Related by context. All words. (Click for frequent words.) 73 probands 69 familial aggregation 68 allele frequencies 68 CC genotype 68 #q# deletion syndrome 68 mutant allele 68 C#Y 67 nonpsychotic 67 HNPCC 67 homozygosity 67 genes predisposing 67 #q# [001] 67 CDH1 66 IgA deficiency 66 heterozygous 66 monozygotic 66 PTPN# 66 heterozygotes 66 multivariate analyzes 66 apolipoprotein E 66 TT genotype 66 rs# [004] 66 multivariable analysis 66 microdeletion 66 ApoE gene 65 T1DM 65 APOE e4 65 APOE genotype 65 monozygotic twins 65 UGT#A# * 65 autosomal recessive 65 MYH9 gene 65 #q#.# deletion syndrome 65 CDKN2A 65 rs# [003] 65 recessive inheritance 65 Multivariate analysis 65 autosomal dominant 65 C#BL/#J 65 homozygotes 65 APOE gene 65 seropositivity 65 apolipoprotein E gene 65 chromosome #q#.# [001] 65 multivariate Cox 64 #p#.# [002] 64 GH deficiency 64 autosomal recessive disease 64 rs# [001] 64 inherited mutations 64 hypogonadotropic hypogonadism 64 DRD2 64 Li Fraumeni syndrome 64 ABCB1 64 CHEK2 64 IL#B 64 5 HTTLPR 64 germline mutations 64 #q#.# [001] 64 #q# deletion 64 DRD2 gene 64 advanced neoplasia 64 neurocognitive impairment 64 hyper IgE syndrome 64 MLH1 64 DRD4 64 euthymic patients 64 dopamine transporter gene 64 MTHFR 64 sCJD 64 GBA mutations 64 familial pancreatic cancer 64 thrombophilia 64 missense mutations 64 genomewide 64 logistic regression analysis 64 microsatellite instability 64 SNP rs# [001] 64 microdeletions 63 idiopathic PAH 63 rs# [002] 63 nondemented 63 dizygotic twins 63 chromosome #q# [002] 63 HLA B# 63 genotyped 63 prostate cancer CaP 63 neoplasias 63 chromosomal anomalies 63 univariate analyzes 63 CNTNAP2 63 heterozygote 63 monozygotic twin 63 histological subtype 63 dyads 63 paternally inherited 63 #p# [003] 63 clinico pathological 63 MSH2 63 Haplogroup 63 penetrance 63 PON1 63 IPAH 63 bivariate analyzes 63 HLA DQ2 63 dopamine receptor gene 63 autosomal dominant inheritance 63 VUR 63 APOE ε4 63 hereditary hemochromatosis 63 colorectal neoplasia 63 nonhereditary 63 euthyroid 63 histologic subtype 63 sporadic ALS 62 V Leiden 62 retrospective cohort 62 SNP rs# [002] 62 nondiabetic 62 allelic variants 62 #p#.# [001] 62 R#W [002] 62 variant allele 62 autistic traits 62 heterozygosity 62 MECP2 gene 62 susceptibility gene 62 genetic polymorphisms 62 TCF#L# gene 62 seronegative 62 normal karyotype 62 antiphospholipid antibodies 62 MMSE score 62 Subgroup analysis 62 HIV HCV coinfected 62 BRCA1 BRCA2 62 Univariate analysis 62 APOE4 62 deleterious mutation 62 schizophreniform disorder 62 #p# [001] 62 ADPKD 62 cryptorchidism 62 comorbid anxiety 62 familial adenomatous polyposis FAP 62 mutated K ras 62 autosomal 62 paraganglioma 62 congenital adrenal hyperplasia CAH 62 hepatocellular carcinomas 62 variant rs# 62 syngeneic 62 Hashimoto thyroiditis 62 BRCA2 mutation 62 alexithymia 62 C. trachomatis 62 apolipoprotein E4 62 DAT1 62 CIN2 + 62 #q# [002] 62 MetS 62 mosaicism 62 neuroblastomas 62 G allele 62 T2DM 62 GABRA2 62 de novo mutations 62 psychiatric comorbidities 62 chromosome #q# [001] 62 serum estradiol 62 susceptibility locus 62 habitual snoring 62 CYP#C# * 62 alleles 62 immunocompetent 62 affective psychosis 62 NNRTI resistance 62 confidence interval #.