Related by context. All words. (Click for frequent words.) 67 LRRK2 gene 66 APOE4 66 BRCA2 gene 66 MECP2 gene 65 mutated gene 65 mtDNA mutations 65 familial ALS 65 TCF#L# gene 65 chromosome abnormality 65 ApoE4 gene 64 susceptibility gene 64 inherited mutations 64 BRCA1 gene 64 Hashimoto thyroiditis 64 familial adenomatous polyposis 64 gene APOE4 63 mutation 63 mutated BRCA1 63 gene mutation 63 inherited predisposition 63 genetic variant 63 ApoE4 63 mutations 62 holoprosencephaly 62 APOE e4 62 GBA mutations 62 Li Fraumeni syndrome 62 sporadic ALS 62 APOE gene 62 genetic mutation 62 genetic abnormality 62 mutant gene 62 PTEN gene 62 CFTR gene 62 de novo mutations 61 familial pancreatic cancer 61 gene mutations 61 BRCA1 mutations 61 genes predisposing 61 HLA B# 61 defective gene 61 G#S [002] 61 LIS1 61 ApoE gene 61 epigenetic changes 61 LQTS 61 apoE4 61 mitochondrial dysfunction 61 p# mutations 61 gene MECP2 61 LRRK2 mutations 61 IgA deficiency 61 gene variant 61 missense mutation 61 CHD7 61 ADPKD 61 VHL gene 60 PTEN mutations 60 genomic deletions 60 CDH1 60 apolipoprotein E 60 BARD1 60 chromosomal aberrations 60 familial hypercholesterolemia 60 APOL1 60 mosaicism 60 myotonic dystrophy 60 fronto temporal dementia 60 CNTNAP2 gene 60 APOE allele 60 #q#.# [001] 60 chromosomal rearrangement 60 ectodermal dysplasia 60 chromosomal defect 60 epigenetic silencing 60 COMT gene 60 dopamine D4 receptor 60 SHANK3 60 MC4R gene 60 BRAF gene 60 HLA DRB1 60 Apert syndrome 60 monozygotic twin 60 PTPN# 60 autosomal recessive 60 mice lacking 60 mitochondrial mutations 60 C#Y 60 BRCA mutation 60 germline mutations 60 FASPS 60 idiopathic PAH 59 BRCA2 gene mutation 59 #q# [001] 59 NF1 gene 59 MYH9 gene 59 LRRK2 mutation 59 genetic defect 59 gene variation 59 TP# mutation 59 MYCN amplification 59 CYP#D# gene 59 MC1R 59 spontaneous mutations 59 progranulin gene 59 proband 59 mutated genes 59 PALB2 59 Wwox 59 APOE 59 microcephalin 59 LRP5 59 breast cancer genes BRCA1 59 hereditary predisposition 59 Lafora disease 59 genetic abnormalities 59 recessive trait 59 BRIP1 59 autosomal dominant disorder 59 MGUS 59 SLC#A# [002] 59 Angelman syndrome 59 CNTNAP2 59 penetrance 59 sCJD 59 basal cell nevus syndrome 59 susceptibility genes 59 APOE ε4 59 ADAM# 59 MeCP2 gene 59 spinocerebellar ataxia 59 genetic polymorphisms 59 chromosomal translocations 59 MSH2 59 MTHFR 59 G6PD deficiency 58 alpha synuclein gene 58 giant danio 58 G allele 58 huntingtin gene 58 sFlt1 58 FMR1 gene 58 apolipoprotein E gene 58 Genetic variants 58 DQB1 * 58 Dravet syndrome 58 chromosome abnormalities 58 medulloblastomas 58 PTEN protein 58 aneuploidy 58 autosomal dominant inheritance 58 frontotemporal dementia 58 SORL1 58 neurodevelopmental disorder 58 GFP gene 58 polycystic ovary syndrome 58 APOE genotype 58 BRCA1 58 Cockayne syndrome 58 gene BRCA2 58 hemochromatosis 58 BRCA mutations 58 HGPS 58 neuroblastoma tumors 58 airway remodeling 58 herpesviruses 58 KIF6 gene 58 NR#A# 58 Peutz Jeghers syndrome 58 virulence genes 58 recessive mutations 58 V Leiden 58 microdeletion 58 