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(Click for frequent words.) 84 gene mutation 82 mutation 79 mutated gene 77 genetic defect 76 genetic mutations 73 mutations 73 genetic variant 73 gene mutations 72 defective gene 72 mutant gene 71 gene 71 genetic abnormality 69 gene variant 68 genetic variation 68 mutated genes 68 genetic trait 67 genes 65 genetic variations 65 gene variation 65 BRCA1 gene 65 genetic defects 65 spontaneous mutation 64 genetic alteration 64 gene variants 64 recessive gene 64 genetic abnormalities 63 genetic variants 63 FMR1 gene 63 genetic disorder 63 mutant protein 62 G#S mutation 61 recessive trait 61 mutant genes 61 huntingtin gene 61 recessive genes 61 BRCA2 gene 61 chromosomal abnormality 61 X chromosome 61 genetic predisposition 61 genetic makeup 61 TP# mutation 61 alleles 61 spontaneous mutations 60 mutated protein 60 Fanconi anemia 60 inherited mutations 60 tumor suppressor gene 60 chromosome abnormality 59 recessive mutations 59 allele 59 genetically 59 epigenetic changes 59 genetic 59 mtDNA mutations 59 achromatopsia 59 HGPS 59 ApoE4 gene 59 hereditary disorder 58 genetic alterations 58 sporadic ALS 58 CFTR gene 58 SORL1 58 parkin gene 58 APOE4 58 autosomal recessive 58 enzyme deficiency 58 breast cancer genes BRCA1 58 chromosomal abnormalities 58 microcephalin 58 susceptibility gene 58 progerin 58 mitochondrial mutations 58 CDH1 58 genetic susceptibility 58 HMGA2 58 chromosome 58 herpes viruses 58 Cockayne syndrome 58 genetic markers 58 familial adenomatous polyposis 57 de novo mutations 57 chromosomal defect 57 MC1R 57 BRCA2 mutation 57 mutant alleles 57 APOE gene 57 familial ALS 57 phenotype 57 Li Fraumeni syndrome 57 molecular pathway 57 protein fragment 57 homozygous 57 LRRK2 gene 57 BRAF gene 57 MECP2 gene 57 epigenetic alterations 57 MC1R gene 57 LIS1 57 SOX3 gene 57 susceptibility genes 57 neurodegenerative disorder 57 VHL gene 57 BRCA1 mutation 57 molecular mechanism 57 chromosomal anomaly 56 autosomal dominant 56 IgA deficiency 56 NF1 gene 56 IGF1 56 Fragile X gene 56 BRCA1 mutations 56 missense mutation 56 receptor protein 56 causative genes 56 mitochondrial genome 56 nonsense mutations 56 IGF2 56 BARD1 56 CYP#E# gene 56 germline mutations 56 herpes virus 56 Kufs disease 56 GBM tumors 56 MLL gene 56 BRCA mutations 56 haplotype 56 myotonic dystrophy 56 somatic mutations 56 recessive mutation 56 receptor gene 56 heterozygous 56 heritable 56 ZNF# 56 Akt1 56 BRCA1 56 RUNX3 56 ApoE4 56 huntingtin protein 56 mitochondrial dysfunction 56 progranulin 55 fetal hemoglobin 55 tumor suppressor protein 55 BRCA mutation 55 dyskeratosis congenita 55 medulloblastomas 55 endogenous retroviruses 55 ADPKD 55 progranulin gene 55 mammary cells 55 mosaicism 55 bacterium 55 MIF protein 55 CHD7 55 HLA genes 55 Angelman syndrome 55 prion disease 55 causative gene 55 PTPN# 55 chromosomal alterations 55 Joubert syndrome 55 p# mutations 55 Genetic mutations 55 SMN1 55 SMN2 55 