#-#.# 62 chromosomal anomaly 62 monocytic 62 parous women 62 chromosome #p# [001] 62 familial ALS 61 missense mutation 61 ADH1B * 61 neurodevelopmental impairment 61 narcolepsy cataplexy 61 maternally transmitted 61 shorter telomere length 61 univariate analysis 61 TP# mutation 61 Klinefelter syndrome 61 neurological abnormalities 61 polygenic 61 adnexal mass 61 haplotype 61 Heritability 61 familial clustering 61 chromosomal aberrations 61 homozygote 61 genetic loci 61 % CI #.#-#.# [007] 61 univariate 61 HLA DR4 61 multivariate logistic regression 61 genetic variants associated 61 BRAF V#E 61 β thalassemia 61 HBeAg negative 61 depressive symptomatology 61 Homozygous 61 gene polymorphism 61 pheochromocytoma 61 recessive mutations 61 aneuploidies 61 CCR5 delta# 61 testicular germ cell 61 LRRK2 mutation 61 TACI mutations 61 nodal metastasis 61 HNSCC 61 invasive carcinomas 61 SLC#A# [002] 61 % CI #.#-#.# [003] 61 acute leukemias 61 homozygous 61 HLA DRB1 * 61 gene MECP2 61 multiple logistic regression 61 HLA identical 61 Multivariate analyzes 61 Framingham Offspring 61 predisposing factor 61 COMT gene 61 BRCA1 mutations 61 chromosomal defect 61 HBeAg 61 gestational diabetes mellitus 61 nondepressed 61 hypermethylated 61 testicular tumors 61 multivariable analyzes 61 urolithiasis 61 prepubertal 61 enterocolitis 61 BARD1 61 monoclonal gammopathy 61 genetic polymorphism 61 etiologic 61 causative mutation 61 covariate 61 Leydig cell 61 SSc 61 highly heritable 60 MEF2A 60 obstructive coronary artery 60 HLA DRB1 60 LRRK2 mutations 60 metaplasia 60 NRTI resistance 60 Y chromosomal 60 MLL2 60 BRCA2 mutation carriers 60 GSTP1 60 sociodemographic variables 60 chromosome #q 60 isoprostane 60 deletion 5q 60 autosomal dominant disorder 60 logistic regression model 60 APOC3 60 alpha1 antitrypsin deficiency 60 relapsed ALL 60 extramedullary 60 cryptogenic 60 fraternal twin pairs 60 hamartomas 60 astrocytomas 60 Asymptomatic 60 MGUS 60 placental malaria 60 aortic atherosclerosis 60 Apolipoprotein E 60 Genetic variants 60 Fragile X gene 60 tumor histology 60 rheumatoid factor 60 airway hyperresponsiveness 60 diagnosed prenatally 60 BRCA2 carriers 60 seroconverted 60 bronchopulmonary dysplasia 60 Clusterin 60 postoperative delirium 60 vesicoureteral reflux 60 maternally inherited 60 thyrotropin levels 60 NMIBC 60 hamartoma 60 diffuse gastric 60 alpha thalassemia 60 phenotype 60 atrophic gastritis 60 chorioamnionitis 60 atypical hyperplasia 60 hemodynamically significant 60 CYP#C# [002] 60 serum selenium 60 hematological relapse 60 diabetes mellitus DM 60 chronicity 60 epididymitis 60 bivariate analysis 60 HFE gene 60 logistic regression analyzes 60 idiopathic pulmonary arterial hypertension 60 sociodemographic factors 60 premorbid 60 lowest tertile 60 functional polymorphism 60 RRM1 60 BRAF V#E mutation 60 BRCA2 mutations 60 DSM IV diagnosis 60 neuropathologic 60 chromosome #p#.