Related by context. All words. (Click for frequent words.) 73 hereditary nonpolyposis colorectal cancer 71 familial adenomatous polyposis 70 MSH2 69 IgA deficiency 69 microsatellite instability 68 thrombophilia 68 MLH1 68 familial ALS 68 BRCA1 mutations 67 MYH9 gene 67 inherited mutations 67 familial pancreatic cancer 67 narcolepsy cataplexy 67 atypical hyperplasia 67 proband 67 CDH1 67 ADPKD 66 myeloproliferative neoplasms 66 BRCA mutation 66 ABCB1 66 germline mutation 66 hereditary nonpolyposis colon cancer 66 hereditary hemochromatosis 66 autosomal recessive 66 germline mutations 66 APOE e4 66 HNSCC 66 sporadic ALS 66 BRAF V#E 66 TCF#L# gene 65 APOL1 65 missense mutations 65 advanced adenoma 65 mtDNA mutations 65 LQTS 65 BRCA2 mutations 65 sCJD 65 MGUS 65 BRCA1 BRCA2 65 mutated BRCA1 65 gallstone disease 65 euthymic patients 64 rs# [004] 64 breast cancer susceptibility genes 64 Li Fraumeni syndrome 64 familial adenomatous polyposis FAP 64 PTPN# 64 smoldering myeloma 64 CIN2 + 64 GBA mutations 64 neoplasias 64 microdeletions 64 CDKN2A 64 VCFS 64 autosomal dominant 64 familial hypercholesterolemia 64 untreated celiac disease 64 histological subtype 64 diabetes mellitus DM 64 autoimmune thyroid 63 Hashimoto thyroiditis 63 genes predisposing 63 MTHFR 63 familial aggregation 63 Li Fraumeni 63 diffuse gastric 63 monogenic 63 advanced adenomas 63 HER2 overexpression 63 BRCA2 carriers 63 somatization disorder 63 TP# mutation 63 advanced neoplasia 63 Cholangiocarcinoma 63 APOE genotype 63 Haptoglobin 63 hereditary predisposition 63 prostate cancer CaP 63 BRCA2 mutation carriers 63 adenomatous polyps 63 colorectal adenoma 63 APOE ε4 63 #q# deletion 63 EoE 63 basal cell nevus syndrome 63 nonmelanoma skin cancers 63 pheochromocytomas 63 leiomyomas 63 #q#.# [001] 63 CP CPPS 63 nonhereditary 63 subclinical atherosclerosis 62 AAT deficiency 62 mesotheliomas 62 somatic mutations 62 Epstein Barr virus EBV 62 susceptibility gene 62 K ras mutations 62 pancreatic adenocarcinoma 62 BRCA1 62 genetic abnormalities 62 myeloproliferative 62 APOE4 62 PCa 62 chorioamnionitis 62 testicular germ cell 62 obstructive coronary artery 62 susceptibility loci 62 genetic syndromes 62 amnestic MCI 62 allele frequencies 62 PCNSL 62 C#Y 62 lung adenocarcinoma 62 rs# [002] 62 affective psychoses 62 malignant pleural mesothelioma 62 microdeletion 62 EBV infection 62 paraganglioma 62 BRCA mutations 62 colorectal cancer CRC 62 Asymptomatic 62 mutated K ras 62 ApoE4 62 Brugada Syndrome 62 renal cell carcinomas 62 breast carcinomas 62 de novo mutations 62 histologic subtype 62 FLT3 mutations 62 CHEK2 62 CC genotype 62 genomewide 62 prostate adenocarcinoma 62 neurocognitive impairment 62 mitochondrial toxicity 62 familial clustering 62 genetic loci 62 vWD 62 etiologic 62 thyroid dysfunction 62 ApoE4 gene 62 mycosis fungoides 62 NAFLD 62 paragangliomas 62 pilocytic astrocytomas 62 autosomal dominant inheritance 62 TGFBR1 * 6A 61 atopic 61 dominantly inherited 61 beta thalassemia 61 thyroiditis 61 Leukemias 61 recurrent miscarriage 61 pulmonary hypertension PH 61 undergone radical prostatectomy 61 chromosomal anomalies 61 hereditary breast cancer 61 Hurthle cell 61 Meckel Gruber 61 gene BRCA2 61 Adenomas 61 probands 61 Brugada syndrome 61 hepatocellular carcinomas 61 HBeAg negative 61 immunodeficiencies 61 CCR5 delta# 61 GSTT1 61 MLL2 61 genetic variants associated 61 chlamydial infection 61 GISTs 61 acute leukemias 61 BRCA2 mutation 61 Nonalcoholic fatty liver 61 peritoneal carcinomatosis 61 aneuploidy 61 essential thrombocythemia 61 lactose malabsorption 61 aneuploidies 61 supratentorial 61 TACI mutations 61 abnormal cytology 61 APOE gene 61 Prostatitis 61 lymphoproliferative disorders 61 UGT#A# * 61 bladder cancers 61 IDH1 mutation 61 hyperplastic 61 T1DM 61 #q#.