Teare MD

Latest

BIOlogical Factors that Limit sustAined Remission in rhEumatoid arthritis (the BIO-FLARE study): Protocol for a non-randomised longitudinal cohort study
Enhancing Social-Emotional outcomes in Early years (E-SEE): Randomized pilot study of incredible years infant and toddler programs
A reply to 'Lung cancer outcomes: Are BMI and race clinically relevant?'
The relationship between body-mass index and overall survival in non-small cell lung cancer by sex, smoking status, and race: A pooled analysis of 20,937 International lung Cancer consortium (ILCCO) patients
Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility
The role of personality functioning in drug misuse treatment engagement
PP14 Soiled airway tracheal intubation and the effectiveness of decontamination (SATIATED) by paramedics: A randomised controlled manikin study
Body mass index (BMI), BMI change, and overall survival in patients with SCLC and NSCLC: A pooled analysis of the International Lung Cancer Consortium
Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci
1 Soiled airway tracheal intubation and the effectiveness of decontamination (SATIATED) by paramedics: A randomised controlled manikin study
Lung cancer risk in never-smokers of European descent is associated With genetic variation in the 5p15.33 TERT-CLPTM1Ll region
Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development
Statistical design and analysis in trials of proportionate interventions: A systematic review
Shared heritability and functional enrichment across six solid cancers
Appropriate statistical methods for analysing partially nested randomised controlled trials with continuous outcomes: A simulation study
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity
Clinical and cost-effectiveness of one-session treatment (OST) versus multisession cognitive-behavioural therapy (CBT) for specific phobias in children: Protocol for a non-inferiority randomised controlled trial
Genetic modifiers of radon-induced lung cancer risk: A genome-wide interaction study in former uranium miners
Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers
Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population
Unit of analysis issues in laboratory-based research
Pleiotropy of genetic variants on obesity and smoking phenotypes: Results from the Oncoarray Project of The International Lung Cancer Consortium
Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study
AHEAD Study: An observational study of the management of anticoagulated patients who suffer head injury
Should all anticoagulated patients with head injury receive a CT scan? Decision-analysis modelling of an observational cohort
Pronounced increase in risk of acute ST-segment elevation myocardial infarction in younger smokers
A candidate gene association study of bone mineral density in an Iranian population
Genetic risk can be decreased: Quitting smoking decreases and delays lung cancer for smokers with high and low CHRNA5 risk genotypes — A meta-analysis
Risk prediction models for lung cancer: A systematic review
The Recognition of STEMI by Paramedics and the Effect of Computer inTerpretation (RESPECT): A randomised crossover feasibility study
Airway clearance techniques used by people with cystic fibrosis in the UK
Associated links among smoking, chronic obstructive pulmonary disease, and small cell lung cancer: A pooled analysis in the International Lung Cancer Consortium
RIPOSTE: A framework for improving the design and analysis of laboratory-based research
Cannabis smoking and lung cancer risk: Pooled analysis in the International Lung Cancer Consortium
Comparison of Nottingham Prognostic Index and Adjuvant Online prognostic tools in young women with breast cancer: Review of a single-institution experience
Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing
Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomised controlled trials
Exploration of the impact of ‘mild phenotypes' on median age at death in the U.K. CF registry
AB0019 A PLS multivariate model to predict RA radiological severity by selecting key predictors from a large panel of SNPS and environmental factors
Circulating cell-free DNA: A potential biomarker in lung cancer
Metaanalysis of the association of smoking and PTPN22 R620W genotype on autoantibody status and radiological erosions in rheumatoid arthritis
Allele-dose association of the C5orf30 rs26232 variant with joint damage in rheumatoid arthritis
The angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian patients with vitiligo: A case–control study and meta-analysis
Increased risk of lung cancer in individuals with a family history of the disease: A pooled analysis from the International Lung Cancer Consortium
Strategies to increase influenza vaccination rates: Outcomes of a nationwide cross-sectional survey of UK general practice
Comparing methods for mapping cis acting polymorphisms using allelic expression ratios
Optimizing the yield and utility of circulating cell-free DNA from plasma and serum
A Bayesian approach to copy-number–polymorphism analysis in nuclear pedigrees
Genomic tests: Unreliable for cancer? A focus on circulating DNA and lung cancer
An expectation-maximization algorithm for the analysis of allelic expression imbalance
Genetic linkage studies
Association of a common variant of the CASP8 gene with reduced risk of breast cancer
Heterozygote excess is repeatedly observed in females at the BRCA2 locus N372H
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13
Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21
Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14
The extent of linkage disequilibrium in four populations with distinct demographic histories
No evidence of germline PTEN mutations in familial prostate cancer
A systematic review of genetic polymorphisms and breast cancer risk
A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: Two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
Analysis of genetic linkage and somatic loss of heterozygosity in affected pairs of first-degree relatives
A genetic register for von Hippel-Lindau disease
An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53
The use of loss of constitutional heterozygosity data to ascertain the location of predisposing genes in cancer families
Cancer incidence in the families of children with Ewing's tumor
Cancer in the families of children with soft tissue sarcoma
Identification of factors associated with high breast cancer risk in the mothers of children with soft tissue sarcoma
The inter-regional epidemiological study of childhood cancer (IRESCC): Case-control study of children with central nervous system tumours
Are germ cell tumors part of the Li-Fraumeni cancer family syndrome?
The inter-regional epidemiological study of childhood cancer (IRESCC): Past medical history in children with cancer