Related by context. All words. (Click for frequent words.) 66 Fragile X gene 66 genes predisposing 63 APOE e4 63 mutated gene 63 autosomal recessive disease 63 recessive genetic 63 APOE4 62 heritable genetic 62 mutation 62 germline mutations 62 Li Fraumeni syndrome 62 inherited mutations 61 defective gene 61 CDH1 61 progranulin gene 61 MEF2A 61 APOE4 gene 61 ApoE4 gene 61 proband 61 CFTR gene 60 BARD1 60 HLA DQ2 60 gene mutation 60 autosomal recessive 60 cardiac channelopathies 60 mutant gene 60 BRCA2 gene 60 MLL2 60 TP# mutation 59 recessive mutation 59 Lafora disease 59 breast cancer genes BRCA1 59 genetic mutation 59 de novo mutations 59 C#Y 59 susceptibility genes 59 KRAS oncogene 59 spontaneous mutations 59 Wolbachia strains 59 spontaneous mutation 59 apolipoprotein E gene 59 Smith Lemli Opitz syndrome 59 mutated BRCA 59 gene mutations 59 MSH2 59 MIF gene 59 mutated genes 58 parkin gene 58 chromosomal anomalies 58 maternally transmitted 58 MYH9 gene 58 LRRK2 gene 58 TCF#L# gene 58 BRCA2 mutation 58 #q# deletion 58 CYP#C# * 58 susceptibility gene 58 recessive trait 58 dominantly inherited 58 Wiskott Aldrich syndrome 58 CDKN2A 58 G#S mutation 58 DICER1 gene 58 MLH1 58 LRP5 58 mutant allele 58 APOE e4 gene 58 NPC1 58 prion gene 58 KIBRA 58 recessive genes 58 Kufs disease 57 mutations 57 Newborn screening 57 CHEK2 57 GPC5 57 MC4R gene 57 G#S [002] 57 SNPs pronounced snips 57 genetic abnormalities 57 BMPR2 57 enteroviral 57 Li Fraumeni 57 maternally inherited 57 DRD2 gene 57 PTPN# 57 ApoE gene 57 HLA B# 57 sporadic ALS 57 retinoblastoma Rb 57 HLA identical 57 GSTM1 gene 57 DAT1 57 APOE gene 57 missense mutations 56 ZNF# 56 MTHFR 56 chromosome abnormality 56 homocystinuria 56 apolipoprotein E 56 JAK mutations 56 causative genes 56 Genetic variation 56 familial dysautonomia 56 causative gene 56 FMR1 gene 56 phenotypic expression 56 ApoE4 allele 56 deleterious mutation 56 BRCA2 gene mutation 56 modifier genes 56 CTVT 56 familial adenomatous polyposis 56 gene BRCA2 56 genomic imprinting 56 premutation 56 apoE4 56 genetic variants associated 56 heterozygote 56 mutant genes 56 monogenic 56 mitochondrial DNA mtDNA 56 microdeletion 56 MLL gene 56 BRCA mutation 56 mitochondrial mutations 56 familial ALS 56 CNTNAP2 56 genetically inherited 56 BRCA1 mutation 56 ApoE4 56 mutated K ras 56 Entamoeba 56 mosaicism 56 CCR5 delta# 56 severe congenital neutropenia 56 SMN1 56 genetic variant 56 PALB2 56 BRIP1 56 somatic mutations 56 TGFBR1 * 6A 55 TMEM#B 55 APOE ε4 55 Spinal muscular atrophy 55 genetic defect 55 genetic defects 55 chordate 55 apoE 55 microdeletions 55 monozygotic twin 55 HHV 6 55 von Hippel Lindau 55 TACI mutations 55 Streptomyces 55 gene rearrangements 55 chromosomal anomaly 55 PTEN mutations 55 hyper IgE syndrome 55 chromosomal regions 55 virulence genes 55 HNPCC 55 ENPP1 55 transgenic rats 55 IL#R 55 WDR# 55 transgenic mouse models 55 BRCA1 gene 55 chromosomal deletions 55 familial pancreatic cancer 55 testicular germ cell 55 nonhereditary 55 LPA gene 55 herpesviruses 55 apolipoprotein E4 55 