Related by context. All words. (Click for frequent words.) 73 familial pancreatic cancer 72 IL#R 72 de novo mutations 72 CHD7 71 CDH1 71 autosomal recessive 71 MTHFR 71 chromosomal anomalies 71 IgA deficiency 71 PTPN# 71 missense mutations 71 aneuploidies 71 nonhereditary 70 KRAS oncogene 70 microdeletion 70 ADPKD 70 hereditary predisposition 70 myopathies 70 TACI mutations 70 G6PD deficiency 70 MLL2 70 developmental abnormalities 69 SCN5A 69 chromosomal rearrangement 69 TSC1 69 germline mutations 69 testicular germ cell 69 LRP5 69 mtDNA mutations 69 MSH2 69 Genetic variants 69 monogenic 69 FGFs 69 genes BRCA1 69 dominantly inherited 69 Genetic mutations 69 #q# deletion 69 TCF#L# gene 69 CCR5 delta# 69 motor neuron degeneration 68 p# mutations 68 chorioamnionitis 68 neuroblastomas 68 LIS1 68 Hashimoto thyroiditis 68 BRIP1 68 epigenetic changes 68 microdeletions 68 untreated celiac disease 68 neurofibromas 68 K ras mutations 68 progressive neurodegenerative disorder 68 Tay Sachs thalassemia 68 KCNQ1 68 familial adenomatous polyposis 68 ABCB1 68 chromosomal anomaly 68 Autoimmune disorders 68 gastric carcinoma 68 maternally inherited 67 missense mutation 67 epigenetic alterations 67 autosomal dominant inheritance 67 VHL gene 67 Fragile X gene 67 HNPCC 67 genetic loci 67 herpesviruses 67 MYH9 gene 67 clefting 67 GBA mutations 67 gene rearrangements 67 spontaneous mutations 67 Genetic variations 67 APOE ε4 67 MLH1 67 Genetic predisposition 67 #q#.# [002] 67 #q#.# [001] 67 autosomal dominant disorder 67 transfusion syndrome 67 breast endometrial 67 TP# mutations 67 ataxias 67 TMEM#B 67 narcolepsy cataplexy 67 NR#A# 67 HGPS 67 molecular abnormalities 67 Meckel Gruber 67 CNTNAP2 67 HbF 67 Li Fraumeni syndrome 67 genetic syndromes 67 Cryptococcus neoformans 67 Carcinoid tumors 67 NKX2 67 fronto temporal dementia 67 inherited predisposition 67 MeCP2 gene 67 Epstein Barr virus EBV 67 polycystic ovarian syndrome PCOS 66 Kufs disease 66 p# mutation 66 breast cancer genes BRCA1 66 MYCN amplification 66 monozygotic twins 66 genetic abnormalities 66 FMR1 gene 66 pathogenic mutations 66 hypermethylated 66 polycystic ovary syndrome PCOS 66 SHANK3 66 mutated BRCA1 66 abnormal methylation 66 familial ALS 66 chromosome #q#.# [001] 66 MECP2 gene 66 DQB1 * 66 mutated K ras 66 holoprosencephaly 66 chromosomal aberrations 66 INF2 66 MEF2A 66 Hutchinson Gilford progeria 66 Leukemias 66 leiomyomas 66 susceptibility gene 66 CFTR gene 66 BCL#A 66 p# activation 66 NOTCH1 66 HFE gene 66 seminomas 66 epithelial tissues 66 causal variants 66 pancreatic endocrine 66 NF1 66 DNA methylation patterns 66 Li Fraumeni 66 leptin deficiency 66 Genetic variation 66 familial hypercholesterolemia 66 TYMS 66 neurological abnormalities 66 testicular tumors 66 hamartomas 66 GPC5 66 CYP#C# [002] 66 SMAD4 66 hyperinsulinism 66 FGFR2 66 JAK2 enzyme 65 epigenetic modification 65 hydrops 65 mosaicism 65 Colon polyps 65 HER2 neu 65 chromosome rearrangements 65 TCF#L# 65 MGUS 65 congenital disorders 65 sortilin 65 CagA 65 autoinflammatory diseases 65 BARD1 65 miRNA genes 65 folate metabolism 65 inherited genetic mutations 65 basal cell nevus syndrome 65 ADAMTS# 65 CDKN2A 65 LRAT 65 neurodevelopmental disorder 65 MC1R 65 nerve degeneration 65 osteosarcomas 65 neuroligins 65 functional polymorphism 65 fatal neuromuscular disorder 65 chromosomal alterations 65 Bacterial vaginosis 65 GNAQ 65 microcephalin 65 virulence genes 65 dysgenesis 65 advanced adenoma 65 Treg cell 65 apolipoprotein E gene 65 #p#.