# deletion syndrome 61 CMV infection 61 KRAS oncogene 61 Gorlin syndrome 61 Fragile X gene 61 ataxias 61 alexithymia 61 Von Willebrand disease 61 IKZF1 61 SRBD 61 #q# [001] 61 genes BRCA1 61 varicoceles 61 SSc 61 BRCA2 gene mutation 61 genomic alterations 61 malignant neoplasm 61 hematopoietic cancers 61 oesophageal adenocarcinoma 61 somatic mutation 61 syndromic 61 atrophic gastritis 61 genetic polymorphisms 61 ApoE gene 61 recessive inheritance 61 mitochondrial disorders 61 nondemented 61 chromosomal aberrations 61 ovarian pancreatic 61 colorectal carcinoma 61 chromosome #q#.# [001] 61 prostate cancer PCa 61 IL#R 61 chromosome abnormality 61 epithelial tumors 61 late onset hypogonadism 61 hyper IgE syndrome 61 somatoform disorders 61 postoperative delirium 61 stratifying patients 61 HLA B# 61 mucinous 61 urolithiasis 61 BRCA1 mutation carriers 61 Klinefelter syndrome 61 BRAF gene 61 motor neuron degeneration 61 T2D 61 basal cell carcinoma BCC 61 cervical carcinoma 61 lobular breast cancer 61 CNTNAP2 60 NMIBC 60 deletion 5q 60 herpesviruses 60 MELAS 60 FXTAS 60 fronto temporal dementia 60 Aneuploidy 60 inherited predisposition 60 psychiatric comorbidity 60 variant rs# 60 FTLD 60 Lafora disease 60 choriocarcinoma 60 Genetic predisposition 60 APOE e4 gene 60 urethritis 60 nonalcoholic steatohepatitis NASH 60 V Leiden 60 nonmetastatic 60 urothelial carcinoma 60 T2DM 60 clinicopathological 60 clinicopathologic 60 primary hyperparathyroidism 60 sporadic Creutzfeldt Jakob 60 1 diabetes T1D 60 Peutz Jeghers syndrome 60 JMML 60 carotid stenosis 60 shorter telomere length 60 Cowden syndrome 60 C. trachomatis 60 autosomal recessive genetic 60 Metastases 60 MetS 60 ARVD 60 varicocele 60 pituitary adenoma 60 PALB2 60 dopamine receptor gene 60 mosaicism 60 Chronic lymphocytic leukemia 60 LRP5 60 generalized epilepsy 60 esophageal squamous cell carcinoma 60 Langerhans cell histiocytosis 60 dyskeratosis congenita 60 CYP#C# [001] 60 BRCA gene mutation 60 thoracic aortic disease 60 chromosomal rearrangement 60 carcinoid tumors 60 haemochromatosis 60 BRCA2 gene 60 Venous thromboembolism 60 penetrance 60 spontaneous mutations 60 non polyposis colorectal 60 maternally inherited 60 KIBRA 60 astrocytomas 60 activating mutation 60 primary biliary cirrhosis 60 neuroblastoma tumors 60 autosomal dominant disorder 60 paraneoplastic 60 elevated CRP 60 SCN5A 60 Chlamydia trachomatis 60 monozygotic twins 60 G6PD deficiency 60 urothelial cancer 60 GNAQ 60 mutation 60 KIF6 gene 60 inherited genetic mutations 60 meningiomas 60 severe congenital neutropenia 60 BARD1 60 LV dysfunction 60 NOMID 60 metachronous 60 FGFR2 60 homozygosity 60 recurrent miscarriages 60 Endometrial cancer 60 apolipoprotein E4 60 Heritability 60 Aortic stenosis 60 proliferative diabetic retinopathy 60 Adjuvant chemotherapy 60 gene rearrangements 60 chromosomal regions 60 colorectal neoplasia 60 overt hypothyroidism 60 congenital toxoplasmosis 60 latent TB infection 60 KRAS mutation 60 generalized vitiligo 60 Sjögren syndrome 60 nonalcoholic