Neuregulin 1 55 Six3 55 chromosomal disorder 55 abnormal hemoglobin 55 Wnt signaling 55 neuroblastomas 55 FASPS 55 SGK1 55 H. pylori 55 retrovirus 55 biochemical signaling pathway 55 pathogenic mutations 55 Dravet syndrome 55 aneuploidies 55 EBV infection 55 ARID1A 54 PALB2 54 protein p# 54 missense mutations 54 degenerative disorder 54 endostatin 54 nonsense mutation 54 HLA B# 54 SOD1 gene 54 enzyme 54 protein encoded 54 lissencephaly 54 mutant allele 54 genes predisposing 54 genomic instability 54 Helicobacter 54 CNVs 54 chromosomal rearrangement 54 NF1 54 genes BRCA1 54 FMRP protein 54 nerve degeneration 54 PTEN gene 54 Prox1 54 HNPCC 54 hypertrophic cardiomyopathy HCM 54 C EBP alpha 54 SMN protein 54 Male pattern baldness 54 primary cilia 54 HFE gene 54 abnormal chromosome 54 chromosomal 54 EZH2 54 epigenetic silencing 54 subtype 54 medulloblastoma 54 tumor suppressor genes 54 FTLD 54 tumors 54 gene p# 54 genotype 54 hereditary deafness 54 toxoplasmosis 54 genetically inherited 54 Fragile X syndrome 54 Epstein Barr virus EBV 54 SOD1 protein 54 autosomal recessive disease 54 germline mutation 54 BRCA genes 54 chromosomal translocations 54 suppressor gene 54 incurable genetic 54 LRAT 54 receptor molecule 54 myostatin gene 54 herpesviruses 54 Peutz Jeghers syndrome 54 micro RNAs 54 mutated 54 genetic disorders 54 autosomal dominant disorder 54 aneuploidy 54 narcolepsy cataplexy 54 BRCA gene 54 anaplastic lymphoma kinase 54 alpha synuclein gene 54 MYH9 gene 54 chromosomal instability 54 apolipoprotein E gene 54 JAK2 mutation 54 gene locus 54 connexin 54 chromosomal aberrations 54 miRNA genes 54 LQTS 54 Brugada syndrome 54 inherited neurological disorder 54 mutated BRCA1 54 ovarian tumors 54 autoantibodies 54 gene expression patterns 54 RPE# 54 apoE4 54 abnormal chromosomes 53 NF2 53 inherited predisposition 53 Toxoplasma 53 mice lacking 53 Leber congenital amaurosis 53 prion proteins 53 abnormalities 53 C1q 53 MEF2A 53 measles virus 53 Plasmodium parasites 53 penetrance 53 GFP gene 53 FTO gene 53 C#Y 53 HbF 53 CCR5 delta# 53 Cryptococcus neoformans 53 breast cancer metastasis 53 gut microbes 53 microRNA molecules 53 holoprosencephaly 53 histone modification 53 colon tumors 53 mtDNA 53 faulty BRCA1 gene 53 chromosome abnormalities 53 familial adenomatous polyposis FAP 53 MeCP2 gene 53 monogenic 53 dopamine receptor gene 53 protein 53 Hashimoto thyroiditis 53 chromosome rearrangements 53 CIB1 53 Lafora disease 53 homozygosity 53 NKT cells 53 parasite 53 BCL#A 53 PTEN mutations 53 Htt 53 TGFBR1 * 6A 53 SORL1 gene 53 p# gene 53 genetic traits 53 Epstein Barr virus 53 GAB2 53 genetic variants associated 53 STAT4 53 MTHFR 53 epigenetic mechanisms 53 brain lesions 53 molecular pathways 53 transcriptional repression 53 aldehyde dehydrogenase 53 MSH2 53 basal cell nevus syndrome 53 trypanosomes 53 apoE 53 Genetic variation 53 congenital disorder 53 SIRT1 gene 53 genetically susceptible 53 multidrug resistance 53 