scholarly article | Q13442814 |
P50 | author | Carlos Caldas | Q9696930 |
Leslie Bernstein | Q60607806 | ||
Paul D P Pharoah | Q61822938 | ||
Xinxue Liu | Q64481663 | ||
Nicholas J. Shaheen | Q64749672 | ||
Anna H Wu | Q89864403 | ||
Harvey A. Risch | Q97531829 | ||
Marilie Gammon | Q104751082 | ||
Douglas A. Corley | Q110251065 | ||
Olof Nyrén | Q114237293 | ||
Stephen Chanock | Q27662321 | ||
David C. Whiteman | Q37837275 | ||
Stuart Macgregor | Q42711014 | ||
Geoffrey Liu | Q51134597 | ||
P2093 | author name string | Thomas L. Vaughan | |
Rui Zhang | |||
Rebecca C. Fitzgerald | |||
Wong-Ho Chow | |||
Weimin Ye | |||
Nicholas K. Hayward | |||
Patricia Harrington | |||
Lynn Onstad | |||
Irene Debiram-Beecham | |||
Pierre Lao-Sirieix | |||
Yvonne Romero | |||
David M. Levine | |||
Brian J. Reid | |||
Alan G. Casson | |||
Cassandra Sather | |||
Isabel Caldas | |||
Laura J. Hardie | |||
Liam J. Murray | |||
Nigel C. Bird | |||
Weronica E. Ek | |||
P2860 | cites work | An integrated encyclopedia of DNA elements in the human genome | Q22122150 |
A family history of Barrett's oesophagus: Another risk factor? | Q58104647 | ||
Functional single-nucleotide polymorphism of epidermal growth factor is associated with the development of Barrett's esophagus and esophageal adenocarcinoma | Q58376620 | ||
Familial Barrett's esophagus associated with adenocarcinoma | Q68079125 | ||
Carcinoma arising in familial Barrett's esophagus | Q71500732 | ||
Familial aggregation of gastroesophageal reflux in patients with Barrett's esophagus and esophageal adenocarcinoma | Q73835483 | ||
Familial clustering of reflux symptoms | Q77424138 | ||
Identification of Barrett's esophagus in relatives by endoscopic screening | Q81036244 | ||
Familial Barrett's adenocarcinoma | Q82853387 | ||
Familial gastroesophageal reflux and development of Barrett's esophagus | Q93566136 | ||
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes | Q24635938 | ||
Genes mirror geography within Europe | Q24644872 | ||
PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
Foxp2 and Foxp1 cooperatively regulate lung and esophagus development | Q28508512 | ||
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. | Q29417009 | ||
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma | Q29417131 | ||
METAL: fast and efficient meta-analysis of genomewide association scans | Q29547217 | ||
Transcriptome genetics using second generation sequencing in a Caucasian population | Q29614413 | ||
Annotation of functional variation in personal genomes using RegulomeDB | Q29614867 | ||
The Creb1 coactivator Crtc1 is required for energy balance and fertility | Q30439853 | ||
Quality control and quality assurance in genotypic data for genome-wide association studies | Q30498925 | ||
A high-performance computing toolset for relatedness and principal component analysis of SNP data | Q30573123 | ||
Barx1-mediated inhibition of Wnt signaling in the mouse thoracic foregut controls tracheo-esophageal septation and epithelial differentiation | Q31028060 | ||
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies | Q34151528 | ||
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus | Q34298428 | ||
GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies | Q34439401 | ||
Iodine in evolution of salivary glands and in oral health | Q35008249 | ||
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping | Q35012994 | ||
High frequency of PIK3R1 and PIK3R2 mutations in endometrial cancer elucidates a novel mechanism for regulation of PTEN protein stability | Q35275603 | ||
p85β phosphoinositide 3-kinase subunit regulates tumor progression | Q36094306 | ||
Complex diseases in gastroenterology and hepatology: GERD, Barrett's, and esophageal adenocarcinoma | Q36160959 | ||
FOXP1: a potential therapeutic target in cancer. | Q36871999 | ||
A functional epidermal growth factor (EGF) polymorphism, EGF serum levels, and esophageal adenocarcinoma risk and outcome | Q36948334 | ||
Altered LKB1/CREB-regulated transcription co-activator (CRTC) signaling axis promotes esophageal cancer cell migration and invasion. | Q39517661 | ||
Expression of epidermal growth factor, transforming growth factor alpha and their receptor in gastro-oesophageal diseases | Q40881497 | ||
Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk | Q44265917 | ||
P4510 | describes a project that uses | genome-wide association study | Q1098876 |
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | adenocarcinoma | Q356033 |
Barrett's esophagus | Q808892 | ||
genome-wide association study | Q1098876 | ||
susceptibility locus | Q62091149 | ||
P304 | page(s) | 1487–1493 | |
P577 | publication date | 2013-12-01 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus | |
P478 | volume | 45 |