steatohepatitis 60 chromosomal anomaly 60 monoclonal gammopathy 60 osteosarcomas 60 intestinal polyps 60 systemic lupus erythematosus SLE 60 pleural mesothelioma 60 lysosomal storage diseases 60 Papillary 59 hypermethylated 59 endometrial hyperplasia 59 Acute myeloid leukemia 59 Chlamydia pneumoniae 59 BRCA2 59 autonomic dysfunction 59 GSTP1 59 Severe Primary IGFD 59 ovarian malignancy 59 malignant lymphoma 59 gestational diabetes mellitus 59 polycystic ovary syndrome PCOS 59 micrometastases 59 clinico pathological 59 cardioembolic stroke 59 SLC#A# [002] 59 DQB1 * 59 atypical ductal hyperplasia 59 LVNC 59 nonsense mutations 59 Kabuki syndrome 59 unexplained mental retardation 59 gastric adenocarcinoma 59 heterozygotes 59 NF1 59 hypermethylation 59 adenoma 59 Cognitive impairment 59 epididymitis 59 breast cancer genes BRCA1 59 heterozygous 59 cardiac channelopathies 59 TP# mutations 59 Apolipoprotein E 59 progressive neurodegenerative disorder 59 androgen deficiency 59 systemic amyloidosis 59 ependymoma 59 testicular tumors 59 AML MDS 59 causative mutations 59 incidentalomas 59 Parkinson Disease PD 59 etiological 59 metaplasia 59 Niemann Pick disease 59 ASCUS 59 KRAS mutations 59 monozygotic twin 59 gene mutations 59 autoimmune thyroiditis 59 gastric carcinoma 59 chromosomal abnormalities 59 HGPIN 59 Hodgkin lymphoma HL 59 congenital abnormalities 59 lymphocytic 59 LHON 59 lung adenocarcinomas 59 #p#.# [002] 59 dysglycemia 59 acute myeloid 59 adenocarcinomas 59 atherogenic dyslipidemia 59 OSAHS 59 prostate carcinoma 59 Multivariate analysis 59 abdominal adiposity 59 NNRTI resistance 59 affective psychosis 59 gastric cancers 59 fetal chromosomal 59 thiopurine 59 neoplasm 59 ε4 59 Hutchinson Gilford progeria 59 SLC#A# [001] 59 ragweed allergic 59 varicella infection 59 XMRV infection 59 LPA gene 59 TCF#L# 59 clefting 59 VaD 59 neuroendocrine cancers 59 PTEN mutations 59 hamartomas 59 rs# [003] 59 DNA methylation patterns 59 BRCA mutation carriers 59 genotype phenotype 59 molecular abnormalities 59 dysthymic disorder 59 colorectal adenomas 59 VUR 59 ALI ARDS 59 transfusion syndrome 59 serous ovarian cancer 59 APOC3 59 pathogenic mutations 59 chronic granulomatous disease 59 chromosomal disorders 59 comorbid disorders 59 papillary carcinoma 59 atherothrombotic disease 59 affective disorders 59 Cytogenetic 59 thymoma 59 precancerous cervical lesions 59 chronic myeloid 59 chronic HBV infection 59 medulloblastomas 59 Hemophilia B 59 myelodysplasia 59 idiopathic PAH 59 LRRK2 gene 59 JAK2 mutation 59 habitual snoring 59 Ischemic 59 neuropsychiatric disorder 59 p# mutations 59 benign breast 59 nonischemic 59 PAOD 59 Colon polyps 59 ectodermal dysplasia 59 microcephalin 59 Leydig cell 59 SOD1 gene 59 clade B 59 tumor histology 59 apolipoprotein E gene 59 autosomal recessive disorder 59 spontaneous mutation 59 B Cell Lymphoma 59 chronic periodontitis 59 microscopic hematuria 59 holoprosencephaly 59 hereditary deafness 59 renal scarring 59 acute rheumatic fever 59 lobular carcinoma 59 chromosomal alterations 59 acute lymphoid leukemia 59 BMPR2 59 PNET 59 affective disorder 59 renal tumors 58 bronchogenic carcinoma 58 TEAEs 58 cytogenic 58 cytogenetic abnormalities 58 precancerous condition 58 myelofibrosis polycythemia vera 58 HER2 positivity 58 HG PIN 58 invasive fungal infection 58 chronic prostatitis 58 invasive ductal 58 genetically inherited 58 causal variants 58 