Tay Sachs disease 53 TCF#L# gene 53 herpes infection 53 YKL 53 KCNE2 53 neural tube defect 53 Mitochondrial DNA 53 Genetic mutation 53 KRAS gene 53 JAK2 enzyme 53 TB bacterium 53 Bardet Biedl syndrome 52 G#S [002] 52 abnormal growths 52 polymorphisms 52 mitochondrial DNA mutations 52 CNTNAP2 52 serotonin receptor 52 CNTNAP2 gene 52 familial pancreatic cancer 52 mutant huntingtin protein 52 PrPSc 52 Meckel Gruber 52 imprinted genes 52 MTHFR gene 52 chitinase 52 methylation 52 recessive genetic 52 microdeletion 52 transthyretin 52 genomic imprinting 52 MC4R gene 52 MAOA gene 52 trypanosome 52 SRY gene 52 TP# gene 52 Ets2 52 Skp2 52 APOE e4 gene 52 progressive neurodegenerative disorder 52 defensin 52 Notch signaling 52 IRAK1 52 Wolbachia 52 antibodies 52 leptin receptors 52 inherited genetic mutation 52 MECP2 52 NKX2 52 PrP 52 retinal degeneration 52 APOE e4 52 RPE# gene 52 beta thalassemia 52 activin 52 Beckwith Wiedemann syndrome 52 epigenetic 52 cardiac hypertrophy 52 FXTAS 52 microdeletions 52 Brugada Syndrome 52 proband 52 chromatin structure 52 varicella zoster virus 52 epigenetically 52 PARP inhibition 52 Vpu 52 xeroderma pigmentosum 52 motor neuron 52 epigenetic modification 52 TACI mutations 52 malaria parasite 52 neural crest cells 52 gene rearrangements 52 OCA2 gene 52 regulates gene expression 52 #q#.# [001] 52 apoC III 52 globin 52 FANCD2 52 malignant transformation 52 molecular abnormalities 52 normal prion protein 52 FGFR2 52 mammary tumors 52 HLA alleles 52 genotoxic stress 52 haplotypes 52 overexpression 52 synapse formation 52 biochemical pathway 52 virulence genes 52 amyloid peptide 52 DICER1 52 DNA methylation 52 hypermethylation 52 spinocerebellar ataxia 52 pigment melanin 52 SMN2 gene 52 Apert syndrome 52 PKM2 52 congenital disorders 52 genomic rearrangements 52 SCN5A 52 heterozygotes 52 SMN1 gene 52 mycobacterium tuberculosis 52 oncogene 52 maternally inherited 52 luminal cells 52 genetic polymorphism 52 collagen VI 52 GSTM1 gene 52 malaria parasite Plasmodium falciparum 52 cyclin D1 52 polymorphism 52 genetic determinants 52 inherited gene mutation 52 pneumococci 52 NRG1 52 Neanderthal genes 52 epigenetic modifications 52 mitochondrial 52 chromosomal regions 52 signaling pathway 52 GRK5 52 LRRK2 mutations 52 RNA molecule 52 neuroglobin 52 BRCA2 52 ChR2 52 bacterium E. coli 52 asymptomatically 52 SOD2 gene 52 zebrafish 52 CHEK2 52 hereditary predisposition 51 signaling molecule 51 placental function 51 sickle hemoglobin 51 mitochondria 51 mycobacterium 51 Ashkenazi Jews 51 atherosclerotic lesions 51 enteroviruses 51 nerve cells 51 BRCA2 gene mutation 51 mitochondrial disease 51 kinase gene 51 breast epithelial cells 51 Hutchinson Gilford Progeria Syndrome 51 IDH1 51 miRNAs 51 heterozygote 51 glutamate signaling 51 proteins 51 TSLP 51 Pten 51 cardiac progenitor cells 51 KLF# 51 Beta thalassemia 51 biochemical cascade 51 IDH mutations 51 Mycoplasma pneumoniae 51 genetically engineered mice 