# 60 receptor gene 60 NPM1 gene 60 Leukemias 60 c KIT 60 HER2 expression 60 MYCN amplification 60 KIF6 gene 60 DQB1 * 60 aetiological 60 LQTS 60 juvenile idiopathic arthritis JIA 60 preoperative PSA 60 maternal serum 60 subclinical atherosclerosis 60 VKORC1 60 Hurthle cell 60 chromosomal regions 60 G6PD deficiency 60 HLA DRB1 SE 60 myeloproliferative 60 familial adenomatous polyposis 60 K#R [002] 60 neuritic 60 subclinical hypothyroidism 60 BMI z 60 HIV uninfected 60 overt hypothyroidism 59 autonomic dysfunction 59 glutamic acid decarboxylase 59 chromosome #q#.# [002] 59 HMGA1 59 variant alleles 59 neuropsychiatric disorder 59 CYP#C# gene 59 microscopic colitis 59 atopy 59 autopsied brains 59 Leydig cells 59 clinicopathologic 59 malignant lymphoma 59 paraneoplastic 59 comorbid depression 59 susceptibility loci 59 nulliparous 59 intraepithelial neoplasia 59 familial hypercholesterolemia 59 conditional logistic regression 59 chromosomal disorders 59 autistic regression 59 microcephalin 59 p = .# [002] 59 mitochondrial DNA mtDNA 59 colorectal adenoma 59 PCR RFLP 59 parkinsonism 59 autoimmune thyroid 59 Sjögren syndrome 59 BRCA mutation 59 G#S mutation 59 human leukocyte antigen HLA 59 Chlamydia pneumoniae 59 e4 allele 59 Brugada Syndrome 59 affective disorders 59 SCN1A 59 T1D 59 recurrent acute pancreatitis 59 PCa 59 advanced adenoma 59 TP# mutations 59 adenomatous polyps 59 clinicopathological 59 comorbid disorders 59 atopic 59 preeclamptic 59 KRAS mutations 59 onset diabetes mellitus 59 Hp2 2 59 Immunohistochemical analysis 59 amnestic MCI 59 KRAS oncogene 59 differentially expressed genes 59 K ras mutations 59 noncarriers 59 orthologs 59 endophenotypes 59 APOE4 gene 59 Child Behavior Checklist 59 nondiabetic patients 59 gene locus 59 genotypic resistance 59 HLA A2 59 haplotypes 59 vWD 59 PTEN mutations 59 catechol O methyltransferase 59 dominantly inherited 59 Legg Calvé Perthes disease 59 MAOA gene 59 MRSA isolates 59 SCN5A 59 monogenic 59 affective psychoses 59 Histologic 59 neurosensory 59 dizygotic 59 prostate carcinoma 59 PNET 59 apolipoprotein E APOE 59 LRAT 59 chromosome abnormality 59 Sydenham chorea 59 nonmetastatic 59 cerebral infarction 59 hematopoietic cancers 59 GPC5 59 Polymorphism 59 psychiatric outpatients 59 BRCA1 mutation carriers 59 leiomyomas 59 thyrotropin 59 pT2 59 nonischemic 59 antibody titer 59 allelic variation 59 neoplasm 59 tumorigenicity 59 ABCB1 gene 59 allelic 59 amnestic 59 frameshift mutation 59 AAT deficiency 59 gene APOE 59 clinicopathological features 59 Gestational 59 COL#A# 59 HRCT 59 % CI #.#-#.# [008] 59 smoldering myeloma 59 supratentorial 59 methylation patterns 59 leptin deficiency 59 PPCM 59 ADRB2 59 chromosomal alterations 59 chromosomal rearrangement 59 allele 59 telomere lengths 59 pretransplant 59 serum retinol 59 hyperprolactinemia 59 neurological manifestations 59 genotypic 59 gene polymorphisms 59 ApoE4 59 BCG vaccinated 59 airway responsiveness 59 papillary renal cell carcinoma 59 NF1 59 IL#R 59 ENPP1 58 BMPR2 58 LV dysfunction 58 melanocytic nevi 58 kidney allograft 58 T1c 58 Wiskott Aldrich syndrome 58 inbreeding coefficient 58 congenital disorders 58 Kaplan Meier analysis 58 hyperplastic 58 NSCLC tumors 58 UGT#B# 58 haplogroups 58 karyotype 58 HBsAg 58 KIBRA 58 antenatal depression 58 spontaneous mutation 58 5q 58 Wwox 58 thiopurine 58 SHANK3 58 HER2 overexpression 58 