# [001] 65 DNA hypomethylation 65 cause cardiac channelopathies 65 neuropsychiatric disorder 65 #q# [001] 65 normal karyotype 65 Peutz Jeghers syndrome 65 BRCA1 mutation carriers 65 beta1 integrin 65 filaggrin 65 sporadic ALS 65 ependymomas 65 VIPR2 65 TGFBR1 * 6A 65 hyper IgE syndrome 65 PTEN mutations 65 SLC#A# [002] 65 von Hippel Lindau 65 genes predisposing 65 Brugada syndrome 65 Clusterin 65 anaplastic lymphoma kinase 65 chromosome #p#.# 65 sCJD 65 Endometrial cancer 65 mutations 65 chromosomal defect 65 BRAF gene 65 PALB2 65 chromosome #q# [002] 65 COX2 65 chromosomal abnormalities 65 LRRK2 gene 65 AAT deficiency 65 nonsense mutation 65 gene BRCA2 65 polymorphic ventricular tachycardia 65 BRCA1 mutations 65 astrocytomas 65 phenotypic expression 65 apoE 65 Neurofibromatosis type 65 WDR# 65 somatic mutations 65 enterocolitis 65 oligodendrogliomas 64 autosomal dominant 64 apoE4 64 Sjögren syndrome 64 MC4R gene 64 germline mutation 64 KIF6 gene 64 IKZF1 64 hypermethylation 64 pre eclamptic 64 methylenetetrahydrofolate reductase 64 spinal muscle atrophy 64 susceptibility genes 64 Celiac sprue 64 activating mutations 64 exocrine 64 lung ovary 64 genetic polymorphisms 64 proband 64 Smad3 64 retinoblastoma Rb 64 cell adhesion molecule 64 penetrance 64 chromosomal deletions 64 Wwox 64 #p#.# [002] 64 chromosomal instability 64 familial predisposition 64 chromosomal disorders 64 GSTT1 64 recessive genetic 64 spinocerebellar ataxia 64 #q#.# deletion syndrome 64 mesotheliomas 64 Childhood Disorder 64 upregulating 64 atypical hyperplasia 64 Tuberous sclerosis 64 Pten 64 chromosomal defects 64 BRCA2 gene 64 Epstein Barr Virus EBV 64 etiologic 64 EoE 64 TP# mutation 64 G#S mutation 64 Zinc deficiency 64 dizygotic twins 64 NOD2 64 BRCA1 gene 64 Fibroblast 64 PDGFR 64 hyperprolactinemia 64 RUNX3 64 Metastases 64 BRCA2 breast cancer 64 Meckel Gruber syndrome 64 autoimmune thyroid 64 GSTP1 64 heterotaxy 64 dopamine D4 receptor 64 APOE e4 64 Hurthle cell 64 mutated genes 64 tryptophan hydroxylase 64 inherit predisposition 64 BRAF V#E 64 mutated gene 64 CYP#D# gene 64 mRNA transcripts 64 severe congenital neutropenia 64 BRCA1 BRCA2 64 adenomatous polyps 64 epigenetically 64 Yamanaka recipe 64 sequence homology 64 mitochondrial mutations 64 BMPR2 64 Polycystic ovary syndrome PCOS 64 Aspergillus species 64 microvascular disease 64 haematopoietic 64 nephronophthisis 64 WAGR syndrome 64 Rh incompatibility 64 GISTs 64 bacteria Streptococcus pneumoniae 64 MLL gene 64 tyrosine phosphorylation 64 tumor suppressor protein 64 phthalate syndrome 64 Polymorphisms 64 ALK mutations 64 sickle cell cystic fibrosis 64 R#W [002] 64 chlamydial infections 64 autosomal recessive disease 64 metabolic abnormalities 64 nonsense mutations 64 genetic abnormality 64 apolipoprotein E4 64 gene mutations 64 PTEN gene 64 DISC1 gene 64 mental retardation epilepsy 64 embryonal 64 BRCA2 gene mutations 64 vWD 64 CALHM1 64 androgen excess 64 fluoroquinolone resistance 64 promoter hypermethylation 64 chromosomal regions 64 conductance