abnormal hemoglobin 55 genetic 55 dyskeratosis congenita 55 APOL1 55 autosomal dominant polycystic kidney 55 CHD7 55 HGPS 55 BRCA gene 55 GATA4 55 SMN1 gene 55 Hypophosphatasia 55 flavivirus 55 monozygotic twins 55 genetic makeups 55 giant danio 55 alpha synuclein toxicity 55 HFE gene 55 KIF6 gene 55 huntingtin gene 55 Beta thalassemia 55 BRCA1 BRCA2 55 klotho 55 Genetic variants 54 disorder thalassemia 54 molecular abnormalities 54 chromosomal aberrations 54 LIS1 54 microcephalin 54 fatal neuromuscular disorder 54 BRCA1 mutations 54 paternally inherited 54 FADS2 gene 54 Diamond Blackfan anemia 54 Meckel Gruber 54 GM1 gangliosidosis 54 causative mutation 54 autoinflammatory 54 APOE epsilon 4 54 Genetic mutations 54 mutated BRCA1 54 Entamoeba histolytica 54 vesicular stomatitis virus 54 IKZF1 54 BRCA1 gene mutation 54 HLA G 54 holoprosencephaly 54 ABCB1 gene 54 hereditary hemochromatosis 54 Hutchinson Gilford progeria 54 MTHFR gene 54 aneuploidies 54 Severe Combined Immunodeficiency 54 murine leukemia virus 54 genetic abnormality 54 ataxia telangiectasia 54 Tay Sachs disease 54 genetic mutations 54 cystic fibrosis Duchenne muscular 54 GSTP1 54 M. pneumoniae 54 causal variants 54 non mutated KRAS 54 CDK4 54 Cryptococcus neoformans 54 klotho gene 54 microfilariae 54 GABRA2 54 chromosomal alterations 54 variant alleles 54 Froguel 54 NR#A# gene 54 Sandhoff disease 54 polydactylism 54 FXTAS 54 pneumococci 54 MSH6 54 LRAT 54 ARID1A 54 gene variants 54 alpha thalassemia 54 HLA DRB1 54 Alu elements 54 recessive gene 54 PTEN gene 54 NF1 gene 54 VHL gene 54 Alport Syndrome 54 SCN1A 54 Dravet syndrome 54 Epstein Barr virus EBV 54 beta thalassemia 54 CALHM1 54 BRCA gene mutation 54 DNA methylation patterns 54 orthologs 54 sickle cell hemoglobin 54 LRRK2 mutation 54 dizygotic twins 53 Genetic predisposition 53 Niemann Pick disease 53 BRCA2 gene mutations 53 reassortants 53 mitochondrial disorders 53 epigenetic alterations 53 susceptibility alleles 53 homozygosity 53 BRCA2 breast cancer 53 fronto temporal dementia 53 lentiviruses 53 DLX5 53 genetic polymorphism 53 childhood acute lymphoblastic 53 positional cloning 53 CYP#E# gene 53 homozygote 53 allelic variants 53 ADAM# 53 mutated protein 53 PARP inhibition 53 C. neoformans 53 Rh factor 53 T. vaginalis 53 polyploid 53 Brugada Syndrome 53 galactosemia 53 tumor suppressor protein 53 abnormal prions 53 HLA molecules 53 promoter hypermethylation 53 human leukocyte antigens 53 congenital CMV infection 53 nonpathogenic 53 familial adenomatous polyposis FAP 53 APOE genotype 53 heritable 53 multigene 53 Salmonella typhi 53 chromosomal translocations 53 DQB1 * 53 ALK gene 53 Single Nucleotide Polymorphisms SNPs 53 FADS2 53 A. fumigatus 53 sCJD 53 HbF 53 undiagnosed celiac disease 53 COMT gene 53 JAK2 gene 53 causative mutations 53 ORMDL3 53 simian immunodeficiency virus 53 heritable diseases 53 ε4 53 IgA deficiency 53 NF1 53 paratuberculosis 53 neuroligins 53 fibrous tangles 53 mutant alleles 53 OPRM1 gene 53 MC1R 53 JAK2 mutation 53 recessively inherited 53 gene