liver histology 58 differential gene expression 58 SIDS infants 58 colorectal carcinoma 58 lymphocytic 58 Suicidal ideation 58 VNTR 58 Genotypic 58 de novo AML 58 cytogenetic abnormalities 58 medulloblastoma tumors 58 coinfection 58 LPA gene 58 adiponectin concentrations 58 poor metabolizers 58 histologically 58 angiographically 58 distinct subtypes 58 progressive neurodegenerative disorder 58 APOE e4 gene 58 Familial Hypercholesterolemia 58 PALB2 58 intima media thickness 58 dysbindin 58 non syndromic 58 gastric carcinomas 58 HBV genotype 58 klotho 58 mtDNA mutations 58 LRRK2 gene 58 HRQL 58 parkinsonian 58 nonobese 58 Sociodemographic 58 intraventricular hemorrhage 58 paragangliomas 58 CNVs 58 behavioral disinhibition 58 GSTT1 58 tertile 58 breast carcinoma 58 GSTM1 gene 58 #q#.# [002] 58 enteroviral 58 invasive ductal 58 HGPIN 58 normal birthweight 58 posttransplant 58 abacavir Ziagen 58 GG genotype 58 pulmonary hypoplasia 58 renal carcinoma 58 BRCA2 gene mutation 58 NAT2 58 Spinal muscular atrophy 58 psychiatric comorbidity 58 T2D 58 Adenomas 58 null mice 58 GSTM1 58 varicocele 58 serum leptin 58 causative mutations 58 gastric adenocarcinoma 58 karyotypes 58 Hutchinson Gilford progeria 58 hereditary predisposition 58 nodal metastases 58 neuroblastoma tumors 58 RhD negative 58 recurrent UTI 58 prognostic factors 58 decompensated cirrhosis 58 acute myeloid 58 ASCUS 58 inhibin 58 arterial thickening 58 immunohistochemical staining 58 serum IGF 58 idiopathic thrombocytopenic purpura 58 von Hippel Lindau 58 neonatal lupus 58 colorectal neoplasms 58 basal cell carcinoma BCC 58 renal cell carcinomas 58 gastric carcinoma 58 microsatellite markers 58 Socioeconomic status 58 dysmorphic features 58 congenital hypothyroidism 58 urothelial carcinoma 58 Meckel Gruber 58 carotid plaques 58 CYP#A# gene 58 thyroglobulin 58 Histological 58 genes differentially expressed 58 differentially regulated 58 nulliparous women 58 germline mutation 58 mutation 58 persistent pulmonary hypertension 58 KIAA# 58 hepatoma 58 HOMA IR 58 GISTs 58 rCBF 58 MYH9 58 % CI #.#-#.# [006] 58 ZNF# 58 ependymoma 58 Lafora disease 58 susceptibility alleles 58 AML MDS 58 recessive genetic 58 ELBW infants 58 SLC#A# [001] 58 Apert syndrome 58 chromosome deletion 58 choriocarcinoma 58 TRAF1 C5 58 lymphocytosis 58 Insulin sensitivity 58 pre eclamptic 58 endometrial thickness 58 elevated ALT 58 herpesviruses 58 independent prognostic marker 58 spontaneous mutations 58 thymoma 58 internalizing disorders 58 medulloblastomas 58 neurocognitive dysfunction 58 transient elastography 58 serum albumin 58 syndromic 58 cerebri 58 #.#ng/ml 58 BRCA mutation carriers 58 serous ovarian cancer 58 CFTR gene 58 subclinical hyperthyroidism 58 Multiple logistic regression 58 C#BL 6 mice 57 biochemical recurrence 57 HGPS 57 cognitively normal 57 ApoE4 gene 57 multivariate adjustment 57 extrapyramidal symptoms 57 Becker muscular dystrophy 57 serum ferritin 57 cerebral microbleeds 57 comorbid ADHD 57 paternal lineage 57 congenital deficiency 57 Arrhythmogenic Right Ventricular Cardiomyopathy 57 Papillary 57 psychosocial functioning 57 SRBD 57 cytopathic 57 recessive mutation 57 CP CPPS 