multivariable analysis 58 invasive carcinoma 58 primary aldosteronism 58 recurrent glioblastoma multiforme 58 mutations 58 MSH6 58 breast endometrial 58 GSTM1 gene 58 congenital adrenal hyperplasia CAH 58 HLA genes 58 causative gene 58 TT genotype 58 bipolar affective disorder 58 nonmelanoma skin cancer 58 Helicobacter pylori infection 58 parkinsonism 58 neoplastic 58 squamous cell carcinoma SCC 58 myeloid leukemia 58 oligodendrogliomas 58 Vitamin D insufficiency 58 ApoE4 allele 58 LRRK2 mutations 58 Congenital Muscular Dystrophy 58 Polycystic ovary syndrome PCOS 58 latent tuberculosis infection 58 post thrombotic syndrome 58 AUDs 58 anovulatory infertility 58 HLA DQ2 58 Myelodysplastic Syndrome 58 impaired fasting glucose 58 atypia 58 Trichomonas vaginalis 58 EGFR mutations 58 papillary thyroid cancer 58 microvascular disease 58 lysosomal storage disease 58 autosomal dominant polycystic kidney 58 HbF 58 myelomeningocele 58 #q# deletion syndrome 58 distant metastasis 58 precancerous cervical 58 subclinical hyperthyroidism 58 chemoresistant 58 TRAF1 C5 58 invasive lobular 58 HLA DRB1 * 58 BRCA1 gene 58 neurofibromas 58 cause cardiac channelopathies 58 pathologic fractures 58 ductal breast cancer 58 de novo AML 58 MALT lymphoma 58 microalbuminuria 58 Lymphocytic 58 androgenetic alopecia 58 GSTM1 58 seminomas 58 homozygous 58 heterotaxy 58 gynecologic malignancy 58 HLA DRB1 58 LTBI 58 chromosomal defect 58 SLNB 58 murine leukemia virus 58 FMR1 gene 58 muscular dystrophy cystic fibrosis 58 intravenous bisphosphonates 58 variant allele 58 Hurler syndrome 58 LRAT 58 IPAH 58 Adenocarcinoma 58 Uterine cancer 58 imatinib resistance 58 human metapneumovirus 58 Sezary syndrome 58 disease NAFLD 58 modifier genes 58 subclinical hypothyroidism 58 polycystic ovary syndrome 58 leukaemias 58 missense mutation 58 CIN3 58 BRAF V#E mutation 58 Becker muscular dystrophy 58 Legg Calvé Perthes disease 58 haplotypes 58 allelic variants 58 inherited genetic mutation 58 colorectal polyps 58 squamous cell lung cancer 58 promoter hypermethylation 58 knee OA 58 benign proliferative breast 58 FLT3 58 endometrial cancers 58 pituitary adenomas 58 TOMM# 58 papillary renal cell carcinoma 58 Arrhythmogenic Right Ventricular Cardiomyopathy 58 seminoma 58 NSCLC tumors 58 homozygous FH 58 endophenotypes 58 frontotemporal dementia 58 optica 58 causative mutation 58 Thyroid nodules 58 Wiskott Aldrich syndrome 58 seropositivity 58 spinocerebellar ataxia 58 coronary calcification 58 AAT Deficiency 58 alpha1 antitrypsin deficiency 58 clinically heterogeneous 58 MYCN amplification 58 rs# [001] 58 HIV HCV coinfected 58 chromosome #p#.# 58 karyotypes 58 myeloproliferative disorders 58 MECP2 gene 58 lung cancer NSCLC 58 Genetic variation 58 post transplant lymphoproliferative 58 virus XMRV 58 NPM1 gene 58 teratoma 58 Hematologic 58 Clusterin 58 compulsive hoarding syndrome 58 chromosome #p# [001] 58 chromosomal mutations 58 monozygotic 58 STAT4 58 metastatic neuroendocrine tumors 58 methylenetetrahydrofolate reductase 58 CagA 58 neuropathologic 58 neuroblastomas 58 chromosome #p# [002] 58 hyperparathyroidism 58 retrospective cohort 58 intraepithelial neoplasia 58 Waldenstrom macroglobulinemia 58 autosomal recessive disease 58 haematologic 58 extramedullary 58 carcinoid tumor 58 leptin deficiency 58 abacavir Ziagen 58 VKORC1 58 intestinal metaplasia 58 PARP inhibition 58 neurologic complications 58 Parkinsonian