Q34744122 | A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis |
Q39531221 | A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population |
Q36753025 | A newly identified susceptibility locus near FOXP1 modifies the association of gastroesophageal reflux with Barrett's esophagus |
Q38368081 | A review of the epidemiology of Barrett's oesophagus and oesophageal adenocarcinoma |
Q40365358 | ACG Clinical Guideline: Diagnosis and Management of Barrett's Esophagus |
Q91517636 | Adaptive Transcriptional Responses by CRTC Coactivators in Cancer |
Q50209263 | An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk. |
Q36551207 | Analyzing the Association of Polymorphisms in the CRYBB2 Gene with Prostate Cancer Risk in African Americans |
Q36029469 | Assessment of Esophageal Adenocarcinoma Risk Using Somatic Chromosome Alterations in Longitudinal Samples in Barrett's Esophagus |
Q41652261 | Association Between Germline Mutation in VSIG10L and Familial Barrett Neoplasia |
Q54232649 | Barrett's Esophagus and Esophageal Adenocarcinoma: How Common Are They Really? |
Q33959620 | Barrett's esophagus and cancer risk: how research advances can impact clinical practice |
Q38363283 | Barrett's esophagus: recent insights into pathogenesis and cellular ontogeny. |
Q38575013 | Biomarkers and novel agents in esophago-gastric cancer: are we making progress? |
Q38213141 | Biomarkers for dysplastic Barrett's: ready for prime time? |
Q88528269 | Biomarkers of Barrett's Esophagus: From the Laboratory to Clinical Practice |
Q91891617 | Centromeric Satellite DNAs: Hidden Sequence Variation in the Human Population |
Q36551285 | Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagus |
Q38940534 | Common Variants Confer Susceptibility to Barrett's Esophagus: Insights from the First Genome-Wide Association Studies |
Q35144975 | Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice |
Q38815316 | Computation of ancestry scores with mixed families and unrelated individuals |
Q37153044 | Constrained Score Statistics Identify Genetic Variants Interacting with Multiple Risk Factors in Barrett's Esophagus |
Q37536975 | Convergent evidence from systematic analysis of GWAS revealed genetic basis of esophageal cancer |
Q55007510 | Correlation between prostate stem cell antigen gene expression and oral squamous cell carcinoma. |
Q64118172 | Cumulative evidence for association between genetic polymorphisms and esophageal cancer susceptibility: A review with evidence from meta-analysis and genome-wide association studies |
Q91474078 | DNA methylation changes in infants between 6 and 52 weeks |
Q39212995 | Deregulation of CRTCs in Aging and Age-Related Disease Risk |
Q89896747 | Detection of LINE-1 hypomethylation in cfDNA of Esophageal Adenocarcinoma Patients |
Q47726498 | Detection of genetic alterations in cfDNA as a possible strategy to monitor the neoplastic progression of Barrett's esophagus |
Q47298550 | Determining Risk of Barrett's Esophagus and Esophageal Adenocarcinoma Based on Epidemiologic Factors and Genetic Variants |
Q38310617 | Diagnostic and Management Implications of Basic Science Advances in Barrett's Esophagus |
Q28079946 | Endoscopic risk factors for neoplastic progression in patients with Barrett's oesophagus |
Q57433696 | Environmentally Induced Alterations in the Epigenome Affecting Obesity and Cancer in Minority Populations |
Q26852690 | Epidemiological studies of esophageal cancer in the era of genome-wide association studies |
Q35893814 | Epidemiology, Diagnosis, and Management of Esophageal Adenocarcinoma |
Q42131289 | Esophageal Cancer: Genomic and Molecular Characterization, Stem Cell Compartment and Clonal Evolution |
Q38734003 | Esophageal Cancer: New Insights into a Heterogenous Disease |
Q26799758 | Esophageal cancer: Risk factors, screening and endoscopic treatment in Western and Eastern countries |
Q38542183 | Esophageal development and epithelial homeostasis |
Q28077495 | Etiology and Prevention of Esophageal Cancer |
Q31028176 | Fitting Proportional Odds Model to Case-Control data with Incorporating Hardy-Weinberg Equilibrium |
Q90133777 | Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases |
Q90701991 | Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in Foxp1 +/- mice |
Q36109030 | Genetic Insights in Barrett's Esophagus and Esophageal Adenocarcinoma |
Q26740556 | Genetic susceptibility to Barrett's oesophagus: Lessons from early studies |
Q47366887 | Genetic variants in miR-196a2 and miR-499 are associated with susceptibility to esophageal squamous cell carcinoma in Chinese Han population |
Q88391279 | Genetic variants of FOXP1 and FOXF1 are associated with the susceptibility of oesophageal adenocarcinoma in Chinese population |
Q34479395 | Genetics and early detection in idiopathic pulmonary fibrosis |