autosomal dominant 58 genetic polymorphism 58 Joubert syndrome 58 FTLD 58 transgenic mouse model 58 hypertrophic cardiomyopathy HCM 58 miRNA genes 58 parkinsonism 58 gene variants 58 NF1 58 MCADD 58 recessive genetic 58 chromosomal anomaly 58 Hutchinson Gilford progeria 58 BRAF mutation 58 HFE gene 58 chromosomal alterations 58 progressive neurodegenerative disorder 58 Six3 58 microchimerism 57 ataxia telangiectasia 57 C. neoformans 57 FXTAS 57 APOE4 gene 57 undiagnosed celiac disease 57 homozygosity 57 chromosomal abnormalities 57 SLC#A# gene [001] 57 dermatomyositis 57 monogenic 57 WT1 57 LKB1 57 DLX5 57 LRAT 57 GSTP1 57 narcolepsy cataplexy 57 neurofibromatosis type 57 mutant genes 57 CHEK2 57 NOD2 57 FGFR2 gene 57 IDH1 mutation 57 neurological abnormalities 57 chromosomal instability 57 SORL1 gene 57 Genetic predisposition 57 STAT4 57 herpes viruses 57 NF2 57 BRCA gene mutation 57 Kufs disease 57 missense mutations 57 C1q 57 Epstein Barr virus EBV 57 HNPCC 57 HbF 57 UGT#A# * 57 MEF2A 57 JAK mutations 57 nonsense mutations 57 apoE 57 TGFBR1 * 6A 57 ALK mutations 57 gene APOE 57 NKX2 57 BDNF gene 57 SERT gene 57 HMGA2 57 mutant allele 57 pseudotumor cerebri 57 dominantly inherited 57 leptin deficiency 57 molecular abnormalities 57 recessive gene 57 neurodegenerative disorder 57 KIBRA 57 neuroligins 57 varicella zoster virus 57 FTO gene 57 KLF# 57 Helicobacter 57 leptin receptor 57 RUNX3 57 BRCA2 mutation 57 GBM tumors 57 IKZF1 57 Fragile X gene 56 RPE# 56 FGFR2 56 GPC5 56 TACI mutations 56 #q# deletion 56 brain lesions 56 Sjögren syndrome 56 hydrops 56 Alzheimers disease 56 malignant transformation 56 airway hyperresponsiveness 56 polymorphic ventricular tachycardia 56 neurofibroma 56 MLH1 56 chromosomal disorder 56 SGK1 56 chromosome #q#.# [001] 56 SMN protein 56 genes BRCA1 56 MTHFR gene 56 promoter hypermethylation 56 ataxias 56 Epstein Barr 56 nondemented 56 IL#R 56 enteroviruses 56 hereditary deafness 56 IGF2 56 chromosome translocations 56 SLC#A# [001] 56 NEIL1 56 Niemann Pick disease 56 aneuploidies 56 WDR# 56 achromatopsia 56 adrenal function 56 ARVD 56 estrogen receptor alpha 56 neurofibromas 56 DRD2 gene 56 TMEM#B 56 ApoE 56 KRAS oncogene 56 genetic variants 56 rs# [002] 56 ORMDL3 56 recessive mutation 56 pRb 56 underlying pathophysiology 56 Foxp3 56 testicular tumors 56 myelodysplasia 56 bowel polyps 56 Meckel Gruber 56 genetic variants associated 56 JAK2 gene 56 rs# [001] 56 Cyclin D1 56 hypermethylation 56 IRS1 56 Cryptococcus neoformans 56 gene predisposing 56 genetic mutations 56 BCL#A 56 galactosemia 56 CYP#B# 56 ovarian hormones 56 tumor suppressor protein 56 alleles 56 prosopagnosia 56 XMRV infection 56 ependymomas 56 spontaneous mutation 56 Klinefelter syndrome 56 motor neuron degeneration 56 tumor suppressor gene 56 abnormal hemoglobin 56 genomic imprinting 56 lymphocyte activation 56 haemochromatosis 56 inherited neurological disorder 56 progerin 56 Li Fraumeni 56 beta thalassemia 56 familial clustering 56 beta1 integrin 56 somatic mutations 56 EBV infection 56 CYP#A# gene 56 hereditary hemochromatosis 56 neuroblastomas 56 microdeletions 56 BRCA2 56 receptor gene 56 Akt3 56 Vitamin B# deficiency 56 mitochondrial disorders 56 genetic alteration 56 parkin gene 56 BRCA1 BRCA2 56 nonhereditary 56 gene p# 56 CYP#E# gene 56 MAOA gene 56 #q#.