Syndromes 58 von Willebrand 58 somatic symptoms 58 tumor recurrence 58 chronic hepatitis cirrhosis 58 Glioblastoma Multiforme GBM 58 parathyroid 58 distinct subtypes 58 nephrogenic 58 cranial irradiation 58 pyloric stenosis 58 neurosyphilis 58 valvular heart 58 superinfection 58 nonalcoholic fatty liver 58 adnexal mass 58 subclinical 58 depressive symptomatology 58 latent celiac disease 57 mitochondrial mutations 57 bladder carcinoma 57 neural tube defect 57 SNP rs# [001] 57 precursor lesions 57 neurological abnormalities 57 neurocognitive deficits 57 ductal adenocarcinoma 57 pathophysiologic 57 PITX2 57 multivessel coronary artery 57 lung carcinomas 57 grade serous ovarian 57 undiagnosed celiac disease 57 Chronic pancreatitis 57 chromosomal instability 57 PPCM 57 epithelial ovarian cancer 57 2 diabetes T2D 57 atypical hemolytic uremic syndrome 57 T1c 57 Acute lymphoblastic leukemia 57 pT2 57 chlamydial infections 57 alcoholic fatty liver 57 juvenile idiopathic arthritis 57 papillary thyroid carcinoma 57 somatization 57 completely resected 57 Celiac sprue 57 dysthymia 57 highly heritable 57 #q#.# [002] 57 autoantibodies 57 recurrent DVT 57 pyelonephritis 57 endometrial carcinoma 57 Irritable bowel syndrome IBS 57 Fanconi syndrome 57 kidney allograft 57 psychiatric outpatients 57 susceptibility genes 57 Irritable bowel syndrome 57 arterial thickening 57 Arrhythmogenic 57 capillary leak 57 systemic scleroderma 57 hallux valgus 57 Hypertrophic 57 abnormal lipid 57 grade cervical intraepithelial 57 Anaplastic 57 GPC5 57 CYP#C# [002] 57 gene APOE 57 BRAF mutation 57 neuropathological 57 chronic GVHD 57 histologically confirmed 57 Acute Promyelocytic Leukemia 57 premalignant lesions 57 presymptomatic 57 ductal carcinomas 57 gene polymorphisms 57 polymorphic ventricular tachycardia 57 differentially expressed genes 57 Alzheimer Disease AD 57 polycystic ovarian syndrome PCOS 57 TMPRSS2 ERG fusion 57 extrapyramidal symptoms 57 follicular lymphoma FL 57 nonadherence 57 galactosemia 57 childhood leukemias 57 bronchopulmonary dysplasia 57 minimally symptomatic 57 immunocompetent 57 genetic mutations 57 Epstein Barr Virus 57 Ovary removal 57 promoter methylation 57 R#W [002] 57 proliferative retinopathy 57 logistic regression analysis 57 Neurofibromatosis type 57 CA MRSA infections 57 acute aortic dissection 57 p# mutation 57 M. pneumoniae 57 bronchopulmonary dysplasia BPD 57 uveal melanoma 57 anemia hemoglobin 57 MYH9 57 missense 57 schizoaffective disorder bipolar 57 subependymal giant cell 57 APOE allele 57 transcranial Doppler ultrasound 57 invasive ductal breast cancer 57 transthyretin amyloidosis 57 Medulloblastoma 57 activating mutations 57 hippocampal atrophy 57 linkage disequilibrium 57 multivariate analyzes 57 cerebral vasospasm 57 chlamydia infection 57 Genetic variants 57 cholangiocarcinoma 57 Osteosarcoma 57 subclinical disease 57 serotype #A 57 differential gene expression 57 HGPS 57 SNCA 57 telomere lengths 57 Dysregulation 57 CaP 57 epithelial ovarian 57 IL#B 57 fructose intolerance 57 contralateral breast cancer 57 chromosome #q# [002] 57 abnormal uterine bleeding 57 colon tumors 57 abnormal p# 57 HIV seropositive 57 microscopic colitis 57 Squamous 57 Glioma 57 Relapsing remitting MS 57 Autoimmune disorders 57 microRNA expression 57 prothrombotic 57 Mantle Cell Lymphoma 57 pheochromocytoma 57 Klinefelter Syndrome 57 adenomyosis 57 PIK3CA 57 tumoral 57 Joubert syndromes 57 lacunar 57 obstructive coronary 57 #p#.