telomeres 49 basal forebrain 49 FMRP protein 49 ADAM# 49 gene deletions 49 physiological 49 C#BL/#J 49 cortices 49 androgen signaling 49 mitochondrial 49 Inappropriate activation 49 Y Chromosome 49 mutated BRCA1 49 clusterin 49 methyltransferase 49 G6PD deficiency 49 budding yeast 49 cybrids 49 K ras mutations 49 p tau 49 resistin 49 Apolipoprotein E 49 causative mutation 49 psychobiological 49 KLF# 49 mitochondrial genomes 49 JAK2 enzyme 49 gene expression patterns 49 NPC1 49 neurofibromas 49 modulatory 49 beta globin 49 mitochondrial DNA mtDNA 49 monoclonal gammopathy 49 SCN1A 49 chlamydial infection 49 BRCA2 mutations 49 atopy 49 undiagnosed celiac disease 49 Chlamydomonas 49 Adiponectin 49 transcriptional regulators 49 mammalian embryos 49 peroxisome 49 lymphocytic 49 POMC gene 49 gene encoding 49 retinol binding protein 49 ectoderm 49 primate lineage 49 μ opioid receptor 49 transgene expression 49 neurodevelopmental disorders 49 TOP2A gene 49 oligodendrogliomas 49 endogenous retroviruses 49 Joubert syndromes 49 lateralized 49 euthymic patients 49 NNRTI resistance 49 somatic 49 Frizzled 49 R#W [002] 49 Toxoplasma 49 biological predisposition 49 thale cress Arabidopsis thaliana 49 basal ganglia 49 previously undescribed 49 TOMM# 49 androgen receptor AR

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