# deletion syndrome 56 poorer prognosis 56 DISC1 gene 56 polycystic ovary syndrome PCOS 56 BRCA1 gene mutation 56 familial adenomatous polyposis FAP 56 folate deficiency 56 neuro degenerative disease 56 Fanconi anemia 56 dopamine receptor gene 56 Clusterin 56 endoplasmic reticulum stress 56 KCNE2 56 leukaemias 56 IGFBP2 56 androgen receptor gene 56 filaggrin gene 56 medulloblastoma tumors 55 CDK4 55 C. pneumoniae 55 APOE4 variant 55 genomic rearrangement 55 nonmelanoma skin cancers 55 hepatic toxicity 55 COX2 55 PARP inhibition 55 maternally inherited 55 untreated celiac disease 55 BRCA2 breast cancer 55 hereditary disorder 55 vitamin B# deficiency 55 APOE e4 allele 55 lobular breast cancer 55 lung adenocarcinoma 55 autoimmune thyroiditis 55 Kabuki syndrome 55 multidrug resistance 55 epigenetically 55 serotonin transporter gene 55 fibrous dysplasia 55 Mycoplasma pneumoniae 55 CC genotype 55 BRCA1 mutation carriers 55 klotho 55 eosinophilic esophagitis 55 cerebellar hypoplasia 55 HHV 6 55 MC1R gene 55 Alzheimer pathology 55 chronic autoimmune disorder 55 Pin1 55 TOMM# 55 DNA methylation patterns 55 Rb gene 55 micro RNAs 55 renal cell carcinomas 55 autosomal recessive disease 55 pathogenic mutations 55 SOD1 gene 55 serotonin receptor 55 behavioral abnormalities 55 endostatin 55 Genetic mutation 55 KCNH2 55 IDH1 55 filaggrin 55 CYP#D# 55 Apolipoprotein E 55 congenital deafness 55 measles virus 55 genetic defects 55 angiosarcoma 55 autistic regression 55 mutated protein 55 otosclerosis 55 tau pathology 55 neural tube defect 55 NFKBIA 55 Hurthle cell 55 Pten 55 protein encoded 55 chorioamnionitis 55 SCN5A 55 apoC III 55 colorectal neoplasia 55 ABCB1 55 dyskeratosis congenita 55 ALK gene 55 S#A# [002] 55 chromosomal abnormality 55 p# mutation 55 epigenetic modification 55 testicular germ cell 55 LPA gene 55 recurrent miscarriages 55 OPRM1 gene 55 germline mutation 55 MIF gene 55 TCF#L# 55 rare chromosomal disorder 55 Leber hereditary optic neuropathy 55 CNVs 55 hamartomas 55 BRCA1 mutation 55 roseola 55 ALDH2 55 paraganglioma 55 nicotinamide 55 Von Willebrand disease 55 hyperemesis 55 GPR# [002] 55 mesotheliomas 55 AAT deficiency 55 predisposing factor 55 infantile hemangioma 55 Brugada syndrome 55 PDE#A 55 subclinical hypothyroidism 55 IRF6 55 p# gene 55 genomic instability 55 immunodeficient 55 genetic susceptibility 55 Retinoblastoma 55 degenerative disorder 55 Cowden syndrome 55 Krabbe Disease 55 MCAD deficiency 55 systemic scleroderma 55 gene polymorphisms 55 Immunohistochemical analysis 55 MIF protein 55 MLL2 55 variable immunodeficiency 55 GSTT1 55 herpes simplex encephalitis 55 chromosome deletion 55 pneumococci 55 alpha thalassemia 55 chromosome #q# [001] 55 enzymatic activity 55 BRAF mutations 55 CFH gene 54 carcinoid tumor 54 Ras oncogene 54 5 HTTLPR 54 