APOE4 53 heterozygotes 53 autosomal dominant inheritance 53 CNTNAP2 gene 53 CNVs 53 PALB2 gene 53 SOD1 gene 53 incurable neurodegenerative disease 53 immunodeficiency diseases 53 BRAC2 53 gene 53 PON1 53 sibling grandparent 53 M. capricolum 53 Myotonic dystrophy 53 sphingolipid 53 C. trachomatis 53 MECP2 gene 53 IDH2 53 CFTR gene mutations 53 K ras gene 53 neurodegenerative disorder 53 antinuclear antibodies 53 homozygous 53 epigenetic modification 53 G6PD deficiency 53 measles virus 53 INF2 53 neurofibrillary 53 BRCA2 carriers 53 mutated p# 53 missense mutation 53 pea aphid 53 FASPS 53 medulloblastoma tumors 53 chronic granulomatous disease 53 budding yeast 53 alleles 53 pathogenic mutations 53 Trypanosoma brucei 53 receptor gene 53 epigenetic changes 53 CYP#D# gene 53 immunodeficiency disorder 53 heterozygous 53 bacterium Listeria 53 chlamydial 53 nucleus Chinnery 53 syngeneic 53 consanguineous marriage 53 Lesch Nyhan syndrome 52 genetic trait 52 Fanconi anemia 52 TP# gene 52 LKB1 52 DNA rearrangements 52 human leukocyte antigen HLA 52 Arabidopsis genome 52 Apobec3 52 HLA DRB1 SE 52 neuroblastomas 52 SHANK3 52 chlamydiosis 52 imprinted genes 52 ribonucleic acid RNA 52 PIK3CA 52 chromosome #q#.# [001] 52 Hsp# [001] 52 LRRK2 mutations 52 congenital blindness 52 familial hypercholesterolemia 52 mycobacterium tuberculosis 52 somatic mutation 52 NPHP 52 chromosome rearrangements 52 presymptomatic 52 SHANK3 gene 52 apoC III 52 autosomal dominant disorder 52 genes BRCA 52 IGF1 52 fruitfly Drosophila 52 CYP#A# gene 52 Pten 52 Heterozygous 52 myeloproliferative neoplasms MPNs 52 neuroblastoma tumors 52 abnormal methylation 52 Leptospira 52 familial clustering 52 Genetic mutation 52 variant allele 52 parasite Toxoplasma gondii 52 haematopoietic 52 myeloproliferative 52 GPI anchored 52 #p#.# [001] 52 CRTC3 52 paramyxovirus 52 splice junctions 52 phthalate syndrome 52 PDGFRA 52 neuro developmental disorders 52 K ras mutations 52 gene variant 52 leptin deficiency 52 Mitochondrial DNA 52 penetrance 52 PTCHD1 gene 52 gene APOE 52 hypermethylated 52 medulloblastomas 52 KIAA# 52 clefting 52 Neurofibromatosis type 52 DGAT1 52 toxoplasma 52 maternally derived 52 SORL1 gene 52 BCL#A 52 lysosomal storage disease 52 inherited predisposition 52 Krabbe Leukodystrophy 52 genetic variants 52 V Leiden 52 prodynorphin 52 JAK2 enzyme 52 C EBP alpha 52 prenatally diagnosed 52 SMN2 gene 52 Single Nucleotide Polymorphisms 52 ALK inhibitors 52 primordial germ cells 52 TIR1 52 Homozygous 52 COL#A# 52 chromosome aberrations 52 epigenetic silencing 52 genes 52 MC1R gene 52 genomewide 52 recessive inheritance 52 congenital disorders 52 TRAF1 C5 52 vitamin D receptor 52 haemochromatosis 52 KLF4 52 recessive genetic disorders 52 glucocorticoid receptors 52 P. reichenowi 52 Wwox 52 ADH1B * 52 adeno associated viruses 52 autosomal 52 gene MECP2 52 GLUT1 52 GSTT1 52 MYBPC3 52 human metapneumovirus 52 bowel polyps 52 anaplastic lymphoma kinase 52 metabolomic profiles 52 clade B 52 WAGR syndrome 52 CAG repeats 52 mitochondrial