regulator 64 excitatory synapses 64 APOL1 64 G6PD 64 Neuregulin 1 64 HLA DRB1 64 spontaneous mutation 64 ORMDL3 64 Hurler syndrome 64 #beta HSD1 64 eotaxin 64 nonischemic 64 KIBRA 64 EBV infection 64 Hip dysplasia 64 underlying pathophysiology 64 neurologic complications 64 BRAF protein 64 nonmelanoma skin cancers 64 micro RNAs 64 progranulin gene 64 paraneoplastic 63 STAT3 signaling 63 FASPS 63 mitochondrial disorders 63 recurrent miscarriages 63 hyperactivation 63 nonmelanoma 63 Glucocorticoids 63 progressive neurodegenerative 63 T1DM 63 histone deacetylases 63 rheumatoid arthritis lupus 63 gene MECP2 63 Joubert syndrome 63 kidney urologic 63 Six3 63 beta catenin protein 63 pathogenic mechanisms 63 epigenetic modifications 63 pRb 63 gene polymorphisms 63 Thyroid disorders 63 immunodeficiencies 63 dysregulated 63 muscular dystrophy cystic fibrosis 63 GBM tumors 63 pituitary adenomas 63 elevated triglyceride levels 63 IRS1 63 constitutively expressed 63 vimentin 63 misregulation 63 JAK mutations 63 myeloproliferative 63 dopamine receptor gene 63 glutamic acid decarboxylase 63 BRCA2 carriers 63 epithelial tumors 63 inherited neurological disorder 63 dyskeratosis congenita 63 HLA DQ2 63 5 HTTLPR 63 TRAF1 C5 63 ovarian dysfunction 63 androgen receptor AR 63 TTR gene 63 varicella infection 63 SOD1 gene 63 lactase deficiency 63 gestational diabetes mellitus 63 inactive X chromosome 63 KCNH2 63 Fibroblast Growth Factor Receptor 63 protein encoded 63 Beta thalassemia 63 Gliomas 63 Dystrophin 63 Premature Aging 63 epilepsies 63 colonic mucosa 63 predisposing factor 63 extramedullary 63 antiphospholipid syndrome 63 IUGR 63 V#F mutation 63 euthymic patients 63 AML MDS 63 neuroendocrine cells 63 ADAM# 63 Irritable bowel syndrome IBS 63 FXTAS 63 inherited retinal degeneration 63 neurodegenerative disorder 63 FGFR4 63 radiosensitive 63 neurofibromin 63 JAK2 gene 63 Vitamin B# deficiency 63 sporadic Creutzfeldt Jakob 63 Malassezia 63 neuronal dysfunction 63 ZNF# 63 non coding RNA 63 myeloproliferative neoplasms 63 Hemangiomas 63 parkinsonism 63 Oxidative damage 63 estrogen receptor alpha 63 leiomyoma 63 intestinal epithelium 63 bacterium Neisseria meningitidis 63 KIAA# 63 mitochondrial defects 63 phenotypic variation 63 C#Y 63 causative genes 63 pilocytic astrocytomas 63 atrophic gastritis 63 causative mutations 63 IRF6 63 gallstone disease 63 chronic granulomatous disease 63 skeletal metastases 63 LQTS 63 genus Plasmodium 63 Medulloblastoma 63 highly heritable 63 Chronic pancreatitis 63 intracellular signal transduction 63 STAT4 63 chromosome abnormalities 63 NF kB signaling 63 Hh pathway 63 clinically heterogeneous 63 connexin 63 Wnt signaling pathway 63 NFKBIA 63 mitochondrial dysfunction 63 fatal myelination disorder 63 MAP kinases 63 Cathepsin B 63 carcinoid tumors 63 lichen planus 63 post transplant lymphoproliferative 63 splice variants 63 thyroid hormone levels 63 Myelodysplastic syndromes MDS 63 renal cell carcinomas 63 heterozygotes 63 adenocarcinomas 63 fibrillin 1 63 PARP inhibition 63 cystic fibrosis chronic pancreatitis 63 Heterozygous 63 alpha synuclein protein 63 epigenetic silencing 63 mucins 63 cisplatin resistant 63 frontotemporal dementia 63 sphingolipid 63 AAT Deficiency 63 congenital adrenal hyperplasia