disease familial dysautonomia 54 JAK2 mutation 54 FOXP3 54 epigenetic markers 54 mammary cancers 54 transthyretin 54 histone deacetylases 54 lichen planus 54 Klotho gene 54 epigenetic alterations 54 mitochondrial toxicity 54 myostatin gene 54 microRNA expression 54 nicotinic receptor 54 EoE 54 Pneumocystis carinii 54 deletion 5q 54 palladin 54 JMML 54 DICER1 54 benign polyps 54 chromosome rearrangements 54 Notch signaling 54 polyglutamine diseases 54 SH#B# 54 medulloblastoma 54 MeCP2 protein 54 Neuregulin 1 54 BMPR2 54 Akt1 54 heterozygotes 54 CYP#C# gene 54 genomewide 54 gene rearrangements 54 heterozygous 54 oxysterols 54 NKX#.# 54 breast cancer gene mutation 54 skeletal malformations 54 Hirschsprung disease 54 cerebral vascular disease 54 varicella infection 54 primary biliary cirrhosis 54 Rh factor 54 GSTM1 gene 54 PB1 F2 54 #p#.# [002] 54 carcinoid 54 ankyrin B 54 familial aggregation 54 recessive genes 54 hyperprolactinemia 54 Male pattern baldness 54 Hurler syndrome 54 hereditary nonpolyposis colorectal cancer 54 Autoimmune disorders 54 Prox1 54 kinase gene 54 genetic variations 54 subclinical hyperthyroidism 54 fetal hemoglobin 54 cardiac channelopathies 54 precocious puberty 54 chlamydial infection 54 5 HTT gene 54 spontaneous remission 54 metabolic abnormality 54 retinitis pigmentosa RP 54 sporadic Creutzfeldt Jakob 54 toxoplasma 54 M. pneumoniae 54 miR #b [001] 54 EGFR gene 54 G6PD 54 IDH mutations 54 Hutchinson Gilford Progeria Syndrome 54 protein p# 54 breast carcinomas 54 NPHP 54 enteroviral infection 54 B7 H3 54 hippocampal function 54 DFMO 54 cyclin E 54 uPAR 54 RPE# gene 54 autosomal recessive genetic 54 SIRT1 gene 54 TSLP 54 WNK1 54 Bardet Biedl Syndrome 54 collagen VI 54 polymorphism 54 asymptomatically 54 K#R [002] 54 PHLPP 54 HPV# 54 ERK signaling 54 hyperinsulinemia 54 elevated CRP 54 IGF1 54 NFkB 54 GRP# 54 cardioembolic stroke 54 thyroid abnormalities 54 somatic mutation 54 neuronal dysfunction 54 intestinal polyps 54 BRAC2 54 Fragile X syndrome 54 Cholangiocarcinoma 54 SCA5 54 circadian genes 54 cyclophilin D 54 folic acid deficiency 54 chronic granulomatous disease 54 Becker muscular dystrophy 54 TH# cells 54 sickle hemoglobin 54 progranulin 54 endometrial cancers 54 Neurofibromatosis type 54 autoimmune thyroid 54 Bacterial vaginosis 54 Wiskott Aldrich syndrome 54 immunodeficiencies 54 degenerative neurological disorder 54 pheochromocytoma 54 previously uncharacterized 54 epigenetic mechanisms 54 MLL gene 54 neuro developmental disorder 54 shorter telomeres 54 diabetic kidney 54 human herpesvirus 54 PDGFR 54 Reye Syndrome 54 inherited gene mutation 54 myeloproliferative neoplasms 54 suppressor gene 54 Vitamin D insufficiency 54 fatal neuromuscular disorder 54 aetiological 54 gene 54 ADAMTS# 54 #p#.