metabolism 52 genetic modifiers 52 gene locus 52 FMR1 52 Yamanaka recipe 52 T. gondii 52 GPR# [002] 52 dysbindin gene 52 chromosome translocations 52 mRNA transcripts 52 autopsied brains 52 apolipoprotein E APOE 52 Karayiorgou 52 laforin 52 mtDNA mutations 52 mitochondrial gene 52 progressive retinal degenerative 52 Rh positive 52 SORL1 52 autistic regression 52 IGFBP2 52 chromosomal defects 52 genetic variations 52 sequenced genomes 52 CFTR cystic fibrosis transmembrane 52 dysbindin 52 gamma globin gene 52 IL#B gene 52 Stuttering tends 52 Saccharomyces 52 invasive secretory carcinoma 52 hereditary spastic paraplegia 52 VKORC1 52 CETP VV 52 human papillomaviruses HPV 52 Cystic fibrosis CF 52 c KIT 52 genetic variation 52 ERBB2 52 vacuolar 52 copper zinc superoxide 52 Hashimoto thyroiditis 52 Prox1 52 histocompatibility 52 filaggrin 52 HMPV 52 germline mutation 52 Salmonella Typhi 52 endogenous retroviruses 52 protein p# 52 PB1 F2 52 S. maltophilia 52 STK# gene 52 MIF protein 52 homozygotes 52 Von Willebrand disease 52 Prion proteins 52 cerebrospinal fluid biomarkers 52 succinate dehydrogenase 52 defensin 52 protein isoforms 52 #q#.# deletion syndrome 52 experimentally infected 52 histone modification 51 genetic syndromes 51 CYP#C# [001] 51 STAT4 51 TrkB 51 hypertrophic cardiomyopathy HCM 51 HLA genes 51 TEL AML1 51 MCAD deficiency 51 probands 51 CCR3 51 Apert syndrome 51 chromosome #p# [001] 51 APOE allele 51 T. brucei 51 5q 51 Rh incompatibility 51 hereditary disorders 51 cause cardiac channelopathies 51 dopamine D4 receptor 51 palladin 51 transmembrane receptor 51 tubercle bacillus 51 BRCA breast cancer 51 transthyretin 51 Drosophila melanogaster 51 genetic makeup 51 hereditary predisposition 51 regulates gene expression 51 staphylococci 51 epigenomes 51 FGFR2 51 Fragile X Syndrome 51 gene deletions 51 abnormal chromosomes 51 ADPKD 51 microscopic colitis 51 G allele 51 SLC#A# [001] 51 KCNQ1 51 Toxoplasma 51 aneuploid cells 51 1 diabetes T1D 51 multidrug resistance 51 DRD4 51 ankyrin repeat 51 genomic alterations 51 5 hydroxymethylcytosine 51 GBA mutations 51 M. genitalium 51 Six3 51 p# activation 51 recessive traits 51 SOD2 gene 51 Chlamydia pneumoniae 51 MYCN amplification 51 UGT#B# 51 chromosomal abnormalities 51 human leukocyte antigen 51 RPE# gene 51 MeCP2 gene 51 narcolepsy cataplexy 51 NEIL1 51 peroxisome 51 Ets2 51 ADRB2 51 TMPRSS2 ERG fusion 51 Francisella 51 C1q 51 H2AX 51 tau protein tangles 51 CYP#C# gene 51 cystic kidney 51 Akt1 51 Folic acid deficiency 51 pancreatic islet 51 HOX genes 51 TRIM5a 51 phenotypic variation 51 NKX#.# 51 sequence homology 51 genetic alterations 51 humanin 51 congenital deafness 51 HLA DR4 immune 51 ß amyloid 51 abnormal proteins 51 SMN protein 51 COX2 51 Ashwell receptor 51 B. fragilis 51 Tay Sachs Disease 51 LMNA 51 alpha defensin 51 Tay Sachs thalassemia 51 number variations CNVs 51 faulty BRCA1 gene 51 monozygotic 51 XMRV retrovirus 51 MYH9 51 SLC#A# [002] 51 EoE 51 mucins 51 HLA gene 51 allele 51 basal cell nevus syndrome 51 R#W [002] 51 genotyping