57 surgically resected 57 IKZF1 57 cell adhesion molecule 57 JAK mutations 57 aged ≥ 57 GLUT1 57 â ‰ ¥ 57 IDH1 mutation 57 prostate cancer PCa 57 thyroid carcinoma 57 enteroviral infection 57 mutated BRCA1 57 IL#B gene 57 psychiatric morbidity 57 mRNA expression 57 multivariate analysis 57 Genetic variation 57 gallstone disease 57 breast cancer subtypes 57 basal cell nevus syndrome 57 transfusion syndrome 57 PDGFRA 57 pyloric stenosis 57 latent celiac disease 57 coinfected 57 odds ratios ORs 57 autosomal recessive genetic 57 leiomyoma 57 cerebellar 57 HeFH 57 histologically proven 57 virological response 57 H#K#me# 57 serologically 57 histopathological 57 TGFBR1 * 6A 57 repeat allele 57 distant metastasis 57 thyroid peroxidase 57 chronic eosinophilic leukemia 57 affective disorder 57 breast cancer genes BRCA1 57 covariates 57 colorectal carcinomas 57 syndromal 57 breast carcinomas 57 RET PTC rearrangements 57 lymphoproliferative disorders 57 SLITRK1 57 multivariable adjusted 57 lacunar 57 sociodemographic characteristics 57 pathologic diagnosis 57 Bonferroni correction 57 immunohistochemical 57 ALT flares 57 2 diabetes T2D 57 polymorphism 57 Logistic regression 57 Brugada syndrome 57 promoter polymorphism 57 HbF 57 vesicoureteral reflux VUR 57 unexplained mental retardation 57 lupus anticoagulant 57 meningiomas 57 TOP2A 57 cardioembolic stroke 57 lymphovascular invasion 57 del 5q 57 muscarinic receptor 57 myeloproliferative neoplasms 57 biopsy Gleason 57 pyelonephritis 57 congenital toxoplasmosis 57 enteropathy 57 aminotransferase 57 Genotypes 57 primitive neuroectodermal tumors 57 collagenous colitis 57 WDR# 57 genetic variant 57 multiple linear regression 57 liver metastasis 57 cranial irradiation 57 Myocardial infarction 57 causative gene 57 unfavorable prognostic 57 transaminase elevations 57 metabolizer 57 International Prognostic Scoring 57 atypical hemolytic uremic syndrome 57 histologic findings 57 gastrointestinal stromal tumors GISTs 57 Cognitive impairment 57 CagA 57 Univariate 57 BPS IC 57 abnormal lipid 57 prolactin levels 57 perinatally 57 OPRM1 gene 57 grade cervical intraepithelial 57 prostate adenocarcinoma 57 suicide attempters 57 congenital abnormalities 57 cervical lymph nodes 57 dysglycemia 57 neuropsychological impairments 57 carotid IMT 57 p# mutation 57 postoperative complication 57 pilocytic astrocytomas 57 fractional anisotropy 57 BMI ≥ 57 prognostic biomarker 57 subclinical 57 colorectal adenomas 57 immunoglobulin G 57 HLA matched 57 dysgenesis 57 brain lesions 57 CYP#D# genotype 57 GABHS 57 plasma adiponectin 57 ECG abnormalities 57 Squamous 57 APOE epsilon 4 57 operable breast cancer 57 elevated triglyceride levels 57 aneurysmal subarachnoid hemorrhage 57 somatic symptoms 57 BRCA mutations 57 advanced adenomas 57 Poisson regression 57 MMSE scores 57 cause cardiac channelopathies 57 BRCA2 gene 57 hyperkinetic disorder 57 XLHED 57 morphologic 57 biochemical relapse 57 microscopic hematuria 57 apoE4 57 metabolomic profiles 57 dopamine D4 receptor 57 pCR 57 2D 4D ratio 57 K ras mutation 57 alpha1 57 completely resected 57 STK# gene 57 S aureus 57 fetuin 57 confidence intervals CIs 57 N. gonorrhoeae 