51 deleterious mutation 51 Wwox 51 LKB1 51 AAT deficiency 51 parainfluenza virus 51 dominantly inherited 51 lactose tolerance 51 IKZF1 51 TMEM#B 51 Wnt pathway 51 chromosomal translocation 51 breast tumors 51 phthalate syndrome 51 proto oncogene 51 deleterious mutations 51 brain malformation 51 hemochromatosis 51 alpha synuclein 51 chronic granulomatous disease 51 fibrodysplasia ossificans progressiva 51 PTEN mutation 51 fatty acid synthesis 51 nematode worm 51 genotypes 51 senescent cells 51 melanoma tumors 51 lipin 51 neural crest 51 JAK mutations 51 PKD1 51 filaggrin 51 hormone leptin 51 chromosome #q#.# [001] 51 Foxp3 51 ApoE 51 hereditary hemochromatosis 51 HLA molecules 51 lung adenocarcinoma 51 causal variants 51 Fragile X Syndrome 51 dystrophin gene 51 mice genetically engineered 51 dysgenesis 51 stathmin 51 filaggrin gene 51 mutant strain 51 Y chromosome 51 MLL2 51 T. gondii 51 neurotransmitter GABA 51 GABAergic neurons 51 gene expression 51 clusterin 51 GATA4 51 polydactylism 51 SNPs 51 neuroblastoma tumors 51 Niemann Pick disease 51 Sjögren syndrome 51 primordial germ cells 51 mitochondrial disorders 51 #q# [001] 51 chromosomes 51 Crouzon syndrome 51 Leber congenital amaurosis LCA 51 APOE4 gene 51 neural cells 51 Genetic testing 51 GSTT1 51 transcriptional repressor 51 MIF gene 51 chromosome translocations 51 APOL1 51 single celled parasite 51 chromosomal anomalies 51 MCAD deficiency 51 exomes 51 MHC genes 51 chromosomal disorders 51 malignant tumors 51 homocystinuria 51 lipofuscin 51 Alu RNA 51 BRCA gene mutation 51 GNAQ 51 calcineurin 51 matriptase 51 transgene 51 chromosomal rearrangements 51 palladin 51 DISC1 gene 51 parasitic worm 51 hormone estrogen 51 germ cells 51 tumor suppressor p# 51 X chromosomes 51 chromosome #q# [002] 51 nestin 51 amyloid protein 51 giant danio 51 Klotho gene 51 mammary cancers 51 osteopontin 51 naturally occurring enzyme 51 PON1 51 TRIM5 51 congenital deafness 51 mutant proteins 51 SHANK3 51 interferon pathway 51 BRIP1 51 dystrophin 51 TCF4 51 OGG1 51 germline cells 51 abnormal proteins 51 RAR beta 51 autoantibody 51 MnSOD 51 klotho 51 Cyclin D1 51 plasma kallikrein 51 NPC1 51 cystic fibrosis transmembrane conductance 51 TTR gene 51 prion protein 51 CYP#B# 51 GRK2 51 bacterium Listeria 51 BRCA1 gene mutation 51 histone deacetylases 51 parasite Trypanosoma cruzi 51 DiGeorge syndrome 51 estrogen receptor alpha 50 NF κB activation 50 familial hypercholesterolemia 50 sortilin 50 breast cancers 50 prion protein gene 50 severe congenital neutropenia 50 polycystic kidneys 50 follistatin 50 #q# [002] 50 dietary restriction 50 Wnts 50 TGF beta pathway 50 NEDD9 50 leptin hormone 50 protozoan parasite 50 micro RNA 50 colorectal tumors 50 Plasmodium parasite 50 KCNQ1 50 SIR2 gene 50 amino acid substitution 50 Apobec3 50 sCJD 50 neuroblastoma cells 50 alternatively spliced 50 beta globin gene 50 degenerative neurological disorder 50 melanopsin 50 Hirschsprung disease 50 