# [001] 54 nNOS 54 congenital adrenal hyperplasia CAH 54 polymyalgia rheumatica 54 CFTR protein 54 hereditary spastic paraplegia 54 N. gonorrhoeae 54 elevated triglyceride levels 54 chromosome #q 54 Htt 54 Beckwith Wiedemann syndrome 54 ischemic colitis 54 atypical hyperplasia 54 ependymoma 54 epigenetic regulation 54 vimentin 54 microsatellite instability 54 adenocarcinomas 54 herpes infection 54 bronchopulmonary dysplasia 54 LRRK2 54 intestinal inflammation 53 E4 variant 53 hamartoma 53 multi infarct dementia 53 thrombophilia 53 TGF ß 53 genes 53 ADDLs 53 autoimmune pancreatitis 53 motor neuron diseases 53 pre cancerous lesion 53 CALHM1 53 synapse formation 53 Proteus syndrome 53 ZNF# 53 IRF6 gene 53 CIB1 53 Alport syndrome 53 nerve degeneration 53 primary progressive aphasia 53 causative genes 53 VIPR2 53 tubercle bacillus 53 MYH9 53 SCD1 53 Congenital Adrenal Hyperplasia 53 Tay Sachs disease 53 gallstone disease 53 Notch1 53 mutated K ras 53 BRCA gene 53 dysautonomia 53 superinfection 53 matriptase 53 neuroendocrine 53 FSGS 53 cerebri 53 T1DM 53 MHC molecules 53 BRAF V#E mutation 53 TSC1 53 EGFR protein 53 ductal adenocarcinoma 53 activating mutations 53 metapneumovirus 53 PCNSL 53 gastric carcinomas 53 Plasmodium parasites 53 JAK2 enzyme 53 Gorlin syndrome 53 NRG1 53 BRCA2 mutations 53 myelogenous leukemia 53 interferon pathway 53 genes encoding 53 Argonaute 53 PKC beta 53 chronic prostatitis 53 Pdx1 53 phthalate syndrome 53 serotonin transporter 53 choroidal vasculopathy 53 HLA B# gene 53 CYP#C# [001] 53 WAGR syndrome 53 mutant huntingtin protein 53 congenital hypothyroidism 53 homozygotes 53 Wnt signaling 53 basal cell carcinomas 53 R#W [002] 53 KLF4 53 GBV C 53 mutant mouse 53 clinically insignificant 53 mastocytosis 53 KCNQ1 53 trophoblast cells 53 fatty liver disease 53 placental function 53 sortilin 53 clefting 53 Henoch purpura 53 squamous cell lung cancer 53 inherited genetic mutation 53 cryptorchidism 53 neurodevelopmental disorders 53 osteopetrosis 53 ERBB2 53 intrauterine infection 53 polycystic kidneys 53 ApoE4 allele 53 Chlamydia pneumoniae 53 metastatic lung cancer 53 non syndromic 53 nephritis 53 #q# [002] 53 dystrophin gene 53 PALB2 gene 53 amyloid deposits 53 euthymic patients 53 cystatin C 53 thyroiditis 53 MECP2 53 K ras mutations 53 presenilin 53 Long QT syndrome 53 MDM2 53 breast cancer susceptibility genes 53 ER alpha 53 behavioral disinhibition 53 persistent pulmonary hypertension 53 systemic mastocytosis 53 Genetic mutations 53 autoantibodies 53 immuno deficiency 53 modifier genes 53 postmenopausal breast cancer 53 progranulin mutations 53 invasive secretory carcinoma 53 autosomal dominant polycystic kidney 53 epithelial barrier 53 chromosomal translocation 53 SCN1A 53 cardiac fibrosis 53 DRD4 53 CYP#C# * 53 DRD2 53 lissencephaly 53 PPAR γ 53 Smad3 53 CXCL5 53 cranial irradiation 53 Epstein Barr virus 53 nongenetic 53 atrophic gastritis 53 nestin 53 chromosomal rearrangements 53 CETP gene 53 DRB1 * 53 myositis 53 epigenetic modifications 53 prostate cancer CaP 53 enterocolitis 53 murine leukemia virus 53 oncomodulin 53 chromosomal deletions 53 liver toxicity 53 Brugada Syndrome 53 atypical parkinsonism 53 FLT3 53 SIRT6 53 human papillomaviruses HPV 53 GSTM1 53 BRCA2 mutation carriers 53 pancreatic endocrine 53 muscarinic receptors 53 medium chain acyl 53 pyloric stenosis 