Q34537405 | Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis |
Q38668307 | Genome-wide association studies of cancer in diverse populations |
Q37191879 | Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma |
Q41826361 | Genomic and Epigenetic Complexity of the FOXF1 Locus in 16q24.1: Implications for Development and Disease. |
Q39530717 | Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma |
Q92350925 | Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data |
Q38831897 | In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer. |
Q89845986 | Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP) |
Q34586242 | Integrative post-genome-wide association analysis of CDKN2A and TP53 SNPs and risk of esophageal adenocarcinoma |
Q52649946 | Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. |
Q88132507 | Leaky transporters and sphincters in Barrett's oesophagus? |
Q48529215 | Letter: future directions for epidemiological studies of Barrett's oesophagus |
Q40056604 | Methodological quality evaluation of systematic reviews or meta-analyses on ERCC1 in non-small cell lung cancer: a systematic review |
Q35651285 | MiRNA-Related SNPs and Risk of Esophageal Adenocarcinoma and Barrett's Esophagus: Post Genome-Wide Association Analysis in the BEACON Consortium |
Q35486982 | Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite |
Q34508850 | Molecular markers and imaging tools to identify malignant potential in Barrett's esophagus |
Q64458449 | No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study |
Q34354158 | Obesity and risk of esophageal adenocarcinoma and Barrett's esophagus: a Mendelian randomization study |
Q39205170 | Obesity-associated digestive cancers: A review of mechanisms and interventions |
Q38816897 | Oesophageal adenocarcinoma and gastric cancer: should we mind the gap? |
Q37720195 | Pathway‑based detection of idiopathic pulmonary fibrosis at an early stage |
Q36290025 | Pleiotropic analysis of cancer risk loci on esophageal adenocarcinoma risk |
Q64926353 | Polymorphism of miRNA and esophageal cancer risk: an updated systemic review and meta-analysis. |
Q33361584 | Polymorphisms in Genes of Relevance for Oestrogen and Oxytocin Pathways and Risk of Barrett's Oesophagus and Oesophageal Adenocarcinoma: A Pooled Analysis from the BEACON Consortium |
Q36470039 | Polymorphisms in genes in the androgen pathway and risk of Barrett's esophagus and esophageal adenocarcinoma |
Q35042479 | Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus |
Q91711671 | Polymorphisms of the BARX1 and ADAMTS17 Locus Genes in Individuals With Gastroesophageal Reflux Disease |
Q47901698 | Polymorphisms of the FOXF1 and MHC locus genes in individuals undergoing esophageal acid reflux assessments |
Q38857539 | Precancer Atlas to Drive Precision Prevention Trials. |
Q35243217 | Precision prevention of oesophageal adenocarcinoma |
Q46923415 | Prognostic impact of FOXF1 polymorphisms in gastric cancer patients |
Q40083252 | Racial Disparity in Gastrointestinal Cancer Risk |
Q26864783 | Recent developments in pathogenesis, diagnosis and therapy of Barrett's esophagus |
Q28076807 | Risk Factors for Barrett's Oesophagus |
Q40879184 | Risk factors for Barrett's esophagus |
Q34036491 | Risk of esophageal adenocarcinoma decreases with height, based on consortium analysis and confirmed by Mendelian randomization |
Q34736608 | Role of LKB1-CRTC1 on glycosylated COX-2 and response to COX-2 inhibition in lung cancer. |
Q28080445 | Screening for Barrett's Esophagus |
Q41660792 | Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma |
Q51048878 | Strategy for prevention of cancers of the esophagus. |
Q36358569 | Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma |
Q36895095 | The Barrett-associated variants at GDF7 and TBX5 also increase esophageal adenocarcinoma risk |
Q39440077 | The Evolving Genomic Landscape of Barrett's Esophagus and Esophageal Adenocarcinoma |
Q38771931 | The Genetics of Barrett's Esophagus: A Familial and Population-Based Perspective |
Q35815874 | The Role of Gastroesophageal Reflux and Other Factors during Progression to Esophageal Adenocarcinoma |
Q37227732 | The characterization of an intestine-like genomic signature maintained during Barrett's-associated adenocarcinogenesis reveals an NR5A2-mediated promotion of cancer cell survival. |
Q54318784 | Translational research on Barrett's esophagus. |
Q33714435 | Trends in esophageal and esophagogastric junction cancer research from 2007 to 2016: A bibliometric analysis |
Q39836449 | Variants of EVER1 and EVER2 (TMC6 and TMC8) and human papillomavirus status in patients with mucosal squamous cell carcinoma of the head and neck |
Q28602015 | ZYG11A serves as an oncogene in non-small cell lung cancer and influences CCNE1 expression |
Search more.