abnormal prions 50 huntingtin 50 pRb 50 mutant worms 50 autosomal dominant inheritance 50 encodes protein 50 TET2 50 myostatin 50 Nrf2 50 insulin resistance 50 lamin 50 Li Fraumeni 50 phenotypic variation 50 N Myc 50 microRNA miR 50 JAK2 gene 50 beta1 integrin 50 WDR# 50 Jhdm2a 50 neural crest stem cells 50 CYP#D# gene 50 metabolic enzymes 50 Sox9 50 spontaneous remission 50 epidermolysis bullosa EB 50 fatty acid synthase 50 CCR5 mutation 50 hydrops 50 inherited neurodegenerative disorder 50 SLC#A# [002] 50 Rickettsia 50 K ras gene 50 SLC#A# gene [001] 50 Leber hereditary optic neuropathy 50 KIBRA 50 TH# cells 50 LRRK2 mutation 50 tumor suppressor 50 CRISPR Cas 50 LMNA 50 disease 50 p# mutation 50 parasite Plasmodium falciparum 50 Leptospira 50 cyclin E 50 BRAF protein 50 Pin1 50 menin 50 frameshift mutation 50 Chromosome 50 protein misfolding 50 retinoic acid 50 S#K# 50 Mitochondrial diseases 50 infectious prion proteins 50 Id1 50 Genetic variants 50 G6PD 50 mitochondrial DNA 50 leukaemic stem cells 50 ALK gene 50 Clusterin 50 karyotype 50 galactosemia 50 eosinophilic esophagitis 50 C. neoformans 50 mutational 50 HOX genes 50 homologs 50 vesicular stomatitis virus 50 MAPK pathway 50 methylation patterns 50 ALDH2 enzyme 50 Hox gene 50 chromosomal defects 50 beta defensin 50 poorer prognosis 50 Hutchinson Gilford progeria 50 EGFR gene 50 neurodevelopmental disorder 50 LRRK2 50 mammary stem cells 50 EGFR mutations 50 CatB 50 Fanconi Anemia 50 inherited retinal degeneration 50 genetically engineered mouse 50 COMT gene 50 transgenic mouse model 50 GBA mutations 50 hyperactivation 50 KCNH2 50 non coding RNA 50 motor neuron degeneration 50 microglial 50 MCADD 50 APOE allele 50 pseudotumor cerebri 50 GPR# [002] 50 NAFLD 50 H#Y 50 neurodegenerative disease 50 synaptogenesis 50 neuropsychiatric disorder 50 neuronal pathways 50 microsporidia 50 Genes 50 hypertrichosis 50 genetic polymorphisms 50 normal prion proteins 50 FGFR1 50 fungal pathogen 50 Notch1 50 CALHM1 50 genetically identical 50 bacterial enzyme 50 CFTR protein 50 positional cloning 50 BRAF V#E 50 SATB1 50 transcriptional activation 50 BRAF mutation 50 microcephaly 50 HLA DRB1 50 mammalian embryos 50 CXCL5 50 p# protein 50 telomere DNA 50 ferroportin 50 AAV2 50 atopy 50 underlying pathophysiology 50 genetic variability 50 protein kinase C 50 Chronic fatigue syndrome 50 ubiquitylation 50 genomes 50 metabolic disorder 50 telomere shortening 50 Klinefelter syndrome 50 Dicer enzyme 50 telomerase enzyme 50 hormone ghrelin 50 fusogen 50 hedgehog pathway 50 microfilariae 50 teratoma 50 murine leukemia virus 50 KRAS oncogene 50 olfactory receptor 50 MDM2 50 GSTP1 50 uPAR 50 medulloblastoma tumors 50 lactase gene 50 microRNAs 50 Argonaute 50 phenotypes 50 misregulation 50 intestinal inflammation 50 trisomy 50 alpha thalassemia 50 SIR2 50 CAG repeats 50 beta amyloid plaques 50 gene APOE4 50 tau proteins 50 estrogen receptor 50 PPAR γ 50 lung tumors 50 BMP4 50 PB1 F2 