53 SMN1 53 primary cilia 53 laforin 53 SHANK3 gene 53 lymphocytic 53 causative gene 53 prion disease 53 PTEN tumor suppressor 53 genotoxic stress 53 cholestasis 53 hypermethylated 53 PrP 53 GPx 53 T#I [002] 53 Treg cell 53 breast endometrial 53 pleural mesothelioma 53 abnormal proteins 53 TP# mutations 53 hyperactivated 53 mutant proteins 53 faulty BRCA1 gene 53 p# activation 53 TT genotype 53 apolipoprotein E4 53 Wilms tumor 53 hypovitaminosis D 53 Wnt signaling pathway 53 TRIM5 53 microbleeds 53 periodontal infection 53 HLA DRB1 * 53 GAB2 53 parainfluenza virus 53 NF kB pathway 53 OGG1 53 SMAD4 53 teratoma 53 Rett syndrome 53 Helicobacter pylori infection 53 Hypophosphatasia 53 sulfasalazine 53 cystic fibrosis transmembrane conductance 53 fibrocytes 53 spinocerebellar ataxia type 53 excitatory synapses 53 fatty acid metabolism 53 neurocognitive impairment 53 PIK3CA 53 progressive neurodegenerative 53 SNCA 53 lysosomal storage diseases 53 pernicious anemia 53 type 1diabetes 53 bronchoalveolar 53 mutant protein 53 genetic syndromes 53 myopathies 53 mutated BRCA 53 Pulmonary hypertension 53 NNRTI resistance 53 transgenic rats 53 retinal dysfunction 53 APOC3 53 SCN9A gene 53 c KIT 53 esophageal squamous cell carcinoma 53 eotaxin 53 allelic variants 53 alpha1 antitrypsin AAT deficiency 53 PNET 53 ferroportin 53 phenotypic variation 52 genetically inherited 52 fetal microchimerism 52 thyroid hormone levels 52 BMP2 52 clusterin 52 Leber congenital amaurosis 52 antisense RNA 52 immunopathology 52 UGT#B# 52 Polycystic ovary syndrome PCOS 52 Candida albicans 52 tau protein 52 mammary gland tumors 52 spastic paraplegia 52 nonsense mutation 52 DiGeorge syndrome 52 hyperalgesia 52 mammary cells 52 caveolin 52 Von Hippel Lindau 52 leukoencephalopathy 52 thyrotropin 52 Multivariate analyzes 52 CCR5 delta# 52 Cushing syndrome 52 immunocompetent 52 PTEN mutation 52 tau mutation 52 interstitial pneumonia 52 pathophysiologic 52 Friedreich ataxia 52 SOD2 gene 52 RANKL 52 KIAA# 52 aldehyde dehydrogenase 52 degenerative neurological diseases 52 incurable genetic 52 X chromosome 52 SOX3 gene 52 papillary carcinoma 52 autoantigens 52 developmental abnormalities 52 Apobec3 52 fetal malformations 52 immunodeficiency 52 adrenal cortex 52 heterotaxy 52 5 HT1A 52 KRAS mutations 52 claudin 52 HSV1 52 prolactin levels 52 agranulocytosis 52 dysbindin 52 degenerative neurological disease 52 placenta praevia 52 lung fibrosis 52 maternally transmitted 52 ABCB1 gene 52 allergic dermatitis 52 childhood leukemias 52 CXCL# 52 abnormal chromosomes 52 gene polymorphism 52 serous ovarian cancer 52 haplotype 52 severe congenital neutropenia 52 cyclin D1 52 neurodevelopmental disability 52 rheumatic disease 52 GNAQ 52 GRK5 52 Retinitis Pigmentosa RP 52 genetic locus 52 CAG repeats 52 HER2 neu 52 clotting disorder 52 SIDS infants 52 chemoresistance 52 antiphospholipid syndrome 52 IL #R 52 MALT lymphoma 52 heterozygote 52 carcinoid tumors 52 immunodeficiency disorder 52 IGFBP 3 52 probands 52 LRP6 52 CEACAM1 52 amyloid deposition 52 muscular dystrophies