57 HIV seropositive 57 MC4R gene 57 kDa protein 57 Niemann Pick disease 57 MADRS score 57 comorbidity 57 CYP#B# 57 adenotonsillectomy 57 infarcts 57 SGPT 57 postnatally 57 definite stent thrombosis 57 APOE allele 57 fetal aneuploidy 57 TYMS 57 alpha1 antitrypsin AAT deficiency 57 IUGR 57 Uterine cancer 57 Adjuvant chemotherapy 57 Haptoglobin 57 PCA3 gene 57 MC1R gene 57 CFTR gene mutations 57 underlying pathophysiology 57 chlamydial infection 57 malignant neoplasm 57 cerebellar hypoplasia 57 AUDs 57 comorbid psychiatric disorders 57 immunostaining 57 fronto temporal dementia 57 leukocytosis 57 constitutively expressed 57 allele frequency 57 MYBPC3 56 nasopharyngeal carcinoma 56 histologic 56 MELAS 56 parous 56 SNHL 56 OPRM1 56 CYP#A# [002] 56 TMPRSS2 ERG fusion 56 ApoE4 allele 56 hMPV 56 UGT#A# 56 methylenetetrahydrofolate reductase 56 HBeAg positive 56 cytologic 56 underwent CABG 56 hippocampal volume 56 IDDM 56 parasitaemia 56 genetic syndromes 56 D#N 56 ovarian carcinoma 56 Upregulation 56 gestational diabetes mellitus GDM 56 microglial 56 DNA methylation patterns 56 T1a 56 subependymal giant cell 56 tumoral 56 proximal colon 56 HLA B 56 sonographic findings 56 intestinal metaplasia 56 femoral neck BMD 56 normotensive 56 genetic relatedness 56 serum urate levels 56 interobserver reliability 56 K#N 56 highest tertile 56 CDK4 56 Subgroup analyzes 56 subscale scores 56 FTLD 56 CYP#D# gene 56 laterality 56 ataxias 56 SE alleles 56 ischemic lesions 56 choroidal neovascularization 56 systemic lupus erythematosus SLE 56 systemic amyloidosis 56 VLBW infants 56 atopic asthma 56 PsA 56 HIV seronegative 56 TEAEs 56 bronchoalveolar 56 metabolizing enzyme 56 NPM1 mutations 56 chromosome #p# [002] 56 radiographic findings 56 anal intraepithelial neoplasia 56 neurodevelopmental disorder 56 klotho gene 56 CYP#C# [001] 56 PDGFR 56 Wistar rats 56 autosomal recessive disorder 56 venous thrombosis 56 Depressive symptoms 56 childhood acute lymphoblastic 56 Logistic regression analysis 56 alveolar epithelial cells 56 etiologic factors 56 Breslow thickness 56 leukemia ALL 56 humoral responses 56 relapsed MM 56 essential thrombocythemia 56 gene APOE4 56 Haplotype 56 cTnI 56 FXTAS 56 histopathologic 56 NR#A# 56 CFH gene 56 coronary stenosis 56 posterior cingulate 56 NAFLD 56 CHEK2 gene 56 chronic myeloid 56 leukemia AML 56 subsyndromal 56 Acute Myeloid Leukaemia AML 56 schizotypal traits 56 hydrops 56 RhD 56 EoE 56 prognostic markers 56 thrombocytopenic 56 ectodermal dysplasia 56 undescended testes 56 PIGF 56 KCNH2 56 superior mesenteric artery 56 extracapsular extension 56 infantile onset 56 aminotransferase levels 56 C#T [002] 56 gene BRCA2 56 lupus erythematosus 56 hydronephrosis 56 hepatorenal syndrome 56 hypercalciuria 56 mild cognitive impairments 56 MC1R 56 CSF biomarkers 56 somatic mutations 56 haemochromatosis 56 enamel defects 56 quetiapine Seroquel 56 FEV ^ sub 56 primary aldosteronism 56 D. melanogaster 56 rebleeding 56 idiopathic membranous nephropathy 56 nongenetic 56 haplogroup 56 bronchoalveolar lavage 56 T#I [002] 56 myocardial infarctions MI 56 nonfatal MI 56 Heterozygous 56 genotype 56 neurodevelopmental outcome