50 INF2 50 APOE 50 regulator CFTR gene 50 myelination 50 FMR1 50 sex hormone estrogen 50 untreated celiac disease 50 Hypophosphatasia 50 PTP1B 50 Krabbe Leukodystrophy 50 Cowden syndrome 49 microglial cells 49 muscular dystrophies 49 Alu elements 49 immunodeficiency 49 Akt3 49 ADAMTS# 49 thyroid hormone 49 piRNAs 49 RANKL 49 retinal ganglion cells 49 CFH gene 49 amyloid plaque 49 microRNAs miRNAs 49 MC4R 49 Hsp# [001] 49 latent TB infection 49 acetylation 49 Bcr Abl 49 airway remodeling 49 CaMKII 49 long QT syndrome 49 Igf2 49 collagen VII 49 adrenal cortex 49 CagA 49 blastomeres 49 FOXP2 gene 49 Mutation 49 ectoderm 49 amyloid deposits 49 TGF beta 49 HCMV 49 gene encoding 49 nicotinamide 49 Heterozygous 49 epithelial tissues 49 neuro degenerative disease 49 granzyme B 49 β amyloid 49 ALK mutations 49 fatty acid metabolism 49 genes encoding 49 melanocyte 49 enzymatic activity 49 leptin 49 synuclein 49 outer membrane proteins 49 granule cells 49 Tregs 49 H#K# methylation 49 Bacteroides 49 tuberculosis bacterium 49 serotonin transporter 49 GPC5 49 HLA B# gene 49 biochemical pathways 49 FOXP2 49 eosinophilic 49 APOE ε4 49 mitochondrial diseases 49 epigenetic inheritance 49 neurofibroma 49 BRCA2 breast cancer 49 allelic variants 49 PIP3 49 shorter telomeres 49 ectopic expression 49 HLA DQ2 49 Bcl2 49 Duchenne muscular dystrophy DMD 49 acute myelogenous leukemia AML 49 neuronal degeneration 49 Ras oncogene 49 colon cancers 49 OCA2 49 Cancerous cells 49 dopamine receptor 49 simian virus 49 anti microbial peptides 49 bacterium Escherichia coli 49 toxoplasma 49 fusion protein 49 Loeys Dietz syndrome 49 genome 49 mucins 49 P. falciparum 49 organism genome 49 prosopagnosia 49 IKK2 49 mRNA transcripts 49 endocannabinoids 49 PCSK9 protein 49 palmitoylation 49 fronto temporal dementia 49 bowel cancers 49 cardiac channelopathies 49 cardiac fibrosis 49 herpes simplex virus 49 CHD5 49 EGFR protein 49 SIRT3 49 noncoding RNAs 49 DNA rearrangements 49 KLF4 49 rhodopsin 49 Smad3 49 UCP2 49 beta catenin 49 epigenetic markers 49 autism susceptibility genes 49 IGFBP2 49 malarial parasite 49 ectodermal dysplasia 49 somatic mutation 49 epigenetic marks 49 Rad# 49 Smad7 49 infective agent 49 Colorectal cancers 49 fatal neurological disorder 49 synaptic function 49 Borrelia burgdorferi 49 Mitochondrial 49 shortened telomeres 49 Dystrophin 49 genomic deletions 49 prion infection 49 Plasmodium falciparum 49 insulin signaling pathway 49 PDGFR 49 gene MECP2 49 CETP gene 49 immunodeficient 49 NOTCH1 49 Retinitis pigmentosa 49 chromosome deletion 49 ataxia telangiectasia 49 mRNAs 49 congenital blindness 49 hormone aldosterone 49 insulin receptors 49 TCF#L# 49 androgen receptor 49 chromosome #q# [001] 49 kisspeptin 49 deacetylation 49 spinal muscular atrophy SMA 49 Kabuki syndrome 49 Rhes 49 WT1 49 TACI 49 ALDH2 49 protein clumps 49 Parkinson disease neurodegenerative disorder 49 DGAT1 49 prion gene 49 RNA sequences 49 amyloid deposition