CAH 63 malignant prostate 63 progranulin mutations 63 neurofibrillary 63 constitutive activation 63 Activating mutations 63 UGT#B# 63 insulin signaling pathway 63 aneuploidy 63 synaptogenesis 63 dysplastic lesions caused 63 MYH9 63 Joubert syndromes 63 ERBB2 63 tRNA synthetases 63 teratogens 63 APOE genotype 63 HER2 expression 62 degenerative neurological diseases 62 SCN9A 62 pancreatic prostate 62 familial clustering 62 klotho 62 SMN1 62 carbohydrate intolerance 62 SORL1 62 differential gene expression 62 granzyme B 62 SLC#A# [001] 62 LKB1 62 monozygotic twin 62 Mycoplasma pneumoniae 62 protein kinase C 62 muscular dystrophies 62 spongiform encephalopathies 62 FTLD 62 gastrointestinal dysfunction 62 recurrent miscarriage 62 HDAC enzymes 62 PKU genetic 62 pheochromocytomas 62 Autoantibodies 62 cell adhesion molecules 62 motor neuron diseases 62 Klinefelter syndrome 62 type 1diabetes 62 IGFBP2 62 chromosomal disorder 62 abnormal chromosomes 62 genomic imprinting 62 medulloblastoma tumors 62 methicillin susceptible Staphylococcus aureus 62 CHEK2 62 DLX5 62 CP CPPS 62 Malignant mesothelioma 62 genotoxic stress 62 Leydig cell 62 paragangliomas 62 primary cilia 62 neuroendocrine cancers 62 metastatic neuroendocrine tumors 62 chromosome deletion 62 genomic variants 62 copper zinc superoxide 62 ERK signaling 62 oral clefts 62 lymphocyte activation 62 ApoE gene 62 endometrial cancers 62 KCNE2 62 hormonal abnormalities 62 gene APOE4 62 SLITRK1 62 V Leiden 62 PCNSL 62 malignant neoplasm 62 genetic alteration 62 TACI 62 amyloid deposition 62 endometrial hyperplasia 62 MIF protein 62 BRCA2 gene mutation 62 SMN protein 62 Pseudomonas syringae 62 Diabetic neuropathy 62 bladder cancers 62 regulator CFTR gene 62 HER2 overexpression 62 MC1R gene 62 endocrine abnormalities 62 ductal breast cancer 62 MMP# 62 aldehyde dehydrogenase 62 BMP2 62 achromatopsia 62 HLA genes 62 anatomical abnormalities 62 Escherichia coli Klebsiella pneumoniae 62 astrocytic 62 ankyrin B 62 LRRK2 mutations 62 IDH2 62 nondemented 62 parkin gene 62 medulloblastomas 62 BRCA2 mutations 62 Upregulation 62 thyrotropin 62 rhinovirus infection 62 Lrp5 62 polyglutamine diseases 62 persistent pulmonary hypertension 62 allelic variants 62 Vitamin D insufficiency 62 PIK3CA 62 mice lacking 62 Aortic stenosis 62 methylation patterns 62 peroxisome 62 prenatally diagnosed 62 colorectal carcinoma 62 downregulation 62 huntingtin gene 62 fibrotic disease 62 homocystinuria 62 APOE4 62 chitinase 62 neural tube defect 62 intestinal polyps 62 N. gonorrhoeae 62 gene mutation 62 Rb gene 62 regulates gene expression 62 glucocorticoid receptors 62 Dpp 62 essential thrombocythemia 62 Folate deficiency 62 C. pneumoniae 62 abnormal prions 62 FMRP protein 62 lymphangiogenesis 62 fetal chromosomal 62 prodynorphin 62 Factor Receptor 62 hypothalamic pituitary 62 obstructive coronary artery 62 GSTM1 62 LPA receptors 62 myelofibrosis polycythemia vera 62 Ribavirin causes 62 GATA4 62 genomic rearrangements 62 Papillary 62 unprovoked seizures 62 Dysregulation 62 microRNA expression 62 ENPP1 62 UGT#A# * 62 ovarian endometrial 62 pancreatic lung 62 granulosa cell 62 CMV infection 62 HMGA2 62 mitochondrial DNA mtDNA 62 serous ovarian cancer 62 ANCA associated 62 RET PTC rearrangements 62 Brugada Syndrome 62 Colorectal cancers 62 Chlamydia pneumoniae 62 genetic mutations 62 periventricular 62 TP# gene 62 mutation 62 immunocompetent 62 recessive inheritance 62 postoperative delirium 62 neuroblastoma tumors 62 Abnormalities 62 progressive neurodegenerative disorders 62 alpha synuclein gene 62 Squamous 62 shortened telomeres 62 NOMID 62 atopic disorders 62 COL#A# 62 neurological disorder affecting 62 familial adenomatous polyposis FAP 62 β1 62 modifier genes 62 neuro developmental disorder 62 peroxisomal 62 progranulin protein 62 pyloric stenosis 62 CNTNAP2 gene 62 neurocognitive impairment 62 unstable detrusor muscle 62 trophoblastic 62 GLUT1 62 CYP#B# 62 pituitary adenoma 62 ALI ARDS 62 transcriptional repression 62 HLA B# 62 FLT3 62 biochemical imbalance 62 CYP#D# 62 aneuploid cells 62 APOE gene 62 endocrine glands 62 cytokine signaling 62 RSV infections 62 Systemic lupus erythematosus SLE 62 genetic alterations 62 Ovarian cysts 62 TGF ß 62 hereditary deafness 62 dysbindin 62 IDH mutations 62 fat malabsorption 62 differentially regulated 62 vitamin D receptors 62 cAMP signaling 62 CDK4 62 amenorrhoea 62 Trichophyton rubrum 62 liver scarring 62 genomic alterations 62 prolonged QT interval 62 CNVs 62 recessive mutations 62 KIT mutations 62 EGFR protein 62 brain lesions 62 thyroid hormone deficiency 62 H. pylori infections 62 caveolin 62 microRNA molecules 62 PON1 62 Fibroblasts 62 heritable variation 62 Apert syndrome 62 stathmin 62 adrenocortical cancer 62 imprinted genes 62 neonatal encephalopathy 62 ovarian hormones 62 dysplasias 62 squamous cell lung cancer 62 susceptibility loci 62 histone modification 62 congenital anomalies 62 recurrent seizures 62 myeloproliferative diseases 62 primary ciliary dyskinesia 62 Imprinted genes 62 gastroenteritis conjunctivitis 61 nonalcoholic steatohepatitis NASH 61 chromosome abnormality 61 Entamoeba 61 myelin insulation 61 TEL AML1 61 epigenetic mechanisms 61 cellular prion protein 61 abnormalities 61 DNA rearrangements 61 adrenal cortex 61 KRAS mutations 61 endocrine tumors 61 SCN1A 61 Immunohistochemical analysis 61 downregulated 61 familial aggregation 61 Jhdm2a 61 hypopituitarism 61 hypokalemia hypomagnesemia 61 penile cancers 61 apoC III 61 oncogenesis 61 Premature menopause 61 CYP#A# gene 61 Basal cell 61 Cysts 61 MTDH 61 pituitary tumors 61 mitochondrial metabolism 61 SETDB1 61 anovulatory infertility 61 histone methylation 61 previously uncharacterized 61 alpha thalassemia 61 synovial cells 61 IFN γ 61 cirrhosis liver failure 61 LDL receptor 61 Sporadic CJD 61 gynecologic malignancy 61 male hormone androgen 61 neuroendocrine 61 interferon pathway 61 Fas ligand 61 misfolding 61 neurofibroma 61 FMR1 61 heritable genetic 61 TRAIL induced apoptosis 61 inherited gene mutation 61 recessive trait 61 deacetylation 61 Pulmonary hypertension 61 anencephaly 61 NFkB 61 Lymphocytic 61 IRAK1 61 lobular breast cancer 61 autistic regression 61 trophoblast cells 61 spinocerebellar ataxia type 61 genetic defects 61 hypoperfusion 61 DHFR 61 reproductive abnormalities 61 Cowden syndrome 61 somatic mutation 61 HOX genes 61 mutant allele 61 endostatin 61 coagulation abnormalities 61 cypin 61 chromosomal rearrangements 61 apolipoprotein E 61 tardive dyskinesia TD 61 hyperplastic 61 enteroviruses 61 HER2 positivity 61 ichthyosis vulgaris 61 irregular menstrual cycles 61 autosomal recessive genetic 61 GAB2 61 hippocampal function 61 calcineurin 61 prostate adenocarcinoma 61 genetically inherited 61 PDE#A 61 intestinal inflammation 61 Hereditary angioedema HAE 61 human papillomaviruses HPV 61 overactivation 61 causative gene 61 Prion proteins 61 precancerous cervical 61 C. neoformans 61 interleukins 61 TMPRSS2 ERG 61 E selectin 61 ARID1A 61 phenotypic variability 61 transthyretin 61 cultured neurons 61 p# deficient 61 dermatophytes 61 Polymorphic Ventricular Tachycardia CPVT 61 allelic variation 61 familial polyposis 61 immunocompromised individuals 61 hyperactivated 61 SRY gene 61 paraganglioma 61 epigenetic regulation 61 endogenous retroviruses 61 bexarotene 61 dentinal hypersensitivity 61 proliferative diabetic retinopathy 61 IKK2 61 embryonal rhabdomyosarcoma 61 cancerous enlargement 61 neuron degeneration 61 abnormal p# 61 PTEN tumor suppressor 61 dysglycemia 61 idiopathic myelofibrosis 61 torsade de pointes 61 Atopic dermatitis 61 chromosomal aberration 61 WT1 61 infertility miscarriages 61 FGFR1 61 neuroinflammatory 61 Prion diseases 61 Magnesium deficiency 61 prothrombotic 61 Barrett mucosa 61 CIB1 61 lung adenocarcinomas 61 adenomyosis 61 Sezary syndrome 61 hepatic lipase 61 cytopathic 61 molar pregnancy 61 abnormal chromosome 61 genetic variants associated 61 idiopathic PAH 61 synuclein 61 RPE# 61 breast cancer susceptibility genes 61 Candida species 61 DEC2 61 Akt signaling 61 RIP1 61 Viral infections 61 Squamous cell 61 Dilated cardiomyopathy 61 proto oncogene 61 somatostatin 61 tumoral 61 fetal malformations 61 prostate carcinogenesis 61 Pancreatic insufficiency 61 uterine ovarian 61 undiagnosed celiac disease 61 progressive degeneration 61 Ets2 61 embryonic tissues 61 cryptogenic 61 CHDs 61 Genetic abnormalities 61 systemic scleroderma 61 leptin receptor 61 breast cancer metastasis 61 aneuploid 61 gene deletions 61 alexithymia 61 sonographic diagnosis 61 γ secretase 61 chromosomal translocations 61 trophoblasts 61 leukaemias 61 ABCB1 gene 61 protein alpha synuclein 61 subclinical hypothyroidism 61 Alpha synuclein 61 genetic defect 61 neurofibromatosis type 61 BRCA2 mutation 61 synaptic function 61 Cyclin E 61 noncoding RNAs 61 mitogen activated protein kinases 61 FUS protein 61 shorter telomere length 61 Chlamydia psittaci 61 mutant huntingtin protein 61 CFTR cystic fibrosis transmembrane 61 disregulation 61 bronchopulmonary dysplasia BPD 61 neural crest 61 Inactivation 61 hereditary nonpolyposis colorectal cancer 61 Gorlin syndrome 61 Mitochondrial diseases 61 papillary carcinoma 61 cholinergic neurons 61 Heavy menstrual bleeding 61 PCOD 61 circadian genes 61 chromatin structure 61 carcinoids 61 neoplastic diseases 61 arterial calcification 61 Plasmodium vivax 61 genomic deletions 61 epithelial barrier 61 TGF b 61 proapoptotic 61 Polycomb proteins 61 Parkinsonian Syndromes 61 bronchopulmonary dysplasia 61 neuro developmental disorders 61 Vascular dementia 61 lupus scleroderma 61 chronic autoimmune disorder 61 apolipoprotein E APOE 61 Brain metastases 61 primary biliary cirrhosis 61 facial clefts 61 leaky gut 61 inactivating mutations 61 autism spectrum disorders ASDs 61 Kv#.#