# [001] 57 alveolar rhabdomyosarcoma 57 PsA 57 Shy Drager syndrome 57 asplenia 57 intestinal biopsy 57 G allele 57 G#S mutation 57 fibrous dysplasia 57 unexplained infertility 57 neurodegenerative disorder 57 non syndromic 57 Generalized Anxiety Disorder 57 recurrent UTI 57 Idiopathic pulmonary fibrosis 57 KRAS wild 57 Bronchiectasis 57 immunohistochemical 57 COL#A# 57 chromosome rearrangements 57 EGFR TKIs 57 malignant fibrous histiocytoma 57 idiopathic myelofibrosis 57 Sleep disordered breathing 57 Hyperlipidemia 57 cerebral infarction 57 PTEN gene 57 coinfection 57 thyroid nodules 57 biochemical abnormalities 57 Fanconi anemia 57 ENPP1 57 streptococcal infections 57 Polycystic Ovary Syndrome 57 precancer 57 hypertrophic cardiomyopathy HCM 57 cardiomyopathies 57 bacteraemia 57 atherothrombotic 57 hormone receptor negative 57 total thyroidectomy 57 subsyndromal 57 HER2 expression 57 ADRB2 57 T1D 57 VTEs 57 Von Hippel Lindau 57 variant alleles 57 relapsed ALL 57 MC1R 57 Loeys Dietz syndrome 57 thromboembolism 57 SNP rs# [002] 57 squamous 57 apolipoprotein E 57 hypovitaminosis D 57 HRCT 57 allelic 57 Major depressive disorder 57 nodal metastases 57 Acute Myeloid Leukaemia AML 57 puerperal psychosis 57 HeFH 57 juvenile idiopathic arthritis JIA 57 mutant allele 57 primary ovarian insufficiency 57 neovascular AMD 57 invasive aspergillosis 57 cervical intraepithelial neoplasia 57 mutated gene 57 noncarriers 57 chronic rhinosinusitis CRS 57 LHRH receptor positive 57 Hepatocellular Carcinoma HCC 57 autosomal 57 pseudotumor cerebri 57 Menopausal hormone therapy 57 diagnosed prenatally 57 Polymorphic Ventricular Tachycardia CPVT 57 BRCA testing 57 breast carcinoma 57 chronic renal insufficiency 57 leukemia ALL 57 inbred strains 57 ovarian breast 57 colorectal cancers 57 NR#A# 57 Morquio 57 noncardiac 57 susceptibility locus 57 prenatally diagnosed 57 mutated genes 57 hepatitis B infection 57 serologic testing 57 lichen planus 57 Polymorphisms 57 Hereditary angioedema HAE 57 CTEPH 57 genetic polymorphism 57 unmeasured confounders 57 etiologic agent 57 bacterial vaginosis BV 57 gene MECP2 57 HIVAN 57 operable breast cancer 57 gastrointestinal stromal tumors GISTs 57 gastrointestinal cancers 57 thyrotropin levels 57 ovarian endometrial 57 DRD2 57 colorectal carcinomas 57 JAK2 gene 57 histocompatibility 57 primary ciliary dyskinesia 57 ETV1 57 Severe Asthma 56 Loeys Dietz 56 genotypic resistance 56 comorbid depression 56 BRCA genes 56 Subtypes 56 leukemia AML 56 transferrin saturation 56 esophageal adenocarcinoma 56 clinicopathological features 56 LEOPARD syndrome 56 metabolic dysfunction 56 CNVs 56 BRAF mutations 56 metastatic prostate 56 underwent radical prostatectomy 56 CHD7 56 cryptogenic 56 neurogenic 56 myopathies 56 postoperative pulmonary 56 androgenic alopecia 56 bacterial prostatitis 56 streptococcal 56 arterial calcification 56 lymphovascular invasion 56 splice junctions 56 lipid abnormalities 56 univariate 56 neuropathies 56 BCR ABL mutations 56 functional gastrointestinal disorders 56 LMNA 56 cortical dysplasia 56 intraventricular hemorrhage 56 aortic atherosclerosis 56 BRIP1 56 liver metastasis 56 Beta thalassemia 56 Framingham Offspring 56 metastatic lung cancer 56 GIST tumors 56 myelogenous leukemia 56 CYP#A# gene 56 Fatty Liver Disease 56 thyroglobulin 56 Multiple logistic regression