gene expression 51 ABCB1 51 Simian Immunodeficiency Virus 51 dopamine transporter gene 51 Y chromosomal 51 gut microbes 51 genetic polymorphisms 51 metabolizing enzyme 51 Rb gene 51 provirus 51 asymptomatic carriers 51 sexually reproducing 51 multiprotein complex 51 nonidentical 51 polymorphisms 51 BChE 51 girl Hagemen 51 BRCA genes 51 haplotypes 51 spinal muscular atrophy SMA 51 FOXP2 gene 51 nondemented 51 mitochondrial defects 51 ALK mutations 51 genotoxic stress 51 N acetyltransferase 51 paraoxonase 51 paramyxoviruses 51 NPM1 gene 51 mammary cells 51 malayi 51 DEAR1 51 NOD mouse 51 inherited gene mutation 51 CHEK2 gene 51 parainfluenza virus 51 C. pneumoniae 51 TCF#L# 51 Htt 51 multigenic 51 globin genes 51 RPE# 51 HER2 neu 51 polycystic kidneys 51 chromosomal defect 51 fully sequenced genomes 51 mitochondrial proteins 50 IDH1 gene 50 resistant isolates 50 aciduria 50 Alpha synuclein 50 beta globin 50 VIPR2 50 autosomal dominant 50 sporadic Creutzfeldt Jakob 50 aneuploidy 50 Clusterin 50 FUS TLS 50 diagnostic biomarker 50 miRNA genes 50 hereditary pancreatitis 50 IKKa 50 GIST tumors 50 E1A 50 synthases 50 Meckel Gruber syndrome 50 HMGCR 50 CEP# 50 Phenylketonuria PKU 50 HLA matched 50 enterovirus infection 50 Genetic variations 50 Chlamydia psittaci 50 PPARγ 50 hereditary nonpolyposis colorectal cancer 50 HipA 50 genetic biomarkers 50 Epstein Barr Virus EBV 50 TH# cells 50 alternatively spliced 50 heterozygosity 50 NFkB 50 RUNX3 50 number variation CNV 50 Glioblastoma multiforme GBM 50 SERT gene 50 Vesivirus 50 herpes viruses 50 myostatin gene 50 microsatellite instability 50 congenital adrenal hyperplasia CAH 50 CYP#B# 50 Alport syndrome 50 SOD1 protein 50 mammary gland tumors 50 pRb 50 constitutively expressed 50 radiolabeled antibodies 50 Apolipoprotein E 50 Canine influenza 50 genetic determinants 50 mice lacking 50 HLA DQ 50 unexplained mental retardation 50 Vpu 50 activating mutations 50 familial hypercholesterolemia FH 50 NR#A# 50 gene expression patterns 50 mammary stem cells 50 Deoxyribonucleic acid 50 Nicotiana benthamiana 50 nonalcoholic fatty liver 50 gene variation 50 small RNAs encoded 50 shiga toxin 50 APOE 50 ApoE 50 FUS protein 50 oncogenic mutations 50 respiratory viral infections 50 chloroplast genome 50 SNP rs# [001] 50 Shendure 50 AAT deficiency 50 MAPCs 50 virulence determinants 50 glutamic acid decarboxylase 50 filoviruses 50 genetically mapped 50 protozoan parasite 50 mammalian embryos 50 susceptibility loci 50 infectious prion proteins 50 Tay Sachs 50 CMV infections 50 HLA DRB1 * 50 Dpp 50 Neisseria 50 chromosomal rearrangement 50 Mutation Analysis 50 XLHED 50 p# mutations 50 neuropsychiatric disorder 50 retrovirus 50 Mycoplasma genitalium 50 aneuploid 50 BRCA2 mutations 50 capsular polysaccharide 50 genes BRCA1 50 SCA5 50 TRIM5 50 trophoblast cells 50 Ras oncogene 50 immuno deficiency 50 #q#.# [001] 50 polyglutamine diseases 50 lactase persistence 50 M. paratuberculosis 50 meiotic recombination 50 beta lactamases 50 mitochondrial genome 50 RNA binding 50 generalized vitiligo 50 defensins 50 lymphocytic choriomeningitis virus LCMV 50 Krabbe leukodystrophy 50 Wnt#b 50 neuro degenerative disease 50 fatal neurodegenerative 50 FUS1 50 defective mitochondria 50 Transcription factors 50 retrovirus XMRV 50 haplotype 50 Leydig cells 50 genetic blueprints 50 D. melanogaster 50 FTO gene 50 PKCi 50 5 methylcytosine 50 chromosome #q 50 Mendelian disorders 50 synuclein 50 tuberculosis bacterium 50 monogenic diabetes 50 CCL#L# 50 transfusion syndrome 50 immunodeficient 50 TGFBR1 50 HLA alleles 50 BRAF V#E 50 TPMT 50 Fanconi anemia FA 50 genomic deletions 50 mesenchymal cell 50 NOTCH1 50 IRS1 50 #q# [001] 50 pilocytic astrocytomas 50 NNRTI resistant virus 50 progressive neurodegenerative 50 protein glycosylation 50 familial aggregation 50 Sonic Hedgehog 50 gastric carcinomas 50 autoinflammatory diseases 50 epistasis 50 Hereditary angioedema 50 endostatin 50 Telomere length 50 humoral responses 50 replicase 50 MnSOD 50 fibrodysplasia ossificans progressiva 50 chromosome abnormalities 50 polyomavirus 50 alpha synuclein gene 50 SOX3 gene 50 reverse vaccinology 50 RET PTC rearrangements 50 DiGeorge syndrome 50 piRNAs 50 molybdenum cofactor deficiency 50 pestis 50 epigenetic regulation 50 DONOHUE My 50 ribosomal RNA 50 thymidine kinase 50 HLAs 50 salivary proteins 50 glycolipid 50 H. influenzae 50 autistic enterocolitis 50 IRAK1 50 genetically altered mouse 50 globin 50 lung adenocarcinoma 50 CC genotype 50 rifamycins 50 histone deacetylases 50 juvenile myelomonocytic leukemia 50 trypanosome 50 Genetic testing 50 corona virus 50 Venter genome 50 perilipin 50 CagA 50 breast cancer gene mutation 50 OGG1 50 HCMV 50 Von Hippel Lindau 50 MCADD 50 FLT3 50 thyroid deficiency 50 leukaemias 50 MECP2 50 cultured neurons 50 leukemic stem cells 50 breast cancer subtypes 50 incurable genetic 50 potent inducer 50 exome sequencing 50 β thalassemia 50 RNA ribonucleic acid 50 replicon 50 sickle hemoglobin 50 SE alleles 50 Leydig cell 50 Neanderthal genes 50 leukemia aplastic anemia 50 deCODEme TM 50 luciferase gene 50 microchimerism 50 MetAP2 50 genetic loci 50 maternal serum 50 Leber congenital amaurosis 50 yeast Saccharomyces cerevisiae 50 susceptibility locus 50 rRNA 50 DICER1 50 Nup# 50 p#/CBP 50 VeraCode 50 Bardet Biedl syndrome 50 Prevotella 50 Leukemias 50 Myb 50 Hypertensive heart 50 HOTAIR 50 HLA B 50 Mycobacterium leprae 50 Smad3 50 4E BP1 50 alveolar rhabdomyosarcoma 50 inbred strains 50 polymorphism 49 divide asymmetrically 49 premature ovarian 49 #p#.# [002] 49 untreated celiac disease 49 conserved sequences 49 SAPAP3 49 chromatin immunoprecipitation ChIP 49 gestational diabetes mellitus 49 Polycystic kidney disease 49 channelopathies 49 hepatitis B infection 49 microbiomes 49 capsid proteins 49 embryonic tissues 49 rotaviruses 49 fetal microchimerism 49 beta amyloid peptides 49 NKX2 49 atopy 49 thrombophilia 49 epigenetic inheritance 49 prognostic markers 49 PARP1 49 Duchenne muscular dystrophy DMD 49 serous ovarian cancer 49